Origin of Concatemeric T7DNA

Bacteriophage T7

Studier, F. W. (1972) · Science · doi:10.1126/science.176.4033.367 · Cited by 592 · see citing works

The genetics and physiology of bacteriophage T7

Studier, F. W. (1969) · Virology · doi:10.1016/0042-6822(69)90104-4 · Cited by 521 · see citing works

Mechanism of DNA chain growth. I. Possible discontinuity and unusual secondary structure of newly synthesized chains.

Okazaki, R., Okazaki, T., SAKABE, K., Sugimoto, K., & Sugino, A. (1968) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.59.2.598 · Cited by 435 · see citing works

Active Center of DNA Polymerase

Kornberg, A. (1969) · Science · doi:10.1126/science.163.3874.1410 · Cited by 413 · see citing works

RNA Synthesis Initiates In Vitro Conversion of M13 DNA to Its Replicative Form

Wickner, W. T., Brutlag, D. L., Schekman, R. W., et al. (1972) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.69.4.965 · Cited by 301 · see citing works

A Possible Role for RNA Polymerase in the Initiation of M13 DNA Synthesis

Brutlag, D. L., Schekman, R. W., & Kornberg, A. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.11.2826 · Cited by 264 · see citing works

CHROMOSOME STRUCTURE IN PHAGE T4, III. TERMINAL REDUNDANCY AND LENGTH DETERMINATION

Streisinger, G., Emrich, J., & Stahl, M. M. (1967) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.57.2.292 · Cited by 251 · see citing works

Enzymes in DNA Metabolism

Richardson, C. C. (1969) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.38.070169.004051 · Cited by 150 · see citing works

Terminal repetition in non-permuted T3 and T7 bacteriophage DNA molecules

Ritchie, D. A., Thomas, C. A., MacHattie, L. A., et al. (1967) · Journal of Molecular Biology · doi:10.1016/s0022-2836(67)80111-6 · Cited by 142 · see citing works

An intermediate in the replication of bacteriophage T7 DNA molecules

Kelly, T. J., & Thomas, C. A. (1969) · Journal of Molecular Biology · doi:10.1016/0022-2836(69)90373-8 · Cited by 135 · see citing works

The Anatomy of Viral DNA Molecules

Thomas, C. A., & MacHattie, L. A. (1967) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.36.070167.002413 · Cited by 120 · see citing works

Gene 6 Exonuclease of Bacteriophage T7

Kerr, C., & Sadowski, P. D. (1972) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)45791-8 · Cited by 113 · see citing works

Initiation and Reinitiation of DNA Synthesis during Replication of Bacteriophage T7

Dressler, D., Wolfson, J. S., & Magazin, M. (1972) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.69.4.998 · Cited by 99 · see citing works

Bacteriophage T7 DNA Replication: A Linear Replicating Intermediate

Wolfson, J. S., Dressler, D., & Magazin, M. (1972) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.69.2.499 · Cited by 86 · see citing works

Structure of the Replicating DNA from Bacteriophage T4

Delius, H., Howe, C. C., & Kozinski, A. W. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.12.3049 · Cited by 83 · see citing works

Structure of branch points in replicating DNA: Presence of single-stranded connections in λ DNA branch points

Inman, R. B., & Schnös, M. (1971) · Journal of Molecular Biology · doi:10.1016/0022-2836(71)90467-0 · Cited by 83 · see citing works

Biosynthesis of DNA

Goulian, M. (1971) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.40.070171.004231 · Cited by 76 · see citing works

Variations in sedimentation patterns among deoxyribonucleic acids synthesized after infection of Escherichia coli by different amber mutants of bacteriophage T7

Hausmann, R., & Larue, K. (1969) · Journal of Virology · doi:10.1128/jvi.3.2.278-281.1969 · Cited by 68 · see citing works

Enzymic synthesis of deoxyribonucleic acid

MITRA, S. P., Reichard, P. A., Inman, R. B., et al. (1967) · Journal of Molecular Biology · doi:10.1016/0022-2836(67)90229-x · Cited by 66 · see citing works

The 5′-terminal dinucleotides of the separated strands of T7 bacteriophage deoxyribonucleic acid

Weiss, B., & Richardson, C. C. (1967) · Journal of Molecular Biology · doi:10.1016/s0022-2836(67)80115-3 · Cited by 66 · see citing works

Chromosome structure in phage T4, II. Terminal redundancy and heterozygosis.

