-
1
-
-
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 et al. DNA variants at the LPL gene locus associate with angiographically-defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population. Arterioscler Thromb 1994; 14: 1090-7.
-
(1994)
Arterioscler Thromb
, vol.14
, pp. 1090-1097
-
-
Mattu, R.K.1
Needham, E.W.A.2
Morgan, R.3
-
2
-
-
0024791116
-
Organization of the human lipoprotein lipase gene and evolution of the lipase gene family
-
Kirchgessner TG, Chuat JC, Heinzmann C et al. Organization of the human lipoprotein lipase gene and evolution of the lipase gene family. Proc Natl Acad Sci USA 1989; 86: 9647-51.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 9647-9651
-
-
Kirchgessner, T.G.1
Chuat, J.C.2
Heinzmann, C.3
-
3
-
-
0024397097
-
Structure of the human lipoprotein lipase gene
-
Deeb SS, Peng R. Structure of the human lipoprotein lipase gene. Biochemistry 1989; 28: 4131-5.
-
(1989)
Biochemistry
, vol.28
, pp. 4131-4135
-
-
Deeb, S.S.1
Peng, R.2
-
5
-
-
0029808302
-
Premature atherosclerosis in patients with familial chylomicronaemia caused by mutations in the lipoprotein lipase gene
-
Benlian P, De Gennes JL, Foubert L, Zhang H, Gagne E, Hayden M. Premature atherosclerosis in patients with familial chylomicronaemia caused by mutations in the lipoprotein lipase gene. N Engl J Med 1996; 335: 848-54.
-
(1996)
N Engl J Med
, vol.335
, pp. 848-854
-
-
Benlian, P.1
De Gennes, J.L.2
Foubert, L.3
Zhang, H.4
Gagne, E.5
Hayden, M.6
-
6
-
-
0028980247
-
The mutant Asn291→Ser human lipoprotein lipase is associated with reduced catalytic activity and does not influence binding to heparin
-
Busca R, Peinado J, Vilella E et al. The mutant Asn291→Ser human lipoprotein lipase is associated with reduced catalytic activity and does not influence binding to heparin. FEBS Letts 1995; 367: 257-62.
-
(1995)
FEBS Letts
, vol.367
, pp. 257-262
-
-
Busca, R.1
Peinado, J.2
Vilella, E.3
-
7
-
-
0006635668
-
Type III hyperlipoproteinaemia in apo E2/E2 homozygotes: Possible role of mutations in the lipoprotein lipase gene
-
Ma Y, Zhang H, Liu MS, Frohlich J, Brunzell JD, Hayden MR. Type III hyperlipoproteinaemia in apo E2/E2 homozygotes: possible role of mutations in the lipoprotein lipase gene. Circulation (Suppl.) 1993; 88: I-I79.
-
(1993)
Circulation (Suppl.)
, vol.88
-
-
Ma, Y.1
Zhang, H.2
Liu, M.S.3
Frohlich, J.4
Brunzell, J.D.5
Hayden, M.R.6
-
8
-
-
0029130943
-
Patients with Apo E3 deficiency (E3/2, and E4/2) who manifest with hyperlipidaemia have increased frequency of an Asn291→Ser mutation in the human LPL gene
-
Zhang H, Reymer PWA, Liu MS et al. Patients with Apo E3 deficiency (E3/2, and E4/2) who manifest with hyperlipidaemia have increased frequency of an Asn291→Ser mutation in the human LPL gene. Arterioscler Thromb Vasc Biol 1995; 15: 1695-703.
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 1695-1703
-
-
Zhang, H.1
Reymer, P.W.A.2
Liu, M.S.3
-
9
-
-
0028853880
-
Interaction of the lipoprotein lipase asparagine 291→serine mutation with body mass index determines elevated plasma triacylglycerol concentrations: A study in hyperlipidemic subjects, myocardial infarction survivors and healthy adults
-
Fisher RM, Mailly F, Peacock RE et al. Interaction of the lipoprotein lipase asparagine 291→serine mutation with body mass index determines elevated plasma triacylglycerol concentrations: a study in hyperlipidemic subjects, myocardial infarction survivors and healthy adults. J Lipid Res 1995; 36: 2104-12.
-
(1995)
J Lipid Res
, vol.36
, pp. 2104-2112
-
-
Fisher, R.M.1
Mailly, F.2
Peacock, R.E.3
-
10
-
-
0029142759
-
A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidaemia
-
Reymer PWA, Groenemeyer BE, Gagne E et al. A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidaemia. Hum Mol Genet 1995; 4: 1543-9.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1543-1549
-
-
Reymer, P.W.A.1
Groenemeyer, B.E.2
Gagne, E.3
-
11
-
-
0029047717
-
A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis
-
Reymer PWA, Gagne E, Groenemeyer BE et al. A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis. Nat Genet 1995; 10: 28-33.
