Genomic integrity and the ageing brain
Abstract
DNA damage is correlated with and may drive the ageing process. Neurons in the brain are postmitotic and are excluded from many forms of DNA repair; therefore, neurons are vulnerable to various neurodegenerative diseases. The challenges facing the field are to understand how and when neuronal DNA damage accumulates, how this loss of genomic integrity might serve as a 'time keeper' of nerve cell ageing and why this process manifests itself as different diseases in different individuals.
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Mutations in DNA repair pathway components lead to neurodevelopment and neurodegenerative diseases.
“mutations in DNA repair pathway components lead to neurodevelopment and neurodegenerative diseases”
From Neuronal DNA double-strand breaks lead to genome structural variations and 3D genome disruption in neurodegeneration (2023) · cites this paper as [107]
Deficient DNA damage repair underlies many neurological disorders, especially age-associated neurodegenerative diseases.
“a wealth of evidence indicates deficient DNA damage repair underlies many neurological disorders, especially age‐associated neurodegenerative diseases.”
From Mechanisms of DNA damage-mediated neurotoxicity in neurodegenerative disease (2022) · cites this paper as Chow & Herrup, 2015
DNA damage and defective DDR push cellular fate toward apoptosis, senescence, or uncontrolled cell division.
“These insults ultimately push cellular fate toward apoptosis, senescence, or uncontrolled cell division”
From Mechanisms of DNA damage-mediated neurotoxicity in neurodegenerative disease (2022) · cites this paper as Chow & Herrup, 2015
Apoptosis, senescence, and uncontrolled cell division are hallmarks of age-associated disease.
“all of which are hallmarks of age‐associated disease”
From Mechanisms of DNA damage-mediated neurotoxicity in neurodegenerative disease (2022) · cites this paper as Chow & Herrup, 2015
Defective DDR pathways can result in toxic genomic rearrangements, transcriptional dysregulation, and the accumulation of unrepaired lesions.
“Defective DDR pathways can result in toxic genomic rearrangements, transcriptional dysregulation, and the accumulation of unrepaired lesions”
From Mechanisms of DNA damage-mediated neurotoxicity in neurodegenerative disease (2022) · cites this paper as Chow & Herrup, 2015
DNA damage seems to be one of the earliest indicators of neuropathology.
“In many cases, DNA damage seems to be one of the earliest indicators of neuropathology”
From Mechanisms of DNA damage-mediated neurotoxicity in neurodegenerative disease (2022) · cites this paper as Chow & Herrup, 2015
A well-established link exists between DNA damage and neurodegenerative diseases.
“A well‐established link exists between DNA damage and neurodegenerative diseases.”
From Mechanisms of DNA damage-mediated neurotoxicity in neurodegenerative disease (2022) · cites this paper as Chow & Herrup, 2015
Cites
2 retracted
Fousteri, M., Vermeulen, W., van Zeeland, A. A., & Mullenders, L. H. F. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.06.029 · Cited by 387 · see citing works
RetractedTOM40 Mediates Mitochondrial Dysfunction Induced by α-Synuclein Accumulation in Parkinson’s Disease
Bender, A., Desplats, P., Spencer, B. J., Rockenstein, E. M., Adame, A., Elstner, M., Laub, C., Mueller, S. K., Koob, A. O., Mante, M., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062277 · Cited by 150 · see citing works
RetractedOkano, M., Bell, D. W., Haber, D. A., & Li, E. (1999) · Cell · doi:10.1016/s0092-8674(00)81656-6 · Cited by 6,143 · see citing works
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139
Rogakou, E. P., Pilch, D. R., Orr, A. H., Ivanova, V. S., & Bonner, W. M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.10.5858 · Cited by 5,438 · see citing works
Genome maintenance mechanisms for preventing cancer
Hoeijmakers, J. H. J. (2001) · Nature · doi:10.1038/35077232 · Cited by 3,939 · see citing works
Mammalian microRNAs predominantly act to decrease target mRNA levels
Guo, H., Ingolia, N. T., Weissman, J. S., & Bartel, D. P. (2010) · Nature · doi:10.1038/nature09267 · Cited by 3,886 · see citing works
A microRNA component of the p53 tumour suppressor network
He, L., He, X., Lim, L. P., de Stanchina, E., Xuan, Z., Liang, Y., Xue, W., Zender, L., Magnus, J., Ridzon, D., et al. (2007) · Nature · doi:10.1038/nature05939 · Cited by 2,692 · see citing works
ATM and related protein kinases: safeguarding genome integrity
Shiloh, Y. (2003) · Nature Reviews Cancer · doi:10.1038/nrc1011 · Cited by 2,577 · see citing works
Understanding the odd science of aging
Kirkwood, T. B. L. (2005) · Cell · doi:10.1016/j.cell.2005.01.027 · Cited by 1,984 · see citing works
MicroRNA profiling: approaches and considerations
Pritchard, C. C., Cheng, H. H., & Tewari, M. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3198 · Cited by 1,765 · see citing works
The DNA Damage Response: Ten Years After
Harper, J. W., & Elledge, S. J. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.11.015 · Cited by 1,705 · see citing works
HDAC2 negatively regulates memory formation and synaptic plasticity
Guan, J.-S., Haggarty, S. J., Giacometti, E., Dannenberg, J.-H., Joseph, N., Gao, J., Nieland, T. J. F., Zhou, Y., Wang, X., Mazitschek, R., et al. (2009) · Nature · doi:10.1038/nature07925 · Cited by 1,644 · see citing works
Genomic Instability and Aging-like Phenotype in the Absence of Mammalian SIRT6
Mostoslavsky, R., Chua, K. F., Lombard, D. B., Pang, W. W., Fischer, M. R., Gellon, L., Liu, P., Mostoslavsky, G., Franco, S., Murphy, M. M., et al. (2006) · Cell · doi:10.1016/j.cell.2005.11.044 · Cited by 1,637 · see citing works
miR-34a repression of SIRT1 regulates apoptosis
Yamakuchi, M., Ferlito, M., & Lowenstein, C. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801613105 · Cited by 1,344 · see citing works
Neural mechanisms of ageing and cognitive decline
Bishop, N. A., Lu, T., & Yankner, B. A. (2010) · Nature · doi:10.1038/nature08983 · Cited by 1,323 · see citing works
Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage
Falck, J., Coates, J., & Jackson, S. P. (2005) · Nature · doi:10.1038/nature03442 · Cited by 1,248 · see citing works
Recovery of learning and memory is associated with chromatin remodelling
Fischer, A., Sananbenesi, F., Wang, X., Dobbin, M., & Tsai, L.-H. (2007) · Nature · doi:10.1038/nature05772 · Cited by 1,227 · see citing works
Xu, G., Bestor, T. H., Bourc’his, D., Hsieh, C., Tommerup, N., Bugge, M., Hultén, M. A., Qu, X., Russo, J. J., & Viégas-Pèquignot, E. (1999) · Nature · doi:10.1038/46052 · Cited by 1,204 · see citing works
Living on a break: cellular senescence as a DNA-damage response
d'Adda di Fagagna, F. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2440 · Cited by 1,170 · see citing works
Oxidative damage to mitochondrial DNA is increased in Alzheimer’s disease
Mecocci, P., MacGarvey, U., & Beal, M. F. (1994) · Annals of Neurology · doi:10.1002/ana.410360510 · Cited by 1,037 · see citing works
Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaks
Celeste, A., Fernandez-Capetillo, O., Kruhlak, M. J., Pilch, D. R., Staudt, D. W., Lee, A., Bonner, R. F., Bonner, W. M., & Nussenzweig, A. (2003) · Nature Cell Biology · doi:10.1038/ncb1004 · Cited by 989 · see citing works
Botuyan, M. V., Lee, J., Ward, I. M., Kim, J., Thompson, J. R., Chen, J., & Mer, G. (2006) · Cell · doi:10.1016/j.cell.2006.10.043 · Cited by 973 · see citing works
DNA hypomethylation leads to elevated mutation rates
Chen, R. Z., Pettersson, U., Beard, C., Jackson‐Grusby, L., & Jaenisch, R. (1998) · Nature · doi:10.1038/25779 · Cited by 950 · see citing works
Cogswell, J. P., Ward, J., Taylor, I. A., Waters, M., Shi, Y., Cannon, B., Kelnar, K., Kemppainen, J., Brown, D., Chen, C., et al. (2008) · Journal of Alzheimer s Disease · doi:10.3233/jad-2008-14103 · Cited by 943 · see citing works
DNA methylation and healthy human aging
Jones, M. J., Goodman, S. J., & Kobor, M. S. (2015) · Aging Cell · doi:10.1111/acel.12349 · Cited by 937 · see citing works
Senescence and apoptosis: dueling or complementary cell fates?
