BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

540 related articles for article (PubMed ID: 16481476)

  • 1. Lamin A/C and emerin are critical for skeletal muscle satellite cell differentiation.
    Frock RL; Kudlow BA; Evans AM; Jameson SA; Hauschka SD; Kennedy BK
    Genes Dev; 2006 Feb; 20(4):486-500. PubMed ID: 16481476
    [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. Expression of emerin and lamins in muscle of patients with different forms of Emery-Dreifuss muscular dystrophy.
    Niebroj-Dobosz I; Fidzianska A; Hausmanowa-Petrusewicz I
    Acta Myol; 2003 Sep; 22(2):52-7. PubMed ID: 14959564
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Abnormal nuclear shape and impaired mechanotransduction in emerin-deficient cells.
    Lammerding J; Hsiao J; Schulze PC; Kozlov S; Stewart CL; Lee RT
    J Cell Biol; 2005 Aug; 170(5):781-91. PubMed ID: 16115958
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy.
    Manilal S; Sewry CA; Pereboev A; Man N; Gobbi P; Hawkes S; Love DR; Morris GE
    Hum Mol Genet; 1999 Feb; 8(2):353-9. PubMed ID: 9949197
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interaction between emerin and nuclear lamins.
    Sakaki M; Koike H; Takahashi N; Sasagawa N; Tomioka S; Arahata K; Ishiura S
    J Biochem; 2001 Feb; 129(2):321-7. PubMed ID: 11173535
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Mutations in the LMNA gene encoding lamin A/C.
    Genschel J; Schmidt HH
    Hum Mutat; 2000 Dec; 16(6):451-9. PubMed ID: 11102973
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.