-
(1995)
Nat Genet
, vol.10
, pp. 28-33
-
-
Reymer, P.W.A.1
Gagne, E.2
Groenemeyer, B.E.3
-
12
-
-
0026428636
-
A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians
-
Ma Y, Henderson H, Murthy V et al. A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians. N Engl J Med 1991; 324: 1761-6.
-
(1991)
N Engl J Med
, vol.324
, pp. 1761-1766
-
-
Ma, Y.1
Henderson, H.2
Murthy, V.3
-
13
-
-
0030946073
-
Development of a direct DNA sequencing method for detecting heterozygous mutations of the human lipoprotein lipase gene
-
Mori A, Takagi A, Ikeda Y, Yamamoto A. Development of a direct DNA sequencing method for detecting heterozygous mutations of the human lipoprotein lipase gene. Clin Biochem 1997; 30: 315-24.
-
(1997)
Clin Biochem
, vol.30
, pp. 315-324
-
-
Mori, A.1
Takagi, A.2
Ikeda, Y.3
Yamamoto, A.4
-
14
-
-
0025239015
-
188) of human lipoprotein lipase imparting functional deficiency
-
188) of human lipoprotein lipase imparting functional deficiency. J Biol Chem 1990; 265: 5910-6.
-
(1990)
J Biol Chem
, vol.265
, pp. 5910-5916
-
-
Emi, M.1
Wilson, D.E.2
Iverius, P.H.3
-
15
-
-
0023665343
-
A rapid method for the purification of DNA from blood
-
Jeanpierre M. A rapid method for the purification of DNA from blood. Nucleic Acids Res 1987; 15: 9611.
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 9611
-
-
Jeanpierre, M.1
-
16
-
-
0023242425
-
An improved method for prenatal diagnosis of genetic diseases by analysis of amplified sequences; application to hemophilia A
-
Kogan SC, Doherty M, Gitschier J. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified sequences; application to hemophilia A. N Engl J Med 1987; 317: 985-90.
-
(1987)
N Engl J Med
, vol.317
, pp. 985-990
-
-
Kogan, S.C.1
Doherty, M.2
Gitschier, J.3
-
17
-
-
0023090942
-
Human lipoprotein lipase complementary DNA sequence
-
Wion KL, Kirchgessner TG, Lusis AJ, Schotz MC, Lawn RM. Human lipoprotein lipase complementary DNA sequence. Science 1987; 235: 1638-41.
-
(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
-
18
-
-
0028889944
-
Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridaemic patients of French Canadian descent
-
Minnich A, Kessling A, Roy M, Giry C, DeLangavant G, Lavinge J. Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridaemic patients of French Canadian descent. J Lipid Res 1995; 36: 117-24.
-
(1995)
J Lipid Res
, vol.36
, pp. 117-124
-
-
Minnich, A.1
Kessling, A.2
Roy, M.3
Giry, C.4
DeLangavant, G.5
Lavinge, J.6
-
19
-
-
0030896983
-
A common substitution (Asn291Ser) in lipoprotein lipase is associated with increased risk of ischaemic heart disease
-
Wittrup HH, Tybjaerg-Hansen A, Abildgaard S, Steffensen R, Schnohr P, Nordestgaard BJ. A common substitution (Asn291Ser) in lipoprotein lipase is associated with increased risk of ischaemic heart disease. J Clin Invest 1997; 99: 1606-13.
-
(1997)
J Clin Invest
, vol.99
, pp. 1606-1613
-
-
Wittrup, H.H.1
Tybjaerg-Hansen, A.2
Abildgaard, S.3
Steffensen, R.4
Schnohr, P.5
Nordestgaard, B.J.6
-
20
-
-
0028883699
-
Lipoprotein lipase gene polymorphisms: Associations with myocardial infarction and lipoprotein levels, the ECTIM study
-
Jemaa R, Fumeron F, Poirier O et al. Lipoprotein lipase gene polymorphisms: associations with myocardial infarction and lipoprotein levels, the ECTIM study. J Lipid Res 1995; 36: 2141-6.
