Lysosomal Acidification Mechanisms

Vacuolar ATPases: rotary proton pumps in physiology and pathophysiology

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AN INTRODUCTION TO TRP CHANNELS

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Pannexin‐1 mediates large pore formation and interleukin‐1β release by the ATP‐gated P2X7 receptor

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X-ray structure of a ClC chloride channel at 3.0 Å reveals the molecular basis of anion selectivity

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Loss of the ClC-7 Chloride Channel Leads to Osteopetrosis in Mice and Man

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Mammalian cell-cycle regulation: several Cdks, numerous cyclins and diverse compensatory mechanisms

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NAADP mobilizes calcium from acidic organelles through two-pore channels

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Gating the Selectivity Filter in ClC Chloride Channels

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The ABC protein turned chloride channel whose failure causes cystic fibrosis

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Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

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Lysosomal ion channels involved in cellular entry and uncoating of enveloped viruses: Implications for therapeutic strategies against SARS-CoV-2

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The role of lysosomal ion channels in lysosome dysfunction

Kendall, R. L., & Holian, A. (2021) · Inhalation Toxicology · doi:10.1080/08958378.2021.1876188 · Cited by 38

Downregulation of ATP6V1A Involved in Alzheimer’s Disease via Synaptic Vesicle Cycle, Phagosome, and Oxidative Phosphorylation

Zhou, Z., Bai, J., Zhong, S., Zhang, R., Kang, K., Zhang, X., Xu, Y., Zhao, C., & Zhao, M. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/5555634 · Cited by 36

Ambient fine particulate matter provokes multiple modalities of cell death via perturbation of subcellular structures

Wāng, Y. (2024) · Environment International · doi:10.1016/j.envint.2024.109193 · Cited by 35

Arginine‐Modified Nanostructured Lipid Carriers with Charge‐Reversal and pH‐Sensitive Membranolytic Properties for Anticancer Drug Delivery

Sun, M., Li, J., Zhang, C., Xie, Y., Qiao, H., Su, Z., Oupický, D., & Ping, Q. N. (2017) · Advanced Healthcare Materials · doi:10.1002/adhm.201600693 · Cited by 35

The HIV-1 accessory proteins Nef and Vpu downregulate total and cell surface CD28 in CD4+ T cells

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Highly selective, red emitting BODIPY-based fluorescent indicators for intracellular Mg 2+ imaging

Lin, Q., & Buccella, D. (2018) · Journal of Materials Chemistry B · doi:10.1039/c8tb01599f · Cited by 36

A modified lysosomal organelle mediates nonlytic egress of reovirus

de Castro, I. F., Tenorio, R., Ortega-González, P., Knowlton, J. J., Zamora, P. F., Lee, C. H., Fernández, J., Dermody, T. S., & Risco, C. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201910131 · Cited by 35

Highly Photostable Fluorescent Tracker with pH-Insensitivity for Long-Term Imaging of Lysosomal Dynamics in Live Cells

Chao, X., Qi, Y., & Zhang, Y. (2020) · ACS Sensors · doi:10.1021/acssensors.0c01588 · Cited by 35

The V-ATPase a3 Subunit: Structure, Function and Therapeutic Potential of an Essential Biomolecule in Osteoclastic Bone Resorption

Chu, A., Zirngibl, R. A., & Manolson, M. F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136934 · Cited by 34

Biomolecular condensates sustain pH gradients at equilibrium through charge neutralisationPreprint

Ausserwӧger, H., Scrutton, R. M., Fischer, C. M., Šneideris, T., Qian, D., de Csilléry, E., Baronaite, I., Saar, K. L., Białek, A. Z., Oeller, M., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.23.595321 · Cited by 35

Mechanisms of the immune response cause by cationic and anionic surface functionalized cellulose nanocrystals using cell-based assays

Despres, H. W., Sabra, A., Anderson, P., Hemraz, U. D., Boluk, Y., Sunasee, R., & Ckless, K. (2018) · Toxicology in Vitro · doi:10.1016/j.tiv.2018.12.009 · Cited by 34

Mechanism of protein cleavage at asparagine leading to protein–protein cross-links

