Short stature explained by dimerization of human growth hormone induced by a p.C53S point mutation
Author:
Funder
Deutsche Forschungsgemeinschaft
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference47 articles.
1. Short stature caused by a biologically inactive mutant growth hormone (GH-C53S);Besson;J. Clin. Endocrinol. Metab,2005
2. Growth failure with normal serum RIA-GH and low somatomedin activity: somatomedin restoration and growth acceleration after exogenous GH;Kowarski;J. Clin. Endocrinol. Metab,1978
3. Human growth-hormone and extracellular domain of its receptor: crystal structure of the complex;de Vos;Science,1992
4. Growth hormone and prolactin: molecular and functional evolution;Forsyth;J. Mammary Gland Biol. Neoplasia,2002
5. Sequences of pituitary and placental lactogenic and growth hormones: evolution from a primordial peptide by gene reduplication;Niall;Proc. Natl. Acad. Sci. U.S.A,1971
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