関連する実験動画

Updated: Jul 9, 2026

Pooled shRNA Screen for Reactivation of MeCP2 on the Inactive X Chromosome
11:15

Pooled shRNA Screen for Reactivation of MeCP2 on the Inactive X Chromosome

Published on: March 2, 2018

男性における非致命的な神経発達障害としてのMECP2の体内の変異は,男性における非致命的な神経発達障害として,MECP2の体内の変異は,男性における非致命的な神経発達障害として,男性における非致命的な神経発達障害として,男性における非

J Clayton-Smith, P Watson, S Ramsden

    Lancet (London, England)
    |October 7, 2000
    PubMed
    まとめ

    男性は,体的モザイク主義により,重度の神経発達障害であるレット症候群を発症することがあります. これは,MECP2遺伝子変異を有する細胞が正常細胞と共存し,罹患した雄の生存を可能にすると起こります.

    さらに関連する動画

    A Non-random Mouse Model for Pharmacological Reactivation of Mecp2 on the Inactive X Chromosome08:27

    A Non-random Mouse Model for Pharmacological Reactivation of Mecp2 on the Inactive X Chromosome

    Published on: May 22, 2019

    An Electrochemiluminescence-Based Assay for MeCP2 Protein Variants07:44

    An Electrochemiluminescence-Based Assay for MeCP2 Protein Variants

    Published on: May 22, 2020

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