review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0168-9525(00)02022-9 |
P698 | PubMed publication ID | 10827453 |
P50 | author | James E. Haber | Q37373309 |
P2093 | author name string | Haber JE | |
P2860 | cites work | Mre11 and Ku70 interact in somatic cells, but are differentially expressed in early meiosis | Q22010601 |
Cell cycle and genetic requirements of two pathways of nonhomologous end-joining repair of double-strand breaks in Saccharomyces cerevisiae | Q24649768 | ||
Double-strand break repair in yeast requires both leading and lagging strand DNA polymerases | Q27934176 | ||
Interhomolog bias during meiotic recombination: meiotic functions promote a highly differentiated interhomolog-only pathway | Q27936249 | ||
The double-strand-break repair model for recombination | Q28267259 | ||
Meiotic chromosomes: integrating structure and function | Q29618524 | ||
The Saccharomyces cerevisiae RAD9 checkpoint reduces the DNA damage-associated stimulation of directed translocations | Q33771893 | ||
Role of yeast SIR genes and mating type in directing DNA double-strand breaks to homologous and non-homologous repair paths. | Q33869149 | ||
Somatic pairing of homologs in budding yeast: existence and modulation | Q35199470 | ||
Collisions between yeast chromosomal loci in vivo are governed by three layers of organization | Q35201786 | ||
Double-strand break repair by interchromosomal recombination: suppression of chromosomal translocations | Q35212139 | ||
Lack of chromosome territoriality in yeast: promiscuous rejoining of broken chromosome ends. | Q35938806 | ||
Homology-directed repair is a major double-strand break repair pathway in mammalian cells | Q36065571 | ||
Rearrangements of highly polymorphic regions near telomeres of Saccharomyces cerevisiae | Q36950194 | ||
DNA length dependence of the single-strand annealing pathway and the role of Saccharomyces cerevisiae RAD59 in double-strand break repair | Q39454427 | ||
Homology search and choice of homologous partner during mitotic recombination | Q39551436 | ||
The role of Schizosaccharomyces pombe Rad32, the Mre11 homologue, and other DNA damage response proteins in non-homologous end joining and telomere length maintenance | Q39728221 | ||
Two alternative pathways of double-strand break repair that are kinetically separable and independently modulated | Q40678286 | ||
Mre11 is essential for the maintenance of chromosomal DNA in vertebrate cells | Q40914610 | ||
Binding of double-strand breaks in DNA by human Rad52 protein | Q40956601 | ||
Gross chromosomal rearrangements in Saccharomyces cerevisiae replication and recombination defective mutants | Q41688249 | ||
Sister chromatid-based DNA repair is mediated by RAD54, not by DMC1 or TID1. | Q41951646 | ||
Expression of Saccharomyces cerevisiae MATa and MAT alpha enhances the HO endonuclease-stimulation of chromosomal rearrangements directed by his3 recombinational substrates. | Q54104293 | ||
Yeast cell-type regulation of DNA repair | Q57579918 | ||
A meiotic recombination checkpoint controlled by mitotic checkpoint genes | Q59098626 | ||
Chromosome pairing via multiple interstitial interactions before and during meiosis in yeast | Q72034931 | ||
Factors affecting ectopic gene conversion in mice | Q74450777 | ||
The many interfaces of Mre11 | Q77654630 | ||
P433 | issue | 6 | |
P921 | main subject | double-strand break repair via nonhomologous end joining | Q14911701 |
P304 | page(s) | 259-264 | |
P577 | publication date | 2000-06-01 | |
P1433 | published in | Trends in Genetics | Q2451468 |
P1476 | title | Partners and pathwaysrepairing a double-strand break | |
P478 | volume | 16 |
Q30426240 | A 21(st) Century View of Evolution |
Q42653271 | A Saccharomyces servazzii clone homologous to Saccharomyces cerevisiae chromosome III spanning KAR4, ARS 304 and SPB1 lacks the recombination enhancer but contains an unknown ORF. |
Q39687331 | A chromosomal position effect on gene targeting in human cells |
Q33739397 | A common copy-number breakpoint of ERBB2 amplification in breast cancer colocalizes with a complex block of segmental duplications |
Q34684278 | A miR-590/Acvr2a/Rad51b axis regulates DNA damage repair during mESC proliferation |
