scholarly article | Q13442814 |
P2093 | author name string | Christopher E West | |
Clifford M Bray | |||
Wanda M Waterworth | |||
Georgina E Drury | |||
P2860 | cites work | The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway | Q22065419 |
The ATM-Chk2-Cdc25A checkpoint pathway guards against radioresistant DNA synthesis | Q24291114 | ||
The MCM-binding protein ETG1 aids sister chromatid cohesion required for postreplicative homologous recombination repair | Q24296748 | ||
ATM activation by DNA double-strand breaks through the Mre11-Rad50-Nbs1 complex | Q24298863 | ||
CDK-dependent phosphorylation of BRCA2 as a regulatory mechanism for recombinational repair | Q24299313 | ||
ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage | Q24306743 | ||
Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro | Q24321787 | ||
Mammalian DNA double-strand break repair protein XRCC4 interacts with DNA ligase IV | Q24323238 | ||
CDK targets Sae2 to control DNA-end resection and homologous recombination | Q24328867 | ||
Molecular aspects of plant adaptation to life in the Chernobyl zone | Q24562105 | ||
Mdc1 couples DNA double-strand break recognition by Nbs1 with its H2AX-dependent chromatin retention | Q24563397 | ||
Recombinational repair of gaps in DNA is asymmetric in Ustilago maydis and can be explained by a migrating D-loop model | Q24605056 | ||
Human CtIP promotes DNA end resection | Q24646062 | ||
Adaptation and impairment of DNA repair function in pollen of Betula verrucosa and seeds of Oenothera biennis from differently radionuclide-contaminated sites of Chernobyl | Q24648330 | ||
High-frequency modification of plant genes using engineered zinc-finger nucleases | Q24654686 | ||
Differential requirements for RAD51 in Physcomitrella patens and Arabidopsis thaliana development and DNA damage repair | Q24670014 | ||
Radioresistance of Deinococcus radiodurans: functions necessary to survive ionizing radiation are also necessary to survive prolonged desiccation | Q24684819 | ||
Dissection of a DNA-damage-induced transcriptional network using a combination of microarrays, RNA interference and computational promoter analysis | Q24812377 | ||
Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes | Q27860662 | ||
Smc5-Smc6 mediate DNA double-strand-break repair by promoting sister-chromatid recombination. | Q27931113 | ||
Distinct roles for SWR1 and INO80 chromatin remodeling complexes at chromosomal double-strand breaks. | Q27934708 | ||
Arabidopsis DNA ligase IV is induced by gamma-irradiation and interacts with an Arabidopsis homologue of the double strand break repair protein XRCC4. | Q27937354 | ||
Ku80: product of the XRCC5 gene and its role in DNA repair and V(D)J recombination | Q28115740 | ||
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139 | Q28131715 | ||
Enhancing Gene Targeting with Designed Zinc Finger Nucleases | Q28202461 | ||
Genome instability and epigenetic modification--heritable responses to environmental stress? | Q37858141 | ||
Arabidopsis RPA2: a genetic link among transcriptional gene silencing, DNA repair, and DNA replication. | Q38319121 | ||
A biochemically defined system for mammalian nonhomologous DNA end joining | Q38333666 | ||
A shared DNA-damage-response pathway for induction of stem-cell death by UVB and by gamma irradiation | Q38342454 | ||
Microarray analysis reveals that TP53- and ATM-mutant B-CLLs share a defect in activating proapoptotic responses after DNA damage but are distinguished by major differences in activating prosurvival responses. | Q38350727 | ||
Non-homologous DNA end joining in plant cells is associated with deletions and filler DNA insertions | Q39721716 | ||
The Arabidopsis AtLIG4 gene is required for the repair of DNA damage, but not for the integration of Agrobacterium T-DNA | Q39792164 | ||
CtIP-BRCA1 modulates the choice of DNA double-strand-break repair pathway throughout the cell cycle. | Q39862482 | ||
Dynamic response of plant genome to ultraviolet radiation and other genotoxic stresses | Q40440702 | ||
Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV | Q40696254 | ||
The origin of interspersed repeats in the human genome | Q41312150 | ||
Functional conservation of the yeast and Arabidopsis RAD54-like genes | Q41792146 | ||
The effect of sequence divergence on recombination between direct repeats in Arabidopsis | Q41862394 | ||
Arabidopsis T-DNA insertional lines for CDC25 are hypersensitive to hydroxyurea but not to zeocin or salt stress | Q41887630 | ||
The role of AtMSH2 in homologous recombination in Arabidopsis thaliana | Q42011370 | ||
A SRS2 homolog from Arabidopsis thaliana disrupts recombinogenic DNA intermediates and facilitates single strand annealing | Q42121359 | ||
Chk1 regulates the S phase checkpoint by coupling the physiological turnover and ionizing radiation-induced accelerated proteolysis of Cdc25A. | Q42439288 | ||
The chromatin assembly factor subunit FASCIATA1 is involved in homologous recombination in plants | Q42598474 | ||
A homolog of ScRAD5 is involved in DNA repair and homologous recombination in Arabidopsis | Q42646846 | ||
An SMC-like protein is required for efficient homologous recombination in Arabidopsis | Q42679489 | ||
Chlorine ions but not sodium ions alter genome stability of Arabidopsis thaliana | Q43102476 | ||
Chromatin remodelling at a DNA double-strand break site in Saccharomyces cerevisiae | Q43230977 | ||
Distinct roles of the ATR kinase and the Mre11-Rad50-Nbs1 complex in the maintenance of chromosomal stability in Arabidopsis. | Q43886386 | ||
Severe developmental defects, hypersensitivity to DNA-damaging agents, and lengthened telomeres in Arabidopsis MRE11 mutants | Q44170735 | ||
AtATM is essential for meiosis and the somatic response to DNA damage in plants | Q44267791 | ||
Ku80‐ and DNA ligase IV‐deficient plants are sensitive to ionizing radiation and defective in T‐DNA integration | Q44445346 | ||
Ku80 plays a role in non-homologous recombination but is not required for T-DNA integration in Arabidopsis | Q44563351 | ||
ATR regulates a G2-phase cell-cycle checkpoint in Arabidopsis thaliana | Q44838357 | ||
The STRUCTURAL MAINTENANCE OF CHROMOSOMES 5/6 complex promotes sister chromatid alignment and homologous recombination after DNA damage in Arabidopsis thaliana | Q44997290 | ||
The role of DNA helicases and their interaction partners in genome stability and meiotic recombination in plants | Q37809933 | ||
Have a break: determinants of meiotic DNA double strand break (DSB) formation and processing in plants | Q37827289 | ||
Induction and repair of DNA double strand breaks: the increasing spectrum of non-homologous end joining pathways | Q37844204 | ||
RAD5A, RECQ4A, and MUS81 have specific functions in homologous recombination and define different pathways of DNA repair in Arabidopsis thaliana | Q45412951 | ||
Epigenetic regulation, somatic homologous recombination, and abscisic acid signaling are influenced by DNA polymerase epsilon mutation in Arabidopsis | Q46108770 | ||
The Mre11/Rad50/Xrs2 complex and non-homologous end-joining of incompatible ends in S. cerevisiae | Q46618397 | ||
BIN4, a novel component of the plant DNA topoisomerase VI complex, is required for endoreduplication in Arabidopsis | Q46869080 | ||
The Rad17 homologue of Arabidopsis is involved in the regulation of DNA damage repair and homologous recombination. | Q47425283 | ||
Characterization of the three Arabidopsis thaliana RAD21 cohesins reveals differential responses to ionizing radiation | Q48099103 | ||
Interaction between Arabidopsis Brca2 and its partners Rad51, Dmc1, and Dss1. | Q48103823 | ||
ATM and ATR. | Q48556004 | ||
Arabidopsis WEE1 kinase controls cell cycle arrest in response to activation of the DNA integrity checkpoint. | Q49065118 | ||
Double-strand break repair in plants is developmentally regulated | Q50481186 | ||
Control of cell proliferation, organ growth, and DNA damage response operate independently of dephosphorylation of the Arabidopsis Cdk1 homolog CDKA;1. | Q51772392 | ||
High efficient gene targeting on the AGAMOUS gene in an ArabidopsisAtLIG4 mutant. | Q52599916 | ||
