...BRCA1, a DNA damage repair sensor and transcription regulator, is in complex with IFI16 in the host cell nucleus, and th...
...BRCA1/2 negative breast cancers is highly relevant for early diagnosis and development of a management plan. Mutations i...
...Brca1 caused the cells to arrest in the G2 phase, suggesting that they may be required for the G2/M transition. In contr...
...BRCA1/2, and TP53, and mutation of a splice donor site in BAP1 and loss of CDKN2A gene. We observed the absence of BAP1 ...
...BRCA1 could lead to impairment of BRCA1 function and provide strong evidence of haploinsufficiency in BRCA1 mutation car...
...BRCA1, BRCA2, CHEK2, NBN, ATM, PALB2, BARD1, and RAD51D, in 202 consecutive patients with triple-negative breast cancers...
...BRCA1). Among them, the downregulation of the E3 ubiquitin ligase DIP1 was closely related to death-associated protein k...
...BRCA1 or BRCA2 mutation who underwent RRSO were identified from a community-based health system in Northern California f...
...BRCA1 variant p.P142H, about female subjects. At the moment, BRCA1 gene variant p.P142H is not certainly classified as n...
...BRCA1/2. Cumulatively, we identified UBE2T as a bona fide FA gene (FANCT) that also may be a rare cancer susceptibility ...
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