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The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair networkFANCE: the link between Fanconi anaemia complex assembly and activityWarsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group MA multiprotein nuclear complex connects Fanconi anemia and Bloom syndromeAnalysis of baseline and cisplatin-inducible gene expression in Fanconi anemia cells using oligonucleotide-based microarrays.Update of the human and mouse Fanconi anemia genesDiagnosis of Fanconi Anemia: Chromosomal Breakage AnalysisA novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transportA novel ubiquitin ligase is deficient in Fanconi anemiaCharacterization, expression and complex formation of the murine Fanconi anaemia gene product FancgImpaired DNA damage-induced nuclear Rad51 foci formation uniquely characterizes Fanconi anemia group D1Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice
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hulumtues
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onderzoeker
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researcher
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հետազոտող
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name
Hans Joenje
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Hans Joenje
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Hans Joenje
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Hans Joenje
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Hans Joenje
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label
Hans Joenje
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Hans Joenje
@en
Hans Joenje
@es
Hans Joenje
@nl
Hans Joenje
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Hans Joenje
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Hans Joenje
@en
Hans Joenje
@es
Hans Joenje
@nl
Hans Joenje
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