-
1
-
-
0026806887
-
Two new alleles in the tetranucleotide repeat polymorphism at the lipoprotein lipase (LPL) locus
-
Ahn, Y. I., Kamboh, M. I. and Ferrell, R. E. (1992) Two new alleles in the tetranucleotide repeat polymorphism at the lipoprotein lipase (LPL) locus. Hum. Genet. 90: 184.
-
(1992)
Hum. Genet.
, vol.90
, pp. 184
-
-
Ahn, Y.I.1
Kamboh, M.I.2
Ferrell, R.E.3
-
2
-
-
0027439342
-
Association of lipoprotein lipase gene variation with the physiological components of the insulin-resistance syndrome in the population of the San Luis Valley, Colorado
-
Ahn, Y. I., Ferrell, R. E., Hamman, R. F. and Kamboh, M. I. (1993a) Association of lipoprotein lipase gene variation with the physiological components of the insulin-resistance syndrome in the population of the San Luis Valley, Colorado. Diabetes Care 16: 1502-1506.
-
(1993)
Diabetes Care
, vol.16
, pp. 1502-1506
-
-
Ahn, Y.I.1
Ferrell, R.E.2
Hamman, R.F.3
Kamboh, M.I.4
-
3
-
-
0027406054
-
Two DNA polymorphisms in the lipoprotein lipase gene and their associations with factors related to cardiovascular disease
-
Ahn, Y. I., Kamboh, M. I., Hamman, R. F., Cole, S. A. and Ferrell, R. E. (1993b) Two DNA polymorphisms in the lipoprotein lipase gene and their associations with factors related to cardiovascular disease. J. Lipid Res. 34: 421-428.
-
(1993)
J. Lipid Res.
, vol.34
, pp. 421-428
-
-
Ahn, Y.I.1
Kamboh, M.I.2
Hamman, R.F.3
Cole, S.A.4
Ferrell, R.E.5
-
4
-
-
0012050333
-
Apoprotein E simulates non receptor triglyceride-rich particle cellular uptake
-
Al-Haideri, M., Granot, E., Schwiegelshoh, B., Vogel, T., Gorecki, M., Goldberg, I. J. and Deckelbaum, R. J. (1993) Apoprotein E simulates non receptor triglyceride-rich particle cellular uptake. Circulation 88: 1-321.
-
(1993)
Circulation
, vol.88
, pp. 1-321
-
-
Al-Haideri, M.1
Granot, E.2
Schwiegelshoh, B.3
Vogel, T.4
Gorecki, M.5
Goldberg, I.J.6
Deckelbaum, R.J.7
-
5
-
-
0025214976
-
Isolation and characterization of the human hepatic lipase gene
-
Ameis, D., Stahnke, G., Kobayashi, J., McLean, J., Lee, G., Buscher, M., Schotz, M. C. and Will, H. (1990) Isolation and characterization of the human hepatic lipase gene. J. Biol. Chem. 265: 6552-6555.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 6552-6555
-
-
Ameis, D.1
Stahnke, G.2
Kobayashi, J.3
McLean, J.4
Lee, G.5
Buscher, M.6
Schotz, M.C.7
Will, H.8
-
6
-
-
0025811179
-
Familial chylomicronemia (type I hyperlipoproteinemia) due to a single missense mutation in the lipoprotein lipase gene
-
Ameis, D., Kobayashi, J., Davis, R. C., Ben Zeev, O., Malloy, M. J., Kane, J. P., Lee, G., Wong, H., Havel, R. J. and Schotz, M. C. (1991) Familial chylomicronemia (type I hyperlipoproteinemia) due to a single missense mutation in the lipoprotein lipase gene. J. Clin. Invest. 87: 1165-1170.
-
(1991)
J. Clin. Invest.
, vol.87
, pp. 1165-1170
-
-
Ameis, D.1
Kobayashi, J.2
Davis, R.C.3
Ben Zeev, O.4
Malloy, M.J.5
Kane, J.P.6
Lee, G.7
Wong, H.8
Havel, R.J.9
Schotz, M.C.10
-
7
-
-
0012019086
-
A de novo mutation in the lipoprotein lipase (LPL) gene causing LPL deficiency
-
Appelman, E. E. G., Bijvoet, S. M., Wiebusch, H., Ma, Y., Reymer, P. W., Bruin, T., Hayden, M. R. and Castelein, J. J. (1994) A de novo mutation in the lipoprotein lipase (LPL) gene causing LPL deficiency. Atherosclerosis 109: 63.
-
(1994)
Atherosclerosis
, vol.109
, pp. 63
-
-
Appelman, E.E.G.1
Bijvoet, S.M.2
Wiebusch, H.3
Ma, Y.4
Reymer, P.W.5
Bruin, T.6
Hayden, M.R.7
Castelein, J.J.8
-
8
-
-
0025268647
-
Coexistence of abnormalities of hepatic lipase and lipoprotein lipase in a large family
-
Auwerx, J. H., Babirak, S. P., Hokanson, J. E., Stahnke, G., Will, H., Deeb, S. S. and Brunzell, J. D. (1990) Coexistence of abnormalities of hepatic lipase and lipoprotein lipase in a large family. Am. J. Hum. Genet. 46: 470-477.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 470-477
-
-
Auwerx, J.H.1
Babirak, S.P.2
Hokanson, J.E.3
Stahnke, G.4
Will, H.5
Deeb, S.S.6
Brunzell, J.D.7
-
9
-
-
0027099736
-
Lipoprotein lipase: Recent contributions from molecular biology
-
Auwerx, J., Leroy, P. and Schoonjans, K. (1992) Lipoprotein lipase: recent contributions from molecular biology. Crit. Rev. Clin. Lab. Sci. 29: 243-268.
-
(1992)
Crit. Rev. Clin. Lab. Sci.
, vol.29
, pp. 243-268
-
-
Auwerx, J.1
Leroy, P.2
Schoonjans, K.3
-
10
-
-
0024383955
-
Detection and characterization of the heterozygote state for lipoprotein lipase deficiency
-
Babirak, S. P., Iverius, P. H., Fujimoto, W. Y. and Brunzell, J. D. (1989) Detection and characterization of the heterozygote state for lipoprotein lipase deficiency. Arteriosclerosis 9: 326-334.
-
(1989)
Arteriosclerosis
, vol.9
, pp. 326-334
-
-
Babirak, S.P.1
Iverius, P.H.2
Fujimoto, W.Y.3
Brunzell, J.D.4
-
11
-
-
0026731011
-
Familial combined hyperlipidemia and abnormal lipoprotein lipase
-
Babirak, S. P., Brown, B. G. Brunzell, J. D. (1992) Familial combined hyperlipidemia and abnormal lipoprotein lipase. Arterioscler. Thromb. 12: 1176-1183.
-
(1992)
Arterioscler. Thromb.
, vol.12
, pp. 1176-1183
-
-
Babirak, S.P.1
Brown, B.G.2
Brunzell, J.D.3
-
12
-
-
0014706551
-
Steroid-induced lipemia. A complication of high-dosage corticosteroid therapy
-
Bagdade, J. D., Porte, D. J. Bierman, E. L. (1970) Steroid-induced lipemia. A complication of high-dosage corticosteroid therapy. Arch. Intern. Med. 125: 129-134.
-
(1970)
Arch. Intern. Med.
, vol.125
, pp. 129-134
-
-
Bagdade, J.D.1
Porte, D.J.2
Bierman, E.L.3
-
13
-
-
0025195637
-
Lipoprotein lipase bethesda: A single amino acid substitution (Ala176→Thr) leads to abnormal heparin binding and loss of enzymic activity
-
Beg, O. U., Meng, M. S., Skarlatos, S. I., Previato, L., Brunzell, J. D., Brewer, H. B., Jr. Fojo, S. S. (1990) Lipoprotein lipase Bethesda: a single amino acid substitution (Ala176→Thr) leads to abnormal heparin binding and loss of enzymic activity. Proc. Natl. Acad. Sci. USA 87: 3474-3478.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 3474-3478
-
-
Beg, O.U.1
Meng, M.S.2
Skarlatos, S.I.3
Previato, L.4
Brunzell, J.D.5
Brewer H.B., Jr.6
Fojo, S.S.7
-
14
-
-
0029027459
-
Receptors for triglyceride-rich lipoproteins and their role in lipoprotein metabolism
-
Beisiegel, U. (1995) Receptors for triglyceride-rich lipoproteins and their role in lipoprotein metabolism. Curr. Opin. Lipidol. 6: 117-122.
-
(1995)
Curr. Opin. Lipidol.
, vol.6
, pp. 117-122
-
-
Beisiegel, U.1
-
15
-
-
0028172032
-
The role of alpha 2M receptor/LRP in chylomicron remnant metabolism
-
Beisiegel, U., Krapp, A., Weber, W. Olivecrona, G. (1994) The role of alpha 2M receptor/LRP in chylomicron remnant metabolism. Ann. NY Acad. Sci. 737: 53-69.
-
(1994)
Ann. NY Acad. Sci.
, vol.737
, pp. 53-69
-
-
Beisiegel, U.1
Krapp, A.2
Weber, W.3
Olivecrona, G.4
-
16
-
-
0017758836
-
Interaction of lipoprotein lipase with heparin-Sepharose. Evaluation of conditions for affinity binding
-
Bengtsson, G. Olivecrona, T. (1977) Interaction of lipoprotein lipase with heparin-Sepharose. Evaluation of conditions for affinity binding. Biochem. J. 167: 109-119.
-
(1977)
Biochem. J.
, vol.167
, pp. 109-119
-
-
Bengtsson, G.1
Olivecrona, T.2
-
17
-
-
0028835707
-
Homozygous deletion of exon 9 causes lipoprotein lipase deficiency; possible intron-Alu recombination
-
Benlian, P., Étienne, J., de Gennes, J. L., Noé, L., Brault, D., Raisonnier, A., Arnault, F., Hamelin, J., Foubert, L., Chuat, J. C., Tsé, C. Galibert, F. (1995) Homozygous deletion of exon 9 causes lipoprotein lipase deficiency; possible intron-Alu recombination. J. Lipid Res. 36: 356-366.
-
(1995)
J. Lipid Res.
, vol.36
, pp. 356-366
-
-
Benlian, P.1
Étienne, J.2
De Gennes, J.L.3
Noé, L.4
Brault, D.5
Raisonnier, A.6
Arnault, F.7
Hamelin, J.8
Foubert, L.9
Chuat, J.C.10
Tsé, C.11
Galibert, F.12
-
18
-
-
0025908609
-
Lipoprotein lipase
-
Bensadoun, A. (1991) Lipoprotein lipase. Annu. Rev. Nutr. 11: 217-237.
-
(1991)
Annu. Rev. Nutr.
, vol.11
, pp. 217-237
-
-
Bensadoun, A.1
-
19
-
-
0026697404
-
Maturation of lipoprotein lipase. Expression of full catalytic activity requires glucose trimming but not translocation to the cis-Golgi compartment
-
Ben Zeev, O., Doolittle, M. H., Davis, R. C., Elovson, J. Schotz, M. C. (1992) Maturation of lipoprotein lipase. Expression of full catalytic activity requires glucose trimming but not translocation to the cis-Golgi compartment. J. Biol. Chem. 267: 6219-6227.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 6219-6227
-
-
Ben Zeev, O.1
Doolittle, M.H.2
Davis, R.C.3
Elovson, J.4
Schotz, M.C.5
-
20
-
-
0027931405
-
Lipoprotein lipase and hepatic lipase: The role of asparagine-linked glycosylation in the expression of a functional enzyme
-
Ben Zeev, O., Stahnke, G., Liu, G., Davis, R. C. Doolittle, M. H. (1994) Lipoprotein lipase and hepatic lipase: the role of asparagine-linked glycosylation in the expression of a functional enzyme. J. Lipid Res. 35: 1511-1523.
-
(1994)
J. Lipid Res.
, vol.35
, pp. 1511-1523
-
-
Ben Zeev, O.1
Stahnke, G.2
Liu, G.3
Davis, R.C.4
Doolittle, M.H.5
-
21
-
-
0026341545
-
Expression de la lipoprotein lipase humaine: Mutations et physiopathologie
-
Bergeron, J., Julien, P. Murthy, M. R. V. (1991) Expression de la lipoprotein lipase humaine: mutations et physiopathologie. Med. Sci. 7: 1061-1068.
-
(1991)
Med. Sci.
, vol.7
, pp. 1061-1068
-
-
Bergeron, J.1
Julien, P.2
Murthy, M.R.V.3
-
22
-
-
0026518064
-
Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of Quebec
-
Bergeron, J., Normand, T., Bharucha, A., Murthy, M. R. V., Julien, P., Gagné, C., Dionne, C., De Braekeleer, M., Brun, D., Hayden, M. R. Lupien, P. J. (1992) Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of Quebec. Clin. Genet. 41: 206-210.
-
(1992)
Clin. Genet.
, vol.41
, pp. 206-210
-
-
Bergeron, J.1
Normand, T.2
Bharucha, A.3
Murthy, M.R.V.4
Julien, P.5
Gagné, C.6
Dionne, C.7
De Braekeleer, M.8
Brun, D.9
Hayden, M.R.10
Lupien, P.J.11
-
23
-
-
0027535121
-
Site-directed mutagenesis of a putative heparin binding domain of avian lipoprotein lipase
-
Berryman, D. E. and Bensadoun, A. (1993) Site-directed mutagenesis of a putative heparin binding domain of avian lipoprotein lipase. J. Biol. Chem. 268: 3272-3276.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 3272-3276
-
-
Berryman, D.E.1
Bensadoun, A.2
-
25
-
-
0028140286
-
Homozygosity for a mutation in the lipoprotein lipase gene (Gly139 → Ser) causes chylomicronaemia in a boy of Spanish descent
-
Bijvoet, S. M., Bruin, T., Tuzgol, S., Bakker, H. D., Hayden, M. R. and Kastelein, J. J. (1994) Homozygosity for a mutation in the lipoprotein lipase gene (Gly139 → Ser) causes chylomicronaemia in a boy of Spanish descent. Hum. Genet. 93: 339-343.
-
(1994)
Hum. Genet.
, vol.93
, pp. 339-343
-
-
Bijvoet, S.M.1
Bruin, T.2
Tuzgol, S.3
Bakker, H.D.4
Hayden, M.R.5
Kastelein, J.J.6
-
26
-
-
0027455653
-
Dietary treatment and growth of hyperchylomicronemic children severely restricted in dietary fat
-
Black, D. M. and Sprecher, D. L. (1993) Dietary treatment and growth of hyperchylomicronemic children severely restricted in dietary fat. Am. J. Dis. Child. 147: 60-62.
-
(1993)
Am. J. Dis. Child.
, vol.147
, pp. 60-62
-
-
Black, D.M.1
Sprecher, D.L.2
-
28
-
-
0026478820
-
Sequence of rat lipoprotein lipase-encoding cDNA
-
Brault, D., Noe, L., Etienne, J., Hamelin, J., Raisonnier, A., Souli, A., Chuat, J. C., Dugail, I., Quignard Boulange, A., Lavau, M. and Galibert, F. (1992) Sequence of rat lipoprotein lipase-encoding cDNA. Gene 121: 237-246.
-
(1992)
Gene
, vol.121
, pp. 237-246
-
-
Brault, D.1
Noe, L.2
Etienne, J.3
Hamelin, J.4
Raisonnier, A.5
Souli, A.6
Chuat, J.C.7
Dugail, I.8
Quignard Boulange, A.9
Lavau, M.10
Galibert, F.11
-
29
-
-
0026672309
-
Regulation of the synthesis, processing and translocation of lipoprotein lipase
-
Braun, J. E. and Severson, D. L. (1992) Regulation of the synthesis, processing and translocation of lipoprotein lipase. Biochem. J. 287: 337-347.
-
(1992)
Biochem. J.
, vol.287
, pp. 337-347
-
-
Braun, J.E.1
Severson, D.L.2
-
30
-
-
0023118950
-
Deficiencies of plasma lipolytic activities
-
Breckenridge, W. C. (1987) Deficiencies of plasma lipolytic activities. Am. Heart J. 113: 567-573.
-
(1987)
Am. Heart J.
, vol.113
, pp. 567-573
-
-
Breckenridge, W.C.1
-
31
-
-
0017888564
-
Hypertriglyceridemia associated with deficiency of apolipoprotein C-II
-
Breckenridge, W. C., Little, J. A., Steiner, G., Chow, A. and Poast, M. (1978) Hypertriglyceridemia associated with deficiency of apolipoprotein C-II. N. Engl. J. Med. 298: 1265-1273.
-
(1978)
N. Engl. J. Med.
, vol.298
, pp. 1265-1273
-
-
Breckenridge, W.C.1
Little, J.A.2
Steiner, G.3
Chow, A.4
Poast, M.5
-
32
-
-
0026674914
-
Nijmegen) resulting in loss of catalytic activity
-
Nijmegen) resulting in loss of catalytic activity. Eur. J. Biochem. 208: 267-272.
-
(1992)
Eur. J. Biochem.
, vol.208
, pp. 267-272
-
-
Bruin, T.1
Kastelein, J.J.2
Van Diermen, D.E.3
Ma, Y.4
Henderson, H.E.5
Stuyt, P.M.6
Stalenhoef, A.F.7
Sturk, A.8
Brunzell, J.D.9
Hayden, M.R.10
-
33
-
-
0027136678
-
Recurrent pancreatitis and chylomicronemia in an extended dutch kindred is caused by a Gly154 → Ser substitution in lipoprotein lipase
-
Bruin, T., Tuzgol, S., van Diermen, D. E., Hoogerbrugge van der Linden, N., Brunzell, J. D., Hayden, M. R. and Kastelein, J. J. (1993) Recurrent pancreatitis and chylomicronemia in an extended Dutch kindred is caused by a Gly154 → Ser substitution in lipoprotein lipase. J. Lipid Res. 34: 2109-2119.
-
(1993)
J. Lipid Res.
, vol.34
, pp. 2109-2119
-
-
Bruin, T.1
Tuzgol, S.2
Van Diermen, D.E.3
Hoogerbrugge Van Der Linden, N.4
Brunzell, J.D.5
Hayden, M.R.6
Kastelein, J.J.7
-
34
-
-
0012050228
-
The role of proline residues in the structure and function of lipoprotein lipase
-
Bruin, T., Appelman, E. E., Blanchard, H., Groot, N. B., Kastelein, J. J. P. and Derewenda, Z. S. (1994a) The role of proline residues in the structure and function of lipoprotein lipase. Atherosclerosis 109: 63.
-
(1994)
Atherosclerosis
, vol.109
, pp. 63
-
-
Bruin, T.1
Appelman, E.E.2
Blanchard, H.3
Groot, N.B.4
Kastelein, J.J.P.5
Derewenda, Z.S.6
-
35
-
-
0028214675
-
A compound heterozygote for lipoprotein lipase deficiency, Va169 → Leu and Gly188 → Glu: Correlation between in vitro LPL activity and clinical expression
-
Bruin, T., Tuzgol, S., Mulder, W. J., van den Ende, A. E., Jansen, H., Hayden, M. R. and Kastelein, J. J. (1994b) A compound heterozygote for lipoprotein lipase deficiency, Va169 → Leu and Gly188 → Glu: correlation between in vitro LPL activity and clinical expression. J. Lipid Res. 35: 438-445.
