Mitochondria in innate immune signaling

Pattern Recognition Receptors and Inflammation

Takeuchi, O., & Akira, S. (2010) · Cell · doi:10.1016/j.cell.2010.01.022 · Cited by 8,895

Innate immune recognition

Janeway, C. A., & Medzhitov, R. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.083001.084359 · Cited by 8,394

Neutrophil Emigration in the Skin, Lungs, and Peritoneum: Different Requirements for CD11/CD18 Revealed by CD18-deficient Mice

Mizgerd, J. P., Kubo, H., Kutkoski, G. J., Bhagwan, S. D., Scharffetter-Kochanek, K., Beaudet, A. L., & Doerschuk, C. M. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.186.8.1357 · Cited by 7,332

Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death

Shi, J., Zhao, Y., Wang, K., Shi, X., Wang, Y., Huang, H., Zhuang, Y., Cai, T., Wang, F., & Shao, F. (2015) · Nature · doi:10.1038/nature15514 · Cited by 6,659

A role for mitochondria in nlrp3 inflammasome activation

Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602

Cyclic GMP-AMP Synthase Is a Cytosolic DNA Sensor That Activates the Type I Interferon Pathway

Sun, L., Wu, J., Du, F., Chen, X., & Chen, Z. J. (2013) · Science · doi:10.1126/science.1232458 · Cited by 4,996

Succinate is an inflammatory signal that induces IL-1β through HIF-1α

Tannahill, G. M., Curtis, A. M., Adamik, J., Palsson-McDermott, E. M., McGettrick, A. F., Goel, G., Frezza, C., Bernard, N. J., Kelly, B., Foley, N. H., et al. (2013) · Nature · doi:10.1038/nature11986 · Cited by 4,176

The RNA helicase RIG-I has an essential function in double-stranded RNA-induced innate antiviral responses

Yoneyama, M., Kikuchi, M., Natsukawa, T., Shinobu, N., Imaizumi, T., Miyagishi, M., Taira, K., Akira, S., & Fujita, T. (2004) · Nature Immunology · doi:10.1038/ni1087 · Cited by 4,022

Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses

Kato, H., Takeuchi, O., Sato, S., Yoneyama, M., Yamamoto, M., Matsui, K., Uematsu, S., Jung, A., Kawai, T., Ishii, K. J., et al. (2006) · Nature · doi:10.1038/nature04734 · Cited by 3,888

Fpr2 exacerbates Streptococcus suis-induced streptococcal toxic shock-like syndrome via attenuation of neutrophil recruitment

Ni, C., Gao, S., Li, X. J., Zheng, Y., Jiang, H., Liu, P., Lv, Q., Huang, W., Li, Q., Ren, Y., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1094331 · Cited by 13

Viroporins Manipulate Cellular Powerhouses and Modulate Innate Immunity

Cedillo‐Barrón, L., García‐Cordero, J., Visoso-Carvajal, G., & León‐Juárez, M. (2024) · Viruses · doi:10.3390/v16030345 · Cited by 12

Crosstalk between Dysfunctional Mitochondria and Proinflammatory Responses during Viral Infections

Sun, Z., Wang, Y., Jin, X. K., Li, S., & Qiu, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179206 · Cited by 14

Somatic NAP1L1 p.D349E promotes cardiac hypertrophy through cGAS-STING-IFN signaling

Lv, C., Alimu, X., Xiao, X., Wang, F., Wang, J., Wang, S., Wu, G., Zhang, Y., Wu, Y., Chen, H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-58453-7 · Cited by 13

Hyperandrogenism triggers mtDNA release to participate in ovarian inflammation via mPTP/cGAS/STING in PCOS

Cai, J., Zhu, Q., Xiang, Y., Weng, L., Liang, N., Hong, X., Xue, M., & Ge, H. (2025) · iScience · doi:10.1016/j.isci.2025.112391 · Cited by 13

Autophagic regulation of neuroinflammation in ischemic stroke

Zheng, Y., Zhou, Z., Han, F., & Chen, Z. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105114 · Cited by 13

Chlamydia psittaci inhibits apoptosis of human neutrophils by activating P2X7 receptor expression

He, Z., Wang, C., Wang, J., Zheng, K., Ding, N., Yu, M., Li, W., Tang, Y., Li, Y., Xiao, J., et al. (2022) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2022.151571 · Cited by 16

