(Q28202356)

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The autosomal dominant hypophosphatemic rickets R176Q mutation in fibroblast growth factor 23 resists proteolytic cleavage and enhances in vivo biological potency

scientific article (publication date: 14 March 2003)

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The autosomal dominant hypophosphatemic rickets R176Q mutation in fibroblast growth factor 23 resists proteolytic cleavage and enhances in vivo biological potency (English)

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autosomal dominant hypophosphatemic rickets

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1 reference

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author name string

Xiu-Ying Bai

1

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Dengshun Miao

2

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David Goltzman

3

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Andrew C Karaplis

4

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language of work or name

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publication date

14 March 2003

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Journal of Biological Chemistry

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278

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11

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9843-9

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Loss of renal phosphate wasting in a child with autosomal dominant hypophosphatemic rickets caused by a FGF23 mutation

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https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Proprotein and prohormone convertases: a family of subtilases generating diverse bioactive polypeptides

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene Is a Secreted Polypeptide Overexpressed by Tumors that Cause Phosphate Wasting

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Cloning of human PEX cDNA. Expression, subcellular localization, and endopeptidase activity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

A simple slide-rule method for the assessment of renal tubular reaborption of phosphate in man

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Molecular cloning of 25-hydroxyvitamin D-3 24-hydroxylase (Cyp-24) from mouse kidney: its inducibility by vitamin D-3

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Mutant FGF-23 responsible for autosomal dominant hypophosphatemic rickets is resistant to proteolytic cleavage and causes hypophosphatemia in vivo.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Oncogenic osteomalacia caused by a phosphaturic mesenchymal tumor of the oral cavity: a case report

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Measurement of mammalian 25-hydroxyvitamin D3 24R-and 1 alpha-hydroxylase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Regulation of the procine 1,25-dihydroxyvitamin D3-24-hydroxylase (CYP24) by 1,25-dihydroxyvitamin D3 and parathyroid hormone in AOK-B50 cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Parathyroid hormone regulates 25-hydroxyvitamin D(3)-24-hydroxylase mRNA by altering its stability

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210490200

21 January 2018

Identifiers

10.1074/JBC.M210490200

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Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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