Lv62
2400 积分 2021-02-23 加入
Analysis of patient‐specific NF1 variants leads to functional insights for Ras signaling that can impact personalized medicine
3小时前
已完结
The predictive role of ERBB2 point mutations in metastatic colorectal cancer: A systematic review
1天前
已完结
The relationship among p53 oligomer formation, structure and transcriptional activity using a comprehensive missense mutation library
6天前
已完结
Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paraganglioma
10天前
已完结
NGS mismapping confounds the clinical interpretation of the PRSS1 p.Ala16Val (c.47C>T) variant in chronic pancreatitis
15天前
已完结
The Protein Interactome of DNMT3A, and Altered Interactions Caused By Missense Mutations Associated with AML and/or the DNMT3A Overgrowth Syndrome
16天前
已关闭
Gene Expression and Benefit of Chemotherapy in Women With Node-Negative, Estrogen Receptor–Positive Breast Cancer
1个月前
已完结
Alectinib for the treatment of papillary thyroid carcinoma harbouring STRN – ALK fusion
1个月前
已完结
Correlative Analysis of ATM, RB1, ERCC2, and FANCC Mutations and Pathologic Complete Response After Neoadjuvant Chemotherapy in Patients with Muscle-invasive Bladder Cancer: Results from the SWOG S1314 Trial
2个月前
已完结
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