about
Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndromeEpidemiologic trends in head and neck cancer and aids in diagnosisInsights into Fanconi Anaemia from the structure of human FANCEFANCI protein binds to DNA and interacts with FANCD2 to recognize branched structuresCellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insightsMolecular profiles of hereditary epithelial ovarian cancers and their implications for the biology of this disease.FANCJ helicase uniquely senses oxidative base damage in either strand of duplex DNA and is stimulated by replication protein A to unwind the damaged DNA substrate in a strand-specific manner.FANCJ (BACH1) helicase forms DNA damage inducible foci with replication protein A and interacts physically and functionally with the single-stranded DNA-binding protein.Bcr/Abl interferes with the Fanconi anemia/BRCA pathway: implications in the chromosomal instability of chronic myeloid leukemia cells.Tumour regression and ERCC1 nuclear protein expression predict clinical outcome in patients with gastro-oesophageal cancer treated with neoadjuvant chemotherapy.The Fanconi anemia protein, FANCG, binds to the ERCC1-XPF endonuclease via its tetratricopeptide repeats and the central domain of ERCC1.Cancer stem cells are enriched in Fanconi anemia head and neck squamous cell carcinomasThe Fanconi anemia pathway and ICL repair: implications for cancer therapy.Damage-dependent regulation of MUS81-EME1 by Fanconi anemia complementation group A protein.Human Fanconi anemia complementation group a protein stimulates the 5' flap endonuclease activity of FEN1.Development of primary early-onset colorectal cancers due to biallelic mutations of the FANCD1/BRCA2 geneProgrammable bio-nanochip-based cytologic testing of oral potentially malignant disorders in Fanconi anemia.Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype.Clinical and molecular characteristics of squamous cell carcinomas from Fanconi anemia patients.Postoperative clinical radiosensitivity in patients with fanconi anemia and head and neck squamous cell carcinoma.A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba MennonitesDiagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger SequencingDOG-1 is the Caenorhabditis elegans BRIP1/FANCJ homologue and functions in interstrand cross-link repairInvestigation of FANCA gene in Fanconi anaemia patients in Iran.Overnight transduction with foamyviral vectors restores the long-term repopulating activity of Fancc-/- stem cells.Contributions of DNA interstrand cross-links to aging of cells and organisms.A recurrent truncating germline mutation in the BRIP1/FANCJ gene and susceptibility to prostate cancer.FANCJ uses its motor ATPase to destabilize protein-DNA complexes, unwind triplexes, and inhibit RAD51 strand exchange.Welcome the family of FANCJ-like helicases to the block of genome stability maintenance proteins.RAD51D- and FANCG-dependent base substitution mutagenesis at the ATP1A1 locus in mammalian cells.FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA.Recent insights into the molecular mechanisms involved in aging and the malignant transformation of adult stem/progenitor cells and their therapeutic implications.Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.FANCJ helicase operates in the Fanconi Anemia DNA repair pathway and the response to replicational stress.Stress and DNA repair biology of the Fanconi anemia pathwayA ChIP-chip approach reveals a novel role for transcription factor IRF1 in the DNA damage response.Cytoprotective effect of honey against chromosomal breakage in fanconi anemia patients in vitro.Identification of Tat-SF1 cellular targets by exon array analysis reveals dual roles in transcription and splicing.Genetic inactivation of the Fanconi anemia gene FANCC identified in the hepatocellular carcinoma cell line HuH-7 confers sensitivity towards DNA-interstrand crosslinking agents.A strategy for molecular diagnostics of Fanconi anemia in Brazilian patients.
P2860
Q24337192-F6462F3C-CB81-4EC8-9F71-4B5AFB648C74Q26852167-0196F111-C128-4CC9-9A3C-4320EB896F1CQ27643858-96697C7C-C3A7-480B-9B4B-0B1577AA9F1DQ28250124-2A6757A6-0370-4228-8D4C-6CC10998D2F3Q28252640-8AF59650-2010-4746-B311-FC1C5FD8F9B6Q30448232-EF156E3C-B175-48D2-B3FE-D3C8BAF0869FQ30863349-AAEC384E-A2A6-4ADC-A7B6-784D367EB51BQ33289084-DBB2BEEE-AA14-45B5-8E1A-0E62B79D910DQ33784347-3A35BCA4-50A2-4C41-9938-0037FB4D4EBCQ33903723-413D28CB-E4C3-40D2-92B1-E8EA32C18E76Q34000660-1DCC49F5-C5DA-4627-8C24-F63AA47F3569Q34432871-DEF67776-A187-4293-BCFF-F80454FD1F35Q35024542-AB6569A5-A744-47BF-BA8A-19A097CE60A1Q35028557-0C43DB22-754A-4CBF-AF6A-9F8C3AB743D5Q35070427-599BEE57-4FE4-4657-A489-853EC5C20AB2Q35150486-923E8F88-FCAA-4B0D-9D0B-B7B11388DE23Q35688626-1B2E40A2-E984-46F3-B710-71B15DF0A367Q35752656-40D457DA-1B07-4FE7-8026-EBFB23266F41Q35821098-B6E17E15-56BE-4002-9801-90A8EBF3199CQ35932551-04E6F0D1-7D75-4B0C-A95F-E3680CDD28DFQ36023433-823E7684-11F9-4CDC-88B4-A79B6AEA222FQ36072260-FE5A5DCE-A1FA-4252-B7E2-5BD0989AE1D6Q36483479-8A6D9820-2AF4-420B-9B48-262E27B2CB3BQ36876769-98064466-9A1D-4A95-9E5E-1DB14CD9533EQ37001945-B62D589F-36D0-4DFC-AA3F-2DB2763DF78AQ37033646-A9CF933A-4B6D-44AD-AD27-C6FF2FA9E89AQ37081107-472DCA07-AFB9-4EED-8E94-1B551CF198B6Q37134364-8546BD8D-06DE-4173-97D4-66BE9C0E447DQ37144651-B81D89C8-7E81-42E0-80F1-1A2AFC39400DQ37218373-D01C84DF-79D3-4B67-AE5E-E0EBE70642BBQ37271577-0F0CEDF4-657A-4520-B23D-5E50A80D7E79Q37310063-2DEFE5EE-F0E8-4178-804E-BDA2F8A32766Q37384036-0B421986-4374-43B1-BE1F-9C3F6244211BQ37391123-63DC8355-659F-46E6-A2ED-8389E7644D90Q38252562-6B38074C-ED7A-4D37-85AF-40EE7A05C059Q38357627-3AE22C07-04D1-4517-A945-CD72D6438AACQ39047849-629551DF-8C2E-4F42-A60D-30391675ADD3Q39600021-33868E06-FA0E-4080-BA28-B91C5E9C9D7CQ39699084-C6B65E27-346A-4331-8F40-FF4C9B106B96Q41023824-EA0086D5-6844-4027-90B9-581F810A8681
P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
The Fanconi anemia pathway of genomic maintenance.
@en
The Fanconi anemia pathway of genomic maintenance.
@nl
type
label
The Fanconi anemia pathway of genomic maintenance.
@en
The Fanconi anemia pathway of genomic maintenance.
@nl
prefLabel
The Fanconi anemia pathway of genomic maintenance.
@en
The Fanconi anemia pathway of genomic maintenance.
@nl
P2093
P921
P356
P1433
P1476
The Fanconi anemia pathway of genomic maintenance
@en
P2093
Hans Joenje
Johan P de Winter
Marieke Levitus
P356
10.1155/2006/974975
P577
2006-01-01T00:00:00Z