Lv4
610 积分 2023-04-06 加入
Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects
1天前
待确认
[Clinical and genetic analysis of a pedigree affected with cytochrome P450 oxidoreductase deficiency]
6个月前
已关闭
Identification of the synonymous variant c.3141G > A in TNRC6B gene that altered RNA splicing by minigene assay
7个月前
已完结
Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations
8个月前
已完结
IDO2-siRNA Carried by Salmonella Combined with Nifuroxazide Attenuates Melanoma Growth
9个月前
已完结
SK1 Inhibitor RB005 Induces Apoptosis in Colorectal Cancer Cells through SK1 Inhibition Dependent and Independent Pathway
9个月前
已完结
Transcriptomics and molecular docking reveal the potential mechanism of lycorine against pancreatic cancer
9个月前
已完结
Common Variable Immunodeficiency
10个月前
已完结
Identification of an IL-1 receptor mutation driving autoinflammation directs IL-1-targeted drug design
10个月前
已完结
Autosomal dominant polycystic kidney disease
10个月前
已完结
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