The SLC26 gene family of multifunctional anion exchangers (Q28205615)

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English	The SLC26 gene family of multifunctional anion exchangers	scientific article (publication date: February 2004)

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instance of

scholarly article

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review article

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Europe PubMed Central

title

The SLC26 gene family of multifunctional anion exchangers (English)

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author name string

David B Mount

series ordinal

1

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Michael F Romero

series ordinal

2

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language of work or name

English

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publication date

February 2004

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published in

Pfluegers Archiv

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volume

447

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issue

5

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page(s)

710-21

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cites work

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Regulation of sulfur assimilation in higher plants: A sulfate transporter induced in sulfate-starved roots plays a central role in Arabidopsis thaliana

1 reference

stated in

PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Oxalate transport via the sulfate/HCO3 exchanger in rabbit renal basolateral membrane vesicles

1 reference

stated in

PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct outcomes of chloride diarrhoea in two siblings with identical genetic background of the disease: implications for early diagnosis and treatment

1 reference

stated in

PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

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Recessive multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279W.

1 reference

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PubMed

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12 December 2020

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Regulation of Na+-independent Cl-/HCO3- exchangers by pH.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of H(+)-coupled formate transport in rabbit renal microvillus membranes

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity for a novel DTDST mutation in a child with a 'broad bone-platyspondylic' variant of diastrophic dysplasia

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prestin is the motor protein of cochlear outer hair cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The STAS domain - a link between anion transporters and antisigma-factor antagonists

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https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestin

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specificity of anion exchange mediated by mouse Slc26a6

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Pendred syndrome gene encodes a chloride-iodide transport protein

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homologous mutations in two diverse sulphate transporters have similar effects.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recognition of unique carboxyl-terminal motifs by distinct PDZ domains

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

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Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal sulfate transport at the basolateral membrane is mediated by anion exchange

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and functional characterization of SLC26A11, a sodium-independent sulfate transporter from high endothelial venules

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a colon mucosa gene that is down-regulated in colon adenomas and adenocarcinomas

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of DRA and AE1 in rat colon by dietary Na depletion

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel amiloride-sensitive sodium-dependent proton secretion in the mouse proximal convoluted tubule

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxalate transport by anion exchange across rabbit ileal brush border

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional expression cloning of the canalicular sulfate transport system of rat hepatocytes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of the murine Slc26a6 anion exchanger: functional comparison with Slc26a1

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogenetic characterization of novel transport protein families revealed by genome analyses

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulatory interaction between the cystic fibrosis transmembrane conductance regulator and HCO3- salvage mechanisms in model systems and the mouse pancreatic duct

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis transmembrane conductance regulator regulates luminal Cl-/HCO3- exchange in mouse submandibular and pancreatic ducts

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The colon anion transporter, down-regulated in adenoma, induces growth suppression that is abrogated by E1A.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Downregulated in adenoma and putative anion transporter are regulated by CFTR in cultured pancreatic duct cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pendrin: an apical Cl-/OH-/HCO3- exchanger in the kidney cortex

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sulfate transport by flounder renal tubule brush border: presence of anion exchange

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolutionary parameters of the transcribed mammalian genome: an analysis of 2,820 orthologous rodent and human sequences

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SLC26A3 mutations in congenital chloride diarrhea

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human DRA Functions as a Sulfate Transporter in Sf9 Insect Cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anion exchange pathways for Cl- transport in rabbit renal microvillus membranes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differences in endolymphatic sac mitochondria-rich cells indicate specific functions.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in PDS causes non-syndromic recessive deafness

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specificities of heparan sulphate proteoglycans in developmental processes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down-regulated in adenoma mediates apical Cl-/HCO3- exchange in rabbit, rat, and human duodenum

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mouse sulfate anion transporter gene Sat1 (Slc26a1): cloning, tissue distribution, gene structure, functional characterization, and transcriptional regulation thyroid hormone

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of pendrin in mouse kidney

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal and intestinal absorptive defects in mice lacking the NHE3 Na+/H+ exchanger

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transport characteristics of the apical anion exchanger of rabbit cortical collecting duct beta-cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Roles of bicarbonate, cAMP, and protein tyrosine phosphorylation on capacitation and the spontaneous acrosome reaction of hamster sperm

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of an apical Cl(-)/HCO3(-) exchanger in the small intestine

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of the PDS gene in Pendred syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fibroblast growth factors induce additional limb development from the flank of chick embryos

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sulfur regulation of the sulfate transporter genes sutA and sutB in Penicillium chrysogenum

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prestin topology: localization of protein epitopes in relation to the plasma membrane

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of Na+/I- symporter and Pendred syndrome genes in trophoblast cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intestinal cancer in patients with a germline mutation in the down-regulated in adenoma (DRA) gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of mouse diastrophic dysplasia sulfate transporter gene induced during osteoblast differentiation by bone morphogenetic protein-2

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic characterization and expression of mouse prestin, the motor protein of outer hair cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of two high affinity sulfate transporters in Saccharomyces cerevisiae.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of apical and basolateral Na(+)-independent Cl-/base exchange in the rabbit superficial proximal straight tubule

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of dietary oxalate to urinary oxalate excretion

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluoroquinolone (ciprofloxacin) secretion by human intestinal epithelial (Caco‐2) cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrogenic sulfate/chloride exchange in Xenopus oocytes mediated by murine AE1 E699Q.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colocalization of the apical Cl-/HCO3- exchanger PAT1 and gastric H-K-ATPase in stomach parietal cells.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural characterization of substrates for the anion exchange transporter in Caco-2 cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prolactin regulation of the pendrin-iodide transporter in the mammary gland

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bicarbonate sulfate exchange in canalicular rat liver plasma membrane vesicles

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12759755

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00424-003-1090-3

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2119114

Dimensions Publication ID

1018545980

0 references

OpenCitations bibliographic resource ID

2119114

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2119114

PubMed publication ID

12759755

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2119114

 

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