Lysosomal Acidification Mechanisms

Vacuolar ATPases: rotary proton pumps in physiology and pathophysiology

Forgac, M. D. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2272 · Cited by 1,626

AN INTRODUCTION TO TRP CHANNELS

Ramsey, I. S., Delling, M., & Clapham, D. E. (2005) · Annual Review of Physiology · doi:10.1146/annurev.physiol.68.040204.100431 · Cited by 1,596

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

Pelegrı́n, P., & Surprenant, A. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601378 · Cited by 1,490

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

Dutzler, R., Campbell, E. B., Cadene, M., Chait, B. T., & MacKinnon, R. (2002) · Nature · doi:10.1038/415287a · Cited by 1,446

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

Kornak, U., Kasper, D., Bösl, M. R., Kaiser, E., Schweizer, M., Schulz, A., Friedrich, W., Delling, G., & Jentsch, T. J. (2001) · Cell · doi:10.1016/s0092-8674(01)00206-9 · Cited by 995

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

Satyanarayana, A., & Kaldis, P. (2009) · Oncogene · doi:10.1038/onc.2009.170 · Cited by 800

NAADP mobilizes calcium from acidic organelles through two-pore channels

Calcraft, P. J., Ruas, M., Pan, Z., Cheng, X., Arredouani, A., Hao, X., Tang, J., Rietdorf, K., Teboul, L., Chuang, K.-T., et al. (2009) · Nature · doi:10.1038/nature08030 · Cited by 760

Gating the Selectivity Filter in ClC Chloride Channels

Dutzler, R., Campbell, E. B., & MacKinnon, R. (2003) · Science · doi:10.1126/science.1082708 · Cited by 727

The ABC protein turned chloride channel whose failure causes cystic fibrosis

Gadsby, D. C., Vergani, P., & Csanády, L. (2006) · Nature · doi:10.1038/nature04712 · Cited by 726

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

Karet, F. E., Finberg, K. E., Nelson, R. D., Nayır, A., Mocan, H. N., Sanjad, S. A., Rodríguez‐Soriano, J., Santos, F., Cremers, C. W. R. J., Pietro, A. D., et al. (1999) · Nature Genetics · doi:10.1038/5022 · Cited by 687

Inspired by nonenveloped viruses escaping from endo-lysosomes: a pH-sensitive polyurethane micelle for effective intracellular trafficking

Song, N., Zhou, L., Li, J., Pan, Z., He, X., Tan, H. S., Wan, X., Li, J., Ran, R., & Fu, Q. (2016) · Nanoscale · doi:10.1039/c6nr00859c · Cited by 26

Inhibition of Amebic Lysosomal Acidification Blocks Amebic Trogocytosis and Cell Killing

Gilmartin, A. A., Ralston, K. S., & Petri, W. A. (2017) · mBio · doi:10.1128/mbio.01187-17 · Cited by 26

Simulation of the Long-Term Fate of Superparamagnetic Iron Oxide-Based Nanoparticles Using Simulated Biological Fluids

Rabel, M., Warncke, P., Grüttner, C., Bergemann, C., Kurland, H., Müller, R., Dugandžić, V., Thamm, J., Müller, F. A., Popp, J., et al. (2019) · Nanomedicine · doi:10.2217/nnm-2018-0382 · Cited by 27

Immobilized Peptide Asparaginyl Ligases Enhance Stability and Facilitate Macrocyclization and Site-Specific Ligation

Hemu, X., To, J., Zhang, X., & Tam, J. P. (2019) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.9b02524 · Cited by 26

BRD4 Inhibition Protects Against Acute Pancreatitis Through Restoring Impaired Autophagic Flux

Shen, S., Li, B., Dai, J., Wu, Z., He, Y., Wen, L., Wang, X., & Hu, G. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00618 · Cited by 26

Azithromycin and ambroxol as potential pharmacotherapy for SARS-CoV-2

Alkotaji, M. M. (2020) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2020.106192 · Cited by 26

Berbamine Hydrochloride inhibits lysosomal acidification by activating Nox2 to potentiate chemotherapy-induced apoptosis via the ROS-MAPK pathway in human lung carcinoma cells

Zhan, Y., Chen, Q., Song, Y., Wei, X., Zhao, T., Chen, B., Li, C., Zhang, W., Jiang, Y., Tan, Y., et al. (2022) · Cell Biology and Toxicology · doi:10.1007/s10565-022-09756-8 · Cited by 24

Photo-activated autophagy-associated tumour cell death by lysosome impairment based on manganese-doped graphene quantum dots

Liang, Q., Yu, F., Cai, H., Wu, X., Ma, M., Li, Z., Tedesco, A. C., Zhu, J., Xu, Q. F., & Bi, H. (2023) · Journal of Materials Chemistry B · doi:10.1039/d2tb02761e · Cited by 26

