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Protein S-nitrosylation: a physiological signal for neuronal nitric oxide

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S-nitrosylated GAPDH initiates apoptotic cell death by nuclear translocation following Siah1 binding

Hara, M. R., Agrawal, N., Kim, S. F., Cascio, M. B., Fujimuro, M., Ozeki, Y., Takahashi, M., Cheah, J. H., Tankou, S. K., Hester, L. D., et al. (2005) · Nature Cell Biology · doi:10.1038/ncb1268 · Cited by 1,079

Inhibition of GAPDH activity by poly(ADP-ribose) polymerase activates three major pathways of hyperglycemic damage in endothelial cells

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Protein S-nitrosylation in health and disease: a current perspective

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Dynamic rerouting of the carbohydrate flux is key to counteracting oxidative stress

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S Phase Activation of the Histone H2B Promoter by OCA-S, a Coactivator Complex that Contains GAPDH as a Key Component

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GAPDH and Autophagy Preserve Survival after Apoptotic Cytochrome c Release in the Absence of Caspase Activation

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Sequence-Specific Binding of Transfer RNA by Glyceraldehyde-3-Phosphate Dehydrogenase

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Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH

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Molecular basis of NMDA receptor-coupled ion channel modulation by S-nitrosylation

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Molecular insights of immune evasion by Orf Virus: the interaction and functional impact of viral OH1 phosphatase on STAT1

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A validated in vitro approach for low-frequency alternating-current stimulation of stem cells: From electrode characterization to biological responses

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Angiotensin-Converting Enzyme in Patients With Early-Stage Psychosis

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Allergenicity assessment of fungal species using immunoclinical and proteomic techniques: a study on Fusarium lateritium

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Proteomic profiling of thyroid tissue in patients with obesity and benign diffuse goiter

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Environmental oxygen affects ex vivo growth and proliferation of mesenchymal progenitors by modulating mitogen-activated protein kinase and mammalian target of rapamycin signaling

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Identification of Protein Targets of S-Nitroso-Coenzyme A-Mediated S-Nitrosation Using Chemoproteomics

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The O-GlcNAcylation of β-actin Ser199 controls nuclear speckle localization and is dysregulated in diabetes

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Cancer Metabolism: A Nexus of Matter, Energy, and Reactive Oxygen Species

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Mind the GAP : Purification and characterization of urea resistant GAPDH during extreme dehydration

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Genomic Organization, Tissue Distribution and Developmental Expression of Glyceraldehyde 3-Phosphate Dehydrogenase Isoforms in Mud Loach Misgurnus mizolepis

Lee, S. Y., Kim, D. S., & Nam, Y. K. (2013) · Fisheries and aquatic sciences · doi:10.5657/fas.2013.0291 · Cited by 2

Ethanol and Acetaminophen Synergistically Induce Hepatic Aggregation and TCH346-Insensitive Nuclear Translocation of GAPDH

Snider, N. T., Portney, D. A., Willcockson, H. H., Maitra, D., Martin, H. C., Greenson, J. K., & Omary, M. B. (2016) · PLoS ONE · doi:10.1371/journal.pone.0160982 · Cited by 2

Cryoprotective Effect of Pyrano-[2,3-C]-Pyrazoles on H2O2 Induced Damage in Tetrahymena thermophila

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The glia club: Validation of polarization biomarkers for human microglia (HMC3) using quantitative real time RT-qPCRPreprint

Franck, E., Storm, J. A., Lu, J., Obtial, M. F., & Wijenayake, S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.26.615202 · Cited by 3

A modular genetic code expansion approach to site-specific lysine acylations

Knecht, P., Nguyen, T.-A., & Lang, K. (2026) · Chem · doi:10.1016/j.chempr.2025.102919 · Cited by 2

The Unique Role of Sperm-Specific GAPDH

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The Highlighted Role of GAPDH and Nitric-Oxide Synthase Regulator Activity in Proton Beam Irradiated Melanoma BLM Cells

