DNA repair deficiency and neurological disease

Instability and decay of the primary structure of DNA

Lindahl, T. (1993) · Nature · doi:10.1038/362709a0 · Cited by 5,679

ATM and ATR Substrate Analysis Reveals Extensive Protein Networks Responsive to DNA Damage

Matsuoka, S., Ballif, B. A., Smogorzewska, A., McDonald, E. R., Hurov, K. E., Luo, J., Bakalarski, C. E., Zhao, Z., Solimini, N., Lerenthal, Y., et al. (2007) · Science · doi:10.1126/science.1140321 · Cited by 3,075

Mechanisms and Functional Implications of Adult Neurogenesis

Zhao, C., Deng, W., & Gage, F. H. (2008) · Cell · doi:10.1016/j.cell.2008.01.033 · Cited by 3,007

Cell-cycle checkpoints and cancer

Kastan, M. B., & Bartek, J. (2004) · Nature · doi:10.1038/nature03097 · Cited by 2,836

A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

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ATM and related protein kinases: safeguarding genome integrity

Shiloh, Y. (2003) · Nature Reviews Cancer · doi:10.1038/nrc1011 · Cited by 2,577

Cellular roles of DNA topoisomerases: a molecular perspective

Wang, J. C. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm831 · Cited by 2,364

ATR: an essential regulator of genome integrity

Cimprich, K. A., & Cortez, D. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2450 · Cited by 1,798

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

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

Bender, A., Krishnan, K. J., Morris, C. M., Taylor, G. A., Reeve, A. K., Perry, R. H., Jaros, E., Hersheson, J. S., Betts, J., Klopstock, T., et al. (2006) · Nature Genetics · doi:10.1038/ng1769 · Cited by 1,570

A mechanism for semaphorin-induced apoptosis: DNA damage of endothelial and myogenic cells in primary cultures from skeletal muscle

Yuan, H. S. H., Katyal, S., & Anderson, J. E. (2018) · Oncotarget · doi:10.18632/oncotarget.25200 · Cited by 9

Non-homologous end joining repair in Xenopus egg extract

Zhu, S., & Peng, A. (2016) · Scientific Reports · doi:10.1038/srep27797 · Cited by 8

Targeting Genome Stability in Melanoma—A New Approach to an Old Field

Osrodek, M., & Woźniak, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073485 · Cited by 11

Homocysteine aggravates DNA damage by impairing the FA/Brca1 Pathway in NE4C murine neural stem cells

Yan, Y., Yin, Y., Feng, X., Chen, Y., Shi, J., Weng, H., & Wang, D. (2020) · International Journal of Medical Sciences · doi:10.7150/ijms.49246 · Cited by 8

Glioblastoma recurrent cells switch between ATM and ATR pathway as an alternative strategy to survive radiation stress

Kaur, E., Ketkar, M., & Dutt, S. (2022) · Medical Oncology · doi:10.1007/s12032-022-01657-4 · Cited by 8

Chronic Alcohol Exposure Decreases 53BP1 Protein Levels Leading to a Defective DNA Repair in Cultured Primary Cortical Neurons

Romero, A. M., Palanca, A., Ruiz‐Soto, M., Llorca, J., Marín, M. P., Renau‐Piqueras, J., Berciano, M. T., & Lafarga, M. (2015) · Neurotoxicity Research · doi:10.1007/s12640-015-9554-8 · Cited by 8

Nbn gene inactivation in the CNS of mouse inhibits the myelinating ability of the mature cortical oligodendrocytes

Liu, B., Chen, X., Wang, Z., & Tong, W. (2013) · Glia · doi:10.1002/glia.22593 · Cited by 9

Nhej1 Deficiency Causes Abnormal Development of the Cerebral Cortex

Waly, B. E., Buhler, E., Haddad, M.-R., & Villard, L. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8919-y · Cited by 8

Nanoparticles for Brain Drug Delivery

Veloso, S. R. S., Ferreira, P. M. T., Martins, J. A., Coutinho, P. J. G., & Castanheira, E. M. S. (2020) · doi:10.1201/9781003119326 · Cited by 8

Protective effects of noradrenaline on benzo[a]pyrene-induced oxidative stress responses in brain tumor cell lines

