Zobrazeno 1 - 5
of 5
pro vyhledávání: '"C. Betard"'
Autor:
François Marceau, I Houde, Marcel Lebel, M Chevrette, Michelle Landry, C Betard, Dimcho Bachvarov, Isabelle Pelletier, J Bergeron
Publikováno v:
Scopus-Elsevier
On the basis of the genomic structure of the human B1 receptor (B1R) for kinins, the presence of possible allelic polymorphisms of this gene was investigated using restriction fragment-length polymorphism and single-strand conformation polymorphism.
Autor:
Ghislaine Roederer, Jacques Genest, Shiqiang Qiu, L. Karayan, Robert Dufour, Jean Davignon, C. Betard, Anne Minnich
Publikováno v:
Arteriosclerosis and Thrombosis: A Journal of Vascular Biology. 14:1258-1263
The 10-kb deletion ("French Canadian mutation") of the low-density lipoprotein (LDL) receptor gene is the most common mutation causing familial hypercholesterolemia among subjects of French Canadian descent. In affected subjects, it results in a null
Autor:
Anna M. Kessling, Madeleine Roy, Suzanne Lussier-Cacan, C. Betard, Ann Chamberland, Jean Davignon
Publikováno v:
Human Genetics. 88:529-536
Familial hypercholesterolemia (FH), at a prevalence of about 1 in 200 in the French-Canadian population, is caused by a 10-kb deletion in the low-density lipoprotein (LDL) receptor gene in 60% of French-Canadian FH heterozygotes. We genotyped 159 FH
Publikováno v:
Atherosclerosis. 119(1)
We investigated the associations between low density lipoprotein (LDL)-receptor gene haplotypes and lipid and lipoprotein levels in French-Canadian individuals with familial hypercholesterolemia (FH). The 112 unrelated patients studied shared the sam
Publikováno v:
Scopus-Elsevier
Structural and functional studies of the gene coding for the low density lipoprotein receptor in patients with familial hypercholesterolemia have uncovered over 180 mutant alleles of the gene. Although the classical familial hypercholesterolemia phen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14dfd152c89fe7f4e20d7c06f9d8e422
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http://www.scopus.com/inward/record.url?eid=2-s2.0-0028949479&partnerID=MN8TOARS