Autosomal dominant growth hormone (GH) deficiency type II: The del32-71-GH deletion mutant suppresses secretion of wild-type GH

Endocrinology

Volumn 141, Issue 3, 2000, Pages 883-890

  Lee, Min S ^a   Wajnrajch, Michael P ^b   Kim, Steve S ^a   Plotnick, Leslie P ^c   Wang, Julie ^b   Gertner, Joseph M ^d   Leibel, Rudolph L ^b,d   Dannies, Priscilla S ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WEILL CORNELL MEDICAL COLLEGE   (United States)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d Department of Pharmacology ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GROWTH HORMONE; PROLACTIN;

ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL STRAIN COS1; CHO CELL; DELETION MUTANT; GENE DELETION; GENE MUTATION; GENETIC TRANSFECTION; GROWTH HORMONE DEFICIENCY; GROWTH HORMONE RELEASE; NEUROSECRETORY CELL; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN PROCESSING; PROTEIN STABILITY; PROTEIN SYNTHESIS; RAT;

EID: 0034465474     PISSN: 00137227     EISSN: None     Source Type: Journal    
DOI: 10.1210/endo.141.3.7380     Document Type: Article

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