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Cytogenetics and Cell Genetics|June 1, 2000
Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35M van Geel, J C van Deutekom, A van Staalduinen, et al.The Journal of Biological Chemistry|November 29, 1996
In the absence of endogenous mouse apolipoprotein E, apolipoprotein E*2(Arg-158 --> Cys) transgenic mice develop more severe hyperlipoproteinemia than apolipoprotein E*3-Leiden transgenic miceB J van Vlijmen, K W van Dijk, H B van't Hof, et al.Human Molecular Genetics|May 1, 1996
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35J C van Deutekom, R J Lemmers, P K Grewal, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|July 15, 2000
Apolipoprotein E2 (Lys146-->Gln) causes hypertriglyceridemia due to an apolipoprotein E variant-specific inhibition of lipolysis of very low density lipoproteins-triglyceridesF de Beer, K W van Dijk, M C Jong, et al.Atherosclerosis|November 24, 1999
Macrophage specific overexpression of the human macrophage scavenger receptor in transgenic mice, using a 180-kb yeast artificial chromosome, leads to enhanced foam cell formation of isolated peritoneal macrophagesM P de Winther, K W van Dijk, B J van Vlijmen, et al.Nutrition & Diabetes|February 10, 2015
Determining the association between adipokine expression in multiple tissues and phenotypic features of non-alcoholic fatty liver disease in obesityM G M Wolfs, N Gruben, S S Rensen, et al.Cell|November 1, 1996
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4R A Ophoff, G M Terwindt, M N Vergouwe, et al.Diabetologia|October 23, 2009
Genetic association analysis of LARS2 with type 2 diabetesE Reiling, B Jafar-Mohammadi, E van 't Riet, et al.Pageof 11