| scholarly article | Q13442814 |
| P50 | author | Ulrich Rothbauer | Q50981601 |
| P2093 | author name string | Heinrich Leonhardt | |
| M Cristina Cardoso | |||
| Oliver Mortusewicz | |||
| P2860 | cites work | Reconstitution of proliferating cell nuclear antigen-dependent repair of apurinic/apyrimidinic sites with purified human proteins | Q22010786 |
| Activity of DNA ligase IV stimulated by complex formation with XRCC4 protein in mammalian cells | Q24320116 | ||
| Mammalian DNA double-strand break repair protein XRCC4 interacts with DNA ligase IV | Q24323238 | ||
| XRCC1 co-localizes and physically interacts with PCNA | Q24563578 | ||
| The N-terminal domain of human DNA ligase I contains the nuclear localization signal and directs the enzyme to sites of DNA replication | Q24597704 | ||
| An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III | Q24615666 | ||
| Molecular cloning and expression of human cDNAs encoding a novel DNA ligase IV and DNA ligase III, an enzyme active in DNA repair and recombination | Q24652220 | ||
| PCNA acts as a stationary loading platform for transiently interacting Okazaki fragment maturation proteins | Q24811726 | ||
| XRCC1 is phosphorylated by DNA-dependent protein kinase in response to DNA damage | Q25257391 | ||
| Genome maintenance mechanisms for preventing cancer | Q28131737 | ||
| A monomeric red fluorescent protein | Q28131782 | ||
| BRCT domain interactions in the heterodimeric DNA repair protein XRCC1-DNA ligase III | Q28188887 | ||
| Spatial organization of the mammalian genome surveillance machinery in response to DNA strand breaks | Q28235091 | ||
| Role of a BRCT domain in the interaction of DNA ligase III-alpha with the DNA repair protein XRCC1 | Q28279796 | ||
| Late embryonic lethality and impaired V(D)J recombination in mice lacking DNA ligase IV | Q28504490 | ||
| Targeted disruption of the gene encoding DNA ligase IV leads to lethality in embryonic mice | Q28510493 | ||
| Mechanism whereby proliferating cell nuclear antigen stimulates flap endonuclease 1 | Q28645598 | ||
| Interaction between PCNA and DNA ligase I is critical for joining of Okazaki fragments and long-patch base-excision repair | Q28645603 | ||
| Aberrant DNA repair and DNA replication due to an inherited enzymatic defect in human DNA ligase I | Q28645712 | ||
| Thermodynamics of human DNA ligase I trimerization and association with DNA polymerase beta | Q28645732 | ||
| In situ analysis of repair processes for oxidative DNA damage in mammalian cells. | Q31111805 | ||
| Recruitment of DNA methyltransferase I to DNA repair sites | Q33217127 | ||
| DNA ligase III is recruited to DNA strand breaks by a zinc finger motif homologous to that of poly(ADP-ribose) polymerase. Identification of two functionally distinct DNA binding regions within DNA ligase III. | Q33869047 | ||
| DNA ligases in the repair and replication of DNA. | Q34006361 | ||
| DNA ligase III as a candidate component of backup pathways of nonhomologous end joining | Q34419519 | ||
| Involvement of XRCC1 and DNA ligase III gene products in DNA base excision repair. | Q34439025 | ||
| Dynamics of DNA replication factories in living cells | Q34508274 | ||
| DNA damage and repair | Q35050625 | ||
| Role of the DNA ligase III zinc finger in polynucleotide binding and ligation. | Q38332424 | ||
| DNA ligase I mediates essential functions in mammalian cells | Q40016859 | ||
| Reduced repair of DNA double-strand breaks by homologous recombination in a DNA ligase I-deficient human cell line | Q40419421 | ||
| DNA polymerase clamp shows little turnover at established replication sites but sequential de novo assembly at adjacent origin clusters | Q40680783 | ||
| Transient association of Ku with nuclear substrates characterized using fluorescence photobleaching | Q40749007 | ||
| Mapping and use of a sequence that targets DNA ligase I to sites of DNA replication in vivo | Q41860526 | ||
| Stimulation of eukaryotic flap endonuclease-1 activities by proliferating cell nuclear antigen (PCNA) is independent of its in vitro interaction via a consensus PCNA binding region | Q43690417 | ||
| Specificity of protein interactions mediated by BRCT domains of the XRCC1 DNA repair protein | Q44563211 | ||
| Solution structure and DNA binding of the zinc-finger domain from DNA ligase IIIalpha | Q45003545 | ||
| Proliferating Cell Nuclear Antigen Facilitates Excision in Long-patch Base Excision Repair | Q57706957 | ||
| Specific function of DNA ligase I in simian virus 40 DNA replication by human cell-free extracts is mediated by the amino-terminal non-catalytic domain | Q95824210 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 3523-3532 | |
| P577 | publication date | 2006-07-19 | |
| P1433 | published in | Nucleic Acids Research | Q135122 |
| P1476 | title | Differential recruitment of DNA Ligase I and III to DNA repair sites | |
| P478 | volume | 34 |
| Q34795353 | A fluorescent two-hybrid assay for direct visualization of protein interactions in living cells |
| Q47772207 | Application of Laser Micro-irradiation for Examination of Single and Double Strand Break Repair in Mammalian Cells |
| Q33557365 | Binding of MBD proteins to DNA blocks Tet1 function thereby modulating transcriptional noise |
| Q33532337 | Biological dose estimation of UVA laser microirradiation utilizing charged particle-induced protein foci |
| Q37122200 | Brain capacity for repair of oxidatively damaged DNA and preservation of neuronal function |
