scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1026170473 |
P356 | DOI | 10.1038/13821 |
P8608 | Fatcat ID | release_ccrsgnyh2jdofpjakxkzvk4qb4 |
P698 | PubMed publication ID | 10508516 |
P2093 | author name string | C Heyting | |
H H Offenberg | |||
M Eijpe | |||
M van Aalderen | |||
W Goedecke | |||
P2860 | cites work | The transcriptional program of sporulation in budding yeast | Q27938344 |
Temporal comparison of recombination and synaptonemal complex formation during meiosis in S. cerevisiae | Q28306536 | ||
SCP2: a major protein component of the axial elements of synaptonemal complexes of the rat | Q28583161 | ||
Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells | Q29617437 | ||
An atypical topoisomerase II from Archaea with implications for meiotic recombination | Q29618230 | ||
The gene encoding a major component of the lateral elements of synaptonemal complexes of the rat is related to X-linked lymphocyte-regulated genes | Q36645944 | ||
Two types of RAS mutants that dominantly interfere with activators of RAS. | Q36654269 | ||
mre11S--a yeast mutation that blocks double-strand-break processing and permits nonhomologous synapsis in meiosis | Q37367245 | ||
A novel mre11 mutation impairs processing of double-strand breaks of DNA during both mitosis and meiosis | Q39631261 | ||
Hdf1, a yeast Ku-protein homologue, is involved in illegitimate recombination, but not in homologous recombination | Q39716405 | ||
Molecular and biochemical characterization of xrs mutants defective in Ku80. | Q40021061 | ||
In situ visualization of DNA double-strand break repair in human fibroblasts | Q41045622 | ||
Double-strand breaks at an initiation site for meiotic gene conversion | Q59068287 | ||
DNA end-joining: from yeast to man | Q63362924 | ||
Identification of joint molecules that form frequently between homologs but rarely between sister chromatids during yeast meiosis | Q64389750 | ||
Spermatogonial stem-cell renewal in the mouse | Q71773555 | ||
The many interfaces of Mre11 | Q77654630 | ||
DNA end-joining catalyzed by human cell-free extracts | Q22008041 | ||
The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks | Q24311761 | ||
Human Rad50 is physically associated with human Mre11: identification of a conserved multiprotein complex implicated in recombinational DNA repair | Q24316169 | ||
Cell cycle and genetic requirements of two pathways of nonhomologous end-joining repair of double-strand breaks in Saccharomyces cerevisiae | Q24649768 | ||
Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family | Q27930009 | ||
Distinct roles of two separable in vitro activities of yeast Mre11 in mitotic and meiotic recombination | Q27930776 | ||
Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis | Q27934770 | ||
Complex formation and functional versatility of Mre11 of budding yeast in recombination | Q27935743 | ||
Relocalization of telomeric Ku and SIR proteins in response to DNA strand breaks in yeast | Q27936427 | ||
The nuclease activity of Mre11 is required for meiosis but not for mating type switching, end joining, or telomere maintenance | Q27937328 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | X-ray repair cross complementing 6 | Q21116645 |
P304 | page(s) | 194-8 | |
P577 | publication date | 1999-10-01 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | Mre11 and Ku70 interact in somatic cells, but are differentially expressed in early meiosis | |
P478 | volume | 23 |
Q35762470 | A means to a DNA end: the many roles of Ku. |
Q33841787 | A mechanism of palindromic gene amplification in Saccharomyces cerevisiae |
Q40575476 | Binding of the DNA-dependent protein kinase catalytic subunit to Holliday junctions |
Q27324477 | COM-1 promotes homologous recombination during Caenorhabditis elegans meiosis by antagonizing Ku-mediated non-homologous end joining |
Q39707017 | Campylobacter jejuni cytolethal distending toxin promotes DNA repair responses in normal human cells |
Q50671994 | Cellular responses to ionizing radiation damage. |
Q92136735 | Challenges and Perspectives in Homology-Directed Gene Targeting in Monocot Plants |
Q34173678 | Checkpoint and DNA-repair proteins are associated with the cores of mammalian meiotic chromosomes |
Q43102476 | Chlorine ions but not sodium ions alter genome stability of Arabidopsis thaliana |
Q35029335 | Choosing the right path: does DNA-PK help make the decision? |
Q34016558 | Chromatin organization and remodeling of interstitial telomeric sites during meiosis in the Mongolian gerbil (Meriones unguiculatus). |
Q37638191 | Collaboration and competition between DNA double‐strand break repair pathways |
