The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Preferential Accumulation of Single-Stranded Regions in Telomeres of Human Fibroblasts
Open accessAbstract
We have demonstrated recently that chronic hyperoxic treatment accelerates the rate of aging of fibroblasts and the rate of telomere shortening in parallel. It was hypothesized that accelerated telomere shortening is due to preferential accumulation of oxidative damage in telomeres. To test this hypothesis, we measured the accumulation of sites sensitive to S1 nuclease treatment in telomeres, in minisatellites, and in the bulk of the genome of fibroblasts under different models of oxidative stress as well as after treatment with the alkylating agent, N-methyl-N'-nitro-N-nitrosoguanidine. A comparison with qualitative data obtained by alkaline electrophoresis reveals that the sites transferred to double-strand breaks by treatment with low concentrations of S1 nuclease are, in fact, single-stranded regions in the DNA. These regions may resemble single-stranded overhangs, gaps, or conventional single-strand breaks. The frequency of single-stranded regions is significantly higher in telomeres than in minisatellites or in the bulk of the genome under all conditions tested. Those regions induced in minisatellites or in the overall genome by a bolus dose of hydrogen peroxide are completely repaired within 24 h. On the other hand, 50 +/- 12% of H2O2-induced single-stranded regions remain unrepaired for at least 19 days in telomeres of human fibroblasts, leading to a significant increase of the telomeric steady-state level of these lesions. This preferential accumulation might significantly contribute to telomere shortening.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“As telomere DNA is particularly sensitive to oxidative damage (Oikawa & Kawanishi, 1999) and single‐strand breaks or other stress‐induced lesions at telomeres are inefficiently repaired (Petersen et al., 1998)”
From P66SHC deletion improves fertility and progeric phenotype of late-generation TERC-deficient mice but not their short lifespan (2016) · cites this paper as Petersen et al., 1998
In the citing paper
“single-stranded breaks have been shown to preferentially accumulate at telomeres in conditions of mild oxidative stress, and such lesions lead to replication fork stalling, resulting in incomplete replication of chromosome ends and thus accelerated telomere shortening (Petersen et al., 1998, von Zglinicki, 2000).”
From Telomeres and cell senescence—size matters not (2017) · cites this paper as Petersen et al., 1998
In the citing paper
“Many studies associate the presence of a great amount of mitochondrial ROS with accumulated single-strand breaks in telomere regions, thus accelerating telomere erosion and cellular senescence [106,107].”
From Role of Age-Related Mitochondrial Dysfunction in Sarcopenia (2020) · cites this paper as [106]
Citations
Cites
The limited in vitro lifetime of human diploid cell strains
Hayflick, L. (1965) · Experimental Cell Research · doi:10.1016/0014-4827(65)90211-9 · Cited by 5,876
Telomeres shorten during ageing of human fibroblasts
Harley, C. B., Futcher, A. B., & Greider, C. W. (1990) · Nature · doi:10.1038/345458a0 · Cited by 5,750
The RNA Component of Human Telomerase
Feng, J., Funk, W. D., Wang, S.-S., Weinrich, S. L., Avilion, A. A., Chiu, C.-P., Adams, R. R., Chang, E., Allsopp, R. C., Yu, J., et al. (1995) · Science · doi:10.1126/science.7544491 · Cited by 2,227
Telomere loss: mitotic clock or genetic time bomb?
Harley, C. B. (1991) · Mutation Research/DNAging · doi:10.1016/0921-8734(91)90018-7 · Cited by 1,139
Oxidative damage to DNA during aging: 8-hydroxy-2'-deoxyguanosine in rat organ DNA and urine.
Fraga, C. G., Shigenaga, M. K., Park, J. W., Degan, P., & Ames, B. N. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4533 · Cited by 1,106
Makarov, V. L., Hirose, Y., & Langmore, J. P. (1997) · Cell · doi:10.1016/s0092-8674(00)81908-x · Cited by 959
Mild hyperoxia shortens telomeres and inhibits proliferation of fibroblasts: a model for senescence?
von Zglinicki, T., Saretzki, G., Döcke, W., & Lotze, C. (1995) · Experimental Cell Research · doi:10.1006/excr.1995.1305 · Cited by 856
Self-citationOxidative DNA damage and senescence of human diploid fibroblast cells.