Childs, B. G., Baker, D. J., Kirkland, J. L., Campisi, J., & van Deursen, J. M. (2014) · The EMBO Reports · doi:10.15252/embr.201439245 · Cited by 915 · see citing works
Tazawa, H., Tsuchiya, N., Izumiya, M., & Nakagama, H. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707351104 · Cited by 902 · see citing works
Methylated lysine 79 of histone H3 targets 53BP1 to DNA double-strand breaks
Huyen, Y., Zgheib, O., DiTullio Jr, R. A., Gorgoulis, V. G., Zacharatos, P., Petty, T. J., Sheston, E. A., Mellert, H. S., Stavridi, E. S., & Halazonetis, T. D. (2004) · Nature · doi:10.1038/nature03114 · Cited by 884 · see citing works
SIRT6 Promotes DNA Repair Under Stress by Activating PARP1
Mao, Z., Hine, C., Tian, X., Van Meter, M., Au, M., Vaidya, A., Seluanov, A., & Gorbunova, V. (2011) · Science · doi:10.1126/science.1202723 · Cited by 867 · see citing works
Telomerase reactivation reverses tissue degeneration in aged telomerase-deficient mice
Jaskelioff, M., Muller, F. L., Paik, J.-H., Thomas, E., Jiang, S., Adams, A. C., Sahin, E., Kost-Alimova, M., Protopopov, A., Cadiñanos, J., et al. (2011) · Nature · doi:10.1038/nature09603 · Cited by 857 · see citing works
An epigenetic blockade of cognitive functions in the neurodegenerating brain
Gräff, J., Rei, D., Guan, J.-S., Wang, W.-Y., Seo, J., Hennig, K. M., Nieland, T. J. F., Fass, D. M., Kao, P. F., Kahn, M., et al. (2012) · Nature · doi:10.1038/nature10849 · Cited by 853 · see citing works
SIRT1 redistribution on chromatin promotes genomic stability but alters gene expression during aging
Oberdoerffer, P., Michan, S., McVay, M., Mostoslavsky, R., Vann, J., Park, S.-K., Hartlerode, A., Stegmuller, J., Hafner, A., Loerch, P., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.025 · Cited by 852 · see citing works
Wang, W., Rajeev, B. W., Stromberg, A. J., Ren, N., Tang, G., Huang, Q., Rigoutsos, I., & Nelson, P. T. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5065-07.2008 · Cited by 827 · see citing works
DNA damage checkpoints: from initiation to recovery or adaptation
Bartek, J., & Lukas, J. (2007) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2007.02.009 · Cited by 784 · see citing works
Impaired DNA Damage Response, Genome Instability, and Tumorigenesis in SIRT1 Mutant Mice
Wang, R.-H., Sengupta, K., Li, C., Kim, H., Cao, L., Xiao, C., Kim, S., Xu, X., Yin, Z., Chilton, B. S., et al. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.09.001 · Cited by 769 · see citing works
Kong, X., Wang, R., Xue, Y., Liu, X., Zhang, H., Chen, Y., Fang, F., & Chang, Y. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011707 · Cited by 718 · see citing works
Defective Mitophagy in XPA via PARP-1 Hyperactivation and NAD+/SIRT1 Reduction
Fang, E. F., Scheibye-Knudsen, M., Brace, L. E., Kassahun, H., SenGupta, T., Nilsen, H., Mitchell, J. R., Croteau, D. L., & Bohr, V. A. (2014) · Cell · doi:10.1016/j.cell.2014.03.026 · Cited by 711 · see citing works
A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis
Gao, Y., Sun, Y., Frank, K. M., Dikkes, P., Fujiwara, Y., Seidl, K. J., Sekiguchi, J. M., Rathbun, G. A., Swat, W., Wang, J., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)81714-6 · Cited by 688 · see citing works
Micro-RNA speciation in fetal, adult and Alzheimer's disease hippocampus
Lukiw, W. J. (2007) · Neuroreport · doi:10.1097/wnr.0b013e3280148e8b · Cited by 662 · see citing works
MicroRNA-125b is a novel negative regulator of p53Preprint
Le, M. T. N., Teh, C., Shyh‐Chang, N., Xie, H., Zhou, B., Korzh, V. P., Lodish, H. F., & Lim, B. (2009) · Genes & Development · doi:10.1101/gad.1767609 · Cited by 655 · see citing works
DNA damage-induced G2–M checkpoint activation by histone H2AX and 53BP1
Fernández-Capetillo, Ó., Chen, H. T., Celeste, A., Ward, I. M., Romanienko, P. J., Morales, J. C., Naka, K., Xia, Z., Camerini‐Otero, R. D., Motoyama, N., et al. (2002) · Nature Cell Biology · doi:10.1038/ncb884 · Cited by 644 · see citing works
Molecular Mechanisms of Mammalian Global Genome Nucleotide Excision Repair
Gillet, L. C. J., & Schärer, O. D. (2006) · Chemical Reviews · doi:10.1021/cr040483f · Cited by 642 · see citing works
miR-29 miRNAs activate p53 by targeting p85α and CDC42
Park, S. Y., Lee, J. H., Ha, M., Nam, J., & Kim, V. N. (2008) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1533 · Cited by 608 · see citing works
DNA Replication Precedes Neuronal Cell Death in Alzheimer's Disease
Yang, Y., Geldmacher, D., & Herrup, K. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02661.2001 · Cited by 607 · see citing works
Self-citationMeiotic recombination in mammals: localization and regulation
Baudat, F., Imai, Y., & de Massy, B. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3573 · Cited by 590 · see citing works
Mosaic Copy Number Variation in Human Neurons
McConnell, M. J., Lindberg, M. R., Brennand, K. J., Piper, J. C., Voet, T., Cowing-Zitron, C., Shumilina, S., Lasken, R. S., Vermeesch, J. R., Hall, I. M., et al. (2013) · Science · doi:10.1126/science.1243472 · Cited by 551 · see citing works
Methylation of Histone H4 Lysine 20 Controls Recruitment of Crb2 to Sites of DNA Damage
Sanders, S. L., Portoso, M., Mata, J., Bähler, J., Allshire, R. C., & Kouzarides, T. (2004) · Cell · doi:10.1016/j.cell.2004.11.009 · Cited by 545 · see citing works
Initiating Cellular Stress Responses
Bakkenist, C. J., & Kastan, M. B. (2004) · Cell · doi:10.1016/j.cell.2004.06.023 · Cited by 544 · see citing works
Ectopic Cell Cycle Proteins Predict the Sites of Neuronal Cell Death in Alzheimer’s Disease Brain
Busser, J., Geldmacher, D. S., & Herrup, K. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-08-02801.1998 · Cited by 543 · see citing works
Self-citationOxidative DNA damage in mild cognitive impairment and late-stage Alzheimer's disease
Lovell, M. A., & Markesbery, W. R. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm821 · Cited by 515 · see citing works
Huse, J. T., Brennan, C., Hambardzumyan, D., Wee, B., Pena, J., Rouhanifard, S. H., Sohn-Lee, C., le Sage, C., Agami, R., Tuschl, T., et al. (2009) · Genes & Development · doi:10.1101/gad.1777409 · Cited by 511 · see citing works
Guarente, L. (2011) · New England Journal of Medicine · doi:10.1056/nejmra1100831 · Cited by 510 · see citing works
Cell cycle regulation in the postmitotic neuron: oxymoron or new biology?
Herrup, K., & Yang, Y. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2124 · Cited by 507 · see citing works
Self-citationTudor, MBT and chromo domains gauge the degree of lysine methylation
Kim, J., Daniel, J. A., Espejo, A. B., Lake, A., Krishna, M., Li, X., Zhang, Y., & Bedford, M. T. (2006) · EMBO Reports · doi:10.1038/sj.embor.7400625 · Cited by 493 · see citing works
Frank, K. M., Sharpless, N. E., Gao, Y., Sekiguchi, J., Ferguson, D. O., Zhu, C., Manis, J. P., Horner, J. W., DePinho, R. A., & Alt, F. W. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)80264-6 · Cited by 492 · see citing works
Suberbielle, E., Sanchez, P. E., Kravitz, A. V., Wang, X., Ho, K., Eilertson, K., Devidze, N., Kreitzer, A. C., & Mucke, L. (2013) · Nature Neuroscience · doi:10.1038/nn.3356 · Cited by 487 · see citing works
Neuronal cell death is preceded by cell cycle events at all stages of Alzheimer’s disease
Yang, Y., Mufson, E. J., & Herrup, K. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-07-02557.2003 · Cited by 483 · see citing works
Self-citationp53-Responsive MicroRNAs 192 and 215 Are Capable of Inducing Cell Cycle Arrest
Braun, C. J., Zhang, X., Savelyeva, I., Wolff, S., Moll, U. M., Schepeler, T., Orntoft, T. F., Andersen, C. L., & Dobbelstein, M. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-1569 · Cited by 467 · see citing works
Epigenetic mechanisms in neurological disease
Jakovcevski, M., & Akbarian, S. (2012) · Nature Medicine · doi:10.1038/nm.2828 · Cited by 450 · see citing works
miR-182-Mediated Downregulation of BRCA1 Impacts DNA Repair and Sensitivity to PARP Inhibitors
Moskwa, P., Buffa, F. M., Pan, Y., Panchakshari, R. A., Gottipati, P., Muschel, R. J., Beech, J. S., Kulshrestha, R., Abdelmohsen, K., Weinstock, D. M., et al. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.12.005 · Cited by 428 · see citing works
Chouliaras, L., Mastroeni, D., Delvaux, E., Grover, A., Kenis, G., Hof, P. R., Steinbusch, H. W. M., Coleman, P. D., Rutten, B. P. F., & van den Hove, D. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.02.021 · Cited by 422 · see citing works
SIRT6 recruits SNF2H to DNA break sites, preventing genomic instability through chromatin remodeling
Toiber, D., Erdel, F., Bouazoune, K., Silberman, D. M., Zhong, L., Mulligan, P., Sebastian, C., Cosentino, C., Martinez-Pastor, B., Giacosa, S., et al. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.06.018 · Cited by 381 · see citing works
Tet family proteins and 5-hydroxymethylcytosine in development and disease
Tan, L., & Shi, Y. G. (2012) · Development · doi:10.1242/dev.070771 · Cited by 377 · see citing works
Alterations in mitochondrial membrane fluidity by lipid peroxidation products
Chen, J. J., & Yu, B. P. (1994) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(94)90167-8 · Cited by 369 · see citing works
Cell Cycle Activation Linked to Neuronal Cell Death Initiated by DNA Damage
Kruman, I. I., Wersto, R. P., Cardozo‐Pelaez, F., Smilenov, L. B., Chan, S. L., Chrest, F. J., Emokpae, R., Gorospe, M., & Mattson, M. P. (2004) · Neuron · doi:10.1016/s0896-6273(04)00017-0 · Cited by 365 · see citing works
McKinnon, P. J. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400210 · Cited by 365 · see citing works
SIRT1 promotes DNA repair activity and deacetylation of Ku70
Jeong, J., Juhn, K., Lee, H., Kim, S. H., Min, B.-H., Lee, K., Cho, M., Park, G. H., & Lee, K.-H. (2007) · Experimental & Molecular Medicine · doi:10.1038/emm.2007.2 · Cited by 356 · see citing works
