scholarly article | Q13442814 |
P50 | author | Reuben S Harris | Q88421845 |
P2093 | author name string | Lei Li | |
P J Hastings | |||
Susan M Rosenberg | |||
Christophe Herman | |||
Jennifer A Halliday | |||
Marcos Hernandez | |||
David Bates | |||
Ryan L Frisch | |||
Kyle M Miller | |||
Elizabeth M Luengas | |||
Chandan Shee | |||
Janet L Gibson | |||
Li-Ya Chiu | |||
David Magnan | |||
Mohan C Joshi | |||
Franklin Gu | |||
Ben D Cox | |||
Huong G Do | |||
Ralf Bernd Nehring | |||
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Mutational processes molding the genomes of 21 breast cancers | Q24620915 | ||
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Megabase chromatin domains involved in DNA double-strand breaks in vivo | Q24680284 | ||
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
Ku80: product of the XRCC5 gene and its role in DNA repair and V(D)J recombination | Q28115740 | ||
Stochastic gene expression in a single cell | Q28131784 | ||
Genomic instability--an evolving hallmark of cancer | Q28274009 | ||
Visualization of DNA double-strand break repair in live bacteria reveals dynamic recruitment of Bacillus subtilis RecF, RecO and RecN proteins to distinct sites on the nucleoids | Q28488848 | ||
Interaction of Ku protein and DNA-dependent protein kinase catalytic subunit with nucleic acids | Q28608946 | ||
Nuclear foci of mammalian recombination proteins are located at single-stranded DNA regions formed after DNA damage | Q28610023 | ||
53BP1 is a reader of the DNA-damage-induced H2A Lys 15 ubiquitin mark | Q29465773 | ||
The importance of repairing stalled replication forks | Q29614220 | ||
Double-strand break end resection and repair pathway choice | Q29614422 | ||
Dynamic changes of BRCA1 subnuclear location and phosphorylation state are initiated by DNA damage | Q29619360 | ||
Nuclear foci of mammalian Rad51 recombination protein in somatic cells after DNA damage and its localization in synaptonemal complexes | Q29620257 | ||
Bleomycin: new perspectives on the mechanism of action | Q30304641 | ||
Independent segregation of the two arms of the Escherichia coli ori region requires neither RNA synthesis nor MreB dynamics. | Q30497367 | ||
APOBEC3B and AID have similar nuclear import mechanisms | Q30514846 | ||
A microhomology-mediated break-induced replication model for the origin of human copy number variation | Q33404060 | ||
Spontaneous DNA breakage in single living Escherichia coli cells | Q33796363 | ||
DNA double-strand breaks caused by replication arrest | Q33886030 | ||
Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
DNA synthesis errors associated with double-strand-break repair | Q33965497 | ||
DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis | Q34340260 | ||
Evidence for APOBEC3B mutagenesis in multiple human cancers | Q34357412 | ||
Heterogeneity in radiation-induced DNA damage and repair in tumor and normal cells measured using the "comet" assay | Q34498804 | ||
Chromosomal Lesion Suppression and Removal in Escherichia coli via Linear DNA Degradation | Q34617452 | ||
Replication stress induces 53BP1-containing OPT domains in G1 cells | Q34854577 | ||
A new method for high-resolution imaging of Ku foci to decipher mechanisms of DNA double-strand break repair | Q34880219 | ||
APOBEC3A can activate the DNA damage response and cause cell-cycle arrest | Q34953340 | ||
Characteristics of Some Multiply Recombination-Deficient Strains of Escherichia coli | Q35157370 | ||
Analysis of the mechanism of interaction of simian Ku protein with DNA | Q35788212 | ||
Clustered mutations in yeast and in human cancers can arise from damaged long single-strand DNA regions. | Q35992079 | ||
Methylcytosine and normal cytosine deamination by the foreign DNA restriction enzyme APOBEC3A | Q36298528 | ||
Replication-transcription conflicts in bacteria. | Q36307709 | ||
Stress-induced mutation via DNA breaks in Escherichia coli: a molecular mechanism with implications for evolution and medicine | Q36496909 | ||
