Evidence for an association between infant mortality and homozygosity for the arctic variant of carnitine palmitoyltransferase 1A

A Selective Sweep on a Deleterious Mutation in CPT1A in Arctic Populations

(2014) Florian J. Clemente et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Association of a Genetic Variant of Carnitine Palmitoyltransferase 1A with Infections in Alaska Native Children

(2013) Bradford D. Gessner et al.   JOURNAL OF PEDIATRICS

Carnitine Palmitoyltransferase I and Sudden Unexpected Infant Death in British Columbia First Nations

(2012) G. B. Sinclair et al.   PEDIATRICS

Associations of obesity with triglycerides and C-reactive protein are attenuated in adults with high red blood cell eicosapentaenoic and docosahexaenoic acids

(2011) Z Makhoul et al.   EUROPEAN JOURNAL OF CLINICAL NUTRITION

Mitochondrial Respiratory Capacity Is a Critical Regulator of CD8+ T Cell Memory Development

(2011) Gerritje J.W. van der Windt et al.   IMMUNITY

Genetic polymorphisms incarnitine palmitoyltransferase 1Agene are associated with variation in body composition and fasting lipid traits in Yup'ik Eskimos

(2011) Dominick J. Lemas et al.   JOURNAL OF LIPID RESEARCH

Impaired fasting tolerance among Alaska native children with a common carnitine palmitoyltransferase 1A sequence variant

(2011) Melanie B. Gillingham et al.   MOLECULAR GENETICS AND METABOLISM

Associations of very high intakes of eicosapentaenoic and docosahexaenoic acids with biomarkers of chronic disease risk among Yup’ik Eskimos

(2010) Zeina Makhoul et al.   AMERICAN JOURNAL OF CLINICAL NUTRITION

Prevalence and Distribution of the c.1436C→T Sequence Variant of Carnitine Palmitoyltransferase 1A among Alaska Native Infants

(2010) Bradford D. Gessner et al.   JOURNAL OF PEDIATRICS

Carnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and Nunavut

(2010) Sorcha A. Collins et al.   MOLECULAR GENETICS AND METABOLISM

Evidence for an Association Between Infant Mortality and a Carnitine Palmitoyltransferase 1A Genetic Variant

(2010) B. D. Gessner et al.   PEDIATRICS

Carnitine palmitoyltransferase IA polymorphism P479L is common in Greenland Inuit and is associated with elevated plasma apolipoprotein A-I

(2009) Chandheeb Rajakumar et al.   JOURNAL OF LIPID RESEARCH

The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations

(2009) Cheryl R. Greenberg et al.   MOLECULAR GENETICS AND METABOLISM

Fatty acid oxidation disorders: maternal health and neonatal outcomes

(2009) R. Scott Rector et al.   Seminars in Fetal & Neonatal Medicine