Pages that link to "Q22253994"
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The following pages link to Ku complex interacts with and stimulates the Werner protein (Q22253994):
Displayed 50 items.
- Werner syndrome RecQ like helicase (Q6591532) (← links)
- X-ray repair cross complementing 5 (Q21116582) (← links)
- X-ray repair cross complementing 6 (Q21116645) (← links)
- A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA (Q24291177) (← links)
- Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity (Q24291787) (← links)
- Biochemical characterization of metnase's endonuclease activity and its role in NHEJ repair (Q24299755) (← links)
- APLF promotes the assembly and activity of non-homologous end joining protein complexes (Q24304501) (← links)
- WRN controls formation of extrachromosomal telomeric circles and is required for TRF2DeltaB-mediated telomere shortening (Q24307499) (← links)
- Werner syndrome protein phosphorylation by abl tyrosine kinase regulates its activity and distribution (Q24318820) (← links)
- The spectrum of WRN mutations in Werner syndrome patients (Q24324195) (← links)
- Physical and functional interactions between Werner syndrome helicase and mismatch-repair initiation factors (Q24338232) (← links)
- Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus (Q24538401) (← links)
- Processing of DNA for nonhomologous end-joining by cell-free extract (Q24556610) (← links)
- Analysis of the unwinding activity of the dimeric RECQ1 helicase in the presence of human replication protein A (Q24563590) (← links)
- Up-regulation of WRN and DNA ligase IIIalpha in chronic myeloid leukemia: consequences for the repair of DNA double-strand breaks (Q24619366) (← links)
- Roles of Werner syndrome protein in protection of genome integrity (Q24643050) (← links)
- Model of human aging: recent findings on Werner's and Hutchinson-Gilford progeria syndromes (Q24644033) (← links)
- Roles of RECQ helicases in recombination based DNA repair, genomic stability and aging (Q24646853) (← links)
- Werner protein recruits DNA polymerase delta to the nucleolus (Q24674594) (← links)
- Human premature aging, DNA repair and RecQ helicases (Q24680996) (← links)
- A conserved and species-specific functional interaction between the Werner syndrome-like exonuclease atWEX and the Ku heterodimer in Arabidopsis (Q24810688) (← links)
- The interaction site of Flap Endonuclease-1 with WRN helicase suggests a coordination of WRN and PCNA (Q24814897) (← links)
- Triplex targeted genomic crosslinks enter separable deletion and base substitution pathways (Q24816234) (← links)
- The biology of DHX9 and its potential as a therapeutic target (Q26749166) (← links)
- The RNA helicase A in malignant transformation (Q26765181) (← links)
- The role of RecQ helicases in non-homologous end-joining (Q26829119) (← links)
- DNA-PK: a dynamic enzyme in a versatile DSB repair pathway (Q26866928) (← links)
- Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice (Q27313716) (← links)
- RecQ helicases in DNA double strand break repair and telomere maintenance (Q27692685) (← links)
- Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions (Q28274227) (← links)
- WRN regulates pathway choice between classical and alternative non-homologous end joining (Q30831557) (← links)
- Telomere instability in a human tumor cell line expressing a dominant-negative WRN protein (Q30953207) (← links)
- Proteomics of herpes simplex virus replication compartments: association of cellular DNA replication, repair, recombination, and chromatin remodeling proteins with ICP8. (Q33202888) (← links)
- Reconstitution of the mammalian DNA double-strand break end-joining reaction reveals a requirement for an Mre11/Rad50/NBS1-containing fraction (Q33559700) (← links)
- Selective blockage of the 3'-->5' exonuclease activity of WRN protein by certain oxidative modifications and bulky lesions in DNA. (Q33616272) (← links)
- Nonhomologous end joining: a good solution for bad ends (Q33625010) (← links)
- Werner syndrome exonuclease catalyzes structure-dependent degradation of DNA. (Q33786685) (← links)
- Delineation of WRN helicase function with EXO1 in the replicational stress response (Q33945750) (← links)
- Cooperation of DNA-PKcs and WRN helicase in the maintenance of telomeric D-loops (Q33965717) (← links)
- The Sgs1 helicase of Saccharomyces cerevisiae inhibits retrotransposition of Ty1 multimeric arrays (Q33969162) (← links)
- Identification of a coiled coil in werner syndrome protein that facilitates multimerization and promotes exonuclease processivity (Q34055963) (← links)
- DNA repair deficiency in neurodegeneration. (Q34183328) (← links)
- Chromatin remodeling, DNA damage repair and aging. (Q34342179) (← links)
- RECQ helicase RECQL4 participates in non-homologous end joining and interacts with the Ku complex (Q34425537) (← links)
- Expression profile of Caenorhabditis elegans mutant for the Werner syndrome gene ortholog reveals the impact of vitamin C on development to increase life span. (Q34460106) (← links)
- Telomeres, chromosome instability and cancer (Q34595437) (← links)
- Collaboration of Werner syndrome protein and BRCA1 in cellular responses to DNA interstrand cross-links (Q34623681) (← links)
- Human RECQ1 interacts with Ku70/80 and modulates DNA end-joining of double-strand breaks (Q34708378) (← links)
- Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing (Q34786864) (← links)
- Developmental modulation of nonhomologous end joining in Caenorhabditis elegans (Q34897855) (← links)