Meiner V - Search Results

1

The association of common SNPs and haplotypes in the CETP and MDR1 genes with lipids response to fluvastatin in familial hypercholesterolemia.

Bercovich D, Friedlander Y, Korem S, Houminer A, Hoffman A, Kleinberg L, Shochat C, Leitersdorf E, Meiner V. Bercovich D, et al. Among authors: meiner v. Atherosclerosis. 2006 Mar;185(1):97-107. doi: 10.1016/j.atherosclerosis.2005.05.025. Epub 2005 Jul 5. Atherosclerosis. 2006. PMID: 16002074 Clinical Trial.

2

Explanations for the discrepancy between variant frequency and homozygous disease occurrence: Lessons from Ashkenazi Jewish data.

Zlotogora J, Harel T, Meiner V. Zlotogora J, et al. Among authors: meiner v. Eur J Med Genet. 2023 Jun;66(6):104765. doi: 10.1016/j.ejmg.2023.104765. Epub 2023 Apr 6. Eur J Med Genet. 2023. PMID: 37028505 Review.

3

Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews.

Birnbaum R, Ezer S, Lotan NS, Eilat A, Sternlicht K, Benyamini L, Reish O, Falik-Zaccai T, Ben-Gad G, Rod R, Segel R, Kim K, Burton B, Keegan CE, Wagner M, Henderson LB, Mor N, Barel O, Hirsch Y, Meiner V, Elpeleg O, Harel T, Mor-Shakad H. Birnbaum R, et al. Among authors: meiner v. J Med Genet. 2024 Feb 21;61(3):289-293. doi: 10.1136/jmg-2023-109504. J Med Genet. 2024. PMID: 37833060

4

Human sterol 27-hydroxylase (CYP27) overexpressor transgenic mouse model. Evidence against 27-hydroxycholesterol as a critical regulator of cholesterol homeostasis.

Meir K, Kitsberg D, Alkalay I, Szafer F, Rosen H, Shpitzen S, Avi LB, Staels B, Fievet C, Meiner V, Björkhem I, Leitersdorf E. Meir K, et al. Among authors: meiner v. J Biol Chem. 2002 Sep 13;277(37):34036-41. doi: 10.1074/jbc.M201122200. Epub 2002 Jul 15. J Biol Chem. 2002. PMID: 12119285 Free article.

5

Identification of a novel mutation in the gene for bone morphogenetic protein receptor II in an Israeli patient with familial primary pulmonary hypertension.

Cahn A, Meiner V, Leitersdorf E, Berkman N. Cahn A, et al. Among authors: meiner v. Isr Med Assoc J. 2004 Mar;6(3):156-9. Isr Med Assoc J. 2004. PMID: 15055271 Free article.

6

Apolipoprotein E genotyping: accurate, simple, high throughput method using ABI Prism SNaPshot Multiplex System.

Ben-Avi L, Durst R, Shpitzen S, Leitersdorf E, Meiner V. Ben-Avi L, et al. Among authors: meiner v. J Alzheimers Dis. 2004 Oct;6(5):497-501. doi: 10.3233/jad-2004-6506. J Alzheimers Dis. 2004. PMID: 15505371 Clinical Trial.

7

SREBP-2 and SCAP isoforms and risk of early onset myocardial infarction.

Friedlander Y, Schwartz SM, Durst R, Meiner V, Robertson AS, Erez G, Leitersdorf E, Siscovick DS. Friedlander Y, et al. Among authors: meiner v. Atherosclerosis. 2008 Feb;196(2):896-904. doi: 10.1016/j.atherosclerosis.2007.02.006. Epub 2007 Mar 26. Atherosclerosis. 2008. PMID: 17383658

8

Rifampicin-induced CYP3A4 activation in CTX patients cannot replace chenodeoxycholic acid treatment.

Szalat A, Gershkovich P, Ben-Ari A, Shaish A, Liberman Y, Boutboul E, Gotkine M, Hoffman A, Harats D, Leitersdorf E, Meiner V. Szalat A, et al. Among authors: meiner v. Biochim Biophys Acta. 2007 Jul;1771(7):839-44. doi: 10.1016/j.bbalip.2007.04.012. Epub 2007 May 1. Biochim Biophys Acta. 2007. PMID: 17553741 Clinical Trial.

9

Leptin, insulin, and obesity-related phenotypes: genetic influences on levels and longitudinal changes.

Friedlander Y, Meiner V, Sharon N, Siscovick DS, Miserez AR. Friedlander Y, et al. Among authors: meiner v. Obesity (Silver Spring). 2009 Jul;17(7):1458-60. doi: 10.1038/oby.2008.672. Epub 2009 Feb 12. Obesity (Silver Spring). 2009. PMID: 19214176 Free article.

10

Increased risk for atherosclerosis of various macrophage scavenger receptor 1 alleles.

Durst R, Neumark Y, Meiner V, Friedlander Y, Sharon N, Polak A, Beeri R, Danenberg H, Erez G, Spitzen S, Ben-Avi L, Leitersdorf E, Lotan C. Durst R, et al. Among authors: meiner v. Genet Test Mol Biomarkers. 2009 Oct;13(5):583-7. doi: 10.1089/gtmb.2009.0048. Genet Test Mol Biomarkers. 2009. PMID: 19715475

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