WRN (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "WRN" in Japanese language version.

Last modified: 02:26:56, 10 December 2023 (UTC)

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5^th place

11^th place

2^nd place

3^rd place

74adsabs.harvard.edu

14^th place

60^th place

630^th place

1,132^nd place

adsabs.harvard.edu (Global: 14^th place; Japanese: 60^th place)

ui.adsabs.harvard.edu

“WRN regulates pathway choice between classical and alternative non-homologous end joining”. Nat Commun 7: 13785. (2016). Bibcode:2016NatCo...713785S. doi:10.1038/ncomms13785. PMC 5150655. PMID 27922005.
“A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity”. Proc. Natl. Acad. Sci. U.S.A. 95 (22): 13097–102. (1998). Bibcode:1998PNAS...9513097L. doi:10.1073/pnas.95.22.13097. PMC 23722. PMID 9789047.
“Inhibition of DNA glycosylases via small molecule purine analogs”. PLOS ONE 8 (12): e81667. (2013). Bibcode:2013PLoSO...881667J. doi:10.1371/journal.pone.0081667. PMC 3857224. PMID 24349107.
“Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer”. Proc. Natl. Acad. Sci. U.S.A. 103 (23): 8822–7. (2006). Bibcode:2006PNAS..103.8822A. doi:10.1073/pnas.0600645103. PMC 1466544. PMID 16723399.

doi.org (Global: 2^nd place; Japanese: 3^rd place)

