Lv11
20 积分 2023-03-05 加入
Autism spectrum disorder phenotype and intellectual disability in females with epilepsy and PCDH-19 mutations
2小时前
待确认
enOsCas12f1-mediated exon skipping for Duchenne muscular dystrophy therapy in humanized mouse model
1个月前
已完结
enOsCas12f1-mediated exon skipping for Duchenne muscular dystrophy therapy in humanized mouse model
1个月前
已完结
Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review
7个月前
已完结
Antisense oligonucleotides restore excitability, GABA signalling and sodium current density in a Dravet syndrome model
8个月前
已完结
PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony ofneurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy
10个月前
已完结
KaryoCreate: A CRISPR-based technology to study chromosome-specific aneuploidy by targeting human centromeres
10个月前
已关闭
CRISPR-Based KCC2 Upregulation Attenuates Drug-Resistant Seizure in Mouse Models of Epilepsy
1年前
已完结
KaryoCreate: A CRISPR-based technology to study chromosome-specific aneuploidy by targeting human centromeres
1年前
已完结
Hypercompact adenine base editors based on transposase B guided by engineered RNA
1年前
已完结
皖公网安备34019202002308
