The Role of PARP-1 and PARP-2 Enzymes in Metabolic Regulation and Disease

Circadian Control of the NAD + Salvage Pathway by CLOCK-SIRT1

Nakahata, Y., Sahar, S., Astarita, G., Kaluzova, M., & Sassone-Corsi, P. (2009) · Science · doi:10.1126/science.1170803 · Cited by 1,198

The secret life of NAD+: an old metabolite controlling new metabolic signaling pathways

Houtkooper, R. H., Cantó, C., Wanders, R. J., & Auwerx, J. (2010) · Endocrine Reviews · doi:10.1210/er.2009-0026 · Cited by 899

The PARP Side of the Nucleus: Molecular Actions, Physiological Outcomes, and Clinical Targets

Krishnakumar, R., & Kraus, W. L. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.06.017 · Cited by 877

PARP-1 inhibition increases mitochondrial metabolism through SIRT1 activation

Bai, P., Cantó, C., Oudart, H., Brunyánszki, A., Cen, Y., Thomas, C., Yamamoto, H., Huber, A., Kiss, B., Houtkooper, R. H., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.03.004 · Cited by 837

Mice lacking the poly(ADP-ribose) polymerase gene are resistant to pancreatic beta-cell destruction and diabetes development induced by streptozocin

Burkart, V., Wang, Z., Radons, J., Heller, B., Herceg, Z., Stingl, L., Wagner, E. F., & Kolb, H. (1999) · Nature Medicine · doi:10.1038/6535 · Cited by 371

Poly(ADP-ribose) polymerase 1 participates in the phase entrainment of circadian clocks to feeding

Asher, G., Reinke, H., Altmeyer, M., Gutierrez-Arcelus, M., Hottiger, M. O., & Schibler, U. (2010) · Cell · doi:10.1016/j.cell.2010.08.016 · Cited by 340

SIRT1 Promotes Cell Survival under Stress by Deacetylation-Dependent Deactivation of Poly(ADP-Ribose) Polymerase 1

Rajamohan, S. B., Pillai, V. B., Gupta, M., Sundaresan, N. R., Birukov, K. G., Samant, S. A., Hottiger, M. O., & Gupta, M. P. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00121-09 · Cited by 313

PARP-2 Regulates SIRT1 Expression and Whole-Body Energy Expenditure

Bai, P., Cantó, C., Brunyánszki, A., Huber, A., Szántó, M., Cen, Y., Yamamoto, H., Houten, S. M., Kiss, B., Oudart, H., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.03.013 · Cited by 260

Amelioration of Diabetes Mellitus in Partially Depancreatized Rats by Poly(ADP-ribose) Synthetase Inhibitors: Evidence of Islet B-Cell Regeneration

Yonemura, Y., Takashima, T., Miwa, K., Miyazaki, I., Yamamoto, H., & Okamoto, H. (1984) · Diabetes · doi:10.2337/diab.33.4.401 · Cited by 170

Metabolism and Receptor Mechanisms of Niacin Action

Boronovskiy, S. E., Сергеевна, К. В., & Nartsissov, Y. R. (2024) · Cell and Tissue Biology · doi:10.1134/s1990519x23700025 · Cited by 12

Beyond monotherapy: An era ushering in combinations of PARP inhibitors with immune checkpoint inhibitors for solid tumors

Zhou, L., Wan, Y., Zhang, L., Meng, H., Yuan, L., Zhou, S., Cheng, W., & Jiang, Y. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116733 · Cited by 10

Biological Functions and Therapeutic Potential of NAD+ Metabolism in Gynecological Cancers

Myong, S., Nguyen, A. Q., & Challa, S. (2024) · Cancers · doi:10.3390/cancers16173085 · Cited by 10

PARylation-mediated post-transcriptional modifications in cancer immunity and immunotherapy

Matsumoto, K., Matsumoto, Y., & Wada, J. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1537615 · Cited by 11

Clinical application of PARP inhibitors and emerging strategies to overcome resistance: a pan-cancer perspective