Monnat RJ (October 2010). “Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology”. Semin. Cancer Biol. 20 (5): 329–39. doi:10.1016/j.semcancer.2010.10.002. PMC 3040982. PMID 20934517.
“Homologous recombination resolution defect in werner syndrome”. Mol. Cell. Biol. 22 (20): 6971–8. (2002). doi:10.1128/mcb.22.20.6971-6978.2002. PMC 139822. PMID 12242278.
“DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells”. J. Biol. Chem. 289 (39): 27314–26. (2014). doi:10.1074/jbc.M114.578823. PMC 4175362. PMID 25122754.
“WRN regulates pathway choice between classical and alternative non-homologous end joining”. Nat Commun 7: 13785. (2016). Bibcode:2016NatCo...713785S. doi:10.1038/ncomms13785. PMC 5150655. PMID 27922005.
“The human Werner syndrome protein stimulates repair of oxidative DNA base damage by the DNA glycosylase NEIL1”. J. Biol. Chem. 282 (36): 26591–602. (2007). doi:10.1074/jbc.M703343200. PMID 17611195.
“Involvement of Werner syndrome protein in MUTYH-mediated repair of oxidative DNA damage”. Nucleic Acids Res. 40 (17): 8449–59. (2012). doi:10.1093/nar/gks648. PMC 3458577. PMID 22753033.
“The Werner syndrome protein: linking the replication checkpoint response to genome stability”. Aging 3 (3): 311–8. (2011). doi:10.18632/aging.100293. PMC 3091524. PMID 21389352.
“Model of human aging: recent findings on Werner's and Hutchinson–Gilford progeria syndromes”. Clin Interv Aging 3 (3): 431–44. (2008). doi:10.2147/CIA.S1957. PMC 2682376. PMID 18982914.
Kristian Moss Bendtsen, Martin Borch Jensen, Alfred May, Lene JuelRasmussen, Ala Trusina, Vilhelm A. Bohr & Mogens H. Jensen (2014). “Dynamics of the DNA repair proteins WRN and BLM in the nucleoplasm and nucleoli”. European Biophysics Journal 43 (10–11): 509–16. doi:10.1007/s00249-014-0981-x. PMC 5576897. PMID 25119658.
“Roles of Werner syndrome protein in protection of genome integrity”. DNA Repair (Amst.) 9 (3): 331–44. (2010). doi:10.1016/j.dnarep.2009.12.011. PMC 2827637. PMID 20075015.
Oshima J (2000). “The Werner syndrome protein: an update”. BioEssays 22 (10): 894–901. doi:10.1002/1521-1878(200010)22:10<894::AID-BIES4>3.0.CO;2-B. PMID 10984715.
“The spectrum of WRN mutations in Werner syndrome patients”. Hum. Mutat. 27 (6): 558–67. (2006). doi:10.1002/humu.20337. PMC 1868417. PMID 16673358.
Lebel M (2001). “Werner syndrome: genetic and molecular basis of a premature aging disorder”. Cell. Mol. Life Sci. 58 (7): 857–67. doi:10.1007/s00018-001-8398-y. PMID 11497235.
“Loss of Werner syndrome protein function promotes aberrant mitotic recombination”. Genes Dev. 15 (8): 933–8. (2001). doi:10.1101/gad.877001. PMC 312674. PMID 11316787.
“Correlation between senescence and DNA repair in cells from young and old individuals and in premature aging syndromes”. Mutat. Res. 316 (1): 37–48. (1994). doi:10.1016/0921-8734(94)90006-x. PMID 7507567.
“A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity”. Proc. Natl. Acad. Sci. U.S.A. 95 (22): 13097–102. (1998). Bibcode:1998PNAS...9513097L. doi:10.1073/pnas.95.22.13097. PMC 23722. PMID 9789047.
“Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51”. Genes Cells 6 (5): 421–30. (2001). doi:10.1046/j.1365-2443.2001.00433.x. PMID 11380620.
“Inhibition of DNA glycosylases via small molecule purine analogs”. PLOS ONE 8 (12): e81667. (2013). Bibcode:2013PLoSO...881667J. doi:10.1371/journal.pone.0081667. PMC 3857224. PMID 24349107.
“Variant base excision repair proteins: contributors to genomic instability”. Seminars in Cancer Biology 20 (5): 320–8. (Oct 2010). doi:10.1016/j.semcancer.2010.10.010. PMC 3254599. PMID 20955798.
“The RAD9-RAD1-HUS1 (9.1.1) complex interacts with WRN and is crucial to regulate its response to replication fork stalling”. Oncogene 31 (23): 2809–23. (2012). doi:10.1038/onc.2011.468. PMC 3272477. PMID 22002307.
“Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest”. EMBO Rep. 1 (1): 80–4. (2000). doi:10.1093/embo-reports/kvd004. PMC 1083680. PMID 11256630.
“The Werner syndrome exonuclease facilitates DNA degradation and high fidelity DNA polymerization by human DNA polymerase δ”. J. Biol. Chem. 287 (15): 12480–90. (2012). doi:10.1074/jbc.M111.332577. PMC 3320997. PMID 22351772.
“Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer”. Proc. Natl. Acad. Sci. U.S.A. 103 (23): 8822–7. (2006). Bibcode:2006PNAS..103.8822A. doi:10.1073/pnas.0600645103. PMC 1466544. PMID 16723399.
“Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins”. J. Biol. Chem. 277 (24): 22035–44. (June 2002). doi:10.1074/jbc.M200914200. PMID 11919194.
“Substrate specificities and identification of putative substrates of ATM kinase family members”. J. Biol. Chem. 274 (53): 37538–43. (Dec 1999). doi:10.1074/jbc.274.53.37538. PMID 10608806.
“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. 277 (21): 18291–302. (May 2002). doi:10.1074/jbc.M111523200. PMID 11889123.
“Stimulation of flap endonuclease-1 by the Bloom's syndrome protein”. J. Biol. Chem. 279 (11): 9847–56. (March 2004). doi:10.1074/jbc.M309898200. PMID 14688284.
“Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity”. EMBO J. 20 (20): 5791–801. (October 2001). doi:10.1093/emboj/20.20.5791. PMC 125684. PMID 11598021.
“Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus”. Nucleic Acids Res. 30 (16): 3583–91. (August 2002). doi:10.1093/nar/gkf482. PMC 134248. PMID 12177300.
“Functional interaction between Ku and the werner syndrome protein in DNA end processing”. J. Biol. Chem. 275 (37): 28349–52. (September 2000). doi:10.1074/jbc.C000289200. PMID 10880505.
“The processing of Holliday junctions by BLM and WRN helicases is regulated by p53”. J. Biol. Chem. 277 (35): 31980–7. (August 2002). doi:10.1074/jbc.M204111200. PMID 12080066.
“p53 Modulates the exonuclease activity of Werner syndrome protein”. J. Biol. Chem. 276 (37): 35093–102. (September 2001). doi:10.1074/jbc.M103332200. PMID 11427532.
“Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA”. Mech. Ageing Dev. 124 (2): 167–74. (February 2003). doi:10.1016/S0047-6374(02)00131-8. PMID 12633936.
“Characterization of the human and mouse WRN 3'-->5' exonuclease”. Nucleic Acids Res. 28 (12): 2396–405. (June 2000). doi:10.1093/nar/28.12.2396. PMC 102739. PMID 10871373.
“Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases”. J. Biol. Chem. 277 (43): 41110–9. (October 2002). doi:10.1074/jbc.M205396200. PMID 12181313.
“A novel protein interacts with the Werner's syndrome gene product physically and functionally”. J. Biol. Chem. 276 (23): 20364–9. (June 2001). doi:10.1074/jbc.C100035200. PMID 11301316.