Patri, M., & Singh, A. (2019) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-019-00378-9 · Cited by 8

Chemotherapy-induced neuronal DNA damage: an intriguing toolbox to elucidate DNA repair mechanisms in the brain

Babu, A., & Urulangodi, M. (2023) · Genome Instability & Disease · doi:10.1007/s42764-023-00110-8 · Cited by 7

A human-specific, concerted repression of microcephaly genes contributes to radiation-induced growth defects in cortical organoids

Ribeiro, J. H., Etlioglu, E., Buset, J., Janssen, A., Puype, H., Berden, L., Mfossa, A. C. M., Vos, W. H. D., Vermeirssen, V., Baatout, S., et al. (2025) · iScience · doi:10.1016/j.isci.2025.111853 · Cited by 7

Brain and induced pluripotent stem cell-derived neural stem cells as an in vitro model of neurodegeneration in ataxia-telangiectasia

Carlessi, L., Poli, E., & Delia, D. (2013) · Experimental Biology and Medicine · doi:10.1177/1535370213480703 · Cited by 7

Prion-induced neurotoxicity: Possible role for cell cycle activity and DNA damage response

Bujdoso, R. (2015) · World Journal of Virology · doi:10.5501/wjv.v4.i3.188 · Cited by 7

Human Developmental Genetics

Tan, W., Gilmore, E. C., & Baris, H. N. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-383834-6.00018-5 · Cited by 9

Neurological Complications in Inborn Errors of Immunity: A Scoping Review of Clinical Spectrum, Pathophysiological Mechanisms, and Therapeutic Strategies

Xiao, N., Huang, X., Chen, L., Zang, W., Guan, M., Li, T., Тузанкина, И. А., Черешнев, В. А., & Liu, G. (2025) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-025-09078-7 · Cited by 6

Human Diseases Induced by Oxidative Damage in DNA

Panda, S., Chatterjee, O., Mukherjee, G., & Chatterjee, S. (2023) · Springer eBooks · doi:10.1007/978-981-19-8520-1_5 · Cited by 6

CITK modulates BRCA1 recruitment at DNA double strand breaks sites through HDAC6

Iegiani, G., Pallavicini, G., Pezzotta, A., Brix, A., Ferraro, A., Gai, M., Boda, E., Bielas, S. L., Pistocchi, A., & Cunto, F. D. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07655-4 · Cited by 6

The Essential DNA Damage Response Complex MRN Is Dispensable for the Survival and Function of Purkinje Neurons

Ding, M., Qing, X., Zhang, G., Baade‐Büttner, C., Gruber, R., Lu, H., Ferguson, D. O., Geis, C., Wang, Z., & Zhou, Z. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.786199 · Cited by 6

Candidate Genes Associated with Delayed Neuropsychomotor Development and Seizures in a Patient with Ring Chromosome 20

Corrêa, T., Venâncio, A. C., Galera, M. F., & Riegel, M. (2020) · Case Reports in Genetics · doi:10.1155/2020/5957415 · Cited by 6

Aag DNA Glycosylase Promotes Alkylation-Induced Tissue Damage Mediated by Parp1

Calvo, J. A., Moroski-Erkul, C. A., Lake, A., Eichinger, L. W., Shah, D., Jhun, I., Limsirichai, P., Bronson, R. T., Christiani, D. C., Meira, L. B., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003413 · Cited by 6

Mitochondrial topoisomerases, nucleoid architecture and mtDNA repair in human disease

Bhattacharjee, S., & Das, B. B. (2025) · Journal of Cell Science · doi:10.1242/jcs.263638 · Cited by 7

Implications of N7-hydrogen and C8-keto on the base pairing, mutagenic potential and repair of 8-oxo-2′-deoxy-adenosine: Investigation by nucleotide analogues

Wu, J., Zhang, M., Song, L., Tan, Y., Taniguchi, Y., Hipolito, C. J., Zhang, Y., & Yin, Y. (2022) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2022.106029 · Cited by 5

Lig3-dependent rescue of mouse viability and DNA double-strand break repair by catalytically inactive Lig4

Medina-Suárez, D., Han, L., O’Reilly, S., Liu, J., Wei, C., Brenière, M., Goff, N. J., Chen, C., Modesti, M., Meek, K., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae1216 · Cited by 5

