| scholarly article | Q13442814 |
| P2093 | author name string | M Jasin | |
| R D Johnson | |||
| P2860 | cites work | Cloning of human, mouse and fission yeast recombination genes homologous to RAD51 and recA | Q24312076 |
| XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages | Q24314738 | ||
| Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair gene | Q24317605 | ||
| Sister chromatids are preferred over homologs as substrates for recombinational repair in Saccharomyces cerevisiae | Q24532829 | ||
| Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae | Q24548535 | ||
| XRCC3 promotes homology-directed repair of DNA damage in mammalian cells | Q24597771 | ||
| Recombinational repair of gaps in DNA is asymmetric in Ustilago maydis and can be explained by a migrating D-loop model | Q24605056 | ||
| Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination | Q24647405 | ||
| Meiotic chromosomes: it takes two to tango | Q27930023 | ||
| Homothallic switching of yeast mating type cassettes is initiated by a double-stranded cut in the MAT locus | Q27930817 | ||
| Identification of double Holliday junctions as intermediates in meiotic recombination. | Q54599520 | ||
| Gene conversion between duplicated genetic elements in yeast | Q59062391 | ||
| Sister chromatid exchanges—A sensitive assay of agents damaging human chromosomes | Q67358556 | ||
| Double-strand break repair in yeast requires both leading and lagging strand DNA polymerases | Q27934176 | ||
| Replication fork pausing and recombination or "gimme a break" | Q28142854 | ||
| Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination | Q28145748 | ||
| Yeast recombination: the association between double-strand gap repair and crossing-over | Q28265497 | ||
| The double-strand-break repair model for recombination | Q28267259 | ||
| Brca1 controls homology-directed DNA repair | Q29614844 | ||
| Rad51-deficient vertebrate cells accumulate chromosomal breaks prior to cell death | Q29614845 | ||
| A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53 | Q29618277 | ||
| Targeted disruption of the Rad51 gene leads to lethality in embryonic mice | Q29618278 | ||
| Cell cycle dependent chromosomal movement in pre-mitotic human T-lymphocyte nuclei | Q33204165 | ||
| Recognition and cleavage site of the intron-encoded omega transposase. | Q33640420 | ||
| Analysis of gene targeting and intrachromosomal homologous recombination stimulated by genomic double-strand breaks in mouse embryonic stem cells | Q33774945 | ||
| Replication and recombination intersect | Q33885019 | ||
| Conservative intrachromosomal recombination between inverted repeats in mouse cells: association between reciprocal exchange and gene conversion | Q33954017 | ||
| Yeast intrachromosomal recombination: long gene conversion tracts are preferentially associated with reciprocal exchange and require the RAD1 and RAD3 gene products. | Q33956010 | ||
| Sister chromatid exchanges are mediated by homologous recombination in vertebrate cells | Q33958829 | ||
| Multiple pathways for repair of DNA double-strand breaks in mammalian chromosomes | Q33960694 | ||
| Expansions and contractions in a tandem repeat induced by double-strand break repair | Q33994800 | ||
| Efficient copying of nonhomologous sequences from ectopic sites via P-element-induced gap repair | Q34336201 | ||
| Homologous and non-homologous recombination differentially affect DNA damage repair in mice | Q35008336 | ||
| Double-strand break repair by interchromosomal recombination: suppression of chromosomal translocations | Q35212139 | ||
| Expression of a site-specific endonuclease stimulates homologous recombination in mammalian cells | Q35550686 | ||
| Homology-directed repair is a major double-strand break repair pathway in mammalian cells | Q36065571 | ||
| Loss of heterozygosity induced by a chromosomal double-strand break | Q36546233 | ||
| Loss of constitutional heterozygosity in human cancer. | Q36549893 | ||
| Stable DNA replication: interplay between DNA replication, homologous recombination, and transcription | Q36574251 | ||
| Inducible expression and cytogenetic effects of the EcoRI restriction endonuclease in Chinese hamster ovary cells | Q36846811 | ||
