Lv6
2480 积分 2021-02-23 加入
Best Practice for Clinical Somatic Variant Interpretation and Reporting
18天前
已完结
Co-occurring EGFR p.E709X Mutation Mediates Primary Resistance to the Third-Generation EGFR-TKIs in EGFR p.G719X-Mutant Patients with Advanced NSCLC
1个月前
已完结
Analysis of patient‐specific NF1 variants leads to functional insights for Ras signaling that can impact personalized medicine
1个月前
已完结
The predictive role of ERBB2 point mutations in metastatic colorectal cancer: A systematic review
1个月前
已完结
The relationship among p53 oligomer formation, structure and transcriptional activity using a comprehensive missense mutation library
1个月前
已完结
Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paraganglioma
1个月前
已完结
NGS mismapping confounds the clinical interpretation of the PRSS1 p.Ala16Val (c.47C>T) variant in chronic pancreatitis
2个月前
已完结
The Protein Interactome of DNMT3A, and Altered Interactions Caused By Missense Mutations Associated with AML and/or the DNMT3A Overgrowth Syndrome
2个月前
已关闭
Gene Expression and Benefit of Chemotherapy in Women With Node-Negative, Estrogen Receptor–Positive Breast Cancer
3个月前
已完结
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