Friedrich, M. G., Wang, Z., Schey, K. L., & Truscott, R. J. W. (2019) · Biochemical Journal · doi:10.1042/bcj20190743 · Cited by 34

NDST3 deacetylates α‐tubulin and suppresses V‐ATPase assembly and lysosomal acidification

Tang, Q., Liu, M., Liu, Y., Hwang, R., Zhang, T., & Wang, J. (2021) · The EMBO Journal · doi:10.15252/embj.2020107204 · Cited by 32

Disturb mitochondrial associated proteostasis: Neurodegeneration and imperfect ageing

Jagtap, Y. A., Kumar, P., Kinger, S., Dubey, A. R., Choudhary, A., Gutti, R. K., Singh, S., Jha, H. C., Poluri, K. M., & Mishra, A. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1146564 · Cited by 36

Expression Patterns and Subcellular Localization of Carbonic Anhydrases Are Developmentally Regulated during Tooth Formation

Reibring, C.-G., Shahawy, M. E., Hallberg, K., Kannius‐Janson, M., Nilsson, J., Parkkila, S., Sly, W. S., Waheed, A., Linde, A., & Gritli-Linde, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096007 · Cited by 34

Rifampicin Attenuates Rotenone-Treated Microglia Inflammation via Improving Lysosomal Function

Liang, Y., Zheng, D., Peng, S., Lin, D., Jing, X., Zeng, Z., Chen, Y., Huang, K., Xie, Y., Zhou, T., et al. (2020) · Toxicology in Vitro · doi:10.1016/j.tiv.2019.104690 · Cited by 33

Towards solving the mystery of peroxisomal matrix protein import

Skowyra, M. L., Feng, P., & Rapoport, T. A. (2024) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.08.005 · Cited by 33

Pharmacological approaches for targeting lysosomes to induce ferroptotic cell death in cancer

Ji, F., Wang, Z.-X., Bin, J.-L., Chen, Y., Ma, J., Deng, J.-H., Huang, X., Zhou, J., & Lu, G. (2024) · Cancer Letters · doi:10.1016/j.canlet.2024.216728 · Cited by 38

G2019S selective LRRK2 kinase inhibitor abrogates mitochondrial DNA damage

Pena, N., Richbourg, T., González-Hunt, C. P., Qi, R., Wren, P. B., Barlow, C., Shanks, N. F., Carlisle, H. J., & Sanders, L. H. (2024) · npj Parkinson s Disease · doi:10.1038/s41531-024-00660-y · Cited by 33

The different roles of V-ATPase a subunits in phagocytosis/endocytosis and autophagy

Chen, Q., Kou, H., Demy, D. L., Liu, W., Li, J., Wen, Z., Herbomel, P., Huang, Z., Zhang, W., & Xu, J. (2024) · Autophagy · doi:10.1080/15548627.2024.2366748 · Cited by 33

Atractylenolide I inhibits angiogenesis and reverses sunitinib resistance in clear cell renal cell carcinoma through ATP6V0D2-mediated autophagic degradation of EPAS1/HIF2α

Li, Q., Zeng, K., Chen, Q., Han, C., Wang, X., Li, B., Miao, J., Zheng, B., Liu, J., Yuan, X., et al. (2024) · Autophagy · doi:10.1080/15548627.2024.2421699 · Cited by 34

Sterile inflammation induced by Carbopol elicits robust adaptive immune responses in the absence of pathogen-associated molecular patterns

Gartlan, K. H., Krashias, G., Wegmann, F., Hillson, W. R., Scherer, E. M., Greenberg, P. D., Eisenbarth, S. C., Moghaddam, A. E., & Sattentau, Q. J. (2016) · Vaccine · doi:10.1016/j.vaccine.2016.03.025 · Cited by 34

Superparamagnetic iron oxide nanoparticles for drug delivery

Chee, C. F., Leo, B. F., & Lai, C. W. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813741-3.00038-8 · Cited by 33

Regulation of Autophagic Flux by the 20S Proteasome

Njomen, E., & Tepe, J. J. (2019) · Cell chemical biology · doi:10.1016/j.chembiol.2019.07.002 · Cited by 33