Ionizing Radiation-Induced Oxidative Stress Alters miRNA Expression
Simone, N. L., Soule, B. P., Ly, D., Saleh, A. D., Savage, J. E., DeGraff, W., Cook, J. A., Harris, C. C., Gius, D. R., & Mitchell, J. B. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006377 · Cited by 329 · see citing works
Chromosomal variation in neurons of the developing and adult mammalian nervous system
Rehen, S. K., McConnell, M. J., Kaushal, D., Kingsbury, M. A., Yang, A. H., & Chun, J. J. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.231487398 · Cited by 328 · see citing works
Robin, J. D., Ludlow, A. T., Batten, K. G., Magdinier, F., Stadler, G., Wagner, K. R., Shay, J. W., & Wright, W. E. (2014) · Genes & Development · doi:10.1101/gad.251041.114 · Cited by 327 · see citing works
DNA repair deficiency and neurological disease
McKinnon, P. J. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2559 · Cited by 323 · see citing works
Constitutional Aneuploidy in the Normal Human Brain
Rehen, S. K., Yung, Y. C., McCreight, M. P., Kaushal, D., Yang, A. H., Almeida, B. S. V., Kingsbury, M. A., Cabral, K. M. D. S., McConnell, M. J., Anliker, B., et al. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4560-04.2005 · Cited by 320 · see citing works
Shioya, M., Obayashi, S., Tabunoki, H., Arima, K., Saito, Y., Ishida, T., & Satoh, J. (2010) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2010.01076.x · Cited by 301 · see citing works
Repression of the miR‐17‐92 cluster by p53 has an important function in hypoxia‐induced apoptosis
Yan, H., Xue, G., Mei, Q., Wang, Y.-Z., Ding, F., Liu, M., Lü, M., Tang, Y., Yu, H., & Sun, S. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.214 · Cited by 299 · see citing works
Yuan, S., Ryder, J. W., Li, B., Wu, X., Fox, N. W., Solenberg, P., Brune, K. A., Paul, S. M., Zhou, Y., Liu, F., et al. (2004) · Biochemistry · doi:10.1021/bi035627j · Cited by 295 · see citing works
Chun, J. J. M., Schatz, D. G., Oettinger, M. A., Jaenisch, R., & Baltimore, D. (1991) · Cell · doi:10.1016/0092-8674(91)90220-s · Cited by 285 · see citing works
Lal, A., Pan, Y., Navarro, F., Dykxhoorn, D. M., Moreau, L. A., Meire, E., Bentwich, Z., Lieberman, J., & Chowdhury, D. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1589 · Cited by 285 · see citing works
Divide and Die: Cell Cycle Events as Triggers of Nerve Cell Death
Herrup, K., Neve, R. L., Ackerman, S. L., & Copani, A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3347-04.2004 · Cited by 285 · see citing works
Self-citationFunctional links between telomeres and proteins of the DNA-damage response
d'Adda di Fagagna, F., Teo, S.-H., & Jackson, S. P. (2004) · Genes & Development · doi:10.1101/gad.1214504 · Cited by 277 · see citing works
The pRb/E2F cell-cycle pathway mediates cell death in Parkinson's disease
Höglinger, G. U., Breunig, J. J., Depboylu, C., Rouaux, C., Michel, P. P., Alvarez-Fischer, D., Boutillier, A.-L., DeGregori, J., Oertel, W. H., Rakic, P., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611671104 · Cited by 276 · see citing works
The sirtuins, oxidative stress and aging: an emerging link
Merksamer, P. I., Liu, Y., He, W., Hirschey, M. D., Chen, D., & Verdin, E. (2013) · Aging · doi:10.18632/aging.100544 · Cited by 275 · see citing works
Wang, X., Liu, P., Zhu, H., Xu, Y., Ma, C., Dai, X., Huang, L., Liu, Y., Zhang, L., & Qin, C. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.08.006 · Cited by 271 · see citing works
Aneuploidy and DNA Replication in the Normal Human Brain and Alzheimer's Disease
Mosch, B., Morawski, M., Mittag, A., Lenz, D., Tárnok, A., & Arendt, T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0379-07.2007 · Cited by 271 · see citing works
SIRT1 Regulates the Function of the Nijmegen Breakage Syndrome Protein
Yuan, Z., Zhang, X. M., Sengupta, N., Lane, W. S., & Seto, E. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.05.029 · Cited by 271 · see citing works
Garcia, A. I., Buisson, M., Bertrand, P., Rimokh, R., Rouleau, É., López, B. S., Lidereau, R., Mikaélian, I., & Mazoyer, S. (2011) · EMBO Molecular Medicine · doi:10.1002/emmm.201100136 · Cited by 265 · see citing works
ATM is down-regulated by N-Myc–regulated microRNA-421
Hu, H., Du, L., Nagabayashi, G., Seeger, R. C., & Gatti, R. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907763107 · Cited by 261 · see citing works
Increased oxidative damage in nuclear and mitochondrial DNA in mild cognitive impairment
Wang, J., Markesbery, W. R., & Lovell, M. A. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03615.x · Cited by 260 · see citing works
Absalon, S., Kochanek, D. M., Raghavan, V., & Krichevsky, A. M. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1327-13.2013 · Cited by 259 · see citing works
Lajer, C. B., Garnæs, E., Friis-Hansen, L. J., Norrild, B., Therkildsen, M. H., Glud, M., Rossing, M., Lajer, H., Svane, D., Skotte, L., et al. (2012) · British Journal of Cancer · doi:10.1038/bjc.2012.109 · Cited by 255 · see citing works
Shimada, M., Niida, H., Zineldeen, D. H., Tagami, H., Tanaka, M., Saito, H., & Nakanishi, M. (2008) · Cell · doi:10.1016/j.cell.2007.12.013 · Cited by 255 · see citing works
SIRT1 collaborates with ATM and HDAC1 to maintain genomic stability in neurons
Dobbin, M. M., Madabhushi, R., Pan, L., Chen, Y., Kim, D., Gao, J., Ahanonu, B., Pao, P.-C., Qiu, Y., Zhao, Y., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3460 · Cited by 250 · see citing works
Oxidative damage in mild cognitive impairment and early Alzheimer's disease
Lovell, M. A., & Markesbery, W. R. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21346 · Cited by 245 · see citing works
Dual control of mitochondrial biogenesis by sirtuin 1 and sirtuin 3
Brenmoehl, J., & Hoeflich, A. (2013) · Mitochondrion · doi:10.1016/j.mito.2013.04.002 · Cited by 240 · see citing works
The ATM Kinase Induces MicroRNA Biogenesis in the DNA Damage Response
Zhang, X., Wan, G., Berger, F. G., He, X., & Lu, X. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.01.020 · Cited by 239 · see citing works
Maintaining genome stability in the nervous system
McKinnon, P. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3537 · Cited by 229 · see citing works
Katchanov, J., Harms, C., Gertz, K. R., Hauck, L., Waeber, C., Hirt, L., Priller, J., von Harsdorf, R., Brück, W., Hörtnagl, H., et al. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05045.2001 · Cited by 227 · see citing works
Characterization of ATM gene mutations in 66 ataxia telangiectasia families
Sandoval, N. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.1.69 · Cited by 226 · see citing works
Sirtuin deacetylases in neurodegenerative diseases of aging
Herskovits, A. Z., & Guarente, L. (2013) · Cell Research · doi:10.1038/cr.2013.70 · Cited by 222 · see citing works
Liu, C., Song, J., Zhang, Y., & Wang, P. (2014) · Molecular Medicine Reports · doi:10.3892/mmr.2014.2484 · Cited by 221 · see citing works
The induction of multiple cell cycle events precedes target-related neuronal death
Herrup, K., & Busser, J. C. (1995) · Development · doi:10.1242/dev.121.8.2385 · Cited by 220 · see citing works
Self-citationNuclear accumulation of HDAC4 in ATM deficiency promotes neurodegeneration in ataxia telangiectasia
Li, J., Chen, J., Ricupero, C. L., Hart, R. P., Schwartz, M. S., Kusnecov, A., & Herrup, K. (2012) · Nature Medicine · doi:10.1038/nm.2709 · Cited by 210 · see citing works
Self-citationIn vivo regulation of amyloid precursor protein neuronal splicing by microRNAs
Smith, P. Y., Hashimi, A. A., Girard, J., Delay, C., & Hébert, S. S. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07097.x · Cited by 209 · see citing works
Iourov, I. Y., Vorsanova, S. G., Liehr, T., & Yurov, Y. B. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.01.003 · Cited by 209 · see citing works
Gu, Y., Sekiguchi, J., Gao, Y., Dikkes, P., Frank, K. M., Ferguson, D. O., Hasty, P., Chun, J. J. M., & Alt, F. W. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.6.2668 · Cited by 198 · see citing works
Nouspikel, T. P., & Hanawalt, P. C. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.5.1562-1570.2000 · Cited by 194 · see citing works
Targeted proteomics for quantification of histone acetylation in A lzheimer's disease
Zhang, K., Schrag, M., Crofton, A. R., Trivedi, R. K., Vinters, H. V., & Kirsch, W. M. (2012) · PROTEOMICS · doi:10.1002/pmic.201200010 · Cited by 191 · see citing works
MicroRNAs and neurodegeneration: role and impact
Abe, M., & Bonini, N. M. (2013) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.08.013 · Cited by 190 · see citing works
Liu, W., Chang, L., Zhu, J.-X., Shu, P., Yin, B., Gong, Y., Qiang, B., Yuan, J., & Peng, X. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.04.034 · Cited by 188 · see citing works
Selective Cell Death of Hyperploid Neurons in Alzheimer’s Disease
Arendt, T., Brückner, M. K., Mosch, B., & Lösche, A. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.090955 · Cited by 187 · see citing works
Opresko, P. L. (2003) · Carcinogenesis · doi:10.1093/carcin/bgg034 · Cited by 187 · see citing works
Park, J. K., Henry, J. C., Jiang, J., Esau, C., Gusev, Y., Lerner, M. R., Postier, R. G., Brackett, D. J., & Schmittgen, T. D. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.02.065 · Cited by 178 · see citing works
EZH2-mediated H3K27 trimethylation mediates neurodegeneration in ataxia-telangiectasia
Li, J., Hart, R. P., Mallimo, E. M., Swerdel, M. R., Kusnecov, A. W., & Herrup, K. (2013) · Nature Neuroscience · doi:10.1038/nn.3564 · Cited by 177 · see citing works
Self-citationShorter telomeres are associated with mortality in those withAPOEϵ4 and dementia
Honig, L. S., Schupf, N., Lee, J. H., Tang, M. X., & Mayeux, R. P. (2006) · Annals of Neurology · doi:10.1002/ana.20894 · Cited by 177 · see citing works
Ectopic localization of phosphorylated histone H3 in Alzheimer's disease: a mitotic catastrophe?
