FGF23 deficiency leads to mixed hearing loss and middle ear malformation in mice (Q30430229)

10 November 2017

FGF23 deficiency leads to mixed hearing loss and middle ear malformation in mice (English)

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10 November 2017

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Andrew C Lysaght

1

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10 November 2017

Quan Yuan

2

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10 November 2017

Yi Fan

3

1 reference

10 November 2017

Neil Kalwani

4

1 reference

10 November 2017

Paul Caruso

5

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10 November 2017

MaryBeth Cunnane

6

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10 November 2017

Beate Lanske

7

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10 November 2017

Konstantina M Stanković

8

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10 November 2017

language of work or name

English

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publication date

22 September 2014

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10 November 2017

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10 November 2017

9

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10 November 2017

9

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10 November 2017

e107681

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Creative Commons Attribution 4.0 International

10 November 2017

start time

22 September 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Parathyroid-specific deletion of Klotho unravels a novel calcineurin-dependent FGF23 signaling pathway that regulates PTH secretion

1 reference

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Panel 3: Recent advances in anatomy, pathology, and cell biology in relation to otitis media pathogenesis

20 June 2018

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A spatial and temporal gradient of Fgf differentially regulates distinct stages of neural development in the zebrafish inner ear

20 June 2018

1 reference

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Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice.

20 June 2018

1 reference

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New developments in aminoglycoside therapy and ototoxicity

20 June 2018

1 reference

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FGF-23/Klotho signaling is not essential for the phosphaturic and anabolic functions of PTH.

20 June 2018

1 reference

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Regulation of phosphate homeostasis by PTH, vitamin D, and FGF23.

20 June 2018

1 reference

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Isolated C-terminal tail of FGF23 alleviates hypophosphatemia by inhibiting FGF23-FGFR-Klotho complex formation

20 June 2018

1 reference

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Adding insult to injury: cochlear nerve degeneration after "temporary" noise-induced hearing loss

20 June 2018

1 reference

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The kidney and ear: emerging parallel functions

20 June 2018

1 reference

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In vivo genetic evidence for klotho-dependent, fibroblast growth factor 23 (Fgf23) -mediated regulation of systemic phosphate homeostasis

20 June 2018

1 reference

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Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).

20 June 2018

1 reference

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Eya4-deficient mice are a model for heritable otitis media

20 June 2018

1 reference

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Klotho as a regulator of oxidative stress and senescence

20 June 2018

1 reference

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Expression and functions of FGF ligands during early otic development.

20 June 2018

1 reference

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Klotho converts canonical FGF receptor into a specific receptor for FGF23

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Regulation of fibroblast growth factor-23 signaling by klotho

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Genetic susceptibility to otitis media

20 June 2018

1 reference

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An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice

20 June 2018

1 reference

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Transgenic mice overexpressing human fibroblast growth factor 23 (R176Q) delineate a putative role for parathyroid hormone in renal phosphate wasting disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Targeted ablation of Fgf23 demonstrates an essential physiological role of FGF23 in phosphate and vitamin D metabolism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Ear and kidney syndromes: molecular versus clinical approach

20 June 2018

1 reference

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Klotho, a gene related to a syndrome resembling human premature aging, functions in a negative regulatory circuit of vitamin D endocrine system

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Roles of fibroblast growth factors in the inner ear.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Insights into ototoxicity. Analogies to nephrotoxicity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Direct expenditures related to otitis media diagnoses: extrapolations from a pediatric medicaid cohort

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171482

Otitis media in 2253 Pittsburgh-area infants: prevalence and risk factors during the first two years of life

20 June 2018

1 reference

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Mineralized tissue cells are a principal source of FGF23.

20 June 2018

1 reference

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Pathogenic role of Fgf23 in Hyp mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0107681

FGF-23 transgenic mice demonstrate hypophosphatemic rickets with reduced expression of sodium phosphate cotransporter type IIa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0107681

Vitamin D-deficient diet rescues hearing loss in Klotho mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0107681

Expression of Klotho protein in the inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0107681

Age-dependent changes in the expression of klotho protein, TRPV5 and TRPV6 in mouse inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0107681

Calcineurin activation contributes to noise-induced hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0107681

Protective effect of calcineurin inhibitors on acoustic injury of the cochlea

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0107681

Impaired hearing in X-linked hypophosphataemic (vitamin-D-resistant) osteomalacia

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0107681

Tumoral calcinosis with hyperphosphatemia. A report of a family with incidence in four siblings

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25243481

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0107681

1 reference

10 November 2017

0 references

1 reference

10 November 2017

PubMed publication ID

25243481

1 reference