Lv1
46 积分 2022-11-07 加入
Deleterious, protein-altering variants in GSPT2 are putatively associated with an X-linked neurodevelopmental disorder with intellectual disability, language impairment, autism and epilepsy
3个月前
已关闭
Differential distribution patterns of CRABP I and CRABP II transcripts during mouse embryogenesis
7个月前
已关闭
Bile acid synthesis impedes tumor-specific T cell responses during liver cancer
9个月前
已完结
Functional characterization of a rare pathogenic variant c.875G > A, p.(Cys292Tyr) in COMP
9个月前
已完结
Functional reconstruction of human AML reveals stem cell origin and vulnerability of treatment-resistant MLL-rearranged leukemia
10个月前
已完结
Disrupting Integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development
10个月前
已完结
Quantitative functional profiling of ERCC2 mutations deciphers cisplatin sensitivity in bladder cancer
10个月前
已完结
SARS1 (SerRS) Causing De Novo Dominant Charcot–Marie–Tooth Disease with Slow Conduction
1年前
已完结
皖公网安备34019202002308