Ogawa, O., Zhu, X., Lee, H., Raina, A. K., Obrenovich, M. E., Bowser, R. P., Ghanbari, H. A., Castellani, R. J., Perry, G. L., & Smith, M. A. (2003) · Acta Neuropathologica · doi:10.1007/s00401-003-0684-3 · Cited by 175 · see citing works
Aneuploid neurons are functionally active and integrated into brain circuitry
Kingsbury, M. A., Friedman, B., McConnell, M. J., Rehen, S. K., Yang, A. H., Kaushal, D., & Chun, J. J. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408171102 · Cited by 175 · see citing works
miR-9 Regulation of BRCA1 and Ovarian Cancer Sensitivity to Cisplatin and PARP Inhibition
Sun, C., Li, N., Yang, Z., Zhou, B., He, Y., Weng, D., Fang, Y., Wu, P., Chen, P., Yang, X., et al. (2013) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djt302 · Cited by 171 · see citing works
Smith, J. A., Park, S., Krause, J. S., & Banik, N. L. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.02.013 · Cited by 167 · see citing works
ATM function and telomere stability
Pandita, T. K. (2002) · Oncogene · doi:10.1038/sj.onc.1205060 · Cited by 164 · see citing works
Alterations in G1 to S Phase Cell-Cycle Regulators during Amyotrophic Lateral Sclerosis
Ranganathan, S., & Bowser, R. P. (2003) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63879-5 · Cited by 160 · see citing works
Cell division in the CNS: Protective response or lethal event in post-mitotic neurons?
Yang, Y., & Herrup, K. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2006.10.002 · Cited by 156 · see citing works
Self-citationLin, F., Li, R., Pan, Z. X., Zhou, B., Yu, D. B., Wang, X. G., Ma, X. S., Han, J., Shen, M., & Liu, H. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038640 · Cited by 155 · see citing works
Wan, G., Mathur, R., Hu, X., Zhang, X., & Lu, X. (2011) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2011.06.002 · Cited by 153 · see citing works
Transcriptional silencing at Saccharomyces telomeres: implications for other organisms
Tham, W., & Zakian, V. A. (2002) · Oncogene · doi:10.1038/sj.onc.1205078 · Cited by 150 · see citing works
DNA Damage and Repair in Alzheimers Disease
Coppede, F., & Migliore, L. (2009) · Current Alzheimer Research · doi:10.2174/156720509787313970 · Cited by 148 · see citing works
Katyal, S., Lee, Y., Nitiss, K. C., Downing, S. M., Li, Y., Shimada, M., Zhao, J., Russell, H. R., Petrini, J. H. J., Nitiss, J. L., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3715 · Cited by 148 · see citing works
Potter, H. (1991) · Europe PMC (PubMed Central) · Cited by 147 · see citing works
Yurov, Y. B., Iourov, I. Y., Monakhov, V. V., Soloviev, I. V., Vm, V., & Vorsanova, S. G. (2005) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.4a6430.2005 · Cited by 144 · see citing works
Du, L.-L., Nakamura, T., & Russell, P. R. (2006) · Genes & Development · doi:10.1101/gad.1422606 · Cited by 141 · see citing works
Enhanced DNA Repair Synthesis in Hyperacetylated Nucleosomes
Ramanathan, B., & Smerdon, M. J. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)60422-3 · Cited by 138 · see citing works
Dyskeratosis congenita as a disorder of telomere maintenance
Nelson, N. D., & Bertuch, A. A. (2011) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2011.06.008 · Cited by 138 · see citing works
DNA polymerase β deficiency leads to neurodegeneration and exacerbates Alzheimer disease phenotypes
Sýkora, P., Misiak, M., Wang, Y., Ghosh, S., Leandro, G. D. S., Liu, D., Tian, J. Y., Baptiste, B. A., Cong, W., Brenerman, B. M., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1356 · Cited by 136 · see citing works
Increased acetyl and total histone levels in post-mortem Alzheimer's disease brain
Narayan, P. J., Lill, C. L., Faull, R. L. M., Curtis, M. A., & Dragunow, M. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.11.023 · Cited by 133 · see citing works
Distinct Patterns of Sirtuin Expression During Progression of Alzheimer’s Disease
Lutz, M. I., Milenković, I., Regelsberger, G., & Kovács, G. G. (2014) · NeuroMolecular Medicine · doi:10.1007/s12017-014-8288-8 · Cited by 131 · see citing works
Human interphase chromosomes: a review of available molecular cytogenetic technologies
Vorsanova, S. G., Yurov, Y. B., & Iourov, I. Y. (2010) · Molecular Cytogenetics · doi:10.1186/1755-8166-3-1 · Cited by 131 · see citing works
Loss of Neuronal Cell Cycle Control in Ataxia-Telangiectasia: A Unified Disease Mechanism
Yang, Y. F., & Herrup, K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4946-04.2005 · Cited by 130 · see citing works
Self-citationWei, Y., Qu, M.-H., Wang, X.-S., Chen, L., Wang, D.-L., Liu, Y., Hua, Q., & He, R.-Q. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002600 · Cited by 129 · see citing works
Gu, X., Sun, J., Li, S., Wu, X., & Li, L. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.10.013 · Cited by 127 · see citing works
Accelerated Age-Related Cognitive Decline and Neurodegeneration, Caused by Deficient DNA Repair
Borgesius, N. Z., de Waard, M. C., van der Pluijm, I., Omrani, A., Zondag, G. C. M., van der Horst, G. T. J., Melton, D. W., Hoeijmakers, J. H. J., Jaarsma, D., & Elgersma, Y. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1589-11.2011 · Cited by 126 · see citing works
Iourov, I. Y., Vorsanova, S. G., Liehr, T., Kolotii, A. D., & Yurov, Y. B. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp207 · Cited by 125 · see citing works
Chromatin structure and DNA damage repair
Dinant, C., Houtsmuller, A. B., & Vermeulen, W. (2008) · Epigenetics & Chromatin · doi:10.1186/1756-8935-1-9 · Cited by 122 · see citing works
DNA end joining activity is reduced in Alzheimer's disease
Shackelford, D. A. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.03.009 · Cited by 120 · see citing works
Zhang, Y., Zhou, J., & Lim, C. U. (2006) · Cell Research · doi:10.1038/sj.cr.7310007 · Cited by 118 · see citing works
Alteration of Gene Expression by Chromosome Loss in the Postnatal Mouse Brain
Kaushal, D., Contos, J. J. A., Treuner, K., Yang, A. H., Kingsbury, M. A., Rehen, S. K., McConnell, M. J., Okabe, M., Barlow, C., & Chun, J. J. M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05599.2003 · Cited by 116 · see citing works
CNS SIRT3 Expression Is Altered by Reactive Oxygen Species and in Alzheimer’s Disease
Weir, H. J. M., Murray, T. K., Kehoe, P. G., Love, S., Verdin, E. M., O’Neill, M. J., Lane, J. D., & Balthasar, N. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048225 · Cited by 115 · see citing works
Chromosome 17 and 21 aneuploidy in buccal cells is increased with ageing and in Alzheimer's disease
Thomas, P., & Fenech, M. F. (2007) · Mutagenesis · doi:10.1093/mutage/gem044 · Cited by 107 · see citing works
To die or grow: Parkinson's disease and cancer
WEST, A., DAWSON, V, & DAWSON, T. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.05.002 · Cited by 106 · see citing works
Chromosome-specific accumulation of aneuploidy in the aging mouse brain
Faggioli, F., Wang, T., Vijg, J., & Montagna, C. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds375 · Cited by 106 · see citing works
Neuronal DNA content variation (DCV) with regional and individual differences in the human brain
Westra, J. W., Rivera, R. R., Bushman, D. M., Yung, Y. C., Peterson, S. E., Barral, S., & Chun, J. J. M. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22436 · Cited by 105 · see citing works
Changes of telomere length with aging
Takubo, K., Aida, J., Izumiyama‐Shimomura, N., Ishikawa, N., Sawabe, M., Kurabayashi, R., Shiraishi, H., Arai, T., & Nakamura, K. (2010) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/j.1447-0594.2010.00605.x · Cited by 103 · see citing works
Zhu, F., Liu, J., Li, J.-P., Xiao, F., Zhang, Z., & Zhang, L. (2013) · Journal of Molecular Neuroscience · doi:10.1007/s12031-013-0155-9 · Cited by 102 · see citing works
Deficiency of the Mre11 DNA repair complex in Alzheimer's disease brains
Jacobsen, E. A., Beach, T. G., Shen, Y., Li, R., & Chang, Y. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.05.023 · Cited by 102 · see citing works
Controlling DNA-end resection: a new task for CDKs
Ferretti, L. P., Lafranchi, L., & Sartori, A. A. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00099 · Cited by 99 · see citing works