Application of magnetic iron oxide nanoparticles: Thrombotic activity, imaging and cytocompatibility of silica-coated and carboxymethyl dextrane-coated particles

Turrina, C., Schoenen, M., Milani, D., Klassen, A., Rojas‐González, D. M., Cvirn, G., Mela, P., Berensmeier, S., Slabu, I., & Schwaminger, S. P. (2023) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2023.113428 · Cited by 26

Real-time monitoring of endogenous cysteine in LPS-induced oxidative stress process with a novel lysosome-targeted fluorescent probe

Yang, Z., Li, J., Li, S., Zhou, J., Cao, Z., Li, L., Zheng, D., Zhao, X., Wang, W., Deng, Y., et al. (2023) · Analytica Chimica Acta · doi:10.1016/j.aca.2023.341819 · Cited by 25

AstragalosideII inhibits autophagic flux and enhance chemosensitivity of cisplatin in human cancer cells

Cui, Y., Wu, C., Xu, D., Wang, M., & Xia, Q. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.03.025 · Cited by 26

Two-Pore Channels: Lessons from Mutant Mouse Models

Ruas, M., Galione, A., & Parrington, J. (2015) · Messenger · doi:10.1166/msr.2015.1041 · Cited by 26

Intracellular pH-Induced Tip-to-Tip Assembly of Gold Nanorods for Enhanced Plasmonic Photothermal Therapy

Ahijado‐Guzmán, R., González‐Rubio, G., Izquierdo, J. G., Bañares, L., López‐Montero, I., Calzado‐Martín, A., Calleja, M., Tardajos, G., & Guerrero‐Martínez, A. (2016) · ACS Omega · doi:10.1021/acsomega.6b00184 · Cited by 26

Temperature and pH dual-stimuli responsive polymeric carriers for drug delivery

Abouelmagd, S. A., Ellah, N. H. A., & El‐Hamid, B. N. A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-08-101995-5.00003-9 · Cited by 26

Molecular evidence for the adaptive evolution in euryhaline bivalves

Zhou, C., Yang, M., Hu, Z., Pu, S., Li, Y., Guo, Y., Zhang, T., & Song, H. (2023) · Marine Environmental Research · doi:10.1016/j.marenvres.2023.106240 · Cited by 25

Insights into the anticancer photodynamic activity of Ir(III) and Ru(II) polypyridyl complexes bearing β-carboline ligands

Sanz-Villafruela, J., Bermejo‐Casadesús, C., Zafon, E., Martı́nez-Alonso, M., Durá, G., Heras, A., Soriano-Díaz, I., Giussani, A., Ortı́, E., Tebar, F., et al. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2024.116618 · Cited by 25

13C NMR detects conformational change in the 100-kD membrane transporter ClC-ec1

Abraham, S. J., Cheng, R. C. K., Chew, T. A., Khantwal, C. M., Liu, C. W., Gong, S., Nakamoto, R. K., & Maduke, M. C. (2015) · Journal of Biomolecular NMR · doi:10.1007/s10858-015-9898-7 · Cited by 27

Weak Organic Acids Decrease Borrelia burgdorferi Cytoplasmic pH, Eliciting an Acid Stress Response and Impacting RpoN- and RpoS-Dependent Gene Expression

Dulebohn, D. P., Richards, C. L., Su, H., Lawrence, K. A., & Gherardini, F. C. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01734 · Cited by 25

Using a Multi‐Shelled Hollow Metal–Organic Framework as a Host to Switch the Guest‐to‐Host and Guest‐to‐Guest Interactions

Liu, X., Zhang, F., Goh, T. W., Li, Y., Shao, Y., Luo, L., Huang, W., Long, Y., Chou, L., & Tsung, C. (2017) · Angewandte Chemie · doi:10.1002/ange.201711600 · Cited by 25

The Roles of ATP13A2 Gene Mutations Leading to Abnormal Aggregation of α-Synuclein in Parkinson’s Disease

Zhang, F., Wu, Z., Long, F., Tan, J., Gong, N., Li, X., & Lin, C. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.927682 · Cited by 29

Steering the azido–tetrazole equilibrium of 4-azidopyrimidines via substituent variation – implications for drug design and azide–alkyne cycloadditions

Thomann, A., Zapp, J., Hutter, M. C., Empting, M., & Hartmann, R. W. (2015) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob01006c · Cited by 25

Lysosomes relax in the cellular suburbs

Gowrishankar, S., & Ferguson, S. M. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201602082 · Cited by 25

In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates

Baranyai, Z., Krátký, M., Vosátka, R., Szabó, E., Senoner, Z., Dávid, S., Stolaříková, J., Vinšová, J., & Bősze, S. E. (2017) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2017.03.047 · Cited by 25

