163 related articles for article (PubMed ID: 14673599)
1. Pathological changes of the myonuclear fibrous lamina and internal nuclear membrane in two cases of autosomal dominant limb-girdle muscular dystrophy with atrioventricular conduction disturbance (LGMD1B).
Matsubara S; Kitaguchi T
Acta Neuropathol; 2004 Feb; 107(2):111-8. PubMed ID: 14673599
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Emerin and the nuclear lamina in muscle and cardiac disease.
Holaska JM
Circ Res; 2008 Jul; 103(1):16-23. PubMed ID: 18596264
[TBL] [Abstract][Full Text] [Related]
7. Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity.
Zhang Q; Bethmann C; Worth NF; Davies JD; Wasner C; Feuer A; Ragnauth CD; Yi Q; Mellad JA; Warren DT; Wheeler MA; Ellis JA; Skepper JN; Vorgerd M; Schlotter-Weigel B; Weissberg PL; Roberts RG; Wehnert M; Shanahan CM
Hum Mol Genet; 2007 Dec; 16(23):2816-33. PubMed ID: 17761684
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin.
Holt I; Clements L; Manilal S; Brown SC; Morris GE
Eur J Hum Genet; 2001 Mar; 9(3):204-8. PubMed ID: 11313760
[TBL] [Abstract][Full Text] [Related]
10. Molecular signatures of Emery-Dreifuss muscular dystrophy.
Wheeler MA; Ellis JA
Biochem Soc Trans; 2008 Dec; 36(Pt 6):1354-8. PubMed ID: 19021555
[TBL] [Abstract][Full Text] [Related]
11. Direct interaction between emerin and lamin A.
Clements L; Manilal S; Love DR; Morris GE
Biochem Biophys Res Commun; 2000 Jan; 267(3):709-14. PubMed ID: 10673356
[TBL] [Abstract][Full Text] [Related]
12. Limb-girdle muscular dystrophy due to emerin gene mutations.
Ura S; Hayashi YK; Goto K; Astejada MN; Murakami T; Nagato M; Ohta S; Daimon Y; Takekawa H; Hirata K; Nonaka I; Noguchi S; Nishino I
Arch Neurol; 2007 Jul; 64(7):1038-41. PubMed ID: 17620497
[TBL] [Abstract][Full Text] [Related]
13. Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle.
Zhang Q; Ragnauth CD; Skepper JN; Worth NF; Warren DT; Roberts RG; Weissberg PL; Ellis JA; Shanahan CM
J Cell Sci; 2005 Feb; 118(Pt 4):673-87. PubMed ID: 15671068
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [The laminopathy saga].
Bonne G
Rev Neurol; 2003 Oct 16-31; 37(8):772-4. PubMed ID: 14593639
[TBL] [Abstract][Full Text] [Related]
16. Nuclear envelope defects in muscular dystrophy.
Roux KJ; Burke B
Biochim Biophys Acta; 2007 Feb; 1772(2):118-27. PubMed ID: 16904876
[TBL] [Abstract][Full Text] [Related]
17. Distribution of emerin during the cell cycle.
Dabauvalle MC; Müller E; Ewald A; Kress W; Krohne G; Müller CR
Eur J Cell Biol; 1999 Oct; 78(10):749-56. PubMed ID: 10569247
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration.
Melcon G; Kozlov S; Cutler DA; Sullivan T; Hernandez L; Zhao P; Mitchell S; Nader G; Bakay M; Rottman JN; Hoffman EP; Stewart CL
Hum Mol Genet; 2006 Feb; 15(4):637-51. PubMed ID: 16403804
[TBL] [Abstract][Full Text] [Related]
20. Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene.
Mercuri E; Brown SC; Nihoyannopoulos P; Poulton J; Kinali M; Richard P; Piercy RJ; Messina S; Sewry C; Burke MM; McKenna W; Bonne G; Muntoni F
Muscle Nerve; 2005 May; 31(5):602-9. PubMed ID: 15770669
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]