Robbins, J. H. (1988) · JAMA · doi:10.1001/jama.1988.03410030100038 · Cited by 99 · see citing works
Cell Cycle Activation in Postmitotic Neurons is Essential for DNA Repair
Schwartz, E. I., Smilenov, L. B., Price, M. A., Osredkar, T., Baker, R. A., Ghosh, S., Shi, F., Vollmer, T. L., Lencinas, A., Stearns, D. M., et al. (2007) · Cell Cycle · doi:10.4161/cc.6.3.3752 · Cited by 96 · see citing works
Krylova, S. M., Musheev, M., Nutiu, R., Li, Y., Lee, G., & Krylov, S. N. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.01.032 · Cited by 96 · see citing works
Changes in nuclear protein acetylation in u.v.-damaged human cells
Ramanathan, B., & Smerdon, M. J. (1986) · Carcinogenesis · doi:10.1093/carcin/7.7.1087 · Cited by 94 · see citing works
Systematic Screen Identifies miRNAs That Target RAD51 and RAD51D to Enhance Chemosensitivity
Huang, J., Wang, Y., Dhillon, K. K., Calses, P. C., Villegas, E., Mitchell, P. S., Tewari, M., Kemp, C. J., & Taniguchi, T. (2013) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-13-0292 · Cited by 93 · see citing works
Xeroderma pigmentosum. Defective DNA repair causes skin cancer and neurodegeneration
Robbins, J. H. (1988) · JAMA · doi:10.1001/jama.260.3.384 · Cited by 92 · see citing works
Role of SIRT1 in homologous recombination
Uhl, M., Csernok, A., DİLSİZ, S. A., Kreienberg, R., Wiesmüller, L., & Gatz, S. A. (2010) · DNA repair · doi:10.1016/j.dnarep.2009.12.020 · Cited by 90 · see citing works
Nestin-CreER Mice Reveal DNA Synthesis by Nonapoptotic Neurons following Cerebral Ischemia–Hypoxia
Burns, K. A., Ayoub, A. E., Breunig, J. J., Adhami, F., Weng, W.-L., Colbert, M. C., RAKIC, P. T., & Kuan, C.-Y. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl164 · Cited by 87 · see citing works
Dynamics of DNA Methylation in Aging and Alzheimer's Disease
Irier, H. A., & Jin, P. (2012) · DNA and Cell Biology · doi:10.1089/dna.2011.1565 · Cited by 84 · see citing works
Yu, Y., Wang, Y., Ren, X., Tsuyada, A., Li, A., Liu, L. J., & Wang, S. E. (2010) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-10-0362 · Cited by 84 · see citing works
The Logic Linking Protein Acetylation and Metabolism
Guarente, L. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.07.007 · Cited by 79 · see citing works
Adlakha, Y. K., & Saini, N. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.46 · Cited by 78 · see citing works
Characterisation of the sites of DNA damage-induced 53BP1 phosphorylation catalysed by ATM and ATR
Jowsey, P. A., Morrice, N. A., Hastie, C. J., McLauchlan, H., Toth, R. L., & Rouse, J. W. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.04.011 · Cited by 78 · see citing works
Wang, S., Zhao, X., Chen, W., Bo, N., WANG, X.-J., Zhao-fu, C., & WU, W. (2014) · Molecular Medicine Reports · doi:10.3892/mmr.2014.2724 · Cited by 77 · see citing works
Liu, R.-L., Dong, Y., Deng, Y.-Z., Wang, W., & Li, W. (2015) · Tumor Biology · doi:10.1007/s13277-015-3152-5 · Cited by 77 · see citing works
Ranganathan, S., Scudiere, S. C., & Bowser, R. P. (2001) · Journal of Alzheimer s Disease · doi:10.3233/jad-2001-3403 · Cited by 76 · see citing works
DNA Damage and Base Excision Repair in Mitochondria and Their Role in Aging
Gredilla, R. (2010) · Journal of Aging Research · doi:10.4061/2011/257093 · Cited by 75 · see citing works
Regulation of the DNA Damage Response by Cyclin-Dependent Kinases
Trovesi, C., Manfrini, N., Falcettoni, M., & Longhese, M. P. (2013) · Journal of Molecular Biology · doi:10.1016/j.jmb.2013.04.013 · Cited by 74 · see citing works
Cell Cycle Proteins Exhibit Altered Expression Patterns in Lentiviral-Associated Encephalitis
Jordan‐Sciutto, K. L., Wang, G., Murphey‐Corb, M., & Wiley, C. A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02185.2002 · Cited by 73 · see citing works
Neuronal expression of cell cycle-related proteins after brain ischaemia in man
Love, S. (2003) · Neuroscience Letters · doi:10.1016/j.neulet.2003.09.004 · Cited by 72 · see citing works
Morano, A., Angrisano, T., Russo, G., Landi, R., Pezone, A., Bartollino, S., Zuchegna, C., Babbio, F., Bonapace, I. M., Allen, B., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt920 · Cited by 72 · see citing works
McConnell, M. J., Kaushal, D., Yang, A. H., Kingsbury, M. A., Rehen, S. K., Treuner, K., Helton, R., Annas, E. G., Chun, J. J. M., & Barlow, C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2263-04.2004 · Cited by 69 · see citing works
The role of ATM and DNA damage in neurons: Upstream and downstream connections
Herrup, K., Li, J., & Chen, J. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.04.012 · Cited by 66 · see citing works
Self-citationHyperphosphorylation Results in Tau Dysfunction in DNA Folding and Protection
Lü, Y., He, H.-J., Zhou, J., Jun-Ye, M. I. A. O., Lü, J., He, Y.-G., Pan, R., Yan, W., Liu, Y. M., & He, R. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-130602 · Cited by 65 · see citing works
Pin, G., Lan, J., Ge, J., Nie, Q., Guo, L., Qiu, Y., & Mao, Q. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.10.020 · Cited by 63 · see citing works
Tomashevski, A., Webster, D. R., Grammas, P., Gorospe, M., & Kruman, I. I. (2010) · Cell Death and Differentiation · doi:10.1038/cdd.2009.221 · Cited by 57 · see citing works
Telomere Dysfunction of Lymphocytes in Patients With Alzheimer Disease
Zhang, J., Kong, Q., Zhang, Z., Ge, P., Ba, D., & He, W. (2003) · Cognitive and Behavioral Neurology · doi:10.1097/00146965-200309000-00004 · Cited by 56 · see citing works
Sublethal Doses of β-Amyloid Peptide Abrogate DNA-dependent Protein Kinase Activity
Cardinale, A., Racaniello, M., Saladini, S., Chiara, G. D., Mollinari, C., de Stefano, M. C., Pocchiari, M., Garaci, E., & Merlo, D. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.276550 · Cited by 54 · see citing works
Telomerase Deficiency Affects Normal Brain Functions in Mice
Lee, J., Jo, Y. S., Sung, Y. H., Hwang, I. K., Kim, H., Kim, S., Yi, S. S., Choi, J.-S., Sun, W., Seong, J. K., et al. (2009) · Neurochemical Research · doi:10.1007/s11064-009-0044-3 · Cited by 53 · see citing works
Chen, B., Duan, L., Yin, G., Tan, J., & Jiang, X. (2013) · Journal of Chemotherapy · doi:10.1179/1973947813y.0000000092 · Cited by 51 · see citing works
Neurobehavioral Changes Resulting from Recombinase Activation Gene 1 Deletion
Cushman, J. D., Lo, J., Huang, Z. L., Wasserfall, C. H., & Petitto, J. M. (2003) · Clinical and Vaccine Immunology · doi:10.1128/cdli.10.1.13-18.2003 · Cited by 51 · see citing works
microRNA-34a promotes DNA damage and mitotic catastrophe
Kofman, A. V., Kim, J., Park, S., Dupart, E., Letson, C. S., Bao, Y., Ding, K., Chen, Q., Schiff, D., Larner, J. M., et al. (2013) · Cell Cycle · doi:10.4161/cc.26459 · Cited by 50 · see citing works
Exceptional stories of microRNAs
Lee, H. (2013) · Experimental Biology and Medicine · doi:10.1258/ebm.2012.012251 · Cited by 47 · see citing works
SIRT6 Minor Allele Genotype Is Associated with >5-Year Decrease in Lifespan in an Aged Cohort
Tennapel, M. J., Lynch, C. F., Burns, T. L., Wallace, R. B., Smith, B. J., Button, A. M., & Domann, F. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0115616 · Cited by 46 · see citing works
Casafont, Í., Palanca, A., Lafarga, V., Berciano, M. T., & Lafarga, M. (2011) · Acta Neuropathologica · doi:10.1007/s00401-011-0869-0 · Cited by 42 · see citing works
Impaired social recognition memory in recombination activating gene 1-deficient mice
McGowan, P. O., Hope, T. A., Meck, W. H., Kelsoe, G. H., & Williams, C. L. (2011) · Brain Research · doi:10.1016/j.brainres.2011.02.054 · Cited by 42 · see citing works
The Effects of SIRT1 on Alzheimer's Disease Models
Dönmez, G. (2012) · International Journal of Alzheimer s Disease · doi:10.1155/2012/509529 · Cited by 38 · see citing works
The DNA-Damage Response to γ-Radiation Is Affected by miR-27a in A549 Cells
Francesco, A. D., Pittà, C. D., Moret, F., Barbieri, V., Celotti, L., & Mognato, M. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140917881 · Cited by 37 · see citing works
Stavenhagen, J. B., & Zakian, V. A. (1998) · Genes & Development · doi:10.1101/gad.12.19.3044 · Cited by 35 · see citing works
