BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 24123753)

  • 1. Epigenetics, fragile X syndrome and transcriptional therapy.
    Tabolacci E; Chiurazzi P
    Am J Med Genet A; 2013 Nov; 161A(11):2797-808. PubMed ID: 24123753
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments.
    Tabolacci E; Pietrobono R; Moscato U; Oostra BA; Chiurazzi P; Neri G
    Eur J Hum Genet; 2005 May; 13(5):641-8. PubMed ID: 15741991
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome.
    Todd PK; Oh SY; Krans A; Pandey UB; Di Prospero NA; Min KT; Taylor JP; Paulson HL
    PLoS Genet; 2010 Dec; 6(12):e1001240. PubMed ID: 21170301
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.
    Coffee B; Zhang F; Warren ST; Reines D
    Nat Genet; 1999 May; 22(1):98-101. PubMed ID: 10319871
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DNA Methylation, Mechanisms of
    Nobile V; Pucci C; Chiurazzi P; Neri G; Tabolacci E
    Biomolecules; 2021 Feb; 11(2):. PubMed ID: 33669384
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome.
    Coffee B; Zhang F; Ceman S; Warren ST; Reines D
    Am J Hum Genet; 2002 Oct; 71(4):923-32. PubMed ID: 12232854
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Reciprocal changes in DNA methylation and hydroxymethylation and a broad repressive epigenetic switch characterize FMR1 transcriptional silencing in fragile X syndrome.
    Brasa S; Mueller A; Jacquemont S; Hahne F; Rozenberg I; Peters T; He Y; McCormack C; Gasparini F; Chibout SD; Grenet O; Moggs J; Gomez-Mancilla B; Terranova R
    Clin Epigenetics; 2016; 8():15. PubMed ID: 26855684
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epigenetics of fragile X syndrome and fragile X-related disorders.
    Kraan CM; Godler DE; Amor DJ
    Dev Med Child Neurol; 2019 Feb; 61(2):121-127. PubMed ID: 30084485
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
    Sheridan SD; Theriault KM; Reis SA; Zhou F; Madison JM; Daheron L; Loring JF; Haggarty SJ
    PLoS One; 2011; 6(10):e26203. PubMed ID: 22022567
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations.
    Tabolacci E; Moscato U; Zalfa F; Bagni C; Chiurazzi P; Neri G
    Eur J Hum Genet; 2008 Dec; 16(12):1487-98. PubMed ID: 18628788
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SIRT1 inhibition alleviates gene silencing in Fragile X mental retardation syndrome.
    Biacsi R; Kumari D; Usdin K
    PLoS Genet; 2008 Mar; 4(3):e1000017. PubMed ID: 18369442
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CGG-repeat dynamics and
    Zhou Y; Kumari D; Sciascia N; Usdin K
    Mol Autism; 2016; 7():42. PubMed ID: 27713816
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unstable mutations in the FMR1 gene and the phenotypes.
    Loesch D; Hagerman R
    Adv Exp Med Biol; 2012; 769():78-114. PubMed ID: 23560306
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Small Molecules Targeting H3K9 Methylation Prevent Silencing of Reactivated
    Kumari D; Sciascia N; Usdin K
    Genes (Basel); 2020 Mar; 11(4):. PubMed ID: 32230785
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Role of CTCF protein in regulating FMR1 locus transcription.
    Lanni S; Goracci M; Borrelli L; Mancano G; Chiurazzi P; Moscato U; Ferrè F; Helmer-Citterich M; Tabolacci E; Neri G
    PLoS Genet; 2013; 9(7):e1003601. PubMed ID: 23874213
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation.
    Tabolacci E; Pomponi MG; Remondini L; Pietrobono R; Nobile V; Pennacchio G; Gurrieri F; Neri G; Genuardi M; Chiurazzi P
    Eur J Hum Genet; 2020 May; 28(5):567-575. PubMed ID: 31804632
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations.
    Brykczynska U; Pecho-Vrieseling E; Thiemeyer A; Klein J; Fruh I; Doll T; Manneville C; Fuchs S; Iazeolla M; Beibel M; Roma G; Naumann U; Kelley N; Oakeley EJ; Mueller M; Gomez-Mancilla B; Bühler M; Tabolacci E; Chiurazzi P; Neri G; Bouwmeester T; Di Giorgio FP; Fodor BD
    Stem Cell Reports; 2016 Dec; 7(6):1059-1071. PubMed ID: 27840045
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene.
    Chiurazzi P; Pomponi MG; Pietrobono R; Bakker CE; Neri G; Oostra BA
    Hum Mol Genet; 1999 Nov; 8(12):2317-23. PubMed ID: 10545613
    [TBL] [Abstract][Full Text] [Related]  

  • 19. FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells.
    Avitzour M; Mor-Shaked H; Yanovsky-Dagan S; Aharoni S; Altarescu G; Renbaum P; Eldar-Geva T; Schonberger O; Levy-Lahad E; Epsztejn-Litman S; Eiges R
    Stem Cell Reports; 2014 Nov; 3(5):699-706. PubMed ID: 25418717
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine.
    Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; Neri G
    Nucleic Acids Res; 2002 Jul; 30(14):3278-85. PubMed ID: 12136110
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.