Rett 综合征相关基因MeCP2 敲除大鼠模型的构建及分析
翟伟， 胡宏秀， 乐亮， 庄峰峰， 王克柱， 赵英， 王凯… - 遗传, 2016 - chinagene.cn
… Generation and analysis of the Rett syndrome-associated MeCP2null rat model … of MeCP2
in brain development and RTT pathogenesis, we aimed to set up the MeCP2-null rat model …
in brain development and RTT pathogenesis, we aimed to set up the MeCP2-null rat model …
[HTML][HTML] MECP2 基因及MECP2 相关疾病
彭镜 - Chinese Journal of Contemporary Pediatrics, 2017 - ncbi.nlm.nih.gov
… 直到1983年，Hagberg等 [2] 在Annals of Neurology报道了类似发育倒退但没有高氨血症的
病例，… Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding …
病例，… Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding …
遗传性神经发育障碍的产后治疗方法
G Levy, B Barak - 中国神经再生研究(英文版), 2021 - sjzsyj.com.cn
… Guy J, Hendrich B, Holmes M, Martin JE, Bird A (2001) A mouse Mecp2-null mutation causes
neurological symptoms that mimic Rett syndrome. Nat Genet 27:322-326. György B, Meijer …
neurological symptoms that mimic Rett syndrome. Nat Genet 27:322-326. György B, Meijer …
[PDF][PDF] 常见精神疾病的大, 小鼠遗传模型研究进展
罗卓慧， 庞硕， 张连峰 - 中国比较医学杂志, 2021 - zgbjyx.cnjournals.com
… Diseases, 2014, 2(1): 45-70. [49] Guy J, Hendrich B, Holmes M, et al. A mouse Mecp2-null
mutation causes neurological symptoms that mimic Rett syndrome [J]. Nat Genet, 2001, 27(3): …
mutation causes neurological symptoms that mimic Rett syndrome [J]. Nat Genet, 2001, 27(3): …
Mecp2 在斑马鱼胚胎神经发育中对NOTCH 信号通路的调控
何丽番， 高海 - 生物技术通报, 2016 - biotech.aiijournal.com
… (Rett syndrome,RTT),是一种神经系统发育异常性疾 病,典型RTT 的临床特征为,出生后6-18 个
月生 长… Our study showed that Mecp2 regulated the differentiation of nerve cells of zebrafish …
月生 长… Our study showed that Mecp2 regulated the differentiation of nerve cells of zebrafish …
脑发育疾病及发病机制
姜义圣， 许执恒 - 遗传, 2019 - chinagene.cn
… the brain, which may result in brain developmental diseases … Rett syndrome: a genetic
update and clinical review focusing … diversity emerging during mouse brain development. Nat …
update and clinical review focusing … diversity emerging during mouse brain development. Nat …
[PDF][PDF] 孤独症谱系障碍实验动物模型研究进展
李燊， 吴海涛 - 中国药理学与毒理学杂志, 2020 - cjpt.magtechjournal.com
… A mouse MeCP2- null mutation causes neurological symptoms that mimic Rett syndrome
[J]. Nat Genet,2001,27(3):322-326. [28] … Mice with truncated MeCP2 recapitulate many Rett …
[J]. Nat Genet,2001,27(3):322-326. [28] … Mice with truncated MeCP2 recapitulate many Rett …
[PDF][PDF] 线粒体功能障碍与孤独症
张洪峰， 张嵘 - Chinese Journal of Biochemistry and Molecular …, 2015 - nri.bjmu.edu.cn
… 综合征和未分类的广泛发育 障碍( pervasive developmental disorder-not otherwise
specified,PDD-NOS) 等统称为孤独症谱系障碍 ( autism spectrum disorders,ASDs) [2],孤独症发病率 …
specified,PDD-NOS) 等统称为孤独症谱系障碍 ( autism spectrum disorders,ASDs) [2],孤独症发病率 …