Arabidopsis DNA double-strand break repair pathways. | Q52858555 | ||
Both ATM and ATR promote the efficient and accurate processing of programmed meiotic double-strand breaks. | Q53481054 | ||
The ATM-mediated DNA-damage response: taking shape. | Q53618038 | ||
Seed aging: chromosome stability and extended viability of seeds stored fully imbided. | Q54009138 | ||
Elevated UV-B radiation reduces genome stability in plants. | Q55034050 | ||
Efficient gene targeting by homologous recombination in rice | Q56900683 | ||
Pathogen-induced systemic plant signal triggers DNA rearrangements | Q59052488 | ||
DNA lesions occur with loss of viability in embryos of ageing rye seed | Q28235124 | ||
NBS1 is involved in DNA repair and plays a synergistic role with ATM in mediating meiotic homologous recombination in plants | Q28239183 | ||
Precise genome modification in the crop species Zea mays using zinc-finger nucleases | Q28243268 | ||
The double-strand-break repair model for recombination | Q28267259 | ||
Cell cycle regulation in plant development | Q28273269 | ||
RAD51 loss of function abolishes gene targeting and de-represses illegitimate integration in the moss Physcomitrella patens | Q28274494 | ||
DNA repair mechanisms in plants: crucial sensors and effectors for the maintenance of genome integrity | Q28284004 | ||
Differing requirements for the Arabidopsis Rad51 paralogs in meiosis and DNA repair | Q28305379 | ||
Non-homologous end-joining proteins are required for Agrobacterium T-DNA integration | Q28364073 | ||
Transgenerational stress memory is not a general response in Arabidopsis | Q28475351 | ||
ATM- and cell cycle-dependent regulation of ATR in response to DNA double-strand breaks | Q29614215 | ||
Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage | Q29614218 | ||
Chimeric nucleases stimulate gene targeting in human cells | Q29615384 | ||
Recruitment of the INO80 complex by H2A phosphorylation links ATP-dependent chromatin remodeling with DNA double-strand break repair | Q29620305 | ||
The biology of chromatin remodeling complexes | Q29620581 | ||
Disruption of the Arabidopsis RAD50 gene leads to plant sterility and MMS sensitivity | Q31908607 | ||
Increase of homologous recombination frequency in vascular tissue of Arabidopsis plants exposed to salt stress | Q33239671 | ||
ATM-mediated transcriptional and developmental responses to gamma-rays in Arabidopsis | Q33283998 | ||
Developmental control of cell division patterns in the shoot apex. | Q33335148 | ||
BRU1, a novel link between responses to DNA damage and epigenetic gene silencing in Arabidopsis. | Q33339924 | ||
Plant DNA polymerase lambda, a DNA repair enzyme that functions in plant meristematic and meiotic tissues | Q33340125 | ||
Tissue-specific regulation of cell-cycle responses to DNA damage in Arabidopsis seedlings | Q33341636 | ||
Tolerance of dividing cells to replication stress in UVB-irradiated Arabidopsis roots: requirements for DNA translesion polymerases eta and zeta | Q33344004 | ||
Gene expression map of the Arabidopsis shoot apical meristem stem cell niche | Q33346789 | ||
Inefficient double-strand DNA break repair is associated with increased fasciation in Arabidopsis BRCA2 mutants | Q33347141 | ||
Suppressor of gamma response 1 (SOG1) encodes a putative transcription factor governing multiple responses to DNA damage | Q33347320 | ||
Hypersensitivity to DNA damage in plant stem cell niches | Q33348230 | ||
Plant stem cell niches: from signalling to execution | Q33349683 | ||
Xrcc1-dependent and Ku-dependent DNA double-strand break repair kinetics in Arabidopsis plants | Q33350093 | ||
The Arabidopsis thaliana checkpoint kinase WEE1 protects against premature vascular differentiation during replication stress | Q33351001 | ||
Capture of genomic and T-DNA sequences during double-strand break repair in somatic plant cells | Q33368852 | ||
Seed longevity: survival and maintenance of high germination ability of dry seeds | Q33377301 | ||