Breaking news: thinking may be bad for DNA

Herrup, K., Chen, J., & Li, J. (2013) · Nature Neuroscience · doi:10.1038/nn.3384 · Cited by 5

A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafish

Shin, U., Choi, Y., Ko, H. S., Myung, K., Lee, S., Cheon, C. K., & Lee, Y. (2023) · Human Genomics · doi:10.1186/s40246-023-00491-7 · Cited by 5

DNA Replication, Repair, and Mutagenesis

Bhagavan, N. V., & Ha, C. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-095461-2.00022-9 · Cited by 5

Correction: Nbn and Atm Cooperate in a Tissue and Developmental Stage-Specific Manner to Prevent Double Strand Breaks and Apoptosis in Developing Brain and Eye

Rodrigues, P. M. G., Grigaravičius, P., Remus, M., Cavalheiro, G. R., Gomes, A. L., Rocha-Martins, M., Frappart, L., Reuß, D., McKinnon, P. J., von Deimling, A., et al. (2013) · PLoS ONE · doi:10.1371/annotation/b38f50e0-04b6-42c5-8b19-50be747a38f3 · Cited by 5

Strawberry (Fragaria ananassaduch.) Alba extract attenuates DNA damage in lymphocytes of patients with Alzheimer’s disease

Živković, L., Bajić, V., Pirković, A., Dekanski, D., Forbes-Hernández, T. Y., Zlatković‐Švenda, M., Perry, G. L., & Spremo‐Potparević, B. (2021) · Journal of Food Biochemistry · doi:10.1111/jfbc.13637 · Cited by 4

XRCC1 Prevents Replication Fork Instability during Misincorporation of the DNA Demethylation Bases 5-Hydroxymethyl-2′-Deoxycytidine and 5-Hydroxymethyl-2′-Deoxyuridine

Peña-Gómez, M. J., Suárez-Pizarro, M., & Rosado, I. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23020893 · Cited by 4

Unraveling DNA Repair Processes In Vivo: Insights from Zebrafish Studies

Shin, U., & Lee, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713120 · Cited by 6

Genomic variation in neurons

Zolzaya, S., Narumoto, A., & Katsuyama, Y. (2023) · Development Growth & Differentiation · doi:10.1111/dgd.12898 · Cited by 4

In vitro dexamethasone treatment does not induce alternative ATM transcripts in cells from Ataxia–Telangiectasia patients

Pozzi, E., Giorgio, E., Mancini, C., Buono, N. L., Augeri, S., Ferrero, M., Gregorio, E. D., Riberi, E., Vinciguerra, M., Nanetti, L., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-77352-z · Cited by 4

Role of Histone Tails and Single Strand DNA Breaks in Nucleosomal Arrest of RNA Polymerase

Gerasimova, N. S., Pestov, N. A., & Studitsky, V. M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032295 · Cited by 4

Mild Hypothermia Attenuates the Anesthetic Isoflurane-Induced Cytotoxicity

Li, C., Dong, Y., Chen, D., Xie, Z., & Zhang, Y. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00015 · Cited by 4

CRISPR/Cas9 technology in neurological disorders: An update for clinicians

Srivastava, A. K., Swarup, V., Kumar, V., Faruq, M., Singh, H. N., & Singh, I. (2020) · Annals of Movement Disorders · doi:10.4103/aomd.aomd_39_19 · Cited by 4

Effects of 5′,8′-Cyclo-2′-Deoxypurines on the Base Excision Repair of Clustered DNA Lesions in Nuclear Extracts of the XPC Cell Line

Kaźmierczak-Barańska, J., Boguszewska, K., Szewczuk, M., & Karwowski, B. T. (2021) · Cells · doi:10.3390/cells10113254 · Cited by 4

The Distinct Signaling Regulatory Roles in the Cortical Atrophy and Cerebellar Apoptosis of Newborn Nbn-Deficient Mice

Liu, B., & Chen, X. (2013) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-013-9971-2 · Cited by 4

Structure-specific nucleases in genome dynamics and strategies for targeting cancers

Sun, H., Luo, M., Zhou, M., Zheng, L., Li, H., Esworthy, R. S., & Shen, B. (2024) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjae019 · Cited by 3

APTX acts in DNA double-strand break repair in a manner distinct from XRCC4

Imamura, R., Saito, M., Shimada, M., Kobayashi, J., Ishiai, M., & Matsumoto, Y. (2023) · Journal of Radiation Research · doi:10.1093/jrr/rrad007 · Cited by 3

New Insight on Entangled DNA Repair Pathways: Stable Silenced Human Cells for Unraveling the DDR Jigsaw

Biard, D. S. F. (2011) · InTech eBooks · doi:10.5772/23681 · Cited by 3

DNA repair deficiency in a newly identified neurological disease

Huang, K. (2010) · Clinical Genetics · doi:10.1111/j.1399-0004.2010.01519_1.x · Cited by 3

JNK Activation by Up-Regulation of iNOS on Cholesterol Accumulation Limits Neurogenesis and Induces Region-Specific DNA Damage Responses in the Subventricular Zone of NPC Mice

Seo, Y., Yang, S., Kim, H., Yu, K., Shin, Y., Kang, S., & Kang, K. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4301 · Cited by 3

Cockayne syndrome

Proietti‐De‐Santis, L., Laugel, V., & Prantera, G. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813796-3.00007-9 · Cited by 3

Chromatin remodeler BRG1 recruits huntingtin to repair DNA double-strand breaks in neuronsPreprint

Pradhan, S., Bush, K. M., Zhang, N., PANDITA, R. K., Tsai, C.-L., Smith-Geater, C., Pandlebury, D. F., Gaikwad, S., Leonard, F., Nie, L., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.19.613927 · Cited by 4

Polystyrene Nanoplastics Induce DNA Damage and Excitotoxicity in Whole-Brain Organoids: The Role of the TLR9/MyD88 Pathway

Wei, Y., Cao, G., Ma, J., Mi, Y., Zhao, Y., Zhang, L., Wang, B., Liu, H., Li, K., Shi, Y., et al. (2025) · Toxics · doi:10.3390/toxics14010005 · Cited by 2

Divergent Roles of Canonical and Non-Canonical Mismatch Repair in Regulating Temozolomide Sensitivity in Glioblastoma

Gupta, S. K., Jain, S., Friedman, T., & Sarkaria, J. N. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27146517 · Cited by 2

DNA Repair, Human Diseases and Aging

Krishnan, V., Liu, B., & Zhou, Z. (2011) · InTech eBooks · doi:10.5772/24565 · Cited by 2

Genomic instability and mitochondrial homeostasis in cancer: does chromatin have a say?

Liu, Y., Li, H., Zimmerman, S. E., & Weyemi, U. (2020) · Molecular & Cellular Oncology · doi:10.1080/23723556.2020.1771959 · Cited by 2

Protein Phosphatase 2ACα Regulates ATR-Mediated Endogenous DNA Damage Response Against Microcephaly

Lin, L., Ding, J., Liu, S., Liu, C., Li, Q., Gao, X., Niu, Y., & Tong, W. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04301-6 · Cited by 2

Tyrosyl-DNA-Phosphodiesterase

Dexheimer, T. S., Huang, S.-Y. N., Das, B. B., & Pommier, Y. G. (2011) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-1-4614-0323-4_16 · Cited by 2

The Dual Role of Survival Genes in Neurons and Cancer Cells: a Strategic Clinical Application of DX2 in Neurodegenerative Diseases and Cancer

Baek, K. (2024) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2024.138 · Cited by 3

Ataxia with Impaired DNA Repair in Adults: A Case Series and Review of the Literature

Нужный, Е. П., Klyushnikov, S. A., Abramycheva, N. Y., Fedotova, E. Y., Andreev, M. N., Vetchinova, A. S., & Illarioshkin, S. N. (2020) · Russian neurological Journal · doi:10.30629/2658-7947-2020-25-2-28-36 · Cited by 1

Cell-to-Cell Communication in Aging: Mechanisms, Impact and Therapeutic Prospects

Mas‐Bargues, C., Sanz‐Ros, J., Huete-Acevedo, J., & Borrás, C. (2024) · Springer eBooks · doi:10.1007/978-3-031-55022-5_8 · Cited by 1