Q54026229 | A new hyperrecombinogenic mutant of Nicotiana tabacum. |
Q34573320 | A role for DNA mismatch repair protein Msh2 in error-prone double-strand-break repair in mammalian chromosomes |
Q34433751 | A role for cell-cycle-regulated histone H3 lysine 56 acetylation in the DNA damage response. |
Q53715599 | A single mutated BRCA1 allele leads to impaired fidelity of double strand break end-joining. |
Q34408074 | A tale of two HSV-1 helicases: roles of phage and animal virus helicases in DNA replication and recombination |
Q27931070 | A yeast gene, MGS1, encoding a DNA-dependent AAA(+) ATPase is required to maintain genome stability. |
Q34425440 | ATM, a central controller of cellular responses to DNA damage. |
Q28201456 | ATM: genome stability, neuronal development, and cancer cross paths |
Q35132648 | ATM: sounding the double-strand break alarm |
Q27932718 | ATR homolog Mec1 controls association of DNA polymerase zeta-Rev1 complex with regions near a double-strand break |
Q34775987 | Accumulation of nuclear DNA damage or neuron loss: molecular basis for a new approach to understanding selective neuronal vulnerability in neurodegenerative diseases |
Q42793585 | Activation of protein kinase Tel1 through recognition of protein-bound DNA ends |
Q34661313 | Adaptive mutation in Saccharomyces cerevisiae |
Q40531809 | Adenoviral-mediated mda-7 expression suppresses DNA repair capacity and radiosensitizes non-small-cell lung cancer cells |
Q64388679 | Allele-specific genome editing using CRISPR-Cas9 is associated with loss of heterozygosity in diploid yeast |
Q51840243 | Arabidopsis RAD51C gene is important for homologous recombination in meiosis and mitosis. |
Q40137186 | Arsenite-induced alterations in Ku70-deficient cells: a model to study genotoxic effects |
Q35830418 | Artemis sheds new light on V(D)J recombination |
Q33945446 | Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency. |
Q36617706 | Ataxia-telangiectasia and related diseases |
Q27919629 | Autophosphorylation of the DNA-dependent protein kinase catalytic subunit is required for rejoining of DNA double-strand breaks |
Q34775325 | BLM helicase-dependent transport of p53 to sites of stalled DNA replication forks modulates homologous recombination |
Q33247050 | Bacillus subtilis SbcC protein plays an important role in DNA inter-strand cross-link repair |
Q54607960 | Biologic activity of a dinuclear Pd(II)-spermine complex toward human breast cancer. |
Q64951143 | Biological Rationale for Targeting MEK/ERK Pathways in Anti-Cancer Therapy and to Potentiate Tumour Responses to Radiation. |
Q24602472 | C. elegans mre-11 is required for meiotic recombination and DNA repair but is dispensable for the meiotic G(2) DNA damage checkpoint |
Q37612335 | CASCADE, a platform for controlled gene amplification for high, tunable and selection-free gene expression in yeast |
Q53922549 | CEN plasmid segregation is destabilized by tethered determinants of Ty 5 integration specificity: a role for double-strand breaks in CEN antagonism. |
Q89873570 | CRISPR/Cas9-mediated genome editing: From basic research to translational medicine |
Q45959772 | CRISPRi repression of nonhomologous end-joining for enhanced genome engineering via homologous recombination in Yarrowia lipolytica. |
Q35018750 | CTG repeat instability and size variation timing in DNA repair-deficient mice |
Q28346450 | Capture of DNA sequences at double-strand breaks in mammalian chromosomes |
Q40464510 | Cell cycle dependence of DNA-dependent protein kinase phosphorylation in response to DNA double strand breaks. |
Q39368114 | Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy |
Q35114513 | Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes |
Q28481640 | Characterization of Rad51 from apicomplexan parasite Toxoplasma gondii: an implication for inefficient gene targeting |
Q36550882 | Chromatin modifications and the DNA damage response to ionizing radiation. |
Q37128128 | Chromatin remodeling finds its place in the DNA double-strand break response |
Q34607379 | Chromatin remodelling beyond transcription: the INO80 and SWR1 complexes. |
Q33299578 | Chromatin structure regulates gene conversion |
