The overexpression of major antioxidant enzymes does not extend the lifespan of mice

A Simple Sequentially Rejective Multiple Test Procedure

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Statistical Models Based on Counting Processes

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Statistical Models Based on Counting Processes

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Extension of murine life span by overexpression of catalase targeted to mitochondria

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Extension of Life-Span by Overexpression of Superoxide Dismutase and Catalase in Drosophila melanogaster

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Trends in oxidative aging theories

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FLP Recombinase-Mediated Induction of Cu/Zn-Superoxide Dismutase Transgene Expression Can Extend the Life Span of Adult Drosophila melanogaster Flies

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Induced Overexpression of Mitochondrial Mn-Superoxide Dismutase Extends the Life Span of Adult Drosophila melanogaster

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Understanding the structure and function of catalases: clues from molecular evolution and in vitro mutagenesis

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Genetic mouse models of extended lifespan

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Role/s of ‘Antioxidant’ Enzymes in Ageing

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MnSOD activity protects mitochondrial morphology of quiescent fibroblasts from age associated abnormalities

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Aging and energetics’ ‘Top 40’ future research opportunities 2010-2013

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Redox regulation in lifespan determination

Karagianni, C., & Bazopoulou, D. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.105761 · Cited by 26

Natural variation in age-related dopamine neuron degeneration is glutathione dependent and linked to life span

Coleman, C. R., Pallos, J., Arreola-Bustos, A., Wang, L., Raftery, D., Promislow, D., & Martin, I. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2403450121 · Cited by 20

Attenuation of liver insoluble protein carbonyls: indicator of a longevity determinant?

Bhattacharya, A., Leonard, S., Tardif, S. D., Buffenstein, R., Fischer, K. E., Richardson, A. G., Austad, S. N., & Chaudhuri, A. R. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00712.x · Cited by 20

Nutritional stress in eukaryotic cells: Oxidative species and regulation of survival in time of scarceness

Ferretti, A. C., Larocca, M. C., & Favre, C. (2011) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2011.11.007 · Cited by 22

Nutrient Sensing and Redox Balance: GCN2 as a New Integrator in Aging

Falcón, P., Escandón, M., Brito, Á., & Matus, S. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/5730532 · Cited by 21

Thioredoxin, oxidative stress, cancer and aging

Flores, L. C., Ortiz, M., Dube, S., Hubbard, G. B., Lee, S., Salmon, A. B., Zhang, Y., & Ikeno, Y. (2012) · Longevity & Healthspan · doi:10.1186/2046-2395-1-4 · Cited by 20

Food Antioxidants and Aging: Theory, Current Evidence and Perspectives

Miyazawa, T., Abe, C., Burdeos, G. C., Matsumoto, A., & Toda, M. (2022) · Nutraceuticals · doi:10.3390/nutraceuticals2030014 · Cited by 20

Future foods, dietary factors and healthspan

Li, K., Wang, C., Wang, Y., Fu, L., & Zhang, N. (2023) · Journal of Future Foods · doi:10.1016/j.jfutfo.2022.12.001 · Cited by 20

Ecological, biomedical and epidemiological approaches to understanding oxidative balance and ageing: what they can teach each other

Cohen, A. A., de Magalhães, J. P., & Gohil, K. (2010) · Functional Ecology · doi:10.1111/j.1365-2435.2010.01761.x · Cited by 19

Thioredoxin overexpression in both the cytosol and mitochondria accelerates age-related disease and shortens lifespan in male C57BL/6 mice

Cunningham, G. M., Flores, L. C., Roman, M. G., Cheng, C., Dube, S., Allen, C., Valentine, J. M., Hubbard, G. B., Bai, Y., Saunders, T. L., et al. (2018) · GeroScience · doi:10.1007/s11357-018-0039-6 · Cited by 19

Different Antioxidant Efficacy of Two MnII-Containing Superoxide Anion Scavengers on Hypoxia/Reoxygenation-Exposed Cardiac Muscle Cells

Becatti, M., Bencini, A., Nistri, S., Conti, L., Fabbrini, M. G., Lucarini, L., Ghini, V., Severi, M., Fiorillo, C., Giorgi, C., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-46476-2 · Cited by 19

Cardiac Cell Senescence and Redox Signaling

Cesselli, D., Aleksova, A., Sponga, S., Cervellin, C., Loreto, C. D., Tell, G., & Beltrami, A. P. (2017) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2017.00038 · Cited by 20

Targeting multiple hallmarks of mammalian aging with combinations of interventions

