(Q40600626)

21 September 2017

title

Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux (English)

1 reference

21 September 2017

Mary P Gillam

1

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21 September 2017

Aniket R Sidhaye

2

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21 September 2017

Eun Jig Lee

3

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21 September 2017

Jonas Rutishauser

4

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21 September 2017

Catherine Waeber Stephan

5

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21 September 2017

Peter Kopp

6

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21 September 2017

language of work or name

English

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publication date

8 January 2004

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Journal of Biological Chemistry

21 September 2017

published in

1 reference

21 September 2017

volume

279

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21 September 2017

issue

13

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21 September 2017

page(s)

13004-13010

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

21 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

A family of mammalian anion transporters and their involvement in human genetic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Prestin is the motor protein of cochlear outer hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Plasma thyrotropin bioactivity in Down's syndrome children with subclinical hypothyroidism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

A mutation in PDS causes non-syndromic recessive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Intracellular anions as the voltage sensor of prestin, the outer hair cell motor protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

The Pendred syndrome gene encodes a chloride-iodide transport protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

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/10.1074%2FJBC.M313648200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Direct repeats as selective response elements for the thyroid hormone, retinoic acid, and vitamin D3 receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Cloning of two human thyroid cDNAs encoding new members of the NADPH oxidase family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Purification of a novel flavoprotein involved in the thyroid NADPH oxidase. Cloning of the porcine and human cdnas

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Identification and Characterization of a Putative Human Iodide Transporter Located at the Apical Membrane of Thyrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Endocrinopathies in the family of endoplasmic reticulum (ER) storage diseases: disorders of protein trafficking and the role of ER molecular chaperones

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

Sulfate Transport Is Not Impaired in Pendred Syndrome Thyrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313648200

21 January 2018

Identifiers

DOI

10.1074/JBC.M313648200

1 reference

21 September 2017

1 reference