Mitochondrial DNA in innate immune responses and inflammatory pathology

Anti-Vascular Endothelial Growth Factors Protect Retinal Pigment Epithelium Cells Against Oxidation by Modulating Nitric Oxide Release and Autophagy

Cillà, S. D., Farruggio, S., Vujosevic, S., Raina, G., Filippini, D. A., Gatti, V., Clemente, N., Mary, D., Vezzola, D., Casini, G., et al. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479441 · Cited by 5,154

Circulating mitochondrial DAMPs cause inflammatory responses to injury

Zhang, Q., Raoof, M., Chen, Y., Sumi, Y., Sursal, T., Junger, W., Brohi, K., Itagaki, K., & Hauser, C. J. (2010) · Nature · doi:10.1038/nature08780 · Cited by 3,812

Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome

Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049

Type I interferons in infectious disease

McNab, F., Mayer-Barber, K., Sher, A., Wack, A., & O'Garra, A. (2015) · Nature Reviews Immunology · doi:10.1038/nri3787 · Cited by 2,780

Regulation and function of the cGAS–STING pathway of cytosolic DNA sensing

Chen, Q., Sun, L., & Chen, Z. J. (2016) · Nature Immunology · doi:10.1038/ni.3558 · Cited by 2,333

Oxidized mitochondrial DNA activates the NLRP3 inflammasome during apoptosis

Shimada, K., Crother, T. R., Karlin, J., Dagvadorj, J., Chiba, N., Chen, S., Ramanujan, V. K., Wolf, A. J., Vergnes, L., Ojcius, D. M., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.01.009 · Cited by 2,282

Mitochondrial DNA stress primes the antiviral innate immune response

West, A. P., Khoury-Hanold, W., Staron, M., Tal, M. C., Pineda, C. M., Lang, S. M., Bestwick, M., Duguay, B. A., Raimundo, N., MacDuff, D. A., et al. (2015) · Nature · doi:10.1038/nature14156 · Cited by 1,975

Mitochondrial form and function

Friedman, J. R., & Nunnari, J. (2014) · Nature · doi:10.1038/nature12985 · Cited by 1,803

Tlr signalling augments macrophage bactericidal activity through mitochondrial ros

West, A. P., Brodsky, I. E., Rahner, C., Woo, D. K., Erdjument-Bromage, H., Tempst, P., Walsh, M. C., Choi, Y., Shadel, G. S., & Ghosh, S. (2011) · Nature · doi:10.1038/nature09973 · Cited by 1,659

Neutrophil extracellular traps enriched in oxidized mitochondrial DNA are interferogenic and contribute to lupus-like disease

Lood, C., Blanco, L. P., Purmalek, M. M., Carmona-Rivera, C., De Ravin, S. S., Smith, C. K., Malech, H. L., Ledbetter, J. A., Elkon, K. B., & Kaplan, M. J. (2016) · Nature Medicine · doi:10.1038/nm.4027 · Cited by 1,570

Identifying mitochondria-related signatures for tuberculosis diagnosis through machine learning on single-cell transcriptomics data and experimental verification

Zhang, X., Zhang, K., Wang, Y., Zhang, B., Huang, Z., & Xu, Y. (2026) · Microbial Pathogenesis · doi:10.1016/j.micpath.2026.108489 · Cited by 1

Leucine-Rich Repeat Kinase 2 (LRRK2) in Glucose Metabolism and Metabolic–Neuroinflammatory Crosstalk

Kawakami, F., Imai, M., Ogata, M., Habata, T., Tamaki, S., Kawashima, R., Kurosaki, Y., Miyai, S., Chatatikun, M., Kyaw, M. P., et al. (2026) · Biomolecules · doi:10.3390/biom16040588 · Cited by 1

Altered mitochondrial ultrastructure in salivary epithelial cells of patients with Sjögren’s disease is associated with mitochondrial DNA release and increased activation of pattern recognition receptors: potential use of tofacitinib as therapy

Carvajal, P., Castro, I., Urra, F., Aguilera, S., González, S., Molina, C., Campos, S., Ramirez, G., Almarza, C., Gutiérrez, J., et al. (2026) · Annals of the Rheumatic Diseases · doi:10.1016/j.ard.2026.03.022 · Cited by 2

Nucleotide metabolism reprogramming in obesity-associated cardiovascular inflammation: a new perspective

