(Q24319800)

7

0 references

Hannes Lohi

1

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Minna Kujala

5

object named as

Minna Kujala

0 references

Ursula Seidler

6

object named as

Ursula Seidler

0 references

author name string

Georg Lamprecht

2

0 references

Daniel Markovich

3

0 references

Anders Heil

American Journal of Physiology - Cell Physiology

4

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language of work or name

English

0 references

publication date

March 2003

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published in

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volume

284

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issue

3

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page(s)

C769-79

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cites work

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

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

Cloning of the full-length coding sequence of rat liver-specific organic anion transporter-1 (rlst-1) and a splice variant and partial characterization of the rat lst-1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

PDZ domains: fundamental building blocks in the organization of protein complexes at the plasma membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

Specificity of anion exchange mediated by mouse Slc26a6

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

Cystic fibrosis of the pancreas. A generalised disturbance of water and electrolyte movement in exocrine tissues.

21 January 2018

2 references

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21 January 2018

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

inferred from DOI database lookup

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

Yes-associated protein 65 localizes p62(c-Yes) to the apical compartment of airway epithelia by association with EBP50

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

The Pendred syndrome gene encodes a chloride-iodide transport protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

Recognition of unique carboxyl-terminal motifs by distinct PDZ domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

Prestin is the motor protein of cochlear outer hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002

inferred from DOI database lookup

7 January 2021

based on heuristic

Genetic Disorders of Membrane Transport III. Congenital chloride diarrhea

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.00270.2002