Panchin, A. Y., Ogmen, A., Blagodatski, A. S., Egorova, A., Batin, M., & Glinin, T. S. (2024) · Aging · doi:10.18632/aging.206078 · Cited by 22

Research progress on the interaction between circadian clock and early vascular aging

Chen, Z., Xiong, Z., & Liu, X. (2021) · Experimental Gerontology · doi:10.1016/j.exger.2021.111241 · Cited by 19

Microphysiological systems for human aging research

Park, S., Laskow, T. C., Chen, J., Guha, P., Dawn, B., & Kim, D. (2024) · Aging Cell · doi:10.1111/acel.14070 · Cited by 21

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

Continuous overexpression of thioredoxin 1 enhances cancer development and does not extend maximum lifespan in male C57BL/6 mice

Flores, L. C., Roman, M. G., Cunningham, G. M., Cheng, C., Dube, S., Allen, C., Remmen, H. V., Hubbard, G. B., Saunders, T. L., & Ikeno, Y. (2018) · Pathobiology of Aging & Age-related Diseases · doi:10.1080/20010001.2018.1533754 · Cited by 18

Targeting redox biology to reverse mitochondrial dysfunction

Marcinek, D. J., & Siegel, M. P. (2013) · Aging · doi:10.18632/aging.100590 · Cited by 18

An Objective Appraisal of the Free Radical Theory of Aging

Lustgarten, M. S., Müller, F. L., & Remmen, H. V. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-378638-8.00008-7 · Cited by 18

The role of mitochondria in longevity and healthspan

Brand, M. D. (2014) · Longevity & Healthspan · doi:10.1186/2046-2395-3-7 · Cited by 17

Developmental drift as a mechanism for aging: lessons from nematodes

Lezzerini, M., Smith, R. L., & Budovskaya, Y. V. (2013) · Biogerontology · doi:10.1007/s10522-013-9462-3 · Cited by 16

Antioxidants: Wonder drugs or quackery?

Azzi, A. (2017) · BioFactors · doi:10.1002/biof.1388 · Cited by 16

Caloric restriction and aging but not overexpression of SOD1 affect hippocampal volumes in mice

Rutten, B. P. F., Brasnjevic, I., Steinbusch, H. W. M., & Schmitz, C. (2010) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2010.08.002 · Cited by 15

About the dangers, costs and benefits of living an aerobic lifestyle

Knoefler, D., Leichert, L. I. O., Thamsen, M., Cremers, C. M., Reichmann, D., Gray, M. J., Wholey, W.-Y., & Jakob, U. (2014) · Biochemical Society Transactions · doi:10.1042/bst20140108 · Cited by 15

Enhancing autophagy by redox regulation extends lifespan in Drosophila

Lennicke, C., Bjedov, I., Grönke, S., Menger, K. E., James, A. M., Castillo-Quan, J. I., van Leeuwen, L. A. G., Foley, A., Buricova, M., Adcott, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60603-w · Cited by 16

Mitochondrial metabolism in aging: Effect of dietary interventions

Cerqueira, F. M., & Kowaltowski, A. J. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.03.009 · Cited by 14

Consolidating multiple evolutionary theories of ageing suggests a need for new approaches to study genetic contributions to ageing decline

Slade, L., Etheridge, T., & Szewczyk, N. J. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102456 · Cited by 15

Intracellular and extracellular redox signals during exercise and aging

Caporossi, D., Jackson, M. J., & Henríquez‐Olguín, C. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.10.283 · Cited by 15

What is the rate-limiting step towards aging? Chemical reaction kinetics might reconcile contradictory observations in experimental aging research

Kunath, S., & Moosmann, B. (2019) · GeroScience · doi:10.1007/s11357-019-00058-2 · Cited by 12

Mechanisms of Mitochondrial Free Radical Production and their Relationship to the Aging Process

Quinlan, C. L., Treberg, J. R., & Brand, M. D. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-378638-8.00003-8 · Cited by 13

Deferoxamine accelerates endothelial progenitor cell senescence and compromises angiogenesis

Lee, Y., Wang, H.-H., Su, C., Lee, H.-I., Chou, Y., Hsieh, C., Liu, W., Shu, K.-T., Chang, K., Yeh, H., et al. (2021) · Aging · doi:10.18632/aging.203469 · Cited by 11

Sestrin2 is a central regulator of mitochondrial stress responses in disease and aging

Machado, I. F., Palmeira, C. M., & Rolo, A. P. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102762 · Cited by 12

