...FANCL and WRN. One patient fulfilled criteria for multi‑locus inherited neoplasia alleles syndrome (MINAS). High‑grade s...
...FANCL-UBE2T complex, and deubiquitination by USP1-UAF1. This review summarizes the functional mechanisms of FANCI across...
...FANCL, FCER2, TLR2) and constructed a recurrence risk score model. Furthermore, we externally validated the risk score m...
...FanclTATΔ) that mimics an allele from a patient with FA. This 3-bp deletion removes a catalytic cysteine in the E3 RING ...
...FANCL, DDX5, SRSF5B) and male-biased genes (STAR, FDX1B, ITGA2B). Furthermore, a competing endogenous RNA (ceRNA) regula...
...FANCL, PALB2, RAD51B, RAD51C, RAD51D, and RAD54L. Biomarker testing patterns and treatment patterns were reported from i...
...FANCL), a ubiquitin E3 ligase that mediates the monoubiquitylation of FANCD2 as an essential step in the FA pathway. The...
...FANCL, FANCM, FANCN/PALB2, FANCO/RAD51C, FANCP/SLX4, FANCQ/XPF, FANCR/RAD51, FANCS/BRCA1, FANCT/UBE2T, FANCU/XRCC2, FANC...
...FANCL-mediated ubiquitin transfer from UBE2T∼Ub to the ID2 complex, without impairing E2 charging or FANCL-UBE2T binding...
...FANCL expression was analyzed at the transcriptional level, and rescue experiments were performed by FANCL overexpressio...
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