Lysosomal cell death mechanisms in aging

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SNAREs — engines for membrane fusion

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Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012

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The role of autophagy in neurodegenerative disease

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Signals from the lysosome: a control centre for cellular clearance and energy metabolism

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Developmental cell death: morphological diversity and multiple mechanisms

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Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function

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Autophagy and Cathepsin D mediated apoptosis contributing to ovarian follicular atresia in the Nile tilapia

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Unwinding the modalities of necrosome activation and necroptosis machinery in neurological diseases

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Inactivation of NSF ATPase Leads to Cathepsin B Release After Transient Cerebral Ischemia

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Imidazole and Benzimidazole Modified Half-Sandwich IridiumIIIN-Heterocyclic Carbene Complexes: Synthesis, Anticancer Application, and Organelle Targeting

Liu, X., Han, Y., Ge, X., & Liu, Z. (2020) · Frontiers in Chemistry · doi:10.3389/fchem.2020.00182 · Cited by 24

Lysosomal Repair in Health and Disease

Xun, J., & Tan, J. X. (2025) · Journal of Cellular Physiology · doi:10.1002/jcp.70044 · Cited by 24

Interruption of endolysosomal trafficking leads to stroke brain injury

Dong, Y., Hu, K., Loke, C. M., Teramoto, H., Liu, C., & Hu, B. R. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113827 · Cited by 23

Cellular compartments challenged by membrane photo-oxidation

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A Vaspin–HSPA1L complex protects proximal tubular cells from organelle stress in diabetic kidney disease

Nakatsuka, A., Yamaguchi, S., Eguchi, J., Kakuta, S., Iwakura, Y., Sugiyama, H., & Wada, J. (2021) · Communications Biology · doi:10.1038/s42003-021-01902-y · Cited by 22

Myocardiocyte autophagy in the context of myocardiocytes regeneration: a potential novel therapeutic strategy

Marzoog, B. A., & Vlasova, T. I. (2022) · Egyptian Journal of Medical Human Genetics · doi:10.1186/s43042-022-00250-8 · Cited by 21

Role of Lysosomal Acidification Dysfunction in Mesenchymal Stem Cell Senescence

Zhang, W., Bai, J., Hang, K., Xu, J., Zhou, C., Li, L., Wang, Z., Wang, Y., Wang, K., & Xue, D. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.817877 · Cited by 21

Methods to Detect Loss of Lysosomal Membrane Integrity

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STAT3 Enhances Sensitivity of Glioblastoma to Drug-Induced Autophagy-Dependent Cell Death

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Recent Advances in Strategies for Imaging Detection and Intervention of Cellular Senescence

Li, J., Bi, Z., Wang, L., Xia, Y., Xie, Y., & Liu, Y. (2022) · ChemBioChem · doi:10.1002/cbic.202200364 · Cited by 19

Cell death classification: A new insight based on molecular mechanisms

Dehghan, S., Kheshtchin, N., Hassannezhad, S., & Soleimani, M. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113860 · Cited by 21

Why autophagy is good for retinal ganglion cells?

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The old second messenger cAMP teams up with novel cell death mechanisms: potential translational therapeutical benefit for Alzheimer’s disease and Parkinson’s disease

Zhang, T., Luu, M. D. A., Dolga, A. M., Eisel, U. L. M., & Schmidt, M. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1207280 · Cited by 16

Dual targeting of tumor cell energy metabolism and lysosomes as an anticancer strategy

Paunović, V., Kosić, M., Misirkic-Marjanovic, M., Trajković, V., & Harhaji-Trajkovic, L. M. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118944 · Cited by 18

Design, synthesis, and evaluation of phosphorescent Ir(III) complexes with anticancer activity

Liu, Z., Li, J., Ge, X., Zhang, S., Xu, Z., & Gao, W. (2019) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2019.110703 · Cited by 16

Replicative Senescence and Expression of Autophagy Genes in Mesenchymal Stromal Cells

Ratushnyy, A. Y., Rudimova, Y. V., & Buravkova, L. B. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920100053 · Cited by 16

