gBRCA1/2 mutations increase the incidence of breast cancer (BC) by interrupting the homologous recombination repair (HRR) pathway. Although gBRCA1 and gBRCA2 BC have similar clinical profiles, differe
Cancer is a genetic disease caused by an accumulation of mutations, however many of these mutations have been identified in pathologically normal tissue. We aim to use laser-capture microscopy (LCM) t
A Crystal structure of OspA mutant Descriptor: DI(HYDROXYETHYL)ETHER, Outer surface protein A Authors: Shiga, S, Makabe, K. Deposit date: 2021-07-16 Release date: 2022-07-20 Last modified: 2024-02-21