Aging: Drugs to Eliminate Methylglyoxal, a Reactive Glucose Metabolite, and Advanced Glycation Endproducts

Dhar, I., & Desai, K. M. (2012) · InTech eBooks · doi:10.5772/34337 · Cited by 14

Aging: The Mitochondrial Connection

Brown, K. V. (2012) · Journal of Clinical & Experimental Pathology · doi:10.4172/2161-0681.s4-003 · Cited by 11

Cur2004-8, a synthetic curcumin derivative, extends lifespan and modulates age-related physiological changes in Caenorhabditis elegans

Kim, B.-K., Kim, S. A., Baek, S.-M., Lee, E. Y., Lee, E. Y., Chung, C. H., Ahn, C. M., & Park, S.-K. (2019) · Drug Discoveries & Therapeutics · doi:10.5582/ddt.2019.01057 · Cited by 10

Neuronal injury from cardiac arrest: aging years in minutes

Cherry, B., Sumien, N., & Mallet, R. T. (2014) · AGE · doi:10.1007/s11357-014-9680-x · Cited by 9

Antioxidant Defense Mechanisms

Jaeschke, H., & Ramachandran, A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.64200-9 · Cited by 10

Murburn posttranslational modifications of proteins: Cellular redox processes and murzyme‐mediated metabolo‐proteomics

Manoj, K. M. (2023) · Journal of Cellular Physiology · doi:10.1002/jcp.30954 · Cited by 8

Applied Healthspan Engineering

Larrick, J. W., & Mendelsohn, A. R. (2010) · Rejuvenation Research · doi:10.1089/rej.2009.0969 · Cited by 8

Cellular oxidative damage is more sensitive to biosynthetic rate than to metabolic rate: A test of the theoretical model on hornworms (Manduca sexta larvae)

Amunugama, K., Jiao, L., Olbricht, G. R., Walker, C., Huang, Y., Nam, P. K.-S., & Hou, C. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.05.015 · Cited by 8

Xanthoxyline prevents aging and neuronal damage by activating autophagy and DAF-16 expression in Caenorhabditis elegans

Kim, H., Lee, S. B., Kim, H. K., & Park, S.-K. (2025) · Animal Cells and Systems · doi:10.1080/19768354.2025.2549756 · Cited by 7

Lifelong soya consumption in males does not increase lifespan but increases health span under a metabolic stress such as type 2 diabetes mellitus

Borrás, C., Abdelaziz, K. M., Díaz, A., Gambini, J., Jové, M., López-Grueso, R., Mas‐Bargues, C., Monleón, D., Pamplona, R., & Viña, J. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111596 · Cited by 7

Sirt2 ablation exacerbates Sod1 knockout-induced progeroid phenotype in mice

Geng, A., Wang, X., Wu, Z., Liu, Z., Huang, X. H., Wang, X., Sun, X., Wang, Y., Chen, J., Jiang, Y., et al. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103770 · Cited by 6

Potentiation of paraquat toxicity by inhibition of the antioxidant defenses and protective effect of the natural antioxidant, 4-hydroxyisopthalic acid in Drosophila melanogaster

Niveditha, S., & Shivanandappa, T. (2022) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2022.109399 · Cited by 6

Symbiotic Origin of Aging

Greenberg, E. F., & Vatolin, S. (2017) · Rejuvenation Research · doi:10.1089/rej.2017.1973 · Cited by 6

Long-term sulforaphane-treatment restores redox homeostasis and prevents cognitive decline in middleaged female and male rats, but cannot revert previous damage in old animals

Santín-Márquez, R., Hernández-Arciga, U., Salas-Venegas, V., Toledo-Pérez, R., López-Cervantes, S. P., Librado‐Osorio, R., Luna‐López, A., López‐Díazguerrero, N. E., Gómez‐González, B., & Königsberg, M. (2022) · Biogerontology · doi:10.1007/s10522-022-09984-9 · Cited by 5

The impact of co-housing on murine aging studies

Luciano, A., & Churchill, G. A. (2025) · GeroScience · doi:10.1007/s11357-024-01480-x · Cited by 6

Superoxide signal orchestrates tetrathiomolybdate-induced longevity via ARGK-1 in Caenorhabditis elegans

Zhou, Y., Zhang, M., Lu, S., Liu, L., Duan, Z., Wei, F., & Li, G. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.07.014 · Cited by 5

Modest inhibition of the growth hormone axis does not affect mitochondrial reactive oxygen species generation or redox state, unlike calorie restriction

