DNA damage and ageing: new-age ideas for an age-old problem

DNA Repair and Mutagenesis

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Instability and decay of the primary structure of DNA

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Genome maintenance mechanisms for preventing cancer

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Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r)

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Senescent cells, tumor suppression, and organismal aging: good citizens, bad neighbors

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The Effect of Retarded Growth Upon the Length of Life Span and Upon the Ultimate Body Size

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IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice

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Understanding the odd science of aging

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Suppression of Aging in Mice by the Hormone Klotho

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The aging process

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Plasma Amyloid Beta 1-42 and DNA Methylation Pattern Predict Accelerated Aging in Young Subjects with Down Syndrome

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New experimental data linking secondhand smoke exposure to lung cancer in nonsmokers

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Dog Aging: A Comprehensive Review of Molecular, Cellular, and Physiological Processes

Guelfi, G., Capaccia, C., Tedeschi, M., Bufalari, A., Leonardi, L., Cenci-Goga, B. T., & Maranesi, M. (2024) · Cells · doi:10.3390/cells13242101 · Cited by 22

p53 regulates diverse tissue-specific outcomes to endogenous DNA damage in mice

Hill, R. J., Bona, N., Smink, J., Webb, H. K., Crisp, A., Garaycoechea, J. I., & Crossan, G. P. (2024) · Nature Communications · doi:10.1038/s41467-024-46844-1 · Cited by 21

Circadian rhythms of body temperature and locomotor activity in aging BALB/c mice: early and late life span predictors

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The role of the reprogramming method and pluripotency state in gamete differentiation from patient-specific human pluripotent stem cells

Mishra, S., Kaçin, E., Stamatiadis, P., Franck, S., der Jeught, M. V., Mertes, H., Pennings, G., Sutter, P. D., Sermon, K., Heindryckx, B., et al. (2018) · Molecular Human Reproduction · doi:10.1093/molehr/gay007 · Cited by 18

An Objective Appraisal of the Free Radical Theory of Aging

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Implications of Cellular Aging in Cardiac Reprogramming

Passaro, F., & Testa, G. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00043 · Cited by 15

In vivo reduction of RAD51‐mediated homologous recombination triggers aging but impairs oncogenesis

Matos-Rodrigues, G. E., Barroca, V., Muhammad, A., Dardillac, E., Allouch, A., Koundrioukoff, S., Lewandowski, D., Despras, E., Guirouilh‐Barbat, J., Frappart, L., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2022110844 · Cited by 17

Nutrients and ageing

Stenvinkel, P., Kooman, J. P., & Shiels, P. G. (2015) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000234 · Cited by 16

E2F1 and p53 Transcription Factors as Accessory Factors for Nucleotide Excision Repair

Vélez-Cruz, R., & Johnson, D. G. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms131013554 · Cited by 15

DNA damage-induced inflammation and nuclear architecture

Stratigi, K., Chatzidoukaki, O., & Garinis, G. A. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.09.008 · Cited by 17

The 19S proteasome subunit Rpn7 stabilizes DNA damage foci upon genotoxic insult

Tsolou, A., Nelson, G., Trachana, V., Chondrogianni, N., Saretzki, G. C., von Zglinicki, T., & Gonos, E. S. (2012) · IUBMB Life · doi:10.1002/iub.1018 · Cited by 16

DNA damage and repair in age-related macular degeneration

Błasiak, J. (2010) · Frontiers in bioscience · doi:10.2741/3789 · Cited by 15

Aging and photo-aging DNA repair phenotype of skin cells—Evidence toward an effect of chronic sun-exposure

Prunier, C., Masson-Genteuil, G., Ugolin, N., Sarrazy, F., & Sauvaigo, S. (2011) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2011.05.005 · Cited by 15

Chance and Causality in Ageing and Longevity

Accardi, G., Aiello, A., Vasto, S., & Caruso, C. (2019) · Springer eBooks · doi:10.1007/978-3-030-20762-5_1 · Cited by 15

Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase

Dhillon, K. K., Sidorova, J. M., Albertson, T., Anderson, J. B., Ladiges, W., Rabinovitch, P. S., Preston, B. D., & Monnat, R. J. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.09.013 · Cited by 14

Electrical Current Signatures of DNA Base Modifications in Single Molecules Immobilized in the α‐Hemolysin Ion Channel

Wolna, A. H., Fleming, A. M., An, N., He, L., White, H. S., & Burrows, C. J. (2013) · Israel Journal of Chemistry · doi:10.1002/ijch.201300022 · Cited by 13

Rapamycin safeguards lymphocytes from DNA damage accumulation in vivo

Chebel, A., Catallo, R., Mabon, C., Bachy, E., Wenner, T., Salles, G., Pouteil‐Noble, C., & Ffrench, M. (2016) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2016.06.004 · Cited by 13

Coordination of cell cycle, DNA repair and muscle gene expression in myoblasts exposed to genotoxic stress

Simonatto, M., Giordani, L., Marullo, F., Minetti, G., Puri, P., & Latella, L. (2011) · Cell Cycle · doi:10.4161/cc.10.14.15948 · Cited by 13

Análise da natureza genotípica de pacientes Xeroderma pigmentosum brasileiros.

