Genetic diseases resulting from disordered FGF23/klotho biology
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference58 articles.
1. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23;White;Nat. Genet.,2000
2. Fibroblast growth factor-23 (FGF23);White,2013
3. Regulation of fibroblastic growth factor 23 expression but not degradation by PHEX;Liu;J. Biol. Chem.,2003
4. Transgenic mice expressing fibroblast growth factor 23 under the control of the alpha1(I) collagen promoter exhibit growth retardation, osteomalacia, and disturbed phosphate homeostasis;Larsson;Endocrinology,2004
5. Mutation of the mouse klotho gene leads to a syndrome resembling ageing;Kuro-o;Nature,1997
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1. Inherited fibroblast growth factor 23 excess;Best Practice & Research Clinical Endocrinology & Metabolism;2023-11
2. Identification of a second Klotho interaction site in the C terminus of FGF23;Cell Reports;2021-01
3. A Normal FGF23 Does Not Preclude Tumor‐Induced Osteomalacia;JBMR Plus;2020-12-23
4. Milk Products in the Treatment of Hypophosphatemic Rickets: A Pilot Study;International Journal of Endocrinology and Metabolism;2019-10-06
5. Clinical aspects of the phosphate transporters NaPi-IIa and NaPi-IIb: mutations and disease associations;Pflügers Archiv - European Journal of Physiology;2018-12-13
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