Chen, Q., Fischer, A., Reagan, J. D., Yan, L. J., & Ames, B. N. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.10.4337 · Cited by 720
Henderson, E. A., Hardin, C. C., Walk, S. K., Tinoco, I., & Blackburn, E. H. (1987) · Cell · doi:10.1016/0092-8674(87)90577-0 · Cited by 684
Telomerase activity in normal leukocytes and in hematologic malignancies
Counter, C. M., Gupta, J., Harley, C., Leber, B. F., & Bacchetti, S. (1995) · Blood · doi:10.1182/blood.v85.9.2315.bloodjournal8592315 · Cited by 604
Flagged first, then by citations
Research works printed but not linked: 1
- von Zglinicki, 1997, Die molekularen Mechanismen der Seneszenz in Zellkultur, Z. Gerontol. Geriatr., 30, 24
Cited by
Sorted by citations
Oxidative stress shortens telomeres
von Zglinicki, T. (2002) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(02)02110-2 · Cited by 2,524
Blackburn, E. H., Epel, E. S., & Lin, J. (2015) · Science · doi:10.1126/science.aab3389 · Cited by 1,596
Mitochondria, oxygen free radicals, disease and ageing
Raha, S., & Robinson, B. H. (2000) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)01674-1 · Cited by 1,066
Trends in oxidative aging theories
Muller, F. L., Lustgarten, M. S., Jang, Y., Richardson, A., & Van Remmen, H. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.03.034 · Cited by 1,053
Hewitt, G., Jurk, D., Marques, F. D. M., Correia-Melo, C., Hardy, T., Gackowska, A., Anderson, R., Taschuk, M., Mann, J., & Passos, J. F. (2012) · Nature Communications · doi:10.1038/ncomms1708 · Cited by 908
Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation
Fumagalli, M., Rossiello, F., Clerici, M., Barozzi, S., Cittaro, D., Kaplunov, J. M., Bucci, G., Dobreva, M., Matti, V., Beausejour, C. M., et al. (2012) · Nature Cell Biology · doi:10.1038/ncb2466 · Cited by 851
Chronic inflammation induces telomere dysfunction and accelerates ageing in mice
Jurk, D., Wilson, C., Passos, J. F., Oakley, F., Correia-Melo, C., Greaves, L., Saretzki, G., Fox, C., Lawless, C., Anderson, R., et al. (2014) · Nature Communications · doi:10.1038/ncomms5172 · Cited by 819
Self-citationMitochondrial dysfunction accounts for the stochastic heterogeneity in telomere-dependent senescence
Passos, J. F., Saretzki, G., Ahmed, S., Nelson, G., Richter, T., Peters, H., Wappler, I., Birket, M. J., Harold, G., Schaeuble, K., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050110 · Cited by 796
“stress-dependent accumulation of single-strand breaks [11]”
Self-citationToussaint, O., Medrano, E. E., & von Zglinicki, T. (2000) · Experimental Gerontology · doi:10.1016/s0531-5565(00)00180-7 · Cited by 713
Self-citationMatthews, C., Gorenne, I., Scott, S., Figg, N., Kirkpatrick, P., Ritchie, A., Goddard, M., & Bennett, M. (2006) · Circulation Research · doi:10.1161/01.res.0000233315.38086.bc · Cited by 615
The impact of oxidative DNA damage and stress on telomere homeostasis
Barnes, R. P., Fouquerel, E., & Opresko, P. L. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.03.013 · Cited by 585
Telomere length assessment: Biomarker of chronic oxidative stress?
Houben, J. M. J., Moonen, H. J. J., van Schooten, F., & Hageman, G. J. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.10.001 · Cited by 577
Accumulation of single-strand breaks is the major cause of telomere shortening in human fibroblasts
von Zglinicki, T., Pilger, R., & Sitte, N. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00207-5 · Cited by 546
Self-citationTelomere Length in Epidemiology: A Biomarker of Aging, Age-Related Disease, Both, or Neither?