DNA-dependent protein kinase and DNA repair: relevance to Alzheimer's disease
Kanungo, J. (2013) · Alzheimer s Research & Therapy · doi:10.1186/alzrt167 · Cited by 35 · see citing works
Potential of chromatin modifying compounds for the treatment of Alzheimer's disease
Karagiannis, T. C., & Ververis, K. (2012) · Pathobiology of Aging & Age-related Diseases · doi:10.3402/pba.v2i0.14980 · Cited by 33 · see citing works
On Somatic Recombination in the Central Nervous System of Transgenic Mice
Abeliovich, A., Gerber, D., Tanaka, O., Katsuki, M., Graybiel, A. M., & Tonegawa, S. (1992) · Science · doi:10.1126/science.1631561 · Cited by 33 · see citing works
Colón-Cesario, M., Wang, J., Ramos, X., Garcia, H. G., Davila, J., Laguna, J., Rosado, C., & de Ortı́z, S. P. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3050-05.2006 · Cited by 32 · see citing works
DNA base excision repair activities in mouse models of Alzheimer's disease
Weissman, L., de Souza-Pinto, N. C., Mattson, M. P., & Bohr, V. A. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2008.02.014 · Cited by 31 · see citing works
Synaptic Proteome Changes in a DNA Repair Deficient Ercc1 Mouse Model of Accelerated Aging
Végh, M. J., de Waard, M. C., van der Pluijm, I., Ridwan, Y. R., Bergamin-Sassen, M. J. M., van Nierop, P., van der Schors, R. C., Li, K. W., Hoeijmakers, J. H. J., Smit, A. B., et al. (2012) · Journal of Proteome Research · doi:10.1021/pr201203m · Cited by 31 · see citing works
Toward an Early Diagnosis and Treatment of Alzheimer’s Disease
Nordberg, A. K. (2003) · International Psychogeriatrics · doi:10.1017/s1041610203009499 · Cited by 31 · see citing works
TLK1B promotes repair of UV-damaged DNA through chromatin remodeling by Asf1.
Sen, S., & Benedetti, A. D. (2006) · BMC Molecular Biology · doi:10.1186/1471-2199-7-37 · Cited by 28 · see citing works
MicroRNA regulation of DNA repair gene expression in 4-aminobiphenyl-treated HepG2 cells
Huan, L. C., Wu, J.-C., Chiou, B., Chen, C.-H., Ma, N. J.-L., Chang, C. Y., Tsen, Y.-K., & Chen, S. (2014) · Toxicology · doi:10.1016/j.tox.2014.05.003 · Cited by 25 · see citing works
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Ageing as a risk factor for neurodegenerative disease
Hou, Y., Dan, X., Babbar, M., Wei, Y., Hasselbalch, S. G., Croteau, D. L., & Bohr, V. A. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-019-0244-7 · Cited by 3,310 · see citing works
Hallmarks of Brain Aging: Adaptive and Pathological Modification by Metabolic States
Mattson, M. P., & Arumugam, T. V. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.05.011 · Cited by 1,242 · see citing works
Mitophagy and Alzheimer’s Disease: Cellular and Molecular Mechanisms
Kerr, J. S., Adriaanse, B. A., Greig, N. H., Mattson, M. P., Cader, M. Z., Bohr, V. A., & Fang, E. F. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.01.002 · Cited by 870 · see citing works
Age, APOE and sex: triad of risk of Alzheimer’s disease.
Riedel, B. C., Thompson, P. M., & Brinton, R. D. (2016) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2016.03.012 · Cited by 627 · see citing works
Mathys, H., Peng, Z., Boix, C. A., Victor, M. B., Leary, N., Babu, S., Abdelhady, G., Jiang, X., Ng, A. P., Ghafari, K., et al. (2023) · Cell · doi:10.1016/j.cell.2023.08.039 · Cited by 495 · see citing works
Hou, Y., Lautrup, S., Cordonnier, S., Wang, Y., Croteau, D. L., Zavala, E., Zhang, Y., Moritoh, K., O’Connell, J. F., Baptiste, B. A., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1718819115 · Cited by 472 · see citing works
Ogrodnik, M., Evans, S. A., Fielder, E., Victorelli, S., Kruger, P., Salmonowicz, H., Weigand, B. M., Patel, A. D., Pirtskhalava, T., Inman, C. L., et al. (2021) · Aging Cell · doi:10.1111/acel.13296 · Cited by 405 · see citing works
The amyloid cascade hypothesis: are we poised for success or failure?
Karran, E., & De Strooper, B. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13632 · Cited by 402 · see citing works
Mitophagy in neurodegeneration and aging
Fivenson, E. M., Lautrup, S., Sun, N., Scheibye-Knudsen, M., Stevnsner, T., Nilsen, H., Bohr, V. A., & Fang, E. F. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.02.007 · Cited by 364 · see citing works
Cellular Senescence in Neurodegenerative Diseases
Martínez‐Cué, C., & Rueda, N. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00016 · Cited by 285 · see citing works
Senatorov, V. V., Friedman, A. R., Milikovsky, D. Z., Ofer, J., Saar-Ashkenazy, R., Charbash, A., Jahan, N., Chin, G., Mihaly, E., Lin, J. M., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aaw8283 · Cited by 257 · see citing works
Mertens, J., Reid, D. A., Lau, S., Kim, Y., & Gage, F. H. (2018) · Annual Review of Genetics · doi:10.1146/annurev-genet-120417-031534 · Cited by 252 · see citing works
Coordination of DNA single strand break repair
Abbotts, R., & Wilson, D. M. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.039 · Cited by 240 · see citing works
Building a lineage from single cells: genetic techniques for cell lineage tracking
Woodworth, M. B., Girskis, K. M., & Walsh, C. A. (2017) · Nature Reviews Genetics · doi:10.1038/nrg.2016.159 · Cited by 236 · see citing works
Mitochondria in the signaling pathways that control longevity and health span
Akbari, M., Kirkwood, T. B. L., & Bohr, V. A. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.100940 · Cited by 232 · see citing works
Alzheimer’s Disease: From Firing Instability to Homeostasis Network Collapse
Frère, S. G. A., & Slutsky, I. (2018) · Neuron · doi:10.1016/j.neuron.2017.11.028 · Cited by 230 · see citing works
Nicotinamide Riboside—The Current State of Research and Therapeutic Uses
Mehmel, M., Jovanović, N. D., & Spitz, U. P. (2020) · Nutrients · doi:10.3390/nu12061616 · Cited by 225 · see citing works
NAD+ biosynthesis, aging, and disease
Johnson, S., & Imai, S. (2018) · F1000Research · doi:10.12688/f1000research.12120.1 · Cited by 178 · see citing works
Serum microRNA miR-501-3p as a potential biomarker related to the progression of Alzheimer’s disease
Hara, N., Kikuchi, M., Miyashita, A., Hatsuta, H., Saito, Y., Kasuga, K., Murayama, S., Ikeuchi, T., & Kuwano, R. (2017) · Acta Neuropathologica Communications · doi:10.1186/s40478-017-0414-z · Cited by 163 · see citing works
DNA-PKcs: A Multi-Faceted Player in DNA Damage Response
Yue, X., Bai, C., Xie, D., Ma, T., & Zhou, P. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.607428 · Cited by 160 · see citing works
Alzheimer’s Disease Pathogenesis: Role of Autophagy and Mitophagy Focusing in Microglia
Eshraghi, M., Adlimoghaddam, A., Mahmoodzadeh, A., Sharifzad, F., Yasavoli-Sharahi, H., Lorzadeh, S., Albensi, B. C., & Ghavami, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073330 · Cited by 158 · see citing works
Genome integrity and disease prevention in the nervous systemPreprint
McKinnon, P. J. (2017) · Genes & Development · doi:10.1101/gad.301325.117 · Cited by 155 · see citing works
Dissecting Aging and Senescence—Current Concepts and Open Lessons
Schmeer, C. W., Kretz, A., Wengerodt, D., Stojiljkovic, M. R., & Witte, O. W. (2019) · Cells · doi:10.3390/cells8111446 · Cited by 148 · see citing works
Vitamin D deficiency accelerates ageing and age‐related diseases: a novel hypothesis
Berridge, M. J. (2017) · The Journal of Physiology · doi:10.1113/jp274887 · Cited by 142 · see citing works
The costs and benefits of senotherapeutics for human health
Raffaele, M., & Vinciguerra, M. (2022) · The Lancet Healthy Longevity · doi:10.1016/s2666-7568(21)00300-7 · Cited by 140 · see citing works
Li, Y., Shen, Y., Hohensinner, P. J., Ju, J., Wen, Z., Goodman, S. B., Zhang, H., Goronzy, J. J., & Weyand, C. M. (2016) · Immunity · doi:10.1016/j.immuni.2016.09.013 · Cited by 138 · see citing works
Dileep, V., Boix, C. A., Mathys, H., Marco, A., Welch, G. M., Meharena, H. S., Loon, A., Jeloka, R., Peng, Z., Bennett, D. A., et al. (2023) · Cell · doi:10.1016/j.cell.2023.08.038 · Cited by 130 · see citing works
Mechanisms of DNA damage-mediated neurotoxicity in neurodegenerative disease
Welch, G., & Tsai, L. (2022) · The EMBO Reports · doi:10.15252/embr.202154217 · Cited by 129 · see citing works