Novel synthesis of platinum complexes and their intracellular delivery to tumor cells by means of magnetic nanoparticles

Quarta, A., Amorín, M., Aldegunde, M. J., Blasi, L., Ragusa, A., Nitti, S., Pugliese, G., Gigli, G., Granja, J. R., & Pellegrino, T. (2019) · Nanoscale · doi:10.1039/c9nr07015j · Cited by 33

Ion Channels and Transporters in Autophagy

Zhang, R., Kang, R., Klionsky, D. J., & Tang, D. (2021) · Autophagy · doi:10.1080/15548627.2021.1885147 · Cited by 33

Translation Inhibitors Activate Autophagy Master Regulators TFEB and TFE3

Dang, T. T., & Back, S. H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222112083 · Cited by 33

CryoEM of endogenous mammalian V-ATPase interacting with the TLDc protein mEAK-7

Tan, Y. Z., Abbas, Y. M., Wu, J., Wu, D., Keon, K. A., Hesketh, G. G., Bueler, S. A., Gingras, A., Robinson, C. V., Grinstein, S., et al. (2022) · Life Science Alliance · doi:10.26508/lsa.202201527 · Cited by 31

HPS6 interacts with dynactin p150Glued to mediate retrograde trafficking and maturation of lysosomes

Li, K., Yang, L., Zhang, C., Niu, Y., Li, W., & Liu, J. (2014) · Journal of Cell Science · doi:10.1242/jcs.141978 · Cited by 33

Cathepsin S attenuates endosomal EGFR signalling: A mechanical rationale for the combination of cathepsin S and EGFR tyrosine kinase inhibitors

Huang, C., Lee, C.-C., Lin, H.-H., & Chang, J. (2016) · Scientific Reports · doi:10.1038/srep29256 · Cited by 33

Liposome-chaperoned cell-free synthesis for the design of proteoliposomes: Implications for therapeutic delivery

Lu, M., Zhao, X., Xing, H., Xun, Z., Yang, T., Cai, C., Wang, D., & Ding, P. (2018) · Acta Biomaterialia · doi:10.1016/j.actbio.2018.03.043 · Cited by 33

Potential targets of microglia in the treatment of neurodegenerative diseases: Mechanism and therapeutic implications

Zhao, W., Liu, Z., Wu, J., Liu, A., & Yan, J. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-01343 · Cited by 37

Role of endolysosomes and pH in the pathogenesis and treatment of glioblastoma

Halcrow, P. W., Datta, G., Ohm, J. E., Soliman, M. L., Chen, X., & Geiger, J. D. (2019) · Cancer Reports · doi:10.1002/cnr2.1177 · Cited by 32

Two-photon AIE probe conjugated theranostic nanoparticles for tumor bioimaging and pH-sensitive drug delivery

Ma, B., Zhuang, W., He, H., Su, X., Yu, T., Hu, J. X., Yang, L., Li, G., & Wang, Y. (2019) · Nano Research · doi:10.1007/s12274-019-2426-4 · Cited by 32

Mini-Review on Lipofuscin and Aging: Focusing on The Molecular Interface, The Biological Recycling Mechanism, Oxidative Stress, and The Gut-Brain Axis Functionality

Ilie, O., Ciobica, A. S., Riga, S., Dhunna, N., McKenna, J., Mavroudis, I. A., Doroftei, B., Ciobanu, A. M., & Riga, D. (2020) · Medicina · doi:10.3390/medicina56110626 · Cited by 34

Interactions between fullerene derivatives and biological systems

Siringan, M. J., Dawar, A., & Zhang, J. (2023) · Materials Chemistry Frontiers · doi:10.1039/d3qm00004d · Cited by 32

Interlaboratory studies on in vitro test methods for estimating in vivo resorption of calcium phosphate ceramics

Ito, A., Sogo, Y., Yamazaki, A., Aizawa, M., Osaka, A., Hayakawa, S., Kikuchi, M., Yamashita, K., Tanaka, Y., Tadokoro, M., et al. (2015) · Acta Biomaterialia · doi:10.1016/j.actbio.2015.07.040 · Cited by 32