-
(1994)
J. Lipid Res.
, vol.35
, pp. 438-445
-
-
Bruin, T.1
Tuzgol, S.2
Mulder, W.J.3
Van Den Ende, A.E.4
Jansen, H.5
Hayden, M.R.6
Kastelein, J.J.7
-
36
-
-
0022589033
-
Severe lipemia induced by tamoxifen
-
Brun, L. D., Gagné, C., Rousseau, C., Moorjani, S. and Lupien, P. J. (1986) Severe lipemia induced by tamoxifen. Cancer 57: 2123-2126.
-
(1986)
Cancer
, vol.57
, pp. 2123-2126
-
-
Brun, L.D.1
Gagné, C.2
Rousseau, C.3
Moorjani, S.4
Lupien, P.J.5
-
37
-
-
0024347052
-
Familial lipoprotein lipase-activity deficiency: Study of total body fatness and subcutaneous fat tissue distribution
-
Brun, L. D., Gagné, C., Julien, P., Tremblay, A., Moorjani, S., Bouchard, C. and Lupien, P. J. (1989) Familial lipoprotein lipase-activity deficiency: study of total body fatness and subcutaneous fat tissue distribution. Metabolism 38: 1005-1009.
-
(1989)
Metabolism
, vol.38
, pp. 1005-1009
-
-
Brun, L.D.1
Gagné, C.2
Julien, P.3
Tremblay, A.4
Moorjani, S.5
Bouchard, C.6
Lupien, P.J.7
-
38
-
-
0002330773
-
Familial lipoprotein lipase deficiency and other causes of chylomicronemia syndrome
-
Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.) McGraw Hill, New York
-
Brunzell, J. D. (1989) Familial lipoprotein lipase deficiency and other causes of chylomicronemia syndrome. The Metabolic Basis of Inherited Disease, 1165-1180, Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.) McGraw Hill, New York
-
(1989)
The Metabolic Basis of Inherited Disease
, pp. 1165-1180
-
-
Brunzell, J.D.1
-
39
-
-
0001033625
-
Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome
-
Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.) McGraw-Hill Inc, New York
-
Brunzell, J. D. (1995) Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome. The Metabolic and Molecular Basis of Inherited Disease, 1913-1932, Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.) McGraw-Hill Inc, New York
-
(1995)
The Metabolic and Molecular Basis of Inherited Disease
, pp. 1913-1932
-
-
Brunzell, J.D.1
-
40
-
-
0020472056
-
Chylomicronemia syndrome: Interaction of genetic and acquired hypertriglyceridemia
-
Brunzell, J. D. and Bierman, E. L. (1982) Chylomicronemia syndrome: interaction of genetic and acquired hypertriglyceridemia. Med. Clin. North Am. 66: 455-468.
-
(1982)
Med. Clin. North Am.
, vol.66
, pp. 455-468
-
-
Brunzell, J.D.1
Bierman, E.L.2
-
41
-
-
0015783897
-
Evidence for a common, saturable, triglyceride removal mechanism for chylomicrons and very low density lipoproteins in man
-
Brunzell, J. D., Hazzard, W. R., Porte, D. and Bierman, E. L. (1973) Evidence for a common, saturable, triglyceride removal mechanism for chylomicrons and very low density lipoproteins in man. J. Clin. Invest. 52: 1578-1585.
-
(1973)
J. Clin. Invest.
, vol.52
, pp. 1578-1585
-
-
Brunzell, J.D.1
Hazzard, W.R.2
Porte, D.3
Bierman, E.L.4
-
42
-
-
0020699657
-
Familial chylomicronemia due to a circulating inhibitor of lipoprotein lipase activity
-
Brunzell, J. D., Miller, N. E., Alaupovic, P., St-Hilaire, R. J., Wang, C. S., Sarson, D. L., Bloom, S. R. and Lewis, B. (1983) Familial chylomicronemia due to a circulating inhibitor of lipoprotein lipase activity. J. Lipid Res. 241: 12-19.
-
(1983)
J. Lipid Res.
, vol.241
, pp. 12-19
-
-
Brunzell, J.D.1
Miller, N.E.2
Alaupovic, P.3
St-Hilaire, R.J.4
Wang, C.S.5
Sarson, D.L.6
Bloom, S.R.7
Lewis, B.8
-
43
-
-
85030208010
-
Familial lipoprotein lipase deficiency
-
Stein, O., Eisenberg, S. and Stein, Y. (eds.) R & L Creative Communications Ltd., Tel Aviv
-
Brunzell, J. D., Peterson, J., Deeb, S. S., Santamarina-Fojo, S., Julien, P., Ma, Y., Henderson, H. E. and Hayden, M. R. (1992) Familial lipoprotein lipase deficiency. In: Atherosclerosis IX. Proceedings of the Ninth International Symposium on Atherosclerosis, pp. 271-273, Stein, O., Eisenberg, S. and Stein, Y. (eds.) R & L Creative Communications Ltd., Tel Aviv.
-
(1992)
Atherosclerosis IX. Proceedings of the Ninth International Symposium on Atherosclerosis
, pp. 271-273
-
-
Brunzell, J.D.1
Peterson, J.2
Deeb, S.S.3
Santamarina-Fojo, S.4
Julien, P.5
Ma, Y.6
Henderson, H.E.7
Hayden, M.R.8
-
44
-
-
0029013289
-
Absence of N-glycosylation at asparagine 43 in human lipoprotein lipase induces its accumulation in the rough endoplasmic reticulum and alters this cellular compartment
-
Busca, R., Pujina, M. A., Pognonee, P., Auwerx, J., Deeb, S. S., Reina, M. and Vilaro, S. (1995) Absence of N-glycosylation at asparagine 43 in human lipoprotein lipase induces its accumulation in the rough endoplasmic reticulum and alters this cellular compartment. J. Lipid Res. 36: 939-951.
-
(1995)
J. Lipid Res.
, vol.36
, pp. 939-951
-
-
Busca, R.1
Pujina, M.A.2
Pognonee, P.3
Auwerx, J.4
Deeb, S.S.5
Reina, M.6
Vilaro, S.7
-
45
-
-
0028305225
-
Human hepatic triglyceride lipase expression reduces high density lipoprotein and aortic cholesterol in cholesterol-fed transgenic mice
-
Busch, S. J., Barnhart, R. L., Martin, G. A., Fitzgerald, M. C., Yates, M. T., Mao, S. J., Thomas, C. E. and Jackson, R. L. (1994) Human hepatic triglyceride lipase expression reduces high density lipoprotein and aortic cholesterol in cholesterol-fed transgenic mice. J. Biol. Chem. 269: 16376-16382.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 16376-16382
-
-
Busch, S.J.1
Barnhart, R.L.2
Martin, G.A.3
Fitzgerald, M.C.4
Yates, M.T.5
Mao, S.J.6
Thomas, C.E.7
Jackson, R.L.8
-
46
-
-
0024468864
-
Structure of the human hepatic triglyceride lipase gene
-
Cai, S. J., Wong, D. M., Chen, S. H. and Chan, L. (1989) Structure of the human hepatic triglyceride lipase gene. Biochemistry 28: 8966-8971.
-
(1989)
Biochemistry
, vol.28
, pp. 8966-8971
-
-
Cai, S.J.1
Wong, D.M.2
Chen, S.H.3
Chan, L.4
-
47
-
-
0015612814
-
Acute pancreatitis with hyperlipidemia: The incidence of lipid abnormalities in acute pancreatitis
-
Cameron, J. L., Capuzzi, D. M., Zuidema, G. D. and Margolis, S. (1973) Acute pancreatitis with hyperlipidemia: the incidence of lipid abnormalities in acute pancreatitis. Ann. Surg. 177: 483-489.
-
(1973)
Ann. Surg.
, vol.177
, pp. 483-489
-
-
Cameron, J.L.1
Capuzzi, D.M.2
Zuidema, G.D.3
Margolis, S.4
-
48
-
-
0026643529
-
Alterations in erythrocyte membrane lipid composition and fluidity in primary lipoprotein lipase deficiency
-
Cantin, B., Brun, L. D., Gagné, C., Murthy, M. R. V., Lupien, P. J. and Julien, P. (1992) Alterations in erythrocyte membrane lipid composition and fluidity in primary lipoprotein lipase deficiency. Biochim. Biophys. Acta 1139: 25-31.
-
(1992)
Biochim. Biophys. Acta
, vol.1139
, pp. 25-31
-
-
Cantin, B.1
Brun, L.D.2
Gagné, C.3
Murthy, M.R.V.4
Lupien, P.J.5
Julien, P.6
-
49
-
-
0029026760
-
Hemolysis in primary lipoprotein lipase deficiency
-
Cantin, B., Boudriau, S., Bertrand, M., Brun, L. D., Gagné, C., Rogers, P. A., Murthy, M. R. V., Lupien, P. J. and Julien, P. (1995) Hemolysis in primary lipoprotein lipase deficiency. Metabolism 44: 652-658.
-
(1995)
Metabolism
, vol.44
, pp. 652-658
-
-
Cantin, B.1
Boudriau, S.2
Bertrand, M.3
Brun, L.D.4
Gagné, C.5
Rogers, P.A.6
Murthy, M.R.V.7
Lupien, P.J.8
Julien, P.9
-
50
-
-
0020683780
-
Severe hypertriglyceridemia: Role of familial and acquired disorders
-
Chait, A. and Brunzell, J. D. (1983) Severe hypertriglyceridemia: role of familial and acquired disorders. Metab. Clin. Exp. 32: 209-213.
-
(1983)
Metab. Clin. Exp.
, vol.32
, pp. 209-213
-
-
Chait, A.1
Brunzell, J.D.2
-
52
-
-
0024438108
-
DNA polymorphisms at the lipoprotein lipase gene: Associations in normal and hypertriglyceridaemic subjects
-
Chamberlain, J. C., Thorn, J. A., Oka, K., Galton, D. J. and Stocks, J. (1989) DNA polymorphisms at the lipoprotein lipase gene: associations in normal and hypertriglyceridaemic subjects. Atherosclerosis 79: 85-91.
-
(1989)
Atherosclerosis
, vol.79
, pp. 85-91
-
-
Chamberlain, J.C.1
Thorn, J.A.2
Oka, K.3
Galton, D.J.4
Stocks, J.5
-
53
-
-
85030205783
-
Origines françaises de la population canadienne, 1608-1759
-
Harris, R. C. and Dechéne, L. (eds.) Les Presses de l'Université de Montréal, Montréal
-
Charbonneau, H. and Robert, N. (1987) Origines françaises de la population canadienne, 1608-1759. In: Atlas Historique du Canada 1. Des Origines à 1800, pp. 118-119, Harris, R. C. and Dechéne, L. (eds.) Les Presses de l'Université de Montréal, Montréal.
-
(1987)
Atlas Historique du Canada 1. Des Origines À
, vol.1800
, pp. 118-119
-
-
Charbonneau, H.1
Robert, N.2
-
54
-
-
0026800903
-
A G → C change at the donor splice site of intron 1 causes lipoprotein lipase deficiency in a southern-Italian family
-
Chimienti, G., Capurso, A., Resta, F. and Pepe, G. (1992) A G → C change at the donor splice site of intron 1 causes lipoprotein lipase deficiency in a southern-Italian family. Biochem. Biophys. Res. Commun. 187: 620-627.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.187
, pp. 620-627
-
-
Chimienti, G.1
Capurso, A.2
Resta, F.3
Pepe, G.4
-
55
-
-
0024508431
-
Chylomicron triglyceride clearance: Comparison of three assessment methods
-
Cohen, J. C. (1989) Chylomicron triglyceride clearance: comparison of three assessment methods. Am. J. Clin. Nutr. 49: 306-313.
-
(1989)
Am. J. Clin. Nutr.
, vol.49
, pp. 306-313
-
-
Cohen, J.C.1
-
56
-
-
0027320936
-
Association of a PvuII RFLP at the lipoprotein lipase locus with fasting insulin levels in hispanic men
-
Cole, S. A., Aston, C. E., Hamman, R. F. and Ferrell, R. E. (1993) Association of a PvuII RFLP at the lipoprotein lipase locus with fasting insulin levels in Hispanic men. Genet. Epidemiol. 10: 177-188.
-
(1993)
Genet. Epidemiol.
, vol.10
, pp. 177-188
-
-
Cole, S.A.1
Aston, C.E.2
Hamman, R.F.3
Ferrell, R.E.4
-
57
-
-
0023522662
-
St. Michael. Familial apolipoprotein CII deficiency associated with premature vascular disease
-
St. Michael. Familial apolipoprotein CII deficiency associated with premature vascular disease. J. Clin. Invest. 80: 1597-1606.
-
(1987)
J. Clin. Invest.
, vol.80
, pp. 1597-1606
-
-
Connelly, P.W.1
Maguire, G.F.2
Little, J.A.3
-
58
-
-
0024360286
-
Avian adipose lipoprotein lipase: cDNA sequence and reciprocal regulation of mRNA levels in adipose and heart
-
Cooper, D. A., Stein, J. C., Strieleman, P. J. and Bensadoun, A. (1989) Avian adipose lipoprotein lipase: cDNA sequence and reciprocal regulation of mRNA levels in adipose and heart. Biochim. Biophys. Acta 1008: 92-101.
-
(1989)
Biochim. Biophys. Acta
, vol.1008
, pp. 92-101
-
-
Cooper, D.A.1
Stein, J.C.2
Strieleman, P.J.3
Bensadoun, A.4
-
59
-
-
0019422161
-
Tissue lipoprotein lipase activity and its action in lipoprotein metabolism
-
Cryer, A. (1981) Tissue lipoprotein lipase activity and its action in lipoprotein metabolism. Int. J. Biochem. 13: 525-541.
-
(1981)
Int. J. Biochem.
, vol.13
, pp. 525-541
-
-
Cryer, A.1
-
60
-
-
0023873364
-
Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase
-
Datta, S., Luo, C. C., Li, W. H., VanTuinen, P., Ledbetter, D. H., Brown, M. A., Chen, S. H., Liu, S. W. and Chan, L. (1988) Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase. J. Biol. Chem. 263: 1107-1110.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 1107-1110
-
-
Datta, S.1
Luo, C.C.2
Li, W.H.3
VanTuinen, P.4
Ledbetter, D.H.5
Brown, M.A.6
Chen, S.H.7
Liu, S.W.8
Chan, L.9
-
61
-
-
0000328589
-
Fibrates: A review of important issues and recent findings
-
Davignon, J. (1994) Fibrates: a review of important issues and recent findings. Can. J. Cardiol. 10: 61B-71B.
-
(1994)
Can. J. Cardiol.
, vol.10
-
-
Davignon, J.1
-
62
-
-
0025115935
-
Combined lipase deficiency in the mouse. Evidence of impaired lipase processing and secretion
-
Davis, R. C., Ben Zeev, O., Martin, D. and Doolittle, M. H. (1990) Combined lipase deficiency in the mouse. Evidence of impaired lipase processing and secretion. J. Biol. Chem. 265: 17960-17966.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 17960-17966
-
-
Davis, R.C.1
Ben Zeev, O.2
Martin, D.3
Doolittle, M.H.4
-
63
-
-
0026802453
-
Chimeras of hepatic lipase and lipoprotein lipase. Domain localization of enzyme-specific properties
-
Davis, R. C., Wong, H., Nikazy, J., Wang, K., Han, Q. and Schotz, M. C. (1992) Chimeras of hepatic lipase and lipoprotein lipase. Domain localization of enzyme-specific properties. J. Biol. Chem. 267: 21499-21504.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 21499-21504
-
-
Davis, R.C.1
Wong, H.2
Nikazy, J.3
Wang, K.4
Han, Q.5
Schotz, M.C.6
-
64
-
-
0000228203
-
Model of evolutionary change in proteins
-
Dayhoff, M. O. (ed.) National Biomedical Research Foundation, Washington, DC
-
Dayhoff, M. O., Schwartz, R. M. and Orcott, B. C. (1978) Model of evolutionary change in proteins. In: Atlas of Protein Sequence and Structure, pp. 345-358, Dayhoff, M. O. (ed.) National Biomedical Research Foundation, Washington, DC.
-
(1978)
Atlas of Protein Sequence and Structure
, pp. 345-358
-
-
Dayhoff, M.O.1
Schwartz, R.M.2
Orcott, B.C.3
-
65
-
-
0025819026
-
Founder effect in familial hyperchylomicronemia among French Canadians of Quebec
-
De Braekeleer, M., Dionne, C., Gagné, C., Julien, P., Brun, D., Murthy, M. R. V. and Lupien, P. J. (1991) Founder effect in familial hyperchylomicronemia among French Canadians of Quebec. Hum. Hered. 41: 168-173.
-
(1991)
Hum. Hered.
, vol.41
, pp. 168-173
-
-
De Braekeleer, M.1
Dionne, C.2
Gagné, C.3
Julien, P.4
Brun, D.5
Murthy, M.R.V.6
Lupien, P.J.7
-
66
-
-
0026700582
-
Triacylglycerol and phospholipid hydrolysis in human plasma lipoproteins: Role of lipoprotein and hepatic lipase
-
Deckelbaum, R. J., Ramakrishnan, R., Eisenberg, S., Olivecrona, T. and Bengtsson Olivecrona, G. (1992) Triacylglycerol and phospholipid hydrolysis in human plasma lipoproteins: role of lipoprotein and hepatic lipase. Biochemistry 31: 8544-8551.
-
(1992)
Biochemistry
, vol.31
, pp. 8544-8551
-
-
Deckelbaum, R.J.1
Ramakrishnan, R.2
Eisenberg, S.3
Olivecrona, T.4
Bengtsson Olivecrona, G.5
-
67
-
-
0024397097
-
Structure of the human lipoprotein lipase gene
-
Erratum, Biochemistry 28: 6786 (1989)
-
Deeb, S. S. and Peng, R. L. (1989) Structure of the human lipoprotein lipase gene. Biochemistry 28: 4131-4135. Erratum, Biochemistry 28: 6786 (1989).
-
(1989)
Biochemistry
, vol.28
, pp. 4131-4135
-
-
Deeb, S.S.1
Peng, R.L.2
-
68
-
-
0012081477
-
Gene mutations in patients with lipoprotein lipase deficiency
-
Deeb, S. S., Reina, M., Petersen, J., Takata, K., Kajiama, G. and Brunzell, J. D. (1991) Gene mutations in patients with lipoprotein lipase deficiency. Arterioscler. Thromb. 11: 1418.
-
(1991)
Arterioscler. Thromb.
