Mouse models of ageing and their relevance to disease
Open accessAbstract
Ageing is a process that gradually increases the organism's vulnerability to death. It affects different biological pathways, and the underlying cellular mechanisms are complex. In view of the growing disease burden of ageing populations, increasing efforts are being invested in understanding the pathways and mechanisms of ageing. We review some mouse models commonly used in studies on ageing, highlight the advantages and disadvantages of the different strategies, and discuss their relevance to disease susceptibility. In addition to addressing the genetics and phenotypic analysis of mice, we discuss examples of models of delayed or accelerated ageing and their modulation by caloric restriction.
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Aging biology differs between rodents and humans, and findings from a mouse model may not fully translate to human liver.
“aging biology differs between rodents and humans, and findings from a mouse model may not fully translate to human liver [5,51,52].”
From Fluorescence-Guided Spatial Mapping of p21-Expressing Senescent Cells in Aged Liver at Single-Cell Resolution (2026) · cites this paper as [52]
The Introduction discusses similarities and differences between mouse and human ageing, and the Summary cautions that mice may not be ideal models of ageing. Those passages support the general concern about translation, but the paper does not establish that findings from a mouse model may fail to translate specifically to human liver. Page numbers are unavailable in our copy. (LLM, conf=0.85)
Experimental — accuracy not yet measuredThe identification of specific mutations causing progeroid syndromes has enabled the development of mouse models that simulate premature aging.
“The identification of specific mutations causing these syndromes has enabled the development of mouse models that simulate premature aging.304”
From Inflammation and aging: signaling pathways and intervention therapies (2023) · cites this paper as [304]
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Safdar, A., Bourgeois, J. M., Ogborn, D. I., Little, J. P., Hettinga, B. P., Akhtar, M., Thompson, J. E., Melov, S., Mocellin, N. J., Kujoth, G. C., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019581108 · Cited by 358 · see citing works
RetractedRETRACTED ARTICLE:Exercise-induced mitochondrial p53 repairs mtDNA mutations in mutator mice
Safdar, A., Khrapko, K., Flynn, J. M., Saleem, A., Lisio, M. D., Johnston, A. P. W., Kratysberg, Y., Samjoo, I. A., Kitaoka, Y., Ogborn, D. I., et al. (2015) · Skeletal Muscle · doi:10.1186/s13395-016-0075-9 · Cited by 66 · see citing works
RetractedInterleukin-10-deficient mice develop chronic enterocolitis
Kühn, R., Löhler, J., Rennick, D. M., Rajewsky, K., & Müller, W. (1993) · Cell · doi:10.1016/0092-8674(93)80068-p · Cited by 4,248 · see citing works
Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases
Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891 · see citing works
Mutation of the mouse klotho gene leads to a syndrome resembling ageing
Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837 · see citing works
Wang, H., Yang, H., Shivalila, C. S., Dawlaty, M. M., Cheng, A. W., Zhang, F., & Jaenisch, R. (2013) · Cell · doi:10.1016/j.cell.2013.04.025 · Cited by 3,495 · see citing works
Extending Healthy Life Span—From Yeast to Humans
Fontana, L., Partridge, L., & Longo, V. D. (2010) · Science · doi:10.1126/science.1172539 · Cited by 3,023 · see citing works
IL-10 inhibits cytokine production by activated macrophages
Fiorentino, D. F., Zlotnik, A., Mosmann, T. R., Howard, M., & O’Garra, A. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.11.3815 · Cited by 2,888 · see citing works
Premature ageing in mice expressing defective mitochondrial DNA polymerase
Trifunovic, A., Wredenberg, A., Falkenberg, M., Spelbrink, J. N., Rovio, A. T., Bruder, C. E., Bohlooly-Y, M., Gidlöf, S., Oldfors, A., Wibom, R., et al. (2004) · Nature · doi:10.1038/nature02517 · Cited by 2,734 · see citing works
Lakatta, E. G., & Levy, D. (2003) · Circulation · doi:10.1161/01.cir.0000048892.83521.58 · Cited by 2,244 · see citing works
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
Eriksson, M., Brown, W. T., Gordon, L. B., Glynn, M. W., Singer, J. I., Scott, L. J., Erdos, M. R., Robbins, C. M., Moses, T. Y., Berglund, P., et al. (2003) · Nature · doi:10.1038/nature01629 · Cited by 2,217 · see citing works
Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging
Kujoth, G. C., Hiona, A., Pugh, T. D., Someya, S., Panzer, K., Wohlgemuth, S. E., Hofer, T., Seo, A. Y., Sullivan, R., Jobling, W. A., et al. (2005) · Science · doi:10.1126/science.1112125 · Cited by 2,165 · see citing works
Telomere Shortening and Tumor Formation by Mouse Cells Lacking Telomerase RNA
Blasco, M. A., Lee, H.-W., Hande, M. P., Samper, E., Lansdorp, P. M., DePinho, R. A., & Greider, C. W. (1997) · Cell · doi:10.1016/s0092-8674(01)80006-4 · Cited by 2,108 · see citing works
Hatori, M., Vollmers, C., Zarrinpar, A., DiTacchio, L., Bushong, E. A., Gill, S., Leblanc, M., Chaix, A., Joens, M., Fitzpatrick, J. A. J., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.019 · Cited by 1,986 · see citing works
Suppression of Aging in Mice by the Hormone Klotho
Kurosu, H., Yamamoto, M., Clark, J. D., Pastor, J. V., Nandi, A., Gurnani, P., McGuinness, O. P., Chikuda, H., Yamaguchi, M., Kawaguchi, H., et al. (2005) · Science · doi:10.1126/science.1112766 · Cited by 1,935 · see citing works
IL-10 acts on the antigen-presenting cell to inhibit cytokine production by Th1 cells
Fiorentino, D. F., Zlotnik, A., Vieira, P., Mosmann, T. R., Howard, M., Moore, K. W., & O’Garra, A. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.146.10.3444 · Cited by 1,858 · see citing works
Lamin A Truncation in Hutchinson-Gilford Progeria
Sandre‐Giovannoli, A. D., Bernard, R., Cau, P., Navarro, C. L., Amiel, J., Boccaccio, I., Lyonnet, S., Stewart, C. L., Münnich, A., Merrer, M. F. L., et al. (2003) · Science · doi:10.1126/science.1084125 · Cited by 1,472 · see citing works
The mitochondrial basis of aging
Sun, N., Youle, R. J., & Finkel, T. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.01.028 · Cited by 1,441 · see citing works
Essential role of mouse telomerase in highly proliferative organs
Lee, H.-W., Blasco, M. A., Gottlieb, G. J., Horner, J. W., Greider, C. W., & DePinho, R. A. (1998) · Nature · doi:10.1038/33345 · Cited by 1,270 · cited 1× · see citing works
“However, late-generation Terc−/− mice did show a shortened lifespan, overall frailty, decreased fertility and tissue atrophy with impaired organ function (Lee et al., 1998).”
BackgroundLi, S., Crenshaw, E. B., Rawson, E. J., Simmons, D. M., Swanson, L. W., & Rosenfeld, M. G. (1990) · Nature · doi:10.1038/347528a0 · Cited by 1,194 · see citing works
Impact of caloric restriction on health and survival in rhesus monkeys from the NIA study
Mattison, J. A., Roth, G. S., Beasley, T. M., Tilmont, E. M., Handy, A. M., Herbert, R. L., Longo, D. L., Allison, D. B., Young, J. E., Bryant, M., et al. (2012) · Nature · doi:10.1038/nature11432 · Cited by 1,145 · see citing works
Berg, D., Davidson, N. M., Kühn, R., Müller, W., Menon, S., Holland, G., Thompson-Snipes, L., Leach, M. W., & Rennick, D. M. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118861 · Cited by 1,125 · see citing works
The Collaborative Cross, a community resource for the genetic analysis of complex traits
Churchill, G. A., Bogue, M. A., Paigen, B. J., Paigen, K., Pan, H.-J., Svenson, K. L., Airey, D. C., Allayee, H., Angel, J. M., Attie, A., et al. (2004) · Nature Genetics · doi:10.1038/ng1104-1133 · Cited by 1,114 · see citing works
Dwarf mice and the ageing process
Brown‐Borg, H. M., Borg, K. E., Meliska, C. J., & Bartke, A. (1996) · Nature · doi:10.1038/384033a0 · Cited by 1,091 · see citing works
Biochemical Adaptations to Endurance Exercise in Muscle
Holloszy, J. O., & Booth, F. W. (1976) · Annual Review of Physiology · doi:10.1146/annurev.ph.38.030176.001421 · Cited by 1,053 · see citing works
Weindruch, R. H., Walford, R. L., Fligiel, S., & Guthrie, D. (1986) · Journal of Nutrition · doi:10.1093/jn/116.4.641 · Cited by 992 · see citing works
Chaix, A., Zarrinpar, A., Miu, P., & Panda, S. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.11.001 · Cited by 956 · see citing works
Rapamycin, But Not Resveratrol or Simvastatin, Extends Life Span of Genetically Heterogeneous Mice
Miller, R. A., Harrison, D. E., Astle, C. M., Baur, J. A., Boyd, A. R., de Cabo, R., Fernandez, E., Flurkey, K., Javors, M. A., Nelson, J. F., et al. (2011) · The Journals of Gerontology: Series A · doi:10.1093/gerona/glq178 · Cited by 896 · see citing works
Hypothalamic programming of systemic ageing involving IKK-β, NF-κB and GnRH
Zhang, G., Li, J., Purkayastha, S., Tang, Y., Zhang, H., Yin, Y., Li, B., Liu, G., & Cai, D. (2013) · Nature · doi:10.1038/nature12143 · Cited by 834 · cited 4× · see citing works
“Mouse models of HGPS are models of laminopathies based on modification of the Lamna gene or its processing enzyme (Zhang et al., 2013a).”