Séchaud, J., Streisinger, G., Emrich, J., et al. (1965) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.54.5.1333 · Cited by 56 · see citing works

The Intracellular Forms of T7 and P22 DNA MoleculesPreprint

Thomas, C. A., Kelly, T. J., & Rhoades, M. (1968) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1968.033.01.048 · Cited by 35 · see citing works

Transformation and DNA Size: Two Controlling Parameters and the Efficiency of the Single Strand IntermediatePreprint

Guild, W. R., Cato, A. E., & Lacks, S. A. (1968) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1968.033.01.072 · Cited by 29 · see citing works

Spontaneous renaturation of newly-synthesized bacteriophage T7 deoxyribonucleic acid

Barzilai, R., & Thomas, C. A. (1970) · Journal of Molecular Biology · doi:10.1016/0022-2836(70)90276-7 · Cited by 25 · see citing works

Additional evidence for two kinds of heterozygotes in phage T4.

Shalitin, C., & Stahl, F. W. (1965) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.54.5.1340 · Cited by 25 · see citing works

Intracellular fate of deoxyribonucleic acid from T7 bacteriophages

Carlson, K. (1968) · Journal of Virology · doi:10.1128/jvi.2.10.1230-1233.1968 · Cited by 22 · see citing works

Equal Incorporation of Both Parental Bacteriophage T7 Deoxyribonucleic Acid Strands into Intracellular Concatemeric Deoxyribonucleic Acid

Ihler, G. M., & Thomas, C. A. (1970) · Journal of Virology · doi:10.1128/jvi.6.6.877-880.1970 · Cited by 14 · see citing works

Terminal Cross-Linking of DNA Strands by an Enzyme System from Escherichia coli Infected with Bacteriophage T4

Weiss, B. (1970) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.65.3.652 · Cited by 12 · see citing works

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 · see citing works

Oxidative stress shortens telomeres

von Zglinicki, T. (2002) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(02)02110-2 · Cited by 2,524 · see citing works

Telomere length predicts replicative capacity of human fibroblasts.

Allsopp, R. C., Vaziri, H., Patterson, C., Goldstein, S., Younglai, E. V., Futcher, A. B., Greider, C. W., & Harley, C. B. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.21.10114 · Cited by 2,200 · see citing works

The essence of senescence: Figure 1.

Kuilman, T., Michaloglou, C., Mooi, W. J., & Peeper, D. S. (2010) · Genes & Development · doi:10.1101/gad.1971610 · Cited by 2,038 · see citing works

hEST2, the Putative Human Telomerase Catalytic Subunit Gene, Is Up-Regulated in Tumor Cells and during Immortalization

Meyerson, M., Counter, C. M., Eaton, E. N., Ellisen, L. W., Steiner, P., Caddle, S. D., Ziaugra, L., Beijersbergen, R. L., Davidoff, M. J., Liu, Q., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80538-3 · Cited by 1,784 · see citing works

The human telomere terminal transferase enzyme is a ribonucleoprotein that synthesizes TTAGGG repeats

Morin, G. B. (1989) · Cell · doi:10.1016/0092-8674(89)90035-4 · Cited by 1,495 · see citing works

Cellular Senescence: Aging, Cancer, and Injury

Calcinotto, A., Kohli, J., Zagato, E., Pellegrini, L., Demaria, M., & Alimonti, A. (2019) · Physiological Reviews · doi:10.1152/physrev.00020.2018 · Cited by 1,270 · see citing works

Reverse Transcriptase Motifs in the Catalytic Subunit of Telomerase

Lingner, J., Hughes, T. R., Shevchenko, A., Mann, M., Lundblad, V., & Cech, T. R. (1997) · Science · doi:10.1126/science.276.5312.561 · Cited by 1,269 · see citing works

Telomeres and Aging

Aubert, G., & Lansdorp, P. M. (2008) · Physiological Reviews · doi:10.1152/physrev.00026.2007 · Cited by 1,188 · see citing works

