Blanc H - Search Results

1

Sequence diversity in 36 candidate genes for cardiovascular disorders.

Cambien F, Poirier O, Nicaud V, Herrmann SM, Mallet C, Ricard S, Behague I, Hallet V, Blanc H, Loukaci V, Thillet J, Evans A, Ruidavets JB, Arveiler D, Luc G, Tiret L. Cambien F, et al. Among authors: blanc h. Am J Hum Genet. 1999 Jul;65(1):183-91. doi: 10.1086/302448. Am J Hum Genet. 1999. PMID: 10364531 Free PMC article.

2

Polymorphisms in the genes encoding platelet-derived growth factor A and alpha receptor.

Herrmann SM, Ricard S, Nicaud V, Brand E, Behague I, Blanc H, Ruidavets JB, Evans A, Arveiler D, Luc G, Poirier O, Cambien F. Herrmann SM, et al. Among authors: blanc h. J Mol Med (Berl). 2000;78(5):287-92. doi: 10.1007/s001090000111. J Mol Med (Berl). 2000. PMID: 10954201

3

The Gln/Arg polymorphism of human paraoxonase (PON 192) is not related to myocardial infarction in the ECTIM Study.

Herrmann SM, Blanc H, Poirier O, Arveiler D, Luc G, Evans A, Marques-Vidal P, Bard JM, Cambien F. Herrmann SM, et al. Among authors: blanc h. Atherosclerosis. 1996 Oct 25;126(2):299-303. doi: 10.1016/0021-9150(96)05917-5. Atherosclerosis. 1996. PMID: 8902155

4

Genetic determination of plasma aldosterone levels in essential hypertension.

Pojoga L, Gautier S, Blanc H, Guyene TT, Poirier O, Cambien F, Benetos A. Pojoga L, et al. Among authors: blanc h. Am J Hypertens. 1998 Jul;11(7):856-60. doi: 10.1016/s0895-7061(98)00048-x. Am J Hypertens. 1998. PMID: 9683048

5

Gene polymorphisms of the renin-angiotensin system in relation to hypertension and parental history of myocardial infarction and stroke: the PEGASE study. Projet d'Etude des Gènes de l'Hypertension Artérielle Sévère à modérée Essentielle.

Tiret L, Blanc H, Ruidavets JB, Arveiler D, Luc G, Jeunemaitre X, Tichet J, Mallet C, Poirier O, Plouin PF, Cambien F. Tiret L, et al. Among authors: blanc h. J Hypertens. 1998 Jan;16(1):37-44. doi: 10.1097/00004872-199816010-00007. J Hypertens. 1998. PMID: 9533415

6

FCRL3 -169CT functional polymorphism in type 1 diabetes and autoimmunity traits.

Duchatelet S, Caillat-Zucman S, Dubois-Laforgue D, Blanc H, Timsit J, Julier C. Duchatelet S, et al. Among authors: blanc h. Biomed Pharmacother. 2008 Mar;62(3):153-7. doi: 10.1016/j.biopha.2007.09.003. Epub 2007 Oct 8. Biomed Pharmacother. 2008. PMID: 17961971

7

Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.

Senée V, Chelala C, Duchatelet S, Feng D, Blanc H, Cossec JC, Charon C, Nicolino M, Boileau P, Cavener DR, Bougnères P, Taha D, Julier C. Senée V, et al. Among authors: blanc h. Nat Genet. 2006 Jun;38(6):682-7. doi: 10.1038/ng1802. Epub 2006 May 21. Nat Genet. 2006. PMID: 16715098

8

Amino acid change associated with the major polymorphic Hinc II site of Oriental and Caucasian mitochondrial DNAs.

Blanc H, Chen KH, D'Amore MA, Wallace DC. Blanc H, et al. Am J Hum Genet. 1983 Mar;35(2):167-76. Am J Hum Genet. 1983. PMID: 6301266 Free PMC article.

9

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.

Zalloua PA, Azar ST, Delépine M, Makhoul NJ, Blanc H, Sanyoura M, Lavergne A, Stankov K, Lemainque A, Baz P, Julier C. Zalloua PA, et al. Among authors: blanc h. Hum Mol Genet. 2008 Dec 15;17(24):4012-21. doi: 10.1093/hmg/ddn304. Epub 2008 Sep 20. Hum Mol Genet. 2008. PMID: 18806274

10

Maternal inheritance of human mitochondrial DNA.

Giles RE, Blanc H, Cann HM, Wallace DC. Giles RE, et al. Among authors: blanc h. Proc Natl Acad Sci U S A. 1980 Nov;77(11):6715-9. doi: 10.1073/pnas.77.11.6715. Proc Natl Acad Sci U S A. 1980. PMID: 6256757 Free PMC article.

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