Q34727255 | Chromosomal aberrations: formation, identification and distribution |
Q33798999 | Combination Platinum-based and DNA Damage Response-targeting Cancer Therapy: Evolution and Future Directions |
Q37226516 | Comparison of nonhomologous end joining and homologous recombination in human cells. |
Q44290667 | Coordinated assembly of Ku and p460 subunits of the DNA-dependent protein kinase on DNA ends is necessary for XRCC4-ligase IV recruitment. |
Q38293573 | DNA cleavage and binding selectivity of a heterodinuclear Pt-Cu(3-Clip-Phen) complex |
Q33350157 | DNA double-strand break repair and the evolution of intron density |
Q34525927 | DNA double-strand break repair from head to tail |
Q28204231 | DNA double-strand breaks: signaling, repair and the cancer connection |
Q39088209 | DNA repair and mutations during quiescence in yeast |
Q24644828 | DNA repair by nonhomologous end joining and homologous recombination during cell cycle in human cells |
Q37122448 | DNA repair in murine embryonic stem cells and differentiated cells |
Q36605661 | DNA repair inhibitors in cancer treatment. |
Q36429457 | DNA repair protein: endo-exonuclease as a new frontier in cancer therapy |
Q54995058 | DNA strand-exchange patterns associated with double-strand break-induced and spontaneous mitotic crossovers in Saccharomyces cerevisiae. |
Q39675323 | DNA substrate dependence of p53-mediated regulation of double-strand break repair |
Q28751993 | DNA transposons: nature and applications in genomics |
Q34020119 | DNA-dependent protein kinase suppresses double-strand break-induced and spontaneous homologous recombination |
Q39977573 | DNA-ligase IV and DNA-protein kinase play a critical role in deficient caspases activation in apoptosis-resistant cancer cells by using doxorubicin |
Q35037441 | Defending genome integrity during S-phase: putative roles for RecQ helicases and topoisomerase III. |
Q33991135 | Deinococcus radiodurans - the consummate survivor |
Q44692120 | Deletion, rearrangement, and gene conversion; genetic consequences of chromosomal double-strand breaks in human cells |
Q39859032 | Dependence of DNA double strand break repair pathways on cell cycle phase in human lymphoblastoid cells |
Q39808916 | Development of a rapid, small-scale DNA repair assay for use on clinical samples |
Q34253229 | Development of serous ovarian cancer is associated with the expression of homologous recombination pathway proteins |
Q39688137 | Displacement of DNA-PKcs from DNA ends by the Werner syndrome protein |
Q44548807 | Distinct pathways of nonhomologous end joining that are differentially regulated by DNA-dependent protein kinase-mediated phosphorylation |
Q64388934 | Diverse patterns of the tandem repeats organization in rye chromosomes |
Q35844894 | Diverse roles for histone H2A modifications in DNA damage response pathways in yeast |
Q34062921 | Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans |
Q36478227 | Double-stranded DNA breaks and gene functions in recombination and meiosis |
Q35507009 | Drosophila MUS312 interacts with the nucleotide excision repair endonuclease MEI-9 to generate meiotic crossovers |
Q42914548 | Dynamic formation of RecA filaments at DNA double strand break repair centers in live cells |
Q35837921 | Effect of ATM and HDAC Inhibition on Etoposide-Induced DNA Damage in Porcine Early Preimplantation Embryos |
Q90221474 | Efficient Single-Gene and Gene Family Editing in the Apicomplexan Parasite Eimeria tenella Using CRISPR-Cas9 |
Q37158752 | Efficient gene replacements in Toxoplasma gondii strains deficient for nonhomologous end joining |
Q39365200 | Engineering biological systems using automated biofoundries |
Q28768697 | Evidence for multiple cycles of strand invasion during repair of double-strand gaps in Drosophila |
Q90292067 | Exonuclease 1 (Exo1) Participates in Mammalian Non-Homologous End Joining and Contributes to Drug Resistance in Ovarian Cancer |
Q39663255 | Expression of DNA repair and apoptosis genes in mitochondrial mutant and normal cells following exposure to ionizing radiation |
Q48718101 | Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays |
Q42043478 | Fen-1 facilitates homologous recombination by removing divergent sequences at DNA break ends |
