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Volumn 40, Issue 10, 1997, Pages 1227-1230
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Mutational analysis of the coding region of the uncoupling protein 2 gene in obese NIDDM patients: Impact of a common amino acid polymorphism on juvenile and maturity onset forms of obesity and insulin resistance
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Author keywords
Amino acid polymorphism; Genetics; Insulin resistance; Obesity; Uncoupling protein 2
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Indexed keywords
ALANINE;
AMINO ACID;
GENE PRODUCT;
UNCOUPLING PROTEIN;
VALINE;
ADULT;
ALLELE;
AMINO ACID SUBSTITUTION;
ARTICLE;
CHROMOSOME 7;
CONTROLLED STUDY;
DIABETIC OBESITY;
FEMALE;
GENE FREQUENCY;
GENE MUTATION;
GENETIC VARIABILITY;
HUMAN;
HUMAN TISSUE;
HYPERINSULINEMIA;
INSULIN DEPENDENT DIABETES MELLITUS;
INSULIN RESISTANCE;
MAJOR CLINICAL STUDY;
MALE;
NON INSULIN DEPENDENT DIABETES MELLITUS;
ONSET AGE;
PRIORITY JOURNAL;
PROTEIN POLYMORPHISM;
SINGLE STRAND CONFORMATION POLYMORPHISM;
ADULT;
AGE OF ONSET;
BLOOD GLUCOSE;
C-PEPTIDE;
DIABETES MELLITUS, TYPE 2;
EUROPEAN CONTINENTAL ANCESTRY GROUP;
FEMALE;
GENOTYPE;
HUMANS;
INSULIN;
INSULIN RESISTANCE;
ION CHANNELS;
MALE;
MEMBRANE TRANSPORT PROTEINS;
MIDDLE AGED;
MITOCHONDRIAL PROTEINS;
MUTATION;
OBESITY;
POLYMORPHISM, GENETIC;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
PROTEINS;
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EID: 9844232617
PISSN: 0012186X
EISSN: None
Source Type: Journal
DOI: 10.1007/s001250050811 Document Type: Article |
Times cited : (74)
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References (10)
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