-
1
-
-
0029920693
-
Lipoprotein lipase and lipolysis: central roles in lipoprotein metabolism and atherogenesis
-
Goldberg I.J. Lipoprotein lipase and lipolysis: central roles in lipoprotein metabolism and atherogenesis. J. Lipid Res. 37 (1996) 693-707
-
(1996)
J. Lipid Res.
, vol.37
, pp. 693-707
-
-
Goldberg, I.J.1
-
2
-
-
0025940314
-
Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein
-
Beisiegel U., Weber W., and Bengtsson-Olivecrona G. Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein. Proc. Natl. Acad. Sci. U. S. A. 88 (1991) 8342-8346
-
(1991)
Proc. Natl. Acad. Sci. U. S. A.
, vol.88
, pp. 8342-8346
-
-
Beisiegel, U.1
Weber, W.2
Bengtsson-Olivecrona, G.3
-
3
-
-
33646689532
-
Lipoprotein lipase bound to apolipoprotein B lipoproteins accelerates clearance of postprandial lipoproteins in humans
-
Zheng C., Murdoch S.J., Brunzell J.D., and Sacks F.M. Lipoprotein lipase bound to apolipoprotein B lipoproteins accelerates clearance of postprandial lipoproteins in humans. Arterioscler. Thromb. Vasc. Biol. 26 (2006) 891-896
-
(2006)
Arterioscler. Thromb. Vasc. Biol.
, vol.26
, pp. 891-896
-
-
Zheng, C.1
Murdoch, S.J.2
Brunzell, J.D.3
Sacks, F.M.4
-
4
-
-
0028819754
-
Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice. Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotes
-
Weinstock P.H., Bisgaier C.L., Aalto-Setala K., Radner H., Ramakrishnan R., Levak-Frank S., Essenburg A.D., Zechner R., and Breslow J.L. Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice. Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotes. J. Clin. Invest. 96 (1995) 2555-2568
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 2555-2568
-
-
Weinstock, P.H.1
Bisgaier, C.L.2
Aalto-Setala, K.3
Radner, H.4
Ramakrishnan, R.5
Levak-Frank, S.6
Essenburg, A.D.7
Zechner, R.8
Breslow, J.L.9
-
5
-
-
0029079312
-
COOH-terminal disruption of lipoprotein lipase in mice is lethal in homozygotes, but heterozygotes have elevated triglycerides and impaired enzyme activity
-
Coleman T., Seip R.L., Gimble J.M., Lee D., Maeda N., and Semenkovich C.F. COOH-terminal disruption of lipoprotein lipase in mice is lethal in homozygotes, but heterozygotes have elevated triglycerides and impaired enzyme activity. J. Biol. Chem. 270 (1995) 12518-12525
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 12518-12525
-
-
Coleman, T.1
Seip, R.L.2
Gimble, J.M.3
Lee, D.4
Maeda, N.5
Semenkovich, C.F.6
-
6
-
-
26244445992
-
S447X beneficial mutation
-
S447X beneficial mutation. Arterioscler. Thromb. Vasc. Biol. 25 (2005) 2143-2150
-
(2005)
Arterioscler. Thromb. Vasc. Biol.
, vol.25
, pp. 2143-2150
-
-
Ross, C.J.1
Liu, G.2
Kuivenhoven, J.A.3
Twisk, J.4
Rip, J.5
van, D.W.6
Excoffon, K.J.7
Lewis, S.M.8
Kastelein, J.J.9
Hayden, M.R.10
-
7
-
-
0030982084
-
Lipoprotein lipase deficiency with pancreatitis in mink: biochemical characterization and pathology
-
Christophersen B., Nordstoga K., Shen Y., Olivecrona T., and Olivecrona G. Lipoprotein lipase deficiency with pancreatitis in mink: biochemical characterization and pathology. J. Lipid Res. 38 (1997) 837-846
-
(1997)
