ライフサイエンスコーパス: sulfate transporter

1 , pendrin has been proposed to function as a sulfate transporter.

2 tion of sulfate uptake and expression of the sulfate transporters.

3 ane glycoprotein and a member of a family of sulfate transporters.

4 ough the interaction between its cytoplasmic sulfate transporter and anti-sigma (STAS) domain and the

5 tructures also show interactions between the Sulfate Transporter and Anti-Sigma factor antagonist (ST

6 ansmembrane (TM) domains and two cytoplasmic sulfate transporter and anti-sigma factor antagonist (ST

7 hway for matrix assembly via modulation of a sulfate transporter and proteoglycan sulfation.

8 panning alpha-helices and a C-terminal STAS (sulfate transporters and anti-sigma-factor) domain homol

9 Sulfate transporters and genes involved in sulfate and M

10 cal for the activity of Arabidopsis thaliana sulfate transporters, and specific lesions in this domai

11 impaired, but deletion of the adjacent STAS (sulfate transporter anti-sigma factor antagonist) domain

12 gulator (CFTR), (R)CFTR, via the Slc26-STAS (sulfate transporter anti-sigma) domain, resulting in mut

13 s of SULTR1;2, which encodes a high-affinity sulfate transporter, are defective in sulfate transport

14 conserved miRNA that targets a low-affinity sulfate transporter (AST68) and three ATP sulfurylases (

15 th treatments also caused up-regulation of a sulfate transporter, but only in the case of sulfur defi

16 member of the sodium-dependent dicarboxylate/sulfate transporter called SDCT2.

17 e exchange of STAS domains between different sulfate transporters, can severely impair transport acti

18 ed sulfate/anion transporters that contain a sulfate transporter domain and are found in a widely dis

19 ral residue substitutions near the conserved sulfate transporter domain of prestin either greatly red

20 nsporter (encoded by DTD; 32%) and the human sulfate transporter 'downregulated in adenoma' (encoded

21 The diastrophic dysplasia sulfate transporter (DTDST) gene encodes a transmembrane

22 Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene have been linked to fou

23 Diastrophic dysplasia sulfate transporter (DTDST) is a sulfate/chloride antipo

24 e identity), the human diastrophic dysplasia sulfate transporter (encoded by DTD; 32%) and the human

25 5'phosphosulfate reductase genes, along with sulfate transporters, especially those involved in sulfa

26 e; however, root proliferation and increased sulfate transporter expression occurred as in S-deficien

27 so tested for effects on selenate uptake and sulfate transporters' expression.

28 d functionally characterized a high-affinity sulfate transporter from the endophytic fungus Serendipi

29 d by a mutation in the diastrophic dysplasia sulfate transporter gene (SLC26A).

30 The sel1 mutants contain lesions in the sulfate transporter gene Sultr1;2 located on the lower a

31 he recently identified diastrophic dysplasia sulfate-transporter gene (DTDST).

32 asing severity caused by lesions in a single sulfate-transporter gene.

33 he sequence analysis classified the Brassica sulfate transporter genes into four different groups.

34 The sulfate transporter genes of Groups 1, 2, and 4 were ind

35 cDNAs corresponding to 12 different sulfate transporter genes representing the complete gene

36 tiana tobacum, which belongs to low affinity sulfate transporter group.

37 The STAS domain in sulfate transporters has significant similarity to bacte

38 SLC26A2 is the primary sodium-independent sulfate transporter in cartilage and bone and is importa

39 ion exome analysis, we identify SLC26A1 as a sulfate transporter in humans and experimentally validat

40 The high expression of sulfate transporters in certain Astragalus species may l

41 Sulfate transporters in plants and animals are structura

42 Sulfate transporters in plants represent a family of pro

43 reased expression of genes encoding specific sulfate transporters in roots and other plant parts.

44 ing or modifying the STAS domain of dominant sulfate transporters in roots of Arabidopsis thaliana.

45 ons 260 and 288, are conserved in all of the sulfate transporters in the family whereas the NaDC cont

46 Sul1 and Sul2 are sulfate transporters in the yeast Saccharomyces cerevisi

47 teractions between residues surrounding the "sulfate transporter motif" is essential for normal prest

48 ing invasive pulmonary aspergillosis since a sulfate transporter mutant strain and a sulfite reductas

49 nine-dependent growth phenotype of the yeast sulfate transporter mutant strain CP154-7B.

50 pecifically, uptake of selenate (probably by sulfate transporters) occurred at a much higher rate tha

51 The A. thaliana Sultr1;2 and Sultr1;1 sulfate transporters rescue the methionine-dependent gro

52 ls all the criteria expected of a functional sulfate transporter responding to sulfur limitation: SiS

53 The expression of the different sulfate transporters showed a complex pattern of tissue

54 logy and the presence of a slightly modified sulfate-transporter signature sequence comprising its pu

55 y analyzing the expression of genes encoding sulfate transporters (STs) of groups 1, 2, and 4 (SlST1.

56 p sulfate and ABA, stomatal conductance, and sulfate transporter (SULTR) expression.

57 One sulfate transporter (SULTR) gene NtaSULTR2 was identifie

58 Plant sulfate transporters (SULTR) mediate absorption and dist

59 , such as late embryogenesis abundant (LEA), sulfate transporters (SULTR), NAM-ATAF-CUC (NAC), and ni

60 d constitutive upregulation in S. pinnata of sulfate transporters SULTR1;2 (root influx) and SULTR2;1

61 icroarray studies identified a high-affinity sulfate transporter (SULTR1;2) among the most robust and

62 ion to its known function as a high-affinity sulfate transporter, SULTR1;2 may have a regulatory role

63 fate assimilation, as well as a low-affinity sulfate transporter, SULTR2;1, is strongly induced by su

64 show that SLC26a2/7 is a ventrally expressed sulfate transporter that promotes a ventral accumulation

65 in has a role in controlling the activity of sulfate transporters, their stability, or their localiza

66 Fusing the STAS domain from other sulfate transporters to Sultr1;2 DeltaSTAS constructs re

67 ux pumps employed to remove cadmium, while a sulfate transporter was down-regulated to reduce nonspec

68 rivation, although the expression of Group 3 sulfate transporters was not affected by the sulfate sta

69 pecies, abundant gene expression of putative sulfate transporters was observed for both Se-hyperaccum

70 d the sphX gene, and transcripts of multiple sulfate transporter were also significantly more abundan

71 quisition genes encoding for a high-affinity sulfate transporter were significantly induced, while de

72 cDNAs for homologs of groups 1 to 4 sulfate transporters were cloned from these Astragalus s