112 related articles for article (PubMed ID: 9452071)
1. Dyslipidemias associated with heterozygous lipoprotein lipase mutations in the French-Canadian population.
Julien P; Gagné C; Murthy MR; Lévesque G; Moorjani S; Cadelis F; Hayden MR; Lupien PJ
Hum Mutat; 1998; Suppl 1():S148-53. PubMed ID: 9452071
[No Abstract] [Full Text] [Related]
2. 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 PH; Lalouel JM
Am J Hum Genet; 1990 Oct; 47(4):721-6. PubMed ID: 2121025
[TBL] [Abstract][Full Text] [Related]
3. Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia.
Hoffer MJ; Bredie SJ; Snieder H; Reymer PW; Demacker PN; Havekes LM; Boomsma DI; Stalenhoef AF; Frants RR; Kastelein JJ
Atherosclerosis; 1998 May; 138(1):91-9. PubMed ID: 9678774
[TBL] [Abstract][Full Text] [Related]
4. A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians.
Ma Y; Henderson HE; Murthy V; Roederer G; Monsalve MV; Clarke LA; Normand T; Julien P; Gagné C; Lambert M
N Engl J Med; 1991 Jun; 324(25):1761-6. PubMed ID: 2038366
[TBL] [Abstract][Full Text] [Related]
5. The common mutations in the lipoprotein lipase gene in Italy: effects on plasma lipids and angiographically assessed coronary atherosclerosis.
Arca M; Campagna F; Montali A; Barillà F; Mangieri E; Tanzilli G; Seccareccia F; Campa PP; Ricci G; Pannitteri G
Clin Genet; 2000 Nov; 58(5):369-74. PubMed ID: 11140837
[TBL] [Abstract][Full Text] [Related]
6. Lipoprotein lipase gene mutations in coronary artery disease.
Minnich A; Baloukas J; Roederer G; Lussier-Cacan S; Davignon J; Genest J
Can J Cardiol; 1998 May; 14(5):711-6. PubMed ID: 9627528
[TBL] [Abstract][Full Text] [Related]
7. Compound heterozygosity for frameshift mutations in the gene for lipoprotein lipase in a patient with early-onset chylomicronemia.
Foubert L; De Gennes JL; Benlian P; Truffert J; Miao L; Hayden MR
Hum Mutat; 1998; Suppl 1():S141-4. PubMed ID: 9452069
[No Abstract] [Full Text] [Related]
8. Hyperlipidemia and pancreatitis during pregnancy in two sisters with a mutation in the lipoprotein lipase gene.
Keilson LM; Vary CP; Sprecher DL; Renfrew R
Ann Intern Med; 1996 Feb; 124(4):425-8. PubMed ID: 8554252
[TBL] [Abstract][Full Text] [Related]
9. A missense mutation (Asp250----Asn) in exon 6 of the human lipoprotein lipase gene causes chylomicronemia in patients of different ancestries.
Ma Y; Wilson BI; Bijvoet S; Henderson HE; Cramb E; Roederer G; Ven Murthy MR; Julien P; Bakker HD; Kastelein JJ
Genomics; 1992 Jul; 13(3):649-53. PubMed ID: 1639392
[TBL] [Abstract][Full Text] [Related]
10. Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene.
Wood S; Schertzer M; Hayden M; Ma Y
Hum Genet; 1993 May; 91(4):312-6. PubMed ID: 8099055
[TBL] [Abstract][Full Text] [Related]
11. Lipoprotein lipase activity in heterozygotes for lipoprotein lipase gene mutations reveals a gender bias.
Murase T; Ebara T; Okubo M
Ann Clin Biochem; 2014 Mar; 51(Pt 2):294-7. PubMed ID: 24081181
[TBL] [Abstract][Full Text] [Related]
12. Heterozygous lipoprotein lipase deficiency: frequency in the general population, effect on plasma lipid levels, and risk of ischemic heart disease.
Nordestgaard BG; Abildgaard S; Wittrup HH; Steffensen R; Jensen G; Tybjaerg-Hansen A
Circulation; 1997 Sep; 96(6):1737-44. PubMed ID: 9323055
[TBL] [Abstract][Full Text] [Related]
13. Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Québec.
Normand T; Bergeron J; Fernandez-Margallo T; Bharucha A; Ven Murthy MR; Julien P; Gagné C; Dionne C; De Braekeleer M; Ma R
Hum Genet; 1992 Aug; 89(6):671-5. PubMed ID: 1511985
[TBL] [Abstract][Full Text] [Related]
14. Identification of compound heterozygous mutations (G188E/W382X) of lipoprotein lipase gene in a Japanese infant with hyperchylomicronemia: the G188E mutation was newly identified in Japanese.
Takagi A; Ikeda Y; Tachi K; Shinozuka T; Yamamoto A
Clin Chim Acta; 1999 Jul; 285(1-2):143-54. PubMed ID: 10481930
[TBL] [Abstract][Full Text] [Related]
15. Extreme diabetic lipaemia associated with a novel lipoprotein lipase gene mutation.
McLean AG; Petersons CJ; Hooper AJ; Burnett JR; Burt MG; Doogue MP
Clin Chim Acta; 2009 Aug; 406(1-2):167-9. PubMed ID: 19447100
[TBL] [Abstract][Full Text] [Related]
16. Assessment of French patients with LPL deficiency for French Canadian mutations.
Foubert L; De Gennes JL; Lagarde JP; Ehrenborg E; Raisonnier A; Girardet JP; Hayden MR; Benlian P
J Med Genet; 1997 Aug; 34(8):672-5. PubMed ID: 9279761
[TBL] [Abstract][Full Text] [Related]
17. Screening for a D9N common mutation in exon 2 of the LPL gene in Thai normolipidemic and hyperlipidemic subjects.
Tirawanchai N; Yamwong P; Pongrapeeporn KU; Likidlilid A; Ong-Ajyooth S; Amornrattana A
J Med Assoc Thai; 2000 Nov; 83 Suppl 2():S54-60. PubMed ID: 11194022
[TBL] [Abstract][Full Text] [Related]
18. Genetics of type III hyperlipoproteinemia.
Feussner G; Piesch S; Dobmeyer J; Fischer C
Genet Epidemiol; 1997; 14(3):283-97. PubMed ID: 9181357
[TBL] [Abstract][Full Text] [Related]
19. Pancreatitis in a child with lipemia due to novel lipoprotein lipase mutations.
Gupta N; Moore D; Hooper AJ; Burnett JR; Metz M
J Pediatr Gastroenterol Nutr; 2010 Apr; 50(4):457-9. PubMed ID: 20179640
[No Abstract] [Full Text] [Related]
20. Detection of missense mutations in the genes for lipoprotein lipase and hepatic triglyceride lipase in patients with dyslipidemia undergoing coronary angiography.
Moennig G; Wiebusch H; Enbergs A; Dorszewski A; Kerber S; Schulte H; Vielhauer C; Haverkamp W; Assmann G; Breithardt G; Funke H
Atherosclerosis; 2000 Apr; 149(2):395-401. PubMed ID: 10729390
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
