-
1
-
-
0002330773
-
Familial lipoprotein lipase deficiency and other causes of chylomicronemia syndrome
-
Stanbury JB, Wyngaarden JB, Fredrickson DS, Goldstein JL, Brown MS, Eds. New York: McGraw-Hill
-
Brunzell JD. Familial lipoprotein lipase deficiency and other causes of chylomicronemia syndrome: In: Stanbury JB, Wyngaarden JB, Fredrickson DS, Goldstein JL, Brown MS, Eds. The metabolic basis of inherited disease. 6th ed. New York: McGraw-Hill Pp. 1165-80; 1986.
-
(1986)
The Metabolic Basis of Inherited Disease. 6th Ed.
, pp. 1165-1180
-
-
Brunzell, J.D.1
-
2
-
-
0024397097
-
Structure of the human lipoprotein lipase gene
-
Deeb SS, Peng R. Structure of the human lipoprotein lipase gene. Biochemistry 1989; 28: 4132-5.
-
(1989)
Biochemistry
, vol.28
, pp. 4132-4135
-
-
Deeb, S.S.1
Peng, R.2
-
3
-
-
0025289589
-
Structure and polymorphic map of human lipoprotein lipase gene
-
Oka K, Tkalcevic GT, Nakano T, Tucker H, Ishimura-Oka K, Brown WV. Structure and polymorphic map of human lipoprotein lipase gene. Biochim Biophys Acta 1990; 1049: 21-6.
-
(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
-
4
-
-
0028174814
-
DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population
-
Mattu RK, Needham EWA, Morgan R, Rees A, Hackshaw AK, Stocks J, Elwood PC, Galton DJ. DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population. Atheroscler Thromb 1994; 14: 1090-7.
-
(1994)
Atheroscler Thromb
, vol.14
, pp. 1090-1097
-
-
Mattu, R.K.1
Needham, E.W.A.2
Morgan, R.3
Rees, A.4
Hackshaw, A.K.5
Stocks, J.6
Elwood, P.C.7
Galton, D.J.8
-
5
-
-
0024438108
-
DNA polymorphisms at the lipoprotein lipase gene: Associations in normal and hypertriglyceridaemic subjects
-
Chamberlain JC, Thorn JA, Oka K, Galton DJ, Stocks J. DNA polymorphisms at the lipoprotein lipase gene: associations in normal and hypertriglyceridaemic subjects. Atherosclerosis 1989; 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
-
6
-
-
0025845830
-
DNA polymorphism haplotypes of the human lipoprotein lipase gene: Possible association with high density lipoprotein levels
-
Heinzmann C, Kirchgessner T, Kwiterovitch PO, Ladias JA, Derby C, Antonarakis SE, Lusis AJ. DNA polymorphism haplotypes of the human lipoprotein lipase gene: possible association with high density lipoprotein levels. Hum Gen 1991; 86: 578-84.
-
(1991)
Hum Gen
, vol.86
, pp. 578-584
-
-
Heinzmann, C.1
Kirchgessner, T.2
Kwiterovitch, P.O.3
Ladias, J.A.4
Derby, C.5
Antonarakis, S.E.6
Lusis, A.J.7
-
8
-
-
0025241155
-
Lipoprotein and hepatic lipase gene variants in coronary atherosclerosis
-
Thorn JA, Chamberlain JC, Alcolado JC, Oka K, Chan L, Stocks J, Galton DJ. Lipoprotein and hepatic lipase gene variants in coronary atherosclerosis. Atherosclerosis 1990; 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
-
9
-
-
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, Lalouel JM. 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. Nucleic Acids Res 1990; 18: 5407-10.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 5407-5410
-
-
Hata, A.1
Robertson, M.2
Emi, M.3
Lalouel, J.M.4
-
10
-
-
0028175553
-
A gene-gender interaction affecting plasma lipoproteins in a genetic isolate
-
Hegele RA, Evans AJ, Tu L, Ip G, Brunt JH, Connelly PW. A gene-gender interaction affecting plasma lipoproteins in a genetic isolate. Arterioscler Thromb 1994; 14: 671-8.
-
(1994)
Arterioscler Thromb
, vol.14
, pp. 671-678
-
-
Hegele, R.A.1
Evans, A.J.2
Tu, L.3
Ip, G.4
Brunt, J.H.5
Connelly, P.W.6
-
11
-
-
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, Yamada N. Mutational analysis of human lipoprotein lipase by carboxy-terminal truncation. J Lipid Res 1993; 34: 1765-72.
-
(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
-
12
-
-
0026337222
-
447 → Ter) in a Turkish family
-
447 → Ter) in a Turkish Family. J Biol Chem 1991; 266: 14418-24.
-
(1991)
J Biol Chem
, vol.266
, pp. 14418-14424
-
-
Faustinella, F.1
Chang, A.2
Biervlie, J.P.V.3
Rosseneu, M.4
Vinaimont, N.5
Smith, L.C.6
Chen, S.7
Chan, L.8
-
13
-
-
0026639516
-
Lipoprotein lipase genotypes for a common premature termination codon mutation detected by PCR-mediated site directed mutagenesis and restriction digestion
-
Stocks J, Thorn JA, Galton DJ. Lipoprotein lipase genotypes for a common premature termination codon mutation detected by PCR-mediated site directed mutagenesis and restriction digestion. J Lipid Res 1992; 33: 853-7.
-
(1992)
J Lipid Res
, vol.33
, pp. 853-857
-
-
Stocks, J.1
Thorn, J.A.2
Galton, D.J.3
-
14
-
-
0026501648
-
A heterozygous mutation (the codon for Ser 447 ≥ a stop codon) in lipoprotein lipase contributes to a defect in lipid interface recognition in a case with type 1 hyperlipidemia
-
Kobayashi J, Nishida T, Ameis D, Stahnke G, Schotz MC, Hashimoto T, Fukamachi I, Yasushi S, Yoshida S. A heterozygous mutation (the codon for Ser 447 ≥ a stop codon) in lipoprotein lipase contributes to a defect in lipid interface recognition in a case with type 1 hyperlipidemia. Biochem Biophys Res Commun 1992; 182: 70-7.
-
(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, T.6
Fukamachi, I.7
Yasushi, S.8
Yoshida, S.9
-
15
-
-
0343660068
-
PCR assay for a polymorphic PvuII site in the LPL gene
-
Johnson JP, Nishina PM, Naggert JK. PCR assay for a polymorphic PvuII site in the LPL gene. Nucleic Acids Res 1992; 18(24): 1769.
-
(1992)
Nucleic Acids Res
, vol.18
, Issue.24
, pp. 1769
-
-
Johnson, J.P.1
Nishina, P.M.2
Naggert, J.K.3
-
16
-
-
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, Bruin T, Tuzgo S, Wilson BI, Roederer G, Liu M-S, Davignon J, Kastelein JJP, Brunzell JD, Hayden MR. 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 1992; 267: 1918-23.
-
(1992)
J Biol Chem
, vol.267
, pp. 1918-1923
-
-
Ma, Y.1
Bruin, T.2
Tuzgo, S.3
Wilson, B.I.4
Roederer, G.5
Liu, M.-S.6
Davignon, J.7
Kastelein, J.J.P.8
Brunzell, J.D.9
Hayden, M.R.10
|