Lv1
18 积分 2022-11-07 加入
Functional reconstruction of human AML reveals stem cell origin and vulnerability of treatment-resistant MLL-rearranged leukemia
1天前
已完结
Disrupting Integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development
12天前
已完结
Quantitative functional profiling of ERCC2 mutations deciphers cisplatin sensitivity in bladder cancer
13天前
已完结
SARS1 (SerRS) Causing De Novo Dominant Charcot–Marie–Tooth Disease with Slow Conduction
2个月前
已完结
Biomimetic Nano‐Immunoactivator via Ionic Metabolic Modulation for Strengthened NIR‐II Photothermal Immunotherapy
11个月前
已完结
Disease‐associated missense variants in ZBTB18 disrupt DNA binding and impair the development of neurons within the embryonic cerebral cortex
1年前
已完结
A novel heterozygous ZBTB18 missense mutation in a family with non-syndromic intellectual disability
1年前
已完结
MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia
1年前
已完结
A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population
1年前
已完结
A novel ATP13A2 variant causing complicated hereditary spastic paraplegia
1年前
已完结
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