DNA ligase 1 deficient plants display severe growth defects and delayed repair of both DNA single and double strand breaks | Q33475120 | ||
The Arabidopsis ATRIP ortholog is required for a programmed response to replication inhibitors | Q33484327 | ||
Transgenerational adaptation of Arabidopsis to stress requires DNA methylation and the function of Dicer-like proteins | Q33538006 | ||
What is stress? Concepts, definitions and applications in seed science | Q33696475 | ||
Ionizing radiation-dependent gamma-H2AX focus formation requires ataxia telangiectasia mutated and ataxia telangiectasia mutated and Rad3-related | Q33768588 | ||
Pathways to meiotic recombination in Arabidopsis thaliana | Q33834760 | ||
High-frequency gene targeting in Arabidopsis plants expressing the yeast RAD54 gene | Q33922824 | ||
A plant DNA ligase is an important determinant of seed longevity | Q34123110 | ||
Involvement of KU80 in T-DNA integration in plant cells. | Q34244956 | ||
Direct activation of the ATM protein kinase by the Mre11/Rad50/Nbs1 complex | Q34311086 | ||
Molecular analysis of telomere fusions in Arabidopsis: multiple pathways for chromosome end-joining | Q34348751 | ||
Identification of a Saccharomyces cerevisiae Ku80 homologue: roles in DNA double strand break rejoining and in telomeric maintenance | Q34411525 | ||
Arabidopsis BRCA2 and RAD51 proteins are specifically involved in defense gene transcription during plant immune responses | Q34450380 | ||
Transgeneration memory of stress in plants. | Q34554779 | ||
Possible role of pectin-containing mucilage and dew in repairing embryo DNA of seeds adapted to desert conditions | Q34627529 | ||
Extreme resistance of bdelloid rotifers to ionizing radiation | Q34764335 | ||
Germination, genetics, and growth of an ancient date seed. | Q34786697 | ||
Involvement of the Arabidopsis SWI2/SNF2 chromatin remodeling gene family in DNA damage response and recombination | Q34895360 | ||
The many functions of SMC proteins in chromosome dynamics | Q34931800 | ||
An Arabidopsis histone H2A mutant is deficient in Agrobacterium T-DNA integration | Q34983158 | ||
Transgenerational response to stress in Arabidopsis thaliana | Q35045665 | ||
Increased frequency of homologous recombination and T-DNA integration in Arabidopsis CAF-1 mutants | Q35191098 | ||
Arabidopsis SNI1 and RAD51D regulate both gene transcription and DNA recombination during the defense response | Q35676871 | ||
Transgene integration in plants: poking or patching holes in promiscuous genomes? | Q35744500 | ||
A tale of two integrations, transgene and T-DNA: gene targeting by homologous recombination in rice | Q35744504 | ||
Functional analysis of maize RAD51 in meiosis and double-strand break repair | Q35911023 | ||
The role of SMC proteins in the responses to DNA damage | Q36015649 | ||
A novel plant gene essential for meiosis is related to the human CtIP and the yeast COM1/SAE2 gene | Q36274706 | ||
The RecQ gene family in plants | Q36349828 | ||
The plant cell cycle--15 years on. | Q36771853 | ||
Efficient transfer of base changes from a vector to the rice genome by homologous recombination: involvement of heteroduplex formation and mismatch correction | Q36824021 | ||
The Arabidopsis AtRAD51 gene is dispensable for vegetative development but required for meiosis | Q36986206 | ||
Single-strand interruptions in replicating chromosomes cause double-strand breaks | Q37093293 | ||
Break-induced replication: what is it and what is it for? | Q37138963 | ||
Snf2 proteins in plants: gene silencing and beyond | Q37266953 | ||
Arabidopsis actin-related protein ARP5 in multicellular development and DNA repair. | Q37423420 | ||
Plant proteins involved in Agrobacterium-mediated genetic transformation | Q37718815 | ||
Mechanisms and regulation of DNA end resection | Q37774547 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 805-822 | |
P577 | publication date | 2011-10-11 | |
P1433 | published in | New Phytologist | Q13548580 |
P1476 | title | Repairing breaks in the plant genome: the importance of keeping it together | |
P478 | volume | 192 |