Three-dimensional modeling of human neurodegeneration: brain organoids coming of age
Grenier, K., Kao, J., & Diamandis, P. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0500-7 · Cited by 127 · see citing works
Incorporation of a nucleoside analog maps genome repair sites in postmitotic human neurons
Reid, D. A., Reed, P. J., Schlachetzki, J. C. M., Nitulescu, I. I., Chou, G., Tsui, E. C., Jones, J. R., Chandran, S., Lu, A. T., McClain, C. A., et al. (2021) · Science · doi:10.1126/science.abb9032 · Cited by 121 · see citing works
Cellular senescence, DNA damage, and neuroinflammation in the aging brain
Zhang, W., Sun, H., Wang, X., Dumont, A. S., & Liu, Q. (2024) · Trends in Neurosciences · doi:10.1016/j.tins.2024.04.003 · Cited by 113 · see citing works
One-Carbon Metabolism: Pulling the Strings behind Aging and Neurodegeneration
Lionaki, E., Ploumi, C., & Tavernarakis, N. (2022) · Cells · doi:10.3390/cells11020214 · Cited by 110 · see citing works
DNA damage in the oligodendrocyte lineage and its role in brain aging
Tse, K.-H., & Herrup, K. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.05.006 · Cited by 108 · see citing works
Self-citationNext generation high throughput DNA damage detection platform for genotoxic compound screening
Sýkora, P., Witt, K. L., Revanna, P., Smith‐Roe, S. L., Dismukes, J., Lloyd, D. G., Engelward, B. P., & Sobol, R. W. (2018) · Scientific Reports · doi:10.1038/s41598-018-20995-w · Cited by 106 · see citing works
Tse, K., & Herrup, K. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14079 · Cited by 104 · see citing works
Self-citationLópez‐Ortiz, S., Pinto-Fraga, J., Valenzuela, P. L., Martín-Hernández, J., Seisdedos, M. M., Garcı́a, Ó., Toschi, N., Giuliano, F. D., Garaci, F. G., Mercuri, N. B., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22062897 · Cited by 101 · see citing works
Engrailed homeoprotein blocks degeneration in adult dopaminergic neurons through LINE‐1 repression
de Thé, F.-X. B., Rekaik, H., Pezé-Heidsieck, E., Massiani-Beaudoin, O., Joshi, R. L., Fuchs, J., & Prochiantz, A. (2018) · The EMBO Journal · doi:10.15252/embj.201797374 · Cited by 94 · see citing works
Clock mediates liver senescence by controlling ER stress
Yuan, G., Hua, B., Cai, T., Xu, L., Li, E., Huang, Y., Sun, N., Yan, Z., Lü, C., & Qian, R. (2017) · Aging · doi:10.18632/aging.101353 · Cited by 90 · see citing works
In Pursuit of Healthy Aging: Effects of Nutrition on Brain Function
Melzer, T. M., Manosso, L. M., Yau, S., Gil‐Mohapel, J., & Brocardo, P. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22095026 · Cited by 90 · see citing works
Review: Somatic mutations in neurodegeneration
Leija‐Salazar, M., Piette, C. E., & Proukakis, C. (2018) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12465 · Cited by 84 · see citing works
Re-thinking the Etiological Framework of Neurodegeneration
Castillo, X., Castro‐Obregón, S., Gutiérrez-Becker, B., Gutiérrez‐Ospina, G., Karalis, N., Khalil, A. A., López‐Noguerola, J. S., Rodríguez, L. L., Martínez‐Martínez, E., Perez‐Cruz, C., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00728 · Cited by 80 · see citing works
Geary, D. C. (2018) · Psychological Review · doi:10.1037/rev0000124 · Cited by 78 · see citing works
Melatonin: Protection against age-related cardiac pathology
Favero, G., Franceschetti, L., Buffoli, B., Moghadasian, M. H., Reiter, R. J., Rodella, L. F., & Rezzani, R. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.11.007 · Cited by 76 · see citing works
Mendes‐Silva, A. P., Pereira, K. S., Araújo, G. T. T., Nicolau, E. D. S., Silva-Ferreira, C. M., Teixeira, A. L., & Diniz, B. S. (2016) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2016.07.017 · Cited by 73 · see citing works
Neurons with Complex Karyotypes Are Rare in Aged Human Neocortex
Chronister, W. D., Burbulis, I. E., Wierman, M. B., Wolpert, M. J., Haakenson, M. F., Smith, A. C. B., Kleinman, J. E., Hyde, T. M., Weinberger, D. R., Bekiranov, S., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.107 · Cited by 72 · see citing works
Connecting the Dots: From DNA Damage and Repair to Aging
Pan, M., Li, K., Lin, S., & Hung, W.-C. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17050685 · Cited by 70 · see citing works
Ontogenetic and Pathogenetic Views on Somatic Chromosomal Mosaicism
Iourov, I. Y., Vorsanova, S. G., Yurov, Y. B., & Kutsev, S. I. (2019) · Genes · doi:10.3390/genes10050379 · Cited by 68 · see citing works
Sexually divergent DNA methylation patterns with hippocampal aging
Masser, D. R., Hadad, N., Porter, H. L., Mangold, C. A., Unnikrishnan, A., Ford, M. M., Giles, C. B., Georgescu, C., Dozmorov, M. G., Wren, J. D., et al. (2017) · Aging Cell · doi:10.1111/acel.12681 · Cited by 68 · see citing works
Monogenic Diseases of DNA Repair
Keijzers, G., Bakula, D., & Scheibye‐Knudsen, M. (2017) · New England Journal of Medicine · doi:10.1056/nejmra1703366 · Cited by 67 · see citing works
Transposable elements as new players in neurodegenerative diseases
Ravel‐Godreuil, C., Znaidi, R., Bonnifet, T., Joshi, R. L., & Fuchs, J. (2021) · FEBS Letters · doi:10.1002/1873-3468.14205 · Cited by 67 · see citing works
Profiling DNA break sites and transcriptional changes in response to contextual fear learning
Stott, R. T., Kritsky, O., & Tsai, L.-H. (2021) · PLOS ONE · doi:10.1371/journal.pone.0249691 · Cited by 62 · see citing works
Research Progress on the Anti-Aging Potential of the Active Components of Ginseng
Su, J., Su, Q., Hu, S., Ruan, X., & Ouyang, S. (2023) · Nutrients · doi:10.3390/nu15153286 · Cited by 58 · see citing works
Somatic mutations in neurons during aging and neurodegeneration
Verheijen, B. M., Vermulst, M., & van Leeuwen, F. W. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1850-y · Cited by 57 · see citing works
Tse, K., Cheng, A., Ma, F., & Herrup, K. (2018) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2017.11.010 · Cited by 56 · see citing works
Self-citationDNA Damage-Induced Neurodegeneration in Accelerated Ageing and Alzheimer’s Disease
Wang, H., Lautrup, S., Caponio, D., Zhang, J., & Fang, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136748 · Cited by 55 · see citing works
Morozko, E. L., Smith-Geater, C., Monteys, A. M., Pradhan, S., Lim, R. G., Langfelder, P., Kachemov, M., Kulkarni, J. A., Zaifman, J., Hill, A. M., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2021836118 · Cited by 54 · see citing works
Ain, Q., Schmeer, C. W., Wengerodt, D., Witte, O. W., & Kretz, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072477 · Cited by 51 · see citing works
Chromosome Instability, Aging and Brain Diseases
Iourov, I. Y., Yurov, Y. B., Vorsanova, S. G., & Kutsev, S. I. (2021) · Cells · doi:10.3390/cells10051256 · Cited by 51 · see citing works
Meo, F. D., Cuciniello, R., Margarucci, S., Bergamo, P., Petillo, O., Peluso, G., Filosa, S., & Crispi, S. (2020) · Antioxidants · doi:10.3390/antiox9040279 · Cited by 50 · see citing works
Retrotransposons as a Source of DNA Damage in Neurodegeneration
Pezé-Heidsieck, E., Bonnifet, T., Znaidi, R., Ravel‐Godreuil, C., Massiani-Beaudoin, O., Joshi, R. L., & Fuchs, J. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.786897 · Cited by 49 · see citing works
Hadad, N., Masser, D. R., Logan, S., Wronowski, B., Mangold, C. A., Clark, N. W., Otalora, L., Unnikrishnan, A., Ford, M. M., Giles, C. B., et al. (2016) · Epigenetics & Chromatin · doi:10.1186/s13072-016-0080-6 · Cited by 48 · see citing works
The Phosphorylated Form of the Histone H2AX (γH2AX) in the Brain from Embryonic Life to Old Age
Merighi, A., Gionchiglia, N., Granato, A., & Lossi, L. (2021) · Molecules · doi:10.3390/molecules26237198 · Cited by 48 · see citing works
The cerebellar degeneration in ataxia-telangiectasia: A case for genome instability
Shiloh, Y. (2020) · DNA repair · doi:10.1016/j.dnarep.2020.102950 · Cited by 47 · see citing works
Failure of DNA double-strand break repair by tau mediates Alzheimer’s disease pathology in vitro
Asada‐Utsugi, M., Uemura, K., Ayaki, T., Uemura, M. T., Minamiyama, S., Hikiami, R., Morimura, T., Shodai, A., Ueki, T., Takahashi, R., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-03312-0 · Cited by 47 · see citing works
