Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q28510251)
Watch
English
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
scientific journal article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
title
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
(English)
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
main subject
Solute carrier family 26, member 4
1 reference
stated in
GOA release 2020-03-11
author name string
L. A. Everett
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
H. Morsli
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
D. K. Wu
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
E. D. Green
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
language of work or name
English
0 references
publication date
17 August 1999
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
volume
96
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
page(s)
9727–9732
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
issue
17
1 reference
stated in
PubMed
PubMed ID
10449762
retrieved
25 January 2017
cites work
The Pendred syndrome gene encodes a chloride-iodide transport protein
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
19 March 2017
Molecular analysis of the PDS gene in Pendred syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
19 March 2017
Two frequent missense mutations in Pendred syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
19 March 2017
A mutation in PDS causes non-syndromic recessive deafness
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
19 March 2017
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
19 March 2017
Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
19 March 2017
Complete nucleotide sequence of band 3 related anion transport protein AE2 from human kidney
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
19 March 2017
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
29 September 2017
Development and maintenance of ear innervation and function: lessons from mutations in mouse and man.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
29 September 2017
Pendred syndrome--100 years of underascertainment?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
29 September 2017
Pendred syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
29 September 2017
Animal models of endolymphatic hydrops
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
29 September 2017
Functional morphology of the epithelium of the spiral prominence. A light, transmission and scanning electron microscope study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
29 September 2017
Production of inner ear fluids
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
29 September 2017
The large vestibular aqueduct syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
29 September 2017
Radiological malformations of the ear in Pendred syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Mechanisms of endolymph secretion.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Development of the mouse inner ear and origin of its sensory organs.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Effects of hypothyroidism on the structural development of the organ of Corti in the rat.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Experimental blockage of the endolymphatic duct and sac and its effect on the inner ear of the guinea pig. A study on endolymphatic hydrops
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Ultrastructure of toe cochlear blood vessels
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Developmental morphology of the mouse inner ear. A scanning electron microscopic observation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Pendred's syndrome. Acoustic, vestibular and radiological findings in 17 unrelated patients.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Pendred's syndrome with episodic vertigo, tinnitus and vomiting and normal bithermal caloric responses.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
The variable intrafamiliar expressivity in Pendred's syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Scanning electron microscopy of the connective tissue along the lateral wall of the mouse cochlear duct with special reference to the external sulcus cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Immunolocalization of Na+,K(+)-ATPase and carbonic anhydrase in the gerbil's vestibular system
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Microcirculation in the labyrinth
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
2 June 2018
Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727
retrieved
21 January 2018
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727
retrieved
21 January 2018
Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727
retrieved
21 January 2018
Localization of bone morphogenetic protein-4 messenger RNA in developing mouse cochlea.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727
retrieved
21 January 2018
Macromolecular transport in the spiral prominence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727
retrieved
21 January 2018
Localization of pH regulating proteins H+ATPase and Cl-/HCO3- exchanger in the guinea pig inner ear.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727
retrieved
21 January 2018
Hearing loss and cochlear abnormalities in the congenital hypothyroid (hyt/hyt) mouse.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727
retrieved
21 January 2018
The fundamental and medical impacts of recent progress in research on hereditary hearing loss.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.96.17.9727
retrieved
21 January 2018
Mondini dysplasia; a clinical and pathological study.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
27 November 2018
Hearing in congenital hypothyroidism.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22278
retrieved
27 November 2018
Destruction of the endolymphatic sac in the cat
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10449762
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Electron microscopy cytochemical studies on electrolyte transport in the lateral cochlear wall
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10449762
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mondini cochlea in Pendred's syndrome. A histological study
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10449762
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Ménière's disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10449762
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.96.17.9727
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3852831
ADS bibcode
1999PNAS...96.9727E
0 references
OpenCitations bibliographic resource ID
3852831
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3852831
PMCID
22278
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3852831
PubMed ID
10449762
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3852831
ResearchGate publication ID
12849611
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit