Citations for
1WRN
Acidic domain of WRNp is critical for autophagy and up-regulates age associated proteins.
Maity J, Das B, Bohr VA, Karmakar P.
DNA Repair (Amst) 68:1-11. doi: 10.1016/j.dnarep.2018.05.003. Epub 2018 May 18. 2018
2RECQL5, WRN
RECQL5 plays co-operative and complementary roles with WRN syndrome helicase.
Popuri V, Huang J, Ramamoorthy M, Tadokoro T, Croteau DL, Bohr VA.
Nucleic Acids Res 45(3):1566. doi: 10.1093/nar/gkw1216. 2017
3WRN
Single-molecule studies reveal reciprocating of WRN helicase core along ssDNA during DNA unwinding.
Wu WQ, Hou XM, Zhang B, Fossé P, René B, Mauffret O, Li M, Dou SX, Xi XG.
Sci Rep 7:43954. doi: 10.1038/srep43954. 2017
4WRN
Residues in the RecQ C-terminal Domain of the Human Werner Syndrome Helicase Are Involved in Unwinding G-quadruplex DNA.
Ketkar A, Voehler M, Mukiza T, Eoff RL.
J Biol Chem 292(8):3154-3163. doi: 10.1074/jbc.M116.767699. Epub 2017 Jan 9. 2017
5BLM, WRN
Bloom's syndrome: Why not premature aging?: A comparison of the BLM and WRN helicases.
de Renty C, Ellis NA.
Ageing Res Rev 33:36-51. doi: 10.1016/j.arr.2016.05.010. Epub 2016 May 26. Review. 2017
6WRN
WRN regulates pathway choice between classical and alternative non-homologous end joining.
Shamanna RA, Lu H, de Freitas JK, Tian J, Croteau DL, Bohr VA.
Nat Commun 7:13785. doi: 10.1038/ncomms13785. 2016
7CDK1, DNA2, EXO1, WRN
CDK1 phosphorylates WRN at collapsed replication forks.
Palermo V, Rinalducci S, Sanchez M, Grillini F, Sommers JA, Brosh RM Jr, Zolla L, Franchitto A, Pichierri P.
Nat Commun 7:12880. doi: 10.1038/ncomms12880. 2016
8BLM, DNA2, WRN
Human DNA2 possesses a cryptic DNA unwinding activity that functionally integrates with BLM or WRN helicases.
Pinto C, Kasaciunaite K, Seidel R, Cejka P.
Elife 5. pii: e18574. doi: 10.7554/eLife.18574. 2016
9WRN
Absence of premature senescence in Werner's syndrome keratinocytes.
Ibrahim B, Sheerin AN, Jennert-Burston K, Bird JL, Massala MV, Illsley M, James SE, Faragher RG.
Exp Gerontol 83:139-47. doi: 10.1016/j.exger.2016.07.017. Epub 2016 Aug 2. 2016
10WRN
The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription.
Tang W, Robles AI, Beyer RP, Gray LT, Nguyen GH, Oshima J, Maizels N, Harris CC, Monnat RJ Jr.
Hum Mol Genet 25(10):2060-2069. Epub 2016 Mar 16. 2016
11ATR, WRN
Replication stress induced site-specific phosphorylation targets WRN to the ubiquitin-proteasome pathway.
Su F, Bhattacharya S, Abdisalaam S, Mukherjee S, Yajima H, Yang Y, Mishra R, Srinivasan K, Ghose S, Chen DJ, Yannone SM, Asaithamby A.
Oncotarget 7(1):46-65. doi: 10.18632/oncotarget.6659. 2016
12BLM, PARP1, RECQL, RECQL4, RECQL5, WRN
RecQ helicases and PARP1 team up in maintaining genome integrity.
Veith S, Mangerich A.
Ageing Res Rev 23(Pt A):12-28. doi: 10.1016/j.arr.2014.12.006. Epub 2014 Dec 30. Review. 2015
13PARP1, RECQL5, WRN
Differential and Concordant Roles for Poly(ADP-Ribose) Polymerase 1 and Poly(ADP-Ribose) in Regulating WRN and RECQL5 Activities.
Khadka P, Hsu JK, Veith S, Tadokoro T, Shamanna RA, Mangerich A, Croteau DL, Bohr VA.
Mol Cell Biol 35(23):3974-89. doi: 10.1128/MCB.00427-15. Epub 2015 Sep 21. 2015
14WRN
The DNA structure and sequence preferences of WRN underlie its function in telomeric recombination events.
