Lv1
70 积分 2022-07-11 加入
Epilepsy due to potential loss of ATP6V1B2 function with mechanistic insight by a Drosophila Vha55 model
1个月前
已完结
Mistargeting and ER retention of CLN7 patient-associated nonsense and sequence deletion mutations as a novel cause for CLN7 disease
1个月前
已完结
GBF1 deficiency causes cataracts in human and mouse
1个月前
已完结
Phenotypic and genotypic analysis of children with methylmalonic academia: A single-center study in China and a recent literature review
1个月前
已完结
Analysis of the 2000 to 2018 autism and developmental disabilities monitoring network surveillance reports: Implications for primary care clinicians
2个月前
已完结
First pathogenic non-coding variant in MMACHC: a functional deletion in the 5'-UTR associated with cobalamin C deficiency
5个月前
已完结
SNAP25 variant I67N: synaptic phenotypes, drug response and proteome changes in human neurons
8个月前
已完结
Sequence variants in HECTD1 result in a variable neurodevelopmental disorder
9个月前
已关闭
GLP1 secretagogue cinnamaldehyde upregulates GLP1/PI3K/AKT and Nrf2 pathways to exert neuroprotection in a rotenone induced mouse model of Parkinson's disease
10个月前
已关闭
皖公网安备34019202002308