Sanders, J. L., & Newman, A. B. (2013) · Epidemiologic Reviews · doi:10.1093/epirev/mxs008 · Cited by 556
Kurz, D. J., Decary, S., Hong, Y., Trivier, E., Akhmedov, A., & Erusalimsky, J. D. (2004) · Journal of Cell Science · doi:10.1242/jcs.01097 · Cited by 499
Ahmed, S. S., Passos, J. F., Birket, M. J., Beckmann, T., Brings, S., Peters, H., Birch‐Machin, M. A., von Zglinicki, T., & Saretzki, G. C. (2008) · Journal of Cell Science · doi:10.1242/jcs.019372 · Cited by 497
Self-citationGomes, N. M. V., Ryder, O. A., Houck, M. L., Charter, S. J., Walker, W., Forsyth, N. R., Austad, S. N., Venditti, C., Pagel, M., Shay, J. W., et al. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00718.x · Cited by 464
Role of Oxidative Stress in Telomere Length Regulation and Replicative Senescence
von Zglinicki, T. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06639.x · Cited by 452
Self-citationIs Telomere Length a Biomarker of Aging? A Review
Mather, K. A., Jorm, A. F., Parslow, R., & Christensen, H. M. (2010) · The Journals of Gerontology Series A · doi:10.1093/gerona/glq180 · Cited by 450
Human cell senescence as a DNA damage response
Zglinicki, T. V., Saretzki, G., Ladhoff, J., Fagagna, F. D. D., & Jackson, S. P. (2005) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.09.034 · Cited by 419
Self-citationTelomeres and cell senescence—size matters not
Victorelli, S., & Passos, J. F. (2017) · EBioMedicine · doi:10.1016/j.ebiom.2017.03.027 · Cited by 413
Stress and telomere shortening: Insights from cellular mechanisms
Lin, J., & Epel, E. S. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101507 · Cited by 418
Sex differences in telomeres and lifespan
Barrett, E. L. B., & Richardson, D. S. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00741.x · Cited by 366
Cellular senescence: all roads lead to mitochondria
Martini, H., & Passos, J. F. (2023) · The FEBS Journal · doi:10.1111/febs.16361 · Cited by 334
Severe Life Stress and Oxidative Stress in the Brain: From Animal Models to Human Pathology
Schiavone, S., Jaquet, V., Trabace, L., & Krause, K. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4720 · Cited by 363
Henle, E. S., Han, Z., Tang, N., Rai, P., Luo, Y., & Linn, S. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.2.962 · Cited by 345
Aging and Immune Function: Molecular Mechanisms to Interventions
Ponnappan, S., & Ponnappan, U. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3228 · Cited by 339
Factors underlying the cell growth-related bystander responses to alpha particles.
Iyer, R. S., Lehnert, B. E., & Svensson, R. (2000) · PubMed · Cited by 346
Monocyte Telomere Shortening and Oxidative DNA Damage in Type 2 Diabetes
Sampson, M., Winterbone, M. S., Hughes, J. C., Dozio, N., & Hughes, D. A. (2006) · Diabetes Care · doi:10.2337/diacare.29.02.06.dc05-1715 · Cited by 343
Erosion of the telomeric single-strand overhang at replicative senescence
Stewart, S. A., Ben-Porath, I., Carey, V. J., O'Connor, B. F., Hahn, W. C., & Weinberg, R. A. (2003) · Nature Genetics · doi:10.1038/ng1127 · Cited by 335
Mitochondrial dysfunction and cell senescence: deciphering a complex relationship
Chapman, J., Fielder, E., & Passos, J. F. (2019) · FEBS Letters · doi:10.1002/1873-3468.13498 · Cited by 325
Schoenmakers, E., Agostini, M., Mitchell, C., Schoenmakers, N., Papp, L., Rajanayagam, O., Padidela, R., Ceron-Gutierrez, L., Doffinger, R., Prevosto, C., et al. (2010) · Journal of Clinical Investigation · doi:10.1172/jci43653 · Cited by 315
DNA damage in telomeres and mitochondria during cellular senescence: is there a connection?
