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Werner syndrome protein is regulated and phosphorylated by DNA-dependent protein kinase.
J Biol Chem. 2001 Oct 12;276(41):38242-8
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Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity.
EMBO J. 2001 Oct 15;20(20):5791-801
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Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation.
J Biol Chem. 2002 May 24;277(21):18291-302
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Junction of RecQ helicase biochemistry and human disease.
J Biol Chem. 2004 Apr 30;279(18):18099-102
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Linkage between Werner syndrome protein and the Mre11 complex via Nbs1.
J Biol Chem. 2004 May 14;279(20):21169-76
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The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine: implications for WRN function.
DNA Repair (Amst). 2004 Jun 3;3(6):629-38
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Physical and functional interaction between the Bloom's syndrome gene product and the largest subunit of chromatin assembly factor 1.
Mol Cell Biol. 2004 Jun;24(11):4710-9
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The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2.
Mol Cell. 2004 Jun 18;14(6):763-74
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Human RECQ5beta, a protein with DNA helicase and strand-annealing activities in a single polypeptide.
EMBO J. 2004 Jul 21;23(14):2882-91
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A retarded rate of DNA chain growth in Bloom's syndrome.
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Functional and physical interaction between WRN helicase and human replication protein A.
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The Werner syndrome protein is involved in RNA polymerase II transcription.
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p14 Arf promotes small ubiquitin-like modifier conjugation of Werners helicase.
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BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity.
EMBO J. 2005 Apr 6;24(7):1465-76
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Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome.
Cell. 2005 Jun 17;121(6):887-98
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Biochemical analysis of the DNA unwinding and strand annealing activities catalyzed by human RECQ1.
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Current advances in unraveling the function of the Werner syndrome protein.
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POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates.
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The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability.
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Phosphorylation of BLM, dissociation from topoisomerase IIIalpha, and colocalization with gamma-H2AX after topoisomerase I-induced replication damage.
Mol Cell Biol. 2005 Oct;25(20):8925-37
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Werner protein protects nonproliferating cells from oxidative DNA damage.
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Gene expression and DNA repair in progeroid syndromes and human aging.
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Repair of formamidopyrimidines in DNA involves different glycosylases: role of the OGG1, NTH1, and NEIL1 enzymes.
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The Pso4 mRNA splicing and DNA repair complex interacts with WRN for processing of DNA interstrand cross-links.
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Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome.
DNA Repair (Amst). 2006 Feb 3;5(2):172-80
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The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta.
Nucleic Acids Res. 2006;34(2):745-54
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Collaboration of Werner syndrome protein and BRCA1 in cellular responses to DNA interstrand cross-links.
Nucleic Acids Res. 2006;34(9):2751-60
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The spectrum of WRN mutations in Werner syndrome patients.
Hum Mutat. 2006 Jun;27(6):558-67
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Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins.
J Biol Chem. 2002 Jun 14;277(24):22035-44
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A nucleolar targeting sequence in the Werner syndrome protein resides within residues 949-1092.
J Cell Sci. 2002 Oct 15;115(Pt 20):3901-7
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Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases.
J Biol Chem. 2002 Oct 25;277(43):41110-9
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DNA damage-induced translocation of the Werner helicase is regulated by acetylation.
J Biol Chem. 2002 Dec 27;277(52):50934-40
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RecQ helicases: caretakers of the genome.
Nat Rev Cancer. 2003 Mar;3(3):169-78
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Werner syndrome protein phosphorylation by abl tyrosine kinase regulates its activity and distribution.
Mol Cell Biol. 2003 Sep;23(18):6385-95
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WRN interacts physically and functionally with the recombination mediator protein RAD52.
J Biol Chem. 2003 Sep 19;278(38):36476-86
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Gene expression profiling in Werner syndrome closely resembles that of normal aging.
Proc Natl Acad Sci U S A. 2003 Oct 14;100(21):12259-64
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Werner protein stimulates topoisomerase I DNA relaxation activity.
Cancer Res. 2003 Nov 1;63(21):7136-46
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Central role for the Werner syndrome protein/poly(ADP-ribose) polymerase 1 complex in the poly(ADP-ribosyl)ation pathway after DNA damage.
Mol Cell Biol. 2003 Dec;23(23):8601-13
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Functional interaction between the Bloom's syndrome helicase and the RAD51 paralog, RAD51L3 (RAD51D).
J Biol Chem. 2003 Nov 28;278(48):48357-66
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The Bloom's syndrome helicase suppresses crossing over during homologous recombination.
Nature. 2003 Dec 18;426(6968):870-4
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Werner syndrome protein contains three structure-specific DNA binding domains.
J Biol Chem. 2003 Dec 26;278(52):52997-3006
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Stimulation of flap endonuclease-1 by the Bloom's syndrome protein.
J Biol Chem. 2004 Mar 12;279(11):9847-56
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Enzymatic mechanism of the WRN helicase/nuclease.
Methods Enzymol. 2006;409:52-85
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Analysis of the DNA unwinding activity of RecQ family helicases.
Methods Enzymol. 2006;409:86-100
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A novel function of DNA repair molecule Nbs1 in terminal differentiation of the lens fibre cells and cataractogenesis.
DNA Repair (Amst). 2006 Aug 13;5(8):885-93
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The Bloom's syndrome helicase can promote the regression of a model replication fork.
