Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model (Q30542953)

17 October 2017

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

1 reference

17 October 2017

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8

Eric D Green

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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

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17 October 2017

Sherry Fleming

5

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17 October 2017

Susan M Wall

6

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17 October 2017

language of work or name

English

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publication date

22 December 2006

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17 October 2017

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17 October 2017

4

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17 October 2017

37

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

17 October 2017

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

PubMed publication ID

17187680

1 reference