798 related articles for article (PubMed ID: 17067998)
1. 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]
2. 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]
3. 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]
4. 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]
5. Emerin inhibits Lmo7 binding to the Pax3 and MyoD promoters and expression of myoblast proliferation genes.
Dedeic Z; Cetera M; Cohen TV; Holaska JM
J Cell Sci; 2011 May; 124(Pt 10):1691-702. PubMed ID: 21525034
[TBL] [Abstract][Full Text] [Related]
6. LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
Mull A; Kim G; Holaska JM
Muscle Nerve; 2015 Feb; 51(2):222-8. PubMed ID: 24825363
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy.
Liang WC; Mitsuhashi H; Keduka E; Nonaka I; Noguchi S; Nishino I; Hayashi YK
Ann Neurol; 2011 Jun; 69(6):1005-13. PubMed ID: 21391237
[TBL] [Abstract][Full Text] [Related]
9. Nuclear membrane protein emerin: roles in gene regulation, actin dynamics and human disease.
Wilson KL; Holaska JM; Montes de Oca R; Tifft K; Zastrow M; Segura-Totten M; Mansharamani M; Bengtsson L
Novartis Found Symp; 2005; 264():51-58; discussion 58-62, 227-30. PubMed ID: 15773747
[TBL] [Abstract][Full Text] [Related]
10. CDNA microarray analysis of gene expression in fibroblasts of patients with X-linked Emery-Dreifuss muscular dystrophy.
Tsukahara T; Tsujino S; Arahata K
Muscle Nerve; 2002 Jun; 25(6):898-901. PubMed ID: 12115980
[TBL] [Abstract][Full Text] [Related]
11. Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy.
Nagano A; Koga R; Ogawa M; Kurano Y; Kawada J; Okada R; Hayashi YK; Tsukahara T; Arahata K
Nat Genet; 1996 Mar; 12(3):254-9. PubMed ID: 8589715
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. The emerin-binding transcription factor Lmo7 is regulated by association with p130Cas at focal adhesions.
Wozniak MA; Baker BM; Chen CS; Wilson KL
PeerJ; 2013; 1():e134. PubMed ID: 24010014
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. How does a g993t mutation in the emerin gene cause Emery-Dreifuss muscular dystrophy?
Holt I; Clements L; Manilal S; Morris GE
Biochem Biophys Res Commun; 2001 Oct; 287(5):1129-33. PubMed ID: 11587540
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion.
Fujimoto S; Ishikawa T; Saito M; Wada Y; Wada I; Arahata K; Nonaka I
Neuropediatrics; 1999 Jun; 30(3):161-3. PubMed ID: 10480214
[TBL] [Abstract][Full Text] [Related]
19. Barrier-to-autointegration factor-like (BAF-L): a proposed regulator of BAF.
Tifft KE; Segura-Totten M; Lee KK; Wilson KL
Exp Cell Res; 2006 Feb; 312(4):478-87. PubMed ID: 16337940
[TBL] [Abstract][Full Text] [Related]
20. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
Mercuri E; Counsell S; Allsop J; Jungbluth H; Kinali M; Bonne G; Schwartz K; Bydder G; Dubowitz V; Muntoni F
Neuropediatrics; 2002 Feb; 33(1):10-4. PubMed ID: 11930270
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
