829 related articles for article (PubMed ID: 15367494)
1. Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.
Broers JL; Peeters EA; Kuijpers HJ; Endert J; Bouten CV; Oomens CW; Baaijens FP; Ramaekers FC
Hum Mol Genet; 2004 Nov; 13(21):2567-80. PubMed ID: 15367494
[TBL] [Abstract][Full Text] [Related]
2. Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction.
Lammerding J; Schulze PC; Takahashi T; Kozlov S; Sullivan T; Kamm RD; Stewart CL; Lee RT
J Clin Invest; 2004 Feb; 113(3):370-8. PubMed ID: 14755334
[TBL] [Abstract][Full Text] [Related]
3. The nuclear membrane and mechanotransduction: impaired nuclear mechanics and mechanotransduction in lamin A/C deficient cells.
Lammerding J; Lee RT
Novartis Found Symp; 2005; 264():264-73; discussion 273-8. PubMed ID: 15773759
[TBL] [Abstract][Full Text] [Related]
4. Nesprin-1 and actin contribute to nuclear and cytoskeletal defects in lamin A/C-deficient cardiomyopathy.
Nikolova-Krstevski V; Leimena C; Xiao XH; Kesteven S; Tan JC; Yeo LS; Yu ZY; Zhang Q; Carlton A; Head S; Shanahan C; Feneley MP; Fatkin D
J Mol Cell Cardiol; 2011 Mar; 50(3):479-86. PubMed ID: 21156181
[TBL] [Abstract][Full Text] [Related]
5. Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium composition.
Holt I; Nguyen TM; Wehnert M; Morris GE
Neuromuscul Disord; 2006 Jun; 16(6):368-73. PubMed ID: 16697197
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genetics of laminopathies.
Ben Yaou R; Muchir A; Arimura T; Massart C; Demay L; Richard P; Bonne G
Novartis Found Symp; 2005; 264():81-90; discussion 90-97, 227-30. PubMed ID: 15773749
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Mutations in the LMNA gene encoding lamin A/C.
Genschel J; Schmidt HH
Hum Mutat; 2000 Dec; 16(6):451-9. PubMed ID: 11102973
[TBL] [Abstract][Full Text] [Related]
10. Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics.
Ho CY; Jaalouk DE; Vartiainen MK; Lammerding J
Nature; 2013 May; 497(7450):507-11. PubMed ID: 23644458
[TBL] [Abstract][Full Text] [Related]
11. Disruption of spermatogenesis in mice lacking A-type lamins.
Alsheimer M; Liebe B; Sewell L; Stewart CL; Scherthan H; Benavente R
J Cell Sci; 2004 Mar; 117(Pt 7):1173-8. PubMed ID: 14996939
[TBL] [Abstract][Full Text] [Related]
12. Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling.
Zwerger M; Jaalouk DE; Lombardi ML; Isermann P; Mauermann M; Dialynas G; Herrmann H; Wallrath LL; Lammerding J
Hum Mol Genet; 2013 Jun; 22(12):2335-49. PubMed ID: 23427149
[TBL] [Abstract][Full Text] [Related]
13. Nuclear lamins, diseases and aging.
Mattout A; Dechat T; Adam SA; Goldman RD; Gruenbaum Y
Curr Opin Cell Biol; 2006 Jun; 18(3):335-41. PubMed ID: 16632339
[TBL] [Abstract][Full Text] [Related]
14. Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.
Arimura T; Helbling-Leclerc A; Massart C; Varnous S; Niel F; Lacène E; Fromes Y; Toussaint M; Mura AM; Keller DI; Amthor H; Isnard R; Malissen M; Schwartz K; Bonne G
Hum Mol Genet; 2005 Jan; 14(1):155-69. PubMed ID: 15548545
[TBL] [Abstract][Full Text] [Related]
15. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
Park YE; Hayashi YK; Goto K; Komaki H; Hayashi Y; Inuzuka T; Noguchi S; Nonaka I; Nishino I
Neuromuscul Disord; 2009 Jan; 19(1):29-36. PubMed ID: 19070492
[TBL] [Abstract][Full Text] [Related]
16. Nuclear envelope proteins and neuromuscular diseases.
Ostlund C; Worman HJ
Muscle Nerve; 2003 Apr; 27(4):393-406. PubMed ID: 12661041
[TBL] [Abstract][Full Text] [Related]
17. [The role of lamins and mutations of LMNA gene in physiological and premature aging].
Sliwińska MA
Postepy Biochem; 2007; 53(1):46-52. PubMed ID: 17718387
[TBL] [Abstract][Full Text] [Related]
18. Mechanical dynamics of single cells during early apoptosis.
Pelling AE; Veraitch FS; Chu CP; Mason C; Horton MA
Cell Motil Cytoskeleton; 2009 Jul; 66(7):409-22. PubMed ID: 19492400
[TBL] [Abstract][Full Text] [Related]
19. Nuclear lamins: laminopathies and their role in premature ageing.
Broers JL; Ramaekers FC; Bonne G; Yaou RB; Hutchison CJ
Physiol Rev; 2006 Jul; 86(3):967-1008. PubMed ID: 16816143
[TBL] [Abstract][Full Text] [Related]
20. Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy.
Cenni V; Sabatelli P; Mattioli E; Marmiroli S; Capanni C; Ognibene A; Squarzoni S; Maraldi NM; Bonne G; Columbaro M; Merlini L; Lattanzi G
J Med Genet; 2005 Mar; 42(3):214-20. PubMed ID: 15744034
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