Zadeh-Esmaeel, M.-M., Shahrokh, S., Azodi, M. Z., & Ahmadi, N. (2019) · Journal of lasers in medical sciences · doi:10.15171/jlms.2019.s13 · Cited by 1

Transcriptomic Insights into Post-Spawning Death and Muscle Atrophy in Ayu (Plecoglossus altivelis)

Liang, J., Fujisawa, M., Toma, S., Asakawa, S., Yoshitake, K., Igarashi, Y., Saito, S., Akutsu, T., Suzuki, K., & Kinoshita, S. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020434 · Cited by 1

Light-evoked activity and BDNF regulate mitochondrial dynamics and mitochondrial localized translation in CNS axons

Kreymerman, A., Weinstein, J. E., Vadgama, N., Shah, S. H., Nahmou, M. M., Belle, K. C., Ji, M. H., Xia, X., Faust, A. E., van der Merwe, Y., et al. (2025) · iScience · doi:10.1016/j.isci.2025.113563 · Cited by 1

Evaluation of Salivary GAPDH as a Predictor Biomarker for Periodontitis

Bellei, E., Bergamini, S., Salvatori, R., & Bertoldi, C. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262110441 · Cited by 1

Multifunctional glyceraldehyde-3-phosphate dehydrogenase (GAPDH) of parasites

Mishra, P., & Joshi, P. (2026) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2026.111732 · Cited by 1

Transcriptome analysis for growth-related genes and SNPs in the Indian catfish Clarias magur

Haldar, C., Ram, R., Pavan‐Kumar, A., Gireesh-Babu, P., KORINGA, P. G., Joshi, C., & Chaudhari, A. (2026) · Aquaculture · doi:10.1016/j.aquaculture.2026.743769 · Cited by 1

In Silico Design and Evaluation of TcGAPDH as a Vaccine Against Chagas Disease: A Reverse Vaccinology Approach

Nava-Cuamatzi, V., Buendia-Corona, R. E., González‐Vázquez, M. C., Cedillo-Ramirez, M. L., & Carabarín‐Lima, A. (2026) · Acta Parasitologica · doi:10.1007/s11686-026-01221-4 · Cited by 1

In Vitro Monitoring of NADH Level in Induced NAFLD Cell Model and Diseased Liver Tissues Using an Organoselenium‐Based Molecular Probe Through Fluorescence Imaging

Dhingra, P., Jaswal, K., Biswas, B., Mondal, I. C., Abebe, A., Sen, A., Mondal, P., & Ghosh, S. (2026) · ChemPhotoChem · doi:10.1002/cptc.202500332 · Cited by 1

From pathology to precision therapy: Contemporary and emerging strategies in Alzheimer's disease treatment

Belavadi, S., & Kadiri, S. K. (2026) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2026.178913 · Cited by 1

Cryptic DNA sequences encode a temperature sensor to regulate mitochondrial suicide during neuronal differentiation

Vujovic, F., Simonian, M. R., Quek, L., Peng, K., Hunter, N., & Farahani, R. H. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-02914-z · Cited by 1

Electrospun Nanofiber Scaffolds for In Vitro 3D Tissue Engineering

Santillan, V. E., Hanumantharao, S. N., Bule, S., Shrestha, R. M., Rodzik, C., Estrada, A. M., Farias, S. L., Tanasova, M., & Rao, S. (2026) · Fibers · doi:10.3390/fib14060065 · Cited by 1

3-Hydroxypropionic acid converts inflammatory macrophage glycolysis into mitochondrial oxidation through GAPDH carboxyethylation

Wu, K., Jia, Y., Lin, Q., Wang, F., Liu, T., Gao, M., Gao, B., Zhu, Y., Xiong, S., Sun, D., et al. (2026) · iScience · doi:10.1016/j.isci.2026.116258 · Cited by 1