InfluentialFlurkey, K., Papaconstantinou, J., Miller, R. A., & Harrison, D. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111158898 · Cited by 826 · see citing works
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 814 · see citing works
Detection of a specific mitochondrial DNA deletion in tissues of older humans
Cortopassi, G. A., & Arnheim, N. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.23.6927 · Cited by 785 · see citing works
Speakman, J. R., & Mitchell, S. E. (2011) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2011.07.001 · Cited by 769 · see citing works
Linking functional decline of telomeres, mitochondria and stem cells during ageing
Sahin, E., & DePinho, R. A. (2010) · Nature · doi:10.1038/nature08982 · Cited by 759 · see citing works
Michikawa, Y., Mazzucchelli, F., Bresolin, N., Scarlato, G., & Attardi, G. M. (1999) · Science · doi:10.1126/science.286.5440.774 · Cited by 725 · see citing works
Caloric restriction reduces age-related and all-cause mortality in rhesus monkeys
Colman, R. J., Beasley, T. M., Kemnitz, J. W., Johnson, S. C., Weindruch, R., & Anderson, R. M. (2014) · Nature Communications · doi:10.1038/ncomms4557 · Cited by 711 · see citing works
Growth Curves and Survival Characteristics of the Animals Used in the Biomarkers of Aging Program
Turturro, A., Witt, W. W., Lewis, S. M., Hass, B. S., Lipman, R. D., & Hart, R. W. (1999) · The Journals of Gerontology Series A · doi:10.1093/gerona/54.11.b492 · Cited by 668 · see citing works
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues.
Cortopassi, G. A., Shibata, D. K., Soong, N.-W., & Arnheim, N. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.16.7370 · Cited by 639 · see citing works
Genetic variability in adult bone density among inbred strains of mice
Beamer, W. G., Donahue, L. R., Rosen, C. J., & Baylink, D. J. (1996) · Bone · doi:10.1016/8756-3282(96)00047-6 · Cited by 630 · see citing works
Miller, R. A., Harrison, D. E., Astle, C. M., Fernández, E., Flurkey, K., Han, M. L., Javors, M. A., Li, X., Nadon, N. L., Nelson, J. F., et al. (2013) · Aging Cell · doi:10.1111/acel.12194 · Cited by 624 · see citing works
Halagappa, V. K. M., Guo, Z., Pearson, M., Matsuoka, Y., Cutler, R. G., LaFerla, F. M., & Mattson, M. P. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.12.019 · Cited by 580 · see citing works
Mutations in PROP1 cause familial combined pituitary hormone deficiency
Wu, W., Cogan, J. D., Pfäffle, R. W., Dasen, J. S., Frisch, H., O’Connell, S. M., Flynn, S. E., Brown, M. R., Mullis, P. E., Parks, J. S., et al. (1998) · Nature Genetics · doi:10.1038/ng0298-147 · Cited by 562 · see citing works
Pendás, A. M., Zhou, Z., Cadiñanos, J., Freije, J. M. P., Wang, J., Hultenby, K., Astudillo, A., Wernerson, A., Rodríguez, F., Tryggvason, K., et al. (2002) · Nature Genetics · doi:10.1038/ng871 · Cited by 554 · see citing works
Premature Aging in Mice Deficient in DNA Repair and Transcription
de Boer, J., Andressoo, J. O., de Wit, J., Huijmans, J., Beems, R. B., van Steeg, H., Weeda, G., van der Horst, G. T. J., van Leeuwen, W., Themmen, A. P. N., et al. (2002) · Science · doi:10.1126/science.1070174 · Cited by 545 · see citing works
Aging, adiposity, and calorie restriction
Fontana, L. (2007) · JAMA · doi:10.1001/jama.297.9.986 · Cited by 526 · see citing works
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.
White, J. K., Gerdin, A.-K., Karp, N. A., Ryder, E., Buljan, M., Bussell, J. N., Salisbury, J., Clare, S., Ingham, N. J., Podrini, C., et al. (2013) · Cell · doi:10.1016/j.cell.2013.06.022 · Cited by 509 · see citing works
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains
Simon, M. M., Greenaway, S., White, J. K., Fuchs, H., Gailus-Durner, V., Wells, S., Sorg, T., Wong, K., Bedu, E., Cartwright, E. J., et al. (2013) · Genome Biology · doi:10.1186/gb-2013-14-7-r82 · Cited by 507 · see citing works
Liao, C., Rikke, B. A., Johnson, T. E., Diaz, V., & Nelson, J. F. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2009.00533.x · Cited by 501 · see citing works
Association of human aging with a functional variant of klotho
Arking, D. E., Krebsová, A., Maçek, M., Maçek, M., Arking, A., Mian, S. I., Fried, L. F., Hamosh, A., Dey, S., McIntosh, I., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.022484299 · Cited by 481 · see citing works
High-Resolution Genetic Mapping Using the Mouse Diversity Outbred Population
Svenson, K. L., Gatti, D. M., Valdar, W. S. J., Welsh, C. E., Cheng, R., Chesler, E. J., Palmer, A. A., McMillan, L., & Churchill, G. A. (2012) · Genetics · doi:10.1534/genetics.111.132597 · Cited by 466 · see citing works
Essential role of limiting telomeres in the pathogenesis of Werner syndrome
Chang, S., Multani, A. S., Cabrera, N. G., Naylor, M. L., Laud, P., Lombard, D., Pathak, S., Guarente, L., & DePinho, R. A. (2004) · Nature Genetics · doi:10.1038/ng1389 · Cited by 462 · see citing works
The diversity outbred mouse population
Churchill, G. A., Gatti, D. M., Munger, S. C., & Svenson, K. L. (2012) · Mammalian Genome · doi:10.1007/s00335-012-9414-2 · Cited by 458 · see citing works
Bergö, M. O., Gavino, B. J., Ross, J., Schmidt, W. K., Hong, C., Kendall, L. V., Mohr, A., Meta, M. D., Genant, H. K., Jiang, Y., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.192460799 · Cited by 443 · see citing works
A genetic and physiological study of impaired glucose homeostasis control in C57BL/6J mice
Toye, A. A., Lippiat, J. D., Proks, P., Shimomura, K., Bentley, L., Hugill, A., Mijat, V., Goldsworthy, M. E., Moir, L., Haynes, A. R., et al. (2005) · Diabetologia · doi:10.1007/s00125-005-1680-z · Cited by 438 · see citing works
Splicing-directed therapy in a new mouse model of human accelerated aging
Osorio, F. G., Navarro, C. L., Cadiñanos, J., López-Mejía, I. C., Quirós, P. M., Bartoli, C., Rivera, J., Tazi, J., Guzmán, G., Varela, I., et al. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002847 · Cited by 432 · see citing works
Duan, W., Guo, Z., Jiang, H., Ware, M., Li, X.-J., & Mattson, M. P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0536856100 · Cited by 428 · see citing works
Yuan, R., Tsaih, S., Petkova, S. B., de Evsikova, C. M., Xing, S., Marion, M. A., Bogue, M. A., Mills, K. D., Peters, L. L., Bult, C. J., et al. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00478.x · Cited by 414 · see citing works
Mitochondrial point mutations do not limit the natural lifespan of mice
Vermulst, M., Bielas, J. H., Kujoth, G. C., Ladiges, W. C., Rabinovitch, P. S., Prolla, T. A., & Loeb, L. A. (2007) · Nature Genetics · doi:10.1038/ng1988 · Cited by 404 · see citing works
Progeria syndromes and ageing: what is the connection?