Xiang, J., Li, J., Guo, Z., Wu, J., Ma, D., Xu, H., Shang, T., Pu, P., Cong, L., Zhou, R., et al. (2026) · Biomarker Research · doi:10.1186/s40364-026-00908-0 · Cited by 11

Impact of the Cellular Zinc Status on PARP-1 Activity and Genomic Stability in HeLa S3 Cells

Wedler, N., Matthäus, T., Strauch, B. M., Dilger, E., Waterstraat, M., Mangerich, A., & Hartwig, A. (2021) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.0c00452 · Cited by 10

Nicotinamide metabolism alterations in bladder cancer: Preliminary studies

Mierzejewska, P., Gawlik-Jakubczak, T., Jabłońska, P., Czajkowski, M., Kutryb-Zając, B. A., Smolenski, R. T., Matuszewski, M., & Slominska, E. M. (2018) · Nucleosides Nucleotides & Nucleic Acids · doi:10.1080/15257770.2018.1535124 · Cited by 10

An Update on Poly(ADP-ribose) Polymerase I-A Brief Review

Negi, P., Lakshmanan, K., Patel, P. K., Rajagopal, K., & Byran, G. (2023) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557523666230221145844 · Cited by 9

Organelle Communication with the Nucleus

Sengupta, S., & Levy, D. L. (2024) · Results and problems in cell differentiation · doi:10.1007/978-3-031-62036-2_1 · Cited by 10

Adaptive regulation of glycerophospholipid metabolism

Zhang, T., Wang, Y., & Ye, C. (2026) · Journal of Cell Science · doi:10.1242/jcs.264300 · Cited by 9

Potential Therapeutic Interventions Targeting NAD+ Metabolism for ALS

Lundt, S., & Ding, S. (2024) · Cells · doi:10.3390/cells13171509 · Cited by 12

Overexpression of NLRC3 enhanced inhibition effect of sevoflurane on inflammation in an ischaemia reperfusion cell model

Li, W., Zhang, Y., Hu, Z., & Xu, Y. (2020) · Folia Neuropathologica · doi:10.5114/fn.2020.100064 · Cited by 9

Association of common SNP rs1136410 in PARP1 gene with the susceptibility to male infertility with oligospermia

Chen, H., Pu, X.-Y., Zhang, R.-P., & Zhou-Cun, A. (2014) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-014-0311-3 · Cited by 9

In Silico Investigation of Potential PARP‐1 Inhibitors from Traditional Chinese Medicine

Chen, K., Sun, M.-F., & Chen, C. Y. (2014) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2014/917605 · Cited by 9

Transcriptional Regulation of the Human Genes that Encode DNA Repair- and Mitochondrial Function-Associated Proteins

Uchiumi, F., Larsen, S. H., & Tanuma, S. (2015) · InTech eBooks · doi:10.5772/59588 · Cited by 10

MicroRNAs Emerge as Modulators of NAD+-Dependent Energy Metabolism in Skeletal Muscle

Svensson, K., & Handschin, C. (2014) · Diabetes · doi:10.2337/db14-0166 · Cited by 9

Dynamics of blood NAD and glutathione in health, disease, aging, and under NAD+-booster treatment

Euro, L., Haimilahti, K., Jansson, S., Forsström, S., Buzková, J., & Suomalainen, A. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104343 · Cited by 9

Is NAD+ a key factor in ovarian aging and dysfunction? Insights and uncertainties from current research

Cordone, V., Vergara, T., Falone, S., Tatone, C., & Emidio, G. D. (2025) · Biology of Reproduction · doi:10.1093/biolre/ioaf140 · Cited by 8

Increased PARP Activity and DNA Damage in NSCLC Patients: The Influence of COPD

Tang, J., Curull, V., Wang, X., Ampurdanés, C., Durán, X., Pijuán, L., Rodríguez-Fuster, A., Aguiló, R., Yélamos, J., & Barreiro, E. (2020) · Cancers · doi:10.3390/cancers12113333 · Cited by 7

