Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency-Reference-Cited by-同舟云学术

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Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency

Published:2013-09 Issue:1-2 Volume:110 Page:191-194
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Frank Graeme R.,Fox Joyce,Candela Ninfa,Jovanovic Zorica,Bochukova Elena,Levine Jeremiah,Papenhausen Peter R.,O'Rahilly Stephen,Farooqi I. Sadaf

Funder

Wellcome Trust

MRC Centre for Obesity and Related Disorders

UK NIHR Cambridge Biomedical Research Centre

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference15 articles.

1. The proprotein convertases, 20years later;Seidah;Methods Mol. Biol.,2011

2. Processing of prothyrotropin-releasing hormone by the family of prohormone convertases;Schaner;J. Biol. Chem.,1997

3. The atypical 16p11.2 deletion: a not so atypical microdeletion syndrome?;Barge-Schaapveld;Am. J. Med. Genet. A,2011

4. PC1 and PC2 are proprotein convertases capable of cleaving proopiomelanocortin at distinct pairs of basic residues;Benjannet;Proc. Natl. Acad. Sci. U. S. A.,1991

5. Cellular localization of the prohormone convertases in the hypothalamic paraventricular and supraoptic nuclei: selective regulation of PC1 in corticotrophin-releasing hormone parvocellular neurons mediated by glucocorticoids;Dong;J. Neurosci.,1997

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