Burtner, C. R., & Kennedy, B. K. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2944 · Cited by 386 · see citing works
Weeda, G., Donker, I., de Wit, J., Morreau, H., Janssens, R. C., Vissers, C. J., Nigg, A. L., STEEG, H. V., Bootsma, D., & Hoeijmakers, J. H. J. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00190-4 · Cited by 380 · see citing works
Kennedy, S. R., Salk, J. J., Schmitt, M. W., & Loeb, L. A. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003794 · Cited by 363 · see citing works
DIABETES MELLITUS AND SIMPLE OPTIC ATROPHY AMONG SIBLINGS: REPORT OF FOUR CASES
Wolfram, D. J. (1938) · Mayo Clinic Proceedings · doi:10.1016/s0025-6196(26)04711-7 · Cited by 344 · see citing works
Caloric restriction attenuates Aβ-deposition in Alzheimer transgenic models
Patel, N. V., Gordon, M. N., Connor, K. E., Good, R. A., Engelman, R. W., Mason, J., Morgan, D. G., Morgan, T. E., & Finch, C. E. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2004.09.014 · Cited by 329 · see citing works
Deletion of Nicotinamide Nucleotide Transhydrogenase
Freeman, H. C., Hugill, A. J., Dear, N. T., Ashcroft, F. M., & Cox, R. (2006) · Diabetes · doi:10.2337/db06-0358 · Cited by 321 · see citing works
Caloric restriction attenuates β‐amyloid neuropathology in a mouse model of Alzheimer's disease
Wang, J., Ho, L., Qin, W., Rocher, A. B., Seror, I., Humala, N., Maniar, K. P., Dolios, G., Wang, R., Hof, P. R., et al. (2005) · The FASEB Journal · doi:10.1096/fj.04-3182fje · Cited by 317 · see citing works
Yang, S. H., Bergö, M. O., Toth, J. I., Qiao, X., Hu, Y., Sandoval, S., Meta, M. D., Bendale, P. M., Gelb, M. H., Young, S. G., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504641102 · Cited by 311 · see citing works
Roers, A., Siewe, L., Strittmatter, E., Deckert, M., Schlüter, D., Stenzel, W., Gruber, A. D., Krieg, T. M., Rajewsky, K., & Müller, W. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20041789 · Cited by 309 · see citing works
Lebel, M., & Leder, P. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.22.13097 · Cited by 304 · see citing works
Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in micePreprint
Chen, Y., Kao, C., Chen, Y.-T., Wang, C., Wu, C.-Y., Tsai, C., Liu, F.-C., Yang, C.-W., Wei, Y., Hsu, M., et al. (2009) · Genes & Development · doi:10.1101/gad.1779509 · Cited by 304 · see citing works
Metabolic reprogramming, caloric restriction and aging
Anderson, R. M., & Weindruch, R. H. (2009) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2009.11.005 · Cited by 300 · see citing works
Calorie restriction and prevention of age‐associated chronic disease
Omodei, D., & Fontana, L. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.03.015 · Cited by 293 · see citing works
Mattson, M. P., Duan, W., & Guo, Z. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01586.x · Cited by 288 · see citing works
Paigen, B., Mitchell, D., Reue, K., Morrow, A. L., Lusis, A. J., & LeBoeuf, R. C. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.11.3763 · Cited by 288 · see citing works
A Homozygous Mutation in a Novel Zinc-Finger Protein, ERIS, Is Responsible for Wolfram Syndrome 2
Amr, S. S., Heisey, C., Zhang, M., Xia, X.-J., Shows, K. H., Ajlouni, K. M., Pandya, A., Satin, L. S., El‐Shanti, H., & Shiang, R. (2007) · The American Journal of Human Genetics · doi:10.1086/520961 · Cited by 284 · see citing works
The International Mouse Phenotyping Consortium: past and future perspectives on mouse phenotyping
Brown, S. D. M., & Moore, M. W. (2012) · Mammalian Genome · doi:10.1007/s00335-012-9427-x · Cited by 282 · see citing works
Dai, D., Chen, T., Wanagat, J., Laflamme, M., Marcinek, D. J., Emond, M. J., Ngo, C. P., Prolla, T. A., & Rabinovitch, P. S. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00581.x · Cited by 280 · see citing works
Henry, K. R., & Chole, R. A. (1980) · International Journal of Audiology · doi:10.3109/00206098009070071 · Cited by 280 · see citing works
Hiona, A., Sanz, A., Kujoth, G. C., Pamplona, R., Seo, A. Y., Hofer, T., Someya, S., Miyakawa, T., Chie, N., Samhan-Arias, A. K., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011468 · Cited by 269 · see citing works
Impact of age and caloric restriction on neurogenesis in the dentate gyrus of C57BL/6 mice
Bondolfi, L., Ermini, F., Long, J. M., Ingram, D. K., & Jucker, M. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00083-6 · Cited by 264 · see citing works
Ishihara, H. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh125 · Cited by 258 · see citing works
Norddahl, G. L., Pronk, C. J., Wahlestedt, M., Sten, G., Nygren, J. M., Ugale, A., Sigvardsson, M., & Bryder, D. (2011) · Cell Stem Cell · doi:10.1016/j.stem.2011.03.009 · Cited by 249 · see citing works
Genotype and age influence the effect of caloric intake on mortality in mice
Forster, M. J., Morris, P., & Sohal, R. S. (2003) · The FASEB Journal · doi:10.1096/fj.02-0533fje · Cited by 236 · see citing works
Riggs, A. C., Bernal‐Mizrachi, E., Ohsugi, M., Wasson, J., Fátrai, S., Welling, C. M., Murray, J., Schmidt, R. E., Herrera, P. L., & Permutt, M. A. (2005) · Diabetologia · doi:10.1007/s00125-005-1947-4 · Cited by 228 · see citing works
Villa‐Bellosta, R., Rivera, J., Osorio, F. G., Acín‐Pérez, R., Enrı́quez, J. A., López-Otı́n, C., & Andrés, V. (2013) · Circulation · doi:10.1161/circulationaha.112.000571 · Cited by 219 · see citing works
The Snell dwarf mutation Pit1dw can increase life span in mice
Flurkey, K., Papaconstantinou, J., & Harrison, D. E. (2002) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(01)00339-6 · Cited by 218 · see citing works
An aging Interventions Testing Program: study design and interim report
Miller, R. A., Harrison, D. E., Astle, C. M., Floyd, R. A., Flurkey, K., Hensley, K., Javors, M. A., Leeuwenburgh, C., Nelson, J. F., Ongini, E., et al. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00311.x · Cited by 217 · see citing works
Trepanowski, J. F., Canale, R. E., Marshall, K. E., Kabir, M. M., & Bloomer, R. J. (2011) · Nutrition Journal · doi:10.1186/1475-2891-10-107 · Cited by 204 · see citing works
Lee, H., & Wei, Y. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-2869-1_14 · Cited by 201 · see citing works
Caloric restriction: powerful protection for the aging heart and vasculature
Weiss, E. P., & Fontana, L. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00685.2011 · Cited by 200 · see citing works
The Physical and Biological Characterization of a Frail Mouse Model
Walston, J. D., Fedarko, N. S., Yang, H., Leng, S. X., Beamer, B. A., Espinoza, S. E., Lipton, A., Zheng, H., & Becker, K. G. (2008) · The Journals of Gerontology Series A · doi:10.1093/gerona/63.4.391 · Cited by 192 · see citing works
Mutations in the <i>WRN</i> Gene in Mice Accelerate Mortality in a p53-Null Background
Lombard, D. B., Beard, C., Johnson, B., Marciniak, R. A., Dausman, J., Bronson, R., Buhlmann, J. E., Lipman, R., Curry, R., Sharpe, A., et al. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.9.3286-3291.2000 · Cited by 187 · see citing works
Leeuwenburgh, C., Pamplona, R., & Sanz, A. (2011) · Journal of Aging Research · doi:10.4061/2011/782946 · Cited by 186 · see citing works
Bygrave, A. E., Rose, K. L., Cortés-Hernández, J., Warren, J. A., Rigby, R. J., Cook, H. T., Walport, M. J., Vyse, T. J., & Botto, M. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020243 · Cited by 186 · see citing works
The mouse as a model organism in aging research: Usefulness, pitfalls and possibilities
Vanhooren, V., & Libert, C. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.03.010 · Cited by 180 · see citing works
Dyskeratosis congenita, stem cells and telomeres
Kirwan, M., & Dokal, I. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.01.010 · Cited by 180 · see citing works
Kasahara, T., Kubota, M., Miyauchi, T., Noda, Y., Mouri, A., Nabeshima, T., & Kato, T. (2006) · Molecular Psychiatry · doi:10.1038/sj.mp.4001824 · Cited by 176 · see citing works
Longley, M. J., Ropp, P. A., Lim, S. E., & Copeland, W. C. (1998) · Biochemistry · doi:10.1021/bi980772w · Cited by 174 · see citing works
Donato, A. J., Walker, A. E., Magerko, K. A., Bramwell, R. C., Black, A. D., Henson, G. D., Lawson, B. R., Lesniewski, L. A., & Seals, D. R. (2013) · Aging Cell · doi:10.1111/acel.12103 · Cited by 169 · see citing works
Passenger Mutations Confound Interpretation of All Genetically Modified Congenic Mice
Berghe, T. V., Hulpiau, P., Martens, L., Vandenbroucke, R. E., Wonterghem, E. V., Perry, S. W., Bruggeman, I., Divert, T., Choi, S. M., Vuylsteke, M., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.06.011 · Cited by 165 · see citing works