Qian, T., Zhang, M., Liu, Y., Guo, D., & Jin, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1829718 · Cited by 1

Viral Mimicry of Alzheimer’s Disease: Innate Sensing of Self-Nucleic Acids as a Driver of Glial Senescence

Abuhassan, Q., Saeed, T. N., Al-Hussainy, A. F., Roopashree, R., Mishra, S., Nanda, A., Mukherjee, G., Rizaev, J., Taher, S. G., Alwan, M., et al. (2026) · Journal of Molecular Neuroscience · doi:10.1007/s12031-026-02532-x · Cited by 1

A Redox Amplification Interface Linking Mitochondrial Dysfunction, Immune-Derived Oxidants, and Biomaterial Electrochemistry in Chronic Inflammation

Mierzejewska, Ż. A., Antonowicz, B., Woźniak, Ł., Lechien, J. R., Vaira, L. A., Dziełak, S., & Borys, J. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27094121 · Cited by 1

Supercharging the metabolic engine: mitochondrial engineering strategies for CAR-T persistence in solid tumors

Chun, S., Yu, S., Lee, H. G., & Kim, M. S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1822668 · Cited by 1

Dual-targeting macrophage membrane nanosystem enhances radiotherapy-induced antitumor immunity via synergistic nuclear and mitochondrial DNA damage

Ju, G., Ding, Q., Gu, H., Liu, R., Liu, X., Wang, Z., Wang, K., Ping, Y., You, J., Yuan, S., et al. (2026) · Biomaterials Science · doi:10.1039/d6bm00279j · Cited by 1

SLC27A3-dependent lipid metabolic reprogramming by trilobatin suppresses microglial mtDNA/TLR9-driven inflammatory activation in traumatic brain injury

Zhang, H., Wang, X.-J., Chu, M.-M., Xing, G.-Y., Qiu, K., Zhang, Y., Zhang, W.-F., Zhang, Y.-T., Liu, X., Li, L., et al. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-026-03826-y · Cited by 1

Ceramide signaling in non-small-cell lung cancer: from dysregulation to targeted therapy

Patil, D. T., & Yadav, K. S. (2026) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-026-05476-6 · Cited by 1

Andes virus and the aging host: lessons from the 2026 outbreak and a framework for age-related disease severity

Quarleri, J. F., Jarmoluk, P., Mazzitelli, I. G., & Delpino, M. V. (2026) · GeroScience · doi:10.1007/s11357-026-02352-2 · Cited by 2

Comparative immune response and disease resistance against Aeromonas hydrophila in Catla catla, Labeo rohita and their intergeneric hybrids

Ahmad, M. K., Zuberi, A., Noorullah, M., Noor, Z., Younas, W., Hussain, A., Uzair, M., & Kamran, M. Z. (2026) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2026.111507 · Cited by 1

Mitochondrial Dysfunction in Autism and Attention-Deficit/Hyperactivity Disorder: Evidence from Genetic, Biochemical, and Neuroimaging Approaches

Ram, T. R., Mu, C., MacEachern, S. J., & Shearer, J. (2026) · Antioxidants · doi:10.3390/antiox15060764 · Cited by 2

Mitochondrial DNA efflux as a potential amplifier of systemic inflammatory network rewiring in heart failure with preserved ejection fraction

Zhao, X., Huang, S., Li, Q., Yang, Y., & Zhang, C. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1866184 · Cited by 1

Aip mutation leads to significant alterations in gene expression, altered sensitivity to Ahr ligands, and early lethality in zebrafish

Perone, D. M., Du, J. K. L., Karchner, S. I., Aluru, N., Stinson, S. R., Truong, L., Hahn, M. E., & Tanguay, R. L. (2026) · Frontiers in Toxicology · doi:10.3389/ftox.2026.1875384 · Cited by 1

Mitochondrial Transcription Factor A Deficiency in T Cells Leads to Activation of the Cyclic Guanosine Monophosphate–Adenosine Monophosphate Synthase/Stimulator of Interferon Genes Pathway and Production of Autoantibodies in Mice

Mashimo, S., Kuwabara, T., Ito, K., Mikami, T., Ishiko, A., & Kondo, M. (2026) · Journal of Immunology Research · doi:10.1155/jimr/2594317 · Cited by 1