Edwards DN, Machwe A, Chen L, Bohr VA, Orren DK.
Nat Commun 6:8331. doi: 10.1038/ncomms9331. 2015
15WRN
WRN translocation from nucleolus to nucleoplasm is regulated by SIRT1 and required for DNA repair and the development of chemoresistance.
Lee SY, Lee H, Kim ES, Park S, Lee J, Ahn B.
Mutat Res 774:40-8. doi: 10.1016/j.mrfmmm.2015.03.001. Epub 2015 Mar 11. 2015
16BLM, DNA2, RMI1, RMI2, WRN
DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells.
Sturzenegger A, Burdova K, Kanagaraj R, Levikova M, Pinto C, Cejka P, Janscak P.
J Biol Chem 289(39):27314-26. doi: 10.1074/jbc.M114.578823. Epub 2014 Aug 13. 2014
17WRN
Transient overexpression of Werner protein rescues starvation induced autophagy in Werner syndrome cells.
Maity J, Bohr VA, Laskar A, Karmakar P.
Biochim Biophys Acta 1842(12 Pt A):2387-94. doi: 10.1016/j.bbadis.2014.09.007. Epub 2014 Sep 23. 2014
18RECQL, WRN
Human RECQL1 participates in telomere maintenance.
Popuri V, Hsu J, Khadka P, Horvath K, Liu Y, Croteau DL, Bohr VA.
Nucleic Acids Res 42(9):5671-88. doi: 10.1093/nar/gku200. Epub 2014 Mar 12. 2014
19BLM, DNA2, WRN
DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells.
Sturzenegger A, Burdova K, Kanagaraj R, Levikova M, Pinto C, Cejka P, Janscak P.
J Biol Chem 289(39):27314-26. doi: 10.1074/jbc.M114.578823. Epub 2014 Aug 13. 2014
20WRN
WRN loss induces switching of telomerase-independent mechanisms of telomere elongation.
Gocha AR, Acharya S, Groden J.
PLoS One 9(4):e93991. doi: 10.1371/journal.pone.0093991. eCollection 2014. 2014
21MUS81, WRN
The WRN and MUS81 proteins limit cell death and genome instability following oncogene activation.
Murfuni I, Nicolai S, Baldari S, Crescenzi M, Bignami M, Franchitto A, Pichierri P.
Oncogene 32(5):610-20. doi: 10.1038/onc.2012.80. Epub 2012 Mar 12. 2013
22RECQL5, WRN
RECQL5 plays co-operative and complementary roles with WRN syndrome helicase.
Popuri V, Huang J, Ramamoorthy M, Tadokoro T, Croteau DL, Bohr VA.
Nucleic Acids Res 41(2):881-99. doi: 10.1093/nar/gks1134. Epub 2012 Nov 23. Erratum in: Nucleic Acids Res. 2016 Dec 6;:. Nucleic Acids Res. 2017 F 2013
23RECQL4, RTS, TERF1, TERF2, WRN
RECQL4, the protein mutated in Rothmund-Thomson syndrome, functions in telomere maintenance.
Ghosh AK, Rossi ML, Singh DK, Dunn C, Ramamoorthy M, Croteau DL, Liu Y, Bohr VA.
J Biol Chem 287(1):196-209. doi: 10.1074/jbc.M111.295063. Epub 2011 Oct 28. 2012
24POLD1, WRN
The Werner syndrome exonuclease facilitates DNA degradation and high fidelity DNA polymerization by human DNA polymerase δ.
Kamath-Loeb AS, Shen JC, Schmitt MW, Loeb LA.
J Biol Chem 287(15):12480-90. doi: 10.1074/jbc.M111.332577. Epub 2012 Feb 17. 2012
25WRN
The Werner syndrome protein promotes CAG/CTG repeat stability by resolving large (CAG)(n)/(CTG)(n) hairpins.
Chan NL, Hou C, Zhang T, Yuan F, Machwe A, Huang J, Orren DK, Gu L, Li GM.
J Biol Chem 287(36):30151-6. doi: 10.1074/jbc.M112.389791. Epub 2012 Jul 11. 2012
26POLN, WRN
Enhancement of human DNA polymerase η activity and fidelity is dependent upon a bipartite interaction with the Werner syndrome protein.
Maddukuri L, Ketkar A, Eddy S, Zafar MK, Griffin WC, Eoff RL.
J Biol Chem 287(50):42312-23. doi: 10.1074/jbc.M112.410332. Epub 2012 Oct 8. 2012
27POT1, WRN
Fission yeast Pot1 and RecQ helicase are required for efficient chromosome segregation.