Self-citationEMPReSS: standardized phenotype screens for functional annotation of the mouse genome
Brown, S. D. M., Chambon, P., & de Angelis, M. H. (2005) · Nature Genetics · doi:10.1038/ng1105-1155 · Cited by 159 · see citing works
Progerin elicits disease phenotypes of progeria in mice whether or not it is farnesylated
Yang, S. H., Andres, D., Spielmann, H. P., Young, S. G., & Fong, L. G. (2008) · Journal of Clinical Investigation · doi:10.1172/jci35876 · Cited by 159 · see citing works
Rippe, C., Lesniewski, L. A., Connell, M. L., LaRocca, T. J., Donato, A. J., & Seals, D. R. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00557.x · Cited by 158 · see citing works
Design of aging intervention studies: the NIA interventions testing program
Nadon, N. L., Strong, R., Miller, R. A., Nelson, J. F., Javors, M. A., Sharp, Z. D., Peralba, J. M., & Harrison, D. E. (2008) · AGE · doi:10.1007/s11357-008-9048-1 · Cited by 156 · see citing works
Ayadi, A., Birling, M., BOTTOMLEY, J. R., Bussell, J., Fuchs, H., Fray, M., Gailus‐Durner, V., Greenaway, S., Houghton, R., Karp, N. A., et al. (2012) · Mammalian Genome · doi:10.1007/s00335-012-9418-y · Cited by 155 · see citing works
de Angelis, M. H., Nicholson, G., Selloum, M., White, J. K., Morgan, H., Ramírez‐Solis, R., Sorg, T., Wells, S., Fuchs, H., Fray, M., et al. (2015) · Nature Genetics · doi:10.1038/ng.3360 · Cited by 146 · see citing works
Harrison, D. E. (1990) · Cited by 146 · see citing works
Strain background effects and genetic modifiers of hearing in mice
Johnson, K. R., Zheng, Q. Y., & Noben‐Trauth, K. (2006) · Brain Research · doi:10.1016/j.brainres.2006.02.021 · Cited by 145 · see citing works
Ionizing radiation and aging: rejuvenating an old idea
Richardson, R. B. (2009) · Aging · doi:10.18632/aging.100081 · Cited by 141 · see citing works
Sharp, Z. D., & Bartke, A. (2005) · The Journals of Gerontology Series A · doi:10.1093/gerona/60.3.293 · Cited by 140 · see citing works
Mitochondrial genome maintenance in health and disease
Copeland, W. C., & Longley, M. J. (2014) · DNA repair · doi:10.1016/j.dnarep.2014.03.010 · Cited by 137 · see citing works
Adding fuel to the fire: the impact of stress on the ageing brain
Prenderville, J. A., Kennedy, P. J., Dinan, T. G., & Cryan, J. F. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2014.11.001 · Cited by 136 · see citing works
Aging research using mouse models
Ackert‐Bicknell, C. L., Anderson, L. C., Sheehan, S., Hill, W. G., Chang, B., Churchill, G. A., Chesler, E. J., Korstanje, R., & Peters, L. L. (2015) · Current Protocols in Mouse Biology · doi:10.1002/9780470942390.mo140195 · Cited by 135 · see citing works
Commercially Available Outbred Mice for Genome-Wide Association Studies
Yalcin, B., Nicod, J., Bhomra, A., Davidson, S. I., Cleak, J., Farinelli, L., Østerås, M., Whitley, A., Wei, Y., Gan, X., et al. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001085 · Cited by 134 · see citing works
Construction of transgenic mice with tissue-specific acceleration of mitochondrial DNA mutagenesis
Zhang, D., Mott, J. L., Chang, S.-W., Denniger, G., Feng, Z., & Zassenhaus, H. P. (2000) · Genomics · doi:10.1006/geno.2000.6333 · Cited by 124 · see citing works
Guo, Z., Mitchell-Raymundo, F., Yang, H., Ikeno, Y., Nelson, J., Diaz, V., Richardson, A., & Reddick, R. (2002) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(02)00008-8 · Cited by 121 · cited 1× · see citing works
“…cardiovascular diseases CVD) The prevalence of cardiomyopathies such as hypertension, therosclerosis, myocardial fibrosis and stroke increases with ageng (Omodei and Fontana, 2011; Lakatta and Levy, 2003; Donato t al., 2013; Guo et al., 2002; Wielinga et al., 2011; McMillen et al., 013).”
BackgroundCaloric restriction: Beneficial effects on brain aging and Alzheimer’s disease
Van Cauwenberghe, C., Vandendriessche, C., Libert, C., & Vandenbroucke, R. E. (2016) · Mammalian Genome · doi:10.1007/s00335-016-9647-6 · Cited by 121 · see citing works
Self-citationFarazi, P. A., Glickman, J. N., Horner, J. W., & DePinho, R. A. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-4608 · Cited by 119 · see citing works
Wu, P., Shen, Q., Dong, S., Xu, Z., Tsien, J. Z., & Hu, Y. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.03.028 · Cited by 116 · see citing works
Zhu, L.-J., Liu, M.-Y., Li, H., Liu, X., Chen, C., Han, Z., Wu, H.-Y., Jing, X., Zhou, H.-H., Suh, H., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097689 · Cited by 114 · see citing works
Hornsby, A., Redhead, Y. T., Rees, D., Ratcliff, M., Reichenbach, A., Wells, T., Francis, L., Amstalden, K. A. Z., Andrews, Z., & Davies, J. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.09.023 · Cited by 112 · see citing works
Sherman, H., Frumin, I., Gutman, R., Chapnik, N., Lorentz, A., Meylan, J., le Coutre, J., & Froy, O. (2010) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2010.01160.x · Cited by 109 · see citing works
Interleukin 10 knockout frail mice develop cardiac and vascular dysfunction with increased age
Sikka, G., Miller, K. L., Steppan, J., Pandey, D., Jung, S. M., Fraser, C. D., Ellis, C. L., Ross, D., Vandegaer, K. M., Bedja, D., et al. (2012) · Experimental Gerontology · doi:10.1016/j.exger.2012.11.001 · Cited by 101 · see citing works
Williams, R. W., Bennett, B., Lu, L., Gu, J., DeFries, J. C., Carosone‐Link, P., Rikke, B. A., Belknap, J. K., & Johnson, T. E. (2004) · Mammalian Genome · doi:10.1007/s00335-004-2380-6 · Cited by 100 · see citing works
Williams, S. L., Huang, J., Edwards, Y. J. K., Ulloa, R. H., Dillon, L. M., Prolla, T. A., Vance, J. M., Moraes, C. T., & Zuchner, S. L. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.11.012 · Cited by 99 · see citing works
Loss of Nfkb1 leads to early onset aging
Bernal, G. M., Wahlstrom, J. S., Crawley, C. D., Cahill, K. E., Pytel, P., Liang, H., Kang, S., Weichselbaum, R. R., & Yamini, B. (2014) · Aging · doi:10.18632/aging.100702 · Cited by 97 · see citing works
In vivo levels of mitochondrial hydrogen peroxide increase with age in mt DNA mutator mice
Logan, A., Shabalina, I. G., Prime, T. A., Rogatti, S., Kalinovich, A., Hartley, R. C., Budd, R. C., Cannon, B., & Murphy, M. P. (2014) · Aging Cell · doi:10.1111/acel.12212 · Cited by 93 · see citing works
Calorie Restriction in Mammals and Simple Model Organisms
Taormina, G., & Mirisola, M. G. (2014) · BioMed Research International · doi:10.1155/2014/308690 · Cited by 90 · see citing works
‘Accelerated aging’: a primrose path to insight?
Miller, R. A. (2004) · Aging Cell · doi:10.1111/j.1474-9728.2004.00081.x · Cited by 87 · see citing works
Understanding Mammalian Genetic Systems: The Challenge of Phenotyping in the Mouse
Brown, S. D. M., Hancock, J. M., & Gates, H. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020118 · Cited by 85 · see citing works
Zhang, H., Kieckhaefer, J. E., & Cao, K. (2012) · Aging Cell · doi:10.1111/acel.12021 · Cited by 85 · see citing works
Rikke, B. A., Liao, C.-Y., McQueen, M. B., Nelson, J. F., & Johnson, T. E. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.04.008 · Cited by 84 · see citing works
Rapamycin extends life- and health span because it slows aging
Blagosklonny, M. V. (2013) · Aging · doi:10.18632/aging.100591 · Cited by 81 · see citing works
Chronic Exercise Modifies Age-Related Telomere Dynamics in a Tissue-Specific Fashion
Ludlow, A. T., Witkowski, S., Marshall, M. R., Wang, Z. J., Lima, L., Pitchford, L. M., Spangenburg, E. E., & Roth, S. M. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls002 · Cited by 77 · see citing works
Inflammation and mortality in a frail mouse model
Ko, F., Yu, Q., Xue, Q., Yao, W., Brayton, C. F., Yang, H., Fedarko, N. S., & Walston, J. D. (2011) · AGE · doi:10.1007/s11357-011-9269-6 · Cited by 74 · see citing works
Wfs1-deficient mice display impaired behavioural adaptation in stressful environment
Luuk, H., Plaas, M., Raud, S., Innos, J., Sütt, S., Lasner, H., Abramov, U., Kurrikoff, K., Kõks, S., & Vasar, E. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.11.007 · Cited by 74 · see citing works
Self-citationMassip, L., Garand, C., Turaga, R. V. N., Deschênes, F., Thorin, É., & Lebel, M. (2005) · Experimental Gerontology · doi:10.1016/j.exger.2005.10.011 · Cited by 73 · see citing works
Petkova, S. B., Yuan, R., Tsaih, S., Schott, W. H., Roopenian, D. C., & Paigen, B. J. (2008) · Physiological Genomics · doi:10.1152/physiolgenomics.00185.2007 · Cited by 73 · see citing works
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.