Passos, J. F., Saretzki, G., & von Zglinicki, T. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm893 · Cited by 344
Self-citationvon Zglinicki, T., Serra, V., Lorenz, M., Saretzki, G. C., Lenzen-Großimlinghaus, R., Gessner, R. V., Risch, A., & Steinhagen‐Thiessen, E. (2000) · Laboratory Investigation · doi:10.1038/labinvest.3780184 · Cited by 305
Self-citationOxidative damage in telomeric DNA disrupts recognition by TRF1 and TRF2
Opresko, P. L. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki273 · Cited by 289
Association of telomere length with type 2 diabetes, oxidative stress and UCP2 gene variation
Salpea, K. D., Talmud, P. J., Cooper, J. A., Maubaret, C. G., Stephens, J. W., Abelak, K., & Humphries, S. E. (2009) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2009.09.070 · Cited by 295
Targeted and Persistent 8-Oxoguanine Base Damage at Telomeres Promotes Telomere Loss and Crisis
Fouquerel, E., Barnes, R. P., Uttam, S., Watkins, S. C., Bruchez, M. P., & Opresko, P. L. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.04.024 · Cited by 275
“, 2012) and reports that telomeres are 15-fold more sensitive to damage than the genome overall (Petersen et al., 1998), we estimate that dye + light produces at least one 8-oxoG per 28-kb telomere.”
BackgroundFactors contributing to the outcome of oxidative damage to nucleic acids
Evans, M. D., & Cooke, M. S. (2004) · BioEssays · doi:10.1002/bies.20027 · Cited by 279
Serra, V., von Zglinicki, T., Lorenz, M., & Saretzki, G. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m207939200 · Cited by 278
Self-citationReplicative senescence: a critical review
Cristofalo, V. J., Lorenzini, A., Allen, R. G., Torres, C. A., & Tresini, M. (2004) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.07.010 · Cited by 285
Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer
Broberg, K., Björk, J., Paulsson, K., Höglund, M., & Albin, M. (2005) · Carcinogenesis · doi:10.1093/carcin/bgi063 · Cited by 255
Senescent human melanocytes drive skin ageing via paracrine telomere dysfunction
Victorelli, S., Lagnado, A., Halim, J., Moore, W., Talbot, D., Barrett, K., Chapman, J., Birch, J., Ogrodnik, M., Meves, A., et al. (2019) · The EMBO Journal · doi:10.15252/embj.2019101982 · Cited by 258
Replicative Aging, Telomeres, and Oxidative Stress
Saretzki, G. C., & von Zglinicki, T. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb02079.x · Cited by 253
Self-citationTelomeres, chromosome instability and cancer
Bailey, S. M. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl303 · Cited by 245
Somatic growth and telomere dynamics in vertebrates: relationships, mechanisms and consequences
Monaghan, P., & Ozanne, S. E. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0446 · Cited by 248
Cellular Senescence: Molecular Mechanisms, In Vivo Significance, and Redox Considerations
Müller, M. K. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2008.2104 · Cited by 243
Mitochondrial dysfunction leads to telomere attrition and genomic instability
Liu, L., Trimarchi, J. R., Smith, P. J. S., & Keefe, D. L. (2002) · Aging Cell · doi:10.1046/j.1474-9728.2002.00004.x · Cited by 237
Role of Age-Related Mitochondrial Dysfunction in Sarcopenia
Ferri, E., Marzetti, E., Calvani, R., Picca, A., Cesari, M., & Arosio, B. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155236 · Cited by 224
Diet, nutrition and telomere length
Paul, L. (2011) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2010.12.001 · Cited by 227
The first molecular details of ALT in human tumor cells
Muntoni, A., & Reddel, R. R. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi266 · Cited by 226
Verfaillie, C. M., Pera, M. F., & Lansdorp, P. M. (2002) · Hematology · doi:10.1182/asheducation-2002.1.369 · Cited by 223
The association between stressors and telomeres in non‐human vertebrates: a meta‐analysis
Chatelain, M., Drobniak, S. M., & Szulkin, M. (2019) · Ecology Letters · doi:10.1111/ele.13426 · Cited by 232
Neutrophils induce paracrine telomere dysfunction and senescence in ROS‐dependent manner
Lagnado, A., Leslie, J., Ruchaud‐Sparagano, M., Victorelli, S., Hirsova, P., Ogrodnik, M., Collins, A. L., Vizioli, M. G., Habiballa, L., Saretzki, G., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2020106048 · Cited by 211
Self-citationHallmarks of telomeres in ageing research
Shay, J., & Wright, W. E. (2007) · The Journal of Pathology · doi:10.1002/path.2090 · Cited by 211
Saretzki, G., Murphy, M. P., & Von Zglinicki, T. (2003) · Aging Cell · doi:10.1046/j.1474-9728.2003.00040.x · Cited by 203
Self-citationStress, DNA damage and ageing — an integrative approach
von Zglinicki, T. (2001) · Experimental Gerontology · doi:10.1016/s0531-5565(01)00111-5 · Cited by 200
Self-citationVascular smooth muscle cell senescence in atherosclerosis
GORENNE, I., KAVURMA, M., SCOTT, S., & BENNETT, M. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.06.004 · Cited by 196
Diabetes, metabolic disease, and telomere length
Cheng, F., Carroll, L. M., Joglekar, M. V., Januszewski, A. S., Wong, K. K., Hardikar, A. A., Jenkins, A. J., & Ronald, C. W. (2020) · The Lancet Diabetes & Endocrinology · doi:10.1016/s2213-8587(20)30365-x · Cited by 196
Gomes, N. M. V., Shay, J. W., & Wright, W. E. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.07.031 · Cited by 197
Ageing, telomeres, senescence, and liver injury
Hoare, M., Das, T., & Alexander, G. (2010) · Journal of Hepatology · doi:10.1016/j.jhep.2010.06.009 · Cited by 184
Coluzzi, E., Colamartino, M., Cozzi, R., Leone, S., Meneghini, C., O’Callaghan, N., & Sgura, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110963 · Cited by 197
Telomeres and chromosome instability
Murnane, J. P. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.05.030 · Cited by 178
Saretzki, G. C., Sitte, N., Merkel, U., Wurm, R. E., & von Zglinicki, T. (1999) · Oncogene · doi:10.1038/sj.onc.1202898 · Cited by 171
Self-citationDNA damage response at telomeres contributes to lung aging and chronic obstructive pulmonary disease
Birch, J., Anderson, R. K., Correia-Melo, C., Jurk, D., Hewitt, G., Marques, F. M., Green, N. J., Moisey, E., Birrell, M. A., Belvisi, M. G., et al. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00293.2015 · Cited by 174
Senescence in Post-Mitotic Cells: A Driver of Aging?
von Zglinicki, T., Wan, T., & Miwa, S. (2021) · Antioxidants & Redox Signaling · doi:10.1089/ars.2020.8048 · Cited by 170
The role of oxidative and nitrosative stress in accelerated aging and major depressive disorder
Maurya, P. K., Noto, C. D. S., Rizzo, L. B., Rios, A. C., Nunes, S. O. V., Barbosa, D. S., Sethi, S., Zeni‐Graiff, M., Mansur, R. B., Maes, M. H. J., et al. (2015) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2015.08.016 · Cited by 174
Mitochondria, telomeres and cell senescence: Implications for lung ageing and disease
Birch, J., Barnes, P. J., & Passos, J. F. (2017) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2017.10.005 · Cited by 174
Telomere length measurement as a clinical biomarker of aging and disease
Fasching, C. L. (2018) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408363.2018.1504274 · Cited by 173
Sabatier, L., Ricoul, M., Pottier, G., & Murnane, J. P. (2005) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-04-0194 · Cited by 160
Genetic regulation of embryo death and senescence
Betts, D. H., & King, W. A. (2001) · Theriogenology · doi:10.1016/s0093-691x(00)00453-2 · Cited by 164
Mitochondria: Are they causal players in cellular senescence?
Correia-Melo, C., & Passos, J. F. (2015) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2015.05.017 · Cited by 160
Telomere Length, Oxidative Damage, Antioxidants and Breast Cancer Risk
Shen, J., Gammon, M. D., Terry, M. B., Wang, Q., Bradshaw, P., Teitelbaum, S. L., Neugut, A. I., & Santella, R. M. (2009) · International Journal of Cancer · doi:10.1002/ijc.24105 · Cited by 159
Deficiency of the DNA repair enzyme ATM in rheumatoid arthritis.
Shao, L., Fujii, H., Colmegna, I., Oishi, H., Goronzy, J. J., & Weyand, C. M. (2009) · Journal of Experimental Medicine · doi:10.1084/jem.20082251 · Cited by 159
Mechanisms of telomere loss and their consequences for chromosome instability
Muraki, K., Nyhan, K. C., Han, L., & Murnane, J. P. (2012) · Frontiers in Oncology · doi:10.3389/fonc.2012.00135 · Cited by 173
Short Telomere Length and Breast Cancer Risk: A Study in Sister Sets
Shen, J., Terry, M. B., Gurvich, I., Liao, Y., Senie, R. T., & Santella, R. M. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-3490 · Cited by 157
Extra-telomeric Functions of Human Telomerase: Cancer, Mitochondria and Oxidative Stress
Saretzki, G. C. (2014) · Current Pharmaceutical Design · doi:10.2174/1381612820666140630095606 · Cited by 162
Self-citationChromosome rearrangements resulting from telomere dysfunction and their role in cancer
Murnane, J. P., & Sabatier, L. (2004) · BioEssays · doi:10.1002/bies.20125 · Cited by 165
Calorie restriction and the exercise of chromatinPreprint
Vaquero, A., & Reinberg, D. (2009) · Genes & Development · doi:10.1101/gad.1807009 · Cited by 157
Armstrong, L., Saretzki, G., Peters, H., Wappler, I., Evans, J., Hole, N., von Zglinicki, T., & Lako, M. (2005) · Stem Cells · doi:10.1634/stemcells.2004-0269 · Cited by 153
Self-citationPavanello, S., Pesatori, A. C., Dioni, L., Hoxha, M., Bollati, V., Siwińska, E., Mielżyńska, D., Bolognesi, C., Bertazzi, P. A., & Baccarelli, A. (2009) · Carcinogenesis · doi:10.1093/carcin/bgp278 · Cited by 148
Tchirkov, A. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg023 · Cited by 143
Mahmoudi, M., Gorenne, I., Mercer, J. R., Figg, N., Littlewood, T. D., & Bennett, M. R. (2008) · Circulation Research · doi:10.1161/circresaha.108.182899 · Cited by 142
DNA damage and repair in atherosclerosis
Mahmoudi, M., MERCER, J., & Bennett, M. R. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.03.002 · Cited by 137
Telomere dysfunction, genome instability and cancer
Annie, L. M. C. (2007) · Frontiers in bioscience · doi:10.2741/2825 · Cited by 137
The role of oxidative damage in mitochondria during aging: a review
Huang, H. (2004) · Frontiers in bioscience · doi:10.2741/1298 · Cited by 136
Gavia-García, G., Rosado-Pérez, J., Arista-Ugalde, T. L., Aguíñiga-Sánchez, I., Santiago‐Osorio, E., & Mendoza-Núñez, V. M. (2021) · Biology · doi:10.3390/biology10040253 · Cited by 148
Human Telomeres Are Hypersensitive to UV-Induced DNA Damage and Refractory to Repair
Rochette, P. J., & Brash, D. E. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000926 · Cited by 133
Permanent embryo arrest: molecular and cellular concepts
Betts, D. H., & Madan, P. (2008) · Molecular Human Reproduction · doi:10.1093/molehr/gan035 · Cited by 131
Asok, A., Bernard, K., Roth, T. L., Rosen, J. B., & Dozier, M. (2013) · Development and Psychopathology · doi:10.1017/s0954579413000011 · Cited by 128
Air Pollution Stress and the Aging Phenotype: The Telomere Connection
Martens, D. S., & Nawrot, T. S. (2016) · Current Environmental Health Reports · doi:10.1007/s40572-016-0098-8 · Cited by 132
Lipofuscin accumulation in proliferating fibroblasts in vitro: an indicator of oxidative stress
Sitte, N., Merker, K., Grune, T., & von Zglinicki, T. (2001) · Experimental Gerontology · doi:10.1016/s0531-5565(00)00253-9 · Cited by 127
Self-citationJennings, B. J., Ozanne, S. E., & Hales, C. N. (2000) · Molecular Genetics and Metabolism · doi:10.1006/mgme.2000.3077 · Cited by 129
Extra-chromosomal telomeric DNA in cells from Atm-/- mice and patients with ataxia-telangiectasia
Hande, M. P. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.5.519 · Cited by 125
Telomeres and telomerase in prostate cancer development and therapy
Graham, M. K., & Meeker, A. K. (2017) · Nature Reviews Urology · doi:10.1038/nrurol.2017.104 · Cited by 125
Telomeres and immunological diseases of aging.
Andrews, N. P., Fujii, H., Goronzy, J. J., & Weyand, C. M. (2010) · Gerontology · doi:10.1159/000268620 · Cited by 108
Accelerated telomere shortening and telomerase activation in Fanconi's anaemia
Leteurtre, F., Li, X., Guardiola, P., Roux, G. L., Sergère, J., Richard, P., Carosella, E. D., & Gluckman, É. (1999) · British Journal of Haematology · doi:10.1046/j.1365-2141.1999.01445.x · Cited by 119
Lo, A. W. I., Sprung, C. N., Fouladi, B., Pedram, M., Sabatier, L., Ricoul, M., Reynolds, G. E., & Murnane, J. P. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.13.4836-4850.2002 · Cited by 118
Telomere length in atherosclerosis and diabetes
Salpea, K. D., & Humphries, S. E. (2009) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2009.12.021 · Cited by 117
Ludwig, A., Saretzki, G. C., Holm, P. S., Tiemann, F., Lorenz, M., Emrich, T., Harley, C. B., & von Zglinicki, T. (2001) · PubMed · doi:10.25405/ncl.34663959 · Cited by 117
Self-citationEffect of Long-Term Hormone Therapy on Telomere Length in Postmenopausal Women
Lee, D., Im, J., Kim, J., Lee, H.-R., & Shim, J. (2005) · Yonsei Medical Journal · doi:10.3349/ymj.2005.46.4.471 · Cited by 114
Metadata
- Authors
- Petersen, S., Saretzki, G., & Zglinicki, T. V.
- Affiliations
- Humboldt-Universität zu Berlin (DE)
- Corresponding author
- Zglinicki, Thomas von
- Venue
- Experimental Cell Research
- Publisher
- Elsevier BV
- Published
- 1998-02
- Volume
- 239
- Issue
- 1
- Pages
- 152-160
- ISSN
- 0014-4827 (ISSN-L)
- OpenAlex
- W2037480531
- Cited by
- 427
- References
- 33
- Citations by year
- 2026: 1 · 2025: 10 · 2024: 9 · 2023: 17 · 2022: 15 · 2021: 14 · 2020: 14 · 2019: 19 · 2018: 18 · 2017: 14 · 2016: 23 · 2015: 15 · 2014: 16 · 2013: 17 · 2012: 20
- FWCI
- 7.99
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Experimental Cell Research (publishedVersion)
- PubMed (publishedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- telomeres, telomere shortening, oxidative DNA damage, hydrogen peroxide, S1 nuclease, minisatellites, N-methyl-N'-nitro-N-nitrosoguanidine, alkylating agents, DNA repair, human fibroblasts, hyperoxia, aging
- MeSH terms
- Cell Line, DNA, Fibroblasts, Humans, Methylnitronitrosoguanidine, Single-Strand Specific DNA and RNA Endonucleases, Telomere, Minisatellite Repeats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review