The telomere terminal transferase of tetrahymena is a ribonucleoprotein enzyme with two kinds of primer specificity

Greider, C. W., & Blackburn, E. H. (1987) · Cell · doi:10.1016/0092-8674(87)90576-9 · Cited by 1,150 · see citing works

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 · see citing works

Telomere end-replication problem and cell aging

Levy, M. Z., Allsopp, R. C., Futcher, A. B., Greider, C. W., & Harley, C. B. (1992) · Journal of Molecular Biology · doi:10.1016/0022-2836(92)90096-3 · Cited by 1,069 · see citing works

Structure and variability of human chromosome ends.

de Lange, T., Shiue, L., Myers, R. M., Cox, D. R., Naylor, S. L., Killery, A. M., & Varmus, H. E. (1990) · Molecular and Cellular Biology · doi:10.1128/mcb.10.2.518 · Cited by 848 · see citing works

Senescence Induced by Altered Telomere State, Not Telomere Loss

Karlseder, J., Smogorzewska, A., & de Lange, T. (2002) · Science · doi:10.1126/science.1069523 · Cited by 796 · see citing works

Hayflick, his limit, and cellular ageing

Shay, J. W., & Wright, W. E. (2000) · Nature Reviews Molecular Cell Biology · doi:10.1038/35036093 · Cited by 764 · see citing works

Roles of telomeres and telomerase in cancer, and advances in telomerase-targeted therapies

Jafri, M. A., Ansari, S. A., Alqahtani, M. H., & Shay, J. W. (2016) · Genome Medicine · doi:10.1186/s13073-016-0324-x · Cited by 716 · see citing works

TELOMERES AND THEIR CONTROL

McEachern, M. J., Krauskopf, A., & Blackburn, E. H. (2000) · Annual Review of Genetics · doi:10.1146/annurev.genet.34.1.331 · Cited by 716 · see citing works

Role of Telomeres and Telomerase in Aging and Cancer

Shay, J. W. (2016) · Cancer Discovery · doi:10.1158/2159-8290.cd-16-0062 · Cited by 668 · see citing works

Telomeres: history, health, and hallmarks of aging

Chakravarti, D., LaBella, K. A., & DePinho, R. A. (2021) · Cell · doi:10.1016/j.cell.2020.12.028 · Cited by 637 · see citing works

Correlating telomerase activity levels with human neuroblastoma outcomes

Hiyama, E., Hiyama, K., Yokoyama, T., Matsuura, Y., Piatyszek, M. A., & Shay, J. W. (1995) · Nature Medicine · doi:10.1038/nm0395-249 · Cited by 611 · see citing works

DNA sequences of telomeres maintained in yeast

Shampay, J., Szostak, J. W., & Blackburn, E. H. (1984) · Nature · doi:10.1038/310154a0 · Cited by 551 · see citing works

A Protein-Counting Mechanism for Telomere Length Regulation in Yeast

Marcand, S., Gilson, E., & Shore, D. (1997) · Science · doi:10.1126/science.275.5302.986 · Cited by 524 · see citing works

Hallmarks of senescence in carcinogenesis and cancer therapy

Shay, J. W., & Roninson, I. B. (2004) · Oncogene · doi:10.1038/sj.onc.1207518 · Cited by 502 · see citing works

Replication and protection of telomeres

Verdun, R. E., & Karlseder, J. (2007) · Nature · doi:10.1038/nature05976 · Cited by 463 · see citing works

Telomere Length as a Marker of Biological Age: State-of-the-Art, Open Issues, and Future Perspectives.