Controlled Generation of Dehydroascorbic Acid: A New Mechanistic Framework for High-Dose Vitamin C Anticancer Therapy

Peskin, A. V. (2026) · Cells · doi:10.3390/cells15131212 · Cited by 1

Six Dehydrogenase Gatekeepers of Carbohydrate Metabolism: Metabolic Integration in Health and Disease

Papaneophytou, C. P., & Petrou, C. C. (2026) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl49369 · Cited by 1

A Function-Centric Framework for Mitochondrial Quality Control

Ozcan, F., Vujovic, F., & Farahani, R. H. (2026) · Biomolecules · doi:10.3390/biom16081116 · Cited by 1

ABA-mediated salt tolerance in Astragalus cicer: From physiological-biochemical responses to key regulatory networks identified by transcriptome profiling and WGCNA

Dong, W., Ma, F., Zhang, Y., Nai, G., Zhao, C., Zhang, Y., & Shi, X. (2026) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2026.111635 · Cited by 1

Differential expression of trypsin-3 and phosrestin II genes in the main malaria vector, Anopheles darlingi, from the Brazilian Amazon region

Ohse, C, K., Matiolli, C. C., C, C., Scarpassa, V. M., Vorholt, S. M., Santos, Volokitina, D. S., Tadei, Wendry Setyadi, P., et al. (2017) · Genetics and Molecular Research · doi:10.4238/gmr16039852 · Cited by 1

Structure-Function Analysis Glyceraldehyde-3-Phosphate Dehydrogenase Homologue GapB in Staphylococcus aureus

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Molecular phylogenetic and in silico analysis of glyceraldeyde-3-phosphate dehydrogenase (GAPDH) gene from northern bobwhite quail (Colinus virginianus)

Kalyanasundaram, A., Henry, B. J., Henry, C., & Kendall, R. J. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-06186-3 · Cited by 1

Evaluation of reference genes suitable for studying mRNAs and microRNAs expression in thyroid neoplasms

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Moonlighting Proteins: Importance and Current Scenarios

Martelli, A. C. F. S., Brambila, B., Barcelos, M. P., Zandonadi, F. D. S., Antão, S. C., Alexandrino, A. V., da Silva, C. H. T. D. P., & Novo‐Mansur, M. T. M. (2024) · Engineering materials · doi:10.1007/978-3-031-75984-0_10 · Cited by 1

Measurements of acrolein adducts resulting from polyamine catabolism

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ANALYSIS OF HOUSEKEEPING GENE STABILIZATION IN ISOLATED MITOCHONDRIA

Ülger, Ö., Fatsa, T., ÖREN, S., & ELÇİ, M. P. (2025) · Ankara Universitesi Eczacilik Fakultesi Dergisi · doi:10.33483/jfpau.1596860 · Cited by 1

Genotoxic effects and transcriptional deregulation of genetic biomarkers in Chironomus riparius larvae exposed to hydroxyl- and amine-terminated generation 3 (G3) polyamidoamine (PAMAM) dendrimers

Planelló, R., Rosal, R., Aquilino, M., & Herrero, Ó. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.145828 · Cited by 1

Affinity‐Driven Covalent Modulator of the Glyceraldehyde‐3‐Phosphate Dehydrogenase (GAPDH) Cascade

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Amelioration for an ignored pitfall in reference gene selection by considering the mean expression and standard deviation of target genes

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The detection of two plasmodium falciparum metabolic enzymes using chicken antibodies.