Retinal Pigment Epithelium Under Oxidative Stress: Chaperoning Autophagy and Beyond

Markitantova, Y. V., & Simirskii, V. N. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26031193 · Cited by 34

STAT3 contributes to lysosomal-mediated cell death in a novel derivative of riccardin D-treated breast cancer cells in association with TFEB

Li, L., Sun, B., Gao, Y., Niu, H., Yuan, H., & Lou, H. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.02.026 · Cited by 32

ATP6V0d2 controls Leishmania parasitophorous vacuole biogenesis via cholesterol homeostasis

Pessoa, C. C., Reis, L. C., Ramos-Sanchez, E. M., Orikaza, C. M., Cortéz, C., Levatti, E. V. D. C., Badaró, A. C. B., Yamamoto, J. U. D. S., D’Almeida, V., Goto, H., et al. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1007834 · Cited by 31

Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies

Lizarraga, S. B., Ma, L., Maguire, A. M., van Dyck, L. I., Wu, Q., Ouyang, Q., Kavanaugh, B. C., Nagda, D., Livi, L. L., Pescosolido, M. F., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.aaw0682 · Cited by 33

Cyclotriphosphazene-Based “Butterfly” Fluorescence Probe for Lysosome Targeting

Liu, P., Wang, L., Chen, L., Su, X., & Shi, X. (2021) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.1c00160 · Cited by 31

Nano-hydroxyapatite accelerates vascular calcification via lysosome impairment and autophagy dysfunction in smooth muscle cells

Liu, Q., Luo, Y., Zhao, Y. F., Xiang, P., Zhu, J., Jing, W., Jin, W., Chen, M., Tang, R., & Yu, H. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.06.004 · Cited by 32

Endocytosis and Enamel Formation

Pham, C.-D., Smith, C. E., Hu, Y., Hu, J. C. ‐., Simmer, J. P., & Chun, Y. P. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00529 · Cited by 30

Antiretroviral Drugs Promote Amyloidogenesis by De-Acidifying Endolysosomes

Liang, H., Ye, Y., Soliman, M. L., Lakpa, K. L., Miller, N., Afghah, Z., Geiger, J. D., & Chen, X. (2019) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-019-09862-1 · Cited by 30

Macrophage dysfunction in cystic fibrosis: Nature or nurture?

Turton, K. B., Ingram, R. J., & Valvano, M. A. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.4ru0620-245r · Cited by 31

Cellular Internalization and Inhibition Capacity of New Anti-Glioma Peptide Conjugates: Physicochemical Characterization and Evaluation on Various Monolayer- and 3D-Spheroid-Based in Vitro Platforms

Baranyai, Z., Biri‐Kovács, B., Krátký, M., Szeder, B., Debreczeni, M. L., Budai, J., Kovács, B., Horváth, L. B., Pári, E., Németh, Z., et al. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c01399 · Cited by 32

Dual Recognition DNA Triangular Prism Nanoprobe: Toward the Relationship between K + and pH in Lysosomes

Li, X., Liu, X., Jia, Y., Luo, X., Chen, H., & Xu, J. (2021) · Analytical Chemistry · doi:10.1021/acs.analchem.1c04056 · Cited by 30

The Toxoplasma plant‐like vacuolar compartment ( PLVAC )

Stasic, A. J., Moreno, S. N. J., Carruthers, V. B., & Dou, Z. (2022) · Journal of Eukaryotic Microbiology · doi:10.1111/jeu.12951 · Cited by 30

The Biology of Lysosomes: From Order to Disorder

Amaral, O., Martins, M. M., Oliveira, A. R., Duarte, A. J., Mondragão-Rodrigues, I., & Macedo, M. F. (2023) · Biomedicines · doi:10.3390/biomedicines11010213 · Cited by 30

A new V-ATPase regulatory mechanism mediated by the Rab interacting lysosomal protein (RILP)

Luca, M. D., & Bucci, C. (2014) · Communicative & Integrative Biology · doi:10.4161/cib.29616 · Cited by 30

A Novel High Content Imaging-Based Screen Identifies the Anti-Helminthic Niclosamide as an Inhibitor of Lysosome Anterograde Trafficking and Prostate Cancer Cell Invasion