Hayashida, T., Komatsu, T., Henmi, Y., Yanagihara‐Outa, K., Kim, A., Chiba, T., Goto, S., Chung, H. Y., & Shimokawa, I. (2011) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/j.1447-0594.2011.00692.x · Cited by 5

Dietary restriction in senolysis and prevention and treatment of disease

Aminzadeh-Gohari, S., Kofler, B., & Herzog, C. M. S. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2153355 · Cited by 5

Clinical & Experimental Pathology

Ren, R., Fedoriw, Y. D., & Willis, M. S. (2012) · Cited by 5

The Role of Scientists in a Human-centered Society

Ramirez, M., & Cayón-Peña, J. (2017) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 5

Multidisciplinary Approach to Aging

Takahashi, R., & Odera, K. (2020) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.19-00193-1 · Cited by 5

Extension of Life Span in Laboratory Mice

Unnikrishnan, A., Deepa, S. S., Herd, H. R., & Richardson, A. G. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811353-0.00019-1 · Cited by 7

Mouse models used to test the role of reactive oxygen species in aging and age-related chronic diseases

Nguyen, H. V. M., Ran, Q., Salmon, A. B., Ahn, B., Chiao, Y. A., Bhaskaran, S., & Richardson, A. G. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.10.269 · Cited by 4

Mitochondrial DNA Repair

Sarah, A. T. (2011) · InTech eBooks · doi:10.5772/23358 · Cited by 4

Species-specific lifespans: Can it be a lottery based on the mode of mitochondrial DNA replication?

Khaidakov, M. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.02.012 · Cited by 4

Level of Certain Oxidants and Antioxidants in Patients with Uterine Fibroids

Çetinkaya, K., Ayral, P. A., Çetinkaya, S. Ç., Yazıhan, N., Fadıloğlu, Ş., Atasever, M., & Erel, Ö. (2019) · Gynecology Obstetrics and Reproductive Medicine · doi:10.21613/gorm.2019.955 · Cited by 4

Flux control in the aging cascade

Moosmann, B. (2021) · Aging · doi:10.18632/aging.202821 · Cited by 4

Photocontrol of Axillary Bud Outgrowth by MicroRNAs: Current State-of-the-Art and Novel Perspectives Gained From the Rosebush Model

Mallet, J., Laufs, P., Leduc, N., & Gourrierec, J. L. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2021.770363 · Cited by 4

Aging in Marine Animals

Philipp, E. E. R., Strahl, J., & Sukhotin, A. A. (2011) · doi:10.1002/9781444345988.ch14 · Cited by 4

Revisiting ROS: duality in organ aging progression

Yu, M., Liu, S., Zhang, C., & Yang, W. J. (2025) · Molecular Biology Reports · doi:10.1007/s11033-025-11342-0 · Cited by 3

Dietary Walnuts Preserve Aspects of Health Span and Alter the Hippocampal Lipidome in Aged High-Fat Diet-Fed Mice

Novaj, A., Engel, M. G., Wang, R., Mao, K., Xue, X., Amir, Y., Atzmon, G., & Huffman, D. M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032314 · Cited by 3

Stem Cell Aging

Rožman, P. J., Jazbec, K., & Jež, M. (2018) · InTech eBooks · doi:10.5772/intechopen.71764 · Cited by 4

Mitochondrial redox signaling: a key player in aging and disease

Vitale, M., Sanz, A., & Scialò, F. (2023) · Aging · doi:10.18632/aging.204659 · Cited by 3

Role of Oxidative Stress in Aging

Knoefler, D., Tienson, H. L., & Jakob, U. (2013) · Springer eBooks · doi:10.1007/978-94-007-5787-5_14 · Cited by 3

The molecular basis of cutaneous aging

Reddy, K. K., & Gilchrest, B. A. (2011) · Expert Review of Dermatology · doi:10.1586/edm.11.48 · Cited by 3

Common Mechanisms for Separate Maculopathies?