Proteostasis in T cell aging

Gressler, A. E., Leng, H., Zinecker, H., & Simon, A. K. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101838 · Cited by 15

Aging and physiological barriers: mechanisms of barrier integrity changes and implications for age-related diseases

Solovev, I. A., Sergeeva, A. D., Geraskina, A., Shaposhnikov, M. V., Vedunova, M. V., Borysova, O., & Moskalev, A. (2024) · Molecular Biology Reports · doi:10.1007/s11033-024-09833-7 · Cited by 19

Ruxolitinib, a promising therapeutic candidate for traumatic brain injury through maintaining the homeostasis of cathepsin B

Peng, J., Gao, C. H., Chen, X., Wang, T., Luo, C., Zhang, M., Chen, X., & Tao, L. (2023) · Experimental Neurology · doi:10.1016/j.expneurol.2023.114347 · Cited by 11

Selective autophagy in type 2 diabetes-associated cognitive dysfunction: Insightful mechanisms and therapies

Luo, L., Que, M., Zeng, L., Wang, X., Sun, T., Zhou, Z., Zhao, Y., Li, S., & Luo, A. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107947 · Cited by 11

H1 Antihistamines—Promising Candidates for Repurposing in the Context of the Development of New Therapeutic Approaches to Cancer Treatment

Trybus, E., & Trybus, W. (2024) · Cancers · doi:10.3390/cancers16244253 · Cited by 12

Artesunate demonstrates neuroprotective effect through activation of lysosomal function and inhibition of cGAS-STING pathway

Wei, H., Chen, Y., Qin, Z., Wang, H., Liu, Y., Song, T., Wu, Y., Hu, W., Huang, X., Lu, G., et al. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110426 · Cited by 11

A Calpain-Like Protein Is Involved in the Execution Phase of Programmed Cell Death of Entamoeba histolytica

Fernández, T. D., Rodríguez, M. A., Monroy, V. S., Gómez-García, M. D. C., Medel, O., & Pérez-Ishiwara, D. G. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00339 · Cited by 11

The potential of Rhodobacter sphaeroides extract as an alternative supplement for cell culture systems

Lee, S., Kim, Y., & Min, J. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.02456-23 · Cited by 9

Macroautophagy and normal aging of the nervous system: Lessons from animal models

Kallergi, E., & Nikoletopoulou, V. (2021) · Cell Stress · doi:10.15698/cst2021.10.257 · Cited by 10

Cell death in development, maintenance, and diseases of the nervous system

Mercau, M. E., Patwa, S., Bhat, K., Ghosh, S., & Rothlin, C. V. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00938-4 · Cited by 9

Nanomaterials-mediated lysosomal regulation: a robust protein-clearance approach for the treatment of Alzheimer’s disease

Hao, M., Chu, J., Zhang, T., Yin, T., Gu, Y., Liang, W., Ji, W., Zhuang, J., Liu, Y., Gao, J., et al. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01736 · Cited by 8

A sequence-activated near-infrared fluorescence probe for precisely tracking in vivo senescence

Nong, J., Li, P., Zhu, M., Li, Y., Wang, C., Zhang, Y., Yan, C., & Guo, Z. (2025) · Chemical Science · doi:10.1039/d5sc05331e · Cited by 8

Maintenance and Decline of Neuronal Lysosomal Function in Aging

Zhong, R., & Richardson, C. E. (2025) · Cells · doi:10.3390/cells14241976 · Cited by 8

A novel biocompatible formate bridged 1D-Cu( ii ) coordination polymer induces apoptosis selectively in human lung adenocarcinoma (A549) cells

Usman, M., Khan, R. A., Khan, M. R., Farah, M. A., BinSharfan, I. I., Alharbi, W., Shaik, J. P., Parine, N. R., Alsalme, A., & Tabassum, S. (2021) · Dalton Transactions · doi:10.1039/d0dt03782f · Cited by 8

