Expression and Cloning of the Human X-Linked Hypophosphatemia Gene cDNA-Reference-Cited by-同舟云学术

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Expression and Cloning of the Human X-Linked Hypophosphatemia Gene cDNA

Published:1997-02 Issue:3 Volume:231 Page:635-639
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Grieff Marvin,Mumm Steven,Waeltz Paul,Mazzarella Richard,Whyte Michael P,Thakker Rajesh V,Schlessinger David

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference25 articles.

1. The Metabolic and Molecular Bases of Inherited Disease, 7th ed.;Rasmussen,1995

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

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

4. Crosstransplantation of kidneys in normal and Hyp mice. Evidence that the Hyp mouse phenotype is unrelated to an intrinsic renal defect.

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1. A New de novo Mosaic Mutation of PHEX Gene: A Case Report of a Boy with Hypophosphatemic Rickets;Endocrine, Metabolic & Immune Disorders - Drug Targets;2023-08

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

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

4. A Unique Mechanism of a Novel Synonymous PHEX Variant Causing X-Linked Hypophosphatemia;The Journal of Clinical Endocrinology & Metabolism;2022-07-27

5. Clinical Evidence for the Benefits of Burosumab Therapy for X-Linked Hypophosphatemia (XLH) and Other Conditions in Adults and Children;Frontiers in Endocrinology;2020-05-28

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