Role of mitochondria in regulating immune response during bacterial infection

Khan, S., Basu, S., Raj, D., & Lahiri, A. (2022) · International review of cytology · doi:10.1016/bs.ircmb.2022.10.004 · Cited by 13

Role of Rab5 early endosomes in regulating Drosophila gut antibacterial response

Joshi, M. K., Viallat-Lieutaud, A., & Royet, J. (2023) · iScience · doi:10.1016/j.isci.2023.107335 · Cited by 12

Characterization of brain resilience in Alzheimer's disease using polygenic risk scores and further improvement by integrating mitochondria-associated loci

Xu, X., Wang, H., Bennett, D. A. A., Zhang, Q., Meng, X., & Zhang, H. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2023.03.002 · Cited by 11

Role of UPRmt and mitochondrial dynamics in host immunity: it takes two to tango

Kumar, M., Sharma, S., & Mazumder, S. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1135203 · Cited by 13

A supervised Bayesian factor model for the identification of multi-omics signatures

Gygi, J. P., Konstorum, A., Pawar, S., Aron, E., Kleinstein, S. H., & Guan, L. (2024) · Bioinformatics · doi:10.1093/bioinformatics/btae202 · Cited by 12

Activation of the mitochondrial unfolded protein response regulates the dynamic formation of stress granules

Lopez-Nieto, M., Sun, Z., Relton, E., Safakli, R. N., Freibaum, B. D., Taylor, J. P., Ruggieri, A., Smyrnias, I., & Locker, N. (2024) · Journal of Cell Science · doi:10.1242/jcs.263548 · Cited by 12

The cell stress and immunity cycle in cancer: Toward next generation of cancer immunotherapy

Laureano, R. S., Vanmeerbeek, I., Sprooten, J., Govaerts, J., Naulaerts, S., & Garg, A. D. (2023) · Immunological Reviews · doi:10.1111/imr.13287 · Cited by 13

Mitochondrial Dysfunction and Cognitive Impairment in Schizophrenia: The Role of Inflammation

Wang, G., Liu, S., Fan, X., Li, J., Xue, Q., Liu, K., Li, X., Yang, Y., Wang, X., Song, M., et al. (2024) · Schizophrenia Bulletin · doi:10.1093/schbul/sbae196 · Cited by 14

Exploring the Molecular Interplay Between Oxygen Transport, Cellular Oxygen Sensing, and Mitochondrial Respiration

Jana, S., & Alayash, A. I. (2025) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0428 · Cited by 12

PGAM5 interacts with Bcl-rambo and regulates apoptosis and mitophagy

Hashino, T., Matsubara, H., Xu, J., Tanaka, R., Kusagawa, E., Ueda, Y., Yoshida, H., & Kataoka, T. (2022) · Experimental Cell Research · doi:10.1016/j.yexcr.2022.113342 · Cited by 11

Endothelial cell activation mediated by cold ischemia-released mitochondria is partially inhibited by defibrotide and impacts on early allograft function following liver transplantation

Villalba-López, F., García‐Bernal, D., Mateo, S. V., Vidal-Correoso, D., Jover-Aguilar, M., Alconchel, F., Martínez-Alarcón, L., López‐López, V., Ríos, A., Cascales-Campos, P. A., et al. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115529 · Cited by 11

Plasma Cell–Free Mitochondrial DNA as a Marker of Geriatric Syndromes in Older Adults With HIV

Johnston, C. D., Siegler, E. L., Rice, M. C., Derry, H. M., Hootman, K. C., Zhu, Y.-S., Burchett, C. O., Choi, M. E., & Glesby, M. J. (2022) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/qai.0000000000002993 · Cited by 10

Immune senescence in multiple myeloma—a role for mitochondrial dysfunction?

Seymour, F., Carmichael, J., Taylor, C., Parrish, C., & Cook, G. (2022) · Leukemia · doi:10.1038/s41375-022-01653-7 · Cited by 11

Research progress on mitochondria regulating tumor immunity

Li, J., Xu, P., & Chen, S. (2024) · Journal of Zhejiang University (Medical Sciences) · doi:10.3724/zdxbyxb-2023-0484 · Cited by 11

Connecting the dots: Mitochondrial transfer in immunity, inflammation, and cancer

Artusa, V., Luca, L. D., Clerici, M., & Trabattoni, D. (2025) · Immunology Letters · doi:10.1016/j.imlet.2025.106992 · Cited by 11