Sex Stratified Neuronal Cultures to Study Ischemic Cell Death Pathways

Fairbanks, S. L., Vest, R. S., Verma, S., Traystman, R. J., & Herson, P. S. (2013) · Journal of Visualized Experiments · doi:10.3791/50758 · Cited by 7

Determination of the relationship between class IV sirtuin genes and growth traits in Chinese black Tibetan sheep

Ma, B., Khan, R., Raza, S. H. A., Gao, Z., Hou, S., Ullah, F., Hassan, M. M., Hassan, M. M., AlGabbani, Q., Alotaibi, M. A., et al. (2021) · Animal Biotechnology · doi:10.1080/10495398.2021.2016434 · Cited by 7

PARP1 911

Bock, F. J., & Chang, P. (2015) · Nature Chemical Biology · doi:10.1038/nchembio.1756 · Cited by 7

Prior heat stress induces moderation of diabetic alterations in glycogen metabolism of rats

Miova, B., Dinevska-Ќovkarovska, S., Djimrevska, A., & Mitev, S. (2013) · Open Life Sciences · doi:10.2478/s11535-013-0260-3 · Cited by 7

In VivoNMR Spectroscopy – Static Aspects

de Graaf, R. A. (2018) · doi:10.1002/9781119382461.ch2 · Cited by 7

Negative ion formation and fragmentation upon dissociative electron attachment to the nicotinamide molecule

Ziegler, P., Pelc, A., Arthur‐Baidoo, E., Ameixa, J., Ončák, M., & Denifl, S. (2021) · RSC Advances · doi:10.1039/d1ra06083j · Cited by 7

Development of New Cancer Treatment by Identifying and Focusing the Genetic Mutations or Altered Expression in Gynecologic Cancers

Tang, Y., Lin, C., & Lai, C. (2021) · Genes · doi:10.3390/genes12101593 · Cited by 5

NAD+ Kinase Enzymes Are Reversible, and NAD+ Product Inhibition Is Responsible for the Observed Irreversibility of the Human Enzyme

Willett, E., Jiang, V., Koder, R. L., & Banta, S. (2022) · Biochemistry · doi:10.1021/acs.biochem.2c00386 · Cited by 6

Serum-dependent and -independent regulation of PARP2

Sun, Q., Gatie, M. I., & Kelly, G. M. (2019) · Biochemistry and Cell Biology · doi:10.1139/bcb-2018-0345 · Cited by 6

siRNA targeting PARP-1 alleviates diabetic peripheral neuropathy in a streptozotocin-induced rat model

Redhwan, M. A. M., Hariprasad, M. G., Samaddar, S., Bafail, D. A., Hard, S. A. A. A., Guha, S., & Dhavale, A. (2024) · Journal of drug targeting · doi:10.1080/1061186x.2024.2431316 · Cited by 7

How ligands regulate the binding of PARP1 with DNA: Deciphering the mechanism at the molecular level

Wang, K., Wu, Y., Lai, L., Wang, X., & Sun, S. (2023) · PLoS ONE · doi:10.1371/journal.pone.0290176 · Cited by 5

PARP inhibition leads to synthetic lethality with key splicing-factor mutations in myelodysplastic syndromes

Zhang, F., Sun, J., Zhang, L., Li, R., Wang, Y., Geng, H., Shen, C., Li, L., & Chen, L. (2024) · British Journal of Cancer · doi:10.1038/s41416-024-02729-0 · Cited by 5

Expression profile of key genes involved in DNA repair mechanisms in bovine cumulus cells cultured with bovine serum albumin or fetal calf serum

Goetten, A. L. F., Koch, J., Rocha, C. C., Mezzalira, A., Price, C. A., Portela, V. M., & Barreta, M. H. (2022) · Reproductive Biology · doi:10.1016/j.repbio.2022.100709 · Cited by 4

Pyrazole Substituted 9-Anilinoacridines as HER2 Inhibitors Targeting Breast Cancer - An in-silico approach

Rajagopal, K., Sri, V. B., Byran, G., & Swaminathan, G. (2021) · Current Drug Research Reviews · doi:10.2174/2589977513666210617160302 · Cited by 5

