PCSK1 Mutations and Human Endocrinopathies: From Obesity to Gastrointestinal Disorders-Reference-Cited by-同舟云学术

PCSK1 Mutations and Human Endocrinopathies: From Obesity to Gastrointestinal Disorders

Published:2016-05-17 Issue:4 Volume:37 Page:347-371
ISSN:0163-769X
Container-title:Endocrine Reviews
language:en
Short-container-title:

Author:

Stijnen Pieter¹,Ramos-Molina Bruno¹,O'Rahilly Stephen²,Creemers John W. M.¹

Affiliation:

1. Laboratory for Biochemical Neuroendocrinology (P.S., B.R.-M., J.W.M.C.), Department of Human Genetics, KU Leuven, Leuven 3000, Belgium

2. Medical Research Council (MRC) Metabolic Diseases Unit (S.O.), Wellcome Trust-MRC Institute of Metabolic Science, National Institute for Health Research, Cambridge Biomedical Research Centre, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, United Kingdom

Publisher

The Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/edrv/article-pdf/37/4/347/10492460/edrv0347.pdf

Reference218 articles.

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3. Peptide Biosynthesis: Prohormone Convertases 1/3 and 2 (Colloquium Series on Neuropeptides);Hoshino,2012

4. Cloning and primary sequence of a mouse candidate prohormone convertase PC1 homologous to PC2, furin, and Kex2: distinct chromosomal localization and messenger RNA distribution in brain and pituitary compared to PC2;Seidah;Mol Endocrinol,1991

5. Identification of a cDNA encoding a second putative prohormone convertase related to PC2 in AtT20 cells and islets of Langerhans;Smeekens;Proc Natl Acad Sci USA,1991

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