Takahashi K, Imano R, Kibe T, Seimiya H, Muramatsu Y, Kawabata N, Tanaka G, Matsumoto Y, Hiromoto T, Koizumi Y, Nakazawa N, Yanagida M, Yukawa M, Tsuchiya E, Ueno M.
Mol Cell Biol 31(3):495-506. Epub 2010 Nov 22. 2011
28RPA1, WRN
Molecular cooperation between the Werner syndrome protein and replication protein A in relation to replication fork blockage.
Machwe A, Lozada E, Wold MS, Li GM, Orren DK.
J Biol Chem 286(5):3497-508. Epub 2010 Nov 24. 2011
29ERCC5, WRN
The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome.
Trego KS, Chernikova SB, Davalos AR, Perry JJ, Finger LD, Ng C, Tsai MS, Yannone SM, Tainer JA, Campisi J, Cooper PK.
Cell Cycle 10(12):1998-2007. Epub 2011 Jun 15. 2011
30RECQL, WRN
RECQL1 and WRN proteins are potential therapeutic targets in head and neck squamous cell carcinoma.
Arai A, Chano T, Futami K, Furuichi Y, Ikebuchi K, Inui T, Tameno H, Ochi Y, Shimada T, Hisa Y, Okabe H.
Cancer Res 71(13):4598-607. Epub 2011 May 13. 2011
31BLM, WRN
The Werner and Bloom syndrome proteins help resolve replication blockage by converting (regressed) holliday junctions to functional replication forks.
Machwe A, Karale R, Xu X, Liu Y, Orren DK.
Biochemistry 50(32):6774-88. Epub 2011 Jul 21. 2011
32ERCC5, WRN, XPG
XPG and WRN: an unexpected partnership.
Kamath-Loeb AS, Loeb LA.
Cell Cycle 10(18):3051. Epub 2011 Sep 15. No abstract available. 2011
33WRN
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.
Friedrich K, Lee L, Leistritz DF, Nürnberg G, Saha B, Hisama FM, Eyman DK, Lessel D, Nürnberg P, Li C, Garcia-F-Villalta MJ, Kets CM, Schmidtke J, Cruz VT, Van den Akker PC, Boak J, Peter D, Compoginis G, Cefle K, Ozturk S, López N, Wessel T, Poot M, Ippel PF, Groff-Kellermann B, Hoehn H, Martin GM, Kubisch C, Oshima J.
Hum Genet 128(1):103-11. Epub 2010 May 5.PMID: 20443122 2010
34TERF2, WRN
Telomeric protein TRF2 protects Holliday junctions with telomeric arms from displacement by the Werner syndrome helicase.
Nora GJ, Buncher NA, Opresko PL.
Nucleic Acids Res 38(12):3984-98. Epub 2010 Mar 9. 2010
35DHX9, WRN
WRN helicase unwinds Okazaki fragment-like hybrids in a reaction stimulated by the human DHX9 helicase.
Chakraborty P, Grosse F.
Nucleic Acids Res 38(14):4722-30. Epub 2010 Apr 12. 2010
36WRN
Identification of a coiled coil in werner syndrome protein that facilitates multimerization and promotes exonuclease processivity.
Perry JJ, Asaithamby A, Barnebey A, Kiamanesch F, Chen DJ, Han S, Tainer JA, Yannone SM.
J Biol Chem 285(33):25699-707. Epub 2010 Jun 1. 2010
37ATM, ATR, RAD51, WRN
ATR and ATM differently regulate WRN to prevent DSBs at stalled replication forks and promote replication fork recovery.
Ammazzalorso F, Pirzio LM, Bignami M, Franchitto A, Pichierri P.
EMBO J 29(18):3156-69. Epub 2010 Aug 27. 2010
38POT1, WRN
Human POT1 is required for efficient telomere C-rich strand replication in the absence of WRN.
Arnoult N, Saintome C, Ourliac-Garnier I, Riou JF, Londoño-Vallejo A.
Genes Dev 23(24):2915-24. 2009
39WRN
The Werner syndrome protein binds replication fork and holliday junction DNAs as an oligomer.
Compton SA, Tolun G, Kamath-Loeb AS, Loeb LA, Griffith JD.
J Biol Chem 283(36):24478-83. Epub 2008 Jul 2. 2008
40MUS81, WRN
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.
Muftuoglu M, Oshima J, von Kobbe C, Cheng WH, Leistritz DF, Bohr VA.
Hum Genet 124(4):369-77. Epub 2008 Sep 23. Review. 2008
41MUS81, WRN
Replication fork stalling in WRN-deficient cells is overcome by prompt activation of a MUS81-dependent pathway.
Franchitto A, Pirzio LM, Prosperi E, Sapora O, Bignami M, Pichierri P.
J Cell Biol 183(2):241-52. Epub 2008 Oct 13. 2008
42WRN
Werner syndrome helicase activity is essential in maintaining fragile site stability.
Pirzio LM, Pichierri P, Bignami M, Franchitto A.
J Cell Biol 180(2):305-14. Epub 2008 Jan 21.PMID: 18209099 2008
43WRN
Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing.
Kusumoto R, Dawut L, Marchetti C, Wan Lee J, Vindigni A, Ramsden D, Bohr VA.
Biochemistry 47(28):7548-56. Epub 2008 Jun 18.PMID: 18558713 2008
44WRN
Telomere dysfunction as a cause of genomic instability in Werner syndrome.
Crabbe L, Jauch A, Naeger CM, Holtgreve-Grez H, Karlseder J.
Proc Natl Acad Sci U S A 104(7):2205-10. Epub 2007 Feb 6. 2007
45WRN, LMNA, PRO1
Werner and Hutchinson-Gilford progeria syndromes: mechanistic basis of human progeroid diseases.
Kudlow BA, Kennedy BK, Monnat RJ Jr.
Nat Rev Mol Cell Biol 8(5):394-404. 2007
46WRN, NEIL1
The Human Werner Syndrome Protein Stimulates Repair of Oxidative DNA Base Damage by the DNA Glycosylase NEIL1.
Das A, Boldogh I, Lee JW, Harrigan JA, Hegde ML, Piotrowski J, de Souza Pinto N, Ramos W, Greenberg MM, Hazra TK, Mitra S, Bohr VA.
J Biol Chem 282(36):26591-602. Epub 2007 Jul 3. 2007
47MSH2, WRN
Physical and functional interactions between Werner syndrome helicase and mismatch-repair initiation factors.
Saydam N, Kanagaraj R, Dietschy T, Garcia PL, Pena-Diaz J, Shevelev I, Stagljar I, Janscak P.
Nucleic Acids Res 35(17):5706-16. Epub 2007 Aug 22. 2007
48WRN
Metal-catalyzed Oxidation of the Werner Syndrome Protein Causes Loss of Catalytic Activities and Impaired Protein-Protein Interactions.
Harrigan JA, Piotrowski J, Di Noto L, Levine RL, Bohr VA.
J Biol Chem 282(50):36403-11. Epub 2007 Oct 2. 2007
49WRN
The role of WRN in DNA repair is affected by post-translational modifications.
Kusumoto R, Muftuoglu M, Bohr VA.
Mech Ageing Dev 128(1):50-7. Epub 2006 Nov 20. Review. 2007
50BGS, BLM, RAPADILINO, RECQL4, WRN
The molecular role of the Rothmund-Thomson-, RAPADILINO- and Baller-Gerold-gene product, RECQL4: recent progress.
Dietschy T, Shevelev I, Stagljar I.
Cell Mol Life Sci 64(7-8):796-802. Review. 2007
51BLM, BLMS, WRN
The Werner and Bloom syndrome proteins catalyze regression of a model replication fork.
Machwe A, Xiao L, Groden J, Orren DK.
Biochemistry 45(47):13939-46. 2006
52WRN
The spectrum of WRN mutations in Werner syndrome patients.
Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, Poot M, Rubin CD, Chen DF, Yang CC, Juch H, Dorn T, Spiegel R, Oral EA, Abid M, Battisti C, Lucci-Cordisco E, Neri G, Steed EH, Kidd A, Isley W, Showalter D, Vittone JL, Konstantinow A, Ring J, Meyer P, Wenger SL, von Herbay A, Wollina U, Schuelke M, Huizenga CR, Leistritz DF, Martin GM, Mian IS, Oshima J.
Hum Mutat 27(6):558-67. 2006
53WRN
A role for WRN in telomere-based DNA damage responses.
Eller MS, Liao X, Liu S, Hanna K, Backvall H, Opresko PL, Bohr VA, Gilchrest BA.
Proc Natl Acad Sci U S A 103(41):15073-8. Epub 2006 Oct 2. 2006
54WRN
The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta.
Harrigan JA, Wilson DM 3rd, Prasad R, Opresko PL, Beck G, May A, Wilson SH, Bohr VA.
