BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 37965930)

  • 61. EEA1 restores homeostatic synaptic plasticity in hippocampal neurons from Rett syndrome mice.
    Xu X; Pozzo-Miller L
    J Physiol; 2017 Aug; 595(16):5699-5712. PubMed ID: 28621434
    [TBL] [Abstract][Full Text] [Related]  

  • 62. The relationship of Rett syndrome and MECP2 disorders to autism.
    Neul JL
    Dialogues Clin Neurosci; 2012 Sep; 14(3):253-62. PubMed ID: 23226951
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome.
    De Felice C; Della Ragione F; Signorini C; Leoncini S; Pecorelli A; Ciccoli L; Scalabrì F; Marracino F; Madonna M; Belmonte G; Ricceri L; De Filippis B; Laviola G; Valacchi G; Durand T; Galano JM; Oger C; Guy A; Bultel-Poncé V; Guy J; Filosa S; Hayek J; D'Esposito M
    Neurobiol Dis; 2014 Aug; 68(100):66-77. PubMed ID: 24769161
    [TBL] [Abstract][Full Text] [Related]  

  • 64. MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders.
    Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H
    Brain Dev; 2012 Jun; 34(6):487-95. PubMed ID: 21982064
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome.
    Johnson BS; Zhao YT; Fasolino M; Lamonica JM; Kim YJ; Georgakilas G; Wood KH; Bu D; Cui Y; Goffin D; Vahedi G; Kim TH; Zhou Z
    Nat Med; 2017 Oct; 23(10):1203-1214. PubMed ID: 28920956
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome.
    Osenberg S; Karten A; Sun J; Li J; Charkowick S; Felice CA; Kritzer M; Nguyen MVC; Yu P; Ballas N
    Proc Natl Acad Sci U S A; 2018 Jun; 115(23):E5363-E5372. PubMed ID: 29769330
    [TBL] [Abstract][Full Text] [Related]  

  • 67. MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.
    Schaevitz LR; Gómez NB; Zhen DP; Berger-Sweeney JE
    Genes Brain Behav; 2013 Oct; 12(7):732-40. PubMed ID: 24283265
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Mirtazapine treatment in a young female mouse model of Rett syndrome identifies time windows for the rescue of early phenotypes.
    Flores Gutiérrez J; Natali G; Giorgi J; De Leonibus E; Tongiorgi E
    Exp Neurol; 2022 Jul; 353():114056. PubMed ID: 35358499
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Pontine norepinephrine defects in Mecp2-null mice involve deficient expression of dopamine beta-hydroxylase but not a loss of catecholaminergic neurons.
    Zhang X; Su J; Rojas A; Jiang C
    Biochem Biophys Res Commun; 2010 Apr; 394(2):285-90. PubMed ID: 20193660
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Brain activity mapping in Mecp2 mutant mice reveals functional deficits in forebrain circuits, including key nodes in the default mode network, that are reversed with ketamine treatment.
    Kron M; Howell CJ; Adams IT; Ransbottom M; Christian D; Ogier M; Katz DM
    J Neurosci; 2012 Oct; 32(40):13860-72. PubMed ID: 23035095
    [TBL] [Abstract][Full Text] [Related]  

  • 71. A selective 5-HT1a receptor agonist improves respiration in a mouse model of Rett syndrome.
    Levitt ES; Hunnicutt BJ; Knopp SJ; Williams JT; Bissonnette JM
    J Appl Physiol (1985); 2013 Dec; 115(11):1626-33. PubMed ID: 24092697
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Pharmacological enhancement of
    Tang X; Drotar J; Li K; Clairmont CD; Brumm AS; Sullins AJ; Wu H; Liu XS; Wang J; Gray NS; Sur M; Jaenisch R
    Sci Transl Med; 2019 Jul; 11(503):. PubMed ID: 31366578
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.
    Bissonnette JM; Schaevitz LR; Knopp SJ; Zhou Z
    Neuroscience; 2014 May; 267():166-76. PubMed ID: 24626160
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Synaptic circuit abnormalities of motor-frontal layer 2/3 pyramidal neurons in a mutant mouse model of Rett syndrome.
    Wood L; Shepherd GM
    Neurobiol Dis; 2010 May; 38(2):281-7. PubMed ID: 20138994
    [TBL] [Abstract][Full Text] [Related]  

  • 75. FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice.
    Deng V; Matagne V; Banine F; Frerking M; Ohliger P; Budden S; Pevsner J; Dissen GA; Sherman LS; Ojeda SR
    Hum Mol Genet; 2007 Mar; 16(6):640-50. PubMed ID: 17309881
    [TBL] [Abstract][Full Text] [Related]  

  • 76. μ opioid receptor activation hyperpolarizes respiratory-controlling Kölliker-Fuse neurons and suppresses post-inspiratory drive.
    Levitt ES; Abdala AP; Paton JF; Bissonnette JM; Williams JT
    J Physiol; 2015 Oct; 593(19):4453-69. PubMed ID: 26175072
    [TBL] [Abstract][Full Text] [Related]  

  • 77. 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]  

  • 78. 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]  

  • 79. Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesis.
    Herrera JA; Ward CS; Wehrens XH; Neul JL
    Hum Mol Genet; 2016 Nov; 25(22):4983-4995. PubMed ID: 28159985
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Multiplex epigenome editing of
    Qian J; Guan X; Xie B; Xu C; Niu J; Tang X; Li CH; Colecraft HM; Jaenisch R; Liu XS
    Sci Transl Med; 2023 Jan; 15(679):eadd4666. PubMed ID: 36652535
    [TBL] [Abstract][Full Text] [Related]  

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