Krause, R. (2012) · ResearchSpace (University of KwaZulu-Natal) · Cited by 1

Molecular steps towards improving prognosis in ovarian cancer

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Native E. coli Glyceraldehyde 3-phosphate dehydrogenase

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Sunshinevirus in Australian snakes: Investigating the link with disease

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Glucose Regulation of Novel Protein Complexes with Potential Roles in the Metabolic Reprogramming of Human Leukemia Cells

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Protein Moonlighting and New Thoughts about Protein Evolution

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Genetic landscape of DNMT3A R882H reveals mechanism of aberrant oligomerizationPreprint

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Characterisation of the novel TPI-GAPDH fusion enzyme in Blastocystis hominis

Evans, K. (2014) · University of Bedfordshire Repository (University of Bedfordshire) · Cited by 1

Reprogramming of energy metabolism by oncogenic Marek's disease virus (MDV) in chicken embryo fibroblasts (CEFs)

Siano, N. (2025) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/8brr-wk43 · Cited by 1

Die kritische Rolle von EPO auf das Überleben, die Funktionalität und die neuronale Differenzierung von mesenchymalen Stammzellen unter neurotoxischen Bedingungen

Schmitt, A. (2013)

Purification and Characterization of Novel Denitrosylases from Yeast and Mammals

Anand, P. (2012) · DukeSpace (Duke University)

Cell Signalling and Pathways Explained in Relation to Music and Musicians

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Caracterização do proteoma nuclear de folhas de cana-de-açúcar (Saccharum spp) de 1 e 4 meses de idade

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The role of NAG-1 in Tumorigenesis

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A conexina 26 e sua relação com outras proteínas no órgão de Corti

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Autophagy in Necrosis: A Force for Survival

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Insights into molecular mechanisms contributing to individual susceptibility to steatohepatitis: Lessons learned from mouse models

Snider, N. T., Weerasinghe, S. V., Singla, A., Leonard, J. M., Hanada, S., & Andrews, P. C. (2012) · Hepatology · doi:10.1002/hep.25707

Effect of the nanohydroxyapatite Formulation NanoXIM.HAp102 on the Proliferation and Osteogenic Differentiation of Human Bone Mesenchymal Stem Cells

Marina, E., & Pires, N. (2013)

Epigenetic basis for the oncogenic potential of IDH mutations

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Caracterização de interações proteína-DNA em tripanossomas.

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Hepatitis Delta Virus: Identification of Host Factors Involved in the Viral Life Cycle, and the Investigation of the Evolutionary Relationship Between HDV and Plant Viroids

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Nuclear Translocation of GAPDH in Retinal Ganglion Cells is an Early Event in Diabetic

Fujikawa, A., & Miyata, Y. (2014)

Reactive dopamine metabolites and neurotoxicity

Vanle, B., Doorn, J. A., Duffel, M. W., Quinn, D. M., Roman, D. L., & Kerns, R. J. (2016) · doi:10.17077/etd.28c5nhya

Proteomics of Sub-cellular Protein Distribution in Oestrogen and Tamoxifen Stimulated MCF-7 Breast Cancer Cells

Alkhanjaf, A. A. M. (2016) · UCL Discovery (University College London)

Proteômica da matriz nuclear espermática suína

de Mendonça, G. S. (2015) · doi:10.14393/ufu.di.2015.325

Lactate dehydrogenase is C-terminally extended by stop codon read-through which targets this isoform into the peroxisomes

George, R. (2016) · doi:10.53846/goediss-5796

Moonlighting GAPDH and Age-Related Neurodegenerative Disease

Sirover, M. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809852-3.00012-1

S-Nitrosothiol Metabolism in Cancer and Therapeutic Implications

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Nitric-Oxide-Mediated Chemosensitization: Gene Therapy Versus Exogenous Introduction of NO Donors

Edwards, M. A., Alshiraihi, I., Schmidt, C., Storsberg, J., & Brown, M. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-811020-1.00001-6

Protection, adaptation or cell death as response to toxins

Sthijns, M. M. J. P. E. (2017) · doi:10.26481/dis.20170915ms

Doberman Hepatitis : Role of Immunological and Genetic Mechanisms

Dyggve, H. (2017) · Työväentutkimus Vuosikirja

Regulation of Skeletal Muscle Carbohydrate Metabolism During Mammalian Hibernation

