Werner syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Werner syndrome" in English language version.

refsWebsite

Global rank English rank

59nih.gov

4^th place

34doi.org

2^nd place

7semanticscholar.org

11^th place

8^th place

5harvard.edu

18^th place

17^th place

1whonamedit.com

2,888^th place

2,730^th place

1zenodo.org

621^st place

380^th place

1biologists.org

3,870^th place

3,434^th place

1jstor.org

26^th place

20^th place

1cornell.edu

332^nd place

246^th place

biologists.org

jcs.biologists.org

Otterlei M, Bruheim P, Ahn B, Bussen W, Karmakar P, Baynton K, Bohr VA (2006). "Werner syndrome protein participates in a complex with RAD51, RAD54, RAD54B and ATR in response to ICL-induced replication arrest" (PDF). J. Cell Sci. 119 (Pt 24): 5137–46. doi:10.1242/jcs.03291. PMID 17118963. S2CID 28357205.

cornell.edu

courses.cit.cornell.edu

"Werner's Syndrome: Treatments". Progeria Information Database. Retrieved April 12, 2014.

doi.org

Norbnop, Phatchara (August 2014). "ZRS 406A>G mutation in patients with tibial hypoplasia, polydactyly and triphalangeal first fingers". Journal of Human Genetics. 59 (8): 467–470. doi:10.1038/jhg.2014.50. PMID 24965254. S2CID 21552381.
Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA (1997). "The Werner syndrome protein is a DNA helicase". Nat. Genet. 17 (1): 100–3. doi:10.1038/ng0997-100. PMID 9288107. S2CID 20587915.
Werner, Otto (1985). "On Cataract in Conjunction with Scleroderma". Werner's Syndrome and Human Aging. Advances in Experimental Medicine and Biology. Vol. 190. pp. 1–14. doi:10.1007/978-1-4684-7853-2_1. ISBN 978-1-4684-7855-6. PMID 3909762.
Hasty P, Campisi J, Hoeijmakers J, van Steeg H, Vijg J (2003). "Aging and genome maintenance: lessons from the mouse?". Science. 299 (5611): 1355–9. doi:10.1126/science.1079161. PMID 12610296. S2CID 840477.
Masala MV, Scapaticci S, Olivieri C, Pirodda C, Montesu MA, Cuccuru MA, Pruneddu S, Danesino C, Cerimele D (2007). "Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster". Eur J Dermatol. 17 (3): 213–6. doi:10.1684/ejd.2007.0155 (inactive 31 January 2024). PMID 17478382.{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)
Navarro CL, Cau P, Lévy N (2006). "Molecular bases of progeroid syndromes". Hum. Mol. Genet. 15 Spec No 2: R151–61. doi:10.1093/hmg/ddl214. PMID 16987878.
Epstein CJ, Martin GM, Schultz AL, Motulsky AG (1966). "Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process". Medicine (Baltimore). 45 (3): 177–221. doi:10.1097/00005792-196605000-00001. PMID 5327241.
Kyng KJ, May A, Kølvraa S, Bohr VA (2003). "Gene expression profiling in Werner syndrome closely resembles that of normal aging". Proc. Natl. Acad. Sci. U.S.A. 100 (21): 12259–64. Bibcode:2003PNAS..10012259K. doi:10.1073/pnas.2130723100. PMC 218746. PMID 14527998.
Kyng K, Croteau DL, Bohr VA (2009). "Werner syndrome resembles normal aging". Cell Cycle. 8 (15): 2319–2323. doi:10.4161/cc.8.15.9148. PMC 4172458. PMID 19633413.
Coppedè, Fabio (August 2013). "The epidemiology of premature aging and associated comorbidities". Clinical Interventions in Aging. 8: 1023–32. doi:10.2147/CIA.S37213. PMC 3760297. PMID 24019745.
Monnat RJ (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.
Chen L, Huang S, Lee L, Davalos A, Schiestl RH, Campisi J, Oshima J (2003). "WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair". Aging Cell. 2 (4): 191–9. doi:10.1046/j.1474-9728.2003.00052.x. PMID 12934712. S2CID 25838286.
Rossi ML, Ghosh AK, Bohr VA (March 2010). "Roles of Werner syndrome protein in protection of genome integrity". DNA Repair (Amst.). 9 (3): 331–44. doi:10.1016/j.dnarep.2009.12.011. PMC 2827637. PMID 20075015.
Goto M, Rubenstein M, Weber J, Woods K, Drayna D (Feb 1992). "Genetic linkage of Werner's syndrome to five markers on chromosome 8". Nature. 355 (6362): 735–8. Bibcode:1992Natur.355..735G. doi:10.1038/355735a0. PMID 1741060. S2CID 4241791.
Bernstein KA, Gangloff S, Rothstein R (2010). "The RecQ DNA helicases in DNA repair". Annu. Rev. Genet. 44: 393–417. doi:10.1146/annurev-genet-102209-163602. PMC 4038414. PMID 21047263.
Chen L, Oshima J (2002). "Werner Syndrome". J. Biomed. Biotechnol. 2 (2): 46–54. doi:10.1155/S1110724302201011. PMC 153784. PMID 12488583.
Pichierri P, Ammazzalorso F, Bignami M, Franchitto A (March 2011). "The Werner syndrome protein: linking the replication checkpoint response to genome stability". Aging. 3 (3): 311–8. doi:10.18632/aging.100293. PMC 3091524. PMID 21389352.
Harris CC (1996). "Structure and function of the p53 tumor suppressor gene: clues for rational cancer therapeutic strategies". J. Natl. Cancer Inst. 88 (20): 1442–55. doi:10.1093/jnci/88.20.1442. PMID 8841019.
Opresko PL, Cheng WH, von Kobbe C, Harrigan JA, Bohr VA (2003). "Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process". Carcinogenesis. 24 (5): 791–802. doi:10.1093/carcin/bgg034. PMID 12771022.
Thompson LH, Schild D (2002). "Recombinational DNA repair and human disease". Mutat. Res. 509 (1–2): 49–78. Bibcode:2002MRFMM.509...49T. doi:10.1016/s0027-5107(02)00224-5. PMID 12427531.
Kusumoto R, Dawut L, Marchetti C, Wan Lee J, Vindigni A, Ramsden D, Bohr VA (2008). "Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing". Biochemistry. 47 (28): 7548–56. doi:10.1021/bi702325t. PMC 2572716. PMID 18558713.
Otterlei M, Bruheim P, Ahn B, Bussen W, Karmakar P, Baynton K, Bohr VA (2006). "Werner syndrome protein participates in a complex with RAD51, RAD54, RAD54B and ATR in response to ICL-induced replication arrest" (PDF). J. Cell Sci. 119 (Pt 24): 5137–46. doi:10.1242/jcs.03291. PMID 17118963. S2CID 28357205.
Harrigan JA, Wilson DM, Prasad R, Opresko PL, Beck G, May A, Wilson SH, Bohr VA (2006). "The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta". Nucleic Acids Res. 34 (2): 745–54. doi:10.1093/nar/gkj475. PMC 1356534. PMID 16449207.
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 (2006). "The spectrum of WRN mutations in Werner syndrome patients". Hum. Mutat. 27 (6): 558–67. doi:10.1002/humu.20337. PMC 1868417. PMID 16673358.
Spillare EA, Robles AI, Wang XW, Shen JC, Yu CE, Schellenberg GD, Harris CC (1999). "p53-mediated apoptosis is attenuated in Werner syndrome cells". Genes Dev. 13 (11): 1355–60. doi:10.1101/gad.13.11.1355. PMC 316776. PMID 10364153.
Salk D, Au K, Hoehn H, Martin GM (1981). "Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism". Cytogenet. Cell Genet. 30 (2): 92–107. doi:10.1159/000131596. PMID 7273860.
Fukuchi K, Martin GM, Monnat RJ (1989). "Mutator phenotype of Werner syndrome is characterized by extensive deletions". Proc. Natl. Acad. Sci. U.S.A. 86 (15): 5893–7. Bibcode:1989PNAS...86.5893F. doi:10.1073/pnas.86.15.5893. PMC 297737. PMID 2762303.
Crabbe L, Jauch A, Naeger CM, Holtgreve-Grez H, Karlseder J (2007). "Telomere dysfunction as a cause of genomic instability in Werner syndrome". Proc. Natl. Acad. Sci. U.S.A. 104 (7): 2205–10. Bibcode:2007PNAS..104.2205C. doi:10.1073/pnas.0609410104. JSTOR 25426449. PMC 1794219. PMID 17284601.
Chan SR, Blackburn EH (2004). "Telomeres and telomerase". Philos. Trans. R. Soc. Lond. B Biol. Sci. 359 (1441): 109–21. doi:10.1098/rstb.2003.1370. PMC 1693310. PMID 15065663.
Multani AS, Chang S (2006). "WRN at telomeres: implications for aging and cancer". J. Cell Sci. 120 (Pt 5): 713–21. doi:10.1242/jcs.03397. PMID 17314245. S2CID 6734884.
Szekely AM, Bleichert F, Nümann A, Van Komen S, Manasanch E, Ben Nasr A, Canaan A, Weissman SM (2005). "Werner protein protects nonproliferating cells from oxidative DNA damage". Mol. Cell. Biol. 25 (23): 10492–506. doi:10.1128/MCB.25.23.10492-10506.2005. PMC 1291253. PMID 16287861.
Davis T, Kipling D (2006). "Werner Syndrome as an example of inflamm-aging: possible therapeutic opportunities for a progeroid syndrome?". Rejuvenation Res. 9 (3): 402–7. doi:10.1089/rej.2006.9.402. PMID 16859481.
Massip L, Garand C, Paquet ER, Cogger VC, O'Reilly JN, Tworek L, Hatherell A, Taylor CG, Thorin E, Zahradka P, Le Couteur DG, Lebel M (2009-09-09). "Vitamin C restores healthy aging in a mouse model for Werner syndrome". FASEB J. 24 (1): 158–72. doi:10.1096/fj.09-137133. PMC 3712979. PMID 19741171.
Coppedè F (August 5, 2013). "The epidemiology of premature aging and associated comorbidities". Clin Interv Aging. 8: 1023–32. doi:10.2147/CIA.S37213. PMC 3760297. PMID 24019745.

harvard.edu

ui.adsabs.harvard.edu

Kyng KJ, May A, Kølvraa S, Bohr VA (2003). "Gene expression profiling in Werner syndrome closely resembles that of normal aging". Proc. Natl. Acad. Sci. U.S.A. 100 (21): 12259–64. Bibcode:2003PNAS..10012259K. doi:10.1073/pnas.2130723100. PMC 218746. PMID 14527998.
Goto M, Rubenstein M, Weber J, Woods K, Drayna D (Feb 1992). "Genetic linkage of Werner's syndrome to five markers on chromosome 8". Nature. 355 (6362): 735–8. Bibcode:1992Natur.355..735G. doi:10.1038/355735a0. PMID 1741060. S2CID 4241791.
Thompson LH, Schild D (2002). "Recombinational DNA repair and human disease". Mutat. Res. 509 (1–2): 49–78. Bibcode:2002MRFMM.509...49T. doi:10.1016/s0027-5107(02)00224-5. PMID 12427531.
Fukuchi K, Martin GM, Monnat RJ (1989). "Mutator phenotype of Werner syndrome is characterized by extensive deletions". Proc. Natl. Acad. Sci. U.S.A. 86 (15): 5893–7. Bibcode:1989PNAS...86.5893F. doi:10.1073/pnas.86.15.5893. PMC 297737. PMID 2762303.
Crabbe L, Jauch A, Naeger CM, Holtgreve-Grez H, Karlseder J (2007). "Telomere dysfunction as a cause of genomic instability in Werner syndrome". Proc. Natl. Acad. Sci. U.S.A. 104 (7): 2205–10. Bibcode:2007PNAS..104.2205C. doi:10.1073/pnas.0609410104. JSTOR 25426449. PMC 1794219. PMID 17284601.

jstor.org

Crabbe L, Jauch A, Naeger CM, Holtgreve-Grez H, Karlseder J (2007). "Telomere dysfunction as a cause of genomic instability in Werner syndrome". Proc. Natl. Acad. Sci. U.S.A. 104 (7): 2205–10. Bibcode:2007PNAS..104.2205C. doi:10.1073/pnas.0609410104. JSTOR 25426449. PMC 1794219. PMID 17284601.

nih.gov

pubmed.ncbi.nlm.nih.gov

Norbnop, Phatchara (August 2014). "ZRS 406A>G mutation in patients with tibial hypoplasia, polydactyly and triphalangeal first fingers". Journal of Human Genetics. 59 (8): 467–470. doi:10.1038/jhg.2014.50. PMID 24965254. S2CID 21552381.
Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA (1997). "The Werner syndrome protein is a DNA helicase". Nat. Genet. 17 (1): 100–3. doi:10.1038/ng0997-100. PMID 9288107. S2CID 20587915.
Werner, Otto (1985). "On Cataract in Conjunction with Scleroderma". Werner's Syndrome and Human Aging. Advances in Experimental Medicine and Biology. Vol. 190. pp. 1–14. doi:10.1007/978-1-4684-7853-2_1. ISBN 978-1-4684-7855-6. PMID 3909762.
Hasty P, Campisi J, Hoeijmakers J, van Steeg H, Vijg J (2003). "Aging and genome maintenance: lessons from the mouse?". Science. 299 (5611): 1355–9. doi:10.1126/science.1079161. PMID 12610296. S2CID 840477.
Masala MV, Scapaticci S, Olivieri C, Pirodda C, Montesu MA, Cuccuru MA, Pruneddu S, Danesino C, Cerimele D (2007). "Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster". Eur J Dermatol. 17 (3): 213–6. doi:10.1684/ejd.2007.0155 (inactive 31 January 2024). PMID 17478382.{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)
Navarro CL, Cau P, Lévy N (2006). "Molecular bases of progeroid syndromes". Hum. Mol. Genet. 15 Spec No 2: R151–61. doi:10.1093/hmg/ddl214. PMID 16987878.
Epstein CJ, Martin GM, Schultz AL, Motulsky AG (1966). "Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process". Medicine (Baltimore). 45 (3): 177–221. doi:10.1097/00005792-196605000-00001. PMID 5327241.
Oshima J, Martin GM, Hisama FM (February 2012) [1993–]. "Werner Syndrome". In Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews. Seattle WA: University of Washington, Seattle. PMID 20301687. NBK1514.
Goto M, Miller RW, Ishikawa Y, Sugano H (1996). "Excess of rare cancers in Werner syndrome (adult progeria)". Cancer Epidemiol. Biomarkers Prev. 5 (4): 239–46. PMID 8722214.
Kyng KJ, May A, Kølvraa S, Bohr VA (2003). "Gene expression profiling in Werner syndrome closely resembles that of normal aging". Proc. Natl. Acad. Sci. U.S.A. 100 (21): 12259–64. Bibcode:2003PNAS..10012259K. doi:10.1073/pnas.2130723100. PMC 218746. PMID 14527998.
Kyng K, Croteau DL, Bohr VA (2009). "Werner syndrome resembles normal aging". Cell Cycle. 8 (15): 2319–2323. doi:10.4161/cc.8.15.9148. PMC 4172458. PMID 19633413.
Coppedè, Fabio (August 2013). "The epidemiology of premature aging and associated comorbidities". Clinical Interventions in Aging. 8: 1023–32. doi:10.2147/CIA.S37213. PMC 3760297. PMID 24019745.
Monnat RJ (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.
Chen L, Huang S, Lee L, Davalos A, Schiestl RH, Campisi J, Oshima J (2003). "WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair". Aging Cell. 2 (4): 191–9. doi:10.1046/j.1474-9728.2003.00052.x. PMID 12934712. S2CID 25838286.
Rossi ML, Ghosh AK, Bohr VA (March 2010). "Roles of Werner syndrome protein in protection of genome integrity". DNA Repair (Amst.). 9 (3): 331–44. doi:10.1016/j.dnarep.2009.12.011. PMC 2827637. PMID 20075015.
Goto M, Rubenstein M, Weber J, Woods K, Drayna D (Feb 1992). "Genetic linkage of Werner's syndrome to five markers on chromosome 8". Nature. 355 (6362): 735–8. Bibcode:1992Natur.355..735G. doi:10.1038/355735a0. PMID 1741060. S2CID 4241791.
Bernstein KA, Gangloff S, Rothstein R (2010). "The RecQ DNA helicases in DNA repair". Annu. Rev. Genet. 44: 393–417. doi:10.1146/annurev-genet-102209-163602. PMC 4038414. PMID 21047263.
Chen L, Oshima J (2002). "Werner Syndrome". J. Biomed. Biotechnol. 2 (2): 46–54. doi:10.1155/S1110724302201011. PMC 153784. PMID 12488583.
Pichierri P, Ammazzalorso F, Bignami M, Franchitto A (March 2011). "The Werner syndrome protein: linking the replication checkpoint response to genome stability". Aging. 3 (3): 311–8. doi:10.18632/aging.100293. PMC 3091524. PMID 21389352.
Harris CC (1996). "Structure and function of the p53 tumor suppressor gene: clues for rational cancer therapeutic strategies". J. Natl. Cancer Inst. 88 (20): 1442–55. doi:10.1093/jnci/88.20.1442. PMID 8841019.
Opresko PL, Cheng WH, von Kobbe C, Harrigan JA, Bohr VA (2003). "Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process". Carcinogenesis. 24 (5): 791–802. doi:10.1093/carcin/bgg034. PMID 12771022.
Thompson LH, Schild D (2002). "Recombinational DNA repair and human disease". Mutat. Res. 509 (1–2): 49–78. Bibcode:2002MRFMM.509...49T. doi:10.1016/s0027-5107(02)00224-5. PMID 12427531.
Kusumoto R, Dawut L, Marchetti C, Wan Lee J, Vindigni A, Ramsden D, Bohr VA (2008). "Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing". Biochemistry. 47 (28): 7548–56. doi:10.1021/bi702325t. PMC 2572716. PMID 18558713.
Otterlei M, Bruheim P, Ahn B, Bussen W, Karmakar P, Baynton K, Bohr VA (2006). "Werner syndrome protein participates in a complex with RAD51, RAD54, RAD54B and ATR in response to ICL-induced replication arrest" (PDF). J. Cell Sci. 119 (Pt 24): 5137–46. doi:10.1242/jcs.03291. PMID 17118963. S2CID 28357205.
Harrigan JA, Wilson DM, Prasad R, Opresko PL, Beck G, May A, Wilson SH, Bohr VA (2006). "The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta". Nucleic Acids Res. 34 (2): 745–54. doi:10.1093/nar/gkj475. PMC 1356534. PMID 16449207.
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 (2006). "The spectrum of WRN mutations in Werner syndrome patients". Hum. Mutat. 27 (6): 558–67. doi:10.1002/humu.20337. PMC 1868417. PMID 16673358.
Spillare EA, Robles AI, Wang XW, Shen JC, Yu CE, Schellenberg GD, Harris CC (1999). "p53-mediated apoptosis is attenuated in Werner syndrome cells". Genes Dev. 13 (11): 1355–60. doi:10.1101/gad.13.11.1355. PMC 316776. PMID 10364153.
Martin GM, Sprague CA, Epstein CJ (1970). "Replicative life-span of cultivated human cells. Effects of donor's age, tissue, and genotype". Lab. Invest. 23 (1): 86–92. PMID 5431223.
Salk D, Au K, Hoehn H, Martin GM (1981). "Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism". Cytogenet. Cell Genet. 30 (2): 92–107. doi:10.1159/000131596. PMID 7273860.
Fukuchi K, Martin GM, Monnat RJ (1989). "Mutator phenotype of Werner syndrome is characterized by extensive deletions". Proc. Natl. Acad. Sci. U.S.A. 86 (15): 5893–7. Bibcode:1989PNAS...86.5893F. doi:10.1073/pnas.86.15.5893. PMC 297737. PMID 2762303.
Crabbe L, Jauch A, Naeger CM, Holtgreve-Grez H, Karlseder J (2007). "Telomere dysfunction as a cause of genomic instability in Werner syndrome". Proc. Natl. Acad. Sci. U.S.A. 104 (7): 2205–10. Bibcode:2007PNAS..104.2205C. doi:10.1073/pnas.0609410104. JSTOR 25426449. PMC 1794219. PMID 17284601.
Chan SR, Blackburn EH (2004). "Telomeres and telomerase". Philos. Trans. R. Soc. Lond. B Biol. Sci. 359 (1441): 109–21. doi:10.1098/rstb.2003.1370. PMC 1693310. PMID 15065663.
Multani AS, Chang S (2006). "WRN at telomeres: implications for aging and cancer". J. Cell Sci. 120 (Pt 5): 713–21. doi:10.1242/jcs.03397. PMID 17314245. S2CID 6734884.
Szekely AM, Bleichert F, Nümann A, Van Komen S, Manasanch E, Ben Nasr A, Canaan A, Weissman SM (2005). "Werner protein protects nonproliferating cells from oxidative DNA damage". Mol. Cell. Biol. 25 (23): 10492–506. doi:10.1128/MCB.25.23.10492-10506.2005. PMC 1291253. PMID 16287861.
Davis T, Kipling D (2006). "Werner Syndrome as an example of inflamm-aging: possible therapeutic opportunities for a progeroid syndrome?". Rejuvenation Res. 9 (3): 402–7. doi:10.1089/rej.2006.9.402. PMID 16859481.
Massip L, Garand C, Paquet ER, Cogger VC, O'Reilly JN, Tworek L, Hatherell A, Taylor CG, Thorin E, Zahradka P, Le Couteur DG, Lebel M (2009-09-09). "Vitamin C restores healthy aging in a mouse model for Werner syndrome". FASEB J. 24 (1): 158–72. doi:10.1096/fj.09-137133. PMC 3712979. PMID 19741171.
Coppedè F (August 5, 2013). "The epidemiology of premature aging and associated comorbidities". Clin Interv Aging. 8: 1023–32. doi:10.2147/CIA.S37213. PMC 3760297. PMID 24019745.

ncbi.nlm.nih.gov

Oshima J, Martin GM, Hisama FM (February 2012) [1993–]. "Werner Syndrome". In Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews. Seattle WA: University of Washington, Seattle. PMID 20301687. NBK1514.
Oshima J, Martin GM, Hisama FM. Werner Syndrome. 2002 Dec 2 [Updated 2012 Dec 13]. In: Pagon RA, Bird TD, Dolan CR, et al., editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993-. Available from:https://www.ncbi.nlm.nih.gov/books/NBK1514/
Kyng KJ, May A, Kølvraa S, Bohr VA (2003). "Gene expression profiling in Werner syndrome closely resembles that of normal aging". Proc. Natl. Acad. Sci. U.S.A. 100 (21): 12259–64. Bibcode:2003PNAS..10012259K. doi:10.1073/pnas.2130723100. PMC 218746. PMID 14527998.
Kyng K, Croteau DL, Bohr VA (2009). "Werner syndrome resembles normal aging". Cell Cycle. 8 (15): 2319–2323. doi:10.4161/cc.8.15.9148. PMC 4172458. PMID 19633413.
Coppedè, Fabio (August 2013). "The epidemiology of premature aging and associated comorbidities". Clinical Interventions in Aging. 8: 1023–32. doi:10.2147/CIA.S37213. PMC 3760297. PMID 24019745.
Monnat RJ (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.
Rossi ML, Ghosh AK, Bohr VA (March 2010). "Roles of Werner syndrome protein in protection of genome integrity". DNA Repair (Amst.). 9 (3): 331–44. doi:10.1016/j.dnarep.2009.12.011. PMC 2827637. PMID 20075015.
Bernstein KA, Gangloff S, Rothstein R (2010). "The RecQ DNA helicases in DNA repair". Annu. Rev. Genet. 44: 393–417. doi:10.1146/annurev-genet-102209-163602. PMC 4038414. PMID 21047263.
Chen L, Oshima J (2002). "Werner Syndrome". J. Biomed. Biotechnol. 2 (2): 46–54. doi:10.1155/S1110724302201011. PMC 153784. PMID 12488583.
Pichierri P, Ammazzalorso F, Bignami M, Franchitto A (March 2011). "The Werner syndrome protein: linking the replication checkpoint response to genome stability". Aging. 3 (3): 311–8. doi:10.18632/aging.100293. PMC 3091524. PMID 21389352.
Kusumoto R, Dawut L, Marchetti C, Wan Lee J, Vindigni A, Ramsden D, Bohr VA (2008). "Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing". Biochemistry. 47 (28): 7548–56. doi:10.1021/bi702325t. PMC 2572716. PMID 18558713.
Harrigan JA, Wilson DM, Prasad R, Opresko PL, Beck G, May A, Wilson SH, Bohr VA (2006). "The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta". Nucleic Acids Res. 34 (2): 745–54. doi:10.1093/nar/gkj475. PMC 1356534. PMID 16449207.
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