325 related articles for article (PubMed ID: 18396274)
1. 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]
2. 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]
3. 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]
4. 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]
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 and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC
BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Laminopathies disrupt epigenomic developmental programs and cell fate.
Perovanovic J; Dell'Orso S; Gnochi VF; Jaiswal JK; Sartorelli V; Vigouroux C; Mamchaoui K; Mouly V; Bonne G; Hoffman EP
Sci Transl Med; 2016 Apr; 8(335):335ra58. PubMed ID: 27099177
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy.
Favreau C; Dubosclard E; Ostlund C; Vigouroux C; Capeau J; Wehnert M; Higuet D; Worman HJ; Courvalin JC; Buendia B
Exp Cell Res; 2003 Jan; 282(1):14-23. PubMed ID: 12490190
[TBL] [Abstract][Full Text] [Related]
11. 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]
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. 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]
14. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].
Onishi Y; Higuchi J; Ogawa T; Namekawa A; Hayashi H; Odakura H; Goto K; Hayashi YK
Rinsho Shinkeigaku; 2002 Feb; 42(2):140-4. PubMed ID: 12424964
[TBL] [Abstract][Full Text] [Related]
15. Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.
Maraldi NM; Lattanzi G; Capanni C; Columbaro M; Merlini L; Mattioli E; Sabatelli P; Squarzoni S; Manzoli FA
Eur J Histochem; 2006; 50(1):1-8. PubMed ID: 16584978
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations.
Scharner J; Brown CA; Bower M; Iannaccone ST; Khatri IA; Escolar D; Gordon E; Felice K; Crowe CA; Grosmann C; Meriggioli MN; Asamoah A; Gordon O; Gnocchi VF; Ellis JA; Mendell JR; Zammit PS
Hum Mutat; 2011 Feb; 32(2):152-67. PubMed ID: 20848652
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy.
Walter MC; Witt TN; Weigel BS; Reilich P; Richard P; Pongratz D; Bonne G; Wehnert MS; Lochmüller H
Neuromuscul Disord; 2005 Jan; 15(1):40-4. PubMed ID: 15639119
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]