RECQ5 helicase promotes resolution of conflicts between replication and transcription in human cells
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Title
RECQ5 helicase promotes resolution of conflicts between replication and transcription in human cells
Authors
Keywords
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Journal
JOURNAL OF CELL BIOLOGY
Volume 214, Issue 4, Pages 401-415
Publisher
Rockefeller University Press
Online
2016-08-09
DOI
10.1083/jcb.201507099
References
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Note: Only part of the references are listed.- Human RecQ Helicases in DNA Repair, Recombination, and Replication
- (2014) Deborah L. Croteau et al. Annual Review of Biochemistry
- RECQL5 Controls Transcript Elongation and Suppresses Genome Instability Associated with Transcription Stress
- (2014) Marco Saponaro et al. CELL
- RNA polymerase II contributes to preventing transcription-mediated replication fork stalls
- (2014) I. Felipe-Abrio et al. EMBO JOURNAL
- Large transcription units unify copy number variants and common fragile sites arising under replication stress
- (2014) Thomas E. Wilson et al. GENOME RESEARCH
- Strand-Specific Analysis Shows Protein Binding at Replication Forks and PCNA Unloading from Lagging Strands when Forks Stall
- (2014) Chuanhe Yu et al. MOLECULAR CELL
- BRCA1 controls homologous recombination at Tus/Ter-stalled mammalian replication forks
- (2014) Nicholas A. Willis et al. NATURE
- Phenotypic characterization of missense polymerase-δ mutations using an inducible protein-replacement system
- (2014) Medini Manohar Ghodgaonkar et al. Nature Communications
- Identification of Early Replicating Fragile Sites that Contribute to Genome Instability
- (2013) Jacqueline H. Barlow et al. CELL
- Transcription-replication encounters, consequences and genomic instability
- (2013) Anne Helmrich et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Single Cell Analysis of Human RAD18-Dependent DNA Post-Replication Repair by Alkaline Bromodeoxyuridine Comet Assay
- (2013) Mónika Mórocz et al. PLoS One
- A Distinct Replication Fork Protection Pathway Connects Fanconi Anemia Tumor Suppressors to RAD51-BRCA1/2
- (2012) Katharina Schlacher et al. CANCER CELL
- DNA replication through hard-to-replicate sites, including both highly transcribed RNA Pol II and Pol III genes, requires the S. pombe Pfh1 helicase
- (2012) N. Sabouri et al. GENES & DEVELOPMENT
- Increased replication initiation and conflicts with transcription underlie Cyclin E-induced replication stress
- (2012) R M Jones et al. ONCOGENE
- The Set2-RPB1 Interaction Domain of Human RECQ5 Is Important for Transcription-Associated Genome Stability
- (2011) M. Li et al. MOLECULAR AND CELLULAR BIOLOGY
- Collisions between Replication and Transcription Complexes Cause Common Fragile Site Instability at the Longest Human Genes
- (2011) Anne Helmrich et al. MOLECULAR CELL
- dsRNA expression in the mouse elicits RNAi in oocytes and low adenosine deamination in somatic cells
- (2011) Jana Nejepinska et al. NUCLEIC ACIDS RESEARCH
- Physical Interaction of RECQ5 Helicase with RAD51 Facilitates Its Anti-recombinase Activity
- (2010) Sybille Schwendener et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- RECQ5 helicase associates with the C-terminal repeat domain of RNA polymerase II during productive elongation phase of transcription
- (2010) Radhakrishnan Kanagaraj et al. NUCLEIC ACIDS RESEARCH
- The helicases DinG, Rep and UvrD cooperate to promote replication across transcription units in vivo
- (2009) Hasna Boubakri et al. EMBO JOURNAL
- Highly Transcribed RNA Polymerase II Genes Are Impediments to Replication Fork Progression in Saccharomyces cerevisiae
- (2009) Anna Azvolinsky et al. MOLECULAR CELL
- Association of human DNA helicase RecQ5β with RNA polymerase II and its possible role in transcription
- (2008) Keiichi Izumikawa et al. BIOCHEMICAL JOURNAL
- Recognition of forked and single-stranded DNA structures by human RAD18 complexed with RAD6B protein triggers its recruitment to stalled replication forks
- (2008) Yuri Tsuji et al. GENES TO CELLS
- Regulation of proliferating cell nuclear antigen ubiquitination in mammalian cells
- (2008) A. Niimi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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