Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes
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Title
Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes
Authors
Keywords
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Journal
BLOOD
Volume 116, Issue 19, Pages 3780-3791
Publisher
American Society of Hematology
Online
2010-07-17
DOI
10.1182/blood-2009-11-256016
References
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Related references
Note: Only part of the references are listed.- How the Fanconi Anemia Pathway Guards the Genome
- (2009) George-Lucian Moldovan et al. Annual Review of Genetics
- Processive and Unidirectional Translocation of Monomeric UvsW Helicase on Single-Stranded DNA†
- (2009) Scott W. Nelson et al. BIOCHEMISTRY
- 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
- (2009) Avvaru N. Suhasini et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- FANCJ Uses Its Motor ATPase to Destabilize Protein-DNA Complexes, Unwind Triplexes, and Inhibit RAD51 Strand Exchange
- (2009) Joshua A. Sommers et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Single-Molecule Analysis Reveals Differential Effect of ssDNA-Binding Proteins on DNA Translocation by XPD Helicase
- (2009) Masayoshi Honda et al. MOLECULAR CELL
- FANCM–FAAP24 and FANCJ: FA proteins that metabolize DNA
- (2009) Abdullah Mahmood Ali et al. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
- Fanconi anemia and its diagnosis
- (2009) Arleen D. Auerbach MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
- Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives
- (2008) A-Yong Cao et al. BREAST CANCER RESEARCH AND TREATMENT
- Structure of the DNA Repair Helicase XPD
- (2008) Huanting Liu et al. CELL
- XPD Helicase Structures and Activities: Insights into the Cancer and Aging Phenotypes from XPD Mutations
- (2008) Li Fan et al. CELL
- A Novel Breast Cancer-Associated BRIP1 (FANCJ/BACH1) Germ-line Mutation Impairs Protein Stability and Function
- (2008) A. De Nicolo et al. CLINICAL CANCER RESEARCH
- FANCJ Is a Structure-specific DNA Helicase Associated with the Maintenance of Genomic G/C Tracts
- (2008) Timothy B. C. London et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Redox Control of the DNA Damage-inducible Protein DinG Helicase Activity via Its Iron-Sulfur Cluster
- (2008) Binbin Ren et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- FANCJ Helicase Defective in Fanconia Anemia and Breast Cancer Unwinds G-Quadruplex DNA To Defend Genomic Stability
- (2008) Y. Wu et al. MOLECULAR AND CELLULAR BIOLOGY
- Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD
- (2008) Stefanie C Wolski et al. PLOS BIOLOGY
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