Newborn serum retinoic acid level is associated with variants of genes in the retinol metabolism pathway

Pediatric Research

Volumn 67, Issue 6, 2010, Pages 598-602

  Manolescu, Daniel C ^a   El Kares, Reyhan ^b   Lakhal Chaieb, Lajmi ^c   Montpetit, Alexandre ^d   Bhat, Pangala V ^a   Goodyer, Paul ^b  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

^b RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^c UNIVERSITÉ LAVAL   (Canada)

^d MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DEHYDROGENASE; ALDEHYDE DEHYDROGENASE 1 FAMILY MEMBER A2; CELLULAR RETINOL BINDING PROTEIN; CELLULAR RETINOL BINDING PROTEIN 2; RETINAL DEHYDROGENASE; RETINOIC ACID; RETINOL; UNCLASSIFIED DRUG;

ARTICLE; ENZYME ACTIVITY; GENETIC ASSOCIATION; GENETIC VARIABILITY; HOMOZYGOSITY; HUMAN; INFANT; PRIORITY JOURNAL; PROTEIN FUNCTION; RECEPTOR BINDING; SINGLE NUCLEOTIDE POLYMORPHISM; UMBILICAL CORD BLOOD; VITAMIN BLOOD LEVEL; VITAMIN METABOLISM;

CHI-SQUARE DISTRIBUTION; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; FETAL BLOOD; GENE FREQUENCY; GENOTYPE; HOMOZYGOTE; HUMANS; INFANT, NEWBORN; MALE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; QUEBEC; RECEPTORS, RETINOIC ACID; RETINAL DEHYDROGENASE; TRETINOIN; VITAMIN A;

EID: 77952542839     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1203/PDR.0b013e3181dcf18a     Document Type: Article

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