Lv4
610 积分 2023-04-06 加入
Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects
2个月前
已完结
[Clinical and genetic analysis of a pedigree affected with cytochrome P450 oxidoreductase deficiency]
8个月前
已关闭
Identification of the synonymous variant c.3141G > A in TNRC6B gene that altered RNA splicing by minigene assay
9个月前
已完结
Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations
10个月前
已完结
IDO2-siRNA Carried by Salmonella Combined with Nifuroxazide Attenuates Melanoma Growth
11个月前
已完结
SK1 Inhibitor RB005 Induces Apoptosis in Colorectal Cancer Cells through SK1 Inhibition Dependent and Independent Pathway
11个月前
已完结
Transcriptomics and molecular docking reveal the potential mechanism of lycorine against pancreatic cancer
11个月前
已完结
Common Variable Immunodeficiency
1年前
已完结
Identification of an IL-1 receptor mutation driving autoinflammation directs IL-1-targeted drug design
1年前
已完结
Autosomal dominant polycystic kidney disease
1年前
已完结
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