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Proceedings of the National Academy of Sciences of the United States of America|August 21, 2008
Role of furin in granular acidification in the endocrine pancreas: identification of the V-ATPase subunit Ac45 as a candidate substrateEls Louagie, Neil A Taylor, Daisy Flamez, et al.
The Biochemical Journal|August 28, 2012
Generation and characterization of non-competitive furin-inhibiting nanobodiesJingjing Zhu, Jeroen Declercq, Bart Roucourt, et al.
Blood|April 21, 2026
Erythroid-produced intact FGF23 is a paracrine inhibitor of erythropoiesisGuillaume Courbon, Jane J Thomas, Eduardo J Duque, et al.
Blood|April 13, 2023
Bone-derived C-terminal FGF23 cleaved peptides increase iron availability in acute inflammationGuillaume Courbon, Jane Joy Thomas, Marta Martinez-Calle, et al.
Human Molecular Genetics|August 8, 2002
A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanismBenjamin G Challis, Lynn E Pritchard, John W M Creemers, et al.
Diabetes|December 5, 2020
Loss of Furin in β-Cells Induces an mTORC1-ATF4 Anabolic Pathway That Leads to β-Cell DysfunctionBas Brouwers, Ilaria Coppola, Katlijn Vints, et al.
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
PREPL deficiency: delineation of the phenotype and development of a functional blood assayLuc Régal, Emma Mårtensson, Isabelle Maystadt, et al.
Diabetes|January 3, 2012
Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesityJohn W M Creemers, Hélène Choquet, Pieter Stijnen, et al.
Cardiovascular Research|April 18, 2024
The proprotein convertase FURIN is a novel aneurysm predisposition gene impairing TGF-β signallingZongsheng He, Arne S IJpma, Dianne Vreeken, et al.
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