Nucleic Acids Res 34(2):745-54. Print 2006. 2006
55WRN, RPA1, BLM
Physical and functional mapping of the replication protein a interaction domain of the werner and bloom syndrome helicases.
Doherty KM, Sommers JA, Gray MD, Lee JW, von Kobbe C, Thoma NH, Kureekattil RP, Kenny MK, Brosh RM Jr.
J Biol Chem 280(33):29494-505. Epub 2005 Jun 17. 2005
56WRN, DHX9
Nuclear DNA helicase II (RNA helicase A) interacts with Werner syndrome helicase and stimulates its exonuclease activity.
Friedemann J, Grosse F, Zhang S.
J Biol Chem 280(35):31303-13. Epub 2005 Jul 1. 2005
57BLM,POT1,WRN
POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates.
Opresko PL, Mason PA, Podell ER, Lei M, Hickson ID, Cech TR, Bohr VA.
J Biol Chem 280(37):32069-80. Epub 2005 Jul 18. 2005
58WRN
Modulation of Werner syndrome protein function by a single mutation in the conserved RecQ domain.
Lee JW, Kusumoto R, Doherty KM, Lin GX, Zeng W, Cheng WH, von Kobbe C, Brosh RM Jr, Hu JS, Bohr VA.
J Biol Chem 280(47):39627-36. Epub 2005 Sep 7. 2005
59WRN
Normal telomere erosion rates at the single cell level in Werner syndrome fibroblast cells.
Baird DM, Davis T, Rowson J, Jones CJ, Kipling D.
Hum Mol Genet 13(14):1515-24. Epub 2004 May 18. 2004
60WRN
Essential role of limiting telomeres in the pathogenesis of Werner syndrome.
Chang S, Multani AS, Cabrera NG, Naylor ML, Laud P, Lombard D, Pathak S, Guarente L, DePinho RA.
Nat Genet 36(8):877-82. Epub 2004 Jul 04. 2004
61WRN, FEN1
In vivo function of the conserved non-catalytic domain of Werner syndrome helicase in DNA replication.
arma S, Sommers JA, Brosh RM Jr.
Hum Mol Genet 13(19):2247-61. Epub 2004 Jul 28. 2004
62WRN
Defective telomere lagging strand synthesis in cells lacking WRN helicase activity.
Crabbe L, Verdun RE, Haggblom CI, Karlseder J.
Science 306(5703):1951-3. 2004
63TERF2, WRN
TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA.
Machwe A, Xiao L, Orren DK.
Oncogene 23(1):149-56. 2004
64WRN
The Werner syndrome protein has separable recombination and survival functions.
Swanson C, Saintigny Y, Emond MJ, Monnat RJ Jr.
DNA Repair (Amst) 3(5):475-82. 2004
65WRN
The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine: implications for WRN function.
Blank A, Bobola MS, Gold B, Varadarajan S, D Kolstoe D, Meade EH, Rabinovitch PS, Loeb LA, Silber JR.
DNA Repair (Amst) 3(6):629-38. 2004
66WRN
The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2.
Opresko PL, Otterlei M, Graakjaer J, Bruheim P, Dawut L, Kolvraa S, May A, Seidman MM, Bohr VA.
Mol Cell 14(6):763-74. 2004
67WRN
The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C.
Kamath-Loeb AS, Welcsh P, Waite M, Adman ET, Loeb LA.
J Biol Chem 279(53):55499-505. Epub 2004 Oct 15. 2004
68WRN
Gene expression profiling in Werner syndrome closely resembles that of normal aging.
Kyng KJ, May A, Kolvraa S, Bohr VA.
Proc Natl Acad Sci U S A 100(21):12259-64. Epub 2003 Oct 03. 2003
69WRN
Neurological complications of Werner's syndrome.
Anderson NE, Haas LF.
J Neurol 250(10):1174-8. 2003
70BLM, MRE11A, NBS1, RAD50, WRN, NBN
Protecting genomic integrity during DNA replication: correlation between Werner's and Bloom's syndrome gene products and the MRE11 complex.
Franchitto A, Pichierri P.
Hum Mol Genet 11(20):2447-53. 2002
71WRN
Biochemical characterization of the DNA substrate specificity of Werner syndrome helicase.
Brosh RM Jr, Waheed J, Sommers JA.
J Biol Chem 277(26):23236-45. Epub 2002 Apr 15. 2002
72WRN, BLM
Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins.
von Kobbe C, Karmakar P, Dawut L, Opresko P, Zeng X, Brosh RM Jr, Hickson ID, Bohr VA.
