Functional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycans
about
Molecular cloning and functional analysis of SUT-1, a sulfate transporter from human high endothelial venulesTat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signalingFunctional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9Functional analysis of nonsynonymous single nucleotide polymorphisms in human SLC26A9Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domainsAcute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytesSpecific loss of chondromodulin-I gene expression in chondrosarcoma and the suppression of tumor angiogenesis and growth by its recombinant protein in vivoPhysiological roles and regulation of mammalian sulfate transportersAutosomal recessive multiple epiphyseal dysplasia with homozygosity for C653S in the DTDST gene: double-layer patella as a reliable signSLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell typesSLC26A7 is a Cl- channel regulated by intracellular pHThe mouse Na(+)-sulfate cotransporter gene Nas1. Cloning, tissue distribution, gene structure, chromosomal assignment, and transcriptional regulation by vitamin DMolecular characterization of the murine Slc26a6 anion exchanger: functional comparison with Slc26a1The solute carrier 26 family of proteins in epithelial ion transport.Roles of Slc13a1 and Slc26a1 sulfate transporters of eel kidney in sulfate homeostasis and osmoregulation in freshwater.Localization of the sulfate/anion exchanger in the rat liver.A key role for membrane transporter NKCC1 in mediating chondrocyte volume increase in the mammalian growth plate.FGFs, heparan sulfate and FGFRs: complex interactions essential for development.Regulated transport of sulfate and oxalate by SLC26A2/DTDST.The clinical chemistry of inorganic sulfate.Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breedSolute carrier family 26 member a2 (Slc26a2) protein functions as an electroneutral SOFormula/OH-/Cl- exchanger regulated by extracellular Cl-.Nonmammalian orthologs of prestin (SLC26A5) are electrogenic divalent/chloride anion exchangers.Role of tubular secretion and carbonic anhydrase in vertebrate renal sulfate excretion.The SLC26 gene family of anion transporters and channels.Sulfate secretion and chloride absorption are mediated by the anion exchanger DRA (Slc26a3) in the mouse cecum.Sulfate transporters involved in sulfate secretion in the kidney are localized in the renal proximal tubule II of the elephant fish (Callorhinchus milii)Association of bone morphogenetic proteins with otosclerosis.Slc26a9--anion exchanger, channel and Na+ transporter.Diverse transport modes by the solute carrier 26 family of anion transporters.Mis-trafficking of bicarbonate transporters: implications to human diseases.The role of intestinal oxalate transport in hyperoxaluria and the formation of kidney stones in animals and man.Congenital chloride-losing diarrhea causing mutations in the STAS domain result in misfolding and mistrafficking of SLC26A3.Novel role for pendrin in orchestrating bicarbonate secretion in cystic fibrosis transmembrane conductance regulator (CFTR)-expressing airway serous cells.Human chondrosarcoma secretes vascular endothelial growth factor to induce tumor angiogenesis and stores basic fibroblast growth factor for regulation of its own growth.Extracellular Cl(-) regulates human SO4 (2-)/anion exchanger SLC26A1 by altering pH sensitivity of anion transport.An anion antiporter model of prestin, the outer hair cell motor protein.Sequence analyses and comparative modeling of fly and worm fibroblast growth factor receptors indicate that the determinants for FGF and heparin binding are retained in evolution.Active sulfate secretion by the intestine of winter flounder is through exchange for luminal chloride.Defects in a new class of sulfate/anion transporter link sulfur acclimation responses to intracellular glutathione levels and cell cycle control.
P2860
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P2860
Functional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycans
description
1998 nî lūn-bûn
@nan
1998 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Functional analysis of diastro ...... ated by sulfated proteoglycans
@en
Functional analysis of diastro ...... ated by sulfated proteoglycans
@nl
type
label
Functional analysis of diastro ...... ated by sulfated proteoglycans
@en
Functional analysis of diastro ...... ated by sulfated proteoglycans
@nl
prefLabel
Functional analysis of diastro ...... ated by sulfated proteoglycans
@en
Functional analysis of diastro ...... ated by sulfated proteoglycans
@nl
P2093
P2860
P356
P1476
Functional analysis of diastro ...... ated by sulfated proteoglycans
@en
P2093
P2860
P304
P356
10.1074/JBC.273.20.12307
P407
P577
1998-05-15T00:00:00Z