Q36247908 | Fission yeast Rhp51 is required for the maintenance of telomere structure in the absence of the Ku heterodimer |
Q36579359 | Five repair pathways in one context: chromatin modification during DNA repair |
Q34615480 | Formation of large palindromic DNA by homologous recombination of short inverted repeat sequences in Saccharomyces cerevisiae |
Q39308016 | Functional analysis of promoter variants in KU70 and their role in cancer susceptibility |
Q27935172 | Functional and genetic analysis of the Saccharomyces cerevisiae RNC1/TRM2: evidences for its involvement in DNA double-strand break repair |
Q39875477 | Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements. |
Q36873831 | Gene conversion and end-joining-repair double-strand breaks in the Caenorhabditis elegans germline |
Q40695823 | Gene repeat expansion and contraction by spontaneous intrachromosomal homologous recombination in mammalian cells |
Q52658229 | Gene targeting in the oil-producing fungus Mortierella alpina 1S-4 and construction of a strain producing a valuable polyunsaturated fatty acid. |
Q52591578 | Gene-targeting in Drosophila validated. |
Q40778006 | Genetic analysis of the DNA-dependent protein kinase reveals an inhibitory role of Ku in late S-G2 phase DNA double-strand break repair |
Q43179154 | Genome editing in plants via designed zinc finger nucleases |
Q52757700 | Genome maintenance functions of the INO80 chromatin remodeller. |
Q28131737 | Genome maintenance mechanisms for preventing cancer |
Q47243146 | Genomic context of paralogous recombination hotspots mediating recurrent NF1 region microdeletion |
Q47202601 | Genomic interspersions determine the size and complexity of transgene loci in transgenic plants produced by microprojectile bombardment |
Q40796022 | Heterogeneity in 2-deoxy-D-glucose-induced modifications in energetics and radiation responses of human tumor cell lines |
Q35851292 | Histone modifications and DNA double-strand break repair |
Q34311675 | Homologous DNA recombination in vertebrate cells |
Q24793756 | Homologous Recombination and Its Role in Carcinogenesis |
Q35604547 | Homologous recombination and gene targeting in plant cells |
Q50802072 | Homologous recombination and non-homologous end-joining repair pathways in bovine embryos with different developmental competence. |
Q34183753 | Homologous recombination as a mechanism of carcinogenesis |
Q28646561 | Homologous recombinational repair of DNA ensures mammalian chromosome stability |
Q37662142 | HuR silencing elicits oxidative stress and DNA damage and sensitizes human triple-negative breast cancer cells to radiotherapy |
Q35538187 | Human and animal models of V(D)J recombination deficiency |
Q35671715 | Human models of inherited immunoglobulin class switch recombination and somatic hypermutation defects (hyper-IgM syndromes). |
Q33203892 | Identification of proteins in the hamster DNA end-binding complex |
Q37583802 | Improvement of a gene targeting system for genetic manipulation in Penicillium digitatum |
Q35632849 | Indecent exposure: when telomeres become uncapped |
Q64387443 | Induction and recovery of double-strand breaks in barley ribosomal DNA |
Q24797982 | Inhibition of double-strand break non-homologous end-joining by cisplatin adducts in human cell extracts |
Q33952928 | Inhibition of histone deacetylases enhances DNA damage repair in SCNT embryos. |
Q40233076 | Inhibition of poly(ADP-ribose)polymerase does not affect the recombination events in CHO xrs6 and wild type cells |
Q36798931 | Involvement of homologous recombination in carcinogenesis. |
Q34895360 | Involvement of the Arabidopsis SWI2/SNF2 chromatin remodeling gene family in DNA damage response and recombination |
Q37259549 | Ionizing radiation induces microhomology-mediated end joining in trans in yeast and mammalian cells |
Q40662139 | Ionizing radiation-induced Rad51 nuclear focus formation is cell cycle-regulated and defective in both ATM(-/-) and c-Abl(-/-) cells |
Q27932980 | Ku interacts with telomerase RNA to promote telomere addition at native and broken chromosome ends |
Q82605776 | Ku70 and Rad51 vary in their importance for the repair of doxorubicin- versus etoposide-induced DNA damage |