Oligodendroglial somatic SNCA copy number gains are associated with inclusions and disease onset in multiple system atrophy

Morley, C., Kalef-Ezra, E., Pérez‐Rodríguez, D., Jaunmuktane, Z., & Proukakis, C. (2026) · Acta Neuropathologica · doi:10.1007/s00401-026-03077-4 · Cited by 1

Epitranscriptomic RNA editing resolves Mus81 DNA repair tradeoffs in heat tolerance and meiosis

Wu, M., Liu, J., Cao, P., Liu, M., Feng, C., Wang, Q., Jiang, C., Xu, J., & Liu, H. (2026) · Nature Communications · doi:10.1038/s41467-026-71219-z · Cited by 1

Expansion of outer cortical CUX2 neurons requires adaptations for DNA repair

Xia, W., Morcom, L. R., Xu, Z., Lu, I.-L., Wang, Q., Hoi, K. K., Wei, M., Zhu, K., Jordan, G. E., Tang, X.-Y., et al. (2026) · Nature · doi:10.1038/s41586-026-10290-4 · Cited by 1

DNA Damage Repair: A Crucial Link to Neurological Disorders

Yang, H., Deng, Y., Chen, W., Zhu, W., & Lu, X. (2026) · The FASEB Journal · doi:10.1096/fj.202504689r · Cited by 1

Mechanisms of Dendrite Degeneration in Amyotrophic Lateral Sclerosis

Lee, S., Shang, Y., & Huang, E. J. (2016) · Springer eBooks · doi:10.1007/978-4-431-56050-0_21 · Cited by 1

Developmental and epileptic encephalopathies in children: clinical, neurophysiological, neuroimaging and genetic characteristics

Kyrylova, L. H., Miroshnikov, О. О., Yuzva, О. О., Badiuk, V. M., Dolenko, O. O., & Bondarenko, Y. M. (2024) · INTERNATIONAL NEUROLOGICAL JOURNAL · doi:10.22141/2224-0713.20.2.2024.1056 · Cited by 1

Microwave Effects on DNA

Behari, J., & Jindal, T. (2017) · Springer eBooks · doi:10.1007/978-3-319-50289-2_3 · Cited by 1

Single-Cell Genomic and Epigenomic DNA Analyses

Geurs, S., Lefevre, T., & Voet, T. (2022) · Neuromethods · doi:10.1007/978-1-0716-2525-5_2 · Cited by 1

Effect of learning on slow gamma propagation between hippocampus and cortex in the wild-type and AD mice

Blinowska, K. J., Kamiński, M., Macrez, N., Marighetto, A., Meyrand, P., & Bem, T. (2022) · Scientific Reports · doi:10.1038/s41598-022-26754-2 · Cited by 1

Targeting the hSSB1-INTS3 Interface: A Computational Screening Driven Approach to Identify Potential Modulators

Barbhuiya, T. K., Beard, S., Shah, E. T., Mason, S. R., Bolderson, E., O'Byrne, K. J., Guddat, L. W., Richard, D. J., Adams, M. N., & Gandhi, N. S. (2024) · ACS Omega · doi:10.1021/acsomega.3c09267 · Cited by 1

Studies of DNA repair strategies in response to complex DNA damages

Bajinskis, A. (2012) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 1

Estudo dos mecanismos moleculares do reparo de quebra de duplas fitas no DNA mitocondrial

dos Santos, V. T. (2015) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.46.2015.tde-23092015-142853 · Cited by 1

Erratum: DNA repair deficiency and neurological disease

McKinnon, P. J. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2592 · Cited by 1

Reactivity of lesions derived from abasic (AP) sites in DNA

Housh, K. (2021) · doi:10.32469/10355/85783 · Cited by 1

Delivery of Nucleic Acids, Such as siRNA and mRNA, Using Complex Formulations

Pattnaik, A., Pany, S., Sanket, A. S., Das, S., Pati, S., & Samal, S. K. (2022) · Methods and principles in medicinal chemistry · doi:10.1002/9783527827855.ch9 · Cited by 1

Novel Roles of Replication Protein A Phosphorylation in the Cellular Response to DNA Damage

Serrano, M. A. (2013) · Digital Commons - East Tennessee State University (East Tennessee State University)

Links Between Injury-Induced Brain Remodeling and Oncogenesis

El-Habr, E. A., & Junier, M. (2014) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4899-7399-3_10

The regulation of RNA Polymerase I-mediated transcription in forebrain neurons.

