(Q24290545)

English

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

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scholarly article

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

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Solute carrier family 26 member 6

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GOA release 2020-03-11

Solute carrier family 26 member 1

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GOA release 2020-03-11

object named as

E Kerkelä

3

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H Lohi

1

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J Kere

6

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Ulpu Saarialho-Kere

4

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U Saarialho-Kere

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author name string

M Kujala

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M Kestilä

5

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language of work or name

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publication date

15 November 2000

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70

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102-12

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1

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Characterization of a novel zinc finger gene (ZNF165) mapping to 6p21 that is expressed specifically in testis

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Prediction of complete gene structures in human genomic DNA

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Human DRA functions as a sulfate transporter in Sf9 insect cells

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Polarized distribution of key membrane transport proteins in the rat submandibular gland

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Regulation of intracellular pH by a neuronal homolog of the erythrocyte anion exchanger

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

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Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

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Acinar lumen pH regulates endocytosis, but not exocytosis, at the apical plasma membrane of pancreatic acinar cells

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A model recognition approach to the prediction of all-helical membrane protein structure and topology

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Prestin is the motor protein of cochlear outer hair cells

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Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

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

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

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DNA sequencing with chain-terminating inhibitors

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Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1)

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Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

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

1 reference

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Regulation of [Na+]i in resting and stimulated submandibular salivary ducts

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

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

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Membrane localization of H+ and HCO3- transporters in the rat pancreatic duct

1 reference

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Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34

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Aligning a DNA sequence with a protein sequence.

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Location of the first genetic locus, PKDr1, controlling autosomal dominant polycystic kidney disease in Han:SPRD cy/+ rat

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

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

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CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

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The PROSITE database, its status in 1997.

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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Electrogenic Na+/HCO3- cotransporters: cloning and physiology

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Two types of chloride channel on duct cells cultured from human fetal pancreas

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

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Protein trafficking and polarity in kidney epithelium: from cell biology to physiology

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Distinct populations of basal keratinocytes express stromelysin-1 and stromelysin-2 in chronic wounds

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Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene

1 reference

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based on heuristic

inferred from DOI database lookup

A PDZ-interacting domain in CFTR is an apical membrane polarization signal

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Evidence for a primary defect of pancreatic HCO3-secretion in cystic fibrosis

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inferred from DOI database lookup

Identifiers

10.1006/GENO.2000.6355

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