Q27324367 | Conditional inactivation of the DNA damage response gene Hus1 in mouse testis reveals separable roles for components of the RAD9-RAD1-HUS1 complex in meiotic chromosome maintenance |
Q34506211 | DNA Double Strand Break Response and Limited Repair Capacity in Mouse Elongated Spermatids |
Q37063328 | DNA damage and repair during lymphoid development: antigen receptor diversity, genomic integrity and lymphomagenesis |
Q40745510 | DNA damage and repair in lymphoblastoid cell lines from normal donors and fragile X syndrome patients |
Q39745562 | DNA damage and toxicogenomic analyses of hydrogen sulfide in human intestinal epithelial FHs 74 Int cells. |
Q35608458 | DNA damage response and repair: insights into strategies for radiation sensitization of gliomas |
Q51971590 | DNA damage response during chromatin remodeling in elongating spermatids of mice. |
Q33975168 | DNA damage-dependent nuclear dynamics of the Mre11 complex |
Q28143901 | DNA ligase IV and XRCC4 form a stable mixed tetramer that functions synergistically with other repair factors in a cell-free end-joining system |
Q46070162 | Deleting Ku70 is milder than deleting Ku80 in p53-mutant mice and cells. |
Q24681223 | Deletion of Ku70, Ku80, or both causes early aging without substantially increased cancer |
Q37510041 | Deletion of individual Ku subunits in mice causes an NHEJ-independent phenotype potentially by altering apurinic/apyrimidinic site repair |
Q47895242 | Differential gene expression of mammalian SPO11/TOP6A homologs during meiosis |
Q44105234 | Disruption of the Arabidopsis AtKu80 gene demonstrates an essential role for AtKu80 protein in efficient repair of DNA double-strand breaks in vivo |
Q42014431 | Division of labor: DNA repair and the cell cycle specific functions of the Mre11 complex. |
Q50481186 | Double-strand break repair in plants is developmentally regulated. |
Q26830517 | Double-strand break repair on sex chromosomes: challenges during male meiotic prophase |
Q53061882 | Dynamics of radiation induced γH2AX foci in chromatin subcompartments of mouse pachytene spermatocytes and round spermatids. |
Q48102360 | Efficiency of nonhomologous DNA end joining varies among somatic tissues, despite similarity in mechanism |
Q41867231 | Enhancement of extra chromosomal recombination in somatic cells by affecting the ratio of homologous recombination (HR) to non-homologous end joining (NHEJ). |
Q35132485 | Envisioning the fourth dimension of the genetic code: the structural biology of macromolecular recognition and conformational switching in DNA repair |
Q36023638 | Expression and possible functions of DNA lesion bypass proteins in spermatogenesis |
Q28365488 | Fission yeast Rad50 stimulates sister chromatid recombination and links cohesion with repair |
Q91991483 | GCNA Interacts with Spartan and Topoisomerase II to Regulate Genome Stability |
Q36072583 | Generation of stable mutants and targeted gene deletion strains in Cryptococcus neoformans through electroporation |
Q34001661 | Genetic analysis of homologous DNA recombination in vertebrate somatic cells |
Q53665792 | Heterogeneous expression of Ku70 in human tissues is associated with morphological and functional alterations of the nucleus. |
Q35571865 | Heteromorphic sex chromosomes: navigating meiosis without a homologous partner |
Q35604547 | Homologous recombination and gene targeting in plant cells |
Q34979828 | Homologous recombination: ends as the means. |
Q28646561 | Homologous recombinational repair of DNA ensures mammalian chromosome stability |
Q39600750 | Human DNA polymerase mu (Pol mu) exhibits an unusual replication slippage ability at AAF lesion |
Q73794909 | Human DNA repair genes |
Q33203137 | Identification of interaction partners and substrates of the cyclin A1-CDK2 complex |
Q24294826 | In vitro and in vivo interactions of DNA ligase IV with a subunit of the condensin complex |
Q53487384 | Increased frequency of asynapsis and associated meiotic silencing of heterologous chromatin in the presence of irradiation-induced extra DNA double strand breaks. |
Q39686949 | Increased telomere length and hypersensitivity to DNA damaging agents in an Arabidopsis KU70 mutant. |
Q37664062 | Initiation of meiotic recombination in mammals |
Q37012010 | Ku70 and non-homologous end joining protect testicular cells from DNA damage |
Q42127065 | Ku80-deleted cells are defective at base excision repair |
Q48503758 | Lhx8 ablation leads to massive autophagy of mouse oocytes associated with DNA damage. |
