language:
Find link is a tool written by Edward Betts.searching for Sulfate transporter 15 found (17 total)
alternate case: sulfate transporter
Achondrogenesis
(340 words)
[view diff]
exact match in snippet
view article
find links to article
type 1B is caused by a similar mutation in SLC26A2, which encodes a sulfate transporter. Achondrogenesis, type 2 is one of several skeletal disorders causedSLC26A8 (393 words) [view diff] exact match in snippet view article find links to article
Pineau C, Becq F, Dorseuil O, Gacon G (Jun 2001). "Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linkedSulfur assimilation (4,104 words) [view diff] exact match in snippet view article find links to article
concentration of sulfate in the cytoplasm is kept rather constant. Distinct sulfate transporter proteins mediate the uptake, transport and subcellular distributionChondrogenesis (1,159 words) [view diff] exact match in snippet view article find links to article
the list of genes that regulate chondrogenesis. The SLC26A2 is a sulfate transporter. Defects result in several forms of osteochondrodysplasia. ChondrogenesisSul1 RNA motif (252 words) [view diff] exact match in snippet view article find links to article
domains (whose gene is named sul1) is believed to function as a sulfate transporter. Other common protein domains function as Serine O-acetyltransferaseChloride anion exchanger (1,139 words) [view diff] exact match in snippet view article find links to article
by this gene is a transmembrane glycoprotein that functions as a sulfate transporter. It is localized to the mucosa of the lower intestinal tract, particularlyTranslocase (3,000 words) [view diff] exact match in snippet view article find links to article
[side 2] + [phosphonate- binding protein][side 1] 7.3.2.3 ABC-type sulfate transporter The expected taxonomic range for this enzyme is: Eukaryota, BacteriaChromosome 5 (2,298 words) [view diff] exact match in snippet view article find links to article
Endothelial cell-specific molecule 1 DTDST: diastrophic dysplasia sulfate transporter EIF4E1B: encoding protein Eukaryotic translation initiation factorList of EC numbers (EC 7) (1,043 words) [view diff] exact match in snippet view article
7.3.2.2: ABC-type phosphonate transporter * EC 7.3.2.3: ABC-type sulfate transporter * EC 7.3.2.4: ABC-type nitrate transporter * EC 7.3.2.5: ABC-typeRACGAP1 (1,608 words) [view diff] exact match in snippet view article find links to article
Toure A, Morin L, Pineau C, et al. (June 2001). "Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linkedMonocarboxylate transporter 10 (501 words) [view diff] exact match in snippet view article find links to article
PMID 11827462. Toure A, Morin L, Pineau C, et al. (2001). "Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linkedDivalent anion–sodium symporter (624 words) [view diff] exact match in snippet view article find links to article
hNaSi-1 carriers has been proposed. Two serine residues in the human sulfate transporter, hNaSi-1 (TC# 2.A.47.1.16; Q9BZW2), one in TMS 5 and one in TMS 6Sulfate permease (1,464 words) [view diff] exact match in snippet view article find links to article
sulfotransferase (TC# 2.A.53.9.1). This SulP homologue is presumably a sulfate transporter. Homologues currently characterized in the SulP family can be foundMultiple epiphyseal dysplasia (2,399 words) [view diff] exact match in snippet view article find links to article
almost 90% of the patients, causing diastrophic dysplasia. It is a sulfate transporter, transmembrane glycoprotein implicated in several chondrodysplasiasTransporter Classification Database (5,159 words) [view diff] case mismatch in snippet view article find links to article
A.120 The Putative Amino Acid Permease (PAAP) Family 2.A.121 The Sulfate Transporter (CysZ) Family 2.A.122 The LrgB/CidB holin-like auxiliary protein