Collier, D. A., Barrett, T. G., Curtis, D., Macleod, A. F., Arranz, M. J., Maassen, J. A., & Bundey, S. (1996) · PubMed Central · Cited by 72 · see citing works
Park, J., Glass, Z., Sayed, K., Michurina, T. V., Lazutkin, A. A., Mineyeva, O. A., Velmeshev, D., Ward, W. F., Richardson, A. G., & Enikolopov, G. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12249 · Cited by 71 · see citing works
Ko, F., Abadir, P. M., Marx, R., Westbrook, R., Cooke, C., Yang, H., & Walston, J. D. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2015.11.010 · Cited by 71 · see citing works
Teixeira, R., Diaz, M. M., Santos, T. D. S., Bernardes, J. T. M., Peixoto, L. G., Bocanegra, O., Bernardino, M., & Espíndola, F. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119025 · Cited by 70 · see citing works
Groeschel, M., & Braam, B. G. (2010) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00208.2010 · Cited by 69 · see citing works
Wfs1 gene deletion causes growth retardation in mice and interferes with the growth hormone pathway
Kõks, S., Soomets, U., Paya-Cano, J. L., Fernandes, C., Luuk, H., Plaas, M., Terasmaa, A., Tillmann, V., Noormets, K., Vasar, E., et al. (2009) · Physiological Genomics · doi:10.1152/physiolgenomics.90407.2008 · Cited by 66 · see citing works
Self-citationSIRT1 is a Highly Networked Protein That Mediates the Adaptation to Chronic Physiological Stress
McBurney, M. W., Clark-Knowles, K. V., Caron, A. Z., & Gray, D. A. (2013) · Genes & Cancer · doi:10.1177/1947601912474893 · Cited by 66 · see citing works
Articular Aging and Osteoarthrosis in Dwarf Mice
Silberberg, R. (2008) · Pathologia et Microbiologia · doi:10.1159/000162458 · Cited by 64 · see citing works
Impact of Exercise Training on Physiological Measures of Physical Fitness in the Elderly
Mendonça, G. V., Pezarat‐Correia, P., Vaz, J. R., Silva, L., de Almeida, I. D., & Heffernan, K. S. (2016) · Current Aging Science · doi:10.2174/1874609809666160426120600 · Cited by 64 · see citing works
Mitochondrial DNA Damage Patterns and Aging: Revising the Evidences for Humans and Mice
Kazachkova, N. (2013) · Aging and Disease · doi:10.14336/ad.2013.0400337 · Cited by 63 · see citing works
Circulating micro RNA signature of genotype‐by‐age interactions in the long‐lived A mes dwarf mouse
Victoria, B., Dhahbi, J. M., López, Y. O. N., Spinel, L., Atamna, H., Spindler, S. R., & Masternak, M. M. (2015) · Aging Cell · doi:10.1111/acel.12373 · Cited by 59 · see citing works
Genetic influence on electrocardiogram time intervals and heart rate in aging mice
Xing, S., Tsaih, S.-W., Yuan, R., Svenson, K. L., Jorgenson, L. M., So, M., Paigen, B. J., & Korstanje, R. (2009) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00681.2008 · Cited by 58 · see citing works
Mouse Genome Informatics (MGI): reflecting on 25 years
Eppig, J. T., Richardson, J. E., Kadin, J. A., Ringwald, M., Blake, J. A., & Bult, C. J. (2015) · Mammalian Genome · doi:10.1007/s00335-015-9589-4 · Cited by 58 · see citing works
Liao, C., & Kennedy, B. K. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-397920-9.00003-2 · Cited by 55 · see citing works
Mouse Loci Associated With Life Span Exhibit Sex-Specific and Epistatic Effects
Jackson, A., Gałecki, A. T., Burke, D., & Miller, R. A. (2002) · The Journals of Gerontology Series A · doi:10.1093/gerona/57.1.b9 · Cited by 51 · see citing works
Tsaih, S., Pezzolesi, M. G., Yuan, R., Warram, J. H., Królewski, A. S., & Korstanje, R. (2009) · Kidney International · doi:10.1038/ki.2009.434 · Cited by 50 · see citing works
Age, experience and genetic background influence treadmill walking in mice
Wooley, C. M., Xing, S., Burgess, R. W., Cox, G. A., & Seburn, K. L. (2008) · Physiology & Behavior · doi:10.1016/j.physbeh.2008.10.020 · Cited by 48 · see citing works
Drake, J. C., Bruns, D. R., Peelor, F. F., Biela, L. M., Miller, R. A., Miller, B. F., & Hamilton, K. L. (2015) · Aging Cell · doi:10.1111/acel.12329 · Cited by 48 · see citing works
Calorie restriction can reverse, as well as prevent, aging cardiomyopathy
Yan, L., Gao, S., Ho, D. W. T., Park, M., Ge, H., Wang, C., Tian, Y., Lai, L., Lorenzo, M. S. D., Vatner, D. E., et al. (2013) · AGE · doi:10.1007/s11357-012-9508-5 · Cited by 47 · see citing works
Doğan, S., Rogozina, O. P., Lokshin, A. E., Grande, J. P., & Cleary, M. P. (2009) · Oncology Letters · doi:10.3892/ol_00000031 · Cited by 46 · see citing works
Multiple-Trait Quantitative Trait Loci Analysis Using a Large Mouse Sibship
Jackson, A., Fornés, A., Gałecki, A. T., Miller, R. A., & Burke, D. (1999) · Genetics · doi:10.1093/genetics/151.2.785 · Cited by 45 · see citing works
Cox, L. S., & Faragher, R. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-7123-x · Cited by 44 · see citing works
Harper, J. M., Durkee, S. J., Dysko, R. C., Austad, S. N., & Miller, R. A. (2006) · The Journals of Gerontology Series A · doi:10.1093/gerona/61.10.1019 · Cited by 44 · see citing works
Long-lived Ames dwarf mice: Oxidative damage to mitochondrial DNA in heart and brain
Sanz, A., Bartke, A., & Barja, G. (2002) · AGE · doi:10.1007/s11357-002-0010-3 · Cited by 43 · see citing works
Recent Progress in Metabolic Signaling Pathways Regulating Aging and Life Span
Newgard, C. B., & Pessin, J. E. (2014) · The Journals of Gerontology Series A · doi:10.1093/gerona/glu058 · Cited by 43 · see citing works
Antiaging, longevity and calorie restriction
Morley, J. E., Chahla, E. J., & AlKaade, S. (2009) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e3283331384 · Cited by 42 · see citing works
Paigen, B. J., Albee, D., Holmes, P. A., & Mitchell, D. (1987) · Biochemical Genetics · doi:10.1007/bf00554352 · Cited by 38 · see citing works
Bogue, M. A., Peters, L. L., Paigen, B. J., Korstanje, R., Yuan, R., Ackert‐Bicknell, C. L., Grubb, S. C., Churchill, G. A., & Chesler, E. J. (2014) · The Journals of Gerontology Series A · doi:10.1093/gerona/glu223 · Cited by 38 · see citing works
Male mice with deleted Wolframin (Wfs1) gene have reduced fertility
Noormets, K., Kõks, S., Kavak, A., Arend, A., Aunapuu, M., Keldrimaa, A., Vasar, E., & Tillmann, V. (2009) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-7-82 · Cited by 35 · see citing works
Self-citationWalker, A. E., Henson, G. D., Reihl, K. D., Nielson, E. I., Morgan, R. G., Lesniewski, L. A., & Donato, A. J. (2013) · AGE · doi:10.1007/s11357-013-9585-0 · Cited by 33 · see citing works
A neurological phenotype in mice with DNA repair gene Ercc1 deficiency
Lawrence, N. J., Sacco, J. J., Brownstein, D. G., Gillingwater, T. H., & Melton, D. W. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.10.005 · Cited by 33 · see citing works
Sex Differences in the Development of Diabetes in Mice with Deleted Wolframin (Wfs1) Gene
Noormets, K., Kõks, S., Muldmaa, M., Mauring, L., Vasar, E., & Tillmann, V. (2010) · Experimental and Clinical Endocrinology & Diabetes · doi:10.1055/s-0030-1265163 · Cited by 32 · see citing works
Self-citationAge‐associated changes in hippocampal‐dependent cognition in D iversity O utbred mice
Koh, M. T., Spiegel, A. M., & Gallagher, M. (2014) · Hippocampus · doi:10.1002/hipo.22311 · Cited by 31 · see citing works
Effects of age and caloric restriction on mitochondrial protein oxidative damage in mice
Li, X., Rebrin, I., Forster, M. J., & Sohal, R. S. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.12.001 · Cited by 30 · see citing works
Common mechanisms for calorie restriction and adenylyl cyclase type 5 knockout models of longevity
Yan, L., Park, J. Y., Dillinger, J., Lorenzo, M. S. D., Yuan, C., Lai, L., Wang, C., Ho, D. W. T., Tian, B., Stanley, W. C., et al. (2012) · Aging Cell · doi:10.1111/acel.12013 · Cited by 29 · see citing works
Miller, R. A., & Chrisp, C. E. (1999) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1999.tb01291.x · Cited by 29 · see citing works
Early life programming of obesity.
Martin‐Gronert, M. S., & Ozanne, S. E. (2013) · PubMed · Cited by 28 · see citing works
Wielinga, P. Y., Yakala, G. K., Heeringa, P., Kleemann, R., & Kooistra, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018432 · Cited by 26 · see citing works
Do Ames dwarf and calorie-restricted mice share common effects on age-related pathology?