IRF1-mediated sensing of oxidized mitochondrial DNA drives macrophage PANoptosis in lung ischemia–reperfusion injury

Zhang, N., Zhang, Z., Yu, J., Fu, Y., Gao, J., Jiang, X., Jin, Y., Chen, C., & Wen, Z. (2026) · APOPTOSIS · doi:10.1007/s10495-026-02401-3 · Cited by 1

Management of Musculoskeletal Injuries with an Inflammatory Damage-Associated Molecular Pattern (DAMP) Etiology

Love, R. J., Sheridan, J., Funk, C., & Young, J.-L. (2026) · Pain and Therapy · doi:10.1007/s40122-026-00880-5 · Cited by 1

Quercetin induces molecular hallmarks of immunogenic cell death and cGAS-STING pathway activation via mitochondrial DNA release in hepatocellular carcinoma cells

Lin, T., Chen, Y., & Huang, Z. (2026) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-026-05815-7 · Cited by 1

M-SYFSF attenuates diabetic kidney disease by suppressing Piezo1-associated cGAS–STING signalling and tubular pyroptosis

Li, Y., Hou, J., Wu, X., Zhang, X., Li, C., Fu, Y., Wang, L., Zhou, M., Chen, H., Jiang, W., et al. (2026) · Phytomedicine · doi:10.1016/j.phymed.2026.158763 · Cited by 1

Glutathione reductase deficiency potentiates the immunogenicity of ferroptosis and cuproptosis via amplified reactive oxygen species accumulation and cGAS-STING pathway activation

Deng, X., Deng, Z., Zhu, B., Hu, R., Ma, J., Li, C., Zhang, P., Li, L., Yang, H., Liu, Y., et al. (2026) · Journal of Hematology & Oncology · doi:10.1186/s13045-026-01840-4 · Cited by 2

Mitochondrial homeodynamics in ageing: mechanisms, resilience, and interventions

Chmielewski, P. P. (2026) · Biogerontology · doi:10.1007/s10522-026-10506-0 · Cited by 2

Bioenergetic impedance: a network physiology framework for stress adaptation, maladaptation, and recovery

Tippairote, T., & Hoonkaew, P. (2026) · Frontiers in Network Physiology · doi:10.3389/fnetp.2026.1967461 · Cited by 1

Physical frailty

Pan, Y., & Ma, L. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823761-8.00004-5 · Cited by 1

Pathogenetic mechanisms of burn disease associated with oxidative membrane damage and ways of their correction

Vilyanen, D. V., Pashkevich, N. I., Borisova‐Mubarakshina, M. M., & Стефанович, О. С. (2023) · Биофизика · doi:10.31857/s0006302923010180 · Cited by 1

The possible link between aluminum phosphide poisoning and NLRP3 inflammasome

Hekmatirad, S., & Abdollahi, M. R. (2024) · Medical Hypotheses · doi:10.1016/j.mehy.2024.111352 · Cited by 1

Loss of STING impairs lactogenic differentiation

Vickers, R. R., Wyatt, G. L., Sanchez, L., VanPortfliet, J. J., West, A. P., & Porter, W. W. (2024) · Development · doi:10.1242/dev.202998 · Cited by 1

Receptor agonist/antagonist-incorporated anticancer nanodrugs: Design, materials, and strategies

Hao, S.-J., Wu, S., Chang, Y.-K., & Wu, F. (2024) · Materials Today · doi:10.1016/j.mattod.2024.11.006 · Cited by 1

Association of Circulating Cell‐Free Mitochondrial DNA With Sudden Sensorineural Hearing Loss

Yang, C., Yang, M., Lin, W., Hwang, C., Lin, Y., Wu, C., Chen, I., & Tsai, M. (2025) · Otolaryngology · doi:10.1002/ohn.1238 · Cited by 1

cGAS: a novel therapeutic target in systemic sclerosis-associated interstitial lung disease

Karampitsakos, Τ., & Herazo‐Maya, J. D. (2025) · European Respiratory Journal · doi:10.1183/13993003.00835-2025 · Cited by 1

Mitochondria as Signaling Platforms

Yoboue, E. D., Manon, S., & Camougrand, N. M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-811752-1.00002-x · Cited by 1

Optimized high‐fidelity 3DPCR to assess potential mitochondrial targeting by activation‐induced cytidine deaminase

Wu, H., Zhang, K., Chen, Y., Li, J., Strout, M. P., & Gu, X. (2020) · FEBS Open Bio · doi:10.1002/2211-5463.12927 · Cited by 1

Transplantation From Older Donors: Can Senolytics Turn Back the Clock?