| Interchromosomal recombination is suppressed in mammalian somatic cells | Q37621753 | ||
| Cytological detection of mutagen-carcinogen exposure by sister chromatid exchange | Q39351911 | ||
| Mouse RAD54 affects DNA double-strand break repair and sister chromatid exchange | Q39452644 | ||
| Homologous recombination is required for the viability of rad27 mutants | Q39726024 | ||
| Sister-chromatid cohesion in mitosis and meiosis | Q40613969 | ||
| Direct-repeat analysis of chromatid interactions during intrachromosomal recombination in mouse cells | Q40640907 | ||
| Alu: structure, origin, evolution, significance and function of one-tenth of human DNA. | Q40998369 | ||
| Integration of a vector containing a repetitive LINE-1 element in the human genome | Q41437885 | ||
| Introduction of double-strand breaks into the genome of mouse cells by expression of a rare-cutting endonuclease | Q42832099 | ||
| Targeted gene replacement in Drosophila via P element-induced gap repair. | Q52444406 | ||
| A targeted disruption of the murine Brca1 gene causes gamma-irradiation hypersensitivity and genetic instability. | Q52533204 | ||
| Measurement of sister chromatid exchanges at very low bromodeoxyuridine substitution levels using a monoclonal antibody in Chinese hamster ovary cells. | Q54288277 | ||
| Sister chromatid exchange as an indicator of mutagenesis | Q54587790 | ||
| P433 | issue | 13 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 3398-3407 | |
| P577 | publication date | 2000-07-01 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells | |
| P478 | volume | 19 |
| Q93055030 | "An End to a Means": How DNA-End Structure Shapes the Double-Strand Break Repair Process |
| Q52572400 | 53BP1 contributes to survival of cells irradiated with X-ray during G1 without Ku70 or Artemis. |
| Q91907550 | 53BP1 nuclear bodies enforce replication timing at under-replicated DNA to limit heritable DNA damage |
| Q57068930 | A Lamin-Binding Ligand Inhibits Homologous Recombination Repair of DNA Double-Strand Breaks |
| Q35672227 | A dual role of BRCA1 in two distinct homologous recombination mediated repair in response to replication arrest |
| Q36052291 | A genetic screen for DNA double-strand break repair mutations in Drosophila |
| Q33635645 | A high-throughput chemical screen with FDA approved drugs reveals that the antihypertensive drug Spironolactone impairs cancer cell survival by inhibiting homology directed repair |
| Q97557558 | A high-throughput small molecule screen identifies farrerol as a potentiator of CRISPR/Cas9-mediated genome editing |
| Q36364209 | A new role for Rrm3 in repair of replication-born DNA breakage by sister chromatid recombination |
| Q37024369 | A phase I followed by a randomized phase II trial of two cycles carboplatin-olaparib followed by olaparib monotherapy versus capecitabine in BRCA1- or BRCA2-mutated HER2-negative advanced breast cancer as first line treatment (REVIVAL): study protoc |
| Q37151375 | A single double-strand break system reveals repair dynamics and mechanisms in heterochromatin and euchromatin |
| Q40895699 | A strand invasion 3' polymerization intermediate of mammalian homologous recombination |
| Q24647310 | ATM and Artemis promote homologous recombination of radiation-induced DNA double-strand breaks in G2 |
| Q54326103 | ATR inhibition preferentially targets homologous recombination-deficient tumor cells. |
| Q33606163 | Aberrant double-strand break repair in rad51 mutants of Saccharomyces cerevisiae |
| Q34207156 | Abundant gene conversion between arms of palindromes in human and ape Y chromosomes. |
| Q42259191 | Acute inactivation of the replicative helicase in human cells triggers MCM8-9-dependent DNA synthesis. |
| Q48007327 | Alternative Lengthening of Telomeres Mediated by Mitotic DNA Synthesis Engages Break-Induced Replication Processes |
| Q40724946 | Alternative pathways for the repair of RAG-induced DNA breaks |
| Q21145054 | Alternative-NHEJ is a mechanistically distinct pathway of mammalian chromosome break repair |
