Isolated congenital ACTH deficiency: a cleavage enzyme defect?
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.1994.tb02499.x/fullpdf
Reference8 articles.
1. A member of the eukaryotic subtilisin family (PC3) has the enzymic properties of the type 1 proinsulin-converting endopeptidase
2. Intraorganellar calcium and pH control proinsulin cleavage in the pancreatic β cell via two distinct site-specific endopeptidases
3. Isolated ACTH deficiency: enzyme defect or chimaeric enzyme?
4. A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
5. Isolated congenital ACTH deficiency: a cleavage enzyme defect?.
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1. Of old and new diseases: genetics of pituitary ACTH excess (Cushing) and deficiency;Clinical Genetics;2007-08-13
2. Molecular Mechanisms of Pituitary Differentiation and Regulation: Implications for Hormone Deficiencies and Hormone Resistance Syndromes;Frontiers of Hormone Research;2006
3. Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained byTPITGene Mutations;The Journal of Clinical Endocrinology & Metabolism;2005-03
4. Human and mouseTPITgene mutations cause early onset pituitary ACTH deficiency;Genes & Development;2003-03-03
5. Tpit, un nouveau membre de la famille des gènes à boîte T, est impliqué dans la déficience isolée en ACTH;médecine/sciences;2001-11
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