J. Lipid Res.
, vol.38
, pp. 837-846
-
-
Christophersen, B.1
Nordstoga, K.2
Shen, Y.3
Olivecrona, T.4
Olivecrona, G.5
-
8
-
-
0029912304
-
A mutation in the lipoprotein lipase gene is the molecular basis of chylomicronemia in a colony of domestic cats
-
Ginzinger D.G., Lewis M.E., Ma Y., Jones B.R., Liu G., and Jones S.D. A mutation in the lipoprotein lipase gene is the molecular basis of chylomicronemia in a colony of domestic cats. J. Clin. Invest. 97 (1996) 1257-1266
-
(1996)
J. Clin. Invest.
, vol.97
, pp. 1257-1266
-
-
Ginzinger, D.G.1
Lewis, M.E.2
Ma, Y.3
Jones, B.R.4
Liu, G.5
Jones, S.D.6
-
9
-
-
0001033625
-
Familial Lipoprotein Lipase Deficiency and Other Causes of the Chylomicronemia Syndrome
-
Sriver C., Baudet A., Sly W., and Valle D. (Eds), McGraw-Hill, New York
-
Brunzell J. Familial Lipoprotein Lipase Deficiency and Other Causes of the Chylomicronemia Syndrome. In: Sriver C., Baudet A., Sly W., and Valle D. (Eds). The Metabolic and Molecular Basis of Inherited Disease. 7th ed. (1995), McGraw-Hill, New York 1913-1932
-
(1995)
The Metabolic and Molecular Basis of Inherited Disease. 7th ed.
, pp. 1913-1932
-
-
Brunzell, J.1
-
10
-
-
0000102874
-
Type III Hyperlipoproteinaemia (Dyslipoproteinemia; Remnant Particle Disease)
-
Betteridge D.J., Illingworth D.R., and Shepherd J.A. (Eds), Arnold Publishers, London, Great Britain
-
Mahley R.W., and Rall S.C. Type III Hyperlipoproteinaemia (Dyslipoproteinemia; Remnant Particle Disease). In: Betteridge D.J., Illingworth D.R., and Shepherd J.A. (Eds). Lipoproteins in Health and Disease (1999), Arnold Publishers, London, Great Britain 719-736
-
(1999)
Lipoproteins in Health and Disease
, pp. 719-736
-
-
Mahley, R.W.1
Rall, S.C.2
-
11
-
-
0020478765
-
Abnormal lipoprotein receptor-binding activity of the human E apoprotein due to cysteine-arginine interchange at a single site
-
Weisgraber K.H., Innerarity T.L., and Mahley R.W. Abnormal lipoprotein receptor-binding activity of the human E apoprotein due to cysteine-arginine interchange at a single site. J. Biol. Chem. 257 (1982) 2518-2521
-
(1982)
J. Biol. Chem.
, vol.257
, pp. 2518-2521
-
-
Weisgraber, K.H.1
Innerarity, T.L.2
Mahley, R.W.3
-
12
-
-
0016635833
-
The biochemical, clinical, and genetic features of type III hyperlipoproteinemia
-
Morganroth J., Levy R.I., and Fredrickson D.S. The biochemical, clinical, and genetic features of type III hyperlipoproteinemia. Ann. Intern. Med. 82 (1975) 158-174
-
(1975)
Ann. Intern. Med.
, vol.82
, pp. 158-174
-
-
Morganroth, J.1
Levy, R.I.2
Fredrickson, D.S.3
-
13
-
-
0029130943
-
Patients with apoE3 deficiency (E2/2, E3/2, and E4/2) who manifest with hyperlipidemia have increased frequency of an Asn 291→Ser mutation in the human LPL gene
-
Zhang H., Reymer P.W., Liu M.S., Forsythe I.J., Groenemeyer B.E., Frohlich J., Brunzell J.D., Kastelein J.J., Hayden M.R., and Ma Y. Patients with apoE3 deficiency (E2/2, E3/2, and E4/2) who manifest with hyperlipidemia have increased frequency of an Asn 291→Ser mutation in the human LPL gene. Arterioscler. Thromb. Vasc. Biol. 15 (1995) 1695-1703
-
(1995)
Arterioscler. Thromb. Vasc. Biol.