| Q39686977 | An xrcc4 defect or Wortmannin stimulates homologous recombination specifically induced by double-strand breaks in mammalian cells. |
| Q48279546 | Arm-specific multicolor fluorescence in situ hybridization reveals widespread chromosomal instability in glioma cell lines |
| Q40007398 | Assaying double-strand break repair pathway choice in mammalian cells using a targeted endonuclease or the RAG recombinase |
| Q92033470 | Assembling nuclear domains: Lessons from DNA repair |
| Q36353114 | Association of Polymorphisms of Phase I Metabolizing Genes with Sister Chromatid Exchanges in Occupational Workers Exposed to Toluene Used in Paint Thinners |
| Q36666191 | Ataxia telangiectasia mutated (ATM) is dispensable for endonuclease I-SceI-induced homologous recombination in mouse embryonic stem cells |
| Q37334605 | BCR-ABL promotes the frequency of mutagenic single-strand annealing DNA repair |
| Q89548686 | BLM has Contrary Effects on Repeat-Mediated Deletions, based on the Distance of DNA DSBs to a Repeat and Repeat Divergence |
| Q37770591 | BRCA1 16 years later: DNA damage-induced BRCA1 shuttling |
| Q34110729 | BRCA1 and BRCA2: breast/ovarian cancer susceptibility gene products and participants in DNA double-strand break repair |
| Q42870831 | BRCA1 and CtIP suppress long-tract gene conversion between sister chromatids |
| Q33986975 | BRCA1 controls homologous recombination at Tus/Ter-stalled mammalian replication forks |
| Q36724941 | BRCA1-Ku80 protein interaction enhances end-joining fidelity of chromosomal double-strand breaks in the G1 phase of the cell cycle |
| Q29618799 | BRCA2 is required for homology-directed repair of chromosomal breaks |
| Q27342280 | BRG1 promotes the repair of DNA double-strand breaks by facilitating the replacement of RPA with RAD51. |
| Q28070584 | Balancing self-renewal against genome preservation in stem cells: How do they manage to have the cake and eat it too? |
| Q37199083 | Bifunctional DNA alkylator 1,3-bis(2-chloroethyl)-1-nitrosourea activates the ATR-Chk1 pathway independently of the mismatch repair pathway |
| Q34658965 | Bloom DNA helicase facilitates homologous recombination between diverged homologous sequences |
| Q99605757 | Canonical and Noncanonical Roles of Fanconi Anemia Proteins: Implications in Cancer Predisposition |
| Q28346450 | Capture of DNA sequences at double-strand breaks in mammalian chromosomes |
| Q33847205 | Cell cycle-dependent induction of homologous recombination by a tightly regulated I-SceI fusion protein |
| Q36447371 | Cellular defects caused by hypomorphic variants of the Bloom syndrome helicase gene BLM. |
| Q24337912 | Cellular localization of human Rad51C and regulation of ubiquitin-mediated proteolysis of Rad51 |
| Q36951670 | Characterization of CHO XPF mutant UV41: influence of XPF heterozygosity on double-strand break-induced intrachromosomal recombination |
| Q81760994 | Characterization of in vivo recombination activities in the mouse embryo |
| Q28205315 | Chromosomal stability and the DNA double-stranded break connection |
| Q90099999 | Chromosome Preference During Homologous Recombination Repair of DNA Double-Strand Breaks in Drosophila melanogaster |
| Q29622881 | Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs |
| Q34282271 | Chromosome instability as a result of double-strand breaks near telomeres in mouse embryonic stem cells |
| Q34373094 | Collaboration of homologous recombination and nonhomologous end-joining factors for the survival and integrity of mice and cells |
| Q37226516 | Comparison of nonhomologous end joining and homologous recombination in human cells. |
| Q36188451 | Complex Breakpoints and Template Switching Associated with Non-canonical Termination of Homologous Recombination in Mammalian Cells. |
| Q40536064 | Conservative homologous recombination preferentially repairs DNA double-strand breaks in the S phase of the cell cycle in human cells |
| Q41549984 | Control of sister chromatid recombination by histone H2AX. |
| Q42738081 | Cooperative roles of vertebrate Fbh1 and Blm DNA helicases in avoidance of crossovers during recombination initiated by replication fork collapse |