ensembl.org (Global: 630^th place; Japanese: 1,132^nd place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000165392 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000031583 - Ensembl, May 2017

nih.gov (Global: 5^th place; Japanese: 11^th place)

pubmed.ncbi.nlm.nih.gov

Monnat RJ (October 2010). “Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology”. Semin. Cancer Biol. 20 (5): 329–39. doi:10.1016/j.semcancer.2010.10.002. PMC 3040982. PMID 20934517.
“Homologous recombination resolution defect in werner syndrome”. Mol. Cell. Biol. 22 (20): 6971–8. (2002). doi:10.1128/mcb.22.20.6971-6978.2002. PMC 139822. PMID 12242278.
“DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells”. J. Biol. Chem. 289 (39): 27314–26. (2014). doi:10.1074/jbc.M114.578823. PMC 4175362. PMID 25122754.
“WRN regulates pathway choice between classical and alternative non-homologous end joining”. Nat Commun 7: 13785. (2016). Bibcode:2016NatCo...713785S. doi:10.1038/ncomms13785. PMC 5150655. PMID 27922005.
“The human Werner syndrome protein stimulates repair of oxidative DNA base damage by the DNA glycosylase NEIL1”. J. Biol. Chem. 282 (36): 26591–602. (2007). doi:10.1074/jbc.M703343200. PMID 17611195.
“Involvement of Werner syndrome protein in MUTYH-mediated repair of oxidative DNA damage”. Nucleic Acids Res. 40 (17): 8449–59. (2012). doi:10.1093/nar/gks648. PMC 3458577. PMID 22753033.
“The Werner syndrome protein: linking the replication checkpoint response to genome stability”. Aging 3 (3): 311–8. (2011). doi:10.18632/aging.100293. PMC 3091524. PMID 21389352.
“Model of human aging: recent findings on Werner's and Hutchinson–Gilford progeria syndromes”. Clin Interv Aging 3 (3): 431–44. (2008). doi:10.2147/CIA.S1957. PMC 2682376. PMID 18982914.
Kristian Moss Bendtsen, Martin Borch Jensen, Alfred May, Lene JuelRasmussen, Ala Trusina, Vilhelm A. Bohr & Mogens H. Jensen (2014). “Dynamics of the DNA repair proteins WRN and BLM in the nucleoplasm and nucleoli”. European Biophysics Journal 43 (10–11): 509–16. doi:10.1007/s00249-014-0981-x. PMC 5576897. PMID 25119658.
“Roles of Werner syndrome protein in protection of genome integrity”. DNA Repair (Amst.) 9 (3): 331–44. (2010). doi:10.1016/j.dnarep.2009.12.011. PMC 2827637. PMID 20075015.
Oshima J (2000). “The Werner syndrome protein: an update”. BioEssays 22 (10): 894–901. doi:10.1002/1521-1878(200010)22:10<894::AID-BIES4>3.0.CO;2-B. PMID 10984715.
“The spectrum of WRN mutations in Werner syndrome patients”. Hum. Mutat. 27 (6): 558–67. (2006). doi:10.1002/humu.20337. PMC 1868417. PMID 16673358.
Lebel M (2001). “Werner syndrome: genetic and molecular basis of a premature aging disorder”. Cell. Mol. Life Sci. 58 (7): 857–67. doi:10.1007/s00018-001-8398-y. PMID 11497235.
“Loss of Werner syndrome protein function promotes aberrant mitotic recombination”. Genes Dev. 15 (8): 933–8. (2001). doi:10.1101/gad.877001. PMC 312674. PMID 11316787.
“Correlation between senescence and DNA repair in cells from young and old individuals and in premature aging syndromes”. Mutat. Res. 316 (1): 37–48. (1994). doi:10.1016/0921-8734(94)90006-x. PMID 7507567.
“A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity”. Proc. Natl. Acad. Sci. U.S.A. 95 (22): 13097–102. (1998). Bibcode:1998PNAS...9513097L. doi:10.1073/pnas.95.22.13097. PMC 23722. PMID 9789047.
“Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51”. Genes Cells 6 (5): 421–30. (2001). doi:10.1046/j.1365-2443.2001.00433.x. PMID 11380620.
“Inhibition of DNA glycosylases via small molecule purine analogs”. PLOS ONE 8 (12): e81667. (2013). Bibcode:2013PLoSO...881667J. doi:10.1371/journal.pone.0081667. PMC 3857224. PMID 24349107.