Ikeno, Y., Hubbard, G. B., Lee, S., Dube, S., Flores, L. C., Roman, M. G., & Bartke, A. (2013) · Pathobiology of Aging & Age-related Diseases · doi:10.3402/pba.v3i0.20833 · Cited by 25 · see citing works
Psychological stress-induced catecholamines accelerates cutaneous aging in mice
Romana‐Souza, B., Lima-Cezar, G. S., & Monte‐Alto‐Costa, A. (2015) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2015.10.004 · Cited by 24 · see citing works
Mitochondrial DNA deletions in mice in men: Substantia nigra is much less affected in the mouse
Guo, X., Kudryavtseva, E., Bodyak, N. D., Nicholas, A., Dombrovsky, I., Yang, D., Kraytsberg, Y., Simon, D. K., & Khrapko, K. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.04.005 · Cited by 23 · see citing works
Papaconstantinou, J., & Hsieh, C.-C. (2015) · Oncotarget · doi:10.18632/oncotarget.6112 · Cited by 6 · see citing works
McMillen, T. S., Minami, E., & LeBoeuf, R. C. (2013) · Nutrition and Diabetes · doi:10.1038/nutd.2013.19 · Cited by 5 · see citing works
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Inflammation and aging: signaling pathways and intervention therapies
Li, X., Li, C., Zhang, W., Wang, Y., Qian, P., & Huang, H. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01502-8 · Cited by 1,443 · see citing works
“The identification of specific mutations causing these syndromes has enabled the development of mouse models that simulate premature aging.(304) For instance, mouse models of HGPS have been created by modifying the Lmna gene or its processing enzyme.”
BackgroundBiomarkers of aging for the identification and evaluation of longevity interventions
Moqri, M., Herzog, C. M. S., Poganik, J. R., Justice, J. N., Belsky, D. W., Higgins‐Chen, A., Moskalev, A., Fuellen, G., Cohen, A. A., Bautmans, I., et al. (2023) · Cell · doi:10.1016/j.cell.2023.08.003 · Cited by 697 · see citing works
Loss of epigenetic information as a cause of mammalian aging
Yang, J.-H., Hayano, M., Griffin, P. T., Amorim, J. A., Bonkowski, M. S., Apostolides, J. K., Salfati, E. L., Blanchette, M., Munding, E. M., Bhakta, M., et al. (2023) · Cell · doi:10.1016/j.cell.2022.12.027 · Cited by 643 · see citing works
Yanai, S., & Endo, S. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.697621 · Cited by 171 · see citing works
Cardiac ageing: extrinsic and intrinsic factors in cellular renewal and senescence
Gude, N. A., Broughton, K. M., Firouzi, F., & Sussman, M. A. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0061-5 · Cited by 166 · see citing works
Senescent cells suppress macrophage-mediated corpse removal via upregulation of the CD47-QPCT/L axis
Schloesser, D., Lindenthal, L., Sauer, J., Chung, K., Chavakis, T., Griesser, E., Baskaran, P., Maier-Habelsberger, U., Fundel‐Clemens, K., Schlotthauer, I., et al. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202207097 · Cited by 113 · see citing works
Regulation of inflammation as an anti‐aging intervention
Neves, J., & Sousa‐Victor, P. (2019) · FEBS Journal · doi:10.1111/febs.15061 · Cited by 108 · see citing works
Jurcău, M. C., Jurcău, A., Cristian, A., Hogea, V. O., Diaconu, R. G., & Nunkoo, V. S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251910535 · Cited by 90 · see citing works
van der Lugt, B., Rusli, F., Lute, C., Lamprakis, A., Salazar, E., Boekschoten, M. V., Hooiveld, G. J., Müller, M., Vervoort, J., Kersten, S., et al. (2018) · Aging · doi:10.18632/aging.101439 · Cited by 72 · see citing works
Telomeres and Longevity: A Cause or an Effect?
Shekhidem, H. A., Sharvit, L. E., Leman, E., Manov, I., Roichman, A., Holtze, S., Huffman, D. M., Cohen, H. Y., Hildebrandt, T. B., Shams, I., et al. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20133233 · Cited by 65 · see citing works
O’Leary, T. P., & Brown, R. E. (2022) · Genes Brain & Behavior · doi:10.1111/gbb.12794 · Cited by 61 · see citing works
Geroprotectors: A role in the treatment of frailty
Trendelenburg, A., Scheuren, A. C., Potter, P. K., Müller, R., & Bellantuono, I. (2019) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2019.03.002 · Cited by 50 · see citing works
Self-citationLoss of Epigenetic Information as a Cause of Mammalian AgingPreprint
Yang, J.-H., Hayano, M., Griffin, P. T., Amorim, J. A., Bonkowski, M. S., Apostolides, J. K., Blanchette, M., Munding, E. M., Bhakta, M. S., Salfati, E., et al. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3951490 · Cited by 45 · see citing works
Nagarajan, P., Agudelo Garcia, P. A., Iyer, C. C., Popova, L. V., Arnold, W. D., & Parthun, M. R. (2019) · Aging Cell · doi:10.1111/acel.12992 · Cited by 43 · see citing works
Age-associated SARS-CoV-2 breakthrough infection and changes in immune response in a mouse model
Chen, Y., Li, C., Liu, F., Ye, Z., Song, W., Lee, A. C.-Y., Shuai, H., Lu, L., To, K. K., Chan, J. F., et al. (2022) · Emerging Microbes & Infections · doi:10.1080/22221751.2022.2026741 · Cited by 43 · see citing works
Reutzel, M., Grewal, R., Dilberger, B., Silaidos, C. V., Joppe, A., & Eckert, G. P. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/4060769 · Cited by 41 · see citing works
Shahini, A., Rajabian, N., Choudhury, D., Shahini, S., Vydiam, K., Nguyen, T. M., Kulczyk, J., Santarelli, T., Ikhapoh, I. A., Zhang, Y., et al. (2021) · Science Advances · doi:10.1126/sciadv.abe5671 · Cited by 41 · see citing works
Tendon Extracellular Matrix Assembly, Maintenance and Dysregulation Throughout Life
Siadat, S. M., Zamboulis, D. E., Thorpe, C. T., Ruberti, J. W., & Connizzo, B. K. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-80614-9_3 · Cited by 42 · see citing works
Glucocorticoid effects on the brain: from adaptive developmental plasticity to allostatic overload
Eachus, H., & Ryu, S. (2024) · Journal of Experimental Biology · doi:10.1242/jeb.246128 · Cited by 37 · see citing works
Iacobini, C., Vitale, M., Haxhi, J., Menini, S., & Pugliese, G. (2024) · Cells · doi:10.3390/cells13090763 · Cited by 38 · see citing works
Changes in the biochemical taste of cytoplasmic and cell-free DNA are major fuels for inflamm-aging
Storci, G., Carolis, S. D., Olivieri, F., & Bonafè, M. (2018) · Seminars in Immunology · doi:10.1016/j.smim.2018.08.003 · Cited by 37 · see citing works
Validation of a geropathology grading system for aging mouse studies
Snyder, J. M., Snider, T. A., Ciol, M. A., Wilkinson, J. E., Imai, D. M., Casey, K. M., Vilches-Moure, J. G., Pettan-Brewer, C., Pillai, S. P. S., Carrasco, S. E., et al. (2019) · GeroScience · doi:10.1007/s11357-019-00088-w · Cited by 35 · see citing works
FTO demethylase activity is essential for normal bone growth and bone mineralization in mice
Sachse, G., Church, C., Stewart, M. E., Cater, H. L., Teboul, L., Cox, R., & Ashcroft, F. M. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2017.11.027 · Cited by 33 · see citing works
Rodent models of frailty and their application in preclinical research
Banga, S., Heinze-Milne, S., & Howlett, S. E. (2019) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2019.01.008 · Cited by 31 · see citing works
Ghanemi, A., Melouane, A., Yoshioka, M., & St‐Amand, J. (2022) · Metabolites · doi:10.3390/metabo12020125 · Cited by 31 · see citing works
DNA repair‐deficient premature aging models display accelerated epigenetic age
Perez, K., Parras, A., Picó, S., Rechsteiner, C., Haghani, A., Brooke, R., Mrabti, C., Schoenfeldt, L., Horvath, S., & Ocampo, A. (2024) · Aging Cell · doi:10.1111/acel.14058 · Cited by 31 · see citing works
Barros, P. R., Costa, T. J. D., Akamine, E. H., & Tostes, R. C. (2021) · Frontiers in Aging · doi:10.3389/fragi.2021.727604 · Cited by 30 · see citing works
Wang, H., Lu, J. L., Stevens, T., Roberts, A., Mandel, J. A., Avula, R., Ma, B., Wu, Y. L., Wang, J., Land, C. V., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112830 · Cited by 28 · see citing works
Aging: therapeutics for a healthy future
Hodgson, R. A., Kennedy, B. K., Masliah, E., Scearce-Levie, K. A., Tate, B. A., Venkateswaran, A., & Braithwaite, S. P. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.11.021 · Cited by 30 · see citing works
CRISPR-Cas9 Mediated Telomere Removal Leads to Mitochondrial Stress and Protein Aggregation
