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 *

199 related articles for article (PubMed ID: 21070191)

  • 21. Mecp2-null mice provide new neuronal targets for Rett syndrome.
    Urdinguio RG; Lopez-Serra L; Lopez-Nieva P; Alaminos M; Diaz-Uriarte R; Fernandez AF; Esteller M
    PLoS One; 2008; 3(11):e3669. PubMed ID: 18989361
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Rett syndrome: insights into genetic, molecular and circuit mechanisms.
    Ip JPK; Mellios N; Sur M
    Nat Rev Neurosci; 2018 Jun; 19(6):368-382. PubMed ID: 29740174
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Brain-derived neurotrophic factor expression and respiratory function improve after ampakine treatment in a mouse model of Rett syndrome.
    Ogier M; Wang H; Hong E; Wang Q; Greenberg ME; Katz DM
    J Neurosci; 2007 Oct; 27(40):10912-7. PubMed ID: 17913925
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains.
    Itoh M; Ide S; Takashima S; Kudo S; Nomura Y; Segawa M; Kubota T; Mori H; Tanaka S; Horie H; Tanabe Y; Goto Y
    J Neuropathol Exp Neurol; 2007 Feb; 66(2):117-23. PubMed ID: 17278996
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ube3a expression is not altered in Mecp2 mutant mice.
    Jordan C; Francke U
    Hum Mol Genet; 2006 Jul; 15(14):2210-5. PubMed ID: 16754645
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Role of epigenetics in Rett syndrome.
    Kubota T; Miyake K; Hirasawa T
    Epigenomics; 2013; 5(5):583-92. PubMed ID: 24059803
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis.
    Alvarez-Saavedra M; Sáez MA; Kang D; Zoghbi HY; Young JI
    Hum Mol Genet; 2007 Oct; 16(19):2315-25. PubMed ID: 17635839
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis.
    Forlani G; Giarda E; Ala U; Di Cunto F; Salani M; Tupler R; Kilstrup-Nielsen C; Landsberger N
    Hum Mol Genet; 2010 Aug; 19(16):3114-23. PubMed ID: 20504995
    [TBL] [Abstract][Full Text] [Related]  

  • 29. MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution.
    Kaufmann WE; Johnston MV; Blue ME
    Brain Dev; 2005 Nov; 27 Suppl 1():S77-S87. PubMed ID: 16182491
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Disruption of MeCP2 attenuates circadian rhythm in CRISPR/Cas9-based Rett syndrome model mouse.
    Tsuchiya Y; Minami Y; Umemura Y; Watanabe H; Ono D; Nakamura W; Takahashi T; Honma S; Kondoh G; Matsuishi T; Yagita K
    Genes Cells; 2015 Dec; 20(12):992-1005. PubMed ID: 26456390
    [TBL] [Abstract][Full Text] [Related]  

  • 31. P152R Mutation Within MeCP2 Can Cause Loss of DNA-Binding Selectivity.
    Franklin D
    Interdiscip Sci; 2019 Mar; 11(1):10-20. PubMed ID: 30673959
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome.
    Moretti P; Levenson JM; Battaglia F; Atkinson R; Teague R; Antalffy B; Armstrong D; Arancio O; Sweatt JD; Zoghbi HY
    J Neurosci; 2006 Jan; 26(1):319-27. PubMed ID: 16399702
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Disruption of DNA-methylation-dependent long gene repression in Rett syndrome.
    Gabel HW; Kinde B; Stroud H; Gilbert CS; Harmin DA; Kastan NR; Hemberg M; Ebert DH; Greenberg ME
    Nature; 2015 Jun; 522(7554):89-93. PubMed ID: 25762136
    [TBL] [Abstract][Full Text] [Related]  

  • 35. MeCP2 and Rett syndrome: reversibility and potential avenues for therapy.
    Gadalla KK; Bailey ME; Cobb SR
    Biochem J; 2011 Oct; 439(1):1-14. PubMed ID: 21916843
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry.
    LaSalle JM; Goldstine J; Balmer D; Greco CM
    Hum Mol Genet; 2001 Aug; 10(17):1729-40. PubMed ID: 11532982
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dynamic changes in Histone H3 lysine 9 acetylation localization patterns during neuronal maturation require MeCP2.
    Thatcher KN; LaSalle JM
    Epigenetics; 2006; 1(1):24-31. PubMed ID: 17464364
    [TBL] [Abstract][Full Text] [Related]  

  • 38. MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation.
    Sheikh TI; de Paz AM; Akhtar S; Ausió J; Vincent JB
    Hum Mol Genet; 2017 Nov; 26(21):4132-4141. PubMed ID: 28973632
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.
    Chang Q; Khare G; Dani V; Nelson S; Jaenisch R
    Neuron; 2006 Feb; 49(3):341-8. PubMed ID: 16446138
    [TBL] [Abstract][Full Text] [Related]  

  • 40. MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome.
    Wan M; Zhao K; Lee SS; Francke U
    Hum Mol Genet; 2001 May; 10(10):1085-92. PubMed ID: 11331619
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.