-
(1995)
J Lipid Res
, vol.36
, pp. 2141-2146
-
-
Jemaa, R.1
Fumeron, F.2
Poirier, O.3
-
21
-
-
0026769994
-
A case-control study of lipoprotein particles in two populations at contrasting risk of coronary heart disease. The ECTIM study
-
Parra HJ, Arveiler D, Evans AE et al. A case-control study of lipoprotein particles in two populations at contrasting risk of coronary heart disease. The ECTIM study. Arterioscler Thromb 1992; 12: 701-7.
-
(1992)
Arterioscler Thromb
, vol.12
, pp. 701-707
-
-
Parra, H.J.1
Arveiler, D.2
Evans, A.E.3
-
22
-
-
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
-
23
-
-
0034183324
-
Relationship of abdominal adiposity and dyslipidemic status in women with a common mutation in the lipoprotein lipase gene
-
The REGICOR investigators
-
Senti M, Bosch M, Aubo C, Elosua R, Masia R, Marrugat J. Relationship of abdominal adiposity and dyslipidemic status in women with a common mutation in the lipoprotein lipase gene. The REGICOR investigators. Atherosclerosis 2000; 150: 135-41.
-
(2000)
Atherosclerosis
, vol.150
, pp. 135-141
-
-
Senti, M.1
Bosch, M.2
Aubo, C.3
Elosua, R.4
Masia, R.5
Marrugat, J.6
-
24
-
-
0027406054
-
Two DNA polymorphisms in the lipoprotein lipase gene and their associations with factors related to cardiovascular disease
-
Ahn YI, Kamboh MI, Hamman RF, Cole SA, Ferrell RE. Two DNA polymorphisms in the lipoprotein lipase gene and their associations with factors related to cardiovascular disease. J Lipid Res 1993; 34: 421-8.
-
(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
-
25
-
-
0029156010
-
Polymorphisms in the lipoprotein lipase gene and their associations with plasma lipid concentrations in 40-year-old Danish men
-
Gerdes C, Gerdes LU, Hansen PS, Faergemann O. Polymorphisms in the lipoprotein lipase gene and their associations with plasma lipid concentrations in 40-year-old Danish men. Circulation 1995; 92: 1765-9.
-
(1995)
Circulation
, vol.92
, pp. 1765-1769
-
-
Gerdes, C.1
Gerdes, L.U.2
Hansen, P.S.3
Faergemann, O.4
-
26
-
-
0036843805
-
Single-nucleotide polymorphisms in the lipoprotein lipase gene associated with coronary heart disease in Chinese
-
Su ZG, Zhang SZ, Hou YP et al. Single-nucleotide polymorphisms in the lipoprotein lipase gene associated with coronary heart disease in Chinese. Eur J Pharmacol 2002; 454: 9-18.
-
(2002)
Eur J Pharmacol
, vol.454
, pp. 9-18
-
-
Su, Z.G.1
Zhang, S.Z.2
Hou, Y.P.3
-
27
-
-
0028937522
-
DNA polymorphisms at the lipoprotein lipase gene are associated with microangiopathy in type 2 (noninsulin-dependent) diabetes mellitus
-
Ukkola O, Savolainen MJ, Salmela PI, von Dickhoff K, Kesaniemi YA. DNA polymorphisms at the lipoprotein lipase gene are associated with microangiopathy in type 2 (noninsulin-dependent) diabetes mellitus. Atherosclerosis 1995; 115: 99-105.
-
(1995)
Atherosclerosis
, vol.115
, pp. 99-105
-
-
Ukkola, O.1
Savolainen, M.J.2
Salmela, P.I.3
Von Dickhoff, K.4
Kesaniemi, Y.A.5
-
28
-
-
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 et al. Detection of three separate DNA polymorphisms in the human lipoprotein lipase gene by gene amplification and restriction endonuclease digestion. J Lipid Res 1992; 33: 1067-72.
-
(1992)
J Lipid Res
, vol.33
, pp. 1067-1072
-
-
Gotoda, T.1
Yamada, N.2
Murase, T.3
-
29
-
-
0028167760
-
Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia
-
Gagne E, Genest J, Zhang H, Clarke LA, Hayden MR. Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia. Arterioscler Thromb 1994; 14: 1250-7.
-
(1994)
Arterioscler Thromb
, vol.14
, pp. 1250-1257
-
-
Gagne, E.1
Genest, J.2
Zhang, H.3
Clarke, L.A.4
Hayden, M.R.5
-
30
-
-
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 MV, Henderson H, Roederer G et al. 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 1990; 86: 728-34.
-
(1990)
J Clin Invest
, vol.86
, pp. 728-734
-
-
Monsalve, M.V.1
Henderson, H.2
Roederer, G.3
|