| Q39457128 | Coupled homologous and nonhomologous repair of a double-strand break preserves genomic integrity in mammalian cells |
| Q27936900 | Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis |
| Q26861805 | DNA DSB repair pathway choice: an orchestrated handover mechanism |
| Q34405417 | DNA double strand break repair and chromosomal translocation: lessons from animal models |
| Q37063485 | DNA double strand break repair inhibition as a cause of heat radiosensitization: re-evaluation considering backup pathways of NHEJ. |
| Q33350157 | DNA double-strand break repair and the evolution of intron density |
| Q34835417 | DNA double-strand break repair by homologous recombination |
| Q34929930 | DNA double-strand break repair signalling: the case of RAD51 post-translational regulation. |
| Q28204231 | DNA double-strand breaks: signaling, repair and the cancer connection |
| Q33947027 | DNA ligase IV-deficient cells are more resistant to ionizing radiation in the absence of Ku70: Implications for DNA double-strand break repair |
| Q40156883 | DNA polymerase beta overexpression stimulates the Rad51-dependent homologous recombination in mammalian cells |
| Q39687447 | DNA polymerases nu and theta are required for efficient immunoglobulin V gene diversification in chicken |
| Q24644828 | DNA repair by nonhomologous end joining and homologous recombination during cell cycle in human cells |
| Q36429457 | DNA repair protein: endo-exonuclease as a new frontier in cancer therapy |
| Q24630816 | DNA replication meets genetic exchange: chromosomal damage and its repair by homologous recombination |
| Q42238198 | DNA replication origin plasticity and perturbed fork progression in human inverted repeats |
| Q39675323 | DNA substrate dependence of p53-mediated regulation of double-strand break repair |
| Q38685731 | Deciphering the Code of the Cancer Genome: Mechanisms of Chromosome Rearrangement |
| Q53963846 | Deficiency in BRCA2 leads to increase in non-conservative homologous recombination. |
| Q44692120 | Deletion, rearrangement, and gene conversion; genetic consequences of chromosomal double-strand breaks in human cells |
| Q35584259 | Development of a targeted flip-in system in avian DT40 cells |
| Q39087801 | Differences in 53BP1 and BRCA1 regulation between cycling and non-cycling cells |
| Q44696976 | Different DNA-PKcs functions in the repair of radiation-induced and spontaneous DSBs within interstitial telomeric sequences. |
| Q40696390 | Different genetic requirements for repair of replication-born double-strand breaks by sister-chromatid recombination and break-induced replication |
| Q39125635 | Differential regulation of short- and long-tract gene conversion between sister chromatids by Rad51C. |
| Q27933564 | Distinct roles for the RSC and Swi/Snf ATP-dependent chromatin remodelers in DNA double-strand break repair |
| Q35728414 | Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility |
| Q36510700 | Distinct roles of chromatin-associated proteins MDC1 and 53BP1 in mammalian double-strand break repair |
| Q28661754 | Double strand break repair functions of histone H2AX |
| Q38400007 | Double-strand break repair assays determine pathway choice and structure of gene conversion events in Drosophila melanogaster |
| Q35071160 | Double-strand break repair by interchromosomal recombination: an in vivo repair mechanism utilized by multiple somatic tissues in mammals |
| Q34264389 | Double-strand break repair: are Rad51/RecA--DNA joints barriers to DNA replication? |
| Q27934450 | Double-strand breaks arising by replication through a nick are repaired by cohesin-dependent sister-chromatid exchange. |
| Q48587042 | EXO1 suppresses double-strand break induced homologous recombination between diverged sequences in mammalian cells |
| Q35944680 | Early events in the DNA damage response |
| Q64388139 | Effects of different doses of X-ray irradiation on cell apoptosis, cell cycle, DNA damage repair and glycolysis in HeLa cells |
| Q63383467 | Equal Sister Chromatid Exchange Is a Major Mechanism of Double-Strand Break Repair in Yeast |
| Q39022234 | Eukaryotic DNA Polymerases in Homologous Recombination |
