These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 23759142)

  • 1. Comparative DNA methylation among females with neurodevelopmental disorders and seizures identifies TAC1 as a MeCP2 target gene.
    Aldinger KA; Plummer JT; Levitt P
    J Neurodev Disord; 2013 Jun; 5(1):15. PubMed ID: 23759142
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The impact of MECP2 mutations in the expression patterns of Rett syndrome patients.
    Ballestar E; Ropero S; Alaminos M; Armstrong J; Setien F; Agrelo R; Fraga MF; Herranz M; Avila S; Pineda M; Monros E; Esteller M
    Hum Genet; 2005 Jan; 116(1-2):91-104. PubMed ID: 15549394
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation.
    Nagarajan RP; Hogart AR; Gwye Y; Martin MR; LaSalle JM
    Epigenetics; 2006; 1(4):e1-11. PubMed ID: 17486179
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Altered methylation pattern of the G6 PD promoter in Rett syndrome.
    Huppke P; Bohlander S; Krämer N; Laccone F; Hanefeld F
    Neuropediatrics; 2002 Apr; 33(2):105-8. PubMed ID: 12075494
    [TBL] [Abstract][Full Text] [Related]  

  • 5. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome.
    Chen L; Chen K; Lavery LA; Baker SA; Shaw CA; Li W; Zoghbi HY
    Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5509-14. PubMed ID: 25870282
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Alpha-Synuclein Gene (SNCA) is a Genomic Target of Methyl-CpG Binding Protein 2 (MeCP2)-Implications for Parkinson's Disease and Rett Syndrome.
    Schmitt I; Evert BO; Sharma A; Khazneh H; Murgatroyd C; Wüllner U
    Mol Neurobiol; 2024 Mar; ():. PubMed ID: 38429622
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Differentiation of multipotent neural stem cells derived from Rett syndrome patients is biased toward the astrocytic lineage.
    Andoh-Noda T; Akamatsu W; Miyake K; Matsumoto T; Yamaguchi R; Sanosaka T; Okada Y; Kobayashi T; Ohyama M; Nakashima K; Kurosawa H; Kubota T; Okano H
    Mol Brain; 2015 May; 8():31. PubMed ID: 26012557
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel alterations in the epigenetic signature of MeCP2-targeted promoters in lymphocytes of Rett syndrome patients.
    Lilja T; Wallenborg K; Björkman K; Albåge M; Eriksson M; Lagercrantz H; Rohdin M; Hermanson O
    Epigenetics; 2013 Mar; 8(3):246-51. PubMed ID: 23348913
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.
    Aldosary M; Al-Bakheet A; Al-Dhalaan H; Almass R; Alsagob M; Al-Younes B; AlQuait L; Mustafa OM; Bulbul M; Rahbeeni Z; Alfadhel M; Chedrawi A; Al-Hassnan Z; AlDosari M; Al-Zaidan H; Al-Muhaizea MA; AlSayed MD; Salih MA; AlShammari M; Faiyaz-Ul-Haque M; Chishti MA; Al-Harazi O; Al-Odaib A; Kaya N; Colak D
    OMICS; 2020 Mar; 24(3):160-171. PubMed ID: 32105570
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome.
    Miyake K; Hirasawa T; Soutome M; Itoh M; Goto Y; Endoh K; Takahashi K; Kudo S; Nakagawa T; Yokoi S; Taira T; Inazawa J; Kubota T
    BMC Neurosci; 2011 Aug; 12():81. PubMed ID: 21824415
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.
    Hogart A; Nagarajan RP; Patzel KA; Yasui DH; Lasalle JM
    Hum Mol Genet; 2007 Mar; 16(6):691-703. PubMed ID: 17339270
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA Methylation Contributes to the Differential Expression Levels of
    Liyanage VRB; Olson CO; Zachariah RM; Davie JR; Rastegar M
    Int J Mol Sci; 2019 Apr; 20(8):. PubMed ID: 31013990
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes.
    Nectoux J; Fichou Y; Rosas-Vargas H; Cagnard N; Bahi-Buisson N; Nusbaum P; Letourneur F; Chelly J; Bienvenu T
    J Cell Mol Med; 2010 Jul; 14(7):1962-74. PubMed ID: 20569274
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease.
    Pejhan S; Rastegar M
    Biomolecules; 2021 Jan; 11(1):. PubMed ID: 33429932
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.
    Swanberg SE; Nagarajan RP; Peddada S; Yasui DH; LaSalle JM
    Hum Mol Genet; 2009 Feb; 18(3):525-34. PubMed ID: 19000991
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MECP2 promoter methylation and X chromosome inactivation in autism.
    Nagarajan RP; Patzel KA; Martin M; Yasui DH; Swanberg SE; Hertz-Picciotto I; Hansen RL; Van de Water J; Pessah IN; Jiang R; Robinson WP; LaSalle JM
    Autism Res; 2008 Jun; 1(3):169-78. PubMed ID: 19132145
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The MeCP2E1/E2-BDNF-
    Pejhan S; Del Bigio MR; Rastegar M
    Front Cell Dev Biol; 2020; 8():763. PubMed ID: 32974336
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
    Amir RE; Van den Veyver IB; Wan M; Tran CQ; Francke U; Zoghbi HY
    Nat Genet; 1999 Oct; 23(2):185-8. PubMed ID: 10508514
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Integrated genome-wide Alu methylation and transcriptome profiling analyses reveal novel epigenetic regulatory networks associated with autism spectrum disorder.
    Saeliw T; Tangsuwansri C; Thongkorn S; Chonchaiya W; Suphapeetiporn K; Mutirangura A; Tencomnao T; Hu VW; Sarachana T
    Mol Autism; 2018; 9():27. PubMed ID: 29686828
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome.
    Filosa S; Pecorelli A; D'Esposito M; Valacchi G; Hajek J
    Free Radic Biol Med; 2015 Nov; 88(Pt A):81-90. PubMed ID: 25960047
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.