Inducin Triggers LC3‐Lipidation and ESCRT‐Mediated Lysosomal Membrane Repair

Corkery, D., Ursu, A., Lucas, B., Grigalunas, M., Kriegler, S., Oliva, R., Dec, R., Koska, S., Pahl, A., Sievers, S., et al. (2023) · ChemBioChem · doi:10.1002/cbic.202300579 · Cited by 7

Lysosomal Degradation of Junctional Proteins

Flores-Maldonado, C., Verdejo‐Torres, O., Campos-Blázquez, J. P., Cabrera, A. R., García‐Hernández, V., Rincón-Heredia, R., & Contreras, R. G. (2017) · InTech eBooks · doi:10.5772/intechopen.69370 · Cited by 8

Organelle-oriented nanomedicines in tumor therapy: Targeting, escaping, or collaborating?

Tan, K., Zhang, H., Yang, J., Wang, H., Li, Y., Ding, G., Gu, P., Yang, S., Li, J., & Fan, X. (2025) · Bioactive Materials · doi:10.1016/j.bioactmat.2025.02.040 · Cited by 8

Lysosomes and lysosomal dysfunction in ageing biology

Steinhauser, M. L., Liu, Y., Rizzo, S. J. S., Chen, B. B., Finkel, T., & Tan, J. X. (2026) · Nature Cell Biology · doi:10.1038/s41556-026-02007-6 · Cited by 9

The Role of Cathepsin B in Ischemia-Reperfusion Injury After Stroke

Gaire, B. P., Subedi, L., Teramoto, H., & Hu, B. R. (2021) · Exon Publications eBooks · doi:10.36255/exonpublications.cerebralischemia.2021.cathepsin · Cited by 7

Spatially Confined Intervention of Cellular Senescence by a Lysosomal Metabolism Targeting Molecular Prodrug for Broad‐Spectrum Senotherapy

Xia, Y., Li, J., Wang, L., Luo, X., Xie, Y., & Liu, Y. (2022) · Angewandte Chemie · doi:10.1002/ange.202115764 · Cited by 7

Lysosome

Matte, Ú. D. S., & Pasqualim, G. (2016) · Journal of Inborn Errors of Metabolism and Screening · doi:10.1177/2326409816679431 · Cited by 7

Role of Cellular Senescence in Parkinson’s Disease: Potential for Disease-Modification Through Senotherapy

Rademacher, D. J., Exline, J. E., & Foecking, E. M. (2025) · Biomedicines · doi:10.3390/biomedicines13061400 · Cited by 8

Inhibition of annexin A7 suppresses senescence‐associated heterochromatin foci formation and senescence through the AMPK/mTOR pathway in human dermal fibroblasts

Li, N., Yan, X., Cui, X., Zhao, C., Lin, Z., & Miao, J. (2023) · Journal of Cellular Biochemistry · doi:10.1002/jcb.30472 · Cited by 6

Biochemical Hallmarks of Oxidative Stress-Induced Overactivation of Xenopus Eggs

Tokmakov, A. A., Awamura, M., & Sato, K. (2019) · BioMed Research International · doi:10.1155/2019/7180540 · Cited by 6

Cell Death: a Molecular Perspective

Zia, Q., Azhar, A., Hassan, N., Jain, P., Singh, M., Mirza, M. A., Ali, A., Parveen, S., Hasan, S., Alothaim, A. S., et al. (2021) · Current Molecular Biology Reports · doi:10.1007/s40610-021-00146-3 · Cited by 6

In vivo analysis of Bisphenol A induced dose-dependent adverse effects in cauda epididymis of mice

Samova, S., Doctor, H., & Verma, R. J. (2018) · Interdisciplinary Toxicology · doi:10.2478/intox-2018-0019 · Cited by 6

ATG9A and ARFIP2 cooperate to regulate PI4P levels for lysosomal repairPreprint

Tito, S. D., Almacellas, E., Yu, D. D., Zhang, W., Millard, E., Hervás, J. H., Pellegrino, E., Panagi, I., Fodge, D., Thurston, T. L. M., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.23.604321 · Cited by 6

High cathepsin A protein expression predicts poor prognosis and tumor recurrence of hepatocellular carcinoma patients after curative hepatectomy.