Vaiserman, A., & Krasnienkov, D. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2020.630186 · Cited by 454 · see citing works

Telomeres, telomerase, and aging: Origin of the theory

Olovnikov, A. M. (1996) · Experimental Gerontology · doi:10.1016/0531-5565(96)00005-8 · Cited by 431 · see citing works

Telomeres and cell senescence—size matters not

Victorelli, S., & Passos, J. F. (2017) · EBioMedicine · doi:10.1016/j.ebiom.2017.03.027 · Cited by 413 · see citing works

Biomarkers of cellular senescence and skin aging

Wang, A. S., & Dreesen, O. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00247 · Cited by 404 · see citing works

Differential Expression of Telomerase Activity in Hematopoietic Progenitors from Adult Human Bone Marrow

Chiu, C., Dragowska, W., Kim, N. W., Vaziri, H., Yui, J., Thomas, T. E., Harley, C. B., & Lansdorp, P. M. (1996) · STEM CELLS · doi:10.1002/stem.140239 · Cited by 388 · see citing works

Telomerase Activity in Hematopoietic Cells Is Associated with Self-Renewal Potential

Morrison, S. J., Prowse, K. R., Ho, P., & Weissman, I. L. (1996) · Immunity · doi:10.1016/s1074-7613(00)80316-7 · Cited by 394 · see citing works

Telomerase-Mediated Telomere Addition In Vivo Requires DNA Primase and DNA Polymerases α and δ

Diede, S. J., & Gottschling, D. E. (1999) · Cell · doi:10.1016/s0092-8674(00)81670-0 · Cited by 379 · see citing works

Telomere Length: A Review of Methods for Measurement

Montpetit, A. J., Alhareeri, A. A., Montpetit, M., Starkweather, A. R., Elmore, L. W., Filler, K., Mohanraj, L., Burton, C. W., Menzies, V. S., Lyon, D. E., et al. (2014) · Nursing Research · doi:10.1097/nnr.0000000000000037 · Cited by 293 · see citing works

Telomere length homeostasis

Hug, N., & Lingner, J. (2006) · Chromosoma · doi:10.1007/s00412-006-0067-3 · Cited by 291 · see citing works

Functional Human Telomeres Are Recognized as DNA Damage in G2 of the Cell Cycle

Verdun, R. E., Crabbe, L., Haggblom, C., & Karlseder, J. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.09.024 · Cited by 284 · see citing works

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 · see citing works

Telomere-driven diseases and telomere-targeting therapies

Martínez, P., & Blasco, M. A. (2017) · Journal of Cell Biology · doi:10.1083/jcb.201610111 · Cited by 257 · see citing works

Telomere and its role in the aging pathways: telomere shortening, cell senescence and mitochondria dysfunction

Zhu, Y., Liu, X., Ding, X., Wang, F., & Geng, X. (2019) · Biogerontology · doi:10.1007/s10522-018-9769-1 · Cited by 255 · see citing works

Telomere dysfunction as a cause of genomic instability in Werner syndrome

Crabbe, L., Jauch, A., Naeger, C. M., Holtgreve-Grez, H., & Karlseder, J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609410104 · Cited by 240 · see citing works

Age-Dependent Telomere Shortening Is Slowed down by Enrichment of Intracellular Vitamin C via Suppression of Oxidative Stress

Furumoto, K., Inoue, E., Nagao, N., Hiyama, E., & Miwa, N. (1998) · Life Sciences · doi:10.1016/s0024-3205(98)00351-8 · Cited by 240 · see citing works

Telomere length in leukocyte subpopulations of patients with aplastic anemia

Brümmendorf, T. H., Maciejewski, J. P., Mak, J., Young, N. S., & Lansdorp, P. M. (2001) · Blood · doi:10.1182/blood.v97.4.895 · Cited by 233 · see citing works

Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia

Calado, R. T., Regal, J. A., Hills, M., Yewdell, W. T., Dalmazzo, L. F., Zago, M. A., Lansdorp, P. M., Hogge, D., Chanock, S. J., Estey, E. H., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807057106 · Cited by 184 · see citing works

Telomerase Activity Concentrates in the Mitotically Active Segments of Human Hair Follicles

Ramirez, R. D., Wright, W. E., Shay, J. W., & Taylor, R. S. (1997) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12285654 · Cited by 174 · see citing works

Progressive telomere shortening and telomerase reactivation during hepatocellular carcinogenesis

Miura, N., Horikawa, I., Nishimoto, A., Ohmura, H., Ito, H., Hirohashi, S., Shay, J. W., & Oshimura, M. (1997) · Cancer Genetics and Cytogenetics · doi:10.1016/s0165-4608(96)00329-9 · Cited by 174 · see citing works

“Social Life” of Senescent Cells: What Is SASP and Why Study It?