Methods of PARP-1 Determination and its Importance in Living Organisms

Zielińska, Z., Ołdak, Ł., & Gorodkiewicz, E. (2022) · Protein and Peptide Letters · doi:10.2174/0929866529666220405160715 · Cited by 5

Harnessing NAD+ Metabolism as Therapy for Cardiometabolic Diseases

Chakraborty, A. D., Minor, K., Nizami, H. L., Chiao, Y. A., & Lee, C. F. (2022) · Current Heart Failure Reports · doi:10.1007/s11897-022-00550-5 · Cited by 6

Nicotinamide adenine dinucleotide attenuates acetaminophen-induced acute liver injury via activation of PARP1, Sirt1, and Nrf2 in mice

Liao, C., Zhang, L., Jiang, R., Da, H., Xu, J., Hu, K., Jiang, S., Li, L., Yang, Y., Huang, J., et al. (2022) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2022-0127 · Cited by 5

Acute nicotinamide riboside supplementation increases human cerebral NAD + levels in vivo

Nanga, R. P. R., Wiers, C. E., Elliott, M. A., Wilson, N. E., Liu, F., Cao, Q., Swago, S., Jacobs, P. S., Armbruster, R. R., Reddy, D., et al. (2024) · Magnetic Resonance in Medicine · doi:10.1002/mrm.30227 · Cited by 4

Zelluläre Mikroskopie der Poly(ADP‐Ribos)ylierung von Proteinen in Echtzeit

Buntz, A., Wallrodt, S., Gwosch, E., Schmalz, M. F., Beneke, S., Ferrando‐May, E., Marx, A., & Zumbusch, A. (2016) · Angewandte Chemie · doi:10.1002/ange.201605282 · Cited by 4

Increased SIRT3 combined with PARP inhibition rescues motor function of SBMA mice

Castro, D. R. G., Mazuk, J. R., Heine, E. M., Simpson, D., Pinches, R. S., Lozzi, C., Hoffman, K. L., Morrin, P., Mathis, D., Lebedev, M. V., et al. (2023) · iScience · doi:10.1016/j.isci.2023.107375 · Cited by 4

Anemonin ameliorates human diploid fibroblasts 2BS and IMR90 cell senescence by PARP1-NAD+-SIRT1 signaling pathway

Zhao, L., Hu, K., Liu, W.-T., Qi, H., Li, G., Chen, J., & Han, L. (2023) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2023.105255 · Cited by 4

Gal‐1 promotes lung cancer cell survival by enhancing PARP1 / H1 .2 interaction to promote DNA repair upon DNA damage response

Chen, Y., Liu, X., Li, B., Xie, X., Jin, X., & Sun, H. Z. (2025) · FEBS Journal · doi:10.1111/febs.70134 · Cited by 4

Fer and FerT: A New Regulatory Link between Sperm and Cancer Cells

Nir, U., Grinshtain, E., & Breitbart, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065256 · Cited by 4

PARP inhibitors target cellular energy metabolism: Mechanisms of action and clinical implications

Li, J., Mu, D., Jin, L. P., Lan, M., Wu, W., Zhang, S., & Dai, Y. (2026) · Translational Oncology · doi:10.1016/j.tranon.2026.102757 · Cited by 4

Therapeutic Potential of ACMSD Inhibitors in NAD+ Deficient Diseases

Chen, M., Zhang, H., & Ji, P. (2025) · Drugs and Drug Candidates · doi:10.3390/ddc4010007 · Cited by 3

NAD+ Boosting Strategies

Rice, J., Lautrup, S., & Fang, E. F. (2024) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-031-66768-8_4 · Cited by 4

SIRT1 in Metabolic Health and Disease

Boutant, M., & Cantó, C. (2016) · Springer eBooks · doi:10.1007/978-94-024-0962-8_4 · Cited by 3

In Silico Family-Wide Profiling and 3D Modelling of the Poly(ADP-Ribose) Polymerase Superfamily