Dixon, W., Feng, S., & Gardner, J. M. (2021) · Transplantation · doi:10.1097/tp.0000000000003538 · Cited by 1

POS0109 IDENTIFICATION OF PRIMARY SJOGREN'S SYNDROME SUBTYPES BY MACHINE LEARNING

Qiu, M. T., Zhang, S. X., Qiao, J., Zhang, J. Q., Song, S., Zhao, R., Chang, M., Zhang, Y., Liu, G., He, P. F., et al. (2021) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2021-eular.2402 · Cited by 1

Borrelia burgdorferi Secretes c-di-AMP as an Extracellular Pathogen-Associated Molecular Pattern to Elicit Type I Interferon Responses in Mammalian HostsPreprint

Priya, R., Ye, M., Raghunandanan, S., Liu, Q., Li, W., Yu, Q., Lou, Y., Sintim, H. O., & Yang, X. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.13.607721 · Cited by 1

STING and VDAC inhibitors attenuate inflammation and ineffective erythropoiesis caused by an altered metabolome in the Nan (EKLF/E339D) mouse model of neonatal anemiaPreprint

Arif, T., Mukherjee, K., Li, X., Catrow, J. L., Cox, J., & Bieker, J. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.11.693792 · Cited by 1

Endothelial RRM2B-dependent mitochondrial DNA signalling drives doxorubicin-cardiotoxicityPreprint

GRAZIANI, S., Bonello, A., Casas, R. B., Risato, G., Tiso, N., Argenton, F., Rampazzo, C., Shinjo, S., Zamberlan, M., Facchinello, N., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.19.700350 · Cited by 1

NLRX1 is an essential, druggable regulator of mitochondrial permeability transitionPreprint

Heap, R. E., Frederick, D. W., Pickering, R. J., Ghidelli‐Disse, S., Searle, K. L., Barber, J. C., Galwey, N. W., Wilhelm, L. P., Triantafilou, K., Triantafilou, M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.24.746860 · Cited by 1

Lysosomal and mitochondrial crosstalk: the role of lysosomal signaling on mitochondrial biogenesis and function

Yambire, K. F. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7142

Modality for Disseminated Intravascular Coagulation and Current Treatment

Dirik, Y., & Kolusarı, P. (2019) · Eastern Journal Of Medicine · doi:10.5505/ejm.2019.24085

Mitochondria transplantation in organ damage and repair

Rossi, A., Porporato, P. E., & Bussolati, B. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819451-5.00001-9

Ovarian Tumor Mitochondria Exhibit Abnormal Phenotypes and Blunted Associations with Biobehavioral FactorsPreprint

Bindra, S., McGill, M. A., Triplett, M. K., Tyagi, A., Thaker, P. H., Dahmoush, L., Goodheart, M. J., Ogden, T., Owusu-Ansah, E., Karan, K. R., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-246331/v1

Prominent Increases of Nuclear DNAJA3and Cytosolic STAT1 with Nucleic Acid Sensors Underlie Innate Immunity Activation in ClpP-null MousePreprint

Maletzko, A., Key, J., Wittig, I., Gispert, S., Koepf, G., Canet-Pons, J., Torres-Odio, S., West, A. P., & Auburger, G. W. J. (2021) · Preprints.org · doi:10.20944/preprints202105.0021.v1

Rol de la mitocondria en la Sepsis

Velarde, G. C., Vélez-Páez, J. L., Montalvo-Villagómez, M., Jara, F., Moscoso, S. X. A., & Páez, P. A. V. (2021) · Movimiento Científico · doi:10.33881/2011-7191.mct.14202

POS0108 PLASMA MITOCHONDRIAL DNA AS A BIOMARKER IN DIAGNOSIS AND FOLLOW-UP OF SYSTEMIC LUPUS ERYTHEMATOSUS

Giaglis, S., Daoudlarian, D., Kyburz, D., Venhoff, N., & Walker, U. A. (2021) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2021-eular.1833

BAM15 treats mouse sepsis and sepsis-AKI, linking circulating mitochondrial DNA and tubule reactive oxygen speciesPreprint