Borodkina, A. V., Deryabin, P. I., Giukova, А. А., & Nikolsky, N. N. (2018) · Acta Naturae · doi:10.32607/20758251-2018-10-1-4-14 · Cited by 170 · see citing works

Roles of telomere biology in cell senescence, replicative and chronological ageing

Liu, J., Wang, L., Wang, Z., & Liu, J.-P. (2019) · Cells · doi:10.3390/cells8010054 · Cited by 164 · see citing works

Comparison of the telomeric repeat amplification protocol (TRAP) to the new TRAP-eze telomerase detection kit

Holt, S. E., Norton, J. C., Wright, W. E., & Shay, J. W. (1996) · Methods in Cell Science · doi:10.1007/bf00132889 · Cited by 131 · see citing works

Mice without telomerase: what can they teach us about human cancer?

Artandi, S. E., & DePinho, R. A. (2000) · Nature Medicine · doi:10.1038/78595 · Cited by 126 · see citing works

The illusion of cell immortality

Hayflick, L. (2000) · British Journal of Cancer · doi:10.1054/bjoc.2000.1296 · Cited by 124 · see citing works

Linear mitochondrial genomes: 30 years down the line

Nosek, J., Tomáška, L., Fukuhara, H., Suyama, Y., & Kováč, L. (1998) · Trends in Genetics · doi:10.1016/s0168-9525(98)01443-7 · Cited by 122 · see citing works

For Better or Worse? Telomerase Inhibition and Cancer

de Lange, T., & Jacks, T. (1999) · Cell · doi:10.1016/s0092-8674(00)81955-8 · Cited by 119 · see citing works

The role of NBS1 in DNA double strand break repair, telomere stability, and cell cycle checkpoint control

Zhang, Y., Zhou, J., & Lim, C. U. (2006) · Cell Research · doi:10.1038/sj.cr.7310007 · Cited by 118 · see citing works

Identification and characterization of negative regulatory elements of the human telomerase catalytic subunit (hTERT) gene promoter: possible role of MZF-2 in transcriptional repression of hTERT

Fujimoto, K., Kyo, S., Takakura, M., Kanaya, T., Kitagawa, Y., Itoh, H., Takahashi, M., & Inoue, M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.13.2557 · Cited by 116 · see citing works

Telomerase Repressor Sequences on Chromosome 3 and Induction of Permanent Growth Arrest in Human Breast Cancer Cells

Cuthbert, A. P., Bond, J., Trott, D. A., Gill, S., Broni, J., Marriott, A., Khoudoli, G., Parkinson, E. K., Cooper, C. S., & Newbold, R. F. (1999) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/91.1.37 · Cited by 114 · see citing works

Small-Molecule PAPD5 Inhibitors Restore Telomerase Activity in Patient Stem Cells

Nagpal, N., Wang, J., Zeng, J., Lo, E., Moon, D. H., Luk, K., Braun, R. O., Burroughs, L. M., Keel, S. B., Reilly, C., et al. (2020) · Cell Stem Cell · doi:10.1016/j.stem.2020.03.016 · Cited by 105 · see citing works

Telomerase and telomeres in aging theory and chronographic aging theory (Review)

Razgonova, M., Zakharenko, A., Golokhvast, K., Thanasoula, M., Sarandi, E., Nikolouzakis, K., Fragkiadaki, P., Tsoukalas, D., Spandidos, D., & Tsatsakis, A. (2020) · Molecular Medicine Reports · doi:10.3892/mmr.2020.11274 · Cited by 89 · see citing works

Role of TERRA in the regulation of telomere length

Wang, C., Zhao, L., & Lu, S. (2015) · International Journal of Biological Sciences · doi:10.7150/ijbs.10528 · Cited by 89 · see citing works

Telomeres Shorten with Age in Rat Cerebellum and Cortex <i>in vivo</i>

Flanary, B. E., & Streit, W. J. (2003) · Journal of Anti-Aging Medicine · doi:10.1089/109454503323028894 · Cited by 85 · see citing works

Reprogramming of Telomerase by Expression of Mutant Telomerase RNA Template in Human Cells Leads to Altered Telomeres That Correlate with Reduced Cell Viability

