A novel Phex mutation in a new mouse model of hypophosphatemic rickets-Reference-Cited by-同舟云学术

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A novel Phex mutation in a new mouse model of hypophosphatemic rickets

Published:2012-05-09 Issue:7 Volume:113 Page:2432-2441
ISSN:0730-2312
Container-title:Journal of Cellular Biochemistry
language:en
Short-container-title:J. Cell. Biochem.

Author:

Owen Celeste,Chen Frieda,Flenniken Ann M.,Osborne Lucy R.,Ichikawa Shoji,Adamson S. Lee,Rossant Janet,Aubin Jane E.

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jcb.24115/fullpdf

Reference48 articles.

1. MEPE, the gene encoding a tumor-secreted protein in oncogenic hypophosphatemic osteomalacia, is expressed in bone;Argiro;Genomics,2001

2. Sclerostin is a locally acting regulator of late-osteoblast/pre-osteocyte differentiation and regulates mineralization through a MEPE-ASARM dependent mechanism;Atkins;J Bone Miner Res,2011

3. Partial rescue of the Hyp phenotype by osteoblast-targeted PHEX (phosphate-regulating gene with homologies to endopeptidases on the X chromosome) expression;Bai;Mol Endocrinol,2002

4. The autosomal dominant hypophosphatemic rickets R176Q mutation in fibroblast growth factor 23 resists proteolytic cleavage and enhances in vivo biological potency;Bai;J Biol Chem,2003

5. Transgenic mice overexpressing human fibroblast growth factor 23 (R176Q) delineate a putative role for parathyroid hormone in renal phosphate wasting disorders;Bai;Endocrinology,2004

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. PHEXL222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease;Genes;2022-07-28

2. Deficiency of Mineralization-Regulating Transcription Factor Trps1 Compromises Quality of Dental Tissues and Increases Susceptibility to Dental Caries;Frontiers in Dental Medicine;2022-04-11

3. Novel PHEX gene locus‐specific database: Comprehensive characterization of vast number of variants associated with X‐linked hypophosphatemia (XLH);Human Mutation;2021-12-05

4. Regulation of fibroblast growth factor 23 (FGF23) in health and disease;FEBS Letters;2019-07-05

5. FGF23 and its role in X-linked hypophosphatemia-related morbidity;Orphanet Journal of Rare Diseases;2019-02-26

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