294 related articles for article (PubMed ID: 16440304)
1. 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; 98(4):810-26. PubMed ID: 16440304
[TBL] [Abstract][Full Text] [Related]
2. 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; 315(14):2373-85. PubMed ID: 19442658
[TBL] [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; 312(2):171-83. PubMed ID: 16289535
[TBL] [Abstract][Full Text] [Related]
4. 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; 14(20):2959-69. PubMed ID: 16126733
[TBL] [Abstract][Full Text] [Related]
5. 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; 15(7):1113-22. PubMed ID: 16481358
[TBL] [Abstract][Full Text] [Related]
6. Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo.
Holt I; Ostlund C; Stewart CL; Man Nt; Worman HJ; Morris GE
J Cell Sci; 2003 Jul; 116(Pt 14):3027-35. PubMed ID: 12783988
[TBL] [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; 304(2):582-92. PubMed ID: 15748902
[TBL] [Abstract][Full Text] [Related]
8. 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; 5(1):46. PubMed ID: 15596010
[TBL] [Abstract][Full Text] [Related]
9. The lamin CxxM motif promotes nuclear membrane growth.
Prüfert K; Vogel A; Krohne G
J Cell Sci; 2004 Dec; 117(Pt 25):6105-16. PubMed ID: 15546914
[TBL] [Abstract][Full Text] [Related]
10. Nuclear titin interacts with A- and B-type lamins in vitro and in vivo.
Zastrow MS; Flaherty DB; Benian GM; Wilson KL
J Cell Sci; 2006 Jan; 119(Pt 2):239-49. PubMed ID: 16410549
[TBL] [Abstract][Full Text] [Related]
11. Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy.
Motsch I; Kaluarachchi M; Emerson LJ; Brown CA; Brown SC; Dabauvalle MC; Ellis JA
Eur J Cell Biol; 2005 Sep; 84(9):765-81. PubMed ID: 16218190
[TBL] [Abstract][Full Text] [Related]
12. RNAi of FACE1 protease results in growth inhibition of human cells expressing lamin A: implications for Hutchinson-Gilford progeria syndrome.
Gruber J; Lampe T; Osborn M; Weber K
J Cell Sci; 2005 Feb; 118(Pt 4):689-96. PubMed ID: 15671064
[TBL] [Abstract][Full Text] [Related]
13. Partial cleavage of A-type lamins concurs with their total disintegration from the nuclear lamina during apoptosis.
Broers JL; Bronnenberg NM; Kuijpers HJ; Schutte B; Hutchison CJ; Ramaekers FC
Eur J Cell Biol; 2002 Dec; 81(12):677-91. PubMed ID: 12553668
[TBL] [Abstract][Full Text] [Related]
14. Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells.
Kandert S; Lüke Y; Kleinhenz T; Neumann S; Lu W; Jaeger VM; Munck M; Wehnert M; Müller CR; Zhou Z; Noegel AA; Dabauvalle MC; Karakesisoglou I
Hum Mol Genet; 2007 Dec; 16(23):2944-59. PubMed ID: 17881656
[TBL] [Abstract][Full Text] [Related]
15. Towards a Drosophila model of Hutchinson-Gilford progeria syndrome.
Beard GS; Bridger JM; Kill IR; Tree DR
Biochem Soc Trans; 2008 Dec; 36(Pt 6):1389-92. PubMed ID: 19021561
[TBL] [Abstract][Full Text] [Related]
16. Lco1 is a novel widely expressed lamin-binding protein in the nuclear interior.
Vlcek S; Foisner R; Wilson KL
Exp Cell Res; 2004 Aug; 298(2):499-511. PubMed ID: 15265697
[TBL] [Abstract][Full Text] [Related]
17. CTP:phosphocholine cytidylyltransferase α (CCTα) and lamins alter nuclear membrane structure without affecting phosphatidylcholine synthesis.
Gehrig K; Ridgway ND
Biochim Biophys Acta; 2011 Jun; 1811(6):377-85. PubMed ID: 21504799
[TBL] [Abstract][Full Text] [Related]
18. Expression of disease-causing lamin A mutants impairs the formation of DNA repair foci.
Manju K; Muralikrishna B; Parnaik VK
J Cell Sci; 2006 Jul; 119(Pt 13):2704-14. PubMed ID: 16772334
[TBL] [Abstract][Full Text] [Related]
19. Effects of expressing lamin A mutant protein causing Emery-Dreifuss muscular dystrophy and familial partial lipodystrophy in HeLa cells.
Bechert K; Lagos-Quintana M; Harborth J; Weber K; Osborn M
Exp Cell Res; 2003 May; 286(1):75-86. PubMed ID: 12729796
[TBL] [Abstract][Full Text] [Related]
20. Nucleocytoplasmic transport in cells with progerin-induced defective nuclear lamina.
Ferri G; Storti B; Bizzarri R
Biophys Chem; 2017 Oct; 229():77-83. PubMed ID: 28712764
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