Circu, M. L., Dykes, S. S., Carroll, J. L., Kelly, K., Galiano, F. J., Greer, A. H., Cardelli, J. A., & El-Osta, H. E. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146931 · Cited by 30

Methods for monitoring Ca2+ and ion channels in the lysosome

Zhong, X. Z., Yang, Y., Sun, X. J., & Dong, X. (2016) · Cell Calcium · doi:10.1016/j.ceca.2016.12.001 · Cited by 31

Novel reversibly switchable fluorescent proteins for RESOLFT and STED nanoscopy engineered from the bacterial photoreceptor YtvA

Gregor, C., Sidenstein, S. C., Andresen, M. A., Sahl, S. J., Danzl, J. G., & Hell, S. W. (2018) · Scientific Reports · doi:10.1038/s41598-018-19947-1 · Cited by 30

Copper toxicity and deficiency: the vicious cycle at the core of protein aggregation in ALS

Min, J.-H., Sarlus, H., & Harris, R. A. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1408159 · Cited by 31

Biomolecular condensates sustain pH gradients at equilibrium through charge neutralization

Ausserwöger, H., Scrutton, R. M., Fischer, C. M., Šneideris, T., Qian, D., de Csilléry, E., Baronaitė, I., Saar, K. L., Białek, A. Z., Oeller, M., et al. (2026) · Nature Chemistry · doi:10.1038/s41557-025-02039-9 · Cited by 71

Select microtubule inhibitors increase lysosome acidity and promote lysosomal disruption in acute myeloid leukemia (AML) cells

Bernard, D., Gebbia, M., Prabha, S., Gronda, M., MacLean, N., Wang, X., Hurren, R., Sukhai, M. A., Cho, E. E., Manolson, M. F., et al. (2015) · APOPTOSIS · doi:10.1007/s10495-015-1123-3 · Cited by 29

Lysosomal and vacuolar sorting: not so different after all!

Lousa, C. D. M., & Denecke, J. (2016) · Biochemical Society Transactions · doi:10.1042/bst20160050 · Cited by 29

Cysteine peptidases of Eudiplozoon nipponicum: a broad repertoire of structurally assorted cathepsins L in contrast to the scarcity of cathepsins B in an invasive species of haematophagous monogenean of common carp

Jedličková, L., Dvořáková, H., Dvořák, J., Kašný, M., Ulrychová, L., Vorel, J., Žárský, V., & Mikeš, L. (2018) · Parasites & Vectors · doi:10.1186/s13071-018-2666-2 · Cited by 29

Cleavage C-terminal to Asp leads to covalent crosslinking of long-lived human proteins

Wang, Z., Friedrich, M. G., Truscott, R. J. W., & Schey, K. L. (2019) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2019.06.009 · Cited by 29

Synergistic anti-breast cancer effect of pulsatilla saponin D and camptothecin through interrupting autophagic–lysosomal function and promoting p62-mediated ubiquitinated protein aggregation

Wang, K., Tu, Y., Wan, J., Chen, M., & He, C. (2019) · Carcinogenesis · doi:10.1093/carcin/bgz140 · Cited by 29

Heat shock factor 4 regulates lysosome activity by modulating the αB-crystallin-ATP6V1A-mTOR complex in ocular lens

Cui, X., Feng, R., Wang, J., Du, C., Pi, X., Chen, D., Li, J., Li, H., Zhang, J., Zhang, J., et al. (2019) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2019.129496 · Cited by 29

Nanoparticle-Mediated Therapeutic Application for Modulation of Lysosomal Ion Channels and Functions

Lee, D., & Hong, J. H. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12030217 · Cited by 30

Repurposing Chloroquine Against Multiple Diseases With Special Attention to SARS-CoV-2 and Associated Toxicity

Kamat, S., & Kumari, M. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.576093 · Cited by 29

A Multifunctional Nanomicelle for Real‐Time Targeted Imaging and Precise Near‐Infrared Cancer Therapy

Tian, J., Ding, L., Ju, H., Yang, Y., Li, X., Shen, Z., Zhu, Z., Yu, J., & Yang, C. J. (2014) · Angewandte Chemie · doi:10.1002/ange.201405490 · Cited by 29

