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649 related items for PubMed ID: 19442658
1. Nuclear protein import is reduced in cells expressing nuclear envelopathy-causing lamin A mutants. Busch A, Kiel T, Heupel WM, Wehnert M, Hübner S. Exp Cell Res; 2009 Aug 15; 315(14):2373-85. PubMed ID: 19442658 [Abstract] [Full Text] [Related]
2. Quantitative analysis of localization and nuclear aggregate formation induced by GFP-lamin A mutant proteins in living HeLa cells. Hübner S, Eam JE, Wagstaff KM, Jans DA. J Cell Biochem; 2006 Jul 01; 98(4):810-26. PubMed ID: 16440304 [Abstract] [Full Text] [Related]
3. Laminopathy-inducing lamin A mutants can induce redistribution of lamin binding proteins into nuclear aggregates. Hübner S, Eam JE, Hübner A, Jans DA. Exp Cell Res; 2006 Jan 15; 312(2):171-83. PubMed ID: 16289535 [Abstract] [Full Text] [Related]
4. The nucleoporin Nup153 is required for nuclear pore basket formation, nuclear pore complex anchoring and import of a subset of nuclear proteins. Walther TC, Fornerod M, Pickersgill H, Goldberg M, Allen TD, Mattaj IW. EMBO J; 2001 Oct 15; 20(20):5703-14. PubMed ID: 11598013 [Abstract] [Full Text] [Related]
5. Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition. Glynn MW, Glover TW. Hum Mol Genet; 2005 Oct 15; 14(20):2959-69. PubMed ID: 16126733 [Abstract] [Full Text] [Related]
6. The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers. Delbarre E, Tramier M, Coppey-Moisan M, Gaillard C, Courvalin JC, Buendia B. Hum Mol Genet; 2006 Apr 01; 15(7):1113-22. PubMed ID: 16481358 [Abstract] [Full Text] [Related]
7. Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization. Broers JL, Kuijpers HJ, Ostlund C, Worman HJ, Endert J, Ramaekers FC. Exp Cell Res; 2005 Apr 01; 304(2):582-92. PubMed ID: 15748902 [Abstract] [Full Text] [Related]
8. The nucleoporin Nup214 sequesters CRM1 at the nuclear rim and modulates NFkappaB activation in Drosophila. Xylourgidis N, Roth P, Sabri N, Tsarouhas V, Samakovlis C. J Cell Sci; 2006 Nov 01; 119(Pt 21):4409-19. PubMed ID: 17032737 [Abstract] [Full Text] [Related]
9. Altered protein dynamics of disease-associated lamin A mutants. Gilchrist S, Gilbert N, Perry P, Ostlund C, Worman HJ, Bickmore WA. BMC Cell Biol; 2004 Dec 13; 5(1):46. PubMed ID: 15596010 [Abstract] [Full Text] [Related]
11. Dysfunction of lamin A triggers a DNA damage response and cellular senescence. Lees-Miller SP. DNA Repair (Amst); 2006 Feb 03; 5(2):286-9. PubMed ID: 16344005 [Abstract] [Full Text] [Related]
13. [The role of lamins and mutations of LMNA gene in physiological and premature aging]. Sliwińska MA. Postepy Biochem; 2007 Feb 03; 53(1):46-52. PubMed ID: 17718387 [Abstract] [Full Text] [Related]
14. The transmembrane nucleoporin NDC1 is required for targeting of ALADIN to nuclear pore complexes. Yamazumi Y, Kamiya A, Nishida A, Nishihara A, Iemura S, Natsume T, Akiyama T. Biochem Biophys Res Commun; 2009 Nov 06; 389(1):100-4. PubMed ID: 19703420 [Abstract] [Full Text] [Related]