Novel chimeric TLR2/NOD2 agonist CL429 exhibited significant radioprotective effects in mice

Cheng, Y., Du, J., Liu, R., Dong, S., Cai, J., Gao, F., & Liu, C. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16252 · Cited by 10

Neospora caninum infection induced mitochondrial dysfunction in caprine endometrial epithelial cells via downregulating SIRT1

Tao, D.-L., Zhao, S., Chen, J., Chen, X., Yang, X., Song, J.-K., Liu, Q., & Zhao, G. (2022) · Parasites & Vectors · doi:10.1186/s13071-022-05406-4 · Cited by 10

The Multi-Faceted Nature of Renalase for Mitochondrial Dysfunction Improvement in Cardiac Disease

Stojanović, D. R., Stojanović, M., Milenković, J., Veličkov, A., Ignjatović, A., & Milojković, M. (2023) · Cells · doi:10.3390/cells12121607 · Cited by 10

Mitochondria dysfunction in circulating tumor cells

Agnoletto, C., & Volinia, S. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.947479 · Cited by 9

TJ-M2010-5 Attenuates Severe Myocardial Ischemia/Reperfusion Injury in Heart Transplantation by Inhibiting MyD88 Homodimerization In Vivo

Yang, H., Zhou, P., Li, Q., Zhou, X., Li, J., Wang, J., Wang, J., Zhao, Y., Yang, B., Zhang, B., et al. (2022) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-022-10246-9 · Cited by 9

Effect of Phosphatidylcholine Nanosomes on Phospholipid Composition of the Plasma Membranes in Liver Cells and Blood Serum in Experimental Atherosclerosis

Leskova, G. F., Kaplun, A. P., Bezrukov, D. A., & Lvovsky, A. I. (2020) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-020-05028-9 · Cited by 9

Urine Cell-Free Mitochondrial DNA as a Marker of Weight Loss and Body Composition in Older Adults With HIV

Johnston, C. D., Siegler, E. L., Rice, M. C., Derry, H. M., Hootman, K. C., Zhu, Y., Burchett, C. O., Gupta, S. K., Choi, M. E., & Glesby, M. J. (2021) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/qai.0000000000002766 · Cited by 9

Actin Cytoskeleton Dynamics and Type I IFN-Mediated Immune Response: A Dangerous Liaison in Cancer?

Trono, P., Tocci, A., Musella, M., Sistigu, A., & Nisticò, P. (2021) · Biology · doi:10.3390/biology10090913 · Cited by 8

Yellow fever virus infection alters mitochondrial network dynamics and trigger IFN-I response via TLR2 pathway

Tomatis, C., Charó, N. L., Ferrer, M. F., Aquila, S., Fuentes, F., Scalise, M. L., Aguiar, M. C. A. M., Valdivieso, G., Silva, E. A. C., & Gomez, R. M. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114699 · Cited by 8

The role of protein acetylation in regulating mitochondrial fusion and fission

Uddin, G. M., Abbas, R., & Shutt, T. E. (2021) · Biochemical Society Transactions · doi:10.1042/bst20210798 · Cited by 8

FGIN-1-27 Mitigates Radiation-induced Mitochondrial Hyperfunction and Cellular Hyperactivation in Cultured Astrocytes

Zhang, S., Deng, Z., Qiu, Y., Lu, G., Wu, J., & Huang, H. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.10.017 · Cited by 10

Crosstalk between myocardial autophagy and sterile inflammation in the development of heart failure

Tang, J., Tam, E., Song, E., Xu, A., & Sweeney, G. (2024) · Autophagy Reports · doi:10.1080/27694127.2024.2320605 · Cited by 7

Regulatory role of PDK1 via integrated gene analysis of mitochondria-immune response in periodontitis

Sun, X., Wu, T., Yang, Z., Chen, S., Zhao, Z., Hu, C., Wu, S., Wu, J., Mao, Y., Liu, J., et al. (2024) · Gene · doi:10.1016/j.gene.2024.148476 · Cited by 8

Gfap Mutation and Astrocyte Dysfunction Lead to a Neurodegenerative Profile with Impaired Synaptic Plasticity and Cognitive Deficits in a Rat Model of Alexander Disease

Berman, R. F., Matson, M. R., Bachman, A. M., Lin, N., Coyne, S., Frelka, A., Pearce, R. A., Messing, A., & Hagemann, T. L. (2025) · eNeuro · doi:10.1523/eneuro.0504-24.2025 · Cited by 10