, vol.15
, pp. 1695-1703
-
-
Zhang, H.1
Reymer, P.W.2
Liu, M.S.3
Forsythe, I.J.4
Groenemeyer, B.E.5
Frohlich, J.6
Brunzell, J.D.7
Kastelein, J.J.8
Hayden, M.R.9
Ma, Y.10
-
14
-
-
0031981240
-
Expression of type III hyperlipoproteinemia in patients homozygous for apolipoprotein E-2 is modulated by lipoprotein lipase and postprandial hyperinsulinemia
-
Brummer D., Evans D., Berg D., Greten H., Beisiegel U., and Mann W.A. Expression of type III hyperlipoproteinemia in patients homozygous for apolipoprotein E-2 is modulated by lipoprotein lipase and postprandial hyperinsulinemia. J. Mol. Med. 76 (1998) 355-364
-
(1998)
J. Mol. Med.
, vol.76
, pp. 355-364
-
-
Brummer, D.1
Evans, D.2
Berg, D.3
Greten, H.4
Beisiegel, U.5
Mann, W.A.6
-
15
-
-
0033049968
-
Lipoprotein lipase compensates for the defective function of apo E variants in vitro by interacting with proteoglycans and lipoprotein receptors
-
Mann W.A., Meyer N., Berg D., Greten H., and Beisiegel U. Lipoprotein lipase compensates for the defective function of apo E variants in vitro by interacting with proteoglycans and lipoprotein receptors. Atherosclerosis 145 (1999) 61-69
-
(1999)
Atherosclerosis
, vol.145
, pp. 61-69
-
-
Mann, W.A.1
Meyer, N.2
Berg, D.3
Greten, H.4
Beisiegel, U.5
-
16
-
-
0032128001
-
Type III hyperlipoproteinemia and spontaneous atherosclerosis in mice resulting from gene replacement of mouse Apoe with human Apoe*2
-
Sullivan P.M., Mezdour H., Quarfordt S.H., and Maeda N. Type III hyperlipoproteinemia and spontaneous atherosclerosis in mice resulting from gene replacement of mouse Apoe with human Apoe*2. J. Clin. Invest. 102 (1998) 130-135
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 130-135
-
-
Sullivan, P.M.1
Mezdour, H.2
Quarfordt, S.H.3
Maeda, N.4
-
17
-
-
4544326444
-
Long-term correction of murine lipoprotein lipase deficiency with AAV1-mediated gene transfer of the naturally occurring LPL(S447X) beneficial mutation
-
Ross C.J., Twisk J., Meulenberg J.M., Liu G., van den O.K., Moraal E., Hermens W.T., Rip J., Kastelein J.J., Kuivenhoven J.A., and Hayden M.R. Long-term correction of murine lipoprotein lipase deficiency with AAV1-mediated gene transfer of the naturally occurring LPL(S447X) beneficial mutation. Hum. Gene Ther. 15 (2004) 906-919
-
(2004)
Hum. Gene Ther.
, vol.15
, pp. 906-919
-
-
Ross, C.J.1
Twisk, J.2
Meulenberg, J.M.3
Liu, G.4
van den, O.K.5
Moraal, E.6
Hermens, W.T.7
Rip, J.8
Kastelein, J.J.9
Kuivenhoven, J.A.10
Hayden, M.R.11
-
18
-
-
33646933211
-
Correction of feline lipoprotein lipase deficiency with adeno-associated virus serotype 1-mediated gene transfer of the lipoprotein lipase S447X beneficial mutation
-
Ross C.J., Twisk J., Bakker A.C., Miao F., Verbart D., Rip J., Godbey T., Dijkhuizen P., Hermens W.T., Kastelein J.J., Kuivenhoven J.A., Meulenberg J.M., and Hayden M.R. Correction of feline lipoprotein lipase deficiency with adeno-associated virus serotype 1-mediated gene transfer of the lipoprotein lipase S447X beneficial mutation. Hum. Gene Ther. 17 (2006) 487-499
-
(2006)
Hum. Gene Ther.