, vol.11
, pp. 1418
-
-
Deeb, S.S.1
Reina, M.2
Petersen, J.3
Takata, K.4
Kajiama, G.5
Brunzell, J.D.6
-
69
-
-
0025097959
-
Partial gene duplication involving exon-Alu interchange results in lipoprotein lipase deficiency
-
Devlin, R. H., Deeb, S., Brunzell, J. and Hayden, M. R. (1990) Partial gene duplication involving exon-Alu interchange results in lipoprotein lipase deficiency. Am. J. Hum. Genet. 46: 112-119.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 112-119
-
-
Devlin, R.H.1
Deeb, S.2
Brunzell, J.3
Hayden, M.R.4
-
70
-
-
0025962224
-
Identification of two separate allelic mutations in the lipoprotein lipase gene of a patient with the familial hyperchylomicronemia syndrome
-
Dichek, H. L., Fojo, S. S., Beg, O. U., Skarlatos, S. I., Brunzell, J. D., Cutler, G. B., Jr. and Brewer, H. B., Jr. (1991) Identification of two separate allelic mutations in the lipoprotein lipase gene of a patient with the familial hyperchylomicronemia syndrome. J. Biol. Chem. 266: 473-477.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 473-477
-
-
Dichek, H.L.1
Fojo, S.S.2
Beg, O.U.3
Skarlatos, S.I.4
Brunzell, J.D.5
Cutler G.B., Jr.6
Brewer H.B., Jr.7
-
71
-
-
0027228272
-
Functional characterization of a chimeric lipase genetically engineered from human lipoprotein lipase and human hepatic lipase
-
Dichek, H. L., Parrott, C., Ronan, R., Brunzell, J. D., Brewer, H. B., Jr. and Santamarina Fojo, S. (1993) Functional characterization of a chimeric lipase genetically engineered from human lipoprotein lipase and human hepatic lipase. J. Lipid Res. 34: 1393-1340.
-
(1993)
J. Lipid Res.
, vol.34
, pp. 1393-11340
-
-
Dichek, H.L.1
Parrott, C.2
Ronan, R.3
Brunzell, J.D.4
Brewer H.B., Jr.5
Santamarina Fojo, S.6
-
72
-
-
0019048236
-
Eruptive xanthomas associated with isotretinoin (13-cis-retinoic acid)
-
Dicken, C. H. and Connolly, S. M. (1980) Eruptive xanthomas associated with isotretinoin (13-cis-retinoic acid). Arch. Dermatol. 116: 951-952.
-
(1980)
Arch. Dermatol.
, vol.116
, pp. 951-952
-
-
Dicken, C.H.1
Connolly, S.M.2
-
73
-
-
0026761495
-
Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Quebec, Canada)
-
Dionne, C., Gagné, C., Julien, P., Murthy, M. R. V., Lambert, M., Roederer, G., Davignon, J., Hayden, M. R., Lupien, P. J. and de Braekeleer, M. (1992) Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Quebec, Canada). Ann. Genet. 35: 89-92.
-
(1992)
Ann. Genet.
, vol.35
, pp. 89-92
-
-
Dionne, C.1
Gagné, C.2
Julien, P.3
Murthy, M.R.V.4
Lambert, M.5
Roederer, G.6
Davignon, J.7
Hayden, M.R.8
Lupien, P.J.9
De Braekeleer, M.10
-
74
-
-
0027550674
-
Genealogy and regional distribution of lipoprotein lipase deficiency in French-Canadians of Quebec
-
Dionne, C., Gagné, C., Julien, P., Murthy, M. R. V., Roederer, G., Davignon, J., Lambert, M., Chitayat, D., Ma, R., Henderson, H., Lupien, P. J., Hayden, M. R. and de Braekeleer, M. (1993) Genealogy and regional distribution of lipoprotein lipase deficiency in French-Canadians of Quebec. Hum. Biol. 65: 29-39.
-
(1993)
Hum. Biol.
, vol.65
, pp. 29-39
-
-
Dionne, C.1
Gagné, C.2
Julien, P.3
Murthy, M.R.V.4
Roederer, G.5
Davignon, J.6
Lambert, M.7
Chitayat, D.8
Ma, R.9
Henderson, H.10
Lupien, P.J.11
Hayden, M.R.12
De Braekeleer, M.13
-
75
-
-
0002473020
-
Lipolytic enzymes and the role of apolipoproteins in the regulation of their activity
-
Rosseneu, M. (ed.) CRC Press, Inc, Boca Raton
-
Dolphin, P. J. (1992) Lipolytic enzymes and the role of apolipoproteins in the regulation of their activity. In: Structure and Function of Apolipoproteins, pp. 295-362, Rosseneu, M. (ed.) CRC Press, Inc, Boca Raton.
-
(1992)
Structure and Function of Apolipoproteins
, pp. 295-362
-
-
Dolphin, P.J.1
-
76
-
-
0026487341
-
Human lipoprotein lipase: The loop covering the catalytic site is essential for interaction with lipid substrates
-
Dugi, K. A., Dichek, H. L., Talley, G. D., Brewer, H. B., Jr. and Santamarina Fojo, S. (1992) Human lipoprotein lipase: the loop covering the catalytic site is essential for interaction with lipid substrates. J. Biol. Chem. 267: 25086-25091.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 25086-25091
-
-
Dugi, K.A.1
Dichek, H.L.2
Talley, G.D.3
Brewer H.B., Jr.4
Santamarina Fojo, S.5
-
77
-
-
0024500560
-
Lipoprotein lipase: A multifunctional enzyme relevant to common metabolic diseases
-
Eckel, R. H. (1989) Lipoprotein lipase: a multifunctional enzyme relevant to common metabolic diseases. N. Engl. J. Med. 320: 1060-1068.
-
(1989)
N. Engl. J. Med.
, vol.320
, pp. 1060-1068
-
-
Eckel, R.H.1
-
78
-
-
0027500451
-
Cloning and sequencing of a full length cDNA encoding ovine lipoprotein lipase
-
Edwards, W. D., Daniels, S. E., Page, R. A., Volpe, C. P., Kille, P., Sweeney, G. E. and Cryer, A. (1993) Cloning and sequencing of a full length cDNA encoding ovine lipoprotein lipase. Biochim. Biophys. Acta 1172: 167-170.
-
(1993)
Biochim. Biophys. Acta
, vol.1172
, pp. 167-170
-
-
Edwards, W.D.1
Daniels, S.E.2
Page, R.A.3
Volpe, C.P.4
Kille, P.5
Sweeney, G.E.6
Cryer, A.7
-
79
-
-
0027962366
-
Molecular screening of the lipoprotein lipase gene in hypertriglyceridemic members of familial noninsulin-dependent diabetes mellitus families
-
Elbein, S. C., Yeager, C., Kwong, L. K., Lingam, A., Inoue, I., Lalouel, J. M. and Wilson, D. E. (1994) Molecular screening of the lipoprotein lipase gene in hypertriglyceridemic members of familial noninsulin-dependent diabetes mellitus families. J. Clin. Endocrinol. Metab. 79: 1450-1456.
-
(1994)
J. Clin. Endocrinol. Metab.
, vol.79
, pp. 1450-1456
-
-
Elbein, S.C.1
Yeager, C.2
Kwong, L.K.3
Lingam, A.4
Inoue, I.5
Lalouel, J.M.6
Wilson, D.E.7
-
80
-
-
0025292715
-
Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene
-
Emi, M., Hata, A., Robertson, M., Iverius, P. H., Hegele, R. and Lalouel, J. M. (1990a) Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene. Am. J. Hum. Genet. 47: 107-111.
-
(1990)
Am. J. Hum. Genet.
, vol.47
, pp. 107-111
-
-
Emi, M.1
Hata, A.2
Robertson, M.3
Iverius, P.H.4
Hegele, R.5
Lalouel, J.M.6
-
81
-
-
0025239015
-
Missense mutation (Gly → Glu188) of human lipoprotein lipase imparting functional deficiency
-
Emi, M., Wilson, D. E., Iverius, P. H., Wu, L., Hata, A., Hegele, R., Williams, R. R. and Lalouel, J. M. (1990b) Missense mutation (Gly → Glu188) of human lipoprotein lipase imparting functional deficiency. J. Biol. Chem. 265: 5910-5916.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 5910-5916
-
-
Emi, M.1
Wilson, D.E.2
Iverius, P.H.3
Wu, L.4
Hata, A.5
Hegele, R.6
Williams, R.R.7
Lalouel, J.M.8
-
82
-
-
0026675606
-
Human lipoprotein lipase. Analysis of the catalytic triad by site-directed mutagenesis of Ser-132, Asp-156, and His-241
-
Emmerich, J., Beg, O. U., Peterson, J., Previato, L., Brunzell, J. D., Brewer, H. B., Jr. and Santamarina Fojo, S. (1992) Human lipoprotein lipase. Analysis of the catalytic triad by site-directed mutagenesis of Ser-132, Asp-156, and His-241. J. Biol. Chem. 267: 4161-4165.
-
(1992)
J. Biol. Chem. 267
, pp. 4161-4165
-
-
Emmerich, J.1
Beg, O.U.2
Peterson, J.3
Previato, L.4
Brunzell, J.D.5
Brewer H.B., Jr.6
Santamarina Fojo, S.7
-
83
-
-
0023510142
-
Molecular cloning and sequence analysis of cDNA encoding lipoprotein lipase of guinea pig
-
Enerback, S., Semb, H., Bengtsson-Olivecrona, G., Carlsson, P., Hermansson, M. L., Olivecrona, T. and Bjursell, G. (1987) Molecular cloning and sequence analysis of cDNA encoding lipoprotein lipase of guinea pig. Gene 58: 1-12.
-
(1987)
Gene
, vol.58
, pp. 1-12
-
-
Enerback, S.1
Semb, H.2
Bengtsson-Olivecrona, G.3
Carlsson, P.4
Hermansson, M.L.5
Olivecrona, T.6
Bjursell, G.7
-
84
-
-
0015819324
-
Suppression of amylase activity by hypertriglyceridemia
-
Fallat, R. W., Nestor, J. W. and Glueck, C. J. (1973) Suppression of amylase activity by hypertriglyceridemia. JAMA 225: 1331-1334.
-
(1973)
JAMA
, vol.225
, pp. 1331-1334
-
-
Fallat, R.W.1
Nestor, J.W.2
Glueck, C.J.3
-
85
-
-
0026337222
-
Catalytic triad residue mutation (Asp156 → Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447 → Ter) in a Turkish family
-
Erratum, J. Biol. Chem. 267: 7194 (1992)
-
Faustinella, F., Chang, A., Van Biervliet, J. P., Rosseneu, M., Vinaimont, N., Smith, L. C., Chen, S. H. and Chan, L. (1991a) Catalytic triad residue mutation (Asp156 → Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447 → Ter) in a Turkish family. J. Biol. Chem. 266: 14418-14424. Erratum, J. Biol. Chem. 267: 7194 (1992).
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 14418-14424
-
-
Faustinella, F.1
Chang, A.2
Van Biervliet, J.P.3
Rosseneu, M.4
Vinaimont, N.5
Smith, L.C.6
Chen, S.H.7
Chan, L.8
-
86
-
-
0025781275
-
Structural and functional roles of highly conserved serines in human lipoprotein lipase. Evidence that serine 132 is essential for enzyme catalysis
-
Faustinella, F., Smith, L. C., Semenkovich, C. F. and Chan, L. (1991b) Structural and functional roles of highly conserved serines in human lipoprotein lipase. Evidence that serine 132 is essential for enzyme catalysis. J. Biol. Chem. 266: 9481-9485.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 9481-9485
-
-
Faustinella, F.1
Smith, L.C.2
Semenkovich, C.F.3
Chan, L.4
-
87
-
-
0026761311
-
Functional topology of a surface loop shielding the catalytic center in lipoprotein lipase
-
Faustinella, F., Smith, L. C. and Chan, L. (1992) Functional topology of a surface loop shielding the catalytic center in lipoprotein lipase. Biochemistry 31: 7219-7223.
-
(1992)
Biochemistry
, vol.31
, pp. 7219-7223
-
-
Faustinella, F.1
Smith, L.C.2
Chan, L.3
-
88
-
-
0027456791
-
Transgenic mice in cardiovascular research
-
Field, L. J. (1983) Transgenic mice in cardiovascular research. Annu. Rev. Physiol. 55: 97-114.
-
(1983)
Annu. Rev. Physiol.
, vol.55
, pp. 97-114
-
-
Field, L.J.1
-
89
-
-
0023664963
-
Two polymorphisms in the human lipoprotein lipase (LPL) gene
-
Fisher, K. L., FitzGerald, G. A. and Lawn, R. M. (1987) Two polymorphisms in the human lipoprotein lipase (LPL) gene. Nucl. Acids Res. 15: 7657.
-
(1987)
Nucl. Acids Res.
, vol.15
, pp. 7657
-
-
Fisher, K.L.1
FitzGerald, G.A.2
Lawn, R.M.3
-
90
-
-
0023227988
-
Pancreatitis associated with isotretinoin-induced hypertriglyceridemia
-
Flynn, W. J., Freeman, P. G. and Wickboldt, L. F. (1987) Pancreatitis associated with isotretinoin-induced hypertriglyceridemia. Ann. Intern. Med. 107: 63.
-
(1987)
Ann. Intern. Med.
, vol.107
, pp. 63
-
-
Flynn, W.J.1
Freeman, P.G.2
Wickboldt, L.F.3
-
91
-
-
13344267520
-
An analysis of mutations underlying lipoprotein lipase (LPL) deficiency in France
-
Foubert, L., Gagné, E., De Gennes, J. L., Ma, Y., Forsythe, I., Liu, M. S., Zhang, H., Dairou, F., Lagarde, J. P., Benlian, P. and Hayden, M. R. (1994) An analysis of mutations underlying lipoprotein lipase (LPL) deficiency in France. Atherosclerosis 109: 67.
-
(1994)
Atherosclerosis
, vol.109
, pp. 67
-
-
Foubert, L.1
Gagné, E.2
De Gennes, J.L.3
Ma, Y.4
Forsythe, I.5
Liu, M.S.6
Zhang, H.7
Dairou, F.8
Lagarde, J.P.9
Benlian, P.10
Hayden, M.R.11
-
92
-
-
0014193061
-
Fat transport in lipoproteins: An integrated approach to mechanisms and disorders
-
Fredrickson, D. S., Levy, R. I. and Lees, R. S. (1967) Fat transport in lipoproteins: an integrated approach to mechanisms and disorders. N. Engl. J. Med. 276: 34-44.
-
(1967)
N. Engl. J. Med.
, vol.276
, pp. 34-44
-
-
Fredrickson, D.S.1
Levy, R.I.2
Lees, R.S.3
-
93
-
-
0024296510
-
Bst NI (Eco RII) RFLP in the lipoprotein lipase gene (LPL)
-
Funke, H., Reckwerth, A., Stapenhorst, D., Schulze Beiering, M., Jansen, M. and Assmann, G. (1988) Bst NI (Eco RII) RFLP in the lipoprotein lipase gene (LPL). Nucl. Acids Res. 16: 2741.
-
(1988)
Nucl. Acids Res.
, vol.16
, pp. 2741
-
-
Funke, H.1
Reckwerth, A.2
Stapenhorst, D.3
Schulze Beiering, M.4
Jansen, M.5
Assmann, G.6
-
94
-
-
0012049990
-
Identification of the molecular defect in a patient with type 1 hyperlipidemia
-
Funke, H., Wiebusch, H., Paulwebe, B. and Assman, G. (1990) Identification of the molecular defect in a patient with Type 1 hyperlipidemia. Arteriosclerosis 10: 830.
-
(1990)
Arteriosclerosis
, vol.10
, pp. 830
-
-
Funke, H.1
Wiebusch, H.2
Paulwebe, B.3
Assman, G.4
-
95
-
-
0017732761
-
Effect of hyperchylomicronemia on the measurement of hemoglobin
-
Gagné, C., Auger, P. L., Moorjani, S., Brun, L. D. and Lupien, P. J. (1977a) Effect of hyperchylomicronemia on the measurement of hemoglobin. Am. J. Clin. Pathol. 68: 584-586.
-
(1977)
Am. J. Clin. Pathol.
, vol.68
, pp. 584-586
-
-
Gagné, C.1
Auger, P.L.2
Moorjani, S.3
Brun, L.D.4
Lupien, P.J.5
-
96
-
-
0017350321
-
Hyperchylomicronémie familiale: Étude de l'activité lipolytique dans une famille
-
Gagné, C., Brun, L. D., Moorjani, S. and Lupien, P. J. (1977b) Hyperchylomicronémie familiale: étude de l'activité lipolytique dans une famille. Un Méd. Can. 106: 333-338.
-
(1977)
Un Méd. Can.
, vol.106
, pp. 333-338
-
-
Gagné, C.1
Brun, L.D.2
Moorjani, S.3
Lupien, P.J.4
-
97
-
-
0024533690
-
Primary lipoprotein-lipase-activity deficiency: Clinical investigation of a French Canadian population
-
Gagné, C., Brun, L. D., Julien, P., Moorjani, S. and Lupien, P. J. (1989) Primary lipoprotein-lipase-activity deficiency: clinical investigation of a French Canadian population. Can. Med. Assoc. J. 140: 405-411.
-
(1989)
Can. Med. Assoc. J.
, vol.140
, pp. 405-411
-
-
Gagné, C.1
Brun, L.D.2
Julien, P.3
Moorjani, S.4
Lupien, P.J.5
-
98
-
-
0028167760
-
Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia
-
Gagné, E., Genest, J., Jr., Zhang, H., Clarke, L. A. and Hayden, M. R. (1994) Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia. Arterioscler. Thromb. 14: 1250-1257.
-
(1994)
Arterioscler. Thromb.
, vol.14
, pp. 1250-1257
-
-
Gagné, E.1
Genest J., Jr.2
Zhang, H.3
Clarke, L.A.4
Hayden, M.R.5
-
99
-
-
0012081829
-
Premature coronary artery disease and high prevalence of monogenic traits for lipid disorders among French Canadians in a North Eastern region of Québec province
-
Gaudet, D., Moorjani, S., Gagné, C., Julien, P., Tremblay, G., Perron, P., Després, J. P. and Lupien, P. J. (1995) Premature coronary artery disease and high prevalence of monogenic traits for lipid disorders among French Canadians in a North Eastern region of Québec province. Atherosclerosis 109: 203.
-
(1995)
Atherosclerosis
, vol.109
, pp. 203
-
-
Gaudet, D.1
Moorjani, S.2
Gagné, C.3
Julien, P.4
Tremblay, G.5
Perron, P.6
Després, J.P.7
Lupien, P.J.8
-
100
-
-
0012050336
-
Point mutations in the lipoprotein lipase (LPL) gene in normal (N) and combined hyperlipidemic (CH) subjects
-
Gehrisch, S., Steinke, M., Kosta, H., Hoche, I., Julius, U. and Jaross, W. (1994) Point mutations in the lipoprotein lipase (LPL) gene in normal (N) and combined hyperlipidemic (CH) subjects. Atherosclerosis 109: 61.
