Single nucleotide polymorphisms of RXRA encoding retinoid X receptor alpha

Journal of Human Genetics

Volumn 46, Issue 7, 2001, Pages 423-425

  Hegele, R A ^a   Cao, H ^a  

^a ROBARTS RESEARCH INSTITUTE   (Canada)

Author keywords

Complex traits; Diabetes; Genomic DNA; Lipodystrophy; Metabolism; Obesity; Sequencing

Indexed keywords

RECEPTOR SUBUNIT; RETINOID X RECEPTOR;

ADIPOCYTE; ARTICLE; CHOLESTEROL METABOLISM; CLINICAL ARTICLE; DIABETES MELLITUS; DNA SEQUENCE; GENE AMPLIFICATION; GENETIC LINKAGE; GENETIC SCREENING; GENETIC VARIABILITY; GLUCOSE HOMEOSTASIS; HUMAN; LIPODYSTROPHY; NUCLEOTIDE SEQUENCE; OBESITY; SINGLE NUCLEOTIDE POLYMORPHISM;

3' UNTRANSLATED REGIONS; CONTINENTAL POPULATION GROUPS; DNA MUTATIONAL ANALYSIS; GENE FREQUENCY; GENOTYPE; HUMANS; INTRONS; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, RETINOIC ACID; RETINOID X RECEPTORS; TRANSCRIPTION FACTORS;

EID: 0034938380     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380170061     Document Type: Article

References (9)

1. Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy
2. Asymmetry in the PPAR-gamma/RXR-alpha crystal structure reveals the molecular basis of heterodimerization among nuclear receptors
3. A gene for congenital generalized lipodystrophy maps to human chromosome 9q34
4. 9-Cis retinoic acid is a high affinity ligand for the retinoid X receptor
5. Localization of the retinoid X receptor alpha gene (RXRA) to chromosome 9q34
6. Nuclear receptor that identifies a novel retinoic acid response pathway
7. A direct repeat in the cellular retinol-binding protein type II gene confers differential regulation by RXR and RAR
8. Regulation of absorption and ABC1-mediated efflux of cholesterol by RXR heterodimers
9. LXR, a nuclear receptor that defines a distinct retinoid response pathway