Smith, S. C. (2012) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/1350

Multiplexing Techniques in Quantitative Proteomics to Study Disease

Evans, A. R. (2015) · D-Scholarship@Pitt (University of Pittsburgh)

3rd International Genome Dynamics in Neuroscience Conference: “DNA repair and neurological disease”

Caldecott, K. W., Bohr, V. A., & McKinnon, P. J. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.07.006

Linking, thinking & fixing: the story about the 2015 Chemistry Nobel Prize and the future of science

Meng, H., & Osborne, O. J. (2015) · 中国科学通报：英文版 · doi:10.1007/s11434-015-0932-7

Neuronal DNA Double Strand Break Damage and Repair Following Sublethal iGluR Activation, and the Neuroprotective Effects of Melatonin

Palchik, G. A. (2013) · DigitalGeorgetown (Georgetown University Library)

La inducción de E2F1 y E2F2 en respuesta al daño al ADN preserva la estabilidad genómica en células neuronales

Castillo, D. S. (2015) · Repositorio Digital Institucional de la Universidad de Buenos Aires (Universidad de Buenos Aires)

Neurons and Neuroglia

Trapp, B. D., & Herrup, K. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00007-1

Introduction to Genetic Diseases

Meisenberg, G., & Simmons, W. H. (2012) · Elsevier eBooks · doi:10.1016/b978-0-323-07155-0.00009-5

Integration of ATM, ATR, and DNA-PKcs Signaling Maintains Genome Integrity During Neurogenesis

Enriquez-Rios, V. D. (2015) · doi:10.21007/etd.cghs.2015.0085

Morphogen and epigenetic regulation of wound healing

Corbett, L. (2015)

Basic Principles of DNA Repair in Toxicology

Dutta, A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.65423-5

Measurement of sensitivity to DNA damaging agents

Sherin Mathew, T. (2017)

EXPLORING GENOME INTEGRITY PATHWAYS IN SACCHAROMYCES CEREVISIAE

Shanmugan, M. K. (2014) · Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) · doi:10.13130/shanmugam-muthukumar_phd2014-01-24

The Saccharomyces cerevisiae Srs2 Helicase Regulates Homologous Recombination through the Disassembly of Recombination Intermediates

Kaniecki, K. (2018) · doi:10.7916/d8q82wj0

Identification of activity-induced Egr3 -dependent genes reveals genes associated with DNA damage response and schizophreniaPreprint

Marballi, K. K., Alganem, K., Brunwasser, S. J., Barkatullah, A., Meyers, K. T., Campbell, J. M., Mccullumsmith, R. R., & Gallitano, A. L. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.01.276626

High-throughput generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genesPreprint

Shin, U., Nakhro, K., Oh, C.-K., Carrington, B., Song, H., Varshney, G., Kim, Y., Song, H., Jeon, S., Robbins, G., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.04.325621

Les maladies de la réparation

Girard, P.-M. (2021) · Bulletin du Cancer · doi:10.1016/j.bulcan.2020.10.020

Epigenetikai faktorok hatásának vizsgálata a Huntington-kór patomechanizmusában Drosophila modellben

Varga, J. (2020) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.10540

The effect of Telomere Lengthening on Genetic Diseases

Bojkovic, M., & Chandra, S. (2021) · Journal of Contemporary Medicine · doi:10.16899/jcm.756562

Genomic Instability and the Oncohistone H3K27M Drive Gliomagenesis in a Murine Model

Pribyl, L. J. (2020) · doi:10.21007/etd.cghs.2020.0515

Contemporary Evolution in CRISPR–CAS9 System Technology and their Uses in Treatment of Human Common Diseases: A Review

Mohammed, Z. S., & Al-Kraity, W. R. H. (2021) · Medico-Legal Update · doi:10.37506/mlu.v21i2.2878

DNA damage in tissue-resident macrophages leads to age-related neurodegenerationPreprint

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