Roederer G - Search Results

1

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, Julien P, Deeb S, Kastelein JJ, Peritz L, Devlin R, Bruin T, Murthy MR, et al. Monsalve MV, et al. Among authors: roederer g. J Clin Invest. 1990 Sep;86(3):728-34. doi: 10.1172/JCI114769. J Clin Invest. 1990. PMID: 1975597 Free PMC article.

2

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, et al. Ma Y, et al. Among authors: roederer g. Genomics. 1992 Jul;13(3):649-53. doi: 10.1016/0888-7543(92)90136-g. Genomics. 1992. PMID: 1639392

3

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 YH, Bruin T, Tuzgol S, Wilson BI, Roederer G, Liu MS, Davignon J, Kastelein JJ, Brunzell JD, Hayden MR. Ma YH, et al. Among authors: roederer g. J Biol Chem. 1992 Jan 25;267(3):1918-23. J Biol Chem. 1992. PMID: 1730727 Free article.

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, et al. Ma Y, et al. Among authors: roederer g. N Engl J Med. 1991 Jun 20;324(25):1761-6. doi: 10.1056/NEJM199106203242502. N Engl J Med. 1991. PMID: 2038366 Free article.

5

Genealogy and regional distribution of lipoprotein lipase deficiency in French-Canadians of Quebec.

Dionne C, Gagné C, Julien P, Murthy MR, Roederer G, Davignon J, Lambert M, Chitayat D, Ma R, Henderson H, et al. Dionne C, et al. Among authors: roederer g. Hum Biol. 1993 Feb;65(1):29-39. Hum Biol. 1993. PMID: 8436388

6

Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Québec, Canada).

Dionne C, Gagné C, Julien P, Murthy MR, Lambert M, Roederer G, Davignon J, Hayden MR, Lupien PJ, de Braekeleer M. Dionne C, et al. Among authors: roederer g. Ann Genet. 1992;35(2):89-92. Ann Genet. 1992. PMID: 1524414

7

Lipoprotein lipase gene mutations in coronary artery disease.

Minnich A, Baloukas J, Roederer G, Lussier-Cacan S, Davignon J, Genest J Jr. Minnich A, et al. Among authors: roederer g. Can J Cardiol. 1998 May;14(5):711-6. Can J Cardiol. 1998. PMID: 9627528

8

Response to HMG CoA reductase inhibitors in heterozygous familial hypercholesterolemia due to the 10-kb deletion ("French Canadian mutation") of the LDL receptor gene.

Karayan L, Qiu S, Betard C, Dufour R, Roederer G, Minnich A, Davignon J, Genest J Jr. Karayan L, et al. Among authors: roederer g. Arterioscler Thromb. 1994 Aug;14(8):1258-63. doi: 10.1161/01.atv.14.8.1258. Arterioscler Thromb. 1994. PMID: 8049186

9

G-->A substitution at position -75 of the apolipoprotein A-I gene promoter. Evidence against a direct effect on HDL cholesterol levels.

Minnich A, DeLangavant G, Lavigne J, Roederer G, Lussier-Cacan S, Davignon J. Minnich A, et al. Among authors: roederer g. Arterioscler Thromb Vasc Biol. 1995 Oct;15(10):1740-5. doi: 10.1161/01.atv.15.10.1740. Arterioscler Thromb Vasc Biol. 1995. PMID: 7583551

10

[Phenotype of apolipoprotein E, hyperlipidemia and atherosclerosis].

Davignon J, Roederer G. Davignon J, et al. Among authors: roederer g. Union Med Can. 1988 Feb 25;117(1):56-61. Union Med Can. 1988. PMID: 3376345 French. No abstract available.

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