Soltys, D. T. (2010) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2010.tde-05082010-114429 · Cited by 13

Delayed γH2AX foci disappearance in mammary epithelial cells from aged women reveals an age-associated DNA repair defect

Anglada, T., Repullés, J., Espinal, A., LaBarge, M. A., Stampfer, M. R., Genescà, A., & Martı́n, M. (2019) · Aging · doi:10.18632/aging.101849 · Cited by 11

FeSTwo, a two-step feature selection algorithm based on feature engineering and sampling for the chronological age regression problem

Wei, Z., Ding, S., Duan, M., Liu, S., Huang, L., & Zhou, F. (2020) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2020.104008 · Cited by 13

DNA damage, inflammation and aging: Insights from mice

Arvanitaki, E. S., Stratigi, K., & Garinis, G. A. (2022) · Frontiers in Aging · doi:10.3389/fragi.2022.973781 · Cited by 14

Stem Cell Aging and Aberrant Differentiation within the Niche

Choi, J., & Artandi, S. E. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.06.006 · Cited by 12

Epigenetic perturbations in aging stem cells

Krauss, S. R., & de Haan, G. (2016) · Mammalian Genome · doi:10.1007/s00335-016-9645-8 · Cited by 14

Pan-Cancer Analysis of Genomic Sequencing Among the Elderly

Wahl, D. R., Nguyen, P. L., Santiago, M., Yousefi, K., Davicioni, E., Shumway, D. A., Speers, C. W., Mehra, R., Feng, F. Y.-C., Osborne, J. R., et al. (2017) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2017.01.002 · Cited by 12

Concise Review: The Epigenetic Contribution to Stem Cell Ageing: Can We Rejuvenate Our Older Cells?

Armstrong, L., Al-Aama, J. Y., Stojković, M., & Lako, M. (2014) · Stem Cells · doi:10.1002/stem.1720 · Cited by 11

TFIIH mutations can impact on translational fidelity of the ribosome

Khalid, F., Phan, T., Qiang, M., Maity, P., Lasser, T., Wiese, S., Penzo, M., Alupei, M. C., Orioli, D., Scharffetter‐­Kochanek, K., et al. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac268 · Cited by 12

Estrés oxidativo mitocondrial y envejecimiento cardíaco

Martín‐Fernández, B., & Gredilla, R. (2018) · Clínica e Investigación en Arteriosclerosis · doi:10.1016/j.arteri.2017.12.002 · Cited by 12

MicroRNA-33 promotes the replicative senescence of mouse embryonic fibroblasts by suppressing CDK6

Xu, S., Huang, H., Li, N., Zhang, B., Jia, Y., Yang, Y.-K., Yuan, Y., Xiong, X., Wang, D., Zheng, H., et al. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.04.016 · Cited by 11

Age- and Lifespan-Dependent Differences in GO Caused DNA Damage in Acheta domesticus

Flasz, B., Dziewięcka, M., Ajay, A. K., Tarnawska, M., Babczyńska, A. I., Kędziorski, A., Napora-Rutkowski, Ł., Ziętara, P., Świerczek, E., & Augustyniak, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010290 · Cited by 11

Mitochondrial oxidative stress and cardiac ageing

Martín‐Fernández, B., & Gredilla, R. (2018) · Clínica e Investigación en Arteriosclerosis (English Edition) · doi:10.1016/j.artere.2017.12.002 · Cited by 10

Laminopathies, other progeroid disorders, and aging: Common pathogenic themes and possible treatments

Neilan, E. G. (2009) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.32702 · Cited by 10

Ganoderma spore lipid ameliorates docetaxel, cisplatin, and 5-fluorouracil chemotherapy-induced damage to bone marrow mesenchymal stem cells and hematopoiesis

Lin, H., Chung, M., Sun, J., Yang, Y., Zhang, L., Pan, X., Wei, M., Cai, S., & Pan, Y. (2024) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-024-04445-x · Cited by 9

