(Q24297211)

GOA release 2020-03-11

author name string

Jean-Baptiste Vincourt

1

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Denis Jullien

2

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Francois Amalric

3

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Jean-Philippe Girard

Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene (SLC26A2): 22 novel mutations, mutation review, associated skeletal phenotypes, and diagnostic relevance

4

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language of work or name

English

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publication date

May 2003

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published in

FASEB Journal

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volume

17

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page(s)

890-2

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issue

8

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cites work

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Functional and biosynthetic changes in endothelial cells of vessels in chronically inflamed tissues: Evidence for endothelial control of lymphocyte entry into diseased tissues

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Fibroblast growth factor-2 interacts with free ribosomal protein S19

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

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/10.1096%2FFJ.02-0787FJE

7 January 2021

Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Molecular cloning of SLC26A7, a novel member of the SLC26 sulfate/anion transporter family, from high endothelial venules and kidney

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Human DRA functions as a sulfate transporter in Sf9 insect cells

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Isolation of a cDNA from Saccharomyces cerevisiae that encodes a high affinity sulphate transporter at the plasma membrane

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

An endothelial ligand for L-selectin is a novel mucin-like molecule

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

High endothelial venules (HEVs): specialized endothelium for lymphocyte migration

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Novel sulfated lymphocyte homing receptors and their control by a Core1 extension beta 1,3-N-acetylglucosaminyltransferase

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

A novel, high endothelial venule-specific sulfotransferase expresses 6-sulfo sialyl Lewis(x), an L-selectin ligand displayed by CD34.

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Sulfation of L-selectin ligands by an HEV-restricted sulfotransferase regulates lymphocyte homing to lymph nodes

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Prestin is the motor protein of cochlear outer hair cells

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Sulphation requirement for GlyCAM-1, an endothelial ligand for L-selectin

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

The Pendred syndrome gene encodes a chloride-iodide transport protein

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

A mutation in PDS causes non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Identification of a chloride-formate exchanger expressed on the brush border membrane of renal proximal tubule cells

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Expression cloning of rat renal Na+/SO4(2-) cotransport

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Plant members of a family of sulfate transporters reveal functional subtypes

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Molecular cloning and functional analysis of SUT-1, a sulfate transporter from human high endothelial venules

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

The Down regulated in Adenoma (dra) gene encodes an intestine-specific membrane sulfate transport protein

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

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/10.1096%2FFJ.02-0787FJE

7 January 2021

Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Immunohistologic and functional characterization of a vascular addressin involved in lymphocyte homing into peripheral lymph nodes

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Sulfotransferases of two specificities function in the reconstitution of high endothelial cell ligands for L-selectin

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Sulfation-dependent recognition of high endothelial venules (HEV)-ligands by L-selectin and MECA 79, and adhesion-blocking monoclonal antibody

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Sulfation of a high endothelial venule-expressed ligand for L-selectin. Effects on tethering and rolling of lymphocytes

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Sulfation and sialylation requirements for a glycoform of CD34, a major endothelial ligand for L-selectin in porcine peripheral lymph nodes

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

pEF-BOS, a powerful mammalian expression vector

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Sulfation in high endothelial venules: cloning and expression of the human PAPS synthetase

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Lymphocyte homing and homeostasis

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021

Binding of L-selectin to the vascular sialomucin CD34.

1 reference

https://api.crossref.org/works/10.1096%2FFJ.02-0787FJE

7 January 2021