Lv3
230 积分 2023-04-24 加入
Cerebral vasculopathy in a Chinese family with neurofibromatosis type I mutation
3个月前
已完结
Cerebral Vasculopathy in Children With Neurofibromatosis Type 1
3个月前
已完结
Expression of the neurofibromatosis I gene product, neurofibromin, in blood vessel endothelial cells and smooth muscle
4个月前
已完结
‘MCC’ protein interacts with E-cadherin and β-catenin strengthening cell–cell adhesion of HCT116 colon cancer cells
4个月前
已完结
RNF213 variant and autophagic impairment: A pivotal link to endothelial dysfunction in Moyamoya disease
5个月前
已完结
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke
5个月前
已完结
A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex
5个月前
已完结
Measurement of chromosomal instability and level of DNA damage in peripheral blood mononuclear cells of endometrial cancer patients
6个月前
已完结
Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans
7个月前
已完结
Three generation families: Analysis of de novo variants in autism
7个月前
已完结
皖公网安备34019202002308