Q37090402 | Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity |
Q38868797 | Low-fidelity alternative DNA repair carcinogenesis theory may interpret many cancer features and anticancer strategies |
Q38221690 | Low-fidelity compensatory backup alternative DNA repair pathways may unify current carcinogenesis theories |
Q40281319 | Low-resolution reconstruction of a synthetic DNA holliday junction. |
Q33963853 | MOF and histone H4 acetylation at lysine 16 are critical for DNA damage response and double-strand break repair |
Q92671094 | MRE11A Isoform Expression Associated with Outcome Following Radiotherapy in Muscle-Invasive Bladder Cancer does not Alter Cell Survival and DNA Double-Strand Break Repair Following Ionising Radiation |
Q34276665 | Maintenance of double-stranded telomeric repeats as the critical determinant for cell viability in yeast cells lacking Ku. |
Q34311686 | Manipulating the mammalian genome by homologous recombination |
Q36177491 | Mdt1 facilitates efficient repair of blocked DNA double-strand breaks and recombinational maintenance of telomeres |
Q28608973 | Mechanisms of human DNA repair: an update |
Q41332522 | Melatonin enhances the developmental competence of porcine somatic cell nuclear transfer embryos by preventing DNA damage induced by oxidative stress. |
Q37034049 | MicroRNA expression and its association with DNA repair in preimplantation embryos |
Q48015614 | Microhomology-mediated end joining: Good, bad and ugly. |
Q28072518 | Mitochondrial DNA damage induced autophagy, cell death, and disease |
Q40407926 | Mitotic cyclins regulate telomeric recombination in telomerase-deficient yeast cells. |
Q28274000 | Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis |
Q24791392 | Mms22p protects Saccharomyces cerevisiae from DNA damage induced by topoisomerase II |
Q36226840 | Molecular aspects of meiotic chromosome synapsis and recombination |
Q45991206 | Mrc1 channels the DNA replication arrest signal to checkpoint kinase Cds1. |
Q52378738 | Multiple Applications of a Transient CRISPR-Cas9 Coupled with Electroporation (TRACE) System in the Cryptococcus neoformans Species Complex. |
Q36028934 | Multiple pathways suppress telomere addition to DNA breaks in the Drosophila germline |
Q28469182 | Multiple-pathway analysis of double-strand break repair mutations in Drosophila |
Q44060421 | Mutagenicity of gamma-radiation, mitomycin C, and etoposide in the Hprt and Tk genes of Tk(+/-) mice |
Q34588653 | Mutations in the extra sex combs and Enhancer of Polycomb genes increase homologous recombination in somatic cells of Drosophila melanogaster |
Q40075000 | NK314, a topoisomerase II inhibitor that specifically targets the alpha isoform. |
Q40716180 | Neocarzinostatin induces Mre11 phosphorylation and focus formation through an ATM- and NBS1-dependent mechanism |
Q36547381 | New tricks for old drugs: the anticarcinogenic potential of DNA repair inhibitors |
Q74185601 | Non-homologous end joining as a mechanism of DNA repair |
Q28364073 | Non-homologous end-joining proteins are required for Agrobacterium T-DNA integration |
Q35075525 | Nonhomologous chromosomal integration of foreign DNA is completely dependent on MUS-53 (human Lig4 homolog) in Neurospora. |
Q92091329 | Overexpression of rice jacalin-related mannose-binding lectin (OsJAC1) enhances resistance to ionizing radiation in Arabidopsis |
Q24635310 | Oxidative stress, mitochondrial dysfunction, and aging |
Q35156963 | PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks |
Q47307969 | POT1 inhibits the efficiency but promotes the fidelity of nonhomologous end joining at non-telomeric DNA regions |
Q28608969 | Pathways of DNA double-strand break repair during the mammalian cell cycle |
Q27932796 | Pds5 is required for homologue pairing and inhibits synapsis of sister chromatids during yeast meiosis |
Q37212174 | Phospholipase D inhibitor enhances radiosensitivity of breast cancer cells |
Q43531552 | Phylogenetic analysis of mitochondrial DNA in a patient with Kearns-Sayre syndrome containing a novel 7629-bp deletion |
Q36547699 | Poly(ADP-ribose) polymerase 1 regulates nuclear reprogramming and promotes iPSC generation without c-Myc |