Kim, H., Ham, S., Jo, M., Lee, G. H., Lee, Y., Shin, J., & Lee, Y. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102093 · Cited by 28 · see citing works
Singh, S. P., Janjuha, S., Chaudhuri, S., Reinhardt, S., Kränkel, A., Dietz, S., Eugster, A., Bilgin, H., Korkmaz, S., Zararsız, G., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-35218-5 · Cited by 28 · see citing works
Curley, M. K., Milne, L., Smith, S. E., J⊘rgensen, A., Frederiksen, H. W., Hadoke, P. W. F., Potter, P. K., & Smith, L. B. (2018) · The FASEB Journal · doi:10.1096/fj.201800612r · Cited by 27 · see citing works
Self-citationAn Appraisal on the Value of Using Nutraceutical Based Senolytics and Senostatics in Aging
Kaur, A., Macip, S., & Stover, C. M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00218 · Cited by 26 · see citing works
Todorovic, S. T., Lončarević‐Vasiljković, N., Jović, M., Sokanovic, S. J., Kanazir, S., & Mladenović, A. (2019) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2019.111195 · Cited by 26 · see citing works
Loss of Chondroitin Sulfate Modification Causes Inflammation and Neurodegeneration in skt Mice
Macke, E. L., Henningsen, E., Jessen, E., Zumwalde, N. A., Landowski, M., Western, D., Russell, W. L., Liu, C., Gruenke, N. P., Doebley, A.-L., et al. (2019) · Genetics · doi:10.1534/genetics.119.302834 · Cited by 25 · see citing works
DNA Break-Induced Epigenetic Drift as a Cause of Mammalian AgingPreprint
Hayano, M., Yang, J.-H., Bonkowski, M. S., Amorim, J. A., Ross, J. M., Coppotelli, G., Griffin, P. T., Chew, Y. C., Guo, W., Yang, X., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/808659 · Cited by 23 · see citing works
Early Adversity and Accelerated Brain Aging: A Mini-Review
Chaudhari, P. R., Singla, A., & Vaidya, V. A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.822917 · Cited by 23 · see citing works
Vascular senescence and ageing: a role for the MEOX proteins in promoting endothelial dysfunction
Northcott, J. M., Czubryt, M. P., & Wigle, J. T. (2017) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2017-0149 · Cited by 21 · see citing works
Infiltrating macrophages contribute to age-related neuroinflammation in C57/BL6 mice
Wolfe, H. E., Minogue, A. M., Rooney, S., & Lynch, M. A. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.05.003 · Cited by 23 · see citing works
Hassan, E. B., Alderghaffar, M., Wauquier, F., Coxam, V., Demontiero, O., Vogrin, S., Wittrant, Y., & Duque, G. (2019) · Aging · doi:10.18632/aging.102299 · Cited by 23 · see citing works
miR‐181b regulates vascular endothelial aging by modulating an MAP3K3 signaling pathway
Zhou, H., Yang, D., Cheng, H. S., McCoy, M. G., Pérez‐Cremades, D., Haemmig, S., Wong, D., Chen, L., & Feinberg, M. W. (2022) · The FASEB Journal · doi:10.1096/fj.202200046r · Cited by 21 · see citing works
Effect of the Resveratrol Rice DJ526 on Longevity
Islam, M. S., Jin, Y., Chung, H., Kim, H., Baek, S.-H., & Hong, S. (2019) · Nutrients · doi:10.3390/nu11081804 · Cited by 21 · see citing works
Eckersley, A., Ozols, M., Chen, P., Tam, V., Ward, L. J., Hoyland, J. A., Trafford, A. W., Yuan, X., Schiller, H. B., Chan, D. T.-M., et al. (2022) · Matrix Biology · doi:10.1016/j.matbio.2022.05.007 · Cited by 19 · see citing works
Łysek-Gładysińska, M., Wieczorek, A., Jóźwik, A., Walaszczyk, A., Jelonek, K., Szczukiewicz-Markowska, G., Horbańczuk, O. K., Pietrowska, M., Widłak, P., & Gabryś, D. (2021) · Cells · doi:10.3390/cells10030502 · Cited by 19 · see citing works
Bone Tissue and the Nervous System: What Do They Have in Common?
Minoia, A., Carbonare, L. D., Schwamborn, J. C., Bolognin, S., & Valenti, M. T. (2022) · Cells · doi:10.3390/cells12010051 · Cited by 19 · see citing works
Zheng, X., Li, Z., Sen, J. B., Samarah, L., Deacon, C. S., Bernardo, J., & Machin, D. R. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1090023 · Cited by 19 · see citing works
Zheng, X., Sen, J. B., Li, Z., Sabouri, M., Samarah, L., Deacon, C. S., Bernardo, J., & Machin, D. R. (2023) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00415.2022 · Cited by 19 · see citing works
Constitutive Dicer1 phosphorylation accelerates metabolism and aging in vivo
Aryal, N. K., Pant, V., Wasylishen, A. R., Parker-Thornburg, J., Baseler, L., El-Naggar, A. K., Liu, B., Kalia, A., Lozano, G., & Arur, S. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1814377116 · Cited by 18 · see citing works
Principles of brain aging: Status and challenges of modeling human molecular changes in mice
Kluever, V., & Fornasiero, E. F. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101465 · Cited by 18 · see citing works
Genetic context modulates aging and degeneration in the murine retina
Marola, O. J., MacLean, M., Cossette, T. L., Diemler, C. A., Hewes, A. A., Reagan, A. M., Kanyinda, J. N., Skelly, D. A., & Howell, G. R. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00800-9 · Cited by 15 · see citing works
New methodologies in ageing research
Osborne, B., Bakula, D., Ezra, M. B., Dresen, C., Hartmann, E., Kristensen, S. M., Mkrtchyan, G. V., Nielsen, M. H., Petr, M. A., & Scheibye‐Knudsen, M. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101094 · Cited by 16 · see citing works
Lessons in aging from Myc knockout mouse models
Prochownik, E. V., & Wang, H. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1244321 · Cited by 14 · see citing works
A researcher's guide to studying sex differences in immune aging
Baker, C., Kim, M., & Benayoun, B. A. (2025) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2025.01.005 · Cited by 14 · see citing works
Quantitative proteomics to study aging in rabbit liver
Amin, B., Ford, K. I., & Robinson, R. A. S. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111227 · Cited by 14 · see citing works
Progress in precision drug delivery systems for neurodegenerative diseases with muscle atrophy
Zhang, G., Hu, F., Zhang, Y., Li, D., Deng, Y., Yang, M., Huang, T., Deng, X., Li, Y., Fu, C., et al. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.111027 · Cited by 12 · see citing works
Phosphatidylethanolamine N-Methyltransferase Knockout Modulates Metabolic Changes in Aging Mice
Zhou, Q., Zhang, F., Kerbl-Knapp, J., Korbelius, M., Kuentzel, K. B., Vujić, N., Akhmetshina, A., Hörl, G., Paar, M., Steyrer, E., et al. (2022) · Biomolecules · doi:10.3390/biom12091270 · Cited by 12 · see citing works
Qiu, G., Zheng, X., Fu, M., Huang, C., & Yang, X. (2019) · Biogerontology · doi:10.1007/s10522-019-09832-3 · Cited by 12 · see citing works
Wu, W., Peng, Y., Zhou, J., Zhang, X., Cao, L., Lin, W., Lu, Y., Wen, J., & Wang, Z. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.689188 · Cited by 12 · see citing works
Targeted Therapeutics Delivery by Exploiting Biophysical Properties of Senescent Cells
Low, J., Chan, B., & Tay, A. K. P. (2021) · Advanced Functional Materials · doi:10.1002/adfm.202107990 · Cited by 11 · see citing works
Dicer1 deficient mice exhibit premature aging and metabolic perturbations in adipocytes
de Cauwer, A., Loustau, T., Erne, W., Pichot, A., Molitor, A. M., Stemmelen, T., Carapito, R., Orend, G., Bahram, S., & Georgel, P. (2022) · iScience · doi:10.1016/j.isci.2022.105149 · Cited by 10 · see citing works
Aging, Parkinson’s Disease, and Models: What Are the Challenges?
Bellantuono, I., Mortiboys, H., Rocha, E. M., Chamoli, M., Chinta, S. J., Andersen, J. K., Wallis, R., Bézard, E., Goldberg, M., Greenamyre, T., et al. (2023) · doi:10.59368/agingbio.20230010 · Cited by 13 · see citing works
Rifaai, R. A., El‐Tahawy, N. F. G., Abozaid, S. M. M., & Abdelwahab, A. (2024) · Microscopy and Microanalysis · doi:10.1093/mam/ozae102 · Cited by 9 · see citing works
Accelerated Aging in Cyclophilin B–Deficient Mice Downstream of p21‐Cip1 /Waf1
Zhang, Y., Pignolo, R. J., & Bram, R. J. (2022) · JBMR Plus · doi:10.1002/jbm4.10674 · Cited by 9 · see citing works
Modelling Osteoporosis in Pre-Clinical Research—Challenges, Trends and New Approaches
Plank, J., Damerau, A., Chacon, M. S., Hoff, P., Buttgereit, F., & Pfeiffenberger, M. (2025) · Cells · doi:10.3390/cells14211649 · Cited by 7 · see citing works
Experimental models for ageing research.
