30 Matching Annotations
  1. Dec 2024
  2. genomemedicine.biomedcentral.com genomemedicine.biomedcentral.com
    Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression
    1
    1. scibot 21 Dec 2024
      RRID:AB_2143849

      DOI: 10.1186/s13073-024-01411-7

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    genomemedicine.biomedcentral.com/articles/10.1186/s13073-024-01411-7
  3. www.sciencedirect.com www.sciencedirect.com
    Acute MeCP2 loss in adult mice reveals transcriptional and chromatin changes that precede neurological dysfunction and inform pathogenesis
    2
    1. scibot 17 Dec 2024
      RRID:AB_2143849

      DOI: 10.1016/j.neuron.2024.11.006

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    2. scibot 17 Dec 2024
      RRID:AB_2143894

      DOI: 10.1016/j.neuron.2024.11.006

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      Curator: @areedewitt04

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    sciencedirect.com/science/article/pii/S0896627324008067
  4. www.sciencedirect.com www.sciencedirect.com
    Spatial organizations of heterochromatin underpin nuclear structural integrity of ventricular cardiomyocytes against mechanical stress
    1
    1. scibot 10 Dec 2024
      RRID:AB_2143849

      DOI: 10.1016/j.celrep.2024.115048

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    sciencedirect.com/science/article/pii/S2211124724013998
  5. Sep 2024
  6. dx.doi.org dx.doi.org
    Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levels
    1
    1. scibot 27 Sep 2024
      RRID:AB_2143849

      DOI: 10.1093/hmg/ddae135

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    dx.doi.org/10.1093/hmg/ddae135
  7. Aug 2024
  8. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Wild-type MeCp2 expression coincides with age-dependent sensory phenotypes in a female mouse model for Rett syndrome
    1
    1. scibot 18 Aug 2024
      RRID:AB_2143849

      DOI: 10.1002/jnr.25190

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    ncbi.nlm.nih.gov/pmc/articles/PMC10332853/
  9. Jul 2024
  10. 52.53.155.43 52.53.155.43
    s41587-024-02313-0-html.html
    1
    1. scibot 30 Jul 2024
      RRID:AB_2143849

      DOI: 10.1038/s41587-024-02313-0

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    52.53.155.43/f657dad9ecdb0995c76c0fa7870c251bdb32d9d3/s41587-024-02313-0-html.html
  11. May 2024
  12. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Mecp2 fine-tunes quiescence exit by targeting nuclear receptors
    1
    1. scibot 17 May 2024
      RRID:AB_2143849

      DOI: 10.7554/eLife.89912

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    ncbi.nlm.nih.gov/pmc/articles/PMC11095939/
  13. www.sciencedirect.com www.sciencedirect.com
    Generation of human induced pluripotent stem cell lines derived from four Rett syndrome patients with MECP2 mutations
    1
    1. scibot 07 May 2024
      RRID:AB_2143849

      DOI: 10.1016/j.scr.2024.103432

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    sciencedirect.com/science/article/pii/S1873506124001302
  14. Mar 2023
  15. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    MeCP2 regulates Gdf11, a dosage-sensitive gene critical for neurological function
    1
    1. scibot 04 Mar 2023
      RRID:AB_2143894

      DOI: 10.7554/eLife.83806

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      Curator: @evieth

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    ncbi.nlm.nih.gov/pmc/articles/PMC9977283/
  16. Jan 2023
  17. www.mdpi.com www.mdpi.com
    The Interactions of the 70 kDa Fragment of Cell Adhesion Molecule L1 with Topoisomerase 1, Peroxisome Proliferator-Activated Receptor γ and NADH Dehydrogenase (Ubiquinone) Flavoprotein 2 Are Involved in Gene Expression and Neuronal L1-Dependent Functions
    1
    1. scibot 28 Jan 2023
      RRID:AB_2143849

      DOI: 10.3390/ijms24032097

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      Curator: @sofiakhan13

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    mdpi.com/1422-0067/24/3/2097
  18. www.mdpi.com www.mdpi.com
    The KDET Motif in the Intracellular Domain of the Cell Adhesion Molecule L1 Interacts with Several Nuclear, Cytoplasmic, and Mitochondrial Proteins Essential for Neuronal Functions
    1
    1. scibot 08 Jan 2023
      RRID:AB_2143849

      DOI: 10.3390/ijms24020932

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    mdpi.com/1422-0067/24/2/932
  19. www.sciencedirect.com www.sciencedirect.com
    Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation
    1
    1. scibot 06 Jan 2023
      RRID:AB_2143849

      DOI: 10.1016/j.celrep.2022.111942

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    sciencedirect.com/science/article/pii/S2211124722018435
  20. Oct 2022
  21. www.pnas.org www.pnas.org
    Targeted RNA editing in brainstem alleviates respiratory dysfunction in a mouse model of Rett syndrome
    1
    1. scibot 13 Oct 2022
      RRID:AB_2143849

      DOI: 10.1073/pnas.2206053119

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    pnas.org/doi/abs/10.1073/pnas.2206053119
  22. Apr 2022
  23. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    The Cell Adhesion Molecule L1 Interacts with Methyl CpG Binding Protein 2 via Its Intracellular Domain
    1
    1. scibot 13 Apr 2022
      RRID:AB_2143849

      DOI: 10.3390/ijms23073554

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    ncbi.nlm.nih.gov/pmc/articles/PMC8998178/
  24. Mar 2022
  25. www.sciencedirect.com www.sciencedirect.com
    A weakened recurrent circuit in the hippocampus of Rett syndrome mice disrupts long-term memory representations
    1
    1. scibot 26 Mar 2022
      RRID:AB_2143849

