Dedicated to the core: understanding the Fanconi anemia complex.
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[1] W. R. Shannon,et al. Cloning of cDNAs for Fanconi's anaemia by functional complementation , 1992, Nature.
[2] W. R. Shannon,et al. Cloning of cDNAs for Fanconi's anaemia by functional complementation , 1992, Nature.
[3] Hans Joenje,et al. Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA , 1996, Nature Genetics.
[4] N. Alon,et al. Erratum: Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA , 1996, Nature Genetics.
[5] F. Kruyt,et al. Involvement of the Fanconi's anemia protein FAC in a pathway that signals to the cyclin B/cdc2 kinase. , 1997, Cancer research.
[6] A. D’Andrea,et al. The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2. , 1997, Blood.
[7] Hans Joenje,et al. The Fanconi anaemia group G gene FANCG is identical with XRCC9 , 1998, Nature Genetics.
[8] A. D’Andrea,et al. The fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[9] C G Mathew,et al. Isolation of a cDNA representing the Fanconi anemia complementation group E gene. , 2000, American journal of human genetics.
[10] P. Hieter,et al. The APC11 RING-H2 finger mediates E2-dependent ubiquitination. , 2000, Molecular biology of the cell.
[11] I. Hickson,et al. Replication Protein A Physically Interacts with the Bloom's Syndrome Protein and Stimulates Its Helicase Activity* , 2000, The Journal of Biological Chemistry.
[12] Hans Joenje,et al. The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM , 2000, Nature Genetics.
[13] S. West,et al. The Bloom's syndrome gene product promotes branch migration of holliday junctions. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[14] M. Grompe,et al. DNA Replication Is Required To Elicit Cellular Responses to Psoralen-Induced DNA Interstrand Cross-Links , 2000, Molecular and Cellular Biology.
[15] Ping Wang,et al. Structure of a c-Cbl–UbcH7 Complex RING Domain Function in Ubiquitin-Protein Ligases , 2000, Cell.
[16] A. D’Andrea,et al. The fanconi anemia proteins FANCA and FANCG stabilize each other and promote the nuclear accumulation of the Fanconi anemia complex. , 2000, Blood.
[17] S. Ganesan,et al. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. , 2001, Molecular cell.
[18] R. Moses,et al. Positional cloning of a novel Fanconi anemia gene, FANCD2. , 2001, Molecular cell.
[19] Linda Hicke,et al. Ubiquitin and proteasomes: Protein regulation by monoubiquitin , 2001, Nature Reviews Molecular Cell Biology.
[20] G. Kupfer,et al. Fanconi Anemia Proteins Localize to Chromatin and the Nuclear Matrix in a DNA Damage- and Cell Cycle-regulated Manner* , 2001, The Journal of Biological Chemistry.
[21] Hans Joenje,et al. FANCE: the link between Fanconi anaemia complex assembly and activity , 2002, The EMBO journal.
[22] C. Mathew,et al. Interaction of FANCD2 and NBS1 in the DNA damage response , 2002, Nature Cell Biology.
[23] A. D’Andrea,et al. S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51. , 2002, Blood.
[24] A. D’Andrea,et al. The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC. , 2002, Blood.
[25] Hans Joenje,et al. Biallelic Inactivation of BRCA2 in Fanconi Anemia , 2002, Science.
[26] I. Hickson,et al. The Bloom's syndrome helicase stimulates the activity of human topoisomerase IIIalpha. , 2002, Nucleic acids research.
[27] A. D’Andrea,et al. The Fanconi anaemia/BRCA pathway , 2003, Nature Reviews Cancer.
[28] Ian D. Hickson,et al. The Bloom's syndrome helicase suppresses crossing over during homologous recombination , 2003, Nature.
[29] Weidong Wang,et al. A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome , 2003, Molecular and Cellular Biology.
[30] J. D. den Dunnen,et al. An alternative to FISH: detecting deletion and duplication carriers within 24 hours , 2003, Journal of medical genetics.
[31] C. Bishop,et al. A novel ubiquitin ligase is deficient in Fanconi anemia , 2003, Nature Genetics.
[32] C. Mathew,et al. Disruption of the Fanconi anemia–BRCA pathway in cisplatin-sensitive ovarian tumors , 2003, Nature Medicine.
[33] H. Youssoufian,et al. Fanconi anaemia proteins: major roles in cell protection against oxidative damage. , 2003, BioEssays : news and reviews in molecular, cellular and developmental biology.
[34] J. Hoeijmakers,et al. A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C protein. , 2003, Genes & development.
[35] I. Hickson. RecQ helicases: caretakers of the genome , 2003, Nature Reviews Cancer.