Epigenetic and redox biomarkers: Novel insights from the MARK-AGE study

Moreno‐Villanueva, M., & Bürkle, A. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.06.006 · Cited by 9

The Radioprotective Effect of Procaine and Procaine-Derived Product Gerovital H3 in Lymphocytes from Young and Aged Individuals

Ungurianu, A., Margina, D. M., Borșa, C., Ionescu, C., von Scheven, G., Oziol, L., Fauré, P., Artur, Y., Bürkle, A., Grădinaru, D., et al. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/3580934 · Cited by 9

Immune response to mutant neo-antigens

Geyer, R. J., Tobet, R., Berlin, R. D., & Srivastava, P. K. (2013) · OncoImmunology · doi:10.4161/onci.26382 · Cited by 9

Measuring the Aging Process in Stem Cells

Liu, Y., Zant, G. E. V., & Liang, Y. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-1785-3_3 · Cited by 9

Nontranscriptional Function of FOXO1/DAF-16 Contributes to Translesion DNA Synthesis

Daitoku, H., Kaneko, Y., Yoshimochi, K., Matsumoto, K., Araoi, S., Sakamaki, J.-I., Takahashi, Y., & Fukamizu, A. (2016) · Molecular and Cellular Biology · doi:10.1128/mcb.00265-16 · Cited by 10

Broken strands, broken minds: Exploring the nexus of DNA damage and neurodegeneration

Stavgiannoudaki, I., Goulielmaki, E., & Garinis, G. A. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103699 · Cited by 8

Aging, longevity and health

Rasmussen, L. J., Sander, M., Wewer, U. M., & Bohr, V. A. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.07.004 · Cited by 8

Endophytes from Malaysian Medicinal Plants as Sources for Discovering Anticancer Agents

Yap, L. S., Lee, W.-L., & Ting, A. S. Y. (2017) · Medicinal and aromatic plants of the world · doi:10.1007/978-981-10-5978-0_10 · Cited by 8

Aging and the Host Response to Implanted Biomaterials

Rao, A. N., Avula, M., & Grainger, D. W. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800196-7.00011-6 · Cited by 8

Signalling DNA Damage

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The Szilard Hypothesis on the Nature of Aging Revisited

Zetterberg, H., Båth, M., Zetterberg, M., Bernhardt, P., & Hammarsten, O. (2009) · Genetics · doi:10.1534/genetics.109.103341 · Cited by 9

Impact of transient down-regulation of DREAM in human embryonic stem cell pluripotency

Fontán‐Lozano, Á., Capilla‐González, V., Aguilera, Y., Mellado-Damas, N., Carrión, Á. M., Soria, B., & Hmadcha, A. (2016) · Stem Cell Research · doi:10.1016/j.scr.2016.03.001 · Cited by 8

Skin Aging and Immune System

Mansouri, P., Chalangari, R., Martits‐Chalangari, K., & Saffarian, Z. (2013) · Springer eBooks · doi:10.1007/978-3-642-39495-9_25 · Cited by 7

Genomic Integrity of Mouse Embryonic Stem Cells

Leyns, L., & Gonzalez, L. (2012) · InTech eBooks · doi:10.5772/37327 · Cited by 10

Mecanismos de envejecimiento vascular: ¿Qué podemos aprender del síndrome de progeria de Hutchinson-Gilford?

del Campo, L., Hamczyk, M. R., Andrés, V., Martínez‐González, J., & Rodrı́guez, C. (2018) · Clínica e Investigación en Arteriosclerosis · doi:10.1016/j.arteri.2017.12.007 · Cited by 7

Premature aging

Vulliamy, T. J. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0091-6 · Cited by 7

Introduction and Perspectives on the Chemistry and Biology of DNA Damage

Geacintov, N. E., & Broyde, S. B. (2010) · Wiley eBooks · doi:10.1002/9783527630110.ch1 · Cited by 7

Methods for Genotoxicity Testing of Environmental Pollutants

Masood, F., Anjum, R., Ahmad, M., & Malik, A. (2011) · Springer eBooks · doi:10.1007/978-94-007-1591-2_7 · Cited by 6

Does juvenile hormone prompt males to oxidative stress?