Azithromycin, a potent autophagy inhibitor for cancer therapy, perturbs cytoskeletal protein dynamics

Takano, N., Hiramoto, M., Yamada, Y., Kokuba, H., Tokuhisa, M., Hino, H., & Miyazawa, K. (2023) · British Journal of Cancer · doi:10.1038/s41416-023-02210-4 · Cited by 29

Recent Development of Advanced Fluorescent Molecular Probes for Organelle-Targeted Cell Imaging

Lu, S., Dai, Z., Cui, Y., & Kong, D. (2023) · Biosensors · doi:10.3390/bios13030360 · Cited by 30

Transmembrane Protein 175, a Lysosomal Ion Channel Related to Parkinson’s Disease

Tang, T., Jian, B., & Liu, Z. (2023) · Biomolecules · doi:10.3390/biom13050802 · Cited by 31

ClC-5: Physiological role and biophysical mechanisms

Pusch, M., & Zifarelli, G. (2014) · Cell Calcium · doi:10.1016/j.ceca.2014.09.007 · Cited by 29

Gene expression profiling of adult female tissues in feeding Rhipicephalus microplus cattle ticks

Stutzer, C., van Zyl, W. A., Olivier, N. A., Richards, S. A., & Maritz-Olivier, C. (2013) · International Journal for Parasitology · doi:10.1016/j.ijpara.2013.01.009 · Cited by 29

Dynamin Regulates Autophagy by Modulating Lysosomal Function

Fang, X., Zhou, J., Liu, W., Duan, X., Gala, U., Sandoval, H., Jaiswal, M., & Tong, C. (2015) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2015.10.005 · Cited by 28

Obatoclax kills anaplastic thyroid cancer cells by inducing lysosome neutralization and necrosis

Champa, D., Orlacchio, A., Patel, B., Ranieri, M., Shemetov, A. A., Verkhusha, V. V., Cuervo, A. M., & Cristofano, A. D. (2016) · Oncotarget · doi:10.18632/oncotarget.9121 · Cited by 29

Design and Synthesis of Soluble and Cell-Permeable PI3Kδ Inhibitors for Long-Acting Inhaled Administration

Perry, M. W. D., Björhall, K., Bonn, B., Carlsson, J., Chen, Y., Eriksson, A., Fredlund, L., Hao, H., Holden, N. S., Karabelas, K., et al. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00401 · Cited by 29

Charge‐Reversal Polymers for Biodelivery

Zhang, B., Wang, K., Si, J., Sui, M., & Shen, Y. (2014) · Wiley eBooks · doi:10.1002/9783527672752.ch9 · Cited by 29

TMEM175: A lysosomal ion channel associated with neurological diseases

Wu, L., Lin, Y., Song, J., Li, L., Rao, X., Wan, W., Wei, G., Hua, F., & Ying, J. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106244 · Cited by 31

A novel marine-derived anti-acute kidney injury agent targeting peroxiredoxin 1 and its nanodelivery strategy based on ADME optimization

Yu, P., Gu, T., Rao, Y., Liang, W., Zhang, X., Jiang, H., Lu, J., She, J., Guo, J., Yang, W., et al. (2024) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2024.03.005 · Cited by 28

Particle uptake by macrophages triggers bifurcated transcriptional pathways that differentially regulate inflammation and lysosomal gene expression

Cobo, I., Murillo‐Saich, J., Alishala, M., Calderon, S., Coras, R., Hemming, B., Inkum, F., Rosas, F., Takei, R., Spann, N. J., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.02.023 · Cited by 30

Cellular uptake and intracellular localization of poly (acrylic acid) nanoparticles in a rainbow trout (Oncorhynchus mykiss) gill epithelial cell line, RTgill-W1

Felix, L. C., Ortega, V. A., & Goss, G. G. (2017) · Aquatic Toxicology · doi:10.1016/j.aquatox.2017.09.008 · Cited by 29

Cerium dioxide (CeO2) nanoparticles decrease arsenite (As(III)) cytotoxicity to 16HBE14o- human bronchial epithelial cells

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