Lv1
50 积分 2024-03-13 加入
Atypical phenotypic characteristics, mutation analysis and treatment in a family of riboflavin transporter deficiency caused by SLC52A3 variants
17天前
已完结
Expression of connexin 30 in the developing mouse cochlea
3个月前
已关闭
Renal clearable CRISPR nanosensor targeting mitochondrial DNA mutation for noninvasive monitoring of tumor progression and metastasis
5个月前
已完结
Interindividual variability in gut microbiome mediates the efficacy of resistant starch on MASLD
5个月前
已完结
Cidea Targeting Protects Cochlear Hair Cells and Hearing Function From Drug‐ and Noise‐Induced Damage
5个月前
已完结
Pyroptosis-Inducing Nanoplatform with Plasmonic-Enhanced Phototherapy for Metastasis-Suppressive Cancer Immunotherapy
5个月前
已完结
Pyroptosis-Inducing Nanoplatform with Plasmonic-Enhanced Phototherapy for Metastasis-Suppressive Cancer Immunotherapy
5个月前
已完结
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
7个月前
已完结
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
7个月前
已完结
The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron
7个月前
已完结
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