900 related articles for article (PubMed ID: 12732141)
21. Nuclear transport of the serum response factor coactivator MRTF-A is downregulated at tensional homeostasis.
McGee KM; Vartiainen MK; Khaw PT; Treisman R; Bailly M
EMBO Rep; 2011 Sep; 12(9):963-70. PubMed ID: 21799516
[TBL] [Abstract][Full Text] [Related]
22. Novel Rho/MRTF/SRF inhibitors block matrix-stiffness and TGF-β-induced fibrogenesis in human colonic myofibroblasts.
Johnson LA; Rodansky ES; Haak AJ; Larsen SD; Neubig RR; Higgins PD
Inflamm Bowel Dis; 2014 Jan; 20(1):154-65. PubMed ID: 24280883
[TBL] [Abstract][Full Text] [Related]
23. Epithelial Protein Lost in Neoplasm alpha (Eplin-alpha) is transcriptionally regulated by G-actin and MAL/MRTF coactivators.
Leitner L; Shaposhnikov D; Descot A; Hoffmann R; Posern G
Mol Cancer; 2010 Mar; 9():60. PubMed ID: 20236507
[TBL] [Abstract][Full Text] [Related]
24. Epithelial cell-cell contacts regulate SRF-mediated transcription via Rac-actin-MAL signalling.
Busche S; Descot A; Julien S; Genth H; Posern G
J Cell Sci; 2008 Apr; 121(Pt 7):1025-35. PubMed ID: 18334560
[TBL] [Abstract][Full Text] [Related]
25. The RhoA/Rho kinase pathway regulates nuclear localization of serum response factor.
Liu HW; Halayko AJ; Fernandes DJ; Harmon GS; McCauley JA; Kocieniewski P; McConville J; Fu Y; Forsythe SM; Kogut P; Bellam S; Dowell M; Churchill J; Lesso H; Kassiri K; Mitchell RW; Hershenson MB; Camoretti-Mercado B; Solway J
Am J Respir Cell Mol Biol; 2003 Jul; 29(1):39-47. PubMed ID: 12600823
[TBL] [Abstract][Full Text] [Related]
26. Nuclear actin network assembly by formins regulates the SRF coactivator MAL.
Baarlink C; Wang H; Grosse R
Science; 2013 May; 340(6134):864-7. PubMed ID: 23558171
[TBL] [Abstract][Full Text] [Related]
27. Rnd3/RhoE expression is regulated by G-actin through MKL1-SRF signaling pathway.
Piquet L; Robbe T; Neaud V; Basbous S; Rosciglione S; Saltel F; Moreau V
Exp Cell Res; 2018 Sep; 370(2):227-236. PubMed ID: 29940177
[TBL] [Abstract][Full Text] [Related]
28. Phosphorylation acts positively and negatively to regulate MRTF-A subcellular localisation and activity.
Panayiotou R; Miralles F; Pawlowski R; Diring J; Flynn HR; Skehel M; Treisman R
Elife; 2016 Jun; 5():. PubMed ID: 27304076
[TBL] [Abstract][Full Text] [Related]
29. Megakaryoblastic leukemia 1, a potent transcriptional coactivator for serum response factor (SRF), is required for serum induction of SRF target genes.
Cen B; Selvaraj A; Burgess RC; Hitzler JK; Ma Z; Morris SW; Prywes R
Mol Cell Biol; 2003 Sep; 23(18):6597-608. PubMed ID: 12944485
[TBL] [Abstract][Full Text] [Related]
30. Prostaglandin E2 inhibits α-smooth muscle actin transcription during myofibroblast differentiation via distinct mechanisms of modulation of serum response factor and myocardin-related transcription factor-A.
Penke LR; Huang SK; White ES; Peters-Golden M
J Biol Chem; 2014 Jun; 289(24):17151-62. PubMed ID: 24802754
[TBL] [Abstract][Full Text] [Related]
31. Induction of megakaryocyte differentiation drives nuclear accumulation and transcriptional function of MKL1 via actin polymerization and RhoA activation.
Smith EC; Teixeira AM; Chen RC; Wang L; Gao Y; Hahn KL; Krause DS
Blood; 2013 Feb; 121(7):1094-101. PubMed ID: 23243284
[TBL] [Abstract][Full Text] [Related]
32. Nuclear actin and myocardin-related transcription factors control disuse muscle atrophy through regulation of Srf activity.
Collard L; Herledan G; Pincini A; Guerci A; Randrianarison-Huetz V; Sotiropoulos A
J Cell Sci; 2014 Dec; 127(Pt 24):5157-63. PubMed ID: 25344251
[TBL] [Abstract][Full Text] [Related]
33. Myocardin-related transcription factor A regulates expression of Bok and Noxa and is involved in apoptotic signalling.
Shaposhnikov D; Descot A; Schilling J; Posern G
Cell Cycle; 2012 Jan; 11(1):141-50. PubMed ID: 22185759
[TBL] [Abstract][Full Text] [Related]
34. Megakaryoblastic leukemia-1/2, a transcriptional co-activator of serum response factor, is required for skeletal myogenic differentiation.
Selvaraj A; Prywes R
J Biol Chem; 2003 Oct; 278(43):41977-87. PubMed ID: 14565952
[TBL] [Abstract][Full Text] [Related]
35. Myocardin-related transcription factors and SRF are required for cytoskeletal dynamics and experimental metastasis.
Medjkane S; Perez-Sanchez C; Gaggioli C; Sahai E; Treisman R
Nat Cell Biol; 2009 Mar; 11(3):257-68. PubMed ID: 19198601
[TBL] [Abstract][Full Text] [Related]
36. Expression profiling of serum inducible genes identifies a subset of SRF target genes that are MKL dependent.
Selvaraj A; Prywes R
BMC Mol Biol; 2004 Aug; 5():13. PubMed ID: 15329155
[TBL] [Abstract][Full Text] [Related]
37. The diaphanous-related formin mDia1 controls serum response factor activity through its effects on actin polymerization.
Copeland JW; Treisman R
Mol Biol Cell; 2002 Nov; 13(11):4088-99. PubMed ID: 12429848
[TBL] [Abstract][Full Text] [Related]
38. Myocardin/MKL family of SRF coactivators: key regulators of immediate early and muscle specific gene expression.
Cen B; Selvaraj A; Prywes R
J Cell Biochem; 2004 Sep; 93(1):74-82. PubMed ID: 15352164
[TBL] [Abstract][Full Text] [Related]
39. Signal-regulated activation of serum response factor is mediated by changes in actin dynamics.
Sotiropoulos A; Gineitis D; Copeland J; Treisman R
Cell; 1999 Jul; 98(2):159-69. PubMed ID: 10428028
[TBL] [Abstract][Full Text] [Related]
40. Mutant actins demonstrate a role for unpolymerized actin in control of transcription by serum response factor.
Posern G; Sotiropoulos A; Treisman R
Mol Biol Cell; 2002 Dec; 13(12):4167-78. PubMed ID: 12475943
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]