[36] Susan M. Gordon,et al. Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems. , 2003, Blood.
[37] Anthony A High,et al. The Fanconi Anemia Core Complex Forms Four Complexes of Different Sizes in Different Subcellular Compartments* , 2004, Journal of Biological Chemistry.
[38] A. D’Andrea,et al. ATR couples FANCD2 monoubiquitination to the DNA-damage response. , 2004, Genes & development.
[39] H. Joenje,et al. Multiple TPR motifs characterize the Fanconi anemia FANCG protein. , 2004, DNA repair.
[40] K. J. Patel,et al. The Fanconi anaemia gene FANCC promotes homologous recombination and error-prone DNA repair. , 2004, Molecular cell.
[41] G. Pals,et al. X-linked inheritance of Fanconi anemia complementation group B , 2004, Nature Genetics.
[42] C. Mathew,et al. Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes. , 2004, Blood.
[43] J. Shabanowitz,et al. FANCG Is Phosphorylated at Serines 383 and 387 during Mitosis , 2004, Molecular and Cellular Biology.
[44] J. Groden,et al. Crosslinks and crosstalk: human cancer syndromes and DNA repair defects. , 2004, Cancer cell.
[45] Mike Tyers,et al. A hitchhiker's guide to the cullin ubiquitin ligases: SCF and its kin. , 2004, Biochimica et biophysica acta.
[46] Q. Waisfisz,et al. The Fanconi Anemia Gene Product FANCF Is a Flexible Adaptor Protein* , 2004, Journal of Biological Chemistry.
[47] K. Komori,et al. Cooperation of the N-terminal Helicase and C-terminal Endonuclease Activities of Archaeal Hef Protein in Processing Stalled Replication Forks* , 2004, Journal of Biological Chemistry.
[48] J. Mi,et al. Phosphorylation of Fanconi Anemia (FA) Complementation Group G Protein, FANCG, at Serine 7 Is Important for Function of the FA Pathway* , 2004, Journal of Biological Chemistry.
[49] A. D’Andrea,et al. Functional Interaction of Monoubiquitinated FANCD2 and BRCA2/FANCD1 in Chromatin , 2004, Molecular and Cellular Biology.
[50] J. Hoeijmakers,et al. Fanconi Anemia (Cross)linked to DNA Repair , 2005, Cell.
[51] J. Pereira-Leal,et al. The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway , 2005, Nature Structural &Molecular Biology.
[52] Dietmar Riedel,et al. Localization of the coactivator Cdh1 and the cullin subunit Apc2 in a cryo-electron microscopy model of vertebrate APC/C. , 2005, Molecular cell.
[53] C. Mathew,et al. A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M , 2005, Nature Genetics.
[54] G. Wider,et al. Ubiquitin-Binding Domains in Y-Family Polymerases Regulate Translesion Synthesis , 2005, Science.
[55] Wah Chiu,et al. Structural analysis of the anaphase-promoting complex reveals multiple active sites and insights into polyubiquitylation. , 2005, Molecular cell.
[56] Susan M. Gordon,et al. FANCC, FANCE, and FANCD2 Form a Ternary Complex Essential to the Integrity of the Fanconi Anemia DNA Damage Response Pathway* , 2005, Journal of Biological Chemistry.
[57] A. D’Andrea,et al. The Fanconi Anemia/BRCA pathway: new faces in the crowd. , 2005, Genes & development.
[58] H. Kitao,et al. A FancD2-monoubiquitin fusion reveals hidden functions of Fanconi anemia core complex in DNA repair. , 2005, Molecular cell.
[59] J. Ott,et al. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia , 2005, Nature Genetics.
[60] J. Mi,et al. The Fanconi anemia core complex associates with chromatin during S phase. , 2005, Blood.
[61] S. Cantor,et al. BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. , 2005, Cancer cell.
[62] A. Horwitz,et al. Direct DNA Binding Activity of the Fanconi Anemia D2 Protein* , 2005, Journal of Biological Chemistry.
[63] C. Mathew,et al. The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J , 2005, Nature Genetics.
[64] J. Labbé,et al. The anaphase-promoting complex: a key factor in the regulation of cell cycle , 2005, Oncogene.
[65] Weidong Wang,et al. Fanconi Anemia Proteins Are Required To Prevent Accumulation of Replication-Associated DNA Double-Strand Breaks , 2006, Molecular and Cellular Biology.
[66] A. Gurtan,et al. The WD40 Repeats of FANCL Are Required for Fanconi Anemia Core Complex Assembly* , 2006, Journal of Biological Chemistry.