Minnich A - Search Results

1

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: minnich a. Arterioscler Thromb. 1994 Aug;14(8):1258-63. doi: 10.1161/01.atv.14.8.1258. Arterioscler Thromb. 1994. PMID: 8049186

2

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. 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

3

New methods for rapid detection of low-density lipoprotein receptor and apolipoprotein B gene mutations causing familial hypercholesterolemia.

Minnich A, Roy M, Chamberland A, Lavigne J, Davignon J. Minnich A, et al. Clin Biochem. 1995 Jun;28(3):277-84. doi: 10.1016/0009-9120(94)00072-4. Clin Biochem. 1995. PMID: 7554246

4

Unexpected consequences of deletion of the first two repeats of the ligand-binding domain from the low density lipoprotein receptor. Evidence from a human mutation.

Sass C, Giroux LM, Lussier-Cacan S, Davignon J, Minnich A. Sass C, et al. Among authors: minnich a. J Biol Chem. 1995 Oct 20;270(42):25166-71. doi: 10.1074/jbc.270.42.25166. J Biol Chem. 1995. PMID: 7559651 Free article.

5

Evidence for a cholesterol-lowering gene in a French-Canadian kindred with familial hypercholesterolemia.

Sass C, Giroux LM, Ma Y, Roy M, Lavigne J, Lussier-Cacan S, Davignon J, Minnich A. Sass C, et al. Among authors: minnich a. Hum Genet. 1995 Jul;96(1):21-6. doi: 10.1007/BF00214181. Hum Genet. 1995. PMID: 7607649

6

Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridemic patients of French Canadian descent.

Minnich A, Kessling A, Roy M, Giry C, DeLangavant G, Lavigne J, Lussier-Cacan S, Davignon J. Minnich A, et al. J Lipid Res. 1995 Jan;36(1):117-24. J Lipid Res. 1995. PMID: 7706936 Free article.

7

Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defect.

Carmena R, Lussier-Cacan S, Roy M, Minnich A, Lingenhel A, Kronenberg F, Davignon J. Carmena R, et al. Among authors: minnich a. Arterioscler Thromb Vasc Biol. 1996 Jan;16(1):129-36. doi: 10.1161/01.atv.16.1.129. Arterioscler Thromb Vasc Biol. 1996. PMID: 8548413

8

Association of an exon 3 mutation (Trp66-->Gly) of the LDL receptor with variable expression of familial hypercholesterolemia in a French Canadian family.

Levy E, Minnich A, Cacan SL, Thibault L, Giroux LM, Davignon J, Lambert M. Levy E, et al. Among authors: minnich a. Biochem Mol Med. 1997 Feb;60(1):59-69. doi: 10.1006/bmme.1996.2549. Biochem Mol Med. 1997. PMID: 9066982

9

Coexisting dysbetalipoproteinemia and familial hypercholesterolemia. Clinical and laboratory observations.

Carmena R, Roy M, Roederer G, Minnich A, Davignon J. Carmena R, et al. Among authors: minnich a. Atherosclerosis. 2000 Jan;148(1):113-24. doi: 10.1016/s0021-9150(99)00212-9. Atherosclerosis. 2000. PMID: 10580177

10

Characterization of inherited scavenger receptor overexpression and abnormal macrophage phenotype in a normolipidemic subject with planar xanthomas.

Giry C, Giroux LM, Roy M, Davignon J, Minnich A. Giry C, et al. Among authors: minnich a. J Lipid Res. 1996 Jul;37(7):1422-35. J Lipid Res. 1996. PMID: 8827515 Free article.

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