Pages that link to "Q24291177"

The following pages link to A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA (Q24291177):

Displaying 49 items.

• Werner syndrome RecQ like helicase (Q6591532) (← links)
• X-ray repair cross complementing 6 (Q21116645) (← links)
• p53 Modulates the exonuclease activity of Werner syndrome protein (Q24291371) (← links)
• Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly(ADP-ribose) polymerase-1 (Q24305550) (← links)
• Asymmetry of DNA replication fork progression in Werner's syndrome (Q24311409) (← links)
• WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing (Q24318651) (← links)
• Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus (Q24538401) (← 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)
• Mycobacterial UvrD1 is a Ku-dependent DNA helicase that plays a role in multiple DNA repair events, including double-strand break repair (Q28486710) (← links)
• RecQ helicases: caretakers of the genome (Q29618390) (← links)
• Coordinate action of the helicase and 3' to 5' exonuclease of Werner syndrome protein (Q30725106) (← links)
• Reconstitution of the mammalian DNA double-strand break end-joining reaction reveals a requirement for an Mre11/Rad50/NBS1-containing fraction (Q33559700) (← links)
• Nonhomologous end joining: a good solution for bad ends (Q33625010) (← links)
• BCR/ABL modifies the kinetics and fidelity of DNA double-strand breaks repair in hematopoietic cells (Q33796384) (← links)
• Non-homologous end joining: emerging themes and unanswered questions (Q33854272) (← links)
• Functional interaction between DNA-PKcs and telomerase in telomere length maintenance (Q34369713) (← links)
• RECQ helicase RECQL4 participates in non-homologous end joining and interacts with the Ku complex (Q34425537) (← links)
• Roles of the Werner syndrome protein in pathways required for maintenance of genome stability (Q34519481) (← links)
• RecQ helicases and cellular responses to DNA damage (Q34994566) (← links)
• RecQ helicases: suppressors of tumorigenesis and premature aging. (Q35152970) (← links)
• Mending the Break: Two DNA Double-Strand Break Repair Machines in Eukaryotes (Q35543795) (← links)
• The Werner Syndrome Helicase-Nuclease--One Protein, Many Mysteries (Q35577695) (← links)
• Developing master keys to brain pathology, cancer and aging from the structural biology of proteins controlling reactive oxygen species and DNA repair. (Q35865533) (← links)
• WRN exonuclease activity is blocked by DNA termini harboring 3' obstructive groups (Q35895249) (← links)
• Analysis of the Xenopus Werner syndrome protein in DNA double-strand break repair (Q36320325) (← links)
• Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability (Q36573932) (← links)
• WRN Exonuclease activity is blocked by specific oxidatively induced base lesions positioned in either DNA strand (Q36859249) (← links)
• Werner syndrome protein, WRN, protects cells from DNA damage induced by the benzene metabolite hydroquinone (Q37091544) (← links)
• RecQ helicases; at the crossroad of genome replication, repair, and recombination (Q37938856) (← links)
• Resolution of complex ends by Nonhomologous end joining - better to be lucky than good? (Q38070431) (← links)
• Bloom's syndrome: Why not premature aging?: A comparison of the BLM and WRN helicases (Q38847700) (← links)
• BCR/ABL stimulates WRN to promote survival and genomic instability. (Q39625105) (← links)
• WRN protein and Werner syndrome (Q39775619) (← links)
• Inhibition of the 5' to 3' exonuclease activity of hEXO1 by 8-oxoguanine (Q39991083) (← links)
• The Ku-binding motif is a conserved module for recruitment and stimulation of non-homologous end-joining proteins (Q40150704) (← links)
• DNA damage-induced translocation of the Werner helicase is regulated by acetylation (Q40696914) (← links)
• Werner and Bloom helicases are involved in DNA repair in a complementary fashion (Q40751512) (← links)
• Depletion of Werner helicase results in mitotic hyperrecombination and pleiotropic homologous and nonhomologous recombination phenotypes (Q42199897) (← links)
• Biochemical characterization of an exonuclease from Arabidopsis thaliana reveals similarities to the DNA exonuclease of the human Werner syndrome protein (Q42606844) (← links)
• DNA repair and the origins of urinary oxidized 2'-deoxyribonucleosides. (Q43045076) (← links)
• Coordinated assembly of Ku and p460 subunits of the DNA-dependent protein kinase on DNA ends is necessary for XRCC4-ligase IV recruitment. (Q44290667) (← links)
• Effect of bulky lesions on DNA: solution structure of a DNA duplex containing a cholesterol adduct (Q44816881) (← links)
• In vivo prooxidant state in Werner syndrome (WS): results from three WS patients and two WS heterozygotes (Q46612416) (← links)
• Werner syndrome protein, the MRE11 complex and ATR: menage-à-trois in guarding genome stability during DNA replication? (Q48026242) (← links)
• The Werner syndrome protein is required for recruitment of chromatin assembly factor 1 following DNA damage (Q48336289) (← links)
• DNase I footprinting and enhanced exonuclease function of the bipartite Werner syndrome protein (WRN) bound to partially melted duplex DNA (Q77211470) (← links)
• Altered nuclear functions in progeroid syndromes: a paradigm for aging research (Q82300194) (← links)