Lv1
38 积分 2023-08-22 加入
FGF9 mutation causes craniosynostosis along with multiple synostoses
20小时前
已完结
[Functional characterization of SLC12A1 gene variants in 3 patients with Bartter syndrome type Ⅰ]
14天前
已完结
Gramine Exerts Cytoprotective Effects and Antioxidant Properties Against H2O2-Induced Oxidative Stress in HEK 293 Cells
2个月前
已完结
SOX9 Promotes Collagen VI Secretion by Upregulating PCOLCE in Neurofibroma
3个月前
已完结
KAT2A coupled with the α-KGDH complex acts as a histone H3 succinyltransferase
4个月前
已完结
KAT2A coupled with the α-KGDH complex acts as a histone H3 succinyltransferase
4个月前
已完结
Hereditary Spherocytosis with Mitochondrial Retention, Increased Oxidative Stress, and Alterations to Bioactive Membrane Lipids
5个月前
已完结
Overexpression of CASP1 triggers acute promyelocytic leukemia cell pyroptosis and differentiation
5个月前
已完结
ERBB3 deficiency causes a multisystemic syndrome in human patient and zebrafish
5个月前
已完结
A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin
5个月前
已完结
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