PCSK1 Mutations and Human Endocrinopathies: From Obesity to Gastrointestinal Disorders

Pieter Stijnen(KU Leuven), John W.M. Creemers(KU Leuven)

Endocrine Reviews

May 17, 2016

10.1210/er.2015-1117

Cited by 174

Related Papers

Metabolic and Behavioural Phenotypes in Nestin-Cre Mice Are Caused by Hypothalamic Expression of Human Growth Hormone

|PLoS ONE|2015|78

Loss of the proprotein convertase Furin in T cells represses mammary tumorigenesis in oncogene-driven triple negative breast cancer

|Cancer Letters|2020|32

Nuclear Localization of the Autism Candidate Gene Neurobeachin and Functional Interaction with the NOTCH1 Intracellular Domain Indicate a Role in Regulating Transcription

|PLoS ONE|2016|29

Platelets of mice heterozygous for neurobeachin, a candidate gene for autism spectrum disorder, display protein changes related to aberrant protein kinase A activity

|Molecular Autism|2013|26

Prolyl endopeptidase-like is a (thio)esterase involved in mitochondrial respiratory chain function

|iScience|2021|23