BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

323 related articles for article (PubMed ID: 17567779)

  • 1. Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy.
    Muchir A; Pavlidis P; Bonne G; Hayashi YK; Worman HJ
    Hum Mol Genet; 2007 Aug; 16(15):1884-95. PubMed ID: 17567779
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy.
    Muchir A; Pavlidis P; Decostre V; Herron AJ; Arimura T; Bonne G; Worman HJ
    J Clin Invest; 2007 May; 117(5):1282-93. PubMed ID: 17446932
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery-Dreifuss muscular dystrophy caused by an LMNA gene mutation.
    Wada E; Matsumoto K; Susumu N; Kato M; Hayashi YK
    J Physiol Sci; 2023 Nov; 73(1):27. PubMed ID: 37940872
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked form of Emery-Dreifuss muscular dystrophy.
    Hayashi YK
    Acta Myol; 2005 Oct; 24(2):98-103. PubMed ID: 16550925
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins.
    Muchir A; Shan J; Bonne G; Lehnart SE; Worman HJ
    Hum Mol Genet; 2009 Jan; 18(2):241-7. PubMed ID: 18927124
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alteration of performance in a mouse model of Emery-Dreifuss muscular dystrophy caused by A-type lamins gene mutation.
    Thomasson R; Vignier N; Peccate C; Mougenot N; Noirez P; Muchir A
    Hum Mol Genet; 2019 Jul; 28(13):2237-2244. PubMed ID: 31220270
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Emery-Dreifuss muscular dystrophy.
    Muchir A; Worman HJ
    Curr Neurol Neurosci Rep; 2007 Jan; 7(1):78-83. PubMed ID: 17217858
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Emery-Dreifuss muscular dystrophy: focal point nuclear envelope.
    Muchir A; Worman HJ
    Curr Opin Neurol; 2019 Oct; 32(5):728-734. PubMed ID: 31460960
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?
    Ben Yaou R; Toutain A; Arimura T; Demay L; Massart C; Peccate C; Muchir A; Llense S; Deburgrave N; Leturcq F; Litim KE; Rahmoun-Chiali N; Richard P; Babuty D; Récan-Budiartha D; Bonne G
    Neurology; 2007 May; 68(22):1883-94. PubMed ID: 17536044
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
    Bonne G; Di Barletta MR; Varnous S; Bécane HM; Hammouda EH; Merlini L; Muntoni F; Greenberg CR; Gary F; Urtizberea JA; Duboc D; Fardeau M; Toniolo D; Schwartz K
    Nat Genet; 1999 Mar; 21(3):285-8. PubMed ID: 10080180
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Emery-Dreifuss muscular dystrophy.
    Puckelwartz M; McNally EM
    Handb Clin Neurol; 2011; 101():155-66. PubMed ID: 21496632
    [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. [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]  

  • 18. Emery-Dreifuss muscular dystrophy.
    Helbling-Leclerc A; Bonne G; Schwartz K
    Eur J Hum Genet; 2002 Mar; 10(3):157-61. PubMed ID: 11973618
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 17.