Q33245589 | Positive selection on the nonhomologous end-joining factor Cernunnos-XLF in the human lineage |
Q37369379 | Possible anti-recombinogenic role of Bloom's syndrome helicase in double-strand break processing |
Q24813430 | Potentiation of gene targeting in human cells by expression of Saccharomyces cerevisiae Rad52 |
Q64068281 | Prediction and identification of recurrent genomic rearrangements that generate chimeric chromosomes in |
Q39778314 | Prediction of clonogenic cell survival curves based on the number of residual DNA double strand breaks measured by gammaH2AX staining |
Q37694126 | Preferential accessibility to specific genomic loci for the repair of double-strand breaks in human cells |
Q64389145 | Programmable DNA repair with CRISPRa/i enhanced homology-directed repair efficiency with a single Cas9 |
Q33948430 | Promiscuous patching of broken chromosomes in mammalian cells with extrachromosomal DNA. |
Q21145041 | Proofreading activity of DNA polymerase Pol2 mediates 3'-end processing during nonhomologous end joining in yeast |
Q30388307 | RAD6 promotes homologous recombination repair by activating the autophagy-mediated degradation of heterochromatin protein HP1. |
Q34563981 | Radiosensitization in prostate cancer: mechanisms and targets |
Q35882372 | Real-Time Evolution of a Subtelomeric Gene Family in Candida albicans |
Q38985539 | Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia |
Q41627974 | Recombination products suggest the frequent occurrence of aberrant gene replacement in the moss Physcomitrella patens |
Q28214575 | Recombinational DNA repair and human disease |
Q33559700 | Reconstitution of the mammalian DNA double-strand break end-joining reaction reveals a requirement for an Mre11/Rad50/NBS1-containing fraction |
Q36515880 | Reduced mismatch repair of heteroduplexes reveals "non"-interfering crossing over in wild-type Saccharomyces cerevisiae |
Q36761497 | Regulation of bacterial RecA protein function |
Q39749064 | Repair System for Noncanonical Purines in Escherichia coli |
Q74082083 | Repair by retrotransposition |
Q38292505 | Repair of sequence-specific 125I-induced double-strand breaks by nonhomologous DNA end joining in mammalian cell-free extracts |
Q37163847 | Repair-mediated duplication by capture of proximal chromosomal DNA has shaped vertebrate genome evolution |
Q36854279 | Replication and protection of telomeres |
Q49829001 | Role of BRCA Mutations in the Modulation of Response to Platinum Therapy |
Q27939650 | Role of Elg1 protein in double strand break repair |
Q43771768 | Role of RAD51 in sister-chromatid exchanges in mammalian cells. |
Q35113329 | Role of homologous recombination in carcinogenesis. |
Q43819402 | S. cerevisiae has three pathways for DNA interstrand crosslink repair |
Q28593511 | SNMIB/Apollo protects leading-strand telomeres against NHEJ-mediated repair |
Q41919979 | Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV. |
Q40134692 | Silencing of endo-exonuclease expression sensitizes mouse B16F10 melanoma cells to DNA damaging agents |
Q38873757 | Single nucleotide polymorphisms in DNA repair genes and putative cancer risk. |
Q34285505 | Sirtuin 6 (SIRT6) rescues the decline of homologous recombination repair during replicative senescence |
Q36525004 | Slow DNA loss in the gigantic genomes of salamanders |
Q74186454 | Somatic and germinal mobility of the RescueMu transposon in transgenic maize |
Q30847802 | Specific recruitment of human cohesin to laser-induced DNA damage |
Q36447830 | Strand exchange activity of human recombination protein Rad52. |
Q27634006 | Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair |
Q33941481 | Suppression of gene amplification and chromosomal DNA integration by the DNA mismatch repair system |
Q40679903 | Suppression of high-fidelity double-strand break repair in mammalian chromosomes by pifithrin-alpha, a chemical inhibitor of p53. |
Q43564059 | Susceptibility of proliferating cells to benzo[a]pyrene-induced homologous recombination in mice. |
Q27936152 | Synergistic effect of TRM2/RNC1 and EXO1 in DNA double-strand break repair in Saccharomyces cerevisiae |
Q52642751 | Taking Drosophila Rad51 for a SPiN. |