Bell, R. A. V. (2014) · doi:10.22215/etd/2014-10455

Nuclear matrix metalloproteinase-2 and investigation of its potential targets in myocardial ischemia-reperfusion injury

Baghirova, S. (2016) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3z892p4f

Characterisation of the streptococcal surface proteins, SEN and GAPDH, and their interaction with host molecules

Cork, A. J. (2011) · Research Online (University of Wollongong)

Impact of Toxoplasma gondii on STAT1 activity and epigenetic regulation during IFN-γ signaling of its host cell

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The Co-Transcriptional Response of Intracellular Group B Streptococcus (GBS) and Monocytes

Prince, D. (2019) · Griffith Research Online · doi:10.25904/1912/1117

Partial catalytic Cys oxidation of human GAPDH

Lia, A., Dowle, A., Taylor, C. F., Santino, A., & Roversi, P. (2020) · Wellcome Open Research · doi:10.12688/wellcomeopenres.15893.1 · Cited by 6

Unconventional ER to Endosomal Trafficking by a Retroviral ProteinPreprint

Xu, W. K., Gou, Y., Lozano, M. M., & Dudley, J. P. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.07.192815

Efecto de elicitores de origen biótico en la transcripción de algunos genes involucrados en los mecanismos de defensa del clavel Dianthus caryophyllus L. al patógeno Fusarium oxysporum f sp dianthi

Monroy-Mena, S. (2020)

Enzymatic Regulation in the Liver of the Freeze-Tolerant Wood Frog in Metabolically Depressed States

Saleem, R. (2020) · doi:10.22215/etd/2020-14149

Evaluation of Reference Genes for Expression Normalization in Psoralea Corylifolia L. under Abiotic StressPreprint

Zhong, Y., Gai, Y., Gao, J., Nie, W., Bao, Z., Wang, W., Xu, X., Wu, J., & He, Y. (2021) · Research Square · doi:10.21203/rs.3.rs-469808/v1

Neurons undergo pathogenic metabolic reprograming in models of familial ALSPreprint

Riechers, S., Mojsilovic‐Petrovic, J., Garjani, M., Medvedeva, V., Dalton, C., Dienel, G. A., & Kalb, R. G. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.20.457111

Identification of Post-translational Modifications of Plasmodium yoeliiGlyceraldehyde-3-phosphate dehydrogenase by Mass Spectrometry

(2017) · Advances in Proteomics and Bioinformatics · doi:10.29011/2690-0092.100003

Characterizing The Role of The Chloride/Bicarbonate Exchanger AE1 in Modulating Tight Junction Properties in Renal Collecting Duct Cells

Lashhab, R. (2021) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-s7b0-et70

GAPDH cooperativity mediates drug resistance and metabolism in Plasmodium fal-ciparum malaria parasitesPreprint

Jezewski, A. J., Guggisberg, A. M., Hodge, D. M., Ghebremichael, N., McLellan, L. K., & John, A. R. O. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.05.467329

Faculty Opinions recommendation of Posttranscriptional control of T cell effector function by aerobic glycolysis.

Berg, L. J. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718022061.793487248

Mitochondrial Proteomics and Transcriptional Analysis of Cytoplasmic Male Sterility in Sugar Beet using iTRAQ and qRT–PCRPreprint

Liu, T., Cheng, D., Han, X., Cui, J., Dai, C., Li, J., & Liang, N. (2022) · Research Square · doi:10.21203/rs.3.rs-1120889/v1

Lipid-mediated nuclear moonlighting of cytosolic glyceraldehyde-3-phosphate dehydrogenase in plant heat responsePreprint

Kim, S., Yao, S., Zhang, Q., & Wang, X. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.31.478510

Selection and Stability Validation of Reference Gene Candidates for Transcriptional Analysis in Rousettus AegyptiacusPreprint