Two mechanisms produce mutation hotspots at DNA breaks in Escherichia coli | Q36713351 | ||
Enzymatic production of deoxyribonucleic acid double-strand breaks after ultraviolet irradiation of Escherichia coli K-12 | Q36762196 | ||
Regulation of DNA repair in hypoxic cancer cells | Q36784378 | ||
Protein-DNA complexes are the primary sources of replication fork pausing in Escherichia coli | Q36820130 | ||
DNA deamination in immunity: AID in the context of its APOBEC relatives. | Q36845658 | ||
Endogenous oxidative stress produces diversity and adaptability in biofilm communities | Q36858633 | ||
R-loops and nicks initiate DNA breakage and genome instability in non-growing Escherichia coli | Q37025967 | ||
Single-strand interruptions in replicating chromosomes cause double-strand breaks | Q37093293 | ||
Multiple Ku orthologues mediate DNA non-homologous end-joining in the free-living form and during chronic infection of Sinorhizobium meliloti | Q37405906 | ||
APOBEC3B is an enzymatic source of mutation in breast cancer. | Q37533713 | ||
More than just a focus: The chromatin response to DNA damage and its role in genome integrity maintenance | Q37942059 | ||
Chromosome translocation, B cell lymphoma, and activation-induced cytidine deaminase | Q38043045 | ||
Replication independent DNA double-strand break retention may prevent genomic instability | Q38345239 | ||
Repair of DNA damage induced by bile salts in Salmonella enterica | Q38583344 | ||
APOBEC3B can impair genomic stability by inducing base substitutions in genomic DNA in human cells. | Q39245074 | ||
Chaperone coexpression plasmids: differential and synergistic roles of DnaK-DnaJ-GrpE and GroEL-GroES in assisting folding of an allergen of Japanese cedar pollen, Cryj2, in Escherichia coli | Q39560568 | ||
53BP1 nuclear bodies form around DNA lesions generated by mitotic transmission of chromosomes under replication stress | Q39593027 | ||
Partial purification and properties of an exonuclease inhibitor induced by bacteriophage Mu-1 | Q39814585 | ||
The loss of gammaH2AX signal is a marker of DNA double strand breaks repair only at low levels of DNA damage | Q40276148 | ||
Quantitative analysis reveals asynchronous and more than DSB-associated histone H2AX phosphorylation after exposure to ionizing radiation. | Q40313015 | ||
Purification of the gam gene-product of bacteriophage Mu and determination of the nucleotide sequence of the gam gene | Q40418427 | ||
The Gam protein of bacteriophage Mu is an orthologue of eukaryotic Ku. | Q40663299 | ||
Sensitization ofEscherichia ColiC to Gamma-radiation by 5-bromouracil Incorporation | Q40829031 | ||
Evidence that the normal route of replication-allowed Red-mediated recombination involves double-chain ends. | Q41351456 | ||
Tumor suppressor p53 binding protein 1 (53BP1) is involved in DNA damage-signaling pathways | Q41861185 | ||
Standard fluorescent imaging of live cells is highly genotoxic | Q42147180 | ||
Localization and dynamic relocalization of mammalian Rad52 during the cell cycle and in response to DNA damage | Q42611090 | ||
Purification of overexpressed gam gene protein from bacteriophage Mu by denaturation-renaturation techniques and a study of its DNA-binding properties | Q42794852 | ||
Identity and function of a large gene network underlying mutagenic repair of DNA breaks | Q42969505 | ||
The TGV transgenic vectors for single-copy gene expression from the Escherichia coli chromosome | Q43694249 | ||
Patterns of chromosomal fragmentation due to uracil-DNA incorporation reveal a novel mechanism of replication-dependent double-stranded breaks | Q46724332 | ||
Localization of RecA in Escherichia coli K-12 using RecA-GFP. | Q50758956 | ||
Binding of Ku protein to DNA. Measurement of affinity for ends and demonstration of binding to nicks. | Q52545931 | ||
Localization of the gam gene of bacteriophage mu and characterisation of the gene product. | Q54438547 | ||
A switch from high-fidelity to error-prone DNA double-strand break repair underlies stress-induced mutation. | Q54478818 | ||
