Published in Appl Physiol Nutr Metab on June 01, 2007
Decreased mitochondrial proton leak and reduced expression of uncoupling protein 3 in skeletal muscle of obese diet-resistant women. Diabetes (2002) 1.10
Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption. Basic Res Cardiol (2010) 1.03
Lamin A/C and cardiac diseases. Curr Opin Cardiol (2006) 0.99
Peroxisome proliferator-activated receptor gamma 2 and acyl-CoA synthetase 5 polymorphisms influence diet response. Obesity (Silver Spring) (2007) 0.93
Sequence analysis of coding and 3' and 5' flanking regions of the epithelial sodium channel alpha, beta, and gamma genes in Dahl S versus R rats. BMC Genet (2007) 0.88
Specific contribution of lamin A and lamin C in the development of laminopathies. Exp Cell Res (2008) 0.85
Functional characterization of a promoter polymorphism that drives ACSL5 gene expression in skeletal muscle and associates with diet-induced weight loss. FASEB J (2009) 0.84
Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation. J Neurol Sci (2008) 0.82
Enhanced expression of epithelial sodium channels in the renal medulla of Dahl S rats. Can J Physiol Pharmacol (2011) 0.80
Lamin A/C mutants disturb sumo1 localization and sumoylation in vitro and in vivo. PLoS One (2012) 0.79
Gene-environment interaction and the metabolic syndrome. Novartis Found Symp (2008) 0.79
Effects of exercise training on molecular markers of lipogenesis and lipid partitioning in fructose-induced liver fat accumulation. J Nutr Metab (2011) 0.79
The TaqIA RFLP is associated with attenuated intervention-induced body weight loss and increased carbohydrate intake in post-menopausal obese women. Appetite (2012) 0.78
Still building on candidate-gene strategy in hypertension? Hypertension (2007) 0.77
A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlation. J Hum Genet (2010) 0.76