-
(1994)
Atherosclerosis
, vol.109
, pp. 61
-
-
Gehrisch, S.1
Steinke, M.2
Kosta, H.3
Hoche, I.4
Julius, U.5
Jaross, W.6
-
101
-
-
0026010003
-
Lipoprotein lipase enables triacylglycerol hydrolysis by perfused newborn rat liver
-
Gimenez Llort, L., Vilanova, J., Skottova, N., Bengtsson Olivecrona, G., Llobera, M. and Robert, M. Q. (1991) Lipoprotein lipase enables triacylglycerol hydrolysis by perfused newborn rat liver. Am. J. Physiol. 261: G641-G647.
-
(1991)
Am. J. Physiol.
, vol.261
-
-
Gimenez Llort, L.1
Vilanova, J.2
Skottova, N.3
Bengtsson Olivecrona, G.4
Llobera, M.5
Robert, M.Q.6
-
102
-
-
0012081478
-
Molecular characterization of a colony of cats with lipoprotein lipase deficiency (LPL) reveals a mutation that impairs catalytic activity and interaction with the LDL receptor related protein (LRP)
-
Ginzinger, D. G., Krapp, A., Zhang, H. F., Gagné, S. E., Beisiegel, U. and Hayden, M. R. (1994) Molecular characterization of a colony of cats with lipoprotein lipase deficiency (LPL) reveals a mutation that impairs catalytic activity and interaction with the LDL receptor related protein (LRP). Atherosclerosis 109: 10.
-
(1994)
Atherosclerosis
, vol.109
, pp. 10
-
-
Ginzinger, D.G.1
Krapp, A.2
Zhang, H.F.3
Gagné, S.E.4
Beisiegel, U.5
Hayden, M.R.6
-
103
-
-
0023135405
-
Effects of estrogen/progestin agents on plasma retinoids and chylomicron remnant metabolism
-
Gleeson, J. M., Dukes, C. S., Elstad, N. L., Chan, I. F. and Wilson, D. E. (1987) Effects of estrogen/progestin agents on plasma retinoids and chylomicron remnant metabolism. Contraception 35: 69-78.
-
(1987)
Contraception
, vol.35
, pp. 69-78
-
-
Gleeson, J.M.1
Dukes, C.S.2
Elstad, N.L.3
Chan, I.F.4
Wilson, D.E.5
-
104
-
-
0014622602
-
A new mechanism of exogenous hypertriglyceridemia
-
Glueck, C. J., Kaplan, A. P., Levy, R. I., Greten, H., Gralnick, H. and Fredrickson, D. S. (1969a) A new mechanism of exogenous hypertriglyceridemia. Ann. Intern. Med. 71: 1051-1062.
-
(1969)
Ann. Intern. Med.
, vol.71
, pp. 1051-1062
-
-
Glueck, C.J.1
Kaplan, A.P.2
Levy, R.I.3
Greten, H.4
Gralnick, H.5
Fredrickson, D.S.6
-
105
-
-
0014559291
-
Acquired type I hyperlipoproteinemia with systemic lupus erythematosus
-
Glueck, C. J., Levy, R. I., Glueck, H. I., Gralnick, H. R., Greten, H. and Fredrickson, D. S. (1969b) Acquired type I hyperlipoproteinemia with systemic lupus erythematosus. Am. J. Med. 47: 318-324.
-
(1969)
Am. J. Med.
, vol.47
, pp. 318-324
-
-
Glueck, C.J.1
Levy, R.I.2
Glueck, H.I.3
Gralnick, H.R.4
Greten, H.5
Fredrickson, D.S.6
-
106
-
-
0024454754
-
Gene polymorphism identified by PvuII in familial lipoprotein lipase deficiency
-
Gotoda, T., Senda, M., Murase, T., Yamada, N., Takaku, F. and Furuichi, Y. (1989) Gene polymorphism identified by PvuII in familial lipoprotein lipase deficiency. Biochem. Biophys. Res. Commun. 164: 1391-1396.
-
(1989)
Biochem. Biophys. Res. Commun.
, vol.164
, pp. 1391-1396
-
-
Gotoda, T.1
Senda, M.2
Murase, T.3
Yamada, N.4
Takaku, F.5
Furuichi, Y.6
-
107
-
-
0012079588
-
Splicing, nonsense and missense mutations in familial lipoprotein lipase deficiency
-
Gotoda, T., Murase, T., Ishibashi, S., Shimario, H., Harada, K. and Yamada, N. (1990) Splicing, nonsense and missense mutations in familial lipoprotein lipase deficiency. Arteriosclerosis 10: 833.
-
(1990)
Arteriosclerosis
, vol.10
, pp. 833
-
-
Gotoda, T.1
Murase, T.2
Ishibashi, S.3
Shimario, H.4
Harada, K.5
Yamada, N.6
-
108
-
-
0026344120
-
Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency
-
Gotoda, T., Yamada, N., Kawamura, M., Kozaki, K., Mori, N., Ishibashi, S., Shimano, H., Takaku, F., Yazaki, Y., Furuichi, Y. and Murase, T. (1991a) Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency. J. Clin. Invest. 88: 1856-1864.
-
(1991)
J. Clin. Invest.
, vol.88
, pp. 1856-1864
-
-
Gotoda, T.1
Yamada, N.2
Kawamura, M.3
Kozaki, K.4
Mori, N.5
Ishibashi, S.6
Shimano, H.7
Takaku, F.8
Yazaki, Y.9
Furuichi, Y.10
Murase, T.11
-
109
-
-
0026316732
-
Occurrence of multiple aberrantly spliced mRNAs upon a donor splice site mutation that causes familial lipoprotein lipase deficiency
-
Gotoda, T., Yamada, N., Murase, T., Inaba, T., Ishibashi, S., Shimano, H., Koga, S., Yazaki, Y., Furuichi, Y. and Takaku, F. (1991b) Occurrence of multiple aberrantly spliced mRNAs upon a donor splice site mutation that causes familial lipoprotein lipase deficiency. J. Biol. Chem. 266: 24757-24762.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 24757-24762
-
-
Gotoda, T.1
Yamada, N.2
Murase, T.3
Inaba, T.4
Ishibashi, S.5
Shimano, H.6
Koga, S.7
Yazaki, Y.8
Furuichi, Y.9
Takaku, F.10
-
110
-
-
0026540588
-
A newly identified null allelic mutation in the human lipoprotein lipase (LPL) gene of a compound heterozygote with familial LPL deficiency
-
Gotoda, T., Yamada, N., Murase, T., Miyake, S., Murakami, R., Kawamura, M., Kozaki, K., Mori, N., Shimano, H., Shimada, M. and Yazaki, Y. (1992a) A newly identified null allelic mutation in the human lipoprotein lipase (LPL) gene of a compound heterozygote with familial LPL deficiency. Biochim. Biophys. Acta 1138: 353-356.
-
(1992)
Biochim. Biophys. Acta
, vol.1138
, pp. 353-356
-
-
Gotoda, T.1
Yamada, N.2
Murase, T.3
Miyake, S.4
Murakami, R.5
Kawamura, M.6
Kozaki, K.7
Mori, N.8
Shimano, H.9
Shimada, M.10
Yazaki, Y.11
-
111
-
-
0026734719
-
Detection of three separate DNA polymorphisms in the human lipoprotein lipase gene by gene amplification and restriction endonuclease digestion
-
Gotoda, T., Yamada, N., Murase, T., Shimano, H., Shimada, M., Harada, K., Kawamura, M., Kozaki, K. and Yazaki, Y. (1992b) Detection of three separate DNA polymorphisms in the human lipoprotein lipase gene by gene amplification and restriction endonuclease digestion. J. Lipid Res. 33: 1067-1072.
-
(1992)
J. Lipid Res.
, vol.33
, pp. 1067-1072
-
-
Gotoda, T.1
Yamada, N.2
Murase, T.3
Shimano, H.4
Shimada, M.5
Harada, K.6
Kawamura, M.7
Kozaki, K.8
Yazaki, Y.9
-
112
-
-
0028292602
-
Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemia
-
Grossman, M., Raper, S. E., Kozarsky, K., Stein, E. A., Engelhardt, J. F., Muller, D., Lupien, P. J. and Wilson, J. M. (1994) Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemia. Nature Genet. 6: 335-341.
-
(1994)
Nature Genet.
, vol.6
, pp. 335-341
-
-
Grossman, M.1
Raper, S.E.2
Kozarsky, K.3
Stein, E.A.4
Engelhardt, J.F.5
Muller, D.6
Lupien, P.J.7
Wilson, J.M.8
-
113
-
-
0025010582
-
Compound heterozygote for lipoprotein lipase deficiency: Ser → Thr244 and transition in 3′ splice site of intron 2 (AG → AA) in the lipoprotein lipase gene
-
Hata, A., Emi, M., Luc, G., Basdevant, A., Gambert, P., Iverius, P. H. and Lalouel, J. M. (1990a) Compound heterozygote for lipoprotein lipase deficiency: Ser → Thr244 and transition in 3′ splice site of intron 2 (AG → AA) in the lipoprotein lipase gene. Am. J. Hum. Genet. 47: 721-726.
-
(1990)
Am. J. Hum. Genet.
, vol.47
, pp. 721-726
-
-
Hata, A.1
Emi, M.2
Luc, G.3
Basdevant, A.4
Gambert, P.5
Iverius, P.H.6
Lalouel, J.M.7
-
114
-
-
0025146957
-
Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: Identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene
-
Hata, A., Robertson, M., Emi, M. and Lalouel, J. M. (1990b) Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene. Nucl. Acids Res. 18: 5407-5411.
-
(1990)
Nucl. Acids Res.
, vol.18
, pp. 5407-5411
-
-
Hata, A.1
Robertson, M.2
Emi, M.3
Lalouel, J.M.4
-
115
-
-
0026733335
-
Missense mutations in exon 5 of the human lipoprotein lipase gene. Inactivation correlates with loss of dimerization
-
Hata, A., Ridinger, D. N., Sutherland, S. D., Emi, M., Kwong, L. K., Shuhua, J., Lubbers, A., Guy Grand, B., Basdevant, A., Iverius, P. H., Wilson, D. E. and Lalouel, J. M. (1992) Missense mutations in exon 5 of the human lipoprotein lipase gene. Inactivation correlates with loss of dimerization. J. Biol. Chem. 267: 20132-20139.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 20132-20139
-
-
Hata, A.1
Ridinger, D.N.2
Sutherland, S.D.3
Emi, M.4
Kwong, L.K.5
Shuhua, J.6
Lubbers, A.7
Guy Grand, B.8
Basdevant, A.9
Iverius, P.H.10
Wilson, D.E.11
Lalouel, J.M.12
-
116
-
-
0027532544
-
Binding of lipoprotein lipase to heparin. Identification of five critical residues in two distinct segments of the amino-terminal domain
-
Hata, A., Ridinger, D. N., Sutherland, S., Emi, M., Shuhua, Z., Myers, R. L., Ren, K., Cheng, T., Inoue, I., Wilson, D. E., Iverius, P. H. and Lalouel, J. M. (1993) Binding of lipoprotein lipase to heparin. Identification of five critical residues in two distinct segments of the amino-terminal domain. J. Biol. Chem. 268: 8447-8457.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 8447-8457
-
-
Hata, A.1
Ridinger, D.N.2
Sutherland, S.3
Emi, M.4
Shuhua, Z.5
Myers, R.L.6
Ren, K.7
Cheng, T.8
Inoue, I.9
Wilson, D.E.10
Iverius, P.H.11
Lalouel, J.M.12
-
117
-
-
0027374750
-
A novel missense mutation in the gene for lipoprotein lipase resulting in a highly conservative amino acid substitution (Asp180 → Glu) causes familial chylomicronemia (type I hyperlipoproteinemia)
-
Haubenwallner, S., Horl, G., Shachter, N. S., Presta, E., Fried, S. K., Hofler, G., Kostner, G. M., Breslow, J. L. and Zechner, R. (1993) A novel missense mutation in the gene for lipoprotein lipase resulting in a highly conservative amino acid substitution (Asp180 → Glu) causes familial chylomicronemia (type I hyperlipoproteinemia). Genomics 18: 392-396.
-
(1993)
Genomics
, vol.18
, pp. 392-396
-
-
Haubenwallner, S.1
Horl, G.2
Shachter, N.S.3
Presta, E.4
Fried, S.K.5
Hofler, G.6
Kostner, G.M.7
Breslow, J.L.8
Zechner, R.9
-
118
-
-
0026768077
-
Molecular genetics of human lipoprotein lipase deficiency
-
Hayden, M. R. and Ma, Y. (1992) Molecular genetics of human lipoprotein lipase deficiency. Mol. Cell. Biochem. 113: 171-176.
-
(1992)
Mol. Cell. Biochem.
, vol.113
, pp. 171-176
-
-
Hayden, M.R.1
Ma, Y.2
-
119
-
-
0024456707
-
A BglII RFLP at the lipoprotein lipase gene
-
Hegele, R. A., Nakamura, Y., Emi, M., Lalouel, J. M. and White, R. (1989a) A BglII RFLP at the lipoprotein lipase gene. Nucl. Acids Res. 17: 8899.
-
(1989)
Nucl. Acids Res.
, vol.17
, pp. 8899
-
-
Hegele, R.A.1
Nakamura, Y.2
Emi, M.3
Lalouel, J.M.4
White, R.5
-
120
-
-
0024815293
-
Two RFLPs at the lipoprotein lipase (LPL) gene
-
Hegele, R. A., Nakamura, Y., Emi, M., Lalouel, J. M. and White, R. (1989b) Two RFLPs at the lipoprotein lipase (LPL) gene. Nucl. Acids Res. 17: 10146.
-
(1989)
Nucl. Acids Res.
, vol.17
, pp. 10146
-
-
Hegele, R.A.1
Nakamura, Y.2
Emi, M.3
Lalouel, J.M.4
White, R.5
-
121
-
-
0023664773
-
RFLP for the human lipoprotein lipase (LPL) gene: HindIII
-
Heinzmann, C., Ladias, J., Antonarakis, S., Kirchgessner, T., Schotz, M. and Lusis, A. J. (1987) RFLP for the human lipoprotein lipase (LPL) gene: HindIII. Nucl. Acids Res. 15: 6763.
-
(1987)
Nucl. Acids Res.
, vol.15
, pp. 6763
-
-
Heinzmann, C.1
Ladias, J.2
Antonarakis, S.3
Kirchgessner, T.4
Schotz, M.5
Lusis, A.J.6
-
122
-
-
0025845830
-
DNA polymorphism haplotypes of the human lipoprotein lipase gene: Possible association with high density lipoprotein levels
-
Heizmann, C., Kirchgessner, T., Kwiterovich, P. O., Ladias, J. A., Derby, C., Antonarakis, S. E. and Lusis, A. J. (1991) DNA polymorphism haplotypes of the human lipoprotein lipase gene: possible association with high density lipoprotein levels. Hum. Genet. 86: 578-584.
-
(1991)
Hum. Genet.
, vol.86
, pp. 578-584
-
-
Heizmann, C.1
Kirchgessner, T.2
Kwiterovich, P.O.3
Ladias, J.A.4
Derby, C.5
Antonarakis, S.E.6
Lusis, A.J.7
-
123
-
-
0025616119
-
Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiency
-
Henderson, H. E., Devlin, R., Peterson, J., Brunzell, J. D. and Hayden, M. R. (1990) Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiency. Mol. Biol. Med. 7: 511-517.
-
(1990)
Mol. Biol. Med.
, vol.7
, pp. 511-517
-
-
Henderson, H.E.1
Devlin, R.2
Peterson, J.3
Brunzell, J.D.4
Hayden, M.R.5
-
124
-
-
0026046258
-
Amino acid substitution (Ile194 → Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric origin
-
Henderson, H. E., Ma, Y., Hassan, M. F., Monsalve, M. V., Marais, A. D., Winkler, F., Gubernator, K., Peterson, J., Brunzell, J. D. and Hayden, M. R. (1991) Amino acid substitution (Ile194 → Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric origin. J. Clin. Invest. 87: 2005-2011.
-
(1991)
J. Clin. Invest
, vol.87
, pp. 2005-2011
-
-
Henderson, H.E.1
Ma, Y.2
Hassan, M.F.3
Monsalve, M.V.4
Marais, A.D.5
Winkler, F.6
Gubernator, K.7
Peterson, J.8
Brunzell, J.D.9
Hayden, M.R.10
-
125
-
-
0026611519
-
The lipoprotein lipase Gly188 → Glu mutation in South Africans of Indian descent: Evidence suggesting common origins and an increased frequency
-
Henderson, H. E., Hassan, F., Berger, G. M. and Hayden, M. R. (1992) The lipoprotein lipase Gly188 → Glu mutation in South Africans of Indian descent: evidence suggesting common origins and an increased frequency. J. Med. Genet. 29: 119-122.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 119-122
-
-
Henderson, H.E.1
Hassan, F.2
Berger, G.M.3
Hayden, M.R.4
-
126
-
-
0027162105
-
Structure-function relationships of lipoprotein lipase: Mutation analysis and mutagenesis of the loop region
-
Henderson, H. E., Ma, Y., Liu, M. S., Clark Lewis, I., Maeder, D. L., Kastelein, J. J., Brunzell, J. D. and Hayden, M. R. (1993) Structure-function relationships of lipoprotein lipase: mutation analysis and mutagenesis of the loop region. J. Lipid Res. 34: 1593-1602.
-
(1993)
J. Lipid Res.
, vol.34
, pp. 1593-1602
-
-
Henderson, H.E.1
Ma, Y.2
Liu, M.S.3
Clark Lewis, I.4
Maeder, D.L.5
Kastelein, J.J.6
Brunzell, J.D.7
Hayden, M.R.8
-
127
-
-
0026572737
-
Structure and evolution of the lipase superfamily
-
Hide, W. A., Chan, L. and Li, W. H. (1992) Structure and evolution of the lipase superfamily. J. Lipid Res. 33: 167-178.
-
(1992)
J. Lipid Res.
, vol.33
, pp. 167-178
-
-
Hide, W.A.1
Chan, L.2
Li, W.H.3
-
128
-
-
0025257612
-
Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI
-
Hixson, J. E. and Vernier, D. T. (1990) Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI. J. Lipid Res. 31: 545-548.
-
(1990)
J. Lipid Res.
, vol.31
, pp. 545-548
-
-
Hixson, J.E.1
Vernier, D.T.2
-
129
-
-
0020593639
-
Initial diagnosis of lipoprotein lipase deficiency in a 75 year-old man
-
Hoeg, J. M., Osborne, J. C. and Gregg, R. E. (1983) Initial diagnosis of lipoprotein lipase deficiency in a 75 year-old man. Am. J. Med. 75: 889-892.
-
(1983)
Am. J. Med.
, vol.75
, pp. 889-892
-
-
Hoeg, J.M.1
Osborne, J.C.2
Gregg, R.E.3
-
130
-
-
0028556785
-
Lipoprotein lipase deficiency due to a 3′ splice site mutation in intron 6 of the lipoprotein lipase gene
-
Hölzl, B., Huber, R., Paulweber, B., Patsch, J. R. and Sandhofer, F. (1994) Lipoprotein lipase deficiency due to a 3′ splice site mutation in intron 6 of the lipoprotein lipase gene. J. Lipid Res. 35: 2161-2169.
