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Scholar Results 1 - 5 of 5 citing Malhotra: Meta-analysis of genome-wide linkage studies of quantitative lipid traits in families.... (0.10 sec) 

Variants in the CD36 gene associate with the metabolic syndrome and high-density …

- oxfordjournals.org
L Love-Gregory, R Sherva, L Sun, J Wasson, … - Human molecular genetics, 2008 - Oxford Univ Press
A region along chromosome 7q was recently linked to components of the metabolic
syndrome (MetS) in several genome-wide linkage studies. Within this region, the
CD36 gene, which encodes a membrane receptor for long-chain fatty acids and ...
Cited by 16 - Related articles - BL Direct - All 9 versions

A genome-wide linkage scan identifies multiple chromosomal regions influencing serum lipid …

- nih.gov
K Aberg, F Dai, G Sun, ED Keighley, SR … - J Lipid Res, 2008 - ASBMB
Page 1. Abbreviations used in the text: total cholesterol (TC), triglyceride
(TG), logarithm of the odds (LOD), cardiovascular disease ...
Cited by 8 - Related articles - All 6 versions

Cellular fatty acid uptake: a pathway under construction

- wustl.edu [PDF] 
X Su, NA Abumrad - Trends in Endocrinology & Metabolism, 2009 - Elsevier
Membrane uptake of long-chain fatty acids (FAs) is the first step in cellular FA
utilization and a point of metabolic regulation. CD36 facilitates a major
fraction of FA uptake by key tissues. This review highlights the ...
Cited by 4 - Related articles - All 10 versions

Genome-wide linkage scan for genes influencing plasma triglyceride levels in the Veterans …


DK Coletta, J Schneider, SL Hu, TD Dyer, S … - Diabetes, 2009 - Am Diabetes Assoc
RESULTS—After adjusting for the significant effects of sex and BMI,
heritability for plasma triglycerides was estimated as 46 ± 7% (P < 0.0001).
Multipoint linkage analysis yielded the strongest evidence for linkage of ...
Cited by 2 - Related articles - All 3 versions

Variants in the FFAR1 gene are associated with beta cell function


M Kalis, P Levéen, V Lyssenko, P Almgren, L … - PLoS ONE, 2007 - pubmedcentral.nih.gov
We re-sequenced the FFAR1 region in 96 subjects (48 healthy and 48 T2D
individuals) and found 13 single nucleotide polymorphisms (SNPs) 8 of which were
not previously described. Two SNPs located in the upstream region of the ...
Cited by 2 - Related articles - All 7 versions


 


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