Li, Y., Xie, L., Huang, T., Zhang, Y., Zhou, J., Qi, B., Wang, X., Chen, Z., & Li, P. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00778 · Cited by 46 · see citing works
Bian, Z., Li, C., Peng, D., Wang, X., & Zhu, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911220 · Cited by 44 · see citing works
Zhao, X., Fan, Y., Vann, P. H., Wong Jessica, M., Sumien, N., & He, J. J. (2020) · Aging and Disease · doi:10.14336/ad.2019.0323 · Cited by 43 · see citing works
Multiple Sclerosis and Aging: The Dynamics of Demyelination and Remyelination
Correale, J. D., & Ysrraelit, M. C. (2022) · ASN NEURO · doi:10.1177/17590914221118502 · Cited by 42 · see citing works
Lemoine, É., Dallaire, F., Yadav, R., Agarwal, R., Kadoury, S., Trudel, D., Guiot, M., Petrecca, K., & Leblond, F. (2019) · The Analyst · doi:10.1039/c9an01144g · Cited by 41 · see citing works
Wong, G. C., & Chow, H. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220203 · Cited by 40 · see citing works
Self-citationFragola, G., Mabb, A. M., Taylor‐Blake, B., Niehaus, J. K., Chronister, W. D., Mao, H., Simon, J. M., Yuan, H., Li, Z., McConnell, M. J., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15794-9 · Cited by 40 · see citing works
DNA Damage-Mediated Neurotoxicity in Parkinson’s Disease
Wang, Z., Li, Y., Pu, J., & Zhang, B. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076313 · Cited by 39 · see citing works
G Protein-Coupled Receptor Systems as Crucial Regulators of DNA Damage Response Processes
Leysen, H., van Gastel, J., Hendrickx, J. O., Santos‐Otte, P., Martin, B., & Maudsley, S. R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19102919 · Cited by 37 · see citing works
Challenges of Repurposing Tetracyclines for the Treatment of Alzheimer’s and Parkinson’s Disease
Markulin, I., Matasin, M., Turk, V. E., & Salković-Petrisic, M. (2022) · Journal of Neural Transmission · doi:10.1007/s00702-021-02457-2 · Cited by 36 · see citing works
DNA damage and neurodegenerative phenotypes in aged Ciz1 null mice
Khan, M. M., Xiao, J., Patel, D., & LeDoux, M. S. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.10.014 · Cited by 34 · see citing works
The link between Mitochondria and Sarcopenia
Kamarulzaman, N. T., & Makpol, S. (2025) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-024-01062-7 · Cited by 33 · see citing works
Zhang, Y., Song, X., & Herrup, K. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-01887-5 · Cited by 33 · see citing works
Self-citationGenomic Mosaicism Formed by Somatic Variation in the Aging and Diseased Brain
Costantino, I. M., Nicodemus, J., & Chun, J. J. M. (2021) · Genes · doi:10.3390/genes12071071 · Cited by 33 · see citing works
Herpes Simplex Virus-Type1 (HSV-1) Impairs DNA Repair in Cortical Neurons
Chiara, G. D., Racaniello, M., Mollinari, C., Marcocci, M. E., Aversa, G., Cardinale, A., Giovanetti, A., Garaci, E., Palamara, A. T., & Merlo, D. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00242 · Cited by 32 · see citing works
Ataxin‐2: A versatile posttranscriptional regulator and its implication in neural function
Lee, J., Kim, M., Itoh, T. Q., & Lim, C. (2018) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1488 · Cited by 30 · see citing works
Geary, D. C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073562 · Cited by 30 · see citing works
Recent insights into the cellular and molecular determinants of aging
Ruan, L., Zhang, X., & Li, R. (2018) · Journal of Cell Science · doi:10.1242/jcs.210831 · Cited by 27 · see citing works
Riancho, J., Vázquez, D. C., Gil-Bea, F. J., Tapia, O., Arozamena, J., Duran-Vian, C., Sedano, M. J., Berciano, M. T., de Munaín, A. L., & Lafarga, M. (2020) · Journal of Neurology · doi:10.1007/s00415-020-09704-8 · Cited by 27 · see citing works
Microrchidia CW-Type Zinc Finger 2, a Chromatin Modifier in a Spectrum of Peripheral Neuropathies
Jacquier, A., Roubille, S., Lomonte, P., & Schaeffer, L. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.896854 · Cited by 26 · see citing works
Eid, J. I., Al-Tuwaijri, M., Mohanty, S., & Das, B. B. (2021) · Heliyon · doi:10.1016/j.heliyon.2021.e06003 · Cited by 26 · see citing works
Baltanás, F. C., Berciano, M. T., Santos, E., & Lafarga, M. (2021) · Biomedicines · doi:10.3390/biomedicines9091157 · Cited by 25 · see citing works
Omega-3 Docosahexaenoic Acid Is a Mediator of Fate-Decision of Adult Neural Stem Cells
Van, A. L., Hachem, M., Lagarde, M., & Bernoud‐Hubac, N. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20174240 · Cited by 25 · see citing works
Mata-Garrido, J., Casafont, Í., Tapia, O., Berciano, M. T., & Lafarga, M. (2016) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0312-9 · Cited by 24 · see citing works
Song, X., Aw, J. T. M., Ma, F., Cheung, M. F., Leung, D., & Herrup, K. (2021) · The Journal of Neuroscience · doi:10.1523/jneurosci.0845-21.2021 · Cited by 23 · see citing works
Self-citationBarańska, A., Pawlos, A., Mokra, K., & Michałowicz, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.869741 · Cited by 23 · see citing works
Cassera, E., Ferrari, E., Vignati, D. A. L., & Capucciati, A. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111366 · Cited by 22 · see citing works
Daniele, S., Costa, B., Pietrobono, D., Giacomelli, C., Iofrida, C., Trincavelli, M. L., Fusi, J., Franzoni, F., & Martini, C. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/3740345 · Cited by 22 · see citing works
Mata-Garrido, J., Tapia, O., Casafont, Í., Berciano, M. T., Cuadrado, A., & Lafarga, M. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0573-6 · Cited by 22 · see citing works
The metabolic engine of cognition: microglia–neuron interactions in health, ageing and disease
Asimakidou, E., Pluchino, S., Silva, B. A., & Peruzzotti‐Jametti, L. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01409-4 · Cited by 21 · see citing works
Amitosenescence and Pseudomitosenescence: Putative New Players in the Aging Process
Wengerodt, D., Schmeer, C. W., Witte, O. W., & Kretz, A. (2019) · Cells · doi:10.3390/cells8121546 · Cited by 21 · see citing works
D’Errico, M., Parlanti, E., Pascucci, B., Filomeni, G., Mastroberardino, P. G., & Dogliotti, E. (2021) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2021.108977 · Cited by 20 · see citing works
Kadhim, M. A., Cagatay, S. T., & Elbakrawy, E. M. (2021) · International Journal of Radiation Biology · doi:10.1080/09553002.2021.1980630 · Cited by 20 · see citing works
Along the microbiota–gut–brain axis: Use of plant polysaccharides to improve mental disorders
Gao, J., Liang, Y., & Liu, P. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.130903 · Cited by 19 · see citing works
Vieira, É. L. M., Mendes‐Silva, A. P., Ferreira, J. D. R., Bertola, L., Barroso, L., Vieira, M., Teixeira, A. L., & Diniz, B. S. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.09.084 · Cited by 19 · see citing works
Omais, S., Jaafar, C., & Ghanem, N. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00144 · Cited by 19 · see citing works
- Authors
- Chow, H.-M., & Herrup, K.
- Affiliations
- Hong Kong University of Science and Technology (HK)
- Corresponding author
- Herrup, Karl
- Venue
- Nature Reviews Neuroscience
- Published
- 2015-10-14
- Volume
- 16
- Issue
- 11
- Pages
- 672-684
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W1758544898
- Semantic Scholar
- 684d55b598f259dc680394ed95b582e198132e4f
- Cited by
- 174
- References
- 202
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 12 · 2023: 9 · 2022: 26 · 2021: 27 · 2020: 16 · 2019: 16 · 2018: 25 · 2017: 17 · 2016: 12
- FWCI
- 1.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Rare & Special e-Zone (The Hong Kong University of Science and Technology) (submittedVersion)
- Funders
- Hong Kong University of Science and Technology
- National Institute of Neurological Disorders and Stroke (NS70193)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Keywords
- brain aging, genome stability, DNA damage, postmitotic neurons, neurodegenerative diseases, DNA damage accumulation
- MeSH terms
- Aging, Animals, Brain, Cell Cycle, DNA Damage, DNA Repair, Humans, Neurodegenerative Diseases, Genomics
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