294 related articles for article (PubMed ID: 16260476)
21. Beta-catenin can bind directly to CRM1 independently of adenomatous polyposis coli, which affects its nuclear localization and LEF-1/beta-catenin-dependent gene expression.
Ki H; Oh M; Chung SW; Kim K
Cell Biol Int; 2008 Apr; 32(4):394-400. PubMed ID: 18262809
[TBL] [Abstract][Full Text] [Related]
22. Nucleocytoplasmic shuttling of phospholipase C-delta1: a link to Ca2+.
Yagisawa H
J Cell Biochem; 2006 Feb; 97(2):233-43. PubMed ID: 16240320
[TBL] [Abstract][Full Text] [Related]
23. Nuclear export is evolutionarily conserved in CVC paired-like homeobox proteins and influences protein stability, transcriptional activation, and extracellular secretion.
Knauer SK; Carra G; Stauber RH
Mol Cell Biol; 2005 Apr; 25(7):2573-82. PubMed ID: 15767664
[TBL] [Abstract][Full Text] [Related]
24. Human topoisomerase IIalpha nuclear export is mediated by two CRM-1-dependent nuclear export signals.
Turner JG; Engel R; Derderian JA; Jove R; Sullivan DM
J Cell Sci; 2004 Jun; 117(Pt 14):3061-71. PubMed ID: 15173319
[TBL] [Abstract][Full Text] [Related]
25. Activation of p38- and CRM1-dependent nuclear export promotes E2F1 degradation during keratinocyte differentiation.
Ivanova IA; Dagnino L
Oncogene; 2007 Feb; 26(8):1147-54. PubMed ID: 16924238
[TBL] [Abstract][Full Text] [Related]
26. Impaired nuclear import of mammalian Dlx4 proteins as a consequence of rapid sequence divergence.
Coubrough ML; Bendall AJ
Exp Cell Res; 2006 Nov; 312(19):3880-91. PubMed ID: 17011548
[TBL] [Abstract][Full Text] [Related]
27. Cytoplasmic localization of calcium/calmodulin-dependent protein kinase I-alpha depends on a nuclear export signal in its regulatory domain.
Stedman DR; Uboha NV; Stedman TT; Nairn AC; Picciotto MR
FEBS Lett; 2004 May; 566(1-3):275-80. PubMed ID: 15147908
[TBL] [Abstract][Full Text] [Related]
28. Topoisomerase II binds importin alpha isoforms and exportin/CRM1 but does not shuttle between the nucleus and cytoplasm in proliferating cells.
Mirski SE; Sparks KE; Friedrich B; Köhler M; Mo YY; Beck WT; Cole SP
Exp Cell Res; 2007 Feb; 313(3):627-37. PubMed ID: 17182034
[TBL] [Abstract][Full Text] [Related]
29. Two separate regions essential for nuclear import of the hnRNP D nucleocytoplasmic shuttling sequence.
Suzuki M; Iijima M; Nishimura A; Tomozoe Y; Kamei D; Yamada M
FEBS J; 2005 Aug; 272(15):3975-87. PubMed ID: 16045768
[TBL] [Abstract][Full Text] [Related]
30. Nup214 is required for CRM1-dependent nuclear protein export in vivo.
Hutten S; Kehlenbach RH
Mol Cell Biol; 2006 Sep; 26(18):6772-85. PubMed ID: 16943420
[TBL] [Abstract][Full Text] [Related]
31. Modulation of nucleocytoplasmic trafficking by retention in cytoplasm or nucleus.
Roth DM; Harper I; Pouton CW; Jans DA
J Cell Biochem; 2009 Aug; 107(6):1160-7. PubMed ID: 19507231
[TBL] [Abstract][Full Text] [Related]
32. Novel shuttling domain in a regulator (RSC1A1) of transporter SGLT1 steers cell cycle-dependent nuclear location.
Filatova A; Leyerer M; Gorboulev V; Chintalapati C; Reinders Y; Müller TD; Srinivasan A; Hübner S; Koepsell H
Traffic; 2009 Nov; 10(11):1599-618. PubMed ID: 19765263
[TBL] [Abstract][Full Text] [Related]
33. Myb-binding protein 1a is a nucleocytoplasmic shuttling protein that utilizes CRM1-dependent and independent nuclear export pathways.
Keough RA; Macmillan EM; Lutwyche JK; Gardner JM; Tavner FJ; Jans DA; Henderson BR; Gonda TJ
Exp Cell Res; 2003 Sep; 289(1):108-23. PubMed ID: 12941609
[TBL] [Abstract][Full Text] [Related]
34. Subcellular localisation of human inositol 1,4,5-trisphosphate 3-kinase C: species-specific use of alternative export sites for nucleo-cytoplasmic shuttling indicates divergent roles of the catalytic and N-terminal domains.
Nalaskowski MM; Windhorst S; Stockebrand MC; Mayr GW
Biol Chem; 2006 May; 387(5):583-93. PubMed ID: 16740130
[TBL] [Abstract][Full Text] [Related]
35. Two motifs essential for nuclear import of the hnRNP A1 nucleocytoplasmic shuttling sequence M9 core.
Iijima M; Suzuki M; Tanabe A; Nishimura A; Yamada M
FEBS Lett; 2006 Feb; 580(5):1365-70. PubMed ID: 16455081
[TBL] [Abstract][Full Text] [Related]
36. Subcellular trafficking signals of constitutive androstane receptor: evidence for a nuclear export signal in the DNA-binding domain.
Xia J; Kemper B
Drug Metab Dispos; 2007 Sep; 35(9):1489-94. PubMed ID: 17567731
[TBL] [Abstract][Full Text] [Related]
37. Identification of the sequence determinants mediating the nucleo-cytoplasmic shuttling of TIAR and TIA-1 RNA-binding proteins.
Zhang T; Delestienne N; Huez G; Kruys V; Gueydan C
J Cell Sci; 2005 Dec; 118(Pt 23):5453-63. PubMed ID: 16278295
[TBL] [Abstract][Full Text] [Related]
38. Transport of galectin-3 between the nucleus and cytoplasm. I. Conditions and signals for nuclear import.
Davidson PJ; Li SY; Lohse AG; Vandergaast R; Verde E; Pearson A; Patterson RJ; Wang JL; Arnoys EJ
Glycobiology; 2006 Jul; 16(7):602-11. PubMed ID: 16473835
[TBL] [Abstract][Full Text] [Related]
39. RNA-binding of the human cytomegalovirus transactivator protein UL69, mediated by arginine-rich motifs, is not required for nuclear export of unspliced RNA.
Toth Z; Lischka P; Stamminger T
Nucleic Acids Res; 2006; 34(4):1237-49. PubMed ID: 16500893
[TBL] [Abstract][Full Text] [Related]
40. Nuclear import and export signals are essential for proper cellular trafficking and function of ZIC3.
Bedard JE; Purnell JD; Ware SM
Hum Mol Genet; 2007 Jan; 16(2):187-98. PubMed ID: 17185387
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]