Suppression of innate immune signaling molecule, MAVS, reduces radiation-induced bystander effect

Jia, R. L., Chen, Y., Jia, C., Hu, B., & Du, Y. (2020) · International Journal of Radiation Biology · doi:10.1080/09553002.2020.1807642 · Cited by 8

Ultrastructural Changes in Mitochondria in Patients with Dilated Cardiomyopathy and Parvovirus B19 Detected in Heart Tissue without Myocarditis

Pawlak, A., Gewartowska, M., Przybylski, M., Kuffner, M., Wiligórska, D., Gil, R. J., Król, Z. J., & Frontczak‐Baniewicz, M. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12020177 · Cited by 8

Mitochondria in Mycobacterium Infection: From the Immune System to Mitochondrial Haplogroups

de Souza, F. G., & Cavalcante, G. C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179511 · Cited by 10

Neurodegeneration, Mitochondria, and Antibiotics

Suarez-Rivero, J. M., López‐Pérez, J., Muela‐Zarzuela, I., Pastor‐Maldonado, C. J., Cilleros-Holgado, P., Gómez-Fernández, D., Álvarez-Córdoba, M., Munuera-Cabeza, M., Talaverón-Rey, M., Povea-Cabello, S., et al. (2023) · Metabolites · doi:10.3390/metabo13030416 · Cited by 9

Identification of Fangjihuangqi Decoction as a late-stage autophagy inhibitor with an adjuvant anti-tumor effect against non-small cell lung cancer

Chen, Q., Liao, Y., Liu, Y., Song, Y., Jiang, J., Zhang, Z., Li, A., Zheng, M., Chen, X., Zhao, T., et al. (2023) · Chinese Medicine · doi:10.1186/s13020-023-00770-4 · Cited by 7

PGC-1α activation to enhance macrophage immune function in mycobacterial infections

Frandsen, J. R., Yuan, Z., Bedi, B., Prasla, Z., Choi, S., Narayanasamy, P., & Sadikot, R. T. (2025) · PLoS ONE · doi:10.1371/journal.pone.0310908 · Cited by 8

Melatonin Exerts Positive Effects on Sepsis Through Various Beneficial Mechanisms

Xu, J., Liang, C., Yao, S., & Wang, F. (2025) · Drug Design Development and Therapy · doi:10.2147/dddt.s509735 · Cited by 7

Mitochondrial Complex I and ROS control neuromuscular function through opposing pre- and postsynaptic mechanisms

Mallik, B., Bhat, S. A., Wang, X., & Frank, C. A. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003388 · Cited by 11

Advances in the Understanding of Mitochondrial Inflammatory Regulation in the Pathogenesis of Alzheimer’s Disease

Zhang, R.-Z., Li, L., Ma, C., Dou, T., Wei, Y.-T., & Yan, X. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s557000 · Cited by 6

Mitochondrial DNA-dependent inflammation in kidney diseases

Luo, S., Yang, M., Zhao, H., Han, Y., Liu, Y., Xiong, X., Chen, W., Li, C., & Sun, L. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108637 · Cited by 7

The status and trends of mitochondrial dynamics research: A global bibliometric and visualized analysis

Guo, Z., Wang, Z., Gao, Z., Feng, T., Gao, Y., Yin, Z., Tian, Z., Liu, Y., Mao, X., & Xiang, C. (2023) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-023-09959-6 · Cited by 7

Human Herpesvirus 6B U26 Inhibits the Activation of the RLR/MAVS Signaling Pathway

Jiang, X., Tang, T., Guo, J., Wang, Y., Li, P., Chen, X., Wang, L. H.-C., Wen, Y., Jia, J., Garbarino, E., et al. (2021) · mBio · doi:10.1128/mbio.03505-20 · Cited by 7

The mitochondrial protease ClpP is a metabolic vulnerability and an immunogenic trigger against multiple myeloma

Perini, T., Zordan, P., Pizzo, R. D., Resnati, M., Viviani, L., Stefanoni, D., Cassina, L., Orfanelli, U., Trudu, M., Oliva, L., et al. (2025) · Blood · doi:10.1182/blood.2024026340 · Cited by 6

NDV inhibited IFN-β secretion through impeding CHCHD10-mediated mitochondrial fusion to promote viral proliferation

