Associated Papers
Harnessing the paradoxical phenotypes of APOE ɛ2 and APOE ɛ4 to identify genetic modifiers in Alzheimer's disease.
Kim YW et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2021
33576571 (PubMed )
Supplement: ALZ-17-831-s002.xlsx › Table_S4
Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population.
Zhou S et al.
Plos One, 2015
Single nucleotide polymorphism in CPT1B and CPT2 genes and its association with blood carnitine levels in acute myocardial infarction patients.
Khan HA et al.
Gene, 2013
A common haplotype of carnitine palmitoyltransferase 1b is associated with the metabolic syndrome.
Auinger A et al.
The British Journal of Nutrition, 2013
Association of the CPT1B gene with skeletal muscle fat infiltration in Afro-Caribbean men.
Miljkovic I et al.
Obesity (silver Spring, Md.), 2009
Variants within the muscle and liver isoforms of the carnitine palmitoyltransferase I (CPT1) gene interact with fat intake to modulate indices of obesity in French-Canadians.
Robitaille J et al.
Journal of Molecular Medicine (berlin, Germany), 2007
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