| Q37446749 | CTG/CAG repeat instability is modulated by the levels of human DNA ligase I and its interaction with proliferating cell nuclear antigen: a distinction between replication and slipped-DNA repair |
| Q90195204 | Cellular Stress Responses in Radiotherapy |
| Q24296083 | Crucial role for DNA ligase III in mitochondria but not in Xrcc1-dependent repair |
| Q64388374 | DNA Ligase 1 is an essential mediator of sister chromatid telomere fusions in G2 cell cycle phase |
| Q50287460 | DNA ligase I ligates single stranded nick in double stranded DNA |
| Q35097944 | DNA ligase III acts as a DNA strand break sensor in the cellular orchestration of DNA strand break repair |
| Q21144955 | DNA ligase III promotes alternative nonhomologous end-joining during chromosomal translocation formation |
| Q37201500 | Damage response of XRCC1 at sites of DNA single strand breaks is regulated by phosphorylation and ubiquitylation after degradation of poly(ADP-ribose). |
| Q34325962 | Detection of ligation products of DNA linkers with 5'-OH ends by denaturing PAGE silver stain |
| Q34555730 | Direct homo- and hetero-interactions of MeCP2 and MBD2. |
| Q35878514 | Disconnecting XRCC1 and DNA ligase III |
| Q35813621 | Distinct kinetics of DNA repair protein accumulation at DNA lesions and cell cycle-dependent formation of γH2AX- and NBS1-positive repair foci |
| Q41894800 | Dynamic as well as stable protein interactions contribute to genome function and maintenance |
| Q33304975 | Feedback-regulated poly(ADP-ribosyl)ation by PARP-1 is required for rapid response to DNA damage in living cells |
| Q37772648 | Functional nuclear architecture studied by microscopy: present and future |
| Q50287380 | Gap-filling DNA synthesis in SDSA |
| Q24298591 | Human RECQL5 participates in the removal of endogenous DNA damage |
| Q64387119 | Interplay between DNA Polymerases and DNA Ligases: Influence on Substrate Channeling and the Fidelity of DNA Ligation |
| Q37149786 | JWA regulates XRCC1 and functions as a novel base excision repair protein in oxidative-stress-induced DNA single-strand breaks |
| Q34343255 | Kinetics of endogenous mouse FEN1 in base excision repair. |
| Q42191835 | Localization of MLH3 at the centrosomes |
| Q40094347 | MeCP2 interacts with HP1 and modulates its heterochromatin association during myogenic differentiation |
| Q39293345 | Mechanisms of DNA damage, repair, and mutagenesis |
| Q47154064 | Meta-analysis of DNA double-strand break response kinetics |
| Q35690306 | Micro-irradiation tools to visualize base excision repair and single-strand break repair |
| Q26786419 | Microirradiation techniques in radiobiological research |
| Q27342027 | Nanoscale histone localization in live cells reveals reduced chromatin mobility in response to DNA damage |
| Q37057512 | Optimal numbers of residues in linkers of DNA polymerase I, T7 primase and DNA polymerase IV |
| Q24653009 | PARP inhibition versus PARP-1 silencing: different outcomes in terms of single-strand break repair and radiation susceptibility |
| Q55615916 | PARP1-dependent recruitment of the FBXL10-RNF68-RNF2 ubiquitin ligase to sites of DNA damage controls H2A.Z loading. |
| Q24619372 | Partial complementation of a DNA ligase I deficiency by DNA ligase III and its impact on cell survival and telomere stability in mammalian cells |
| Q57885869 | Phosphorylation of Thyroid Hormone Receptor-associated Nuclear Receptor Corepressor Holocomplex by the DNA-dependent Protein Kinase Enhances Its Histone Deacetylase Activity |
| Q38770753 | Poly(ADP-ribosyl)ation of Methyl CpG Binding Domain Protein 2 Regulates Chromatin Structure. |
| Q30831106 | Recruitment of DNA repair synthesis machinery to sites of DNA damage/repair in living human cells |
| Q33388647 | Recruitment of RNA polymerase II cofactor PC4 to DNA damage sites |
| Q45314247 | Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) |
| Q33310274 | Sequential recruitment of the repair factors during NER: the role of XPG in initiating the resynthesis step. |
| Q29615347 | Single-strand break repair and genetic disease |
| Q92761157 | Systematic analysis of DNA damage induction and DNA repair pathway activation by continuous wave visible light laser micro-irradiation |
| Q42761123 | TET-mediated oxidation of methylcytosine causes TDG or NEIL glycosylase dependent gene reactivation |
| Q30575324 | Targeting and tracing of specific DNA sequences with dTALEs in living cells. |
| Q26782011 | The Role of the COP9 Signalosome and Neddylation in DNA Damage Signaling and Repair |
| Q90542763 | The Sole DNA Ligase in Entamoeba histolytica Is a High-Fidelity DNA Ligase Involved in DNA Damage Repair |
| Q36562914 | The highly conserved nuclear lamin Ig-fold binds to PCNA: its role in DNA replication |
| Q35943962 | The nucleosome binding protein HMGN1 interacts with PCNA and facilitates its binding to chromatin |
| Q92711495 | Tunable light and drug induced depletion of target proteins |
| Q28087342 | Ubiquitylation, neddylation and the DNA damage response |
| Q28483649 | Versatile toolbox for high throughput biochemical and functional studies with fluorescent fusion proteins |
| Q33299607 | XRCC1 and PCNA are loading platforms with distinct kinetic properties and different capacities to respond to multiple DNA lesions |
| Q33970153 | XRCC1 coordinates disparate responses and multiprotein repair complexes depending on the nature and context of the DNA damage |
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