ライフサイエンスコーパス: c-Yes

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1 he expression of the src family kinase (SFK) c-Yes.

2 The magnitude of c-Yes activation correlated with the degree of invasion

3 c-Yes activities and protein levels are elevated in huma

4 henotype, we determined whether NT stimulate c-Yes activity in human MeWo melanoma cells and two vari

5 Metastatic TXM-13 and TXM-18 increased c-Yes activity in response to NGF.

6 atic 70W subline had an intrinsically higher c-Yes activity than parental MeWo or poorly metastatic 3

7 analogous myristoylated peptide derived from c-Yes also has no inhibitory activity.

8 change in expression of the related kinases c-Yes and c-Lyn, and proliferation rates were similar in

9 lated cell motility of triple-null Src(-/-), c-Yes(-/-), and Fyn(-/-) fibroblasts was dependent on c-

10 ously expressed Src tyrosine kinases (c-Src, c-Yes, and c-Fyn) regulate intestinal cell growth and di

11 rophic agonist, increased activity of c-Src, c-Yes, and Fyn within minutes and promoted a selective r

12 dy into these cells and found that only anti-c-Yes antibody blocked GLUT4 translocation (70% decrease

13 ed, we microinjected anti-c-Src, -c-Fyn, or -c-Yes antibody into these cells and found that only anti

14 These results identify c-Yes as a cellular protein that is involved in WNV asse

15 In NIH3T3 fibroblasts, c-Src, Fyn, and c-Yes associate with the activated PDGF receptor, are su

16 calized with the nonreceptor tyrosine kinase c-Yes at cell junction areas and formed an immunoprecipi

17 Unlike c-Src, Hck, Lyn, and c-Yes bind more generally to beta1A, beta2, and beta3 cy

18 RNA interference mediated knock-down of c-Yes, but not c-Src, and similarly reduced virus yield,

19 cells reconstituted individually with c-Src, c-Yes, c-Fyn, and wild type or phosphorylation site muta

20 revealed that it partitions differently than c-yes, demonstrating that the brush border src kinases a

21 sorbent assay, whereas the overexpression of c-Yes did not modify this interaction.

22 Together, these data suggest that altered c-Yes expression may play a role in the malignant progre

23 rafts and displacement of the SFK, Fyn, and c-Yes from caveolae/lipid rafts.

24 The Src family kinases c-Src, c-Yes, Fyn, and Lyn were expressed and activated by tran

25 lly, human NGF and neurotrophin-3 stimulated c-Yes in brain-metastatic 70W cells.

26 To further examine NT stimulation of c-Yes in melanoma cells, three additional cell lines wer

27 henotype and that NT enhance the activity of c-Yes in signaling penetration into the matrix of NT-ric

28 nd formed an immunoprecipitable complex with c-Yes in vivo.

29 educed virus yield, specifically implicating c-Yes in WNV production.

30 d in medium without Ca(2+) or treated with a c-Yes inhibitor, CGP77675.

31 we show that the nonreceptor tyrosine kinase c-Yes is contained within EBP50 protein complexes by ass

32 ls, and that the nonreceptor tyrosine kinase c-Yes is involved in the regulation of this process.

33 c-Yes kinase was further induced by the prototypic human

34 inct from that resulting from suppression of c-Yes kinase.

35 , containing the nonreceptor tyrosine kinase c-Yes, may regulate apical signal transduction pathways

36 ntrast electroporation of antibodies against c-Yes or c-Fyn had no effect.

37 sferase reporter, while expression of either c-Yes or Fyn was considerably less effective in this reg

38 The c-Yes proto-oncogene (pp62c-Yes) encodes a non-receptor-

39 The c-src and c-yes proto-oncogenes encode 60 000 and 62 000 Dalton no

40 Since overexpression of an activated form of c-Yes resulted in tyrosine phosphorylation of p53BP-2, w

41 ccludin itself, ZO-1, protein kinase C-zeta, c-Yes, the regulatory subunit of phosphatidylinositol 3-

42 A constitutively active form of c-Yes was observed to decrease the binding affinity betw

43 thymidylate synthase and its adjacent gene, c-Yes, was detected in the resistant cell lines.

44 o recruits non-membrane proteins such as the c-Yes/YAP-65 complex, members of the phospholipase Cbeta

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