329 related articles for article (PubMed ID: 17462627)
1. Distinct functional domains in nesprin-1alpha and nesprin-2beta bind directly to emerin and both interactions are disrupted in X-linked Emery-Dreifuss muscular dystrophy.
Wheeler MA; Davies JD; Zhang Q; Emerson LJ; Hunt J; Shanahan CM; Ellis JA
Exp Cell Res; 2007 Aug; 313(13):2845-57. PubMed ID: 17462627
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Nesprins: tissue-specific expression of epsilon and other short isoforms.
Duong NT; Morris GE; Lam le T; Zhang Q; Sewry CA; Shanahan CM; Holt I
PLoS One; 2014; 9(4):e94380. PubMed ID: 24718612
[TBL] [Abstract][Full Text] [Related]
5. Emerin binding to Btf, a death-promoting transcriptional repressor, is disrupted by a missense mutation that causes Emery-Dreifuss muscular dystrophy.
Haraguchi T; Holaska JM; Yamane M; Koujin T; Hashiguchi N; Mori C; Wilson KL; Hiraoka Y
Eur J Biochem; 2004 Mar; 271(5):1035-45. PubMed ID: 15009215
[TBL] [Abstract][Full Text] [Related]
6. Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.
Puckelwartz MJ; Kessler E; Zhang Y; Hodzic D; Randles KN; Morris G; Earley JU; Hadhazy M; Holaska JM; Mewborn SK; Pytel P; McNally EM
Hum Mol Genet; 2009 Feb; 18(4):607-20. PubMed ID: 19008300
[TBL] [Abstract][Full Text] [Related]
7. The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane.
Fairley EA; Kendrick-Jones J; Ellis JA
J Cell Sci; 1999 Aug; 112 ( Pt 15)():2571-82. PubMed ID: 10393813
[TBL] [Abstract][Full Text] [Related]
8. Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis.
Zhou C; Li C; Zhou B; Sun H; Koullourou V; Holt I; Puckelwartz MJ; Warren DT; Hayward R; Lin Z; Zhang L; Morris GE; McNally EM; Shackleton S; Rao L; Shanahan CM; Zhang Q
Hum Mol Genet; 2017 Jun; 26(12):2258-2276. PubMed ID: 28398466
[TBL] [Abstract][Full Text] [Related]
9. Nesprin-2 Giant (NUANCE) maintains nuclear envelope architecture and composition in skin.
Lüke Y; Zaim H; Karakesisoglou I; Jaeger VM; Sellin L; Lu W; Schneider M; Neumann S; Beijer A; Munck M; Padmakumar VC; Gloy J; Walz G; Noegel AA
J Cell Sci; 2008 Jun; 121(11):1887-98. PubMed ID: 18477613
[TBL] [Abstract][Full Text] [Related]
10. Distinct functional domains in emerin bind lamin A and DNA-bridging protein BAF.
Lee KK; Haraguchi T; Lee RS; Koujin T; Hiraoka Y; Wilson KL
J Cell Sci; 2001 Dec; 114(Pt 24):4567-73. PubMed ID: 11792821
[TBL] [Abstract][Full Text] [Related]
11. FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy.
Ziat E; Mamchaoui K; Beuvin M; Nelson I; Azibani F; Spuler S; Bonne G; Bertrand AT
J Neuromuscul Dis; 2016 Nov; 3(4):497-510. PubMed ID: 27911330
[TBL] [Abstract][Full Text] [Related]
12. LINC complex alterations in DMD and EDMD/CMT fibroblasts.
Taranum S; Vaylann E; Meinke P; Abraham S; Yang L; Neumann S; Karakesisoglou I; Wehnert M; Noegel AA
Eur J Cell Biol; 2012 Aug; 91(8):614-28. PubMed ID: 22555292
[TBL] [Abstract][Full Text] [Related]
13. The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype.
Fairley EA; Riddell A; Ellis JA; Kendrick-Jones J
J Cell Sci; 2002 Jan; 115(Pt 2):341-54. PubMed ID: 11839786
[TBL] [Abstract][Full Text] [Related]
14. Lmo7 is an emerin-binding protein that regulates the transcription of emerin and many other muscle-relevant genes.
Holaska JM; Rais-Bahrami S; Wilson KL
Hum Mol Genet; 2006 Dec; 15(23):3459-72. PubMed ID: 17067998
[TBL] [Abstract][Full Text] [Related]
15. Linker of nucleoskeleton and cytoskeleton (LINC) complex-mediated actin-dependent nuclear positioning orients centrosomes in migrating myoblasts.
Chang W; Antoku S; Östlund C; Worman HJ; Gundersen GG
Nucleus; 2015; 6(1):77-88. PubMed ID: 25587885
[TBL] [Abstract][Full Text] [Related]
16. Emery-Dreifuss muscular dystrophy mutations impair TRC40-mediated targeting of emerin to the inner nuclear membrane.
Pfaff J; Rivera Monroy J; Jamieson C; Rajanala K; Vilardi F; Schwappach B; Kehlenbach RH
J Cell Sci; 2016 Feb; 129(3):502-16. PubMed ID: 26675233
[TBL] [Abstract][Full Text] [Related]
17. Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.
Maraldi NM; Lattanzi G; Sabatelli P; Ognibene A; Columbaro M; Capanni C; Rutigliano C; Mattioli E; Squarzoni S
Eur J Histochem; 2003; 47(1):3-16. PubMed ID: 12685553
[TBL] [Abstract][Full Text] [Related]
18. Functional domains of the nucleus: implications for Emery-Dreifuss muscular dystrophy.
Maraldi NM; Lattanzi G; Sabatelli P; Ognibene A; Squarzoni S
Neuromuscul Disord; 2002 Nov; 12(9):815-23. PubMed ID: 12398831
[TBL] [Abstract][Full Text] [Related]
19. Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery-Dreifuss muscular dystrophy.
Wolff N; Gilquin B; Courchay K; Callebaut I; Worman HJ; Zinn-Justin S
FEBS Lett; 2001 Jul; 501(2-3):171-6. PubMed ID: 11470279
[TBL] [Abstract][Full Text] [Related]
20. Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophy.
Meinke P; Schneiderat P; Srsen V; Korfali N; Lê Thành P; Cowan GJ; Cavanagh DR; Wehnert M; Schirmer EC; Walter MC
Neuromuscul Disord; 2015 Feb; 25(2):127-36. PubMed ID: 25454731
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