-
(1994)
J. Lipid Res.
, vol.35
, pp. 2161-2169
-
-
Hölzl, B.1
Huber, R.2
Paulweber, B.3
Patsch, J.R.4
Sandhofer, F.5
-
131
-
-
0012081291
-
Hyperlipidemia in patients with acute pancreatitis
-
Howard, J. M., Ehrlich, E., Spitzer, J. J. and Singh, L. M. (1964) Hyperlipidemia in patients with acute pancreatitis. Ann. Surg. 160: 210-214.
-
(1964)
Ann. Surg.
, vol.160
, pp. 210-214
-
-
Howard, J.M.1
Ehrlich, E.2
Spitzer, J.J.3
Singh, L.M.4
-
132
-
-
0025265399
-
Identification and metabolic characteristics of an apolipoprotein C-II variant isolated from a hypertriglyceridemic subject
-
Huff, M. W., Evans, A. J., Wolfe, B. M., Connelly, P. W., Maguire, G. F. and Strong, W. L. (1990) Identification and metabolic characteristics of an apolipoprotein C-II variant isolated from a hypertriglyceridemic subject. J. Lipid Res. 31: 385-396.
-
(1990)
J. Lipid Res.
, vol.31
, pp. 385-396
-
-
Huff, M.W.1
Evans, A.J.2
Wolfe, B.M.3
Connelly, P.W.4
Maguire, G.F.5
Strong, W.L.6
-
133
-
-
0026613038
-
A missense mutation (Trp86 → Arg) in exon 3 of the lipoprotein lipase gene: A cause of familial chylomicronemia
-
Ishimura Oka, K., Faustinella, F., Kihara, S., Smith, L. C., Oka, K. and Chan, L. (1992a) A missense mutation (Trp86 → Arg) in exon 3 of the lipoprotein lipase gene: a cause of familial chylomicronemia. Am. J. Hum. Genet. 50: 1275-1280.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 1275-1280
-
-
Ishimura Oka, K.1
Faustinella, F.2
Kihara, S.3
Smith, L.C.4
Oka, K.5
Chan, L.6
-
134
-
-
0026611574
-
A missense (Asp250 → asn) mutation in the lipoprotein lipase gene in two unrelated families with familial lipoprotein lipase deficiency
-
Ishimura Oka, K., Semenkovich, C. F., Faustinella, F., Goldberg, I. J., Shachter, N., Smith, L. C., Coleman, T., Hide, W. A., Brown, W. V., Oka, K. and Chan, L. (1992b) A missense (Asp250 → Asn) mutation in the lipoprotein lipase gene in two unrelated families with familial lipoprotein lipase deficiency. J. Lipid Res. 33: 745-754.
-
(1992)
J. Lipid Res.
, vol.33
, pp. 745-754
-
-
Ishimura Oka, K.1
Semenkovich, C.F.2
Faustinella, F.3
Goldberg, I.J.4
Shachter, N.5
Smith, L.C.6
Coleman, T.7
Hide, W.A.8
Brown, W.V.9
Oka, K.10
Chan, L.11
-
135
-
-
0023778715
-
Relationship between lipoprotein lipase activity and plasma sex steroid level in obese women
-
Iverius, P. H. and Brunzell, J. D. (1988) Relationship between lipoprotein lipase activity and plasma sex steroid level in obese women. J. Clin. Invest. 82: 1106-1112.
-
(1988)
J. Clin. Invest.
, vol.82
, pp. 1106-1112
-
-
Iverius, P.H.1
Brunzell, J.D.2
-
136
-
-
0021094722
-
Occurence of idiopathic familial hyperchylomicronemia in a cat
-
Jones, B., Wallace, A., Harding, D. R., Hancock, W. S. and Campbell, C. H. (1983) Occurence of idiopathic familial hyperchylomicronemia in a cat. Vet. Rec. 112: 543-547.
-
(1983)
Vet. Rec.
, vol.112
, pp. 543-547
-
-
Jones, B.1
Wallace, A.2
Harding, D.R.3
Hancock, W.S.4
Campbell, C.H.5
-
137
-
-
0026786139
-
High frequency of lipoprotein lipase deficiency in the Quebec population
-
Julien, P. (1992) High frequency of lipoprotein lipase deficiency in the Quebec population. Can. J. Cardiol. 8: 675-676.
-
(1992)
Can. J. Cardiol.
, vol.8
, pp. 675-676
-
-
Julien, P.1
-
138
-
-
0003100073
-
Mutations of the lipoprotein lipase gene as a cause of dyslipidemias in the Québec population
-
Julien, P., Gagné, C., Murthy, M. R. V., Cantin, B., Cadelis, F., Moorjani, S. and Lupien, P. J. (1994) Mutations of the lipoprotein lipase gene as a cause of dyslipidemias in the Québec population. Can. J. Cardiol. 10: 54-60.
-
(1994)
Can. J. Cardiol.
, vol.10
, pp. 54-60
-
-
Julien, P.1
Gagné, C.2
Murthy, M.R.V.3
Cantin, B.4
Cadelis, F.5
Moorjani, S.6
Lupien, P.J.7
-
139
-
-
0012019362
-
Lipoprotein lipase gene haplotypes and dyslipoproteinemias: Study of a French-Canadian cohort
-
Woodford, F. P., Davignon, J. and Sniderman, A. (eds.) Elsevier, Amsterdam
-
Julien, P., Savanurmath, C. J., Halappanavar, S. P., Murthy, M. R. V., Lévesque, G., Cadelis, F., Gagné, C. and Lupien, P. J. (1995a) Lipoprotein lipase gene haplotypes and dyslipoproteinemias: study of a French-Canadian cohort. In: Atherosclerosis X. Proceedings of the 10th International Symposium on Atherosclerosis, pp. 254-257, Woodford, F. P., Davignon, J. and Sniderman, A. (eds.) Elsevier, Amsterdam.
-
(1995)
Atherosclerosis X. Proceedings of the 10th International Symposium on Atherosclerosis
, pp. 254-257
-
-
Julien, P.1
Savanurmath, C.J.2
Halappanavar, S.P.3
Murthy, M.R.V.4
Lévesque, G.5
Cadelis, F.6
Gagné, C.7
Lupien, P.J.8
-
140
-
-
4244182550
-
Effect of obesity on plasma triglyceride levels in familial lipoprotein lipase deficiency
-
Julien, P., Vohl, M. C., Lévesque, G., Després, J. P., Murthy, M. R. V., Gagné, C., Gaudet, D., Brun, D., Cadelis, F., Moorjani, S. and Lupien, P. J. (1995b) Effect of obesity on plasma triglyceride levels in familial lipoprotein lipase deficiency. Atherosclerosis 115: S8.
-
(1995)
Atherosclerosis
, vol.115
-
-
Julien, P.1
Vohl, M.C.2
Lévesque, G.3
Després, J.P.4
Murthy, M.R.V.5
Gagné, C.6
Gaudet, D.7
Brun, D.8
Cadelis, F.9
Moorjani, S.10
Lupien, P.J.11
-
141
-
-
0024603077
-
Autoimmune hyperchylomicronemia
-
Kihara, S., Matsuzawa, Y., Kubo, M., Nozaki, S., Funahashi, T., Yamashita, S., Sho, N. and Tarui, S. (1989) Autoimmune hyperchylomicronemia. N. Engl. J. Med. 320: 1255-1259.
-
(1989)
N. Engl. J. Med.
, vol.320
, pp. 1255-1259
-
-
Kihara, S.1
Matsuzawa, Y.2
Kubo, M.3
Nozaki, S.4
Funahashi, T.5
Yamashita, S.6
Sho, N.7
Tarui, S.8
-
142
-
-
0023664546
-
The sequence of cDNA encoding lipoprotein lipase. A member of a lipase gene family
-
Kirchgessner, T. G., Svenson, K. L., Lusis, A. J. and Schotz, M. C. (1987) The sequence of cDNA encoding lipoprotein lipase. A member of a lipase gene family. J. Biol. Chem. 262: 8463-8466.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 8463-8466
-
-
Kirchgessner, T.G.1
Svenson, K.L.2
Lusis, A.J.3
Schotz, M.C.4
-
143
-
-
0024791116
-
Organization of the human lipoprotein lipase gene and evolution of the lipase gene family
-
Kirchgessner, T. G., Chuat, J. C., Heinzmann, C., Etienne, J., Guilhot, S., Svenson, K., Ameis, D., Pilon, C., d'Auriol, L., Andalibi, A., Schotz, M. C., Galibert, F. and Lusis, A. J. (1989) Organization of the human lipoprotein lipase gene and evolution of the lipase gene family. Proc. Natl. Acad. Sci. USA 86: 9647-9651.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 9647-9651
-
-
Kirchgessner, T.G.1
Chuat, J.C.2
Heinzmann, C.3
Etienne, J.4
Guilhot, S.5
Svenson, K.6
Ameis, D.7
Pilon, C.8
D'Auriol, L.9
Andalibi, A.10
Schotz, M.C.11
Galibert, F.12
Lusis, A.J.13
-
144
-
-
0026501648
-
A heterozygous mutation (the codon for Ser447 → a stop codon) in lipoprotein lipase contributes to a defect in lipid interface recognition in a case with type I hyperlipidemia
-
Kobayashi, J., Nishida, T., Ameis, D., Stahnke, G., Schotz, M. C., Hashimoto, H., Fukamachi, I., Shirai, K., Saito, Y. and Yoshida, S. (1992) A heterozygous mutation (the codon for Ser447 → a stop codon) in lipoprotein lipase contributes to a defect in lipid interface recognition in a case with type I hyperlipidemia. Biochem. Biophys. Res. Commun. 182: 70-77.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.182
, pp. 70-77
-
-
Kobayashi, J.1
Nishida, T.2
Ameis, D.3
Stahnke, G.4
Schotz, M.C.5
Hashimoto, H.6
Fukamachi, I.7
Shirai, K.8
Saito, Y.9
Yoshida, S.10
-
145
-
-
0027338158
-
A missense mutation (Ala334 → Thr) in exon 7 of the lipoprotein lipase gene in a case with type I hyperlipidemia
-
Kobayashi, J., Sasaki, N., Tashiro, J., Inadera, H., Saito, Y. and Yoshida, S. (1993) A missense mutation (Ala334 → Thr) in exon 7 of the lipoprotein lipase gene in a case with type I hyperlipidemia. Biochem. Biophys. Res. Commun. 191: 1046-1054.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.191
, pp. 1046-1054
-
-
Kobayashi, J.1
Sasaki, N.2
Tashiro, J.3
Inadera, H.4
Saito, Y.5
Yoshida, S.6
-
146
-
-
0027992648
-
A naturally occurring mutation at the second base of codon asparagine 43 in the proposed N-linked glycosylation site of human lipoprotein lipase: In vivo evidence that asparagine 43 is essential for catalysis and secretion
-
Kobayashi, J., Inadera, H., Fujita, Y., Talley, G., Morisaki, N., Yoshida, S., Saito, Y., Fojo, S. S. and Brewer, H. B., Jr. (1994) A naturally occurring mutation at the second base of codon asparagine 43 in the proposed N-linked glycosylation site of human lipoprotein lipase: in vivo evidence that asparagine 43 is essential for catalysis and secretion. Biochem. Biophys. Res. Commun. 205: 506-515.
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.205
, pp. 506-515
-
-
Kobayashi, J.1
Inadera, H.2
Fujita, Y.3
Talley, G.4
Morisaki, N.5
Yoshida, S.6
Saito, Y.7
Fojo, S.S.8
Brewer H.B., Jr.9
-
147
-
-
0023240529
-
Cloning of rat hepatic lipase cDNA: Evidence for a lipase gene family
-
Komaromy, M. C. and Schotz, M. C. (1987) Cloning of rat hepatic lipase cDNA: evidence for a lipase gene family. Proc. Natl. Acad. Sci. USA 84: 1526-1530.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 1526-1530
-
-
Komaromy, M.C.1
Schotz, M.C.2
-
148
-
-
0027494060
-
Mutational analysis of human lipoprotein lipase by carboxy-terminal truncation
-
Kozaki, K., Gotoda, T., Kawamura, M., Shimano, H., Yazaki, Y., Ouchi, Y., Orimo, H. and Yamada, N. (1993) Mutational analysis of human lipoprotein lipase by carboxy-terminal truncation. J. Lipid Res. 34: 1765-1772.
-
(1993)
J. Lipid Res.
, vol.34
, pp. 1765-1772
-
-
Kozaki, K.1
Gotoda, T.2
Kawamura, M.3
Shimano, H.4
Yazaki, Y.5
Ouchi, Y.6
Orimo, H.7
Yamada, N.8
-
149
-
-
0017327454
-
Subclinical chronic pancreatitis in type I hyperlipoproteinemia
-
Kraus, R. M. and Levy, R. I. (1977) Subclinical chronic pancreatitis in type I hyperlipoproteinemia. Am. J. Med. 62: 144-149.
-
(1977)
Am. J. Med.
, vol.62
, pp. 144-149
-
-
Kraus, R.M.1
Levy, R.I.2
-
150
-
-
0026581783
-
Lipoprotein lipase and hepatic triglyceride lipase: Molecular and genetic aspects
-
Lalouel, J. M., Wilson, D. E. and Iverius, P. (1992) Lipoprotein lipase and hepatic triglyceride lipase: molecular and genetic aspects. Curr. Opin. Lipidol. 3: 86-95.
-
(1992)
Curr. Opin. Lipidol.
, vol.3
, pp. 86-95
-
-
Lalouel, J.M.1
Wilson, D.E.2
Iverius, P.3
-
151
-
-
0343970363
-
A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency
-
Langlois, S., Deeb, S., Brunzell, J. D., Kastelein, J. J. and Hayden, M. R. (1989) A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency. Proc. Natl. Acad. Sci. USA 86: 948-952.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 948-952
-
-
Langlois, S.1
Deeb, S.2
Brunzell, J.D.3
Kastelein, J.J.4
Hayden, M.R.5
-
152
-
-
0016514563
-
Diagnosis of pancreatitis masqued by hyperlipidemia
-
Lesser, P. B. and Warshaw, A. L. (1975) Diagnosis of pancreatitis masqued by hyperlipidemia. Ann. Intern. Med. 82: 795-798.
-
(1975)
Ann. Intern. Med.
, vol.82
, pp. 795-798
-
-
Lesser, P.B.1
Warshaw, A.L.2
-
153
-
-
0028264289
-
A rapid restriction site screening method for the Pro207 → Leu mutation in the lipoprotein lipase gene
-
Levesque, G., Julien, P., Deshaies, Y., Lupien, P. J. and Murthy, M. R. V. (1994) A rapid restriction site screening method for the Pro207 → Leu mutation in the lipoprotein lipase gene. Hum. Mutat. 3: 416-417.
-
(1994)
Hum. Mutat.
, vol.3
, pp. 416-417
-
-
Levesque, G.1
Julien, P.2
Deshaies, Y.3
Lupien, P.J.4
Murthy, M.R.V.5
-
154
-
-
0024296399
-
Pvu-II RFLP at the human lipoprotein lipase (LPL) gene locus
-
Li, S. R., Oka, K., Galton, D. and Stocks, J. (1988a) Pvu-II RFLP at the human lipoprotein lipase (LPL) gene locus. Nucl. Acids Res. 16: 2358.
-
(1988)
Nucl. Acids Res.
, vol.16
, pp. 2358
-
-
Li, S.R.1
Oka, K.2
Galton, D.3
Stocks, J.4
-
155
-
-
0024244655
-
Bst-1 RFLP at the human lipoprotein lipase (LPL) gene locus
-
Li, S., Oka, K., Galton, D. and Stocks, J. (1988b) Bst-1 RFLP at the human lipoprotein lipase (LPL) gene locus. Nucl. Acids Res. 16: 11856.
-
(1988)
Nucl. Acids Res.
, vol.16
, pp. 11856
-
-
Li, S.1
Oka, K.2
Galton, D.3
Stocks, J.4
-
156
-
-
0028286780
-
Alteration of lipid profiles in plasma of transgenic mice expressing human lipoprotein lipase
-
Liu, M. S., Jirik, F. R., LeBoeuf, R. C., Henderson, H., Castellani, L. W., Lusis, A. J., Ma, Y., Forsythe, I. J., Zhang, H., Kirk, E., Brunzell, J. D. and Hayden, M. R. (1994) Alteration of lipid profiles in plasma of transgenic mice expressing human lipoprotein lipase. J. Biol. Chem. 269: 11417-11424.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 11417-11424
-
-
Liu, M.S.1
Jirik, F.R.2
LeBoeuf, R.C.3
Henderson, H.4
Castellani, L.W.5
Lusis, A.J.6
Ma, Y.7
Forsythe, I.J.8
Zhang, H.9
Kirk, E.10
Brunzell, J.D.11
Hayden, M.R.12
-
157
-
-
0027401019
-
Chymotryptic cleavage of lipoprotein lipase. Identification of cleavage sites and functional studies of the truncated molecule
-
Lookene, A. and Bengtsson Olivecrona, G. (1993) Chymotryptic cleavage of lipoprotein lipase. Identification of cleavage sites and functional studies of the truncated molecule. Eur. J. Biochem. 213: 185-194.
-
(1993)
Eur. J. Biochem.
, vol.213
, pp. 185-194
-
-
Lookene, A.1
Bengtsson Olivecrona, G.2
-
158
-
-
0026428636
-
A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians
-
Ma, Y., Henderson, H. E., Murthy, M. R. V., Roederer, G., Monsalve, M. V., Clarke, L. A., Normand, T., Julien, P., Gagné, C., Lambert, M., Davignon, J., Lupien, P. J., Brunzell, J. D. and Hayden, M. R. (1991) A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians. N. Engl. J. Med. 324: 1761-1766.
-
(1991)
N. Engl. J. Med.
, vol.324
, pp. 1761-1766
-
-
Ma, Y.1
Henderson, H.E.2
Murthy, M.R.V.3
Roederer, G.4
Monsalve, M.V.5
Clarke, L.A.6
Normand, T.7
Julien, P.8
Gagné, C.9
Lambert, M.10
Davignon, J.11
Lupien, P.J.12
Brunzell, J.D.13
Hayden, M.R.14
-
159
-
-
0026555046
-
Two naturally occurring mutations at the first and second bases of codon aspartic acid 156 in the proposed catalytic triad of human lipoprotein lipase. In vivo evidence that aspartic acid 156 is essential for catalysis
-
Ma, Y. H., Bruin, T., Tuzgol, S., Wilson, B. I., Roederer, G., Liu, M. S., Davignon, J., Kastelein, J. J., Brunzell, J. D. and Hayden, M. R. (1992a) Two naturally occurring mutations at the first and second bases of codon aspartic acid 156 in the proposed catalytic triad of human lipoprotein lipase. In vivo evidence that aspartic acid 156 is essential for catalysis. J. Biol. Chem. 267: 1918-1923.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 1918-1923
-
-
Ma, Y.H.1
Bruin, T.2
Tuzgol, S.3
Wilson, B.I.4
Roederer, G.5
Liu, M.S.6
Davignon, J.7
Kastelein, J.J.8
Brunzell, J.D.9
Hayden, M.R.10
-
160
-
-
0026611411
-
A missense mutation (Asp250 → Asn) in exon 6 of the human lipoprotein lipase gene causes chylomicronemia in patients of different ancestries
-
Ma, Y., Wilson, B. I., Bijvoet, S., Henderson, H. E., Cramb, E., Roederer, G., Murthy, M. R. V., Julien, P., Bakker, H. D., Kastelein, J. J., Brunzell, J. D. and Hayden, M. R. (1992b) A missense mutation (Asp250 → Asn) in exon 6 of the human lipoprotein lipase gene causes chylomicronemia in patients of different ancestries. Genomics 13: 649-653.