Luo, L., Wang, X., Wang, H., Yang, C., Zhang, Y., Li, X., & Xu, Z. (2022) · PubMed Central · Cited by 5

Aberrant lipid accumulation and retinal pigment epithelium dysfunction in PRCD-deficient mice

Motipally, S. I., Kolson, D. R., Guan, T., & Kolandaivelu, S. (2024) · Experimental Eye Research · doi:10.1016/j.exer.2024.110016 · Cited by 5

Identifying the programmed cell death index of hepatocellular carcinoma for prognosis and therapy response improvement by machine learning: a bioinformatics analysis and experimental validation

Shi, Y., Feng, Y., Qiu, P., Zhao, K., Li, X., Deng, Z., & Wang, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1298290 · Cited by 5

Editorial: Crystal death: it's not always the inflammasome…

Schmidt, F. I., & Ploegh, H. L. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.3ce0117-022r · Cited by 5

Involvement of TGF-β, mTOR, and inflammatory mediators in aging alterations during myxomatous mitral valve disease in a canine model

Grzeczka, A., Graczyk, S., & Kordowitzki, P. (2025) · GeroScience · doi:10.1007/s11357-025-01520-0 · Cited by 6

Semax peptide targets the μ opioid receptor gene Oprm1 to promote deubiquitination and functional recovery after spinal cord injury in female mice

Liu, R., Chen, Y., Huang, H., Li, X., Lv, J., Jiang, L., Jiang, H., Wu, C., Chen, W., Xu, H., et al. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70122 · Cited by 4

VPS13C/PARK23 initiates lipid transfer and membrane remodeling for efficient lysosomal repair

Adeosun, O. A., Schröer, C., Südhoff, E., Bergenthal, F., Sommer, K., Döffinger, E., Fiedler, B., Hilderink, A., Lehmann, A., Pohle, L.-S., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-75145-y · Cited by 5

“Micro-managing” immune activation and protein turnover: microglial lysosomes in the context of health and disease

Somodji, E. A., & Gowrishankar, S. (2026) · npj Dementia · doi:10.1038/s44400-026-00086-8 · Cited by 6

Ubiquitination-activated TAB–TAK1–IKK–NF-κB axis modulates gene expression for cell survival in the lysosomal damage responsePreprint

Endo, A., Takahashi, C., Ishibashi, N., Nishito, Y., Yamano, K., Tanaka, K., & Yoshida, Y. (2025) · eLife · doi:10.7554/elife.106901.3 · Cited by 13

Starvation-induced autophagy modulates spermatogenesis and sperm quality in Nile tilapia

Sales, C. F., Pinheiro, A. P. B., Ribeiro, Y. M., Moreira, D. P., Luz, R. K., Melo, R. M. C., & Rizzo, E. (2023) · Theriogenology · doi:10.1016/j.theriogenology.2023.11.030 · Cited by 4

Lysosomes’ fallback strategies: more than just survival or death

Wang, Q., Wang, R., Hu, H., Huo, X., & Wang, F. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1559504 · Cited by 3

The novel effects of the cardiovascular drug ranolazine on the alleviation of age-related cognitive decline and the underlying mechanisms

Yue, X., Wu, S., Yin, Y., Zhao, X. J., Li, E., Liu, G., Zan, X., Yu, Q., He, P. F., & Zhang, C. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.178007 · Cited by 3

Multifactorial Imaging Analysis as a Platform for Studying Cellular Senescence Phenotypes

Shatalova, R. O., Larin, I. I., & Shevyrev, D. (2025) · Journal of Imaging · doi:10.3390/jimaging11100351 · Cited by 3

Intermittent hypobaric pressure induces selective senescent cell death and alleviates age-related osteoporosis