| Q30872875 | Evidence for a fast, intrachromosomal conversion mechanism from mapping of nucleotide variants within a homogeneous alpha-satellite DNA array |
| Q48718101 | Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays |
| Q34812078 | Extensive loss of heterozygosity is suppressed during homologous repair of chromosomal breaks |
| Q41628920 | FANCJ helicase controls the balance between short- and long-tract gene conversions between sister chromatids. |
| Q35161876 | Fanconi anemia FANCG protein in mitigating radiation- and enzyme-induced DNA double-strand breaks by homologous recombination in vertebrate cells |
| Q33551464 | Fanconi anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination |
| Q42043478 | Fen-1 facilitates homologous recombination by removing divergent sequences at DNA break ends |
| Q27935172 | Functional and genetic analysis of the Saccharomyces cerevisiae RNC1/TRM2: evidences for its involvement in DNA double-strand break repair |
| Q39787462 | Functional relation among RecQ family helicases RecQL1, RecQL5, and BLM in cell growth and sister chromatid exchange formation |
| Q33761695 | Functional relationships of FANCC to homologous recombination, translesion synthesis, and BLM |
| Q24803093 | Gene conversion and deletion frequencies during double-strand break repair in human cells are controlled by the distance between direct repeats |
| Q40695823 | Gene repeat expansion and contraction by spontaneous intrachromosomal homologous recombination in mammalian cells |
| Q28287955 | Genetic steps of mammalian homologous repair with distinct mutagenic consequences |
| Q47108896 | Genome-wide mapping of sister chromatid exchange events in single yeast cells using Strand-seq |
| Q28649852 | Gradual implementation of the meiotic recombination program via checkpoint pathways controlled by global DSB levels |
| Q60919860 | Guidelines for DNA recombination and repair studies: Cellular assays of DNA repair pathways |
| Q40134125 | HSV-1 amplicon-mediated post-transcriptional inhibition of Rad51 sensitizes human glioma cells to ionizing radiation |
| Q34137518 | Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination |
| Q24307401 | Highlight: BRCA1 and BRCA2 proteins in breast cancer |
| Q33334428 | Highly conserved regimes of neighbor-base-dependent mutation generated the background primary-structural heterogeneities along vertebrate chromosomes |
| Q52596113 | Histone H3 lysine 36 methyltransferase mobilizes NER factors to regulate tolerance against alkylation damage in fission yeast. |
| Q28563892 | Histone H3K56 acetylation, Rad52, and non-DNA repair factors control double-strand break repair choice with the sister chromatid |
| Q34668555 | Holliday junction processing activity of the BLM-Topo IIIalpha-BLAP75 complex |
| Q24793756 | Homologous Recombination and Its Role in Carcinogenesis |
| Q28085364 | Homologous recombination and human health: the roles of BRCA1, BRCA2, and associated proteins |
| Q50802072 | Homologous recombination and non-homologous end-joining repair pathways in bovine embryos with different developmental competence. |
| Q35084078 | Homologous recombination conserves DNA sequence integrity throughout the cell cycle in embryonic stem cells |
| Q40258601 | Homologous recombination is required for AAV-mediated gene targeting |
| Q39364366 | Homologous recombination repairs secondary replication induced DNA double-strand breaks after ionizing radiation. |
| Q47425709 | Homologous recombination-mediated repair of DNA double-strand breaks operates in mammalian mitochondria |
| Q28646561 | Homologous recombinational repair of DNA ensures mammalian chromosome stability |
| Q35026393 | Homologous repair of DNA damage and tumorigenesis: the BRCA connection |
| Q24295050 | Human SMC5/6 complex promotes sister chromatid homologous recombination by recruiting the SMC1/3 cohesin complex to double-strand breaks |
| Q91736932 | Identification Of Natural Compound Derivative For Inhibition Of XLF And Overcoming Chemoresistance In Colorectal Cancer Cells |
| Q24321883 | Identification of functional domains in the RAD51L2 (RAD51C) protein and its requirement for gene conversion |