“Variant base excision repair proteins: contributors to genomic instability”. Seminars in Cancer Biology 20 (5): 320–8. (Oct 2010). doi:10.1016/j.semcancer.2010.10.010. PMC 3254599. PMID 20955798.
“The RAD9-RAD1-HUS1 (9.1.1) complex interacts with WRN and is crucial to regulate its response to replication fork stalling”. Oncogene 31 (23): 2809–23. (2012). doi:10.1038/onc.2011.468. PMC 3272477. PMID 22002307.
“Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest”. EMBO Rep. 1 (1): 80–4. (2000). doi:10.1093/embo-reports/kvd004. PMC 1083680. PMID 11256630.
“The Werner syndrome exonuclease facilitates DNA degradation and high fidelity DNA polymerization by human DNA polymerase δ”. J. Biol. Chem. 287 (15): 12480–90. (2012). doi:10.1074/jbc.M111.332577. PMC 3320997. PMID 22351772.
“Excess of rare cancers in Werner syndrome (adult progeria)”. Cancer Epidemiol. Biomarkers Prev. 5 (4): 239–46. (1996). PMID 8722214.
“The Werner's Syndrome RecQ helicase/exonuclease at the nexus of cancer and aging”. Hawaii Med J 70 (3): 52–5. (2011). PMC 3071901. PMID 21365542.
“Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer”. Proc. Natl. Acad. Sci. U.S.A. 103 (23): 8822–7. (2006). Bibcode:2006PNAS..103.8822A. doi:10.1073/pnas.0600645103. PMC 1466544. PMID 16723399.
“Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins”. J. Biol. Chem. 277 (24): 22035–44. (June 2002). doi:10.1074/jbc.M200914200. PMID 11919194.
“Substrate specificities and identification of putative substrates of ATM kinase family members”. J. Biol. Chem. 274 (53): 37538–43. (Dec 1999). doi:10.1074/jbc.274.53.37538. PMID 10608806.
“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. 277 (21): 18291–302. (May 2002). doi:10.1074/jbc.M111523200. PMID 11889123.
“Stimulation of flap endonuclease-1 by the Bloom's syndrome protein”. J. Biol. Chem. 279 (11): 9847–56. (March 2004). doi:10.1074/jbc.M309898200. PMID 14688284.
“Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity”. EMBO J. 20 (20): 5791–801. (October 2001). doi:10.1093/emboj/20.20.5791. PMC 125684. PMID 11598021.
“Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus”. Nucleic Acids Res. 30 (16): 3583–91. (August 2002). doi:10.1093/nar/gkf482. PMC 134248. PMID 12177300.
“Functional interaction between Ku and the werner syndrome protein in DNA end processing”. J. Biol. Chem. 275 (37): 28349–52. (September 2000). doi:10.1074/jbc.C000289200. PMID 10880505.
“The processing of Holliday junctions by BLM and WRN helicases is regulated by p53”. J. Biol. Chem. 277 (35): 31980–7. (August 2002). doi:10.1074/jbc.M204111200. PMID 12080066.
“p53 Modulates the exonuclease activity of Werner syndrome protein”. J. Biol. Chem. 276 (37): 35093–102. (September 2001). doi:10.1074/jbc.M103332200. PMID 11427532.
“Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA”. Mech. Ageing Dev. 124 (2): 167–74. (February 2003). doi:10.1016/S0047-6374(02)00131-8. PMID 12633936.
“Characterization of the human and mouse WRN 3'-->5' exonuclease”. Nucleic Acids Res. 28 (12): 2396–405. (June 2000). doi:10.1093/nar/28.12.2396. PMC 102739. PMID 10871373.
“Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases”. J. Biol. Chem. 277 (43): 41110–9. (October 2002). doi:10.1074/jbc.M205396200. PMID 12181313.
“A novel protein interacts with the Werner's syndrome gene product physically and functionally”. J. Biol. Chem. 276 (23): 20364–9. (June 2001). doi:10.1074/jbc.C100035200. PMID 11301316.

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov