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Endocrinology|December 31, 2005
Agouti-related protein is posttranslationally cleaved by proprotein convertase 1 to generate agouti-related protein (AGRP)83-132: interaction between AGRP83-132 and melanocortin receptors cannot be influenced by syndecan-3John W M Creemers, Lynn E Pritchard, Amy Gyte, et al.
Frontiers in Medicine|December 20, 2023
Cushing's syndrome caused by ACTH precursors secreted from a pancreatic yolk sac tumor in an adult-a case report and literature reviewJohnny Yau Cheung Chang, Chariene Shao Lin Woo, Wing Sun Chow, et al.
Cell Death & Disease|October 21, 2020
EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewalRoberto Paredes, James R Kelly, Bethany Geary, et al.
Nucleic Acids Research|June 26, 2018
EVI1 carboxy-terminal phosphorylation is ATM-mediated and sustains transcriptional modulation and self-renewal via enhanced CtBP1 associationRoberto Paredes, Marion Schneider, Adam Stevens, et al.
The Journal of Clinical Endocrinology and Metabolism|June 23, 2022
Obesity and Hyperphagia With Increased Defective ACTH: A Novel POMC VariantEline S van der Valk, Lotte Kleinendorst, Patric J D Delhanty, et al.
Diabetes|January 27, 2011
Deletion of Lkb1 in pro-opiomelanocortin neurons impairs peripheral glucose homeostasis in miceMarc Claret, Mark A Smith, Claude Knauf, et al.
Cell Death & Disease|June 16, 2017
Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruptionStefan Meyer, Adam Stevens, Roberto Paredes, et al.
The Journal of Clinical Investigation|November 18, 2003
Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiencyRobert S Jackson, John W M Creemers, I Sadaf Farooqi, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 27, 2015
Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencingLaurence M Nunn, Luis R Lopes, Petros Syrris, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 18, 2020
A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndromeSara Cuvertino, Verity Hartill, Alice Colyer, et al.
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