J Biol Chem. 2006 Aug 11;281(32):22839-46
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Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability.
Biochem J. 2006 Sep 15;398(3):319-37
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Nucleic Acids Res. 2006;34(15):4106-14
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A role for WRN in telomere-based DNA damage responses.
Proc Natl Acad Sci U S A. 2006 Oct 10;103(41):15073-8
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Human RECQ5beta helicase promotes strand exchange on synthetic DNA structures resembling a stalled replication fork.
Nucleic Acids Res. 2006;34(18):5217-31
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Synthesis, DNA polymerase incorporation, and enzymatic phosphate hydrolysis of formamidopyrimidine nucleoside triphosphates.
J Am Chem Soc. 2006 Nov 15;128(45):14606-11
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DNA helicases required for homologous recombination and repair of damaged replication forks.
Annu Rev Genet. 2006;40:279-306
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Dynamic roles for G4 DNA in the biology of eukaryotic cells.
Nat Struct Mol Biol. 2006 Dec;13(12):1055-9
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Werner syndrome protein participates in a complex with RAD51, RAD54, RAD54B and ATR in response to ICL-induced replication arrest.
J Cell Sci. 2006 Dec 15;119(Pt 24):5137-46
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A positive involvement of RecQL4 in UV-induced S-phase arrest.
DNA Cell Biol. 2006 Dec;25(12):696-703
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DNA Cell Biol. 2007 Jan;26(1):1-18
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Different quaternary structures of human RECQ1 are associated with its dual enzymatic activity.
PLoS Biol. 2007 Feb;5(2):e20
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Telomere dysfunction as a cause of genomic instability in Werner syndrome.
Proc Natl Acad Sci U S A. 2007 Feb 13;104(7):2205-10
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WRN exonuclease activity is blocked by DNA termini harboring 3' obstructive groups.
Mech Ageing Dev. 2007 Mar;128(3):259-66
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J Cell Sci. 2007 Mar 1;120(Pt 5):713-21
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The molecular role of the Rothmund-Thomson-, RAPADILINO- and Baller-Gerold-gene product, RECQL4: recent progress.
Cell Mol Life Sci. 2007 Apr;64(7-8):796-802
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The broken genome: genetic and pharmacologic approaches to breaking DNA.
Ann Med. 2007;39(3):208-18
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The Werner syndrome protein is required for recruitment of chromatin assembly factor 1 following DNA damage.
Oncogene. 2007 May 31;26(26):3811-22
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Role of the BLM helicase in replication fork management.
DNA Repair (Amst). 2007 Jul 1;6(7):936-44
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Werner syndrome protein interacts functionally with translesion DNA polymerases.
Proc Natl Acad Sci U S A. 2007 Jun 19;104(25):10394-9
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Epigenetic gene silencing in cancer: the DNA hypermethylome.
Hum Mol Genet. 2007 Apr 15;16 Spec No 1:R50-9
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Werner syndrome protein prevents DNA breaks upon chromatin structure alteration.
Aging Cell. 2007 Aug;6(4):471-81
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Role for the Werner syndrome protein in the promotion of tumor cell growth.
Mech Ageing Dev. 2007 Jul-Aug;128(7-8):423-36
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Interplay between wrn and the checkpoint in s-phase.
Ital J Biochem. 2007 Jun;56(2):130-40
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The human Werner syndrome protein stimulates repair of oxidative DNA base damage by the DNA glycosylase NEIL1.
J Biol Chem. 2007 Sep 7;282(36):26591-602
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The impact of a negligent G2/M checkpoint on genomic instability and cancer induction.
Nat Rev Cancer. 2007 Nov;7(11):861-9
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RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments.
Genes Dev. 2007 Dec 1;21(23):3073-84
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The mechanism of human nonhomologous DNA end joining.
J Biol Chem. 2008 Jan 4;283(1):1-5
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A RECQ5-RNA polymerase II association identified by targeted proteomic analysis of human chromatin.
Proc Natl Acad Sci U S A. 2008 Jun 24;105(25):8580-4
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Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer.
Proc Natl Acad Sci U S A. 2006 Jun 6;103(23):8822-7
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Ku complex interacts with and stimulates the Werner protein.
Genes Dev. 2000 Apr 15;14(8):907-12
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Selective blockage of the 3'-->5' exonuclease activity of WRN protein by certain oxidative modifications and bulky lesions in DNA.
Nucleic Acids Res. 2000 Jul 15;28(14):2762-70
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Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity.
J Biol Chem. 2000 Aug 4;275(31):23500-8
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Werner syndrome exonuclease catalyzes structure-dependent degradation of DNA.
Nucleic Acids Res. 2000 Sep 1;28(17):3260-8
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DNA repair mechanisms.
Maturitas. 2001 Feb 28;38(1):17-22; discussion 22-3
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Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence.
J Biol Chem. 2001 May 11;276(19):16439-46
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Werner syndrome cells are sensitive to DNA cross-linking drugs.
FASEB J. 2001 May;15(7):1224-6
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Potential role for the BLM helicase in recombinational repair via a conserved interaction with RAD51.
J Biol Chem. 2001 Jun 1;276(22):19375-81
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The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases.
Nucleic Acids Res. 2001 Jul 1;29(13):2843-9
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