| Q51617856 | In vitro and in vivo effects of melatonin on sister chromatid exchange in human blood lymphocytes exposed to hypoxia. |
| Q42534610 | Incorporation of large heterologies into heteroduplex DNA during double-strand-break repair in mouse cells |
| Q64389376 | Induction of Chromosomal Translocations with CRISPR-Cas9 and Other Nucleases: Understanding the Repair Mechanisms That Give Rise to Translocations |
| Q35682308 | Induction of chromosomal translocations in mouse and human cells using site-specific endonucleases |
| Q40551414 | Influence of DNA double-strand break rejoining on clonogenic survival and micronucleus yield in human cell lines. |
| Q33945630 | Influence of homologous recombinational repair on cell survival and chromosomal aberration induction during the cell cycle in gamma-irradiated CHO cells |
| Q36003205 | Initiation of DNA double strand break repair: signaling and single-stranded resection dictate the choice between homologous recombination, non-homologous end-joining and alternative end-joining |
| Q35950053 | Interchromosomal crossover in human cells is associated with long gene conversion tracts |
| Q38953062 | Interchromosomal homology searches drive directional ALT telomere movement and synapsis. |
| Q35049371 | Intron evolution in Neurospora: the role of mutational bias and selection |
| Q35748440 | Inviting instability: Transposable elements, double-strand breaks, and the maintenance of genome integrity. |
| Q24793684 | Ku and the Stability of the Genome |
| Q33510904 | Limiting the persistence of a chromosome break diminishes its mutagenic potential |
| Q34134350 | Loss of heterozygosity in somatic cells of the mouse. An important step in cancer initiation? |
| Q37425607 | Mammalian Rif1 contributes to replication stress survival and homology-directed repair |
| Q34311686 | Manipulating the mammalian genome by homologous recombination |
| Q33909967 | Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophy |
| Q34317108 | Mechanisms of double-strand break repair in somatic mammalian cells |
| Q28608973 | Mechanisms of human DNA repair: an update |
| Q33769217 | Mechanisms of recombination between diverged sequences in wild-type and BLM-deficient mouse and human cells |
| Q64098402 | Mechanistic modelling supports entwined rather than exclusively competitive DNA double-strand break repair pathway |
| Q38618828 | Meiotic Recombination: The Essence of Heredity |
| Q28573938 | Meiotic cohesin REC8 marks the axial elements of rat synaptonemal complexes before cohesins SMC1beta and SMC3 |
| Q37034049 | MicroRNA expression and its association with DNA repair in preimplantation embryos |
| Q36209738 | Mismatch repair-dependent processing of methylation damage gives rise to persistent single-stranded gaps in newly replicated DNA. |
| Q28274000 | Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis |
| Q73943675 | Mitotic maneuvers in the light |
| Q42391798 | Molecular analysis of sister chromatid recombination in mammalian cells |
| Q43246216 | Molecular cross-talk among chromosome fragility syndromes |
| Q48148060 | Mosaic Analysis in Drosophila |
| Q34081887 | Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences |
| Q40691380 | Nbs1 is essential for DNA repair by homologous recombination in higher vertebrate cells |
| Q35026390 | Nijmegen breakage syndrome gene, NBS1, and molecular links to factors for genome stability |
| Q28765557 | No slave to sex |
| Q39756406 | Non-homologous end joining as an important mutagenic process in cell cycle-arrested cells |
| Q37334922 | PARP is activated at stalled forks to mediate Mre11-dependent replication restart and recombination. |
| Q27301083 | Pairing of homologous regions in the mouse genome is associated with transcription but not imprinting status |
| Q34500845 | Parp-1 protects homologous recombination from interference by Ku and Ligase IV in vertebrate cells |
| Q28608969 | Pathways of DNA double-strand break repair during the mammalian cell cycle |
| Q33631833 | Pattern of breast cancer susceptibility gene 1 expression is a potential prognostic biomarker in resectable pancreatic ductal adenocarcinoma |