J Biol Chem 277(24):22035-44. Epub 2002 Mar 27. 2002
73WRN, FEN1
Biochemical characterization of the WRN-FEN-1 functional interaction.
Brosh RM Jr, Driscoll HC, Dianov GL, Sommers JA.
Biochemistry 41(40):12204-16. 2002
74TERF2, BLM, WRN
Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases.
Opresko PL, von Kobbe C, Laine JP, Harrigan J, Hickson ID, Bohr VA.
J Biol Chem 277(43):41110-9. Epub 2002 Aug 13. 2002
75WRN
The Werner syndrome helicase/exonuclease (WRN) disrupts and degrades D-loops in vitro.
Orren DK, Theodore S, Machwe A.
Biochemistry 41(46):13483-8. 2002
76WRN, PRKAR1B
Regulation of the Werner helicase through a direct interaction with a subunit of protein kinase A.
Nguyen DT, Rovira II, Finkel T.
FEBS Lett 521(1-3):170-4. 2002
77WRN, XRCC5
A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA.
Orren DK, Machwe A, Karmakar P, Piotrowski J, Cooper MP, Bohr VA.
Nucleic Acids Res 29(9):1926-1934. 2001
78WRN
The Werner syndrome gene and global sequence variation.
Passarino G, Shen P, Van Kirk JB, Lin AA, De Benedictis G, Cavalli Sforza LL, Oefner PJ, Underhill PA.
Genomics 71(1):118-22. 2001
79BLM, WRN
The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases.
Mohaghegh P, Karow JK, Brosh Jr RM Jr, Bohr VA, Hickson ID.
Nucleic Acids Res 29(13):2843-9. 2001
80FEN1, WRN
Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity.
Brosh RM Jr, von Kobbe C, Sommers JA, Karmakar P, Opresko PL, Piotrowski J, Dianova I, Dianov GL, Bohr VA.
EMBO J 20(20):5791-801. 2001
81PRKDC, WRN
Werner syndrome protein is regulated and phosphorylated by DNA-dependent protein kinase.
Yannone SM, Roy S, Chan DW, Murphy MB, Huang S, Campisi J, Chen DJ.
J Biol Chem 276(41):38242-8. 2001
82ATM, ATR, TREX1, WRN
ATR and ATRIP: partners in checkpoint signaling.
Cortez D, Guntuku S, Qin J, Elledge SJ.
Science 294(5547):1713-6. 2001
83WRN
Telomerase prevents the accelerated cell ageing of werner syndrome fibroblasts.
Wyllie FS, Jones CJ, Skinner JW, Haughton MF, Wallis C, Wynford-Thomas D, Faragher RG, Kipling D.
Nat Genet 24(1):16-7. No abstract available 2000
84POLD1, WRN
Functional interaction between the Werner Syndrome protein and DNA polymerase delta.
Kamath-Loeb AS, Johansson E, Burgers PM, Loeb LA.
Proc Natl Acad Sci U S A 97(9):4603-8. 2000
85SLC2A1, WRN
Association of impaired phosphatidylinositol 3-kinase activity in GLUT1-containing vesicles with malinsertion of glucose transporters into the plasma membrane of fibroblasts from a patient with severe insulin resistance and clinical features of Werner syndrome.
Kausch C, Hamann A, Uphues I, Niendorf A, Muller-Wieland D, Joost HG, Algenstaedt P, Dreyer M, Rudiger HW, Haring HU, Eckel J, Matthaei S.
J Clin Endocrinol Metab 85(2):905-18. 2000
86TSG8B, WRN
Chromosome translocations in breast cancer with breakpoints at 8p12.
Courtay-Cahen C, Morris JS, Edwards PA.
Genomics 66(1):15-25. 2000
87POLD2, WRN
Werner protein recruits DNA polymerase delta to the nucleolus.
Szekely AM, Chen YH, Zhang C, Oshima J, Weissman SM.
Proc Natl Acad Sci U S A 97(21):11365-70. 2000
88WRN
Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, and atherosclerosis.
Castro E, Edland SD, Lee L, Ogburn CE, Deeb SS, Brown G, Panduro A, Riestra R, Tilvis R, Louhija J, Penttinen R, Erkkola R, Wang L, Martin GM, Oshima J.
Am J Med Genet 95(4):374-80. 2000
89WRN
The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases.
Shen JC, Loeb LA.
Trends Genet 16(5):213-20. Review. 2000
90WRN
Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest.
Constantinou A, Tarsounas M, Karow JK, Brosh RM, Bohr VA, Hickson ID, West SC.
