Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy

Diabetes

Volumn 47, Issue 7, 1998, Pages 1145-1151

  Shyng, Show Ling ^a   Ferrigni, Tycho ^a   Shepard, Jeremiah B ^a   Nestorowicz, Ann ^b   Glaser, Benjamin ^c   Permutt, M Alan ^a   Nichols, Colin G ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b ELI LILLY AND COMPANY   (United States)

^c HEBREW UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

SULFONYLUREA DERIVATIVE;

ANALYTIC METHOD; ANIMAL CELL; ARTICLE; BRAIN INJURY; COMPLEX FORMATION; GENE MUTATION; GLUCOSE BLOOD LEVEL; HYPERINSULINEMIA; HYPOGLYCEMIA; INSULIN RELEASE; MEMBRANE DEPOLARIZATION; METABOLIC REGULATION; NONHUMAN; PANCREAS ISLET BETA CELL; PANCREAS RESECTION; PRIORITY JOURNAL; RAT; SITE DIRECTED MUTAGENESIS; STRUCTURE ACTIVITY RELATION;

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATE; ALLELES; ANIMALS; ATP-BINDING CASSETTE TRANSPORTERS; COS CELLS; CRICETINAE; DIAZOXIDE; HUMANS; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; INFANT, NEWBORN; INSULIN; MICE; MUTAGENESIS, SITE-DIRECTED; PANCREAS; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG; RUBIDIUM RADIOISOTOPES; TRANSFECTION;

EID: 0031799545     PISSN: 00121797     EISSN: None     Source Type: Journal    
DOI: 10.2337/diabetes.47.7.1145     Document Type: Article

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