scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Mayura Meerang | Q45990859 |
P2093 | author name string | Kristijan Ramadan | |
P2860 | cites work | HERC2 coordinates ubiquitin-dependent assembly of DNA repair factors on damaged chromosomes | Q24292928 |
A role for the deubiquitinating enzyme USP28 in control of the DNA-damage response | Q24299489 | ||
RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins | Q24300411 | ||
RNF8 transduces the DNA-damage signal via histone ubiquitylation and checkpoint protein assembly | Q24300428 | ||
The MMS22L-TONSL complex mediates recovery from replication stress and homologous recombination | Q24306030 | ||
Identification of the MMS22L-TONSL complex that promotes homologous recombination | Q24306091 | ||
A genome-wide camptothecin sensitivity screen identifies a mammalian MMS22L-NFKBIL2 complex required for genomic stability | Q24306107 | ||
The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage | Q24309181 | ||
RNF168 binds and amplifies ubiquitin conjugates on damaged chromosomes to allow accumulation of repair proteins | Q24309287 | ||
RNAi-based screening identifies the Mms22L-Nfkbil2 complex as a novel regulator of DNA replication in human cells | Q24309443 | ||
PA200, a nuclear proteasome activator involved in DNA repair | Q24536971 | ||
ATM damage response and XLF repair factor are functionally redundant in joining DNA breaks | Q24596775 | ||
DNA resection in eukaryotes: deciding how to fix the break | Q24603592 | ||
The DNA-damage response in human biology and disease | Q24606586 | ||
Mammalian SUMO E3-ligases PIAS1 and PIAS4 promote responses to DNA double-strand breaks | Q24608599 | ||
A PP4-phosphatase complex dephosphorylates gamma-H2AX generated during DNA replication | Q24626425 | ||
E3 ligase Rad18 promotes monoubiquitination rather than ubiquitin chain formation by E2 enzyme Rad6 | Q27667304 | ||
RING domain E3 ubiquitin ligases | Q27860546 | ||
The DNA Damage Response: Making It Safe to Play with Knives | Q27861055 | ||
Inhibition of proteasomal degradation of rpn4 impairs nonhomologous end-joining repair of DNA double-strand breaks | Q27929905 | ||
Proteasome nuclear activity affects chromosome stability by controlling the turnover of Mms22, a protein important for DNA repair | Q27932933 | ||
Regulatory mechanisms controlling biogenesis of ubiquitin and the proteasome | Q27934022 | ||
The DNA damage response: putting checkpoints in perspective | Q28131713 | ||
Breaking the chains: structure and function of the deubiquitinases | Q28131738 | ||
SIAH-1 interacts with CtIP and promotes its degradation by the proteasome pathway | Q28189105 | ||
Regulation of DNA double-strand break repair pathway choice | Q28262730 | ||
Genomic instability--an evolving hallmark of cancer | Q28274009 | ||
Characterization of homologous recombination induced by replication inhibition in mammalian cells | Q28343741 | ||
Recognition and processing of ubiquitin-protein conjugates by the proteasome | Q29547616 | ||
Ubiquitin-binding domains - from structures to functions | Q29614829 | ||
Building ubiquitin chains: E2 enzymes at work | Q29619578 | ||
A dynamic ubiquitin equilibrium couples proteasomal activity to chromatin remodeling | Q30480384 | ||
Disassembly of MDC1 foci is controlled by ubiquitin-proteasome-dependent degradation | Q39945678 | ||
Inhibition of proteasome activity induces concerted expression of proteasome genes and de novo formation of Mammalian proteasomes | Q40658264 | ||
Ultraviolet radiation-induced ubiquitination and proteasomal degradation of the large subunit of RNA polymerase II. Implications for transcription-coupled DNA repair | Q41056225 | ||
The interface between the ubiquitin family and the DNA damage response | Q42331790 | ||
The structure-specific endonuclease Mus81 contributes to replication restart by generating double-strand DNA breaks | Q46952804 | ||
CHIP-mediated degradation and DNA damage-dependent stabilization regulate base excision repair proteins. | Q51574887 | ||
HERC2 is an E3 ligase that targets BRCA1 for degradation. | Q53312505 | ||
Inhibitors of the proteasome suppress homologous DNA recombination in mammalian cells. | Q53527230 | ||
Proteasome Involvement in the Repair of DNA Double-Strand Breaks | Q57209659 | ||
Ubiquitin linkages make a difference | Q57269932 | ||
Cdc48/p97 promotes reformation of the nucleus by extracting the kinase Aurora B from chromatin | Q59096950 | ||
Genetic analysis of BRCA1 ubiquitin ligase activity and its relationship to breast cancer susceptibility | Q33231274 | ||
Proteasome function is required for DNA damage response and fanconi anemia pathway activation | Q33292777 | ||
Turnover of BRCA1 involves in radiation-induced apoptosis | Q33789102 | ||
