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
2个月前
已关闭
Differential distribution patterns of CRABP I and CRABP II transcripts during mouse embryogenesis
6个月前
已关闭
Bile acid synthesis impedes tumor-specific T cell responses during liver cancer
8个月前
已完结
Functional characterization of a rare pathogenic variant c.875G > A, p.(Cys292Tyr) in COMP
8个月前
已完结
Functional reconstruction of human AML reveals stem cell origin and vulnerability of treatment-resistant MLL-rearranged leukemia
8个月前
已完结
Disrupting Integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development
8个月前
已完结
Quantitative functional profiling of ERCC2 mutations deciphers cisplatin sensitivity in bladder cancer
8个月前
已完结
SARS1 (SerRS) Causing De Novo Dominant Charcot–Marie–Tooth Disease with Slow Conduction
10个月前
已完结
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