Cloning of Human PEXcDNA-Reference-Cited by-同舟云学术

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Cloning of Human PEXcDNA

Published:1998-05 Issue:22 Volume:273 Page:13729-13737
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Lipman Mark L.,Panda Dibyendu,Bennett Hugh P.J.,Henderson Janet E.,Shane Elizabeth,Shen Yingnian,Goltzman David,Karaplis Andrew C.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference35 articles.

1. X-linked hypophosphataemia: A homologous phenotype in humans and mice with unusual organ-specific gene dosage

2. Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets.

3. The Gy mutation: another cause of X-linked hypophosphatemia in mouse.

4. A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

5. cDNA Cloning of the MurinePexGene Implicated in X-Linked Hypophosphatemia and Evidence for Expression in Bone

Cited by 128 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. Clinical disorders of phosphate homeostasis;Feldman and Pike's Vitamin D;2024

2. Single-cell RNA sequencing identifies Fgf23-expressing osteocytes in response to 1,25-dihydroxyvitamin D3 treatment;Frontiers in Physiology;2023-01-27

3. Pathogenic Variants of the PHEX Gene;Endocrines;2022-08-08

4. Genetic analysis combined with 3D‐printing assistant surgery in diagnosis and treatment for an X‐linked hypophosphatemia patient;Journal of Clinical Laboratory Analysis;2022-02-02

5. Improving the diagnosis of X-linked hypophosphatemia: recommendations to optimize diagnostic flow and clinician/geneticist cooperation in the Italian clinical practice;AboutOpen;2021-04-19

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