      DOI: 10.1016/j.neuron.2022.02.014

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    sciencedirect.com/science/article/pii/S0896627322001799
  26. Aug 2021
  27. www.jneurosci.org www.jneurosci.org
    CREB Signaling Is Involved in Rett Syndrome Pathogenesis
    1
    1. scibot 08 Aug 2021
      AB_2143849

      DOI: 10.1523/JNEUROSCI.3735-16.2017

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    jneurosci.org/content/37/13/3671
  28. Jul 2021
  29. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Fluoxetine increases brain MeCP2 immuno-positive cells in a female Mecp2 heterozygous mouse model of Rett syndrome through endogenous serotonin
    1
    1. scibot 23 Jul 2021
      RRID:AB_2143849

      DOI: 10.1038/s41598-021-94156-x

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    ncbi.nlm.nih.gov/pmc/articles/PMC8290043/
  30. Feb 2021
  31. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Whole brain delivery of an instability-prone Mecp2 transgene improves behavioral and molecular pathological defects in mouse models of Rett syndrome
    1
    1. scibot 25 Feb 2021
      RRID:AB_2143849

      DOI: 10.7554/eLife.52629

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    ncbi.nlm.nih.gov/pmc/articles/PMC7117907/
  32. Jan 2021
  33. elifesciences.org elifesciences.org
    Deleting Mecp2 from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice
    1
    1. scibot 30 Jan 2021
      RRID:AB_2143849

      DOI: 10.7554/eLife.64833

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      Curator: @evieth

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      RRID:AB_2143849 RRIDCUR:Validated
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    elifesciences.org/articles/64833
  34. Sep 2020
  35. academic.oup.com academic.oup.com
    Sex-dependent mechanisms of glucocorticoid regulation of the mouse hypothalamic corticotropin-releasing hormone gene
    1
    1. scibot 26 Sep 2020
      RRID:AB_2143849

      DOI: 10.1210/endocr/bqz012

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      Curator: @ethanbadger

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      RRIDCUR:Validated RRID:AB_2143849
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    academic.oup.com/endo/article/161/1/bqz012/5637506
  36. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Vitamin D Supplementation Rescues Aberrant NF-κB Pathway Activation and Partially Ameliorates Rett Syndrome Phenotypes in Mecp2 Mutant Mice
    1
    1. scibot 16 Sep 2020
      RRID:AB_2143849

      DOI: 10.1523/ENEURO.0167-20.2020

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      Curator: @evieth

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      RRIDCUR:Validated RRID:AB_2143849
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    ncbi.nlm.nih.gov/pmc/articles/PMC7253640/
  37. www.sciencedirect.com www.sciencedirect.com
    In Vivo Repair of a Protein Underlying a Neurological Disorder by Programmable RNA Editing
    1
    1. scibot 16 Sep 2020
      RRID:AB_2143849

      DOI: 10.1016/j.celrep.2020.107878

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      Curator: @Naa003

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      RRIDCUR:Validated RRID:AB_2143849
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    sciencedirect.com/science/article/pii/S2211124720308597
  38. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Losing Dnmt3a dependent methylation in inhibitory neurons impairs neural function by a mechanism impacting Rett syndrome
    1
    1. scibot 05 Sep 2020
      RRID:AB_2143849

      DOI: 10.7554/eLife.52981

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    ncbi.nlm.nih.gov/pmc/articles/PMC7065908/
  39. Jan 2020
  40. www.sciencedirect.com www.sciencedirect.com
    Generation of four H1 hESC sublines carrying a hemizygous knock-out/mutant MECP2
    1
    1. scibot 13 Jan 2020
      RRID:AB_2143849

      DOI: 10.1016/j.scr.2019.101533

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      RRID:AB_2143849 RRIDCUR:Validated
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    sciencedirect.com/science/article/pii/S1873506119301631
  41. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    miR-132 couples the circadian clock to daily rhythms of neuronal plasticity and cognition
    1
    1. scibot 13 Jan 2020
      RRID:AB_2143849

      DOI: 10.1101/lm.047191.117

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    ncbi.nlm.nih.gov/pmc/articles/PMC5903403/
  42. www.eneuro.org www.eneuro.org
    Mecp2 deletion from cholinergic neurons selectively impairs recognition memory and disrupts cholinergic modulation of the perirhinal cortex
    1
    1. scibot 13 Jan 2020
      RRID:AB_2143849

      DOI: 10.1523/ENEURO.0134-19.2019

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      Curator: @evieth

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    eneuro.org/content/6/6/ENEURO.0134-19.2019
  43. www.sciencedirect.com www.sciencedirect.com
    In Vivo Single-Cell Genotyping of Mouse Cortical Neurons Transfected with CRISPR/Cas9
    1
    1. scibot 13 Jan 2020
      RRID:AB_2143849

      DOI: 10.1016/j.celrep.2019.06.038

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      Curator: @ethanbadger

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    sciencedirect.com/science/article/pii/S2211124719308046
  44. www.sciencedirect.com www.sciencedirect.com
    The Osteogenic Niche Is a Calcium Reservoir of Bone Micrometastases and Confers Unexpected Therapeutic Vulnerability
    1
    1. scibot 13 Jan 2020
      RRID:AB_2143849

      DOI: 10.1016/j.ccell.2018.10.002

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      Curator: @Jmenke

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    sciencedirect.com/science/article/pii/S1535610818304689
  45. Nov 2018
  46. www.jneurosci.org www.jneurosci.org
    Epigenetic Promoter DNA Methylation of miR-124 Promotes HIV-1 Tat-Mediated Microglial Activation via MECP2-STAT3 Axis
    1
    1. scibot 05 Nov 2018
      RRID:AB_2143849

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    jneurosci.org/content/38/23/5367