Friedrichs, V., Balkema‐Buschmann, A., Dorhoi, A., & Pei, G. (2021) · Research Square · doi:10.21203/rs.3.rs-604945/v1

Verification of the Availability of Individual Proteins for Quantitative Analysis in Brains Preserved in Two Different Brain Banks Using GAPDH and GFAPPreprint

Nagaoka, A., Kunii, Y., Hino, M., Izumi, R., Shishido, R., Ishibashi, M., Hatano, M., Sainouchi, M., Kakita, A., & Yabe, H. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3929219

Activated Phosphoryl Groups and Biosynthetic Paths to ATP

(2020) · Royal Society of Chemistry eBooks · doi:10.1039/9781839162312-00177

Faculty Opinions recommendation of Nuclear moonlighting of cytosolic glyceraldehyde-3-phosphate dehydrogenase regulates Arabidopsis response to heat stress.

Leister, D., & Kleine, T. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738312265.793578695

The Effect of Deprenyl and Isatin Administration to Mice on the Proteomic Profile of Liver Isatin-Binding Proteins

Бунеева, О. А., Kopylov, A. T., Zgoda, V. G., & Medvedev, A. E. (2018) · Biochemistry (Moscow) Supplement Series B Biomedical Chemistry · doi:10.1134/s1990750818040108

Nuclear GAPDH in cortical microglia mediates stress-induced cognitive inflexibilityPreprint

Ramos, A., Ishizuka, K., Namkung, H., Hayes, L. N., Saito, A., Hayashida, A., Srivastava, R., Elkins, N., Palen, T., Carloni, E., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.21.497065

Myelin gene expression across murine post-natal brain development: Validating reliable QPCR methods

Smith, S. E. (2022) · doi:10.24124/2022/59339

The gene expression fluctuations of glyceraldehyde-3-phosphate dehydrogenase in drought-stressed-basil cultivarsPreprint

Khakdan, F., Shirazi, Z., & Ranjbar, M. (2023) · Research Square · doi:10.21203/rs.3.rs-2485190/v1

Parasitological, epidemiological, and hematological findings in Spix's yellow-toothed cavy (Galea spixii Wangler, 1831) in the State of Paraiba, northeastern Brazil

Gomes, C. C. S., Vieira, T. S. W. J., Coradi, V. D. S., Barboza, S. D. C. R., da Silva, H. T. F. N. P., Lima, T. D. S., Lucena, R. B., Vieira, R. F. D. C., & Guerra, R. R. (2022) · Semina Ciências Agrárias · doi:10.5433/1679-0359.2022v43n6p2671

C–O Bond Formation and Reactivity: A Family of Related Functional Groups

(2023) · Royal Society of Chemistry eBooks · doi:10.1039/bk9781839169502-00088

Role of the glycolytic protein, glyceraldehyde-3-phosphate dehydrogenase, in normal cell function and in cell pathology

Sirover, M. A. (1997) · Journal of Cellular Biochemistry · doi:10.1002/(sici)1097-4644(19970801)66:2 · Cited by 245

New nuclear functions of the glycolytic protein, glyceraldehyde‐3‐phosphate dehydrogenase, in mammalian cells

Sirover, M. A. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20399 · Cited by 329

GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE, APOPTOSIS, AND NEURODEGENERATIVE DISEASES

Chuang, D., Hough, C. J., & Senatorov, V. V. (2004) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.45.120403.095902 · Cited by 299

Glyceraldehyde-3-phosphate dehydrogenase: Nuclear translocation participates in neuronal and nonneuronal cell death

Sawa, A., Khan, A. A., Hester, L. D., & Snyder, S. H. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.21.11669 · Cited by 316

Use of Glyceraldehyde 3-Phosphate Dehydrogenase (GAPDH) as Internal Control in Western-Blot Experiments?

Ghalamfarsa, G. (2015) · Journal of Cancer Prevention & Current Research · doi:10.15406/jcpcr.2015.02.00061