Meng, B., Qu, Y., Yang, B., Fu, C., He, Y., Li, J., Wan, R., Li, X., Xue, Z., Cao, Z., et al. (2026) · Nature Biomedical Engineering · doi:10.1038/s41551-025-01584-5 · Cited by 4

Autophagosome turnover requires Arp2/3 complex-mediated maintenance of lysosomal integrity

Theodore, C. J., Wagner, L. H., & Campellone, K. G. (2026) · Molecular Biology of the Cell · doi:10.1091/mbc.e24-03-0109 · Cited by 3

Multifunctional applications of difluoroboron β-diketonate complexes

Zeng, L., Zhang, Y.-Q., Teng, K., Niu, L., & Yang, Q. (2026) · Chemical Communications · doi:10.1039/d5cc06502j · Cited by 3

α-hemolysin targets LGALS3 (galectin 3) to promote intracellular survival of Staphylococcus aureus via lysosomal disruption and autophagy inhibition

Zhang, Y., Zhao, Z., Han, P., Qi, J., Zhang, M., Wang, L., Meng, Y., Li, J., Yang, Y. S., Chen, L., et al. (2026) · Autophagy · doi:10.1080/15548627.2026.2642331 · Cited by 3

Dealing with damaged lysosomes : Impact of lysosomal membrane stability in health and disease

Eriksson, I. (2022) · Linköping University medical dissertations · doi:10.3384/9789179291792 · Cited by 3

The PITT pathway: Keeping lysosomes young

Yang, H., & Tan, J. X. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.1097 · Cited by 2

Functional Activity of Non-Proliferating Mesenchymal Stromal Cells Cultured at Different Densities

Ездакова, М. И., Zornikova, K. V., Валентинович, Б. С., & Andreeva, E. R. (2021) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-021-05102-w · Cited by 3

Linear ubiquitination at damaged lysosomes induces local NF-κB activation and controls cell survivalPreprint

Zein, L., Dietrich, M., Balta, D., Bader, V., Scheuer, C., Zellner, S., Weinelt, N., Vandrey, J., Mari, M. C., Behrends, C., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.06.560832 · Cited by 3

Plant flavonoid effects on the non-apoptotic mechanisms of regulated cell death

Białek, W., Czechowicz, P., Grzyb, J., Sławski, J., Collawn, J. F., & Bartoszewski, R. (2025) · Phytochemistry Reviews · doi:10.1007/s11101-025-10140-7 · Cited by 4

A multi-type programmed cell death gene signature predicts survival and reveals therapeutic targets in osteosarcoma

Wu, C. (2025) · Discover Oncology · doi:10.1007/s12672-025-02944-y · Cited by 2

Reductive stress and apoptotic activities in bivalve mollusc Unio tumidus exposed to the combination of microplastics, antibiotic salinomycin and heatingPreprint

Martyniuk, V., Matskiv, T., Yunko, K., Khoma, V., Gnatyshyna, L., Faggio, C., & Stoliar, O. B. (2023) · Research Square · doi:10.21203/rs.3.rs-3156761/v1 · Cited by 2

The impact of dietary restriction on transcriptional profiles of hematopoietic stem cells in aged female mice

Yu, C., Qiu, X., Tao, S., Wu, Y., He, S., Wang, Q., Tang, D., & Wang, Y. (2025) · Biogerontology · doi:10.1007/s10522-025-10263-6 · Cited by 3

Visualizing and mapping cell death: Biochemical tools, techniques and assays

Soni, S., Tiwari, A. K., Singh, A. P., & Upadhyay, A. (2025) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2025.06.018 · Cited by 1

Integrated bioinformatics and experimental validation identify lysosome and immune infiltration-related genes as therapeutic targets in late-onset major depressive disorder

Hu, J.-Z., Gao, Y., Song, X.-N., Wang, D., Du, X.-Z., Wang, X., Hu, X., & Liu, S. (2025) · Scientific Reports · doi:10.1038/s41598-025-10283-9 · Cited by 1