Martínez‐Lendech, N., Osorio‐Beristain, M., Franco, B., Pedraza‐Reyes, M., Obregón, A., & Contreras-Garduño, J. A. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.194530 · Cited by 6

Ubiquitin Recognition by the Cockayne Syndrome Group B Protein: Binding Will Set You Free

Graybuck, L. T., & Weiner, A. M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.05.025 · Cited by 6

Cellular Mechanisms of Age-Related Hearing Loss

Melgar–Rojas, P., Alvarado, J. C., Fuentes‐Santamaría, V., & Juiz, J. M. (2015) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-13473-4_15 · Cited by 6

Nuclear DNA Damage and Ageing

Agathangelou, K., Apostolou, Z., & Garinis, G. A. (2018) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-981-13-2835-0_10 · Cited by 7

Expression of progerin does not result in an increased mutation rate

Deniaud, E., Boumendil, C., Boyle, S., & Bickmore, W. A. (2017) · Chromosome Research · doi:10.1007/s10577-017-9556-x · Cited by 6

Age-Dependent Variation of Telomere Length and DNA Damage in Chicken

Makarenko, M., Usatov, A. V., Getmantseva, L., Chistyakov, V. A., Klimenko, A. I., & Vasilenko, V. N. (2017) · OnLine Journal of Biological Sciences · doi:10.3844/ojbsci.2017.387.393 · Cited by 5

Combining a novel ensemble model and multiplex methylation SNaPshot assays for saliva age prediction and cross-platform data analysis

Xiao, B., Zhou, Y., Zhang, Z., Wang, X., Xiang, J., Lv, Z., Liao, M., Luo, H., & Song, F. (2025) · BMC Genomics · doi:10.1186/s12864-025-11713-8 · Cited by 4

Aging and Protein Kinases

Engin, A. B., & Engin, A. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-49844-3_2 · Cited by 4

Sirtuins and the prevention of immunosenescence

Lasigliè, D. (2021) · Vitamins and hormones · doi:10.1016/bs.vh.2020.12.011 · Cited by 5

SIRT1, IGFBP-3 and CAV1 Promoter DNA Methylation in Aging

Gigek, C. O. (2014) · Translational Medicine · doi:10.4172/2161-1025.1000133 · Cited by 4

Predicted Cellular Interactors of the Endogenous Retrovirus-K Integrase Enzyme

Benoit, I., Brownell, S., & Douville, R. N. (2021) · Microorganisms · doi:10.3390/microorganisms9071509 · Cited by 4

Research Progress on Aging Mechanisms

Wang, Q., Zhou, F., Xie, W., Zhao, X., & Liu, X. (2016) · Advances in Aging Research · doi:10.4236/aar.2016.52005 · Cited by 4

Detection of Nuclear Envelope Alterations in Senescence

Bárcena, C., Osorio, F. G., & Freije, J. M. P. (2012) · Methods in molecular biology · doi:10.1007/978-1-62703-239-1_16 · Cited by 4

Active transcriptomic and proteomic reprogramming in theC. elegansnucleotide excision repair mutant xpa-1

Kassahun, H., & Nilsen, H. L. (2013) · Worm · doi:10.4161/worm.27337 · Cited by 4

The Hallmarks of Cancer Revisited Through Systems Biology and Network Modelling

Auffray, C., Ideker, T., Galas, D. J., & Hood, L. (2011) · Springer eBooks · doi:10.1007/978-94-007-1567-7_9 · Cited by 4

The Emergence of GeroMIRs: A Group of MicroRNAs Implicated in Aging

Ugalde, A. P., Kwarciak, A., Caravia, X. M., López-Otı́n, C., & Ramsay, A. J. (2013) · Wiley eBooks · doi:10.1002/9781118300312.ch5 · Cited by 5

Applications of physiological bases of aging to forensic science

Zapico, S. C., Ubelaker, D. H. V., & Adserias‐Garriga, J. (2020) · doi:10.1002/9781119482062.ch13 · Cited by 4

Specific Low/Endogenous Replication Stress Response Protects Genomic Stability via Controlled ROS Production in an Adaptive Way and Is Dysregulated in Transformed Cells

López, B. S. (2025) · Cells · doi:10.3390/cells14151183 · Cited by 3

Developmental and lifelong dioxin exposure induces measurable changes in cardiac structure and function in adulthood

de Gannes, M., Koch, S. E., Puga, A., & Rubinstein, J. (2021) · Scientific Reports · doi:10.1038/s41598-021-89825-w · Cited by 3

A Simple, High‐Yield Synthesis of DNA Duplexes Containing a Covalent, Thermally Cleavable Interstrand Cross‐Link at a Defined Location

Varela, J. G., & Gates, K. S. (2015) · Angewandte Chemie · doi:10.1002/ange.201502566 · Cited by 3

Mechanisms of vascular aging: What can we learn from Hutchinson-Gilford progeria syndrome?