EMBO Rep 1(1):80-4. 2000
91WRN
Polymorphisms at the Werner locus : I. Newly identified polymorphisms, ethnic variability of 1367Cy/arg, and its stability in a population of Finnish centenarians.
Castro E, et al.
Am J Med Genet 82 : 399-403. 1999
92WRN
WRN mutations in Werner syndrome.
Moser MJ, et al.
Hum Mutat 13 : 271-279. 1999
93WRN
Werner syndrome helicase contains a 5'-->3' exonuclease activity that digests DNA and RNA strands in DNA/DNA and RNA/DNA duplexes dependent on unwinding.
Suzuki N, et al.
Nucleic Acids Res 27(11):2361-2368. 1999
94WRN
Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines.
Prince PR, et al.
Hum Genet 105(1-2):132-8. 1999
95WRN
The Werner syndrome protein is involved in RNA polymerase II transcription.
Balajee AS, Machwe A, May A, Gray MD, Oshima J, Martin GM, Nehlin JO, Brosh R, Orren DK, Bohr VA.
Mol Biol Cell 10(8):2655-68 1999
96WRN
Detection by epitope-defined monoclonal antibodies of Werner DNA helicases in the nucleoplasm and their upregulation by cell transformation and immortalization.
Shiratori M, Sakamoto S, Suzuki N, Tokutake Y, Kawabe Y, Enomoto T, Sugimoto M, Goto M, Matsumoto T, Furuichi Y.
J Cell Biol 144(1):1-9 1999
97TP53, WRN
Physical and functional interaction between p53 and the Werner's syndrome protein.
Blander G, Kipnis J, Leal JF, Yu CE, Schellenberg GD, Oren M.
J Biol Chem 274(41):29463-9. 1999
98WRN
Physical map of the human chromosome 8p12-p21 encompassing tumor suppressor and Werner's syndrome gene loci.
Ichikawa K, et al.
DNA Res 5 : 103-113. 1998
99WRN
Characterization of Werner syndrome protien DNA helicase activity : directionality, substrate dependence and stimulation by replication protein A.
Shen JC, et al.
Nucleic Acids Res 26 : 2879-2885. 1998
100WRN
Nucleolar localization of the Werner syndrome protein in human cells.
Marciniak RA, et al.
Proc Natl Acad Sci U S A 95 : 6887-6892. 1998
101WRN
Structure and function of the human Werner syndrome gene promoter : evidence for transcriptional modulation.
Wang L, et al.
Nucleic Acids Res 26 : 3480-3485. 1998
102WRN
Replication focus-forming activity 1 and the Werner syndrome gene product.
Yan H, et al.
Nat Genet 19 : 375-379. 1998
103WRN
The premature ageing syndrome protein, WRN, is a 3'-5' exonuclease.
Huang S, et al.
Nat Genet 20 : 114-116. 1998
104BLM, RECQL4, RECQL5, WRN
Cloning of two new human helicase genes of the RecQ family : biological significance of multiple species in higher eukaryotes.
Kitao S, Ohsugi I, Ichikawa K, Goto M, Furuichi Y, Shimamoto A.
Genomics 54 : 443-452. 1998
105WRN
Werner syndrome protein. II. Characterization of the integral 3'-->5' DNA exonuclease.
Kamath-Loeb AS, et al.
J Biol Chem 273 : 34145-34150. 1998
106WRN
Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.
Shen JC, et al.
J Biol Chem 273 : 34139-34144. 1998
107WRN
Analysis of helicase gene mutations in Japanese Werner's syndrome patients.
Goto M, et al.
Hum Genet 99 : 191-193. 1997
108WRN
Mutations in the consensus helicase domains of the Werner syndrome gene.
Yu CE, et al.
Am J Hum Genet 60 : 330-341. 1997
109WRN
Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population.
Ye L, et al.
Am J Med Genet 68 : 494-498. 1997
110WRN
Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population.
Matsumoto T, Imamura O, Yamabe Y, Kuromitsu J, Tokutake Y, Shimamoto A, Suzuki N, Satoh M, Kitao S, Ichikawa K, Kataoka H, Sugawara K, Thomas W, Mason B, Tsuchihashi Z, Drayna D, Sugawara M, Sugimoto M, Furuichi Y, Goto M.
Hum Genet 100(1):123-30. 1997
111D8S339, WRN
A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus.
Bruskiewich R, et al.
Genome 40 : 77-83. 1997
112WRN
Impaired nuclear localization of defective DNA helicases in Werner's syndrome.
Matsumoto T, Shimamoto A, Goto M, Furuichi Y.