Marušić, L., Anton, M., Tidy, A., Wang, P., Villeponteau, B., & Bacchetti, S. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.11.6394 · Cited by 74 · see citing works

Development of Retinoblastoma in the Absence of Telomerase Activity

Gupta, J., Han, L.-P., Wang, P., Gallie, B. L., & Bacchetti, S. (1996) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/88.16.1152 · Cited by 74 · see citing works

Hiding at the ends of yeast chromosomes: Telomeres, nucleases and checkpoint pathways

Lydall, D. (2003) · Journal of Cell Science · doi:10.1242/jcs.00765 · Cited by 72 · see citing works

Reduction of leucocyte telomere length in radiographic hand osteoarthritis: a population-based study

Zhai, G., Aviv, A., Hunter, D. J., Hart, D. J., Gardner, J. P., Kimura, M., Lu, X., Valdes, A. M., & Spector, T. D. (2006) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2006.056903 · Cited by 72 · see citing works

Telomerase is active in normal gastrointestinal mucosa and not up-regulated in precancerous lesions

Bachor, C., Bachor, O. A., & Boukamp, P. (1999) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s004320050302 · Cited by 68 · see citing works

Epigenetic ageing is distinct from senescence-mediated ageing and is not prevented by telomerase expression

Kabacik, S., Horvath, S., Cohen, H., & Raj, K. (2018) · Aging · doi:10.18632/aging.101588 · Cited by 68 · see citing works

Telomerase treatment prevents lung profibrotic pathologies associated with physiological aging

Piñeiro-Hermida, S., Autilio, C., Martínez, P., Bosch, F., Pérez-Gil, J., & Blasco, M. A. (2020) · Journal of Cell Biology · doi:10.1083/jcb.202002120 · Cited by 60 · see citing works

Do symptoms of depression predict telomere length? Evidence from the west of Scotland twenty-07 study

Phillips, A. C., Robertson, T., Carroll, D., Der, G., Shiels, P. G., McGlynn, L., & Benzeval, M. (2013) · Psychosomatic Medicine · doi:10.1097/psy.0b013e318289e6b5 · Cited by 55 · see citing works

Senescence and the Pro-tumorigenic Stroma

Alspach, E., Fu, Y., & Stewart, S. A. (2013) · Critical Reviews in Oncogenesis · doi:10.1615/critrevoncog.2014010630 · Cited by 47 · see citing works

Exploring the anti-aging effects of fisetin in telomerase-deficient progeria mouse model

Zhao, R., Kou, H., Jiang, D., & Wang, F. (2023) · PeerJ · doi:10.7717/peerj.16463 · Cited by 18 · see citing works

Concatemerization and packaging of bacteriophage T7 DNA in vitro: determination of the concatemers' length and appearance kinetics by use of rotating gel electrophoresis

Son, M., Hayes, S. J., & Serwer, P. (1988) · Virology · doi:10.1016/0042-6822(88)90392-3 · Cited by 25 · see citing works

Two-Way Gold Nanoparticle Label-Free Sensing of Specific Sequence and Small Molecule Targets Using Switchable Concatemers

Zhu, L., Shao, X., Luo, Y., et al. (2017) · ACS Chemical Biology · doi:10.1021/acschembio.7b00060 · Cited by 32 · see citing works

The Ends on Herpesvirus DNA Replicative Concatemers Contain pac2 cis Cleavage/Packaging Elements and Their Formation Is Controlled by Terminal cis Sequences

McVoy, M. A., Nixon, D. E., Hur, J. K., et al. (2000) · Journal of Virology · doi:10.1128/jvi.74.3.1587-1592.2000 · Cited by 42 · see citing works

Formation and Characterization of DNA-Concatemers

Sun, L., Becker, H.-D., Kim, A. A., et al. (2012) · Biophysical Journal · doi:10.1016/j.bpj.2011.11.3476

Formation of concatemers of lambda phage DNA in a recombination-deficient system

Segawa, T., & Tomizawa, J.-I. (1971) · Molecular and General Genetics MGG · doi:10.1007/bf00433104 · Cited by 6 · see citing works