Yu, X., Jiang, H., Li, J., Ding, J., Chen, K., Ding, Z., & Xu, X. (2023) · Veterinary Microbiology · doi:10.1016/j.vetmic.2023.109973 · Cited by 6

Mitochondria dysfunction: A trigger for cardiovascular diseases in systemic lupus erythematosus

Wang, H., Tang, R., Pan, Q., Yin, Q., Feng, J., & Deng, L. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113722 · Cited by 7

Somatic Mutations of Hematopoietic Cells Are an Additional Mechanism of Body Aging, Conducive to Comorbidity and Increasing Chronification of Inflammation

Yegorov, Y. E., Poznyak, A. V., Bezsonov, E. E., Zhuravlev, A. D., Nikiforov, N. G., Vishnyakova, K. S., & Orekhov, A. N. (2022) · Biomedicines · doi:10.3390/biomedicines10040782 · Cited by 6

Quantifying Regulated Mitochondrial Fission in Macrophages

Afroz, S. F., Condon, N. D., Sweet, M. J., & Kapétanovic, R. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2449-4_18 · Cited by 6

Identification and validation of the mitochondrial function related hub genes by unsupervised machine learning and multi-omics analyses in lung adenocarcinoma

Jin, X., Zhang, H., Sui, Q., Li, M., Liang, J., Hu, Z., Cheng, Y., Zheng, Y., Chen, Z., Lin, M., et al. (2022) · Heliyon · doi:10.1016/j.heliyon.2022.e11966 · Cited by 6

Studies on the effects of bone marrow stem cells on mitochondrial function and the alleviation of ARDS

Zhang, K., Gao, Y., Deng, Y., Zhou, X. J., Zhu, C., He, Z., & Lv, D. (2020) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-020-03888-3 · Cited by 6

Human Norovirus NTPase Antagonizes Interferon-β Production by Interacting With IkB Kinase ε

Zheng, Z., Li, Y., Zhang, M., Liu, Y., Fu, M., Gong, S., & Hu, Q. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.687933 · Cited by 5

Mitochondrial proteins as biomarkers of cellular senescence and age-associated diseases

Panfilova, A. S., Zubareva, T., Mironova, E. S., Mazzoccoli, G., Marasco, M. G. P., Balazovskaia, S., Yablonsky, P., & Kvetnoy, I. M. (2025) · Aging · doi:10.18632/aging.206305 · Cited by 8

Molecular Mechanisms of cGAS-STING Axis and Mitochondrial Dysfunction-Related Diseases in Humans: A Comprehensive Review

Shen, X., Chen, H., Zheng, J., Ma, Y., Tang, Z., Sun, H., Zhang, Q. Y., Zhang, J., & Song, T. (2025) · Current Neuropharmacology · doi:10.2174/011570159x388747250830161230 · Cited by 6

Mitochondrial Genetics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association

Fetterman, J. L., Chinnery, P. F., McClellan, R., Wallace, D. C., Suomalainen, A., Ojala, T. H., Lewis, S. C., & Ballinger, S. W. (2025) · Circulation · doi:10.1161/cir.0000000000001393 · Cited by 7

Mitochondrial DNA Copy Number Variations in Gastrointestinal Tract Cancers: Potential Players

Alikhani, M., Touati, E., Karimipoor, M., Vosough, M., & Mohammadi, M. (2021) · Journal of Gastrointestinal Cancer · doi:10.1007/s12029-021-00707-w · Cited by 5

Effects of dietary chloroquine on fish growth, hepatic intermediary metabolism, antioxidant and inflammatory responses in turbot

Sui, Z., Wang, X., Zhang, X., Zhou, H., Liu, C., Mai, K., & He, G. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.109068 · Cited by 5

MyD88 protein destabilization mitigates NF-κB-dependent protection against macrophage apoptosis

Lainšček, D., Horvat, S., Dolinar, K., Ivanovski, F., Romih, R., Pirkmajer, S., Jerala, R., & Manček‐Keber, M. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01930-1 · Cited by 5

Structural basis for the regulatory mechanism of mammalian mitochondrial respiratory chain megacomplex-I2III2IV2

Zhang, L., Guo, R., Xiao, C. L., Li, J., Gu, J., & Yang, M. (2024) · hLife · doi:10.1016/j.hlife.2024.03.003 · Cited by 7

A review of nutritional recommendations for scuba divers

Brenner, R. J., Balan, K. A., Andersen, M. P. L., Dugrenot, E., Vrijdag, X. C. E., van Waart, H., & Tillmans, F. (2024) · Journal of the International Society of Sports Nutrition · doi:10.1080/15502783.2024.2402386 · Cited by 5

