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Common nonsynonymous variants in PCSK1 confer risk of obesity

article

Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism

scientific article published on 08 December 2016

Hyperphagia and early-onset obesity due to a novel homozygous missense mutation in prohormone convertase 1/3.

artículo científico publicado en 2007

Missense variants in CMS22 patients reveal that PREPL has both enzymatic and nonenzymatic functions

artículo científico publicado en 2024

Mutations in the amino-terminal region of proopiomelanocortin (POMC) in patients with early-onset obesity impair POMC sorting to the regulated secretory pathway

artículo científico publicado en 2008

STAT6 and Furin Are Successive Triggers for the Production of TGF-β by T Cells

artículo científico publicado en 2018

Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency

artículo científico publicado en 2003

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