BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 23720823)

  • 1. FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.
    Neguembor MV; Xynos A; Onorati MC; Caccia R; Bortolanza S; Godio C; Pistoni M; Corona DF; Schotta G; Gabellini D
    J Mol Cell Biol; 2013 Oct; 5(5):294-307. PubMed ID: 23720823
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation.
    Bodega B; Ramirez GD; Grasser F; Cheli S; Brunelli S; Mora M; Meneveri R; Marozzi A; Mueller S; Battaglioli E; Ginelli E
    BMC Biol; 2009 Jul; 7():41. PubMed ID: 19607661
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Direct interplay between two candidate genes in FSHD muscular dystrophy.
    Ferri G; Huichalaf CH; Caccia R; Gabellini D
    Hum Mol Genet; 2015 Mar; 24(5):1256-66. PubMed ID: 25326393
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Epigenetic Regulation by
    Qi H; Liu H; Pullamsetti SS; Günther S; Kuenne C; Atzberger A; Sommer N; Hadzic S; Günther A; Weissmann N; Zhou Y; Yuan X; Braun T
    Circulation; 2021 Sep; 144(13):1042-1058. PubMed ID: 34247492
    [TBL] [Abstract][Full Text] [Related]  

  • 5. FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1).
    Feeney SJ; McGrath MJ; Sriratana A; Gehrig SM; Lynch GS; D'Arcy CE; Price JT; McLean CA; Tupler R; Mitchell CA
    PLoS One; 2015; 10(2):e0117665. PubMed ID: 25695429
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD).
    Pistoni M; Shiue L; Cline MS; Bortolanza S; Neguembor MV; Xynos A; Ares M; Gabellini D
    PLoS Genet; 2013; 9(1):e1003186. PubMed ID: 23300487
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The histone H4K20 methyltransferase SUV4-20H1/KMT5B is required for multiciliated cell differentiation in Xenopus.
    Angerilli A; Tait J; Berges J; Shcherbakova I; Pokrovsky D; Schauer T; Smialowski P; Hsam O; Mentele E; Nicetto D; Rupp RA
    Life Sci Alliance; 2023 Jul; 6(7):. PubMed ID: 37116939
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein.
    Hanel ML; Sun CY; Jones TI; Long SW; Zanotti S; Milner D; Jones PL
    Differentiation; 2011 Feb; 81(2):107-18. PubMed ID: 20970242
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Specificity of the SUV4-20H1 and SUV4-20H2 protein lysine methyltransferases and methylation of novel substrates.
    Weirich S; Kudithipudi S; Jeltsch A
    J Mol Biol; 2016 Jun; 428(11):2344-2358. PubMed ID: 27105552
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD).
    Jones TI; Parilla M; Jones PL
    PLoS One; 2016; 11(3):e0150938. PubMed ID: 26942723
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.
    Gabellini D; D'Antona G; Moggio M; Prelle A; Zecca C; Adami R; Angeletti B; Ciscato P; Pellegrino MA; Bottinelli R; Green MR; Tupler R
    Nature; 2006 Feb; 439(7079):973-7. PubMed ID: 16341202
    [TBL] [Abstract][Full Text] [Related]  

  • 12. GRIP1-associated SET-domain methyltransferase in glucocorticoid receptor target gene expression.
    Chinenov Y; Sacta MA; Cruz AR; Rogatsky I
    Proc Natl Acad Sci U S A; 2008 Dec; 105(51):20185-90. PubMed ID: 19074285
    [TBL] [Abstract][Full Text] [Related]  

  • 13. AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy.
    Bortolanza S; Nonis A; Sanvito F; Maciotta S; Sitia G; Wei J; Torrente Y; Di Serio C; Chamberlain JR; Gabellini D
    Mol Ther; 2011 Nov; 19(11):2055-64. PubMed ID: 21829175
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Suv4-20h1 promotes G1 to S phase transition by downregulating p21
    Wu Y; Wang Y; Liu M; Nie M; Wang Y; Deng Y; Yao B; Gui T; Li X; Ma L; Guo C; Ma C; Ju J; Zhao Q
    Oncol Lett; 2018 May; 15(5):6123-6130. PubMed ID: 29616094
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Muscular dystrophy candidate gene FRG1 is critical for muscle development.
    Hanel ML; Wuebbles RD; Jones PL
    Dev Dyn; 2009 Jun; 238(6):1502-12. PubMed ID: 19097195
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene.
    Nicetto D; Hahn M; Jung J; Schneider TD; Straub T; David R; Schotta G; Rupp RA
    PLoS Genet; 2013; 9(1):e1003188. PubMed ID: 23382689
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells.
    Xynos A; Neguembor MV; Caccia R; Licastro D; Nonis A; Di Serio C; Stupka E; Gabellini D
    J Cell Sci; 2013 May; 126(Pt 10):2236-45. PubMed ID: 23525014
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites.
    Liu Q; Jones TI; Tang VW; Brieher WM; Jones PL
    J Cell Sci; 2010 Apr; 123(Pt 7):1116-23. PubMed ID: 20215405
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Regulation of Skeletal Muscle Stem Cell Quiescence by Suv4-20h1-Dependent Facultative Heterochromatin Formation.
    Boonsanay V; Zhang T; Georgieva A; Kostin S; Qi H; Yuan X; Zhou Y; Braun T
    Cell Stem Cell; 2016 Feb; 18(2):229-42. PubMed ID: 26669898
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cross-species Analyses Unravel the Complexity of H3K27me3 and H4K20me3 in the Context of Neural Stem Progenitor Cells.
    Rhodes CT; Sandstrom RS; Huang SA; Wang Y; Schotta G; Berger MS; Lin CA
    Neuroepigenetics; 2016 Jun; 6():10-25. PubMed ID: 27429906
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.