, vol.17
, pp. 487-499
-
-
Ross, C.J.1
Twisk, J.2
Bakker, A.C.3
Miao, F.4
Verbart, D.5
Rip, J.6
Godbey, T.7
Dijkhuizen, P.8
Hermens, W.T.9
Kastelein, J.J.10
Kuivenhoven, J.A.11
Meulenberg, J.M.12
Hayden, M.R.13
-
19
-
-
27744446128
-
Gene therapy for lipoprotein lipase deficiency: working toward clinical application
-
Rip J., Nierman M.C., Sierts J.A., Petersen W., Den Oever K.V., Raalte D.V., Ross C.J., Hayden M.R., Bakker A.C., Dijkhuizen P., Hermens W.T., Twisk J., Stroes E., Kastelein J.J., Kuivenhoven J.A., and Meulenberg J.M. Gene therapy for lipoprotein lipase deficiency: working toward clinical application. Hum. Gene Ther. 16 (2005) 1276-1286
-
(2005)
Hum. Gene Ther.
, vol.16
, pp. 1276-1286
-
-
Rip, J.1
Nierman, M.C.2
Sierts, J.A.3
Petersen, W.4
Den Oever, K.V.5
Raalte, D.V.6
Ross, C.J.7
Hayden, M.R.8
Bakker, A.C.9
Dijkhuizen, P.10
Hermens, W.T.11
Twisk, J.12
Stroes, E.13
Kastelein, J.J.14
Kuivenhoven, J.A.15
Meulenberg, J.M.16
-
21
-
-
0033962912
-
Phenotypic correction of feline lipoprotein lipase deficiency by adenoviral gene transfer
-
Liu G., Ashbourne Excoffon K.J., Wilson J.E., McManus B.M., Rogers Q.R., Miao L., Kastelein J.J., Lewis M.E., and Hayden M.R. Phenotypic correction of feline lipoprotein lipase deficiency by adenoviral gene transfer. Hum. Gene Ther. 11 (2000) 21-32
-
(2000)
Hum. Gene Ther.
, vol.11
, pp. 21-32
-
-
Liu, G.1
Ashbourne Excoffon, K.J.2
Wilson, J.E.3
McManus, B.M.4
Rogers, Q.R.5
Miao, L.6
Kastelein, J.J.7
Lewis, M.E.8
Hayden, M.R.9
-
22
-
-
33845261493
-
A rapid method of total lipid extraction and purification
-
Bligh E., and Dyer W. A rapid method of total lipid extraction and purification. Can. J. Med. Sci. 37 (1959) 911-917
-
(1959)
Can. J. Med. Sci.
, vol.37
, pp. 911-917
-
-
Bligh, E.1
Dyer, W.2
-
23
-
-
0029142737
-
Muscle-specific overexpression of lipoprotein lipase causes a severe myopathy characterized by proliferation of mitochondria and peroxisomes in transgenic mice
-
Levak-Frank S., Radner H., Walsh A., Stollberger R., Knipping G., Hoefler G., Sattler W., Weinstock P.H., Breslow J.L., and Zechner R. Muscle-specific overexpression of lipoprotein lipase causes a severe myopathy characterized by proliferation of mitochondria and peroxisomes in transgenic mice. J. Clin. Invest. 96 (1995) 976-986
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 976-986
-
-
Levak-Frank, S.1
Radner, H.2
Walsh, A.3
Stollberger, R.4
Knipping, G.5
Hoefler, G.6
Sattler, W.7
Weinstock, P.H.8
Breslow, J.L.9
Zechner, R.10
-
24
-
-
0030858781
-
Muscle-specific overexpression of human lipoprotein lipase in mice causes increased intracellular free fatty acids and induction of peroxisomal enzymes
-
Hoefler G., Noehammer C., Levak-Frank S., el Shabrawi Y., Schauer S., Zechner R., and Radner H. Muscle-specific overexpression of human lipoprotein lipase in mice causes increased intracellular free fatty acids and induction of peroxisomal enzymes. Biochimie 79 (1997) 163-168
-
(1997)
Biochimie
, vol.79
, pp. 163-168
-
-
Hoefler, G.1
Noehammer, C.2
Levak-Frank, S.3
el Shabrawi, Y.4
Schauer, S.5
Zechner, R.6
Radner, H.7
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