-
(1992)
Genomics
, vol.13
, pp. 649-653
-
-
Ma, Y.1
Wilson, B.I.2
Bijvoet, S.3
Henderson, H.E.4
Cramb, E.5
Roederer, G.6
Murthy, M.R.V.7
Julien, P.8
Bakker, H.D.9
Kastelein, J.J.10
Brunzell, J.D.11
Hayden, M.R.12
-
161
-
-
0027299427
-
Gene-environment interaction in the conversion of a mild-to-severe phenotype in a patient homozygous for a Ser172 → Cys mutation in the lipoprotein lipase gene
-
Ma, Y., Liu, M. S., Ginzinger, D., Frohlich, J., Brunzell, J. D. and Hayden, M. R. (1993) Gene-environment interaction in the conversion of a mild-to-severe phenotype in a patient homozygous for a Ser172 → Cys mutation in the lipoprotein lipase gene. J. Clin. Invest. 91: 1953-1958.
-
(1993)
J. Clin. Invest.
, vol.91
, pp. 1953-1958
-
-
Ma, Y.1
Liu, M.S.2
Ginzinger, D.3
Frohlich, J.4
Brunzell, J.D.5
Hayden, M.R.6
-
162
-
-
0028149288
-
Mutagenesis in four candidate heparin binding regions (residues 279-282, 291-304, 390-393 and 439-448) and identification of residues affecting heparin binding of human lipoprotein lipase
-
Ma, Y., Henderson, H. E., Liu, M. S., Zhang, H., Forsythe, I. J., Clarke-Lewis, I., Hayden, M. R. and Brunzell, J. D. (1994a) Mutagenesis in four candidate heparin binding regions (residues 279-282, 291-304, 390-393 and 439-448) and identification of residues affecting heparin binding of human lipoprotein lipase. J. Lipid Res. 35: 2049-2059.
-
(1994)
J. Lipid Res.
, vol.35
, pp. 2049-2059
-
-
Ma, Y.1
Henderson, H.E.2
Liu, M.S.3
Zhang, H.4
Forsythe, I.J.5
Clarke-Lewis, I.6
Hayden, M.R.7
Brunzell, J.D.8
-
163
-
-
0028158096
-
Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries
-
Ma, Y., Liu, M. S., Chitayat, D., Bruin, T., Beisiegel, U., Benlian, P., Foubert, L., De Gennes, J. L., Funke, H., Forsythe, I., Blaichman, S., Papanikolaou, M., Erkelens, D. W., Kastelein, J., Brunzell, J. D. and Hayden, M. R. (1994b) Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries. Hum. Mutât. 3: 52-58.
-
(1994)
Hum. Mutât
, vol.3
, pp. 52-58
-
-
Ma, Y.1
Liu, M.S.2
Chitayat, D.3
Bruin, T.4
Beisiegel, U.5
Benlian, P.6
Foubert, L.7
De Gennes, J.L.8
Funke, H.9
Forsythe, I.10
Blaichman, S.11
Papanikolaou, M.12
Erkelens, D.W.13
Kastelein, J.14
Brunzell, J.D.15
Hayden, M.R.16
-
164
-
-
0028230993
-
2 isoform
-
2 isoform. J. Lipid Res. 35: 1066-1075.
-
(1994)
J. Lipid Res.
, vol.35
, pp. 1066-1075
-
-
Ma, Y.1
Ooi, T.C.2
Liu, M.S.3
Zhang, H.4
McPherson, R.5
Edwards, A.L.6
Forsythe, I.J.7
Frohlich, J.8
Brunzell, J.D.9
Hayden, M.R.10
-
165
-
-
0028915838
-
A common variant in the gene for lipoprotein lipase (Asp9 → Asn). Functional implications and prevalance in normal and hyperlipidemic subjects
-
Mailly, F., Tugrul, Y., Reymer, P. W. A., Bruin, T., Seed, M., Groenemeyer, B. F., Asplund-Carlson, A., Vallance, D., Winder, A. F., Miller, G. J., Kastelein, J. J. P., Hamsten, A., Olivecrona, G., Humphries, S. E. and Talmud, P. J. (1995) A common variant in the gene for lipoprotein lipase (Asp9 → Asn). Functional implications and prevalance in normal and hyperlipidemic subjects. Arterioscler. Thromb. Vasc. Biol. 15: 468-478.
-
(1995)
Arterioscler. Thromb. Vasc. Biol.
, vol.15
, pp. 468-478
-
-
Mailly, F.1
Tugrul, Y.2
Reymer, P.W.A.3
Bruin, T.4
Seed, M.5
Groenemeyer, B.F.6
Asplund-Carlson, A.7
Vallance, D.8
Winder, A.F.9
Miller, G.J.10
Kastelein, J.J.P.11
Hamsten, A.12
Olivecrona, G.13
Humphries, S.E.14
Talmud, P.J.15
-
166
-
-
0016342403
-
The nature and metabolism of the carbohydrate-peptide linkages of glycoprotein
-
Marshall, R. D. (1974) The nature and metabolism of the carbohydrate-peptide linkages of glycoprotein. Biochem. Soc. Symp. 40: 17-26.
-
(1974)
Biochem. Soc. Symp.
, vol.40
, pp. 17-26
-
-
Marshall, R.D.1
-
167
-
-
0023807332
-
Isolation and cDNA sequence of human postheparin plasma hepatic triglyceride lipase
-
Martin, G. A., Busch, S. J., Meredith, G. D., Cardin, A. D., Blankenship, D. T., Mao, S. J., Rechtin, A. E., Woods, C. W., Racke, M. M., Schafer, M. P., Fitzgerald, M. C., Burke, D. M., Flanagan, M. A. and Jackson, R. L. (1988) Isolation and cDNA sequence of human postheparin plasma hepatic triglyceride lipase. J. Biol. Chem. 263: 10907-10914.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 10907-10914
-
-
Martin, G.A.1
Busch, S.J.2
Meredith, G.D.3
Cardin, A.D.4
Blankenship, D.T.5
Mao, S.J.6
Rechtin, A.E.7
Woods, C.W.8
Racke, M.M.9
Schafer, M.P.10
Fitzgerald, M.C.11
Burke, D.M.12
Flanagan, M.A.13
Jackson, R.L.14
-
168
-
-
0025181841
-
Synthesis of inactive nonsecretable high mannosetype lipoprotein lipase by cultured brown adipocytes of combined lipase-deficient cld/cld mice
-
Masuno, H., Blanchette Mackie, E. J., Chernick, S. S. and Scow, R. O. (1990) Synthesis of inactive nonsecretable high mannosetype lipoprotein lipase by cultured brown adipocytes of combined lipase-deficient cld/cld mice. J. Biol. Chem. 265: 1628-1638.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 1628-1638
-
-
Masuno, H.1
Blanchette Mackie, E.J.2
Chernick, S.S.3
Scow, R.O.4
-
169
-
-
0028174814
-
DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population
-
Mattu, R. K., Needham, E. W., Morgan, R., Rees, A., Hackshaw, A. K., Stocks, J., Elwood, P. C. and Galton, D. J. (1994) DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population. Arterioscler. Thromb. 14: 1090-1097.
-
(1994)
Arterioscler. Thromb.
, vol.14
, pp. 1090-1097
-
-
Mattu, R.K.1
Needham, E.W.2
Morgan, R.3
Rees, A.4
Hackshaw, A.K.5
Stocks, J.6
Elwood, P.C.7
Galton, D.J.8
-
170
-
-
0024333252
-
Structure of canine pancreatic lipase gene
-
Mickle, F. S., Weidenbach, F., Swarovsky, B., LaForge, K. S. and Scheele, G. A. (1989) Structure of canine pancreatic lipase gene. J. Biol. Chem. 264: 12895-12901.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 12895-12901
-
-
Mickle, F.S.1
Weidenbach, F.2
Swarovsky, B.3
LaForge, K.S.4
Scheele, G.A.5
-
171
-
-
0027535752
-
Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities
-
Miesenböck, G., Holzl, B., Foger, B., Brandstatter, E., Paulweber, B., Sandhofer, F. and Patsch, J. R. (1993) Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities. J. Clin. Invest. 91: 448-455.
-
(1993)
J. Clin. Invest.
, vol.91
, pp. 448-455
-
-
Miesenböck, G.1
Holzl, B.2
Foger, B.3
Brandstatter, E.4
Paulweber, B.5
Sandhofer, F.6
Patsch, J.R.7
-
172
-
-
0028889944
-
Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridemic patients of French Canadian descent
-
Minnich, A., Kessling, A., Roy, M., Giry, C., DeLangavant, G., Lavigne, J., Lussier-Cacan, S. and Davignon, J. (1995) Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridemic patients of French Canadian descent. J. Lipid Res. 36: 117-124.
-
(1995)
J. Lipid Res.
, vol.36
, pp. 117-124
-
-
Minnich, A.1
Kessling, A.2
Roy, M.3
Giry, C.4
DeLangavant, G.5
Lavigne, J.6
Lussier-Cacan, S.7
Davignon, J.8
-
173
-
-
0028447920
-
DNA polymorphisms at the lipoprotein lipase gene and their association with quantitative variation in plasma high-density lipoproteins and triacylglycerides
-
Mitchell, R. J., Earl, L., Bray, P., Fripp, Y. J. and Williams, J. (1994) DNA polymorphisms at the lipoprotein lipase gene and their association with quantitative variation in plasma high-density lipoproteins and triacylglycerides. Hum. Biol. 66: 383-397.
-
(1994)
Hum. Biol.
, vol.66
, pp. 383-397
-
-
Mitchell, R.J.1
Earl, L.2
Bray, P.3
Fripp, Y.J.4
Williams, J.5
-
174
-
-
0016384016
-
Massive hyperlipidemia during estrogen therapy
-
Molitch, M. E., Oill, P. and Odell, W. D. (1974) Massive hyperlipidemia during estrogen therapy. JAMA 227: 522-525.
-
(1974)
JAMA
, vol.227
, pp. 522-525
-
-
Molitch, M.E.1
Oill, P.2
Odell, W.D.3
-
175
-
-
0025053164
-
A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries
-
Monsalve, M. V., Henderson, H., Roederer, G., Julien, P., Deeb, S., Kastelein, J. J., Peritz, L., Devlin, R., Bruin, T., Murthy, M. R. V., Gagné, C., Davignon, J., Lupien, P. J., Brunzell, J. D. and Hayden, M. R. (1990) A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries. J. Clin. Invest. 86: 728-734.
-
(1990)
J. Clin. Invest.
, vol.86
, pp. 728-734
-
-
Monsalve, M.V.1
Henderson, H.2
Roederer, G.3
Julien, P.4
Deeb, S.5
Kastelein, J.J.6
Peritz, L.7
Devlin, R.8
Bruin, T.9
Murthy, M.R.V.10
Gagné, C.11
Davignon, J.12
Lupien, P.J.13
Brunzell, J.D.14
Hayden, M.R.15
-
176
-
-
0012048485
-
Association of lipoprotein lipase gene polymorphism in intron 3 with hypertriglyceridemia
-
Nakamura, T., Yasuoka, N., Suehiro, T., Nakauchi, Y., Yamamoto, M., Kumon, Y. and Hashimoto, K. (1994) Association of lipoprotein lipase gene polymorphism in intron 3 with hypertriglyceridemia. Atherosclerosis 109: 62.
-
(1994)
Atherosclerosis
, vol.109
, pp. 62
-
-
Nakamura, T.1
Yasuoka, N.2
Suehiro, T.3
Nakauchi, Y.4
Yamamoto, M.5
Kumon, Y.6
Hashimoto, K.7
-
177
-
-
0027685966
-
Dinucleoticle repeat polymorphisms at the lipoprotein lipase (LPL) locus
-
Narcisi, T. M., Schotz, M. C., Scott, J. and Shoulders, C. C. (1993) Dinucleoticle repeat polymorphisms at the lipoprotein lipase (LPL) locus. Hum. Genet. 92: 312-313.
-
(1993)
Hum. Genet.
, vol.92
, pp. 312-313
-
-
Narcisi, T.M.1
Schotz, M.C.2
Scott, J.3
Shoulders, C.C.4
-
178
-
-
0028179511
-
The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity
-
Nevin, D. N., Brunzell, J. D. and Deeb, S. S. (1994) The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity. Arterioscler. Thromb. 14: 869-873.
-
(1994)
Arterioscler. Thromb.
, vol.14
, pp. 869-873
-
-
Nevin, D.N.1
Brunzell, J.D.2
Deeb, S.S.3
-
179
-
-
0007574360
-
Familial lipoprotein lipase deficiency and related disorders of chylomicron metabolism
-
Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds.) McGraw-Hill, New York
-
Nikkila, E. A. (1983) Familial lipoprotein lipase deficiency and related disorders of chylomicron metabolism. In: The Metabolic Basis of Inherited Disease, pp. 604-642, Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds.) McGraw-Hill, New York.
-
(1983)
The Metabolic Basis of Inherited Disease
, pp. 604-642
-
-
Nikkila, E.A.1
-
181
-
-
0026786773
-
Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Quebec
-
Normand, T., Bergeron, J., Fernandez Margallo, T., Bharucha, A., Murthy, M. R. V., Julien, P., Gagné, C., Dionne, C., De Braekeleer, M., Ma, R., Hayden, M. R. and Lupien, P. J. (1992) Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Quebec. Hum. Genet. 89: 671-675.
-
(1992)
Hum. Genet.
, vol.89
, pp. 671-675
-
-
Normand, T.1
Bergeron, J.2
Fernandez Margallo, T.3
Bharucha, A.4
Murthy, M.R.V.5
Julien, P.6
Gagné, C.7
Dionne, C.8
De Braekeleer, M.9
Ma, R.10
Hayden, M.R.11
Lupien, P.J.12
-
182
-
-
0027301838
-
The alpha 2-macroglobulin receptor/low density lipoprotein receptor-related protein binds lipoprotein lipase and beta-migrating very low density lipoprotein associated with the lipase
-
Nykjaer, A., Bengtsson Olivecrona, G., Lookene, A., Moestrup, S. K., Petersen, C. M., Weber, W., Beisiegel, U. and Gliemann, J. (1993) The alpha 2-macroglobulin receptor/low density lipoprotein receptor-related protein binds lipoprotein lipase and beta-migrating very low density lipoprotein associated with the lipase. J. Biol. Chem. 268: 15048-15055.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 15048-15055
-
-
Nykjaer, A.1
Bengtsson Olivecrona, G.2
Lookene, A.3
Moestrup, S.K.4
Petersen, C.M.5
Weber, W.6
Beisiegel, U.7
Gliemann, J.8
-
183
-
-
0024401660
-
Nucleotide sequence of PvuII polymorphic site at the human lipoprotein lipase gene locus
-
Oka, K., Tkalcevic, G. T., Stocks, J., Galton, D. J. and Brown, W. V. (1989) Nucleotide sequence of PvuII polymorphic site at the human lipoprotein lipase gene locus. Nucl. Acids Res. 17: 6752.
-
(1989)
Nucl. Acids Res.
, vol.17
, pp. 6752
-
-
Oka, K.1
Tkalcevic, G.T.2
Stocks, J.3
Galton, D.J.4
Brown, W.V.5
-
184
-
-
0025289589
-
Structure and polymorphic map of human lipoprotein lipase gene
-
Erratum, Biochim. Biophys. Acta. 1090: 357 (1991)
-
Oka, K., Tkalcevic, G. T., Nakano, T., Tucker, H., Ishimura Oka, K. and Brown, W. V. (1990) Structure and polymorphic map of human lipoprotein lipase gene. Biochim. Biophys. Acta 1049: 21-26. Erratum, Biochim. Biophys. Acta. 1090: 357 (1991).
-
(1990)
Biochim. Biophys. Acta
, vol.1049
, pp. 21-26
-
-
Oka, K.1
Tkalcevic, G.T.2
Nakano, T.3
Tucker, H.4
Ishimura Oka, K.5
Brown, W.V.6
-
185
-
-
0025938441
-
Corrigendum: Structure and polymorphic map of human lipoprotein lipase gene
-
Oka, K., Tkalcevic, G., Nakano, T., Tucker, H., Ishimura-Oka, K. and Virgil, W. (1991) Corrigendum: structure and polymorphic map of human lipoprotein lipase gene. Biochim. Biophys. Acta 1090: 357.
-
(1991)
Biochim. Biophys. Acta
, vol.1090
, pp. 357
-
-
Oka, K.1
Tkalcevic, G.2
Nakano, T.3
Tucker, H.4
Ishimura-Oka, K.5
Virgil, W.6
-
186
-
-
0002440672
-
Lipoprotein lipase from milk - The model enzyme in lipoprotein lipase research
-
Borensztajn, J. (ed.) Evener Publishers, Inc., Chicago
-
Olivecrona, T. and Bengtsson-Olivecrona, G. (1987) Lipoprotein lipase from milk - The model enzyme in lipoprotein lipase research. In: Lipoprotein Lipase, pp. 15-58, Borensztajn, J. (ed.) Evener Publishers, Inc., Chicago.
-
(1987)
Lipoprotein Lipase
, pp. 15-58
-
-
Olivecrona, T.1
Bengtsson-Olivecrona, G.2
-
189
-
-
0026540411
-
The α/β hydrolase fold
-
Ollis, D. L., Cheah, E., Cygler, M., Dijkstva, B., Frolow, F., Franken, S. M., Harel, M., Remington, S. J., Silman, I., Schrag, G., Sussman, J. L., Verschueren, K. H. G. and Goldman, A. (1992) The α/β hydrolase fold. Protein Eng. 5: 197-211.
-
(1992)
Protein Eng.
, vol.5
, pp. 197-211
-
-
Ollis, D.L.1
Cheah, E.2
Cygler, M.3
Dijkstva, B.4
Frolow, F.5
Franken, S.M.6
Harel, M.7
Remington, S.J.8
Silman, I.9
Schrag, G.10
Sussman, J.L.11
Verschueren, K.H.G.12
Goldman, A.13
-
190
-
-
0022366273
-
Studies on inactivation of lipoprotein lipase: Role of the dimer to monomer dissociation
-
Osborne, J. C., Jr., Bengtsson-Olivecrona, G., Lee, N. S. and Olivecrona, T. (1985) Studies on inactivation of lipoprotein lipase: role of the dimer to monomer dissociation. Biochemistry 24: 5606-5611.