Adaptive mutation by deletions in small mononucleotide repeats. | Q54630365 | ||
Recombination in adaptive mutation. | Q54635736 | ||
A modified neutral comet assay: elimination of lysis at high temperature and validation of the assay with anti-single-stranded DNA antibody. | Q55035907 | ||
Accumulation of Ku70 at DNA double-strand breaks in living epithelial cells | Q64386695 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e01222 | |
P577 | publication date | 2013-10-29 | |
P1433 | published in | eLife | Q2000008 |
P1476 | title | Engineered proteins detect spontaneous DNA breakage in human and bacterial cells | |
P478 | volume | 2 |
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Q36123927 | An APOBEC3A hypermutation signature is distinguishable from the signature of background mutagenesis by APOBEC3B in human cancers |
Q35844586 | An ultra-dense library resource for rapid deconvolution of mutations that cause phenotypes in Escherichia coli. |
Q64388197 | Bacteria-to-Human Protein Networks Reveal Origins of Endogenous DNA Damage |
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Q36289433 | Bactericidal Antibiotics Induce Toxic Metabolic Perturbations that Lead to Cellular Damage |
Q42124332 | Biased Gene Conversion in Rhizobium etli Is Caused by Preferential Double-Strand Breaks on One of the Recombining Homologs. |
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Q38692105 | CRISPR-Cas adaptation: insights into the mechanism of action |
Q27316519 | Chromothripsis from DNA damage in micronuclei. |
Q38883743 | Consequences of Cas9 cleavage in the chromosome of Escherichia coli |
Q39210590 | DNA Replication in Mycobacterium tuberculosis |
Q38379038 | DNA damage foci: Meaning and significance. |
Q64388893 | Fluorescent fusions of the N protein of phage Mu label DNA damage in living cells |
Q35268535 | Functions that protect Escherichia coli from DNA-protein crosslinks |
Q60919860 | Guidelines for DNA recombination and repair studies: Cellular assays of DNA repair pathways |
Q37574376 | Holliday junction trap shows how cells use recombination and a junction-guardian role of RecQ helicase |
Q41562658 | Improved base excision repair inhibition and bacteriophage Mu Gam protein yields C:G-to-T:A base editors with higher efficiency and product purity. |
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Q35913829 | Interactions and Localization of Escherichia coli Error-Prone DNA Polymerase IV after DNA Damage |
Q36606214 | Ionizing radiation-induced DNA injury and damage detection in patients with breast cancer |
Q55604192 | Iron chelation increases the tolerance of Escherichia coli to hyper-replication stress. |
Q40668340 | Live cell imaging of SOS and prophage dynamics in isogenic bacterial populations |
Q28593605 | Mammalian polymerase θ promotes alternative NHEJ and suppresses recombination |
Q89825438 | Methodologies for detecting environmentally induced DNA damage and repair |
Q35657323 | MioC and GidA proteins promote cell division in E. coli |
Q28088790 | Molecular mechanism and clinical impact of APOBEC3B-catalyzed mutagenesis in breast cancer |
Q36013147 | Mutation Processes in 293-Based Clones Overexpressing the DNA Cytosine Deaminase APOBEC3B. |
Q35113119 | Nucleosome acidic patch promotes RNF168- and RING1B/BMI1-dependent H2AX and H2A ubiquitination and DNA damage signaling. |
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Q47673536 | Phenotypes of dnaXE145A Mutant Cells Indicate that the Escherichia coli Clamp Loader Has a Role in the Restart of Stalled Replication Forks. |
Q39510912 | Profiling DNA damage response following mitotic perturbations |
Q41928270 | Proteins pinpoint double strand breaks |
Q35912619 | Rapid pairing and resegregation of distant homologous loci enables double-strand break repair in bacteria. |
Q35952270 | Repair of transposable phage Mu DNA insertions begins only when the E. coli replisome collides with the transpososome |
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