Kam, C. M. T., Tauber, A. L., Oosthuizen, D. L., Levonis, S. M., & Schweiker, S. S. (2020) · Future Medicinal Chemistry · doi:10.4155/fmc-2020-0274 · Cited by 3

Correlation of poly (adenosine diphosphate[ADP]-ribose) polymerase expression and prognosis in ovarian cancer: A systematic review and meta-analysis

Zhang, J., Wei, Z., & Zhang, Z. (2022) · Journal of Gynecology Obstetrics and Human Reproduction · doi:10.1016/j.jogoh.2022.102344 · Cited by 3

Modification Effect of PARP4 and ERCC1 Gene Polymorphisms on the Relationship between Particulate Matter Exposure and Fasting Glucose Level

Kim, J. H., Lee, S., & Hong, Y. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19106241 · Cited by 3

Network of nicotinamide mononucleotide biosynthesis: substrate tracking, rate-limiting enzyme, and regulatory strategy

Zhang, P., Ye, Z., Tian, Z., Liu, Q., & Huang, Y. (2025) · Synthetic and Systems Biotechnology · doi:10.1016/j.synbio.2025.04.005 · Cited by 2

Uridine 5’-monophosphate (UMP) synthesis connects nucleotide metabolism to programmed cell death in C. elegans

Jiang, H.-S., Han, H., Chen, C., Hsu, K.-L., Kan, H.-T., Lin, W., Wu, M.-H., Tsai, S., Wu, J.-C., & Wu, Y. (2025) · Cell Death and Differentiation · doi:10.1038/s41418-025-01564-x · Cited by 2

Mechanisms of NAD+ Homeostasis in Aging and Disease

McReynolds, M. R. (2026) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-112525-013335 · Cited by 2

Metabolic exhaustion and immune ageing in rheumatoid arthritis

Weyand, C. M., & Goronzy, J. J. (2026) · Nature Reviews Rheumatology · doi:10.1038/s41584-026-01402-5 · Cited by 2

A Cytological Atlas of the Human Liver Proteome from PROTEOMESKY-LIVERHu 2.0, a Publicly Available Database

Lao, Y., Li, Y., Wang, W., Ren, L., Qian, X., He, F., Chen, X., & Jiang, Y. (2022) · Journal of Proteome Research · doi:10.1021/acs.jproteome.2c00190 · Cited by 2

Nicotinamide Mononucleotide Alleviates Angiotensin II-Induced Human Aortic Smooth Muscle Cell Senescence in a Microphysiological Model

Yin, X., Abudupataer, M., Yang, M., Xiang, B., Lai, H., Wang, C., Li, J., & Zhu, K. (2023) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000001400 · Cited by 2

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

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

Regulatory Roles of PARP-1 and Lipids in Epigenetic Mechanisms

Mennella, M. R. F., Masi, A., & Ferreri, C. (2017) · Springer eBooks · doi:10.1007/978-3-319-31143-2_37-1 · Cited by 2

Design, Synthesis and Evaluation of Potential Inhibitors for Poly(ADP-Ribose) Polymerase Members 1 and 14

Kam, C. M. T., Tauber, A. L., Levonis, S. M., & Schweiker, S. S. (2020) · Future Medicinal Chemistry · doi:10.4155/fmc-2020-0218 · Cited by 2

Role of Poly(ADP-Ribose) in Catalyzing Starvation-Induced Autophagy

Rodríguez-Vargas, J. M., & Oliver, F. J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-805421-5.00003-3 · Cited by 2

Pharmacological Approaches for Modulating Sirtuins

Kane, A. E., & Sinclair, D. A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813499-3.00006-x · Cited by 2

Poly (ADP-ribose) Polymerase Inhibition in Advanced Urothelial Carcinoma

Tripathi, A., & Lerner, S. P. (2023) · JCO Precision Oncology · doi:10.1200/po.23.00293 · Cited by 2

Novel inhibitors of PARP1 and PARP14: design, synthesis, and potentiation of cisplatin efficacy in cancer