-
(1985)
Biochemistry
, vol.24
, pp. 5606-5611
-
-
Osborne J.C., Jr.1
Bengtsson-Olivecrona, G.2
Lee, N.S.3
Olivecrona, T.4
-
191
-
-
0014904411
-
Evidence for the chylomicron origin in lipids accumulating in diabetic eruptive xanthomas: A correlative lipid biochemical, histochemical and electron microscopic study
-
Parker, F., Bagdade, J. D., Odland, G. F. and Bierman, E. L. (1970) Evidence for the chylomicron origin in lipids accumulating in diabetic eruptive xanthomas: a correlative lipid biochemical, histochemical and electron microscopic study. J. Clin. Invest. 49: 2172-2187.
-
(1970)
J. Clin. Invest.
, vol.49
, pp. 2172-2187
-
-
Parker, F.1
Bagdade, J.D.2
Odland, G.F.3
Bierman, E.L.4
-
192
-
-
0020533322
-
Combined lipase deficiency (cld): A lethal mutation on chromosome 17 of the mouse
-
Paterniti, J. R., Brown, W. V. and Ginsberg, H. N. (1983) Combined lipase deficiency (cld): a lethal mutation on chromosome 17 of the mouse. Science 221: 167-169.
-
(1983)
Science
, vol.221
, pp. 167-169
-
-
Paterniti, J.R.1
Brown, W.V.2
Ginsberg, H.N.3
-
193
-
-
0026715049
-
Adipose cell size and distribution in familial lipoprotein lipase deficiency
-
Peeva, E., Brun, L. D., Murthy, M. R. V., Després, J. P., Normand, T., Gagné, C., Lupien, P. J. and Julien, P. (1992) Adipose cell size and distribution in familial lipoprotein lipase deficiency. Int. J. Obes. Relat. Metab. Disord. 16: 737-744.
-
(1992)
Int. J. Obes. Relat. Metab. Disord.
, vol.16
, pp. 737-744
-
-
Peeva, E.1
Brun, L.D.2
Murthy, M.R.V.3
Després, J.P.4
Normand, T.5
Gagné, C.6
Lupien, P.J.7
Julien, P.8
-
194
-
-
0027184221
-
Correct usage of a mutated G + 1 splice site and transcript quantitation in a lipoprotein lipase-deficient patient
-
Pepe, G. and Chimienti, G. (1993) Correct usage of a mutated G + 1 splice site and transcript quantitation in a lipoprotein lipase-deficient patient. Hum. Mol. Genet. 2: 1455-1459.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1455-1459
-
-
Pepe, G.1
Chimienti, G.2
-
195
-
-
0028279410
-
A new italian case of lipoprotein lipase deficiency: A Leu365 → Val change resulting in loss of enzyme activity
-
Pepe, G., Chimienti, G., Resta, F., Di Perna, V., Tarricone, C., Lovecchio, M., Colacicco, A. M. and Capurso, A. (1994) A new Italian case of lipoprotein lipase deficiency: a Leu365 → Val change resulting in loss of enzyme activity. Biochem. Biophys. Res. Commun. 199: 570-576.
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.199
, pp. 570-576
-
-
Pepe, G.1
Chimienti, G.2
Resta, F.3
Di Perna, V.4
Tarricone, C.5
Lovecchio, M.6
Colacicco, A.M.7
Capurso, A.8
-
196
-
-
0012081829
-
Does lipoprotein lipase deficiency interfere with growth in the very low birth weight premature infant?
-
Perron, P., Gaudet, D., Gagné, C., Moorjani, S., Julien, P., Tremblay, G. and Lupien, P. J. (1994a) Does lipoprotein lipase deficiency interfere with growth in the very low birth weight premature infant? Atherosclerosis 109: 203.
-
(1994)
Atherosclerosis
, vol.109
, pp. 203
-
-
Perron, P.1
Gaudet, D.2
Gagné, C.3
Moorjani, S.4
Julien, P.5
Tremblay, G.6
Lupien, P.J.7
-
197
-
-
0012054104
-
Effect of feeding on plasma triglyceride level in very low birth weight premature twins born with lipoprotein lipase deficiency
-
Perron, P., Gaudet, D., Moorjani, S., Julien, P., Tremblay, G., Gagné, C. and Lupien, P. J. (1994b) Effect of feeding on plasma triglyceride level in very low birth weight premature twins born with lipoprotein lipase deficiency. Atherosclerosis 109: 142.
-
(1994)
Atherosclerosis
, vol.109
, pp. 142
-
-
Perron, P.1
Gaudet, D.2
Moorjani, S.3
Julien, P.4
Tremblay, G.5
Gagné, C.6
Lupien, P.J.7
-
198
-
-
0028068081
-
A novel missense mutation in the C-terminal domain of lipoprotein lipase (Glu410 → Val) leads to enzyme inactivation and familial chylomicronemia
-
Previato, L., Guardamagna, O., Dugi, K. A., Ronan, R., Talley, G. D., Santamarina Fojo, S. and Brewer, H. B., Jr. (1994) A novel missense mutation in the C-terminal domain of lipoprotein lipase (Glu410 → Val) leads to enzyme inactivation and familial chylomicronemia. J. Lipid Res. 35: 1552-1560.
-
(1994)
J. Lipid Res.
, vol.35
, pp. 1552-1560
-
-
Previato, L.1
Guardamagna, O.2
Dugi, K.A.3
Ronan, R.4
Talley, G.D.5
Santamarina Fojo, S.6
Brewer H.B., Jr.7
-
199
-
-
0017107002
-
Reversal of decreased human adipose tissue lipoprotein lipase and hypertriglyceridemia after treatment of hypothyroidism
-
Pykalisto, O., Goldgerg, A. P. and Brunzell, J. D. (1976) Reversal of decreased human adipose tissue lipoprotein lipase and hypertriglyceridemia after treatment of hypothyroidism. J. Clin. Endocrinol. Metab. 43: 591-600.
-
(1976)
J. Clin. Endocrinol. Metab.
, vol.43
, pp. 591-600
-
-
Pykalisto, O.1
Goldgerg, A.P.2
Brunzell, J.D.3
-
200
-
-
0027053075
-
Molecular basis of familial chylomicronemia: Mutations in the lipoprotein lipase and apolipoprotein C-II genes
-
Reina, M., Brunzell, J. D. and Deeb, S. S. (1992) Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes. J. Lipid Res. 33: 1823-1832.
-
(1992)
J. Lipid Res.
, vol.33
, pp. 1823-1832
-
-
Reina, M.1
Brunzell, J.D.2
Deeb, S.S.3
-
201
-
-
0029047717
-
A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis
-
Reymer, P. W., Gagné, É., Groenmeyer, B. E., Zhang, H., Forsyth, I., Jansen, H., Seidell, J. C., Kromhout, D., Lie, K. E., Kastelein, J. and Hayden, M. R. (1995) A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis. Nature Genetics 10: 28-33.
-
(1995)
Nature Genetics
, vol.10
, pp. 28-33
-
-
Reymer, P.W.1
Gagné, E.2
Groenmeyer, B.E.3
Zhang, H.4
Forsyth, I.5
Jansen, H.6
Seidell, J.C.7
Kromhout, D.8
Lie, K.E.9
Kastelein, J.10
Hayden, M.R.11
-
202
-
-
0022416122
-
Exon shuffling and intron insertion in serine protease genes
-
Rogers, J. (1985) Exon shuffling and intron insertion in serine protease genes. Nature 315: 458-459.
-
(1985)
Nature
, vol.315
, pp. 458-459
-
-
Rogers, J.1
-
203
-
-
0030006214
-
Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL (Asp9 → Asn, Tyr262 → His)
-
Rouis, M., Lohse, P., Dugi, K. A., Lohse, P., Beg, O. U., Ronan, R., Talley, G. D., Brunzell, J. D. and Santamarina Fojo, S. (1996) Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL (Asp9 → Asn, Tyr262 → His). J. Lipid Res. 37: 651-661.
-
(1996)
J. Lipid Res.
, vol.37
, pp. 651-661
-
-
Rouis, M.1
Lohse, P.2
Dugi, K.A.3
Lohse, P.4
Beg, O.U.5
Ronan, R.6
Talley, G.D.7
Brunzell, J.D.8
Santamarina Fojo, S.9
-
204
-
-
0017326566
-
Type I hyperlipoproteinemia in a 8-day-old infant
-
Sadan, N., Brucker, M. M., Arber, I., Joseph, D., Franco, S. and Shapiro, M. S. (1977) Type I hyperlipoproteinemia in a 8-day-old infant. J. Pediat. 90: 775-777.
-
(1977)
J. Pediat.
, vol.90
, pp. 775-777
-
-
Sadan, N.1
Brucker, M.M.2
Arber, I.3
Joseph, D.4
Franco, S.5
Shapiro, M.S.6
-
205
-
-
0026667238
-
Genetic dyslipoproteinemias: Role of lipoprotein lipase and apolipoprotein C-II
-
Santamarina-Fojo, S. (1992) Genetic dyslipoproteinemias: role of lipoprotein lipase and apolipoprotein C-II. Curr. Opin. Lipidol. 3: 186-195.
-
(1992)
Curr. Opin. Lipidol.
, vol.3
, pp. 186-195
-
-
Santamarina-Fojo, S.1
-
206
-
-
0028327343
-
Structure, function and role of lipoprotein lipase in lipoprotein metabolism
-
Santamarina-Fojo, S. and Dugi, K. A. (1994) Structure, function and role of lipoprotein lipase in lipoprotein metabolism. Curr. Opin. Lipidol. 5: 117-125.
-
(1994)
Curr. Opin. Lipidol.
, vol.5
, pp. 117-125
-
-
Santamarina-Fojo, S.1
Dugi, K.A.2
-
207
-
-
0025483209
-
Primary hyperlipoproteinemia type I in the neonatal period
-
Schluter, B., Trowitzsch, E. and Andler, W. (1990) [Primary hyperlipoproteinemia Type I in the neonatal period]. Klin. Padiatr. 202: 355-360.
-
(1990)
Klin. Padiatr.
, vol.202
, pp. 355-360
-
-
Schluter, B.1
Trowitzsch, E.2
Andler, W.3
-
208
-
-
0027050122
-
Underrecognition of chylomicronemia as a cause of acute pancreatitis
-
Searles, G. E. and Ooi, T. C. (1992) Underrecognition of chylomicronemia as a cause of acute pancreatitis. Can. Med. Assoc. J. 147: 1806-1808.
-
(1992)
Can. Med. Assoc. J.
, vol.147
, pp. 1806-1808
-
-
Searles, G.E.1
Ooi, T.C.2
-
209
-
-
0025264381
-
In vitro expression and sitespecific mutagenesis of the cloned human lipoprotein lipase gene. Potential N-linked glycosylation site asparagine 43 is important for both enzyme activity and secretion
-
Semenkovich, C. F., Luo, C. C., Nakanishi, M. K., Chen, S. H., Smith, L. C. and Chan, L. (1990) In vitro expression and sitespecific mutagenesis of the cloned human lipoprotein lipase gene. Potential N-linked glycosylation site asparagine 43 is important for both enzyme activity and secretion. J. Biol. Chem. 265: 5429-5433.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 5429-5433
-
-
Semenkovich, C.F.1
Luo, C.C.2
Nakanishi, M.K.3
Chen, S.H.4
Smith, L.C.5
Chan, L.6
-
210
-
-
0023370756
-
Molecular cloning and sequence of a cDNA coding for bovine lipoprotein lipase
-
Senda, M., Oka, K., Brown, W. V., Qasba, P. K. and Furuichi, Y. (1987) Molecular cloning and sequence of a cDNA coding for bovine lipoprotein lipase. Proc. Natl. Acad. Sci. USA 84: 4369-4373.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 4369-4373
-
-
Senda, M.1
Oka, K.2
Brown, W.V.3
Qasba, P.K.4
Furuichi, Y.5
-
211
-
-
0028331148
-
Overexpression of apolipoprotein CII causes hypertriglyceridemia in transgenic mice
-
Shachter, N. S., Hayek, T., Leff, T., Smith, J. D., Rosenberg, D. W., Walsh, A., Ramakrishnan, R., Goldberg, I. J., Ginsberg, H. N. and Breslow, J. L. (1994) Overexpression of apolipoprotein CII causes hypertriglyceridemia in transgenic mice. J. Clin. Invest. 93: 1683-1690.
-
(1994)
J. Clin. Invest.
, vol.93
, pp. 1683-1690
-
-
Shachter, N.S.1
Hayek, T.2
Leff, T.3
Smith, J.D.4
Rosenberg, D.W.5
Walsh, A.6
Ramakrishnan, R.7
Goldberg, I.J.8
Ginsberg, H.N.9
Breslow, J.L.10
-
212
-
-
0027466627
-
Mechanism of action of fibrates
-
Shepherd, J. (1993) Mechanism of action of fibrates. Postgrad. Med. J. 69: S34-S41.
-
(1993)
Postgrad. Med. J.
, vol.69
-
-
Shepherd, J.1
-
213
-
-
0027296725
-
Overexpression of human lipoprotein lipase in transgenic mice. Resistance to diet-induced hypertriglyceridemia and hypercholesterolemia
-
Shimada, M., Shimano, H., Gotoda, T., Yamamoto, K., Kawamura, M., Inaba, T., Yazaki, Y. and Yamada, N. (1993) Overexpression of human lipoprotein lipase in transgenic mice. Resistance to diet-induced hypertriglyceridemia and hypercholesterolemia. J. Biol. Chem. 268: 17924-17929.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 17924-17929
-
-
Shimada, M.1
Shimano, H.2
Gotoda, T.3
Yamamoto, K.4
Kawamura, M.5
Inaba, T.6
Yazaki, Y.7
Yamada, N.8
-
214
-
-
0026466913
-
Type I hyperlipoproteinemia caused by lipoprotein lipase defect in lipid-interface recognition was relieved by administration of medium-chain triglyceride
-
Shirai, K., Kobayashi, J., Inadera, H., Ohkubo, Y., Mori, S., Saito, Y. and Yoshida, S. (1992) Type I hyperlipoproteinemia caused by lipoprotein lipase defect in lipid-interface recognition was relieved by administration of medium-chain triglyceride. Metabolism 41: 1161-1164.
-
(1992)
Metabolism
, vol.41
, pp. 1161-1164
-
-
Shirai, K.1
Kobayashi, J.2
Inadera, H.3
Ohkubo, Y.4
Mori, S.5
Saito, Y.6
Yoshida, S.7
-
215
-
-
0002988897
-
Peripheral triglyceride clearance, the adipsin-ASP pathway, and type IV hyperlipoproteinemia
-
Bagdade, J. D., Braverman, L. E., Cianflone, K., Horton, E. S., Julien, P., Kannan, C. R., Landsberg, L., Molitch, M. E., Nathan, D. M., Odell, W. D., Poehlman, E. T., Rogol, A. D., Ryan, W. G. and Sniderman, A. D. (eds.) Mosby-Year Book Inc., St. Louis
-
Sniderman, A. D., Julien, P. and Cianflone, K. (1995) Peripheral triglyceride clearance, the adipsin-ASP pathway, and type IV hyperlipoproteinemia. In: Year Book of Endocrinology, 1995, pp. xix-xxxvii, Bagdade, J. D., Braverman, L. E., Cianflone, K., Horton, E. S., Julien, P., Kannan, C. R., Landsberg, L., Molitch, M. E., Nathan, D. M., Odell, W. D., Poehlman, E. T., Rogol, A. D., Ryan, W. G. and Sniderman, A. D. (eds.) Mosby-Year Book Inc., St. Louis.
-
(1995)
Year Book of Endocrinology, 1995
-
-
Sniderman, A.D.1
Julien, P.2
Cianflone, K.3
-
216
-
-
0026611813
-
Trp64 → nonsense mutation in the lipoprotein lipase gene
-
Sprecher, D. L., Kobayashi, J., Rymaszewski, M., Goldberg, I. J., Harris, B. V., Bellet, P. S., Ameis, D., Yunker, R. L., Black, D. M., Stein, E. A., Scholtz, M. C. and Wiginton, D. A. (1992) Trp64 → nonsense mutation in the lipoprotein lipase gene. J. Lipid Res. 33: 859-866.
-
(1992)
J. Lipid Res.
, vol.33
, pp. 859-866
-
-
Sprecher, D.L.1
Kobayashi, J.2
Rymaszewski, M.3
Goldberg, I.J.4
Harris, B.V.5
Bellet, P.S.6
Ameis, D.7
Yunker, R.L.8
Black, D.M.9
Stein, E.A.10
Scholtz, M.C.11
Wiginton, D.A.12
-
217
-
-
0025803837
-
Effect of N-linked glycosylation on hepatic lipase activity
-
Stahnke, G., Davis, R. C., Doolittle, M. H., Wong, H., Schotz, M. C. and Will, H. (1991) Effect of N-linked glycosylation on hepatic lipase activity. J. Lipid Res. 32: 477-484.
-
(1991)
J. Lipid Res.
, vol.32
, pp. 477-484
-
-
Stahnke, G.1
Davis, R.C.2
Doolittle, M.H.3
Wong, H.4
Schotz, M.C.5
Will, H.6
-
218
-
-
0017110316
-
A simple and precise method of determining true sodium, potassium and chloride concentrations in hyperlipidemia
-
Steffes, M. W. and Frier, E. F. (1976) A simple and precise method of determining true sodium, potassium and chloride concentrations in hyperlipidemia. J. Lab. Clin. Med. 88: 683-688.
-
(1976)
J. Lab. Clin. Med.
, vol.88
, pp. 683-688
-
-
Steffes, M.W.1
Frier, E.F.2
-
219
-
-
0021962316
-
Milk and plasma lipid composition in a lactating patient with type I hyperlipoproteinemia
-
Steiner, G., Myher, J. J. and Kuksis, A. (1985) Milk and plasma lipid composition in a lactating patient with type I hyperlipoproteinemia. Am. J. Clin. Nutr. 41: 121-128.
-
(1985)
Am. J. Clin. Nutr.
, vol.41
, pp. 121-128
-
-
Steiner, G.1
Myher, J.J.2
Kuksis, A.3
-
220
-
-
0022497913
-
Pancreatitis induced by oestrogen in a patient with type I hyperlipoproteinaemia
-
Stuyt, P. M., Demacker, P. N. and Stalenhoef, A. F. (1986) Pancreatitis induced by oestrogen in a patient with type I hyperlipoproteinaemia. Br. Med. J. 293: 734.
-
(1986)
Br. Med. J.
, vol.293
, pp. 734
-
-
Stuyt, P.M.1
Demacker, P.N.2
Stalenhoef, A.F.3
-
221
-
-
0022262519
-
Cassette of 8 exons shared by genes for LDL receptor and EGF precursor
-
Sudof, T. C., Russel, D. W., Goldstein, J. L., Brown, M. S., Sanchez-Pescador, R. and Bell, G. (1985) Cassette of 8 exons shared by genes for LDL receptor and EGF precursor. Science 228:893-895.