Körtvely, E., & Ueffing, M. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-0631-0_9 · Cited by 3

The nuanced role of mitochondrial ROS in modulating aging and aging hallmarks

Müller-Eigner, A., Morin, E., Morton, K. S., & Wojtovich, A. P. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104319 · Cited by 2

Regulation of Aging Processes: A Perspective of Dietary Restriction Models

Shimokawa, I. (2024) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.23-00165-3 · Cited by 2

Manganese Superoxide Dismutase (MnSOD) and Its Importance in Mitochondrial Function and Cancer

Holley, A. K., & Clair, D. K. S. (2016) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-30705-3_3 · Cited by 2

Neuroinflammation and oxidative stress in the aging brain: Linking in metabolism, stem cells, proteostasis, and stress adaptation

d’Avila, J. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-817780-8.00004-9 · Cited by 2

Unraveling the mode of action of medicinal plants in delaying age-related diseases using model organisms

Prasanth, M. I., Sivamaruthi, B. S., Kesika, P., Rosmol, P. S., & Tencomnao, T. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819590-1.00002-1 · Cited by 2

A metabolic and mitochondrial angle on aging

Duarte, A. I., Sadowska‐Bartosz, I., Karkucińska‐Więckowska, A., Lebiedzińska, M., Palmeira, C. M., Rolo, A. P., Kabiri, Y., Zavan, B., Pinton, P., Borges, F., et al. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823761-8.00024-0 · Cited by 3

Upstream migrant sea lamprey (Petromyzon marinus) show signs of increasing oxidative stress but maintain aerobic capacity with age

Borowiec, B. G., McDonald, A. E., & Wilkie, M. P. (2023) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2023.111503 · Cited by 1

Role of Oxidative Stress in Vascular Endothelial Cells Through Aging – a Double-Edged Sword

Thorin, É., & Thorin‐Trescases, N. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_66 · Cited by 1

Evolutionary Orthodoxy: How and Why the Evolutionary Theory of Aging Went Astray

Mitteldorf, J. (2014) · Current Aging Science · doi:10.2174/1874609807666140521105844 · Cited by 1

Molecular Signature of Aging Driven by Wnt Signaling Pathway: Lessons from Nematodes

Lezzerini, M., & Budovskaya, Y. V. (2019) · Healthy ageing and longevity · doi:10.1007/978-3-030-24970-0_22 · Cited by 1

Aging mechanism

Zeliger, H. I. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91890-9.00002-7 · Cited by 1

Exploring juventology: unlocking the secrets of youthspan and longevity programs

Brandhorst, S., & Longo, V. D. (2024) · Frontiers in Aging · doi:10.3389/fragi.2024.1379289 · Cited by 2

The Long and the Short of It: How Oxidative Stress Drives Cellular Senescence, Ageing, and Lifespan of Animals

Costantini, D. (2024) · Fascinating life sciences · doi:10.1007/978-3-031-65183-0_10 · Cited by 2

Retard of D-Galactose-Induced Aging in Mice by Whey Hydrolysates

Liu, J., Miao, Y., & Zhao, Z. (2011) · Advanced materials research · doi:10.4028/www.scientific.net/amr.415-417.43 · Cited by 1

Update on the Free Radical Theory of Aging – The Role of Oxidative Stress in Age-Related Hearing Loss

Han, C. J., & Someya, S. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_182 · Cited by 1

Free Radicals in Aging – An Evolutionary Perspective

Csiszár, A., & Ungvari, Z. I. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_14 · Cited by 1

Selective Antioxidative Effect of Hydrogen

Sun, Q., Han, W., & Nakao, A. (2015) · Springer eBooks · doi:10.1007/978-94-017-9691-0_5 · Cited by 1

Molecular mechanisms of aging in MTDNA mutator mice

Edgar, D. (2011) · Figshare · Cited by 1

Efectos del sulforafano sobre la velocidad de conducción nerviosa y su relación con el estado redox en la corteza cerebral e hipocampo de ratas viejas

Santín-Márquez, R. (2018) · doi:10.24275/uami.7d278t04p · Cited by 1

Efectos del sulforafano sobre el estado redox y la inflamación en el sistema nervioso central de ratas Wistar viejas

Santín-Márquez, R. (2023) · doi:10.24275/uami.ht24wj673 · Cited by 1

Quantifying the Impact of Co-Housing on Murine Aging StudiesPreprint

Luciano, A., & Churchill, G. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.06.606373 · Cited by 1

Catalytic Processes and Human Diseases

Duca, G. G. (2012) · Springer series in chemical physics · doi:10.1007/978-3-642-24629-6_4

The Janus Face of Insulin in Brain

Duarte, A. I., Candeias, E., Correia, S. C., Santos, R. X., Carvalho, C., Cardoso, S., Plácido, A. I., Santos, M. S., Oliveira, C. R., & Moreira, P. I. (2013) · Wiley eBooks · doi:10.1002/9781118395318.ch5

Dietary- and fasting-based interventions as novel approaches to improve the efficacy of cancer treatment

Brandhorst, S. (2013) · DuEPublico (University of Duisburg-Essen)

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Journal compilation © Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland 2009 Blackwell

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