BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

273 related articles for article (PubMed ID: 22103509)

  • 1. The LINC complex and human disease.
    Meinke P; Nguyen TD; Wehnert MS
    Biochem Soc Trans; 2011 Dec; 39(6):1693-7. PubMed ID: 22103509
    [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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes.
    Haque F; Mazzeo D; Patel JT; Smallwood DT; Ellis JA; Shanahan CM; Shackleton S
    J Biol Chem; 2010 Jan; 285(5):3487-98. PubMed ID: 19933576
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Contribution of SUN1 mutations to the pathomechanism in muscular dystrophies.
    Li P; Meinke P; Huong le TT; Wehnert M; Noegel AA
    Hum Mutat; 2014 Apr; 35(4):452-61. PubMed ID: 24375709
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Dynamics and molecular interactions of linker of nucleoskeleton and cytoskeleton (LINC) complex proteins.
    Ostlund C; Folker ES; Choi JC; Gomes ER; Gundersen GG; Worman HJ
    J Cell Sci; 2009 Nov; 122(Pt 22):4099-108. PubMed ID: 19843581
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. An Emerin LEM-Domain Mutation Impairs Cell Response to Mechanical Stress.
    Essawy N; Samson C; Petitalot A; Moog S; Bigot A; Herrada I; Marcelot A; Arteni AA; Coirault C; Zinn-Justin S
    Cells; 2019 Jun; 8(6):. PubMed ID: 31185657
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Global loss of a nuclear lamina component, lamin A/C, and LINC complex components SUN1, SUN2, and nesprin-2 in breast cancer.
    Matsumoto A; Hieda M; Yokoyama Y; Nishioka Y; Yoshidome K; Tsujimoto M; Matsuura N
    Cancer Med; 2015 Oct; 4(10):1547-57. PubMed ID: 26175118
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization.
    Meinke P; Mattioli E; Haque F; Antoku S; Columbaro M; Straatman KR; Worman HJ; Gundersen GG; Lattanzi G; Wehnert M; Shackleton S
    PLoS Genet; 2014 Sep; 10(9):e1004605. PubMed ID: 25210889
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Increased solubility of lamins and redistribution of lamin C in X-linked Emery-Dreifuss muscular dystrophy fibroblasts.
    Markiewicz E; Venables R; Mauricio-Alvarez-Reyes ; Quinlan R; Dorobek M; Hausmanowa-Petrucewicz I; Hutchison C
    J Struct Biol; 2002; 140(1-3):241-53. PubMed ID: 12490172
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
    Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F
    Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 14.