213 related articles for article (PubMed ID: 9742093)
1. Involvement of the tyrosine kinase fer in cell adhesion.
Rosato R; Veltmaat JM; Groffen J; Heisterkamp N
Mol Cell Biol; 1998 Oct; 18(10):5762-70. PubMed ID: 9742093
[TBL] [Abstract][Full Text] [Related]
2. p120 Catenin-associated Fer and Fyn tyrosine kinases regulate beta-catenin Tyr-142 phosphorylation and beta-catenin-alpha-catenin Interaction.
Piedra J; Miravet S; Castaño J; Pálmer HG; Heisterkamp N; García de Herreros A; Duñach M
Mol Cell Biol; 2003 Apr; 23(7):2287-97. PubMed ID: 12640114
[TBL] [Abstract][Full Text] [Related]
3. Cell volume-dependent phosphorylation of proteins of the cortical cytoskeleton and cell-cell contact sites. The role of Fyn and FER kinases.
Kapus A; Di Ciano C; Sun J; Zhan X; Kim L; Wong TW; Rotstein OD
J Biol Chem; 2000 Oct; 275(41):32289-98. PubMed ID: 10921917
[TBL] [Abstract][Full Text] [Related]
4. Continuous association of cadherin with beta-catenin requires the non-receptor tyrosine-kinase Fer.
Xu G; Craig AW; Greer P; Miller M; Anastasiadis PZ; Lilien J; Balsamo J
J Cell Sci; 2004 Jul; 117(Pt 15):3207-19. PubMed ID: 15226396
[TBL] [Abstract][Full Text] [Related]
5. Tyrosine phosphorylation and src family kinases control keratinocyte cell-cell adhesion.
Calautti E; Cabodi S; Stein PL; Hatzfeld M; Kedersha N; Paolo Dotto G
J Cell Biol; 1998 Jun; 141(6):1449-65. PubMed ID: 9628900
[TBL] [Abstract][Full Text] [Related]
6. Expression of Src family kinases and their putative substrates in the human preosteoclastic cell line FLG 29.1.
Jeschke M; Brandi ML; Susa M
J Bone Miner Res; 1998 Dec; 13(12):1880-9. PubMed ID: 9844106
[TBL] [Abstract][Full Text] [Related]
7. Mice devoid of fer protein-tyrosine kinase activity are viable and fertile but display reduced cortactin phosphorylation.
Craig AW; Zirngibl R; Williams K; Cole LA; Greer PA
Mol Cell Biol; 2001 Jan; 21(2):603-13. PubMed ID: 11134346
[TBL] [Abstract][Full Text] [Related]
8. Protein kinase C-Fyn kinase cascade mediates the oleic acid-induced disassembly of neonatal rat cardiomyocyte adherens junctions.
Hsu KL; Fan HJ; Chen YC; Huang YS; Chen CH; Wu JC; Wang SM
Int J Biochem Cell Biol; 2009 Jul; 41(7):1536-46. PubMed ID: 19166962
[TBL] [Abstract][Full Text] [Related]
9. Interaction of nonreceptor tyrosine-kinase Fer and p120 catenin is involved in neuronal polarization.
Lee SH
Mol Cells; 2005 Oct; 20(2):256-62. PubMed ID: 16267401
[TBL] [Abstract][Full Text] [Related]
10. Regulation of complexed and free catenin pools by distinct mechanisms. Differential effects of Wnt-1 and v-Src.
Papkoff J
J Biol Chem; 1997 Feb; 272(7):4536-43. PubMed ID: 9020180
[TBL] [Abstract][Full Text] [Related]
11. The homeodomain transcription factors Cdx1 and Cdx2 induce E-cadherin adhesion activity by reducing beta- and p120-catenin tyrosine phosphorylation.
Ezaki T; Guo RJ; Li H; Reynolds AB; Lynch JP
Am J Physiol Gastrointest Liver Physiol; 2007 Jul; 293(1):G54-65. PubMed ID: 17463179
[TBL] [Abstract][Full Text] [Related]
12. Synapses are regulated by the cytoplasmic tyrosine kinase Fer in a pathway mediated by p120catenin, Fer, SHP-2, and beta-catenin.
Lee SH; Peng IF; Ng YG; Yanagisawa M; Bamji SX; Elia LP; Balsamo J; Lilien J; Anastasiadis PZ; Ullian EM; Reichardt LF
J Cell Biol; 2008 Dec; 183(5):893-908. PubMed ID: 19047464
[TBL] [Abstract][Full Text] [Related]
13. Insulin-like growth factor I stimulates tyrosine phosphorylation of p130(Cas), focal adhesion kinase, and paxillin. Role of phosphatidylinositol 3'-kinase and formation of a p130(Cas).Crk complex.
Casamassima A; Rozengurt E
J Biol Chem; 1998 Oct; 273(40):26149-56. PubMed ID: 9748296
[TBL] [Abstract][Full Text] [Related]
14. Identification of a new catenin: the tyrosine kinase substrate p120cas associates with E-cadherin complexes.
Reynolds AB; Daniel J; McCrea PD; Wheelock MJ; Wu J; Zhang Z
Mol Cell Biol; 1994 Dec; 14(12):8333-42. PubMed ID: 7526156
[TBL] [Abstract][Full Text] [Related]
15. Identification of Fer tyrosine kinase localized on microtubules as a platelet endothelial cell adhesion molecule-1 phosphorylating kinase in vascular endothelial cells.
Kogata N; Masuda M; Kamioka Y; Yamagishi A; Endo A; Okada M; Mochizuki N
Mol Biol Cell; 2003 Sep; 14(9):3553-64. PubMed ID: 12972546
[TBL] [Abstract][Full Text] [Related]
16. Tyrosine phosphorylation regulates the adhesions of ras-transformed breast epithelia.
Kinch MS; Clark GJ; Der CJ; Burridge K
J Cell Biol; 1995 Jul; 130(2):461-71. PubMed ID: 7542250
[TBL] [Abstract][Full Text] [Related]
17. CrkII regulates focal adhesion kinase activation by making a complex with Crk-associated substrate, p130Cas.
Iwahara T; Akagi T; Fujitsuka Y; Hanafusa H
Proc Natl Acad Sci U S A; 2004 Dec; 101(51):17693-8. PubMed ID: 15598735
[TBL] [Abstract][Full Text] [Related]
18. Complexes of focal adhesion kinase (FAK) and Crk-associated substrate (p130(Cas)) are elevated in cytoskeleton-associated fractions following adhesion and Src transformation. Requirements for Src kinase activity and FAK proline-rich motifs.
Polte TR; Hanks SK
J Biol Chem; 1997 Feb; 272(9):5501-9. PubMed ID: 9038154
[TBL] [Abstract][Full Text] [Related]
19. p130Cas, a substrate associated with v-Src and v-Crk, localizes to focal adhesions and binds to focal adhesion kinase.
Harte MT; Hildebrand JD; Burnham MR; Bouton AH; Parsons JT
J Biol Chem; 1996 Jun; 271(23):13649-55. PubMed ID: 8662921
[TBL] [Abstract][Full Text] [Related]
20. Galpha12 and Galpha13 stimulate Rho-dependent tyrosine phosphorylation of focal adhesion kinase, paxillin, and p130 Crk-associated substrate.
Needham LK; Rozengurt E
J Biol Chem; 1998 Jun; 273(23):14626-32. PubMed ID: 9603980
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]