(Q30542953)

17 October 2017

Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model (English)

1 reference

17 October 2017

0 references

1 reference

8

Eric D Green

1 reference

17 October 2017

9

Philine Wangemann

1 reference

17 October 2017

Rajanikanth J Maganti

4

object named as

Rajanikanth J Maganti

1 reference

17 October 2017

7

Lorraine A Everett

1 reference

17 October 2017

Sairam V Jabba

1

1 reference

17 October 2017

Alisha Oelke

2

1 reference

17 October 2017

Ruchira Singh

3

1 reference

17 October 2017

Sherry Fleming

5

1 reference

17 October 2017

Susan M Wall

6

1 reference

17 October 2017

language of work or name

English

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publication date

22 December 2006

1 reference

17 October 2017

1 reference

17 October 2017

4

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17 October 2017

37

1 reference

https://scigraph.springernature.com/pub.10.1186/1741-7015-4-37

17 October 2017

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cites work

Intercalated cell H+/OH- transporter expression is reduced in Slc26a4 null mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Macrophages in inflammation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Histological basis of the porcine femoral artery for vascular research.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

ASSOCIATION OF CONGENITAL DEAFNESS WITH GOITRE (PENDRED'S SYNDROME) A STUDY OF 207 FAMILIES.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Sugar transport by mammalian members of the SLC26 superfamily of anion-bicarbonate exchangers

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Enlarged vestibular aqueduct: a radiological marker of pendred syndrome, and mutation of the PDS gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin 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=1796619

The Pendred syndrome gene encodes a chloride-iodide transport protein

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Inner ear defects induced by null mutation of the isk gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1796619

20 June 2018

DEAF-MUTISM AND GOITRE

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-4-37

Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-4-37

Prolactin regulation of the pendrin-iodide transporter in the mammary gland

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-4-37

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-4-37

Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-4-37

Rapid recruitment of inflammatory monocytes is independent of neutrophil migration

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-4-37

Mononuclear phagocytes migrate into the murine cochlea after acoustic trauma

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-4-37

Innate immunity contributes to cochlear adaptive immune responses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-4-37

Na(+)/I(-) symporter and Pendred syndrome gene and protein expressions in human extra-thyroidal tissues

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17187680

12 December 2020

inferred from PubMed ID database lookup

Expression of PDS/Pds, the Pendred syndrome gene, in endometrium

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17187680

12 December 2020

inferred from PubMed ID database lookup

Localization of pendrin in mouse kidney

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17187680

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1186/1741-7015-4-37

1 reference

Dimensions Publication ID

17 October 2017

1020837007

0 references

Fatcat ID

release_sa5vufqr25bz5diohzy6tjbmq4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/sa5vufqr25bz5diohzy6tjbmq4

24 November 2022

mapped directly with Wikidata item

1 reference

17 October 2017

1 reference