Lv1
44 积分 2023-09-27 加入
KEAP1/NRF2 signaling pathway mutations in cervical cancer
3天前
已完结
Saturation genome editing-based clinical classification of BRCA2 variants
1个月前
已完结
Maternal MLH3 dysfunction drives unexplained recurrent pregnancy loss via impaired oocyte maturation and defective decidualization
2个月前
已完结
[Characterization of PIK3CA/AKT1/PTEN gene mutations in hormone receptor- positive/HER2-negative breast cancer]
3个月前
已完结
The Y606C RET mutation causes a receptor gain of function
3个月前
已完结
PRT3789 Is a First-in-Human SMARCA2-Selective Degrader That Induces Synthetic Lethality in SMARCA4 -Mutated Cancers
4个月前
已完结
Prenatal Cell-Free DNA Sequencing and Intrahepatic Cholangiocarcinoma
4个月前
已关闭
Pediatric glioblastoma in the setting of constitutional mismatch-repair deficiency treated with upfront lomustine and nivolumab
4个月前
已完结
Acquired gene alterations in patients treated with ribociclib plus endocrine therapy or endocrine therapy alone using baseline and end-of-treatment circulating tumor DNA samples in the MONALEESA-2, -3, and -7 trials
4个月前
已完结
Tazemetostat in advanced epithelioid sarcoma with loss of INI1/SMARCB1: an international, open-label, phase 2 basket study
5个月前
已完结