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V Meiner

Showing results (31-40 of 42) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 30, 2018
Role of late amniocentesis in the era of modern genomic technologiesH Daum, A Ben David, M Nadjari, et al.
Human Genetics|March 1, 1993
A missense mutation in the low density lipoprotein receptor gene causes familial hypercholesterolemia in Sephardic JewsE Leitersdorf, A Reshef, V Meiner, et al.
European Journal of Clinical Pharmacology|January 1, 1993
Efficacy and safety of high dose fluvastatin in patients with familial hypercholesterolaemiaE Leitersdorf, S Eisenberg, O Eliav, et al.
The Journal of Clinical Investigation|June 1, 1993
Frameshift and splice-junction mutations in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis in Jews or Moroccan originE Leitersdorf, A Reshef, V Meiner, et al.
Journal of Lipid Research|November 5, 1997
Tissue expression studies on the mouse acyl-CoA: cholesterol acyltransferase gene (Acact): findings supporting the existence of multiple cholesterol esterification enzymes in miceV Meiner, C Tam, M D Gunn, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 24, 2020
Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnanciesS Stern, N Hacohen, V Meiner, et al.
American Journal of Human Genetics|August 1, 1991
A common Lithuanian mutation causing familial hypercholesterolemia in Ashkenazi JewsV Meiner, D Landsberger, N Berkman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2001
Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type CV Meiner, S Shpitzen, H Mandel, et al.
Atherosclerosis|February 10, 2006
The discrete and combined effect of SREBP-2 and SCAP isoforms in the control of plasma lipids among familial hypercholesterolaemia patientsR Durst, A Jansen, G Erez, et al.
International Journal of Obesity (2005)|November 3, 2010
Phenotypic and genetic variation in leptin as determinants of weight regainG Erez, A Tirosh, A Rudich, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 30, 2018
Role of late amniocentesis in the era of modern genomic technologiesH Daum, A Ben David, M Nadjari, et al.
Human Genetics|March 1, 1993
A missense mutation in the low density lipoprotein receptor gene causes familial hypercholesterolemia in Sephardic JewsE Leitersdorf, A Reshef, V Meiner, et al.
European Journal of Clinical Pharmacology|January 1, 1993
Efficacy and safety of high dose fluvastatin in patients with familial hypercholesterolaemiaE Leitersdorf, S Eisenberg, O Eliav, et al.
The Journal of Clinical Investigation|June 1, 1993
Frameshift and splice-junction mutations in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis in Jews or Moroccan originE Leitersdorf, A Reshef, V Meiner, et al.
Journal of Lipid Research|November 5, 1997
Tissue expression studies on the mouse acyl-CoA: cholesterol acyltransferase gene (Acact): findings supporting the existence of multiple cholesterol esterification enzymes in miceV Meiner, C Tam, M D Gunn, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 24, 2020
Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnanciesS Stern, N Hacohen, V Meiner, et al.
American Journal of Human Genetics|August 1, 1991
A common Lithuanian mutation causing familial hypercholesterolemia in Ashkenazi JewsV Meiner, D Landsberger, N Berkman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2001
Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type CV Meiner, S Shpitzen, H Mandel, et al.
Atherosclerosis|February 10, 2006
The discrete and combined effect of SREBP-2 and SCAP isoforms in the control of plasma lipids among familial hypercholesterolaemia patientsR Durst, A Jansen, G Erez, et al.
International Journal of Obesity (2005)|November 3, 2010
Phenotypic and genetic variation in leptin as determinants of weight regainG Erez, A Tirosh, A Rudich, et al.
Pageof 5