(Q41791767)

10 October 2017

title

Protein localization of SLC26A2 (DTDST) in rat kidney (English)

1 reference

10 October 2017

Jeannie M Chapman

1

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10 October 2017

Lawrence P Karniski

series ordinal

2

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10 October 2017

publication date

6 April 2010

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10 October 2017

number of pages

7

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Histochemistry and Cell Biology

inferred from page(s)

published in

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10 October 2017

volume

133

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10 October 2017

issue

5

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10 October 2017

page(s)

541-547

1 reference

https://scigraph.springernature.com/pub.10.1007/s00418-010-0694-x

10 October 2017

exact match

0 references

cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00418-010-0694-X

Pathways for oxalate transport in rabbit renal microvillus membrane vesicles

21 January 2018

1 reference

12 December 2020

Calcium oxalate urolithiasis in mice lacking anion transporter Slc26a6

1 reference

12 December 2020

The SLC26 gene family of multifunctional anion exchangers

1 reference

12 December 2020

Linking receptor-mediated endocytosis and cell signaling: evidence for regulated intramembrane proteolysis of megalin in proximal tubule

1 reference

12 December 2020

Mechanisms of stimulation of proximal tubule chloride transport by formate and oxalate

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias

1 reference

12 December 2020

Effects of sulfate and chloride on three separate oxalate transporters reconstituted from rabbit renal cortex

1 reference

12 December 2020

The human renal sodium sulfate cotransporter (SLC13A1; hNaSi-1) cDNA and gene: organization, chromosomal localization, and functional characterization.

1 reference

12 December 2020

A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Renal and intestinal transport defects in Slc26a6-null mice

1 reference

12 December 2020

Detection of two forms of GP330. Their role in Heymann nephritis.

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

The down-regulated in adenoma (DRA) gene encodes an intestine-specific membrane glycoprotein

1 reference

12 December 2020

Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene: correlation between sulfate transport activity and chondrodysplasia phenotype.

1 reference

12 December 2020

Specificity and regulation of renal sulfate transporters

1 reference

12 December 2020

Essential roles of CFEX-mediated Cl(-)-oxalate exchange in proximal tubule NaCl transport and prevention of urolithiasis

1 reference

12 December 2020

Functional expression and cellular distribution of diastrophic dysplasia sulfate transporter (DTDST) gene mutations in HEK cells.

1 reference

12 December 2020

Immunolocalization of Na/SO4-cotransport (NaSi-1) in rat kidney

1 reference

12 December 2020

Immunolocalization of anion transporter Slc26a7 in mouse kidney

1 reference

12 December 2020

Mouse down-regulated in adenoma (DRA) is an intestinal Cl(-)/HCO(3)(-) exchanger and is up-regulated in colon of mice lacking the NHE3 Na(+)/H(+) exchanger

1 reference

12 December 2020

Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea.

1 reference

12 December 2020

The pathogenic antigen of Heymann nephritis is a membrane glycoprotein of the renal proximal tubule brush border

1 reference

12 December 2020

Hyposulfatemia, growth retardation, reduced fertility, and seizures in mice lacking a functional NaSi-1 gene.

1 reference

12 December 2020

Immunolocalization of sat-1 sulfate/oxalate/bicarbonate anion exchanger in the rat kidney

1 reference

12 December 2020

Recessively inherited multiple epiphyseal dysplasia with normal stature, club foot, and double layered patella caused by a DTDST mutation

1 reference

12 December 2020

10.1007/S00418-010-0694-X

Identifiers

DOI

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release_utk5ah7ra5dshf5q3swkuufpcy

10 October 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/utk5ah7ra5dshf5q3swkuufpcy

24 November 2022

mapped directly with Wikidata item

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