Lv2
126 积分 2023-10-07 加入
Single-cell RNA sequencing reveals the landscape of biomarker in allergic rhinitis patient undergoing intracervical lymphatic immunotherapy and related pan-cancer analysis
13天前
已完结
Subtypes of SERPINC1 mutations and the thrombotic phenotype of inherited antithrombin deficient individuals in Chinese Han population
1个月前
已完结
Distinctive regional-specific PROS1 mutation spectrum in Southern China
1个月前
已关闭
The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene
1个月前
已完结
Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency
1个月前
已完结
Causative genetic mutations for antithrombin deficiency and their clinical background among Japanese patients
1个月前
已完结
Association study of miR-146a, miR-149, miR-196a2, and miR-499 polymorphisms with venous thromboembolism in a Korean population
1个月前
已完结
Clinical Manifestation and Mutation Spectrum of 53 Unrelated Pedigrees with Protein S Deficiency in China
1个月前
已完结
Screening and functional exploration of prothrombin Arg596 related mutations in Chinese venous thromboembolism patients
1个月前
已完结
Single-cell RNA-seq reveals abnormal differentiation of keratinocytes and increased inflammatory differentiated keratinocytes in atopic dermatitis
1个月前
已完结
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