BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

276 related articles for article (PubMed ID: 23535822)

  • 1. Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.
    Cohen TV; Gnocchi VF; Cohen JE; Phadke A; Liu H; Ellis JA; Foisner R; Stewart CL; Zammit PS; Partridge TA
    Hum Mol Genet; 2013 Jul; 22(14):2852-69. PubMed ID: 23535822
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lamin A/C Assembly Defects in
    Bertrand AT; Brull A; Azibani F; Benarroch L; Chikhaoui K; Stewart CL; Medalia O; Ben Yaou R; Bonne G
    Cells; 2020 Mar; 9(4):. PubMed ID: 32244403
    [No Abstract]   [Full Text] [Related]  

  • 3. The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C-LAP2α complex in mice.
    Pilat U; Dechat T; Bertrand AT; Woisetschläger N; Gotic I; Spilka R; Biadasiewicz K; Bonne G; Foisner R
    J Cell Sci; 2013 Apr; 126(Pt 8):1753-62. PubMed ID: 23444379
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.
    Owens DJ; Messéant J; Moog S; Viggars M; Ferry A; Mamchaoui K; Lacène E; Roméro N; Brull A; Bonne G; Butler-Browne G; Coirault C
    Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33396724
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy.
    Gnocchi VF; Scharner J; Huang Z; Brady K; Lee JS; White RB; Morgan JE; Sun YB; Ellis JA; Zammit PS
    PLoS One; 2011 Feb; 6(2):e16651. PubMed ID: 21364987
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells.
    Janin A; Bauer D; Ratti F; Valla C; Bertrand A; Christin E; Chopin E; Streichenberger N; Bonne G; Gache V; Cohen T; Méjat A
    Sci Rep; 2018 Apr; 8(1):5618. PubMed ID: 29618840
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Loss of nucleoplasmic LAP2alpha-lamin A complexes causes erythroid and epidermal progenitor hyperproliferation.
    Naetar N; Korbei B; Kozlov S; Kerenyi MA; Dorner D; Kral R; Gotic I; Fuchs P; Cohen TV; Bittner R; Stewart CL; Foisner R
    Nat Cell Biol; 2008 Nov; 10(11):1341-8. PubMed ID: 18849980
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Postnatal development of mice with combined genetic depletions of lamin A/C, emerin and lamina-associated polypeptide 1.
    Wang Y; Shin JY; Nakanishi K; Homma S; Kim GJ; Tanji K; Joseph LC; Morrow JP; Stewart CL; Dauer WT; Worman HJ
    Hum Mol Genet; 2019 Aug; 28(15):2486-2500. PubMed ID: 31009944
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiple novel functions of lamina associated polypeptide 2α in striated muscle.
    Gotic I; Foisner R
    Nucleus; 2010; 1(5):397-401. PubMed ID: 21326822
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Depletion of A-type lamins and Lap2α reduces 53BP1 accumulation at UV-induced DNA lesions and Lap2α protein is responsible for compactness of irradiated chromatin.
    Bártová E; Legartová S; Krejčí J; Řezníčková P; Kovaříková AS; Suchánková J; Fedr R; Smirnov E; Hornáček M; Raška I
    J Cell Biochem; 2018 Nov; 119(10):8146-8162. PubMed ID: 29923310
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Laminopathies disrupt epigenomic developmental programs and cell fate.
    Perovanovic J; Dell'Orso S; Gnochi VF; Jaiswal JK; Sartorelli V; Vigouroux C; Mamchaoui K; Mouly V; Bonne G; Hoffman EP
    Sci Transl Med; 2016 Apr; 8(335):335ra58. PubMed ID: 27099177
    [TBL] [Abstract][Full Text] [Related]  

  • 17. THE ROLE OF LMNA MUTATIONS IN MYOGENIC DIFFERENTIATION OF PRIMARY SATELLITE CELLS AND C2C12 CELLS.
    Perepelina KI; Smolina NA; Zabirnik AS; Dmitrieva RI; Malashicheva AB; Kostareva AA
    Tsitologiia; 2017; 59(2):117-24. PubMed ID: 30199159
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes.
    Bernasconi P; Carboni N; Ricci G; Siciliano G; Politano L; Maggi L; Mongini T; Vercelli L; Rodolico C; Biagini E; Boriani G; Ruggiero L; Santoro L; Schena E; Prencipe S; Evangelisti C; Pegoraro E; Morandi L; Columbaro M; Lanzuolo C; Sabatelli P; Cavalcante P; Cappelletti C; Bonne G; Muchir A; Lattanzi G
    Nucleus; 2018 Jan; 9(1):292-304. PubMed ID: 29693488
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Laminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects.
    Decostre V; Ben Yaou R; Bonne G
    Acta Myol; 2005 Oct; 24(2):104-9. PubMed ID: 16550926
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.