| Q41857124 | Peptide aptamer mimicking RAD51-binding domain of BRCA2 inhibits DNA damage repair and survival in Trypanosoma brucei |
| Q24685242 | Poly(ADP-ribose) polymerase (PARP-1) has a controlling role in homologous recombination |
| Q27933654 | Post-replicative repair involves separase-dependent removal of the kleisin subunit of cohesin |
| Q36302317 | Precise hit: adeno-associated virus in gene targeting |
| Q36824054 | Processing of triplex-directed psoralen DNA interstrand crosslinks by recombination mechanisms |
| Q33948430 | Promiscuous patching of broken chromosomes in mammalian cells with extrachromosomal DNA. |
| Q36387773 | Quantitative live cell imaging reveals a gradual shift between DNA repair mechanisms and a maximal use of HR in mid S phase. |
| Q35856709 | RAD18 and poly(ADP-ribose) polymerase independently suppress the access of nonhomologous end joining to double-strand breaks and facilitate homologous recombination-mediated repair. |
| Q37800769 | RAD51C: a novel cancer susceptibility gene is linked to Fanconi anemia and breast cancer |
| Q92608468 | RAP80 and BRCA1 PARsylation protect chromosome integrity by preventing retention of BRCA1-B/C complexes in DNA repair foci |
| Q34762756 | RAP80-directed tuning of BRCA1 homologous recombination function at ionizing radiation-induced nuclear foci |
| Q36418906 | RING finger nuclear factor RNF168 is important for defects in homologous recombination caused by loss of the breast cancer susceptibility factor BRCA1 |
| Q24338859 | RPA mediates recombination repair during replication stress and is displaced from DNA by checkpoint signalling in human cells |
| Q47264611 | Rad51 overexpression promotes alternative double-strand break repair pathways and genome instability |
| Q30453366 | Rad52 partially substitutes for the Rad51 paralog XRCC3 in maintaining chromosomal integrity in vertebrate cells |
| Q33263102 | Rad52-mediated DNA annealing after Rad51-mediated DNA strand exchange promotes second ssDNA capture |
| Q37062358 | Rapid, Stabilizing Palindrome Rearrangements in Somatic Cells by the Center-Break Mechanism |
| Q34108141 | Recombination at double-strand breaks and DNA ends: conserved mechanisms from phage to humans. |
| Q35132661 | Recombination between two chromosomes: implications for genomic integrity in mammalian cells |
| Q24680716 | Recombinational DNA Repair in Cancer and Normal Cells: The Challenge of Functional Analysis |
| Q28214575 | Recombinational DNA repair and human disease |
| Q34638449 | Reconstitution of recombination-associated DNA synthesis with human proteins. |
| Q24522689 | Recql5 and Blm RecQ DNA helicases have nonredundant roles in suppressing crossovers |
| Q38906341 | Regulation of Single-Strand Annealing and its Role in Genome Maintenance |
| Q35200273 | Regulators of homologous recombination repair as novel targets for cancer treatment. |
| Q28478289 | Repair at single targeted DNA double-strand breaks in pluripotent and differentiated human cells |
| Q48305491 | Repair of Site-Specific DNA Double-Strand Breaks in Barley Occurs via Diverse Pathways Primarily Involving the Sister Chromatid. |
| Q28209896 | Repair of double-strand breaks by homologous recombination in mismatch repair-defective mammalian cells |
| Q90375281 | Repair of multiple simultaneous double-strand breaks causes bursts of genome-wide clustered hypermutation |
| Q37096201 | Repeat expansion by homologous recombination in the mouse germ line at palindromic sequences |
| Q37052095 | Restoration of CAPAN-1 cells with functional BRCA2 provides insight into the DNA repair activity of individuals who are heterozygous for BRCA2 mutations |
| Q39744882 | Rev1 is essential for DNA damage tolerance and non-templated immunoglobulin gene mutation in a vertebrate cell line. |
| Q28508150 | Role for the mammalian Swi5-Sfr1 complex in DNA strand break repair through homologous recombination |
| Q39820516 | Role of Mre11 in chromosomal nonhomologous end joining in mammalian cells |
| Q43771768 | Role of RAD51 in sister-chromatid exchanges in mammalian cells. |
| Q57537928 | Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease |
| Q35113329 | Role of homologous recombination in carcinogenesis. |