Mechanisms of double-strand break repair in somatic mammalian cells | Q34317108 | ||
NF-kappa B as a therapeutic target in multiple myeloma | Q34521393 | ||
Ku80 removal from DNA through double strand break-induced ubiquitylation | Q34804030 | ||
BRCA1 ubiquitinates its phosphorylation-dependent binding partner CtIP | Q34863348 | ||
Proteasome inhibitors in cancer therapy | Q34939959 | ||
Crosstalk between histone modifications during the DNA damage response. | Q34973824 | ||
Nucleotide excision repair-induced H2A ubiquitination is dependent on MDC1 and RNF8 and reveals a universal DNA damage response | Q35006034 | ||
Intracellular localization of proteasomes | Q35097620 | ||
The development of proteasome inhibitors as anticancer drugs | Q35773857 | ||
RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signaling | Q36089253 | ||
Ubc13/Rnf8 ubiquitin ligases control foci formation of the Rap80/Abraxas/Brca1/Brcc36 complex in response to DNA damage | Q36696336 | ||
Role for proteasome activator PA200 and postglutamyl proteasome activity in genomic stability. | Q36945044 | ||
The NBS1-ATM connection revisited | Q36946417 | ||
Control of DNA polymerase lambda stability by phosphorylation and ubiquitination during the cell cycle | Q36946963 | ||
Mechanisms of dealing with DNA damage-induced replication problems | Q37335165 | ||
RAD18 transmits DNA damage signalling to elicit homologous recombination repair | Q37344711 | ||
Regulatory ubiquitylation in response to DNA double-strand breaks | Q37397281 | ||
Distinct ubiquitin ligases act sequentially for RNA polymerase II polyubiquitylation | Q37424165 | ||
Targeting the ubiquitin system in cancer therapy | Q37424802 | ||
Principles of ubiquitin and SUMO modifications in DNA repair. | Q37424808 | ||
The ubiquitin landscape at DNA double-strand breaks | Q37425595 | ||
The proteasomal system. | Q37446143 | ||
Proteasome-dependent processing of topoisomerase I-DNA adducts into DNA double strand breaks at arrested replication forks | Q37459929 | ||
DUBs and cancer: the role of deubiquitinating enzymes as oncogenes, non-oncogenes and tumor suppressors | Q37485753 | ||
Targeting the DNA damage response in cancer | Q37526958 | ||
Physical and functional association of RNA polymerase II and the proteasome | Q37645638 | ||
The ubiquitous role of ubiquitin in the DNA damage response | Q37807639 | ||
Coping with DNA double strand breaks | Q37813243 | ||
The anaphase-promoting complex/cyclosome controls repair and recombination by ubiquitylating Rhp54 in fission yeast | Q39024019 | ||
The SUMO modification pathway is involved in the BRCA1 response to genotoxic stress. | Q39762239 | ||
Mammalian 26S proteasomes remain intact during protein degradation | Q39924238 | ||
P433 | issue | 18 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | ubiquitin-proteasome system | Q47175589 |
P304 | page(s) | 2868-2875 | |
P577 | publication date | 2011-04-28 | |
P1433 | published in | FEBS Letters | Q1388051 |
P1476 | title | Degradation-linked ubiquitin signal and proteasome are integral components of DNA double strand break repair: New perspectives for anti-cancer therapy | |
P478 | volume | 585 |
Q36545969 | Bortezomib-mediated down-regulation of telomerase and disruption of telomere homeostasis contributes to apoptosis of malignant cells |
Q26773104 | Colorectal Carcinogenesis, Radiation Quality, and the Ubiquitin-Proteasome Pathway |
Q28258706 | Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system |
Q26850193 | Improving the efficacy of chemoradiation with targeted agents |
Q35737515 | Involvement of the nuclear proteasome activator PA28γ in the cellular response to DNA double-strand breaks |
Q35200009 | Loss of urokinase receptor sensitizes cells to DNA damage and delays DNA repair |
Q28080823 | NKG2D and DNAM-1 Ligands: Molecular Targets for NK Cell-Mediated Immunotherapeutic Intervention in Multiple Myeloma |
Q90580737 | Precoce and opposite response of proteasome activity after acute or chronic exposure of C. elegans to γ-radiation |
Q47113405 | Proteome Stability as a Key Factor of Genome Integrity |
Q35161624 | Regulation of the DNA damage response by ubiquitin conjugation |
Q36804013 | Role of p97/VCP (Cdc48) in genome stability |
Q28246908 | Should I stay or should I go: VCP/p97-mediated chromatin extraction in the DNA damage response |
Q39371142 | Structure and Function of p97 and Pex1/6 Type II AAA+ Complexes. |
Q42276650 | Termination of DNA replication forks: "Breaking up is hard to do". |
Q34226618 | The ubiquitin-selective segregase VCP/p97 orchestrates the response to DNA double-strand breaks. |
Q53181384 | p97/VCP- and Lys48-linked polyubiquitination form a new signaling pathway in DNA damage response. |
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