Q38868797 | Low-fidelity alternative DNA repair carcinogenesis theory may interpret many cancer features and anticancer strategies |
Q29618789 | Mechanism and control of meiotic recombination initiation |
Q64388742 | Mei1 is epistatic to Dmc1 during mouse meiosis |
Q36198265 | Meiosis: inducing variation by reduction |
Q28573938 | Meiotic cohesin REC8 marks the axial elements of rat synaptonemal complexes before cohesins SMC1beta and SMC3 |
Q38000414 | Meiotic double strand breaks repair in sexually reproducing eukaryotes: we are not all equal |
Q35541520 | Meiotic functions of RAD18. |
Q35015835 | Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22) |
Q35543795 | Mending the Break: Two DNA Double-Strand Break Repair Machines in Eukaryotes |
Q27313888 | Mll5 is required for normal spermatogenesis |
Q36226840 | Molecular aspects of meiotic chromosome synapsis and recombination |
Q36792626 | Molecular targets and mechanisms of radiosensitization using DNA damage response pathways |
Q28506028 | Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages |
Q27930222 | NEJ1 controls non-homologous end joining in Saccharomyces cerevisiae |
Q46582502 | OsDMC1 Is Not Required for Homologous Pairing in Rice Meiosis. |
Q47423101 | PLU-1, a transcriptional repressor and putative testis-cancer antigen, has a specific expression and localisation pattern during meiosis. |
Q33927291 | Partners and pathwaysrepairing a double-strand break. |
Q30881342 | Polymerase eta deficiency in the xeroderma pigmentosum variant uncovers an overlap between the S phase checkpoint and double-strand break repair |
Q33829179 | Post-meiotic DNA double-strand breaks occur in Tetrahymena, and require Topoisomerase II and Spo11. |
Q39155608 | Prophase I: Preparing Chromosomes for Segregation in the Developing Oocyte |
Q47765927 | RAG proteins shepherd double-strand breaks to a specific pathway, suppressing error-prone repair, but RAG nicking initiates homologous recombination |
Q35094244 | Rap1-independent telomere attachment and bouquet formation in mammalian meiosis |
Q33912842 | Recombination: a frank view of exchanges and vice versa. |
Q36900915 | Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis. |
Q38328608 | Regulation of homologous integration in yeast by the DNA repair proteins Ku70 and RecQ. |
Q44170735 | Severe developmental defects, hypersensitivity to DNA-damaging agents, and lengthened telomeres in Arabidopsis MRE11 mutants |
Q37098468 | Sex chromosome inactivation in germ cells: emerging roles of DNA damage response pathways |
Q37187725 | Spermiogenesis and DNA repair: a possible etiology of human infertility and genetic disorders |
Q33914715 | Structural insights into NHEJ: building up an integrated picture of the dynamic DSB repair super complex, one component and interaction at a time |
Q91188176 | Super-Mendelian inheritance mediated by CRISPR-Cas9 in the female mouse germline |
Q34615813 | Telomere binding of checkpoint sensor and DNA repair proteins contributes to maintenance of functional fission yeast telomeres. |
Q33937428 | Telomere dysfunction triggers developmentally regulated germ cell apoptosis. |
Q36761799 | Telomere regulation and function during meiosis |
Q53671345 | Testicular expression of small ubiquitin-related modifier-1 (SUMO-1) supports multiple roles in spermatogenesis: silencing of sex chromosomes in spermatocytes, spermatid microtubule nucleation, and nuclear reshaping. |
Q35621644 | The CAF-1 and Hir Histone Chaperones Associate with Sites of Meiotic Double-Strand Breaks in Budding Yeast |
Q48117756 | The Exonuclease Homolog OsRAD1 Promotes Accurate Meiotic Double-Strand Break Repair by Suppressing Nonhomologous End Joining. |
Q43919127 | The Ku70 DNA-repair protein is involved in centromere function in a grasshopper species. |
Q55033314 | The Kudos of non-homologous end-joining. |
Q34609697 | The Saccharomyces cerevisiae mre11(ts) allele confers a separation of DNA repair and telomere maintenance functions |
Q35980970 | The life and death of DNA-PK. |
Q24291484 | The role of DNA polymerase activity in human non-homologous end joining |
Q61812011 | Transition from a meiotic to a somatic-like DNA damage response during the pachytene stage in mouse meiosis |
Q36002411 | Two separable functions of Ctp1 in the early steps of meiotic DNA double-strand break repair |
Q33984271 | Tying up loose ends: nonhomologous end-joining in Saccharomyces cerevisiae |
Q36011232 | Up-regulation of the Ku heterodimer in Drosophila testicular cyst cells |
Q28506423 | ZIP4H (TEX11) deficiency in the mouse impairs meiotic double strand break repair and the regulation of crossing over |
Search more.