Associated Papers
In the context of the triple burden of malnutrition: A systematic review of gene-diet interactions and nutritional status.
Tan PY et al.
Critical Reviews in Food Science and Nutrition, 2024
Polymorphisms in CPT1B and CPT2 have no significant effect on plasma carnitine levels in Japanese cancer patients.
Hishida A et al.
Nagoya Journal of Medical Science, 2019
Genetic Variation of Fatty Acid Oxidation and Obesity, A Literature Review.
Freitag Luglio H
International Journal of Biomedical Science : Ijbs, 2016
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
Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines.
Duan J et al.
Scientific Reports, 2013
23422947 (PubMed )
Supplement: srep01318-s2.xls › S7
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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