198 related articles for article (PubMed ID: 18808171)
1. Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cells.
Cenni V; Bertacchini J; Beretti F; Lattanzi G; Bavelloni A; Riccio M; Ruzzene M; Marin O; Arrigoni G; Parnaik V; Wehnert M; Maraldi NM; de Pol A; Cocco L; Marmiroli S
J Proteome Res; 2008 Nov; 7(11):4727-35. PubMed ID: 18808171
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Remodelling of the nuclear lamina and nucleoskeleton is required for skeletal muscle differentiation in vitro.
Markiewicz E; Ledran M; Hutchison CJ
J Cell Sci; 2005 Jan; 118(Pt 2):409-20. PubMed ID: 15654018
[TBL] [Abstract][Full Text] [Related]
6. Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects.
Håkelien AM; Delbarre E; Gaustad KG; Buendia B; Collas P
Exp Cell Res; 2008 May; 314(8):1869-80. PubMed ID: 18396274
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Differentiation of C2C12 myoblasts expressing lamin A mutated at a site responsible for Emery-Dreifuss muscular dystrophy is improved by inhibition of the MEK-ERK pathway and stimulation of the PI3-kinase pathway.
Favreau C; Delbarre E; Courvalin JC; Buendia B
Exp Cell Res; 2008 Apr; 314(6):1392-405. PubMed ID: 18294630
[TBL] [Abstract][Full Text] [Related]
9. Functional analysis of phosphorylation sites in human lamin A controlling lamin disassembly, nuclear transport and assembly.
Haas M; Jost E
Eur J Cell Biol; 1993 Dec; 62(2):237-47. PubMed ID: 7925482
[TBL] [Abstract][Full Text] [Related]
10. Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene.
Kandert S; Wehnert M; Müller CR; Buendia B; Dabauvalle MC
Eur J Cell Biol; 2009 Oct; 88(10):593-608. PubMed ID: 19589617
[TBL] [Abstract][Full Text] [Related]
11. A-type lamins and signaling: the PI 3-kinase/Akt pathway moves forward.
Marmiroli S; Bertacchini J; Beretti F; Cenni V; Guida M; De Pol A; Maraldi NM; Lattanzi G
J Cell Physiol; 2009 Sep; 220(3):553-61. PubMed ID: 19479937
[TBL] [Abstract][Full Text] [Related]
12. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
Bakay M; Wang Z; Melcon G; Schiltz L; Xuan J; Zhao P; Sartorelli V; Seo J; Pegoraro E; Angelini C; Shneiderman B; Escolar D; Chen YW; Winokur ST; Pachman LM; Fan C; Mandler R; Nevo Y; Gordon E; Zhu Y; Dong Y; Wang Y; Hoffman EP
Brain; 2006 Apr; 129(Pt 4):996-1013. PubMed ID: 16478798
[TBL] [Abstract][Full Text] [Related]
13. The protein kinase Akt/PKB regulates both prelamin A degradation and Lmna gene expression.
Bertacchini J; Beretti F; Cenni V; Guida M; Gibellini F; Mediani L; Marin O; Maraldi NM; de Pol A; Lattanzi G; Cocco L; Marmiroli S
FASEB J; 2013 Jun; 27(6):2145-55. PubMed ID: 23430973
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Expression of a mutant lamin A that causes Emery-Dreifuss muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts.
Favreau C; Higuet D; Courvalin JC; Buendia B
Mol Cell Biol; 2004 Feb; 24(4):1481-92. PubMed ID: 14749366
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Tethering by lamin A stabilizes and targets the ING1 tumour suppressor.
Han X; Feng X; Rattner JB; Smith H; Bose P; Suzuki K; Soliman MA; Scott MS; Burke BE; Riabowol K
Nat Cell Biol; 2008 Nov; 10(11):1333-40. PubMed ID: 18836436
[TBL] [Abstract][Full Text] [Related]
20. Phosphorylation of the p34(cdc2) target site on goldfish germinal vesicle lamin B3 before oocyte maturation.
Yamaguchi A; Katsu Y; Matsuyama M; Yoshikuni M; Nagahama Y
Eur J Cell Biol; 2006 Jun; 85(6):501-17. PubMed ID: 16600424
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
