Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear (Q28510251)

GOA release 2020-03-11

author name string

L. A. Everett

1

1 reference

25 January 2017

H. Morsli

2

1 reference

25 January 2017

D. K. Wu

3

1 reference

25 January 2017

E. D. Green

Proceedings of the National Academy of Sciences of the United States of America

4

1 reference

25 January 2017

language of work or name

English

0 references

publication date

17 August 1999

1 reference

25 January 2017

1 reference

25 January 2017

96

1 reference

25 January 2017

17

1 reference

25 January 2017

9727–9732

1 reference

25 January 2017

The Pendred syndrome gene encodes a chloride-iodide transport protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Molecular analysis of the PDS gene in Pendred syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Two frequent missense mutations in Pendred syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

A mutation in PDS causes non-syndromic recessive deafness

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Complete nucleotide sequence of band 3 related anion transport protein AE2 from human kidney

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Development and maintenance of ear innervation and function: lessons from mutations in mouse and man.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Pendred syndrome--100 years of underascertainment?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Animal models of endolymphatic hydrops

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Functional morphology of the epithelium of the spiral prominence. A light, transmission and scanning electron microscope study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Production of inner ear fluids

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

The large vestibular aqueduct syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Radiological malformations of the ear in Pendred syndrome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Mechanisms of endolymph secretion.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Development of the mouse inner ear and origin of its sensory organs.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Effects of hypothyroidism on the structural development of the organ of Corti in the rat.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Experimental blockage of the endolymphatic duct and sac and its effect on the inner ear of the guinea pig. A study on endolymphatic hydrops

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Ultrastructure of toe cochlear blood vessels

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Developmental morphology of the mouse inner ear. A scanning electron microscopic observation

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Pendred's syndrome. Acoustic, vestibular and radiological findings in 17 unrelated patients.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Pendred's syndrome with episodic vertigo, tinnitus and vomiting and normal bithermal caloric responses.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

The variable intrafamiliar expressivity in Pendred's syndrome.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Scanning electron microscopy of the connective tissue along the lateral wall of the mouse cochlear duct with special reference to the external sulcus cells

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Immunolocalization of Na+,K(+)-ATPase and carbonic anhydrase in the gerbil's vestibular system

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Microcirculation in the labyrinth

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome.

2 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727

Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727

Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre)

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727

Localization of bone morphogenetic protein-4 messenger RNA in developing mouse cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727

Macromolecular transport in the spiral prominence

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727

Localization of pH regulating proteins H+ATPase and Cl-/HCO3- exchanger in the guinea pig inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727

Hearing loss and cochlear abnormalities in the congenital hypothyroid (hyt/hyt) mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727

The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727

Mondini dysplasia; a clinical and pathological study.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Hearing in congenital hypothyroidism.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278

Destruction of the endolymphatic sac in the cat

27 November 2018

1 reference

PubMed

12 December 2020

Electron microscopy cytochemical studies on electrolyte transport in the lateral cochlear wall

1 reference

PubMed

12 December 2020

Mondini cochlea in Pendred's syndrome. A histological study

1 reference

PubMed

12 December 2020

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.96.17.9727

1 reference

3852831

ADS bibcode

1999PNAS...96.9727E

0 references

3852831

1 reference

1 reference

1 reference