✦ LIBER ✦

Abnormal regulation of the LDL-R and HMG CoA reductase genes in subjects with familial hypercholesterolemia with the “French Canadian Mutation”

✍ Scribed by Yu, Lu; Qiu, Shiqiang; Genest, Jacques

Book ID: 123504565
Publisher: Elsevier Science
Year: 1996
Tongue: English
Weight: 282 KB
Volume: 27
Category: Article
ISSN: 1558-3597
DOI: 10.1016/S0735-1097(96)82469-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Coordinate regulation of expression of t

Coordinate regulation of expression of the LDL receptor and HMG-CoA reductase genes in heterozygous familial hypercholesterolemia with the ‘French Canadian’ mutation

✍ L. Yu; S. Qiu; J. Genest Jr. 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 150 KB

Liver transplantation in a subject with

Liver transplantation in a subject with familial hypercholesterolemia carrying the homozygous p.W577R LDL-receptor gene mutation

✍ Hartmut H-J. Schmidt; Uwe J.F. Tietge; Janine Buettner; Hannelore Barg-Hock; Gis 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 123 KB

Effect of atorvastatin on serum lipid pr

Effect of atorvastatin on serum lipid profile and HMG-CoA reductase gene expression in peripheral blood mononuclear cells in subjects with heterozygous familial hypercholesterolemia

✍ Salazar, L.A.; Hirata, M.H.; Forti, N.; Diament, J.; Giannini, S.D.; Hirata, R.D 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 314 KB

Mutation analysis in 36 unrelated Spanis

Mutation analysis in 36 unrelated Spanish subjects with familial hypercholesterolemia: Identification of 3 novel mutations in the LDL receptor gene

✍ Pilar Mozas; Ana Cenarro; Fernando Civeira; Sergio Castillo; Emilio Ros; Miguel 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 39 KB 👁 2 views

We used the single strand conformation polymorphism (SSCP) method to investigate 36 apparently unrelated Spanish patients with familial hypercholesterolemia (FH) for mutations in the promoter region and the 18 exons and their flanking intron sequences of the low density lipoprotein receptor (LDLR) g

Association of an Exon 3 Mutation (Trp66

Association of an Exon 3 Mutation (Trp66 → Gly) of the LDL Receptor with Variable Expression of Familial Hypercholesterolemia in a French Canadian Family

✍ Emile Levy; Anne Minnich; Suzanne Lussier Cacan; Louise Thibault; Louise-Marie G 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 152 KB

Impact of a common mutation of the LDL r

Impact of a common mutation of the LDL receptor gene, in French-Canadian patients with familial hypercholesterolemia, on means, variances and correlations among traits of lipid metabolism

✍ Madeleine Roy; Charles F. Sing; C. Betard; Jean Davignon 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 884 KB