| Q24646853 | Roles of RECQ helicases in recombination based DNA repair, genomic stability and aging |
| Q91291846 | Rpd3L and Hda1 histone deacetylases facilitate repair of broken forks by promoting sister chromatid cohesion |
| Q27931613 | SMC1 coordinates DNA double-strand break repair pathways |
| Q24791574 | Screening the yeast genome for new DNA-repair genes |
| Q37012717 | Securin is a target of the UV response pathway in mammalian cells |
| Q37725418 | Sensitizing thermochemotherapy with a PARP1-inhibitor. |
| Q38315392 | Sequence homology and microhomology dominate chromosomal double-strand break repair in African trypanosomes |
| Q55511176 | Shepherding DNA ends: Rif1 protects telomeres and chromosome breaks. |
| Q34285505 | Sirtuin 6 (SIRT6) rescues the decline of homologous recombination repair during replicative senescence |
| Q45883259 | Site-specific DNA double-strand break generated by I-SceI endonuclease enhances ectopic homologous recombination in Pyricularia oryzae |
| Q38615359 | Small molecules enhance CRISPR/Cas9-mediated homology-directed genome editing in primary cells |
| Q37143077 | Spatial separation of replisome arrest sites influences homologous recombination quality at a Tus/Ter-mediated replication fork barrier |
| Q33796363 | Spontaneous DNA breakage in single living Escherichia coli cells |
| Q34175345 | Spontaneous DNA damage, genome instability, and cancer--when DNA replication escapes control. |
| Q53666385 | Spontaneous and gamma-ray-induced sister chromatid exchanges in patients with carcinoma of cervix uteri. |
| Q40390945 | Spontaneous homologous recombination is induced by collapsed replication forks that are caused by endogenous DNA single-strand breaks |
| Q35142782 | Spontaneous mitotic homologous recombination at an enhanced yellow fluorescent protein (EYFP) cDNA direct repeat in transgenic mice |
| Q29618612 | Srs2 and Sgs1-Top3 suppress crossovers during double-strand break repair in yeast |
| Q42534161 | Strand Invasion and DNA Synthesis From the Two 3′ Ends of a Double-Strand Break in Mammalian Cells |
| Q51822845 | Strand invasion involving short tract gene conversion is specifically suppressed in BRCA2-deficient hamster cells. |
| Q33279471 | Stripped-down DNA repair in a highly reduced parasite |
| Q90182031 | Studying DNA Double-Strand Break Repair: An Ever-Growing Toolbox |
| Q39949544 | Suppression of retroviral infection by the RAD52 DNA repair protein |
| Q92286222 | Synaptonemal Complex-Deficient Drosophila melanogaster Females Exhibit Rare DSB Repair Events, Recurrent Copy-Number Variation, and an Increased Rate of de Novo Transposable Element Movement |
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| Q29547237 | The Bloom's syndrome helicase suppresses crossing over during homologous recombination |
| Q24650576 | The Dot1 histone methyltransferase and the Rad9 checkpoint adaptor contribute to cohesin-dependent double-strand break repair by sister chromatid recombination in Saccharomyces cerevisiae |
| Q28254892 | The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells |
| Q26747443 | The Knowns Unknowns: Exploring the Homologous Recombination Repair Pathway in Toxoplasma gondii |
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| Q34619271 | The homologous chromosome is an effective template for the repair of mitotic DNA double-strand breaks in Drosophila |
| Q35132597 | The interplay between nonhomologous end-joining and cell cycle checkpoint factors in development, genomic stability, and tumorigenesis |
| Q36718848 | The involvement of DNA-damage and -repair defects in neurological dysfunction |
| Q33539979 | The involvement of human RECQL4 in DNA double-strand break repair |
| Q34931800 | The many functions of SMC proteins in chromosome dynamics |
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| Q57729646 | XRCC4 in G1 suppresses homologous recombination in S/G2, in G1 checkpoint-defective cells |
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| Q37687078 | gammaH2AX: a sensitive molecular marker of DNA damage and repair |
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