Diet induces hepatocyte protection in fatty liver disease via modulation of PTEN signaling (Review)

Ikeda, Y., Murakami, M., Nakagawa, Y., Tsuji, A., Kitagishi, Y., & Matsuda, S. (2020) · Biomedical Reports · doi:10.3892/br.2020.1299 · Cited by 5

No impact of cancer and plague-relevant FPR1 polymorphisms on COVID-19

Petrazzuolo, A., Naour, J. L., Vacchelli, E., Gaussem, P., Ellouze, S., Jourdi, G., Solary, É., Fontenay, M., Smadja, D. M., & Kroemer, G. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1857112 · Cited by 5

Short-chain acyl-CoA dehydrogenase initiates mtDNA demethylation and leakage to fuel antitumor immunity in colorectal cancer

Yang, F., Wang, M., Hu, S., Guan, X., Zhao, K., Zhou, Y., Yao, H., Zhang, T., Li, L., Jing-yuan, G., et al. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02675-8 · Cited by 5

Mitochondrial dysfunction in neurodegenerative disorders: mechanisms and therapeutic advances

Tong, Y., He, J. N., Zhou, L., Zhang, J., Ho, B. M., Du, L., Yip, Y. W. Y., Bisnauthsing, H., Chan, P. P. M., Tham, C. C. Y., et al. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00480-x · Cited by 5

Repeated exposures to PM2.5 alter the mitochondria and the influenza-mediated interferon response in an air-liquid interface bronchial epithelium

Chivé, C., Eon-Bertho, A., Martίn-Faivre, L., Tête, A., Izabelle, C., Sallenave, J., García-Verdugo, I., & Baeza‐Squiban, A. (2025) · Environmental Pollution · doi:10.1016/j.envpol.2025.126687 · Cited by 5

Autism Spectrum Disorders: Role of Pre- and Post-Natal GammaDelta (γδ) T Cells and Immune Regulation

Anderson, G., & Medina, S. R. B. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666191102170125 · Cited by 4

Serum of COVID-19 patients changes neuroinflammation and mitochondrial homeostasis markers in hippocampus of aged rats

Montenegro, Y. H. A., Bobermin, L. D., Sesterheim, P., Salvato, R. S., Anschau, F., de Oliveira, M. J. S., Wyse, Â. T. D. S., Netto, C. A., Gonçalves, C.-A. S., Quincozes‐Santos, A., et al. (2023) · Journal of NeuroVirology · doi:10.1007/s13365-023-01156-w · Cited by 4

Pseudomonas aeruginosa-induced mitochondrial dysfunction inhibits proinflammatory cytokine secretion and enhances cytotoxicity in mouse macrophages in a reactive oxygen species (ROS)-dependent way

Yang, H., Wang, Y., Fan, H., Liu, F., Feng, H., Li, X., Chu, M., Pan, E., Teng, D., Chen, H., et al. (2023) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2300051 · Cited by 5

Trypanosoma cruzi reprograms mitochondrial metabolism within the anterior midgut of its vector Rhodnius prolixus during the early stages of infection

Ouali, R., Vieira, L. R., Salmon, D., & Bousbata, S. (2024) · Parasites & Vectors · doi:10.1186/s13071-024-06415-1 · Cited by 4

Mitochondria/lysosome dual-organelle labelling esterase probe for monitoring cell viability and evaluating lung cancer drug efficiency

He, M., Wang, J., Wang, L., Hu, B., Shen, X., & Chen, H. (2024) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2024.125379 · Cited by 4

Mitochondrial Function and Root-Filled Teeth – Detrimental and Unknown Interfaces in Systemic Immune Diseases

Lechner, J., & Mayer, W. (2020) · International Journal of General Medicine · doi:10.2147/ijgm.s258170 · Cited by 4

Challenges of mitochondrial DNA editing in mammalian cells: focus on treatment of cardiovascular disease

Khotina, V. A., Ekta, M. B., Baig, M. S., Wu, W., Grechko, A. V., & Sukhorukov, V. N. (2022) · Vessel Plus · doi:10.20517/2574-1209.2022.28 · Cited by 5

Mitochondrial DNA Copy Number Variations and Serum Pepsinogen Levels for Risk Assessment in Gastric Cancer

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