Tsuji, N., Tsuji, T., Yamashita, T., Hu, X., Yuen, P. S. T., & Star, R. A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.06.451287

Quantitation and Characterization of Cell-Free Mitochondrial DNA in Plasma by Deep SequencingPreprint

Daly, G. T., Pastukh, V. M., Tan, Y. B., Francis, C. M., Aggen, C. Z., Groark, S. C., Edwards, C., Hamo, M., Simmons, J. D., Kutcher, M., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-668341/v1

STING pathway and modulation for cancer immunotherapy

Su, T., Ahmed, N. T., Zhou, S., Liu, X., & Zhu, G. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823397-9.00011-9

Multi-Omics Analysis Identifies Essential Regulators of Mitochondrial Stress Response in Two Wild-Type C. Elegans StrainsPreprint

Gao, A. W., Alam, G. E., Lalou, A., Li, T. Y., Molenaars, M., Zhu, Y., Overmyer, K. A., Shishkova, E., Hof, K., Sleiman, M. S. B., et al. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3917209

Pro-apoptotic caspase deficiency reveals a cell-extrinsic mechanism of NK cell regulationPreprint

Olsen, T. M., Tan, W. H., Knudsen, A. C., & Rongvaux, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.09.459676

Extracellular release of mitochondrial DNA is triggered by cigarette smoke and is detected in COPDPreprint

Giordano, L., Gregory, A. D., Pérez-Verdaguer, M., Ware, S. A., Harvey, H., DeVallance, E., Brzóska, T., Sundd, P., Zhang, Y., Sciurba, F. C., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.04.462069

A conserved role of CBP/p300 in mitochondrial stress response and longevityPreprint

Li, T. Y., Sleiman, M. S. B., Li, H., Gao, A. W., Mottis, A., Bachmann, A., Alam, G. E., Goeminne, L. J. E., Li, X., Schoonjans, K., et al. (2020) · doi:10.21203/rs.3.rs-86465/v1

Faculty Opinions recommendation of Mitochondrial double-stranded RNA triggers antiviral signalling in humans.

Fitzgerald, K. D. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733687707.793549454 · Cited by 33

Mitochondrial dysfunction and its consequences in the context of neurodegeneration

Key, J. (2021) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.62414

Faculty Opinions recommendation of L1 drives IFN in senescent cells and promotes age-associated inflammation.

Zhang, M., & Xuan, Z. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735010803.793558596

Mitochondrial DNA

Mishra, A. (2017) · Springer eBooks · doi:10.1007/978-3-319-47829-6_162-1

Faculty Opinions recommendation of L1 drives IFN in senescent cells and promotes age-associated inflammation.

Pieters, J., & Mode, R. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735010803.793558622

Borrelia burgdorferi engages mammalian type I interferon responses via the cGAS-STING pathwayPreprint

Farris, L. C., Torres-Odio, S., Adams, L. G., West, A. P., & Hyde, J. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.13.491896

RT-PCR-assisted quantification of type I IFN responses in irradiated cancer cells

Galassi, C., Ruan, Y., Sato, A., Jiménez‐Cortegana, C., Klapp, V., Bloy, N., Guilbaud, E., Petroni, G., Buqué, A., Galluzzi, L., et al. (2022) · Methods in cell biology · doi:10.1016/bs.mcb.2022.05.005

Mitochondrial DNA

Mishra, A. (2022) · Springer eBooks · doi:10.1007/978-3-319-55065-7_162

Could neutrophil extracellular traps drive the development of autism?

Pastorek, M., Drobná, D., & Celec, P. (2022) · Medical Hypotheses · doi:10.1016/j.mehy.2022.110929

Mitochondrial networks of microglia adapt in a sex-specific manner upon injury-induced stress and UCP2 knockoutPreprint

Maes, M. E., Colombo, G., Uiterkamp, F. E. S., Sternberg, F., Venturino, A., Pohl, E. E., & Siegert, S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.22.504738

Progress in the correlation of mitochondrial dysfunction and diabetic kidney disease

Shu-yan, Z. (2022) · International Journal of Frontiers in Medicine · doi:10.25236/ijfm.2022.040410

SBT-272 improves TDP-43 pathology in the ALS motor cortex by modulating mitochondrial integrity, motility, and functionPreprint

