(Q28207018)

English

SLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell types

scientific article (publication date: August 2001)

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scholarly article

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SLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell types (English)

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1 reference

based on heuristic

inferred from title

diastrophic dysplasia

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based on heuristic

inferred from title

object named as

J Kere

5

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author name string

S Haila

1

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J Hästbacka

2

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T Böhling

3

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M L Karjalainen-Lindsberg

4

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U Saarialho-Kere

6

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language of work or name

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publication date

August 2001

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Journal of Histochemistry and Cytochemistry

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49

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8

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973-82

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Sulfate transport in human placenta: further evidence for a sodium-independent mechanism

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

Altered sulfate transport via anion exchange in CFPAC is corrected by retrovirus-mediated CFTR gene transfer

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

Ultrastructural localization of glycosaminoglycans in human term placenta

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

Heparan sulfate oligosaccharides require 6-O-sulfation for promotion of basic fibroblast growth factor mitogenic activity

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

Undersulfation of proteoglycans synthesized by chondrocytes from a patient with achondrogenesis type 1B homozygous for an L483P substitution in the diastrophic dysplasia sulfate transporter.

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

Functional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycans

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

The Pendred syndrome gene encodes a chloride-iodide transport protein

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

Prestin is the motor protein of cochlear outer hair cells

1 reference

https://api.crossref.org/works/10.1177%2F002215540104900805

21 January 2018

Identifiers

10.1177/002215540104900805

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