Toniolo, L., Sirago, G., & Giacomello, E. (2023) · PubMed · doi:10.14670/hh-18-576 · Cited by 7 · see citing works
Loss of Calponin 2 causes premature ovarian insufficiency in mice
Hsieh, T., & Jin, J. (2024) · Journal of Ovarian Research · doi:10.1186/s13048-024-01346-y · Cited by 7 · see citing works
From Elixirs to Geroscience: A Historical and Molecular Perspective on Anti-Aging Medicine
Nicoletti, G. R. P., Mangano, K., Nicoletti, F., & Cavalli, E. (2025) · Molecules · doi:10.3390/molecules30244728 · Cited by 7 · see citing works
Bertran‐Gonzalez, J., Dinale, C., & Matamales, M. (2023) · Current Biology · doi:10.1016/j.cub.2023.04.020 · Cited by 7 · see citing works
Avallone, R., Rustichelli, C., Filaferro, M., & Vitale, G. (2024) · Molecules · doi:10.3390/molecules29174190 · Cited by 6 · see citing works
Plausible Links Between Metabolic Networks, Stem Cells, and Longevity
Kucia, M., & Ratajczak, M. Z. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-31206-0_15 · Cited by 6 · see citing works
Carr, L. M., Mustafa, S., Care, A., & Collins‐Praino, L. E. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.04.023 · Cited by 5 · see citing works
Bernhard, M., Okorie, O., Tseng, W., Chen, M., Danon, J. N., Cui, M., Lashbrooks, E., Yang, Y., & Wang, B. (2024) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00294.2024 · Cited by 5 · see citing works
Husseiny, I. M. E., Kholy, S. E., Mohamed, A. Z., Meshrif, W. S., & Elbrense, H. (2022) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2022.03.006 · Cited by 5 · see citing works
Jaramillo‐Rangel, G., Chávez-Briones, M.-D.-L., Ancer-Arellano, A., Miranda-Maldonado, I. C., & Ortega‐Martínez, M. (2023) · Biomedicines · doi:10.3390/biomedicines11072075 · Cited by 5 · see citing works
Palma, J., Maciejewska, D., Zgutka, K., Piotrowska, K., Skonieczna‐Żydecka, K., & Stachowska, E. (2023) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2023.106764 · Cited by 5 · see citing works
Using Computational Models to Study Aging
Auley, M. T. M., & Mooney, K. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811353-0.00007-5 · Cited by 5 · see citing works
Reproductive toxicology: keeping up with our changing world
Miller, L. B., Feuz, M. B., Meyer, R. G., & Meyer‐Ficca, M. L. (2024) · Frontiers in Toxicology · doi:10.3389/ftox.2024.1456687 · Cited by 8 · see citing works
Otsuka, T., & Matsui, H. (2025) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2025.112087 · Cited by 6 · see citing works
Age-induced P-bodies become detrimental and shorten the lifespan of yeastPreprint
Choi, J., Wang, S., Li, Y., Hao, N., & Zid, B. M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.05.467477 · Cited by 4 · see citing works
The Converging Roles of Nucleases and Helicases in Genome Maintenance and the Aging Process
Margariti, A., Daniil, P., & Rampias, T. N. (2025) · Life · doi:10.3390/life15111729 · Cited by 3 · see citing works
The role of gut microbiota on skeletal muscle strength in LDLR knockdown aging mice
Li, Y., Fang, Z., Luo, Y., Liu, H., Zhao, D., Feng, T., Zhang, X., Mo, S., Fang, X., Huang, L., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-00059-6 · Cited by 3 · see citing works
Potential impact of underlying diseases influencing ADME in nonclinical safety assessment
Cho, S. H., Jo, H., Hwang, Y. J., Kim, C., Jo, Y. H., & Yun, J.-W. (2024) · Food and Chemical Toxicology · doi:10.1016/j.fct.2024.114636 · Cited by 3 · see citing works
Low birth weight and reduced postnatal nutrition lead to cardiac dysfunction in piglets
McPeek, A. C., Patton, B., Columbus, D. A., Olver, T. D., Rodrigues, L. A., Sands, J., Weber, L. P., & Ferguson, D. P. (2023) · Journal of Animal Science · doi:10.1093/jas/skad364 · Cited by 3 · see citing works
RNase 2/EDN cleaves tRNA anticodon loops to generate immunoactive RNAsPreprint
Shigematsu, M., Minami, A., Kawamura, T., Shah, S. D., Ogawa, T., Deshpande, D. A., & Kirino, Y. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/815803 · Cited by 3 · see citing works
The aging lung mucosa: A proteomics studyPreprint
Garcia‐Vilanova, A., Olmo-Fontánez, A. M., Moliva, J. I., Allué‐Guardia, A., Singh, H., Merrit, R. E., Caceres, D. M., Peters, J. I., Wang, Y., Schlesinger, L. S., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.14.460375 · Cited by 3 · see citing works
Zhavoronkov, A. A., Wilczok, D., Ren, F., & Galkin, F. (2025) · Aging · doi:10.18632/aging.206301 · Cited by 2 · see citing works
Tuna, B. G., Keles, N. A., Cicekdal, M. B., Doğan, S., & Kõks, S. (2025) · PLoS ONE · doi:10.1371/journal.pone.0331898 · Cited by 1 · see citing works
Self-citationPalma, J., Skonieczna‐Żydecka, K., Maciejewska, D., Zgutka, K., Piotrowska, K., & Stachowska, E. (2026) · Nutrients · doi:10.3390/nu18030518 · Cited by 2 · see citing works
Experimental model systems to study vascular aging
Tuna, B. G., Rey, A. B. A., Julve, J., Borrell-Pagés, M., Praet, M. V., Riches‐Suman, K., Roks, A. J. M., Rochfort, K. D., Keles, N. A., Tura-Ceide, O., et al. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103256 · Cited by 2 · see citing works
Self-citationBhoumik, S., Kesherwani, R., & Rizvi, S. I. (2024) · Indian Journal of Clinical Biochemistry · doi:10.1007/s12291-024-01220-0 · Cited by 2 · see citing works
Age-related differences in retinal function and structure in C57BL/6J and Thy1-YFPh mice
Lee, P. Y., & Bui, B. V. (2024) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2024.06.005 · Cited by 2 · see citing works
Generation and Identification of Mutations Resulting in Chronic and Age‐Related Phenotypes in Mice
Blease, A., NICOL, T., Falcone, S., Starbuck, B., Greenaway, S., Hutchinson, M., & Potter, P. K. (2018) · Current Protocols in Mouse Biology · doi:10.1002/cpmo.42 · Cited by 2 · see citing works
Self-citationWang, H., Lu, J. L., Stevens, T., Roberts, A., Mandel, J. A., Avula, R., Ma, B., Wu, Y. L., Wang, J., Land, C. V., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.30.526354 · Cited by 2 · see citing works
Age-Related RPE changes in Wildtype C57BL/6J Mice between 2 and 32 MonthsPreprint
Shelton, D. A., Gefke, I., Summers, V. R., Kim, Y., Yu, H., Getz, Y., Ferdous, S., Donaldson, K. J., Liao, K., Papania, J. T., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.30.574142 · Cited by 2 · see citing works
Chen, I., Lu, W., Hsiao, F., Chen, L.-K., Parini, A., Santin, Y., Guiard, B. P., Pradère, J., Vellas, B. J., Rolland, Y., et al. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103183 · Cited by 1 · see citing works
Navarro, H. G., Doğan, S., Tuna, B. G., Potter, P. K., Kõks, G., & Kõks, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11433-3 · Cited by 1 · see citing works
Self-citation(Re)modeling high-salt diet-induced hypertension in mice
Power, G. J., & Padilla, J. (2023) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00093.2023 · Cited by 1 · see citing works
Hsu, J.-E., Wang, B., Hwang, Y., Cheng, W., Zhao, Q., Si, Y., Xu, M., Kang, H.-M., & Lee, J. H. (2026) · Biomolecules · doi:10.3390/biom16040579
On the molecular mechanisms of hematopoietic stem cell aging
Lazare, S. (2018) · University of Groningen research database (University of Groningen / Centre for Information Technology)
O’Connor, J., Herrera, G., Jávega, B., & Martínez‐Romero, A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811353-0.00058-0
- Authors
- Kõks, S., Dogan, S., Tuna, B. G., González-Navarro, H., Potter, P., & Vandenbroucke, R. E.
- Affiliations
- Estonian University of Life Sciences (EE)
- Mary Lyon Centre at MRC Harwell (GB)
- Ghent University (BE)
- Corresponding author
- Vandenbroucke, Roosmarijn E.
- Venue
- Mechanisms of Ageing and Development
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 160
- Pages
- 41-53
- ISSN
- 0047-6374 (ISSN-L)
- OpenAlex
- W2529858651
- Cited by
- 125
- References
- 182
- Citations by year
- 2026: 12 · 2025: 11 · 2024: 16 · 2023: 16 · 2022: 15 · 2021: 15 · 2020: 6 · 2019: 18 · 2018: 12 · 2017: 4
- FWCI
- 1.13
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Mechanisms of Ageing and Development (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion, cc-by)
- Murdoch University Research Portal (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Antioxidants, Aging, Portulaca oleracea
- Keywords
- aging, accelerated aging, caloric restriction, disease susceptibility, phenotypic characterization
- MeSH terms
- Aging, Animals, Humans, Models, Biological, Mice
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.
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