Gautam, M., Genç, B., Helmold, B., Ahrens, A., Kuka, J., Makrecka‐Kuka, M., Günay, A., Koçak, N., Aguilar-Wickings, I. R., Keefe, D., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.04.510854

N-acetylserotonin inhibits oxidized mitochondrial DNA-induced neuroinflammation by activating the AMPK/PGC-1α/TFAM pathway in neonatal hypoxic-ischemic brain injury model

Jing, X., Luo, X., Fang, C., & Zhang, B. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109878

An Immunogenic Cell Death-Related Genes Signature: Predicting Prognosis in Patients with Cervical CancerPreprint

Chen, C., & Yang, L. (2023) · Research Square · doi:10.21203/rs.3.rs-2620356/v1

Research Progress of NLRP3 Inflammasome in Radiation Damage

姜, 佳. (2023) · Advances in Clinical Medicine · doi:10.12677/acm.2023.134871

Efeito da tolerância ao Lipopolissacarídeo (LPS) no desacoplamento mitocondrial da sepse

Silvestre, A. C. S. (2023) · doi:10.11606/d.5.2023.tde-25052023-165839

Study Progress of Coronary Artery Damage in Kawasaki Disease

Lu, R., Gao, C., Zhang, B., & Jiao, F. (2023) · Asian Journal of Pediatric Research · doi:10.9734/ajpr/2023/v13i4285

Estudo da atividade biológica de inibidores de cisteíno catepsinas antineoplásicos em linhagens celulares de câncer de pâncreas (MIA PaCa-2 e BxPC-3)

Laroca, B. A. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.82.2022.tde-10102023-093131

Molecular Basis of Mitochondrial Diseases Exemplified by Mutation of the Translation Factor Cox14

Witte, S. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10162

Neutrophil Extracellular Trap Formation after Sterile Insults in Lung, Liver, Heart and Kidney: A Mini-Review

Seki, R., & Nishizawa, K. (2019) · Annals of Biomedical Research · doi:10.61545/abr-2-117

Mechanisms of organic dust induced neuroinflammation

Massey, N. (2021) · doi:10.31274/td-20240329-498

Additional file 1 of Decreased MFN2 activates the cGAS-STING pathway in diabetic myocardial ischaemia–reperfusion by triggering the release of mitochondrial DNA

Xiong, Y., Leng, Y., Tian, H. M., Deng, X., Li, W., Li, W., & Xia, Z. (2023) · Figshare · doi:10.6084/m9.figshare.23849567

Elevated Expression of Piezo1 Activates the cGAS-STING Pathway in Chondrocytes by Releasing Mitochondrial DNAPreprint

Sun, L., Wang, Y., Kan, T., Wang, H., Cui, J., Wang, L., Liu, C., Li, H., Yu, Z., & Yan, M. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4884647

Disruption of mitochondrial folate metabolism leads to mitochondrial DNA leakage and activation of apoptotic or inflammatory pathwaysPreprint

Hwang, S., Baker, C. D., & Field, M. S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.30.605854

Neurological Impact of Type I Interferon Dysregulation

Mylonas, A. (2024) · IntechOpen eBooks · doi:10.5772/intechopen.1006023

Causes and Consequences of Perturbations of the Mitochondrial Genome

King, D. E., Copeland, W. C., Wallace, K. B., & Meyer, J. N. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00128-5

Nucleotide coordinated polymers, a ROS-based immunomodulatory antimicrobial, doubly kill Pseudomonas aeruginosa biofilms of implant infections

Chen, J., Tang, X., Sun, Q., Ji, X., Wang, X., Liu, Z., Zhang, X. D., Xu, H.-J., Yang, F., Sun, J. L., et al. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.10.026

Mitochondria-derived vesicles: from quality control to inflammation and extracellular vesicles

Todkar, K. J., Amari, L., & Germain, M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15260-3.00007-7

The effect of sevoflurane and propofol on serum nuclear and mitochondrial DNA in pediatric patients with craniosynostosis

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Additional file 3 of Mitochondrial DNA drives noncanonical inflammation activation via cGAS–STING signaling pathway in retinal microvascular endothelial cells

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Additional file 2 of Mitochondrial DNA drives noncanonical inflammation activation via cGAS–STING signaling pathway in retinal microvascular endothelial cells

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Additional file 2 of Intravitreal injection of mitochondrial DNA induces cell damage and retinal dysfunction in rats

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