-
(1985)
Science
, vol.228
, pp. 893-895
-
-
Sudof, T.C.1
Russel, D.W.2
Goldstein, J.L.3
Brown, M.S.4
Sanchez-Pescador, R.5
Bell, G.6
-
222
-
-
0026580924
-
Molecular studies on primary lipoprotein lipase (LPL) deficiency. One base deletion (G916) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript
-
Takagi, A., Ikeda, Y., Tsutsumi, Z., Shoji, T. and Yamamoto, A. (1992) Molecular studies on primary lipoprotein lipase (LPL) deficiency. One base deletion (G916) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript. J. Clin. Invest. 89: 581-591.
-
(1992)
J. Clin. Invest.
, vol.89
, pp. 581-591
-
-
Takagi, A.1
Ikeda, Y.2
Tsutsumi, Z.3
Shoji, T.4
Yamamoto, A.5
-
224
-
-
0026562161
-
Trypsin treatment may impair the interfacial activation action of lipoprotein lipase
-
Tashiro, J., Kobayashi, J., Shirai, K., Saito, Y., Nakamura, H., Morimoto, Y. and Yoshida, S. (1992) Trypsin treatment may impair the interfacial activation action of lipoprotein lipase. J. Biochem. Tokyo 111: 509-514.
-
(1992)
J. Biochem. Tokyo
, vol.111
, pp. 509-514
-
-
Tashiro, J.1
Kobayashi, J.2
Shirai, K.3
Saito, Y.4
Nakamura, H.5
Morimoto, Y.6
Yoshida, S.7
-
225
-
-
0022591495
-
The classification of amino acid conservation
-
Taylor, W. R. (1986) The classification of amino acid conservation. J. Theor. Biol. 119: 205-218.
-
(1986)
J. Theor. Biol.
, vol.119
, pp. 205-218
-
-
Taylor, W.R.1
-
226
-
-
0027972310
-
A novel amino acid substitution (His183 → Gln) in exon 5 of the lipoprotein lipase gene results in loss of catalytic activity: Phenotypic expression of the mutant gene in a heterozygous state
-
Tenkanen, H., Taskinen, M. R., Antikainen, M., Ulmanen, I., Kontula, K. and Ehnholm, C. (1994) A novel amino acid substitution (His183 → Gln) in exon 5 of the lipoprotein lipase gene results in loss of catalytic activity: phenotypic expression of the mutant gene in a heterozygous state. J. Lipid Res. 35: 220-228.
-
(1994)
J. Lipid Res.
, vol.35
, pp. 220-228
-
-
Tenkanen, H.1
Taskinen, M.R.2
Antikainen, M.3
Ulmanen, I.4
Kontula, K.5
Ehnholm, C.6
-
227
-
-
0025241155
-
Lipoprotein and hepatic lipase gene variants in coronary atherosclerosis
-
Thorn, J. A., Chamberlain, J. C., Alcolado, J. C., Oka, K., Chan, L., Stocks, J. and Galton, D. J. (1990) Lipoprotein and hepatic lipase gene variants in coronary atherosclerosis. Atherosclerosis 85: 55-60.
-
(1990)
Atherosclerosis
, vol.85
, pp. 55-60
-
-
Thorn, J.A.1
Chamberlain, J.C.2
Alcolado, J.C.3
Oka, K.4
Chan, L.5
Stocks, J.6
Galton, D.J.7
-
228
-
-
0026537381
-
Role of apolipoprotein E in hepatic lipase catalyzed hydrolysis of phospholipid in high-density lipoproteins
-
Thuren, T., Weisgraber, K. H., Sisson, P. and Waite, M. (1992) Role of apolipoprotein E in hepatic lipase catalyzed hydrolysis of phospholipid in high-density lipoproteins. Biochemistry 31: 2332-2338.
-
(1992)
Biochemistry
, vol.31
, pp. 2332-2338
-
-
Thuren, T.1
Weisgraber, K.H.2
Sisson, P.3
Waite, M.4
-
229
-
-
0028167871
-
Apolipoprotein CII-Padova (Tyr37 → stop) as a cause of chylomicronaemia in an Italian kindred from Siculiana
-
Tuzgol, S., Bijvoet, S. M., Bruin, T., Kastelein, J. J. and Hayden, M. R. (1994) Apolipoprotein CII-Padova (Tyr37 → stop) as a cause of chylomicronaemia in an Italian kindred from Siculiana. J. Med. Genet. 31: 622-626.
-
(1994)
J. Med. Genet.
, vol.31
, pp. 622-626
-
-
Tuzgol, S.1
Bijvoet, S.M.2
Bruin, T.3
Kastelein, J.J.4
Hayden, M.R.5
-
230
-
-
0026687923
-
Structure of the pancreatic lipase-procolipase complex
-
van Tilbeurgh, H., Sarda, L., Verger, R. and Cambillau, C. (1992) Structure of the pancreatic lipase-procolipase complex. Nature 359: 159-162.
-
(1992)
Nature
, vol.359
, pp. 159-162
-
-
Van Tilbeurgh, H.1
Sarda, L.2
Verger, R.3
Cambillau, C.4
-
231
-
-
0027200087
-
Interfacial activation of the lipaseprolipase complex by mixed miscelles revealed by X-ray crystallography
-
van Tilbeurgh, H., EglofF, M. P., Martinez, C., Rugani, N., Verger, R. and Cambillau, C. (1993) Interfacial activation of the lipaseprolipase complex by mixed miscelles revealed by X-ray crystallography. Nature 362: 814-820.
-
(1993)
Nature
, vol.362
, pp. 814-820
-
-
Van Tilbeurgh, H.1
Egloff, M.P.2
Martinez, C.3
Rugani, N.4
Verger, R.5
Cambillau, C.6
-
232
-
-
0028129833
-
Lipoprotein lipase. Molecular model based on the pancreatic lipase X-ray structure: Consequences for heparin binding and catalysis
-
van Tilbeurgh, H., Roussel, A., Lalouel, J. M. and Cambillau, C. (1994) Lipoprotein lipase. Molecular model based on the pancreatic lipase X-ray structure: consequences for heparin binding and catalysis. J. Biol. Chem. 269: 4626-4633.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 4626-4633
-
-
Van Tilbeurgh, H.1
Roussel, A.2
Lalouel, J.M.3
Cambillau, C.4
-
233
-
-
0002175277
-
Pancreatic lipases
-
Borgström, B. and Brockman, H. (eds.) Elsevier Science Publishers B.V., Amsterdam
-
Verger, R. (1984) Pancreatic lipases. In: Lipases, pp. 82-150, Borgström, B. and Brockman, H. (eds.) Elsevier Science Publishers B.V., Amsterdam.
-
(1984)
Lipases
, pp. 82-150
-
-
Verger, R.1
-
234
-
-
0023945473
-
Synthesis of lipoprotein lipase in the liver of newborn rats and localization of the enzyme by immunofluorescence
-
Vilaro, S., Llobera, M., Bengtsson-Olivecrona, G. and Olivecrona, T. (1988) Synthesis of lipoprotein lipase in the liver of newborn rats and localization of the enzyme by immunofluorescence. Biochem. J. 249: 549-556.
-
(1988)
Biochem. J.
, vol.249
, pp. 549-556
-
-
Vilaro, S.1
Llobera, M.2
Bengtsson-Olivecrona, G.3
Olivecrona, T.4
-
236
-
-
0016756911
-
Inhibition of serum and urine amylase activity in pancreatitis with hyperlipidemia
-
Warshaw, A. L., Bellini, C. A. and Lesser, P. B. (1975) Inhibition of serum and urine amylase activity in pancreatitis with hyperlipidemia. Ann. Surg. 182: 72-75.
-
(1975)
Ann. Surg.
, vol.182
, pp. 72-75
-
-
Warshaw, A.L.1
Bellini, C.A.2
Lesser, P.B.3
-
237
-
-
0026572179
-
Management of patients with severe hypertriglyceridaemia during pregnancy: Report of two cases with familial lipoprotein lipase deficiency
-
Watts, G. F., Morton, K., Jackson, P. and Lewis, B. (1992) Management of patients with severe hypertriglyceridaemia during pregnancy: report of two cases with familial lipoprotein lipase deficiency. Br. J. Obstet. Gynaecol. 99: 163-166.
-
(1992)
Br. J. Obstet. Gynaecol.
, vol.99
, pp. 163-166
-
-
Watts, G.F.1
Morton, K.2
Jackson, P.3
Lewis, B.4
-
238
-
-
0012047122
-
Mutations in the lipoprotein lipase gene are not restricted to patients with type 1 hyperlipidemia
-
Wiebusch, H., Funke, H., Kastelein, J. J. P., Bruin, T., Pometta, D., Armstrong, V. and Assman, G. (1992) Mutations in the lipoprotein lipase gene are not restricted to patients with type 1 hyperlipidemia. Circulation 86: 1-609.
-
(1992)
Circulation
, vol.86
, pp. 1-609
-
-
Wiebusch, H.1
Funke, H.2
Kastelein, J.J.P.3
Bruin, T.4
Pometta, D.5
Armstrong, V.6
Assman, G.7
-
239
-
-
0026717599
-
Mechanisms by which lipoprotein lipase alters cellular metabolism of lipoprotein(a), low density lipoprotein, and nascent lipoproteins. Roles for low density lipoprotein receptors and heparan sulfate proteoglycans
-
Williams, K. J., Fless, G. M., Petrie, K. A., Snyder, M. L., Brocia, R. W. and Swenson, T. L. (1992) Mechanisms by which lipoprotein lipase alters cellular metabolism of lipoprotein(a), low density lipoprotein, and nascent lipoproteins. Roles for low density lipoprotein receptors and heparan sulfate proteoglycans. J. Biol. Chem. 267: 13284-13292.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 13284-13292
-
-
Williams, K.J.1
Fless, G.M.2
Petrie, K.A.3
Snyder, M.L.4
Brocia, R.W.5
Swenson, T.L.6
-
240
-
-
0021023902
-
Phenotypic heterogeneity in the extended pedigree of a proband with lipoprotein lipase deficiency
-
Wilson, D. E., Edwards, C. Q. and Chan, I. F. (1983) Phenotypic heterogeneity in the extended pedigree of a proband with lipoprotein lipase deficiency. Metabolism 32: 1107-1114.
-
(1983)
Metabolism
, vol.32
, pp. 1107-1114
-
-
Wilson, D.E.1
Edwards, C.Q.2
Chan, I.F.3
-
241
-
-
0025167797
-
Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation
-
Wilson, D. E., Emi, M., Iverius, P. H., Hata, A., Wu, L. L, Hillas, E., Williams, R. R. and Lalouel, J. M. (1990) Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation. J. Clin. Invest. 86: 735-750.
-
(1990)
J. Clin. Invest.
, vol.86
, pp. 735-750
-
-
Wilson, D.E.1
Emi, M.2
Iverius, P.H.3
Hata, A.4
Wu, L.L.5
Hillas, E.6
Williams, R.R.7
Lalouel, J.M.8
-
242
-
-
0027227835
-
Mutations in exon 3 of the lipoprotein lipase gene segregating in a family with hypertriglyceridemia, pancreatitis, and noninsulin-dependent diabetes
-
Wilson, D. E., Hata, A., Kwong, L. K., Lingam, A., Shuhua, J., Ridinger, D. N., Yeager, C., Kaltenborn, K. C., Iverius, P. H. and Lalouel, J. M. (1993) Mutations in exon 3 of the lipoprotein lipase gene segregating in a family with hypertriglyceridemia, pancreatitis, and noninsulin-dependent diabetes. J. Clin. Invest. 92: 203-211.
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 203-211
-
-
Wilson, D.E.1
Hata, A.2
Kwong, L.K.3
Lingam, A.4
Shuhua, J.5
Ridinger, D.N.6
Yeager, C.7
Kaltenborn, K.C.8
Iverius, P.H.9
Lalouel, J.M.10
-
243
-
-
0028607216
-
Genetic predisposition to hyperlipidaemia in diabetes: The end of the beginning?
-
Wilson, D. E., Kwong, L. K., Elbein, S. C. and Lalouel, J. M. (1994) Genetic predisposition to hyperlipidaemia in diabetes: the end of the beginning? J. Intern. Med. Suppl. 736: 53-61.
-
(1994)
J. Intern. Med. Suppl.
, vol.736
, pp. 53-61
-
-
Wilson, D.E.1
Kwong, L.K.2
Elbein, S.C.3
Lalouel, J.M.4
-
244
-
-
0026842933
-
Ex vivo gene therapy of familial hypercholesterolemia
-
Wilson, J. M., Grossman, M., Raper, S. E., Baker, J. R., Newton, R. S. and Thoene, J. G. (1992) Ex vivo gene therapy of familial hypercholesterolemia. Hum. Gene Ther. 3: 179-222.
-
(1992)
Hum. Gene Ther.
, vol.3
, pp. 179-222
-
-
Wilson, J.M.1
Grossman, M.2
Raper, S.E.3
Baker, J.R.4
Newton, R.S.5
Thoene, J.G.6
-
245
-
-
0025062291
-
Structure of human pancreatic lipase
-
Winkler, F. K., D'Arcy, A. and Hunziker, W. (1990) Structure of human pancreatic lipase. Nature 343: 771-774.
-
(1990)
Nature
, vol.343
, pp. 771-774
-
-
Winkler, F.K.1
D'Arcy, A.2
Hunziker, W.3
-
246
-
-
0023090942
-
Human lipoprotein lipase complementary DNA sequence
-
Wion, K. L., Kirchgessner, T. G., Lusis, A. J., Schotz, M. C. and Lawn, R. M. (1987) Human lipoprotein lipase complementary DNA sequence. Science 235: 1638-1641.
-
(1987)
Science
, vol.235
, pp. 1638-1641
-
-
Wion, K.L.1
Kirchgessner, T.G.2
Lusis, A.J.3
Schotz, M.C.4
Lawn, R.M.5
-
247
-
-
0026323335
-
Domain exchange: Characterization of a chimeric lipase of hepatic lipase and lipoprotein lipase
-
Wong, H., Davis, R. C., Nikazy, J., Seebart, K. E. and Schotz, M. C. (1991) Domain exchange: characterization of a chimeric lipase of hepatic lipase and lipoprotein lipase. Proc. Natl. Acad. Sci. USA 88: 11290-11294.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 11290-11294
-
-
Wong, H.1
Davis, R.C.2
Nikazy, J.3
Seebart, K.E.4
Schotz, M.C.5
-
248
-
-
0024453682
-
Structure of bovine milk lipoprotein lipase
-
Yang, C. Y., Gu, Z. W., Yang, H. X., Rohde, M. F., Gotto, A. M., Jr. and Pownall, H. J. (1989) Structure of bovine milk lipoprotein lipase. J. Biol. Chem. 264: 16822-16827.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 16822-16827
-
-
Yang, C.Y.1
Gu, Z.W.2
Yang, H.X.3
Rohde, M.F.4
Gotto A.M., Jr.5
Pownall, H.J.6
-
249
-
-
0029045344
-
A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activity
-
Yang, W. S., Nevin, D. N., Peng, R., Brunzell, J. D. and Deeb, S. S. (1995) A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activity. Proc. Natl. Acad. Sci. USA 92: 4462-4466.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 4462-4466
-
-
Yang, W.S.1
Nevin, D.N.2
Peng, R.3
Brunzell, J.D.4
Deeb, S.S.5
-
250
-
-
0027193327
-
Prevention of raised low-density lipoprotein cholesterol in a patient with familial hypercholesterolaemia and lipoprotein lipase deficiency
-
Zambon, A., Torres, A., Bijvoet, S., Gagné, C., Moorjani, S., Lupien, P. J., Hayden, M. R. and Brunzell, J. D. (1993) Prevention of raised low-density lipoprotein cholesterol in a patient with familial hypercholesterolaemia and lipoprotein lipase deficiency. Lancet 341: 1119-1121.
-
(1993)
Lancet
, vol.341
, pp. 1119-1121
-
-
Zambon, A.1
Torres, A.2
Bijvoet, S.3
Gagné, C.4
Moorjani, S.5
Lupien, P.J.6
Hayden, M.R.7
Brunzell, J.D.8
-
251
-
-
0001925044
-
In vitro mutagenesis studies defining residues of lipoprotein lipase critical for mediation of the binding of lipoproteins to the LDL receptor-related protein (LRP)
-
Zhang, H., Krapp, A., Ma, Y., Ginzinger, D., Beisiegel, U. and Hayden, M. R. (1994a) In vitro mutagenesis studies defining residues of lipoprotein lipase critical for mediation of the binding of lipoproteins to the LDL receptor-related protein (LRP). Atherosclerosis 109: 66.
-
(1994)
Atherosclerosis
, vol.109
, pp. 66
-
-
Zhang, H.1
Krapp, A.2
Ma, Y.3
Ginzinger, D.4
Beisiegel, U.5
Hayden, M.R.6
-
252
-
-
0001925044
-
Lipoprotein profiles in transgenic mice expressing human lipoprotein lipase on a regular and high fat diet
-
Zhang, H., Leboeuf, R. C., Liu, M., Jirik, F. R., Henderson, H., Castellani, L. W., Lusis, A. J., Forsythe, I., Ma, Y., Kirk, E. and Brunzell, J. D. (1994b) Lipoprotein profiles in transgenic mice expressing human lipoprotein lipase on a regular and high fat diet. Atherosclerosis 109: 66.
-
(1994)
Atherosclerosis
, vol.109
, pp. 66
-
-
Zhang, H.1
Leboeuf, R.C.2
Liu, M.3
Jirik, F.R.4
Henderson, H.5
Castellani, L.W.6
Lusis, A.J.7
Forsythe, I.8
Ma, Y.9
Kirk, E.10
Brunzell, J.D.11
-
253
-
-
0018649439
-
Atherogenesis: A postprandial phenomenon
-
Zilversmith, D. B. (1979) Atherogenesis: a postprandial phenomenon. Circulation 60: 473-485.
-
(1979)
Circulation
, vol.60
, pp. 473-485
-
-
Zilversmith, D.B.1
-
254
-
-
0028225873
-
Transgenic mice expressing human lipoprotein lipase driven by the mouse metallothionein promoter. A phenotype associated with increased perinatal mortality and reduced plasma very low density lipoprotein of normal size
-
Zsigmond, E., Scheffler, E., Forte, T. M., Potenz, R., Wu, W. and Chan, L. (1994) Transgenic mice expressing human lipoprotein lipase driven by the mouse metallothionein promoter. A phenotype associated with increased perinatal mortality and reduced plasma very low density lipoprotein of normal size. J. Biol. Chem. 269: 18757-18766.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 18757-18766
-
-
Zsigmond, E.1
Scheffler, E.2
Forte, T.M.3
Potenz, R.4
Wu, W.5
Chan, L.6
-
255
-
-
0025120708
-
Tetranucleotide repeat polymorphism in the LPL gene
-
Zuliani, G. and Hobbs, H. H. (1990) Tetranucleotide repeat polymorphism in the LPL gene. Nucl. Acids Res. 18: 4958.
-
(1990)
Nucl. Acids Res.
, vol.18
, pp. 4958
-
-
Zuliani, G.1
Hobbs, H.H.2
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