|Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
|The genomic organization of the Fanconi anemia group A (FAA) gene.
|Sequence variation in the Fanconi anemia gene FAA.
|Mutations of the Fanconi anemia group A gene (FAA) in Italian patients.
|Identification of Alu-mediated deletions in the Fanconi anemia gene FAA.
|Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions.
|Functional activity of the Fanconi anemia protein FAA requires FAC binding and nuclear localization.
|The Fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation.
|Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients.
|Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.
|A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulation.
|High frequency of large intragenic deletions in the Fanconi anemia group A gene.
|Novel mutations of the FANCG gene causing alternative splicing in Japanese Fanconi anemia.
|Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients.
|A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome.
|Complete sequencing and characterization of 21,243 full-length human cDNAs.
|The Fanconi anemia proteins functionally interact with the protein kinase regulated by RNA (PKR).
|The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
|X-linked inheritance of Fanconi anemia complementation group B.
|The sequence and analysis of duplication-rich human chromosome 16.
|A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.
|ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage.
|Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
|HES1 is a novel interactor of the Fanconi anemia core complex.
|Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.
|DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome.
|Regulation of Rev1 by the Fanconi anemia core complex.
|FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway.
|A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network.
|Toward a comprehensive characterization of a human cancer cell phosphoproteome.