Q36155030 | Targeted Genome Editing via CRISPR in the Pathogen Cryptococcus neoformans. |
Q37904200 | Targeted endoradiotherapy using nucleotides |
Q30828323 | Targeted engineering of the Caenorhabditis elegans genome following Mos1-triggered chromosomal breaks |
Q38361193 | Telomeric DNA ends are essential for the localization of Ku at telomeres in fission yeast |
Q21145244 | Temporal analysis of meiotic DNA double-strand break formation and repair in Drosophila females |
Q36986206 | The Arabidopsis AtRAD51 gene is dispensable for vegetative development but required for meiosis |
Q37356265 | The Fanconi anemia protein interaction network: casting a wide net. |
Q37397475 | The PTEN phosphatase functions cooperatively with the Fanconi anemia proteins in DNA crosslink repair |
Q24813831 | The RING finger ATPase Rad5p of Saccharomyces cerevisiae contributes to DNA double-strand break repair in a ubiquitin-independent manner |
Q39753325 | The Rad51 pathway of telomerase-independent maintenance of telomeres can amplify TG1-3 sequences in yku and cdc13 mutants of Saccharomyces cerevisiae. |
Q33969162 | The Sgs1 helicase of Saccharomyces cerevisiae inhibits retrotransposition of Ty1 multimeric arrays |
Q24794005 | The accumulation of MMS-induced single strand breaks in G1 phase is recombinogenic in DNA polymerase beta defective mammalian cells |
Q24630851 | The architecture of the human Rad54-DNA complex provides evidence for protein translocation along DNA |
Q27935474 | The beta-lactamase motif in Snm1 is required for repair of DNA double-strand breaks caused by interstrand crosslinks in S. cerevisiae |
Q43030078 | The carboxyl terminal of the archaeal nuclease NurA is involved in the interaction with single-stranded DNA-binding protein and dimer formation |
Q34282411 | The crystal structures of DNA Holliday junctions. |
Q37606970 | The dual role of HOP2 in mammalian meiotic homologous recombination |
Q37922086 | The generation of mitochondrial DNA large-scale deletions in human cells. |
Q74420964 | The genome's best friend |
Q36810416 | The histone deacetylase inhibitor PCI-24781 as a putative radiosensitizer in pediatric glioblastoma cell lines. |
Q37100245 | The interplay of DNA polymerase λ in diverse DNA damage repair pathways in higher plant genome in response to environmental and genotoxic stress factors |
Q27933902 | The karyopherin Kap142p/Msn5p mediates nuclear import and nuclear export of different cargo proteins |
Q35980970 | The life and death of DNA-PK. |
Q35545852 | The mTOR inhibitor rapamycin suppresses DNA double-strand break repair |
Q40899818 | The mechanism of gene targeting in Physcomitrella patens: homologous recombination, concatenation and multiple integration |
Q35597111 | The mechanisms of immune diversification and their disorders |
Q36231119 | The repair of DNA damages/modifications during the maturation of the immune system: lessons from human primary immunodeficiency disorders and animal models. |
Q24537586 | The transcriptional histone acetyltransferase cofactor TRRAP associates with the MRN repair complex and plays a role in DNA double-strand break repair |
Q94474051 | Timed inhibition of CDC7 increases CRISPR-Cas9 mediated templated repair |
Q38351157 | Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs |
Q46246407 | Unique molecular mechanisms for maintenance and alteration of genetic information in the budding yeast Saccharomyces cerevisiae |
Q34099636 | Untargeted mutation of the maternally derived mouse hypervariable minisatellite allele in F1 mice born to irradiated spermatozoa |
Q39936122 | Vanillins--a novel family of DNA-PK inhibitors |
Q37096545 | What causes mitochondrial DNA deletions in human cells? |
Q35120155 | Who's on first in the cellular response to DNA damage? |
Q78025737 | Wild-type levels of Spo11-induced DSBs are required for normal single-strand resection during meiosis |
Q24302150 | XLF interacts with the XRCC4-DNA ligase IV complex to promote DNA nonhomologous end-joining |
Q35222177 | Yeast recombination pathways triggered by topoisomerase II-mediated DNA breaks |
Q36280699 | p21 promotes error-free replication-coupled DNA double-strand break repair |
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