Selective Autophagy: A Potential Player in Cutaneous Wound Healing

Jin, W., Ren, D., Yu, M., Li, Y., Zhang, W., & Guo, S. (2025) · Advances in Wound Care · doi:10.1177/21621918251372954 · Cited by 1

Lysosomal dysfunction in diabetes and diabetic complications

Chen, X., Huang, L., Xiao, Z., & Liu, L. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1794600 · Cited by 1

Subtype-specific secretion of extracellular vesicles by LRRK2 and Rab GTPases under lysosomal stress

Sakurai, M., Kuwahara, T., Suenaga, S., Takatori, S., Tomita, T., Shalit, T., Tengstrand, E., Hsieh, F., & Iwatsubo, T. (2026) · iScience · doi:10.1016/j.isci.2026.117203 · Cited by 1

Vacuolar H + -ATPase Preserves Cardiolipin Homeostasis Through the Lysosomal-Mitochondrial Axis to Restrain Cardiac Aging

Tie, H., Hou, M., Li, Y., Pan, M., Neumann, D., Liu, R., Zhang, J., Hoes, M. F., Nabben, M., Glatz, J. F. C., et al. (2026) · Circulation · doi:10.1161/circulationaha.125.078376 · Cited by 1

BMP4, SGSH, and SLC11A2 are Predicted to Be Biomarkers of Aging Associated with Programmed Cell Death

Öktem, E. K. (2023) · Journal of Molecular Neuroscience · doi:10.1007/s12031-023-02148-5 · Cited by 1

Studying Cellular Senescence Using the Model Organism Drosophila melanogaster

Louka, X. P., Gumeni, S., & Trougakos, I. P. (2025) · Methods in molecular biology · doi:10.1007/978-1-0716-4426-3_17 · Cited by 2

Circulatory factors in stroke protection and recovery

He, J., Liu, Q., Guo, J., Wu, D., & 郭艳苏 (2025) · Brain Research · doi:10.1016/j.brainres.2025.149594 · Cited by 1

Ubiquitination-activated TAB–TAK1–IKK–NF-κB axis modulates gene expression for cell survival in the lysosomal damage responsePreprint

Endo, A., Takahashi, C., Nishito, Y., Tanaka, K., & Yoshida, Y. (2025) · eLife · doi:10.7554/elife.106901.1 · Cited by 1

Distinct lysosomal dysfunction patterns of GRN deficiency in the CNS implicate progranulin in cell type–specific protein sortingPreprint

Werthmann, G. C., & Herz, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.29.696915 · Cited by 2

The endolysosomal system in neuronal physiology and pathology

Sanchez, S. V. (2019)

Relationship between various pathways of cellular death at distinct stages of ontogenesis in normal state and systemic diseases of connective tissue

Shishkin, V. I., Nazarov, P. G., Malenkov, Y. A., Шишкин, В. А., Kudryavtseva, G. V., & Kartunen, А. A. (2020) · Medical Immunology (Russia) · doi:10.15789/1563-0625-rbv-1904

Pathogenesis of age-related macular degeneration

Li, W. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822061-0.00002-5

Kinetic Modeling of Mitochondrial-Reticular Network Dynamics

Kudryavtseva, G. V., Malenkov, Y. A., Shishkin, V. V., Shishkin, V. I., & Kartunen, А. A. (2021) · BIOPHYSICS · doi:10.1134/s0006350921020135

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How to Build a Neuron

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Evaluating Cell Death Signaling by Immunofluorescence in a Rat Model of Ischemic Stroke

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Pathways to Repair or Remove Lysosomes Damaged by Extracellular Fine Particles

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Life of the cell: Is it important how cells die?

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Knowing cell death mechanisms and their applications in the management of disease

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Ubiquitination-activated TAB–TAK1–IKK–NF-κB axis modulates gene expression for cell survival in the lysosomal damage responsePreprint

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Microglial activation and lysosomal dysfunction in hemorrhagic stroke

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Neuromelanin: Bridging catecholamine metabolism and neurodegeneration in Parkinson's disease

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Lysosomes and lysosomal cathepsins in cell death

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