del Campo, L., Hamczyk, M. R., Andrés, V., Martínez‐González, J., & Rodrı́guez, C. (2018) · Clínica e Investigación en Arteriosclerosis (English Edition) · doi:10.1016/j.artere.2017.12.005 · Cited by 4

Mitochondrial modulators

Naumova, N., Koliada, A. K., Kuzub, N., & Vaiserman, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823679-6.00012-6 · Cited by 3

Age-related decline in the expression of BRG1, ATM and ATR are partially reversed by dietary restriction in the livers of female mice

Swer, P. B., Kharbuli, B., Syiem, D., & Sharma, R. (2024) · Biogerontology · doi:10.1007/s10522-024-10117-7 · Cited by 4

Cell and Molecular Aging

Rai, P., & Troen, B. R. (2011) · Springer eBooks · doi:10.1007/978-1-4419-6999-6_2 · Cited by 3

π-Stacking effects on the EPR parameters of a prototypical DNA spin label.

Frecuş, B., Rinkevičius, Ž., & Ågren, H. (2013) · Physical Chemistry, Chemical Physics - PCCP · doi:10.1039/c3cp51129d · Cited by 3

Free-radical redox timer, sirtuins and aging: from chemistry of free radicals to systems theory of reliability

Koltover, V. K., & Skipa, T. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-814118-2.00023-9 · Cited by 3

Mechanisms of genome instability in Hutchinson-Gilford progeria

Zhang, H., & Cao, K. (2016) · Frontiers in Biology · doi:10.1007/s11515-016-1435-x · Cited by 2

Effect of Aging on Meiosis Progression, Developmental Competence and DNA Double-Strand Breaks in Mouse Oocytes

Gao, L., Jia, G., Huang, Z., Yue, M., Zhang, C., Zhu, S., & Fu, X. (2020) · Pakistan Journal of Zoology · doi:10.17582/journal.pjz/20180816030855 · Cited by 2

PRPF19 modulates morphology and growth behavior in a cell culture model of human skin

Kleißl, L., Weinmüllner, R., Lämmermann, I., Dingelmaier‐Hovorka, R., Jafarmadar, M., Ghalbzouri, A. E., Stary, G., Grillari, J., & Dellago, H. (2023) · Frontiers in Aging · doi:10.3389/fragi.2023.1154005 · Cited by 2

Multitasking Roles for Poly(ADP-ribosyl)ation in Aging and Longevity

Mangerich, A., & Bürkle, A. (2015) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-319-14151-0_6 · Cited by 2

The Stem Cell Hypothesis of Aging

Meiliana, A., & Wijaya, A. (2010) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v2i1.108 · Cited by 2

Epigenetic Significance of Chromatin Organization During Cellular Aging and Organismal Lifespan

Georgieva, M., Staneva, D., & Miloshev, G. A. (2016) · Springer eBooks · doi:10.1007/978-3-319-25325-1_2 · Cited by 2

Use of the Micronucleus Assay in Occupational Studies Involving Exposure to Genotoxic Chemicals – an Overview

Wultsch, G., Knasmüller, S., Setayesh, T., Mišík, M., & Nersesyan, A. K. (2019) · Royal Society of Chemistry eBooks · doi:10.1039/9781788013604-00403 · Cited by 2

An update on clinical applications of iPSCs from a genomic point of view

Yoshihara, M., & Murakawa, Y. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-99892-5.00001-3 · Cited by 2

A Multilevel Approach to the Causes of Genetic Instability in Stem Cells

González, E. A. P. (2022) · Springer eBooks · doi:10.1007/978-981-16-6016-0_26-1 · Cited by 2

A Multilevel Approach to the Causes of Genetic Instability in Stem Cells

González, E. A. P. (2022) · Springer eBooks · doi:10.1007/978-981-19-2655-6_26 · Cited by 3

Metformin Modulates the Mechanisms of Ageing

Cătoi, A. F., Andreicuț, A. D., Vodnar, D. C., Szabó, K., Corina, A., Arsene, A. L., Ștefan, S., Stoica, R. A., & Rizzo, M. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.89431 · Cited by 2

Genetic Aspects of Ageing

Pickard, B. S., & Blackwood, D. (2010) · Wiley eBooks · doi:10.1002/9780470669600.ch9 · Cited by 2

Role of mitophagy and mitochondria in aging and cellular senescence

Liang, X. F., Poulton, J., & Lechuga‐Vieco, A. V. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15260-3.00006-5 · Cited by 1

Translational Fidelity Mediated Regulation of ER-Stress by Dph3

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