Kam, C. M. T., Tauber, A. L., Zunk, M., McDermott, C., Levonis, S. M., & Schweiker, S. S. (2024) · Future Medicinal Chemistry · doi:10.1080/17568919.2024.2437972 · Cited by 1

Oxidative stress-induced proinflammatory secretion from retinal pigment epithelium disrupts NAD+ metabolism via CD38 on macrophages leading to immune microenvironment dysregulation

Lin, R., Liang, F., Hu, C., Jiang, L., Wan, Z., Xu, Z., Luo, Y., Ma, J., Wu, Y., Cai, W., et al. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.11.041 · Cited by 1

The effect of obesity and aging on NAD+/Sirtuin metabolism transcription and DNA methylation in subcutaneous adipose tissue of monozygotic twin pairs discordant for BMI

Lapatto, H. A. K., van der Kolk, B. W., Muniandy, M., Heinonen, S., Heikkinen, A., Alvarez, M., Lee, S. H., Jokinen, R., Lundbom, J., Kuula, J., et al. (2026) · International Journal of Obesity · doi:10.1038/s41366-025-02007-w · Cited by 1

Auto-Modification of Poly (ADP-Ribose) Polymerase and Membrane Lipid Composition as Diagnostic Tools to Measure the Physio-Pathological State of the Cell

Bianchi, A. R. (2014) · Journal of Microbial & Biochemical Technology · doi:10.4172/1948-5948.1000148 · Cited by 1

Poly(ADP-Ribose) Polymerases-Inhibitor Talazoparib Inhibits Muscle Atrophy and Fatty Infiltration in a Tendon Release Infraspinatus Sheep Model: A Pilot Study

Olthof, M. G. L., Hasler, A., Valdivieso, P., Flück, M., Gerber, C., Gehrke, R. S., Klein, K., von Rechenberg, B., Snedeker, J. G., & Wieser, K. (2024) · Metabolites · doi:10.3390/metabo14040187 · Cited by 1

The Rate of NAD+ Breakdown Is Maintained Constant against Deletion or Overexpression of NAD+-Degrading Enzymes in Mammalian Cells

Hara, N., Osago, H., Hiyoshi, M., & Kobayashi‐Miura, M. (2024) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.70.295 · Cited by 1

Oxidative stress and PARP activation in the lungs is an early event in COVID-19 pneumonia

Juhász, P., Bohus, P., Sipos, A., Curtin, N. J., Méhes, G., & Bai, P. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.06.010 · Cited by 1

Toxicoproteomic Analysis of Poly(ADP-Ribose)-Associated Proteins Induced by Oxidative Stress in Human Proximal Tubule Cells

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Regulatory Roles of PARP-1 and Lipids in Epigenetic Mechanisms

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Insulin Signaling, Epigenetics, and Human Diseases

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The effects of acute nicotinamide riboside supplementation on substrate utilisation and 5km time-trial performance

Gray, E. L. (2019) · University of Birmingham Institutional Research Archive (University of Birmingham) · Cited by 1

A Case Study of Familiar Gastrointestinal Pathologies at Risk of Cancer. Early Detection of Degenerative Signals by Oxidative Stress BiomarkersPreprint

Ferreri, C., Marone, M., Confalone, E., Maio, A. D., Chatgilialoglu, C., & Mennella, M. R. F. (2019) · Preprints.org · doi:10.20944/preprints201912.0390.v1 · Cited by 1

Role of Inflammation and Inflammasomes in Bone Pathophysiology

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A Case Study of Familiar Gastrointestinal Pathologies at Risk of Cancer. Early Detection of Degenerative Signals by Oxidative Stress BiomarkersPreprint

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The Involvement of Anti-Oxidative Response and Mitochondrial Dynamics in the Pathogenesis of Friedreich’s Ataxia: Relevance to the Development of Future Therapeutics

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Identification of Poly(ADP-Ribose)-Associated Proteins and their Potential Role in ROS-Mediated Cell Death

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A Cytological Atlas of Human Liver Proteome from PROTEOME SKY-LIVER Hu 2.0, A Publicly Available DatabasePreprint

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