Nat Genet 16(4):335-6. 1997
113WRN
The Werner syndrome protein is a DNA helicase.
Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA.
Nat Genet 17(1):100-3. 1997
114WRN
Werner syndrome : characterization of mutations in the WRN gene in an affected family.
Meisslitzer C, Ruppitsch W, Weirich-Schwaiger H, Weirich HG, Jabkowsky J, Klein G, Schweiger M, Hirsch-Kauffmann M.
Eur J Hum Genet 5(6):364-70. 1997
115GTF2E2, NRG1, NEFL, FGFR1, POLB, PPP2CB, WRN
Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome.
Imbert A, et al.
Genomics 32 : 29-38. 1996
116WRN
Positional cloning of the Werner's syndrome gene.
Yu CE, et al.
Science 272 : 258-262. 1996
117WRN, POLB
A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8.
Chaffanet M, et al.
Cytogenet Cell Genet 72 : 63-68. 1996
118WRN
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping : lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.
Goddard KAB, et al.
Am J Hum Genet 58 : 1286-1302. 1996
119D8S2138, D8S2144, D8S2150, D8S2156, D8S2162, D8S2168, D8S2174, D8S2180, D8S2186, D8S2192, D8S2196, D8S2206, WRN
Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.
Nakura J, et al.
Genomics 36 : 130-141. 1996
120WRN
Cloning the gene for Werner syndrome : a disease with many symptoms of premature aging.
Lombard DB, et al.
Trends in Genet 12 : 283-286. 1996
121WRN, D8S2134
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Yu CE, et al.
Genomics 35 : 431-440. 1996
122WRN
Homozygous and compound heterozygous mutations at the Werner syndrome locus.
Oshima J, et al.
Hum Mol Genet 5 : 1909-1913. 1996
123WRN
Estimation of the physical distance between major genomic markers in the Werner syndrome locus (8p11.2-12) by dual-color FISH analysis.
Tokutake Y, et al.
Jpn J Hum Genet 41 : 291-297. 1996
124BLM, WRN
Human homologues of yeast helicase.
Lu J, et al.
Nature 383 : 678-679. 1996
125WRN, D8S1055
Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN) : chromosome microdissection and homozygosity mapping.
Ye L, et al.
Genomics 28 : 566-569. 1995
126WRN
FFA-1, a protein that promotes the formation of replication centers within nuclei.
Yan H, et al.
Science 269 : 1883-1885. 1995
127WRN, TSG8B, TSG8A
Deletion mapping of chromosome 8p in colorectal carcinoma and dysplasia arising in ulcerative colitis, prostatic carcinoma, and malignant fibrous histiocytomas.
Chang M, et al.
Am J Pathol 144 : 1-6. 1994
128WRN
Evidence against DNA polymerase beta as a candidate gene for Werner syndrome.
Chang M, et al.
Hum Genet 93 : 507-512. 1994
129WRN, POLB
Identification of mutations in DNA polymerase beta mRNAs from patients with Werner syndrome.
Sadakane Y, Maeda K, Kuroda Y, Hori K.
Biochem Biophys Res Commun 200(1):219-25. 1994
130WRN
Integrated mapping analysis of the Werner syndrome region of chromosome 8.
Oshima J, et al.
Genomics 23 : 100-113. 1994
131WRN
Homozygosity mapping of the Werner syndrome locus (WRN).
Nakura J, et al.
Genomics 23 : 600-608. 1994
132WRN
Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22.
Nagano K, et al.
Jpn J Hum Genet 38 : 391-397. 1993
133WRN
A genetic analysis of the Werner syndrome region on human chromosome 8p.
Thomas W, et al.
Genomics 16 : 685-690. 1993
134WRN
Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8.
Nakura J, et al.
Gerontology 39 : 11-15. 1993
135WRN
Genetic linkage of Werner's syndrome to five markers on chromosome 8.
Goto M, et al.
Nature 355 : 735-738. 1992
136WRN
Homozygosity mapping and Werner's syndrome.
Schellenberg GD, et al.
Lancet 339 : 1002. 1992
137WRN
Ophthalmological aspects in patients with Werner's syndrome.
Ruprecht KW.
Arch Gerontol Geriatr 9 : 263-270. 1989
138WRN
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's Syndrome.
Scappaticci S, Cerimele D, Fraccaro M.
Hum Genet 62(1):16-24. 1982
139WRN
Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism.
Salk D, Au K, Hoehn H, Martin GM.
Cytogenet Cell Genet 30(2):92-107. 1981