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注意：仅列出部分参考文献，下载原文获取全部文献信息。Mutations in the Gene Encoding the E2 Conjugating Enzyme UBE2T Cause Fanconi Anemia
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Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia
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The Fanconi Anemia Protein FANCM Is Controlled by FANCD2 and the ATR/ATM Pathways
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Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment
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Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24
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Fanconi anemia proteins stabilize replication forks
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FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway
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Deubiquitination of FANCD2 is required for DNA crosslink repair
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FANCI is a second monoubiquitinated member of the Fanconi anemia pathway
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Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair
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Human Tim/Timeless-interacting protein, Tipin, is required for efficient progression of S phase and DNA replication checkpoint
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The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway
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ATR couples FANCD2 monoubiquitination to the DNA-damage response
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DNA replication defects, spontaneous DNA damage, and ATM-dependent checkpoint activation in replication protein A-deficient cells
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