Functional characterization of lysosomal interaction of Akt with VRK2

Hirata, N., Suizu, F., Matsuda‐Lennikov, M., Tanaka, T., Edamura, T., Ishigaki, S., Donia, T., Lithanatudom, P., Obuse, C., Iwanaga, T., et al. (2018) · Oncogene · doi:10.1038/s41388-018-0330-0 · Cited by 27

Multiwalled carbon nanotubes for combination therapy: a biodistribution and efficacy pilot study

Biagiotti, G., Pisaneschi, F., Gammon, S. T., Machetti, F., Ligi, M. C., Giambastiani, G., Tuci, G., Powell, E., Piwnica-Worms, H. M., Pranzini, E., et al. (2019) · Journal of Materials Chemistry B · doi:10.1039/c8tb03299h · Cited by 25

Convection-enhanced delivery of liposomal drugs for effective treatment of glioblastoma multiforme

Han, Y., & Park, J. (2020) · Drug Delivery and Translational Research · doi:10.1007/s13346-020-00773-w · Cited by 26

UsingDrosophilaModels of Amyloid Toxicity to Study Autophagy in the Pathogenesis of Alzheimer’s Disease

O’Keefe, L. V., & Denton, D. (2018) · BioMed Research International · doi:10.1155/2018/5195416 · Cited by 25

Carbon dots with tunable excitation-independent fluorescence and organelle-specific targeting via core graphitization and surface groups engineering

Sun, M.-Y., Tian, B., Li, X., Li, Y., Yu, L., Guo, X.-L., Miao, Q., Li, H., & Liang, H. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.153729 · Cited by 24

A host organelle integrates stolen chloroplasts for animal photosynthesis

Allard, C. A., Thies, A. B., Mitra, R., Vaelli, P. M., Leto, O. D., Walsh, B. L., Laetz, E. M. J., Tresguerres, M., Lee, A. S. Y., & Bellono, N. W. (2025) · Cell · doi:10.1016/j.cell.2025.06.003 · Cited by 24

Endocytosis is essential for cysteine-deprivation-induced ferroptosis

Liu, X., Zhao, Z., Bian, Z., Benthani, F. A., Hu, Y., Liang, D., & Jiang, X. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.08.006 · Cited by 24

TRPV1 activation mitigates hypoxic injury in mouse cardiomyocytes by inducing autophagy through the AMPK signaling pathway

Wei, J., Lin, J., Zhang, J., Tang, D., Xiang, F., Cui, L., Zhang, Q., Yuan, H., Song, H., Lv, Y., et al. (2020) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00161.2019 · Cited by 24

Heterogeneity of ferrous iron‐containing endolysosomes and effects of endolysosome iron on endolysosome numbers, sizes, and localization patterns

Halcrow, P. W., Kumar, N., Afghah, Z., Fischer, J. P., Khan, N., Chen, X., Meucci, O., & Geiger, J. D. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15583 · Cited by 23

Cytoplasmic DNA in cancer cells: Several pathways that potentially limit DNase2 and TREX1 activities

Anindya, R. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2022.119278 · Cited by 24

Modulation of anti-cardiac fibrosis immune responses by changing M2 macrophages into M1 macrophages

Chen, S., Wang, K., Fan, Z., Zhou, T., Li, R., Zhang, B., Chen, J., Chi, J., Wei, K., Liu, J., et al. (2024) · Molecular Medicine · doi:10.1186/s10020-024-00858-z · Cited by 26

A parasitic helminth-derived peptide that targets the macrophage lysosome is a novel therapeutic option for autoimmune disease

Alvarado, R., O’Brien, B. A., Tanaka, A., Dalton, J. P., & Donnelly, S. (2014) · Immunobiology · doi:10.1016/j.imbio.2014.11.008 · Cited by 24

Overexpression of V-ATPase B2 attenuates lung injury/fibrosis by stabilizing lysosomal membrane permeabilization and increasing collagen degradation

Lee, J.-U., Hong, J., Shin, H., Ryu, C.-B., Park, S., & Jeong, S. H. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00776-2 · Cited by 23

Synthetic Nanoassemblies for Regulating Organelles: From Molecular Design to Precision Therapeutics

Guo, Y., Li, P., Guo, X., Yao, C., & Yang, D. (2024) · ACS Nano · doi:10.1021/acsnano.4c10194 · Cited by 25

Engineered Reactive Oxygen Species (ROS)‐Responsive Artificial H+/Cl− Ion Channels for Targeted Cancer Treatment

Jia, C., Luo, D., Zhou, J., Xie, X., Lam, H. Y. I., Li, P., Mu, Y., Zeng, Z., & Ren, C. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202419800 · Cited by 23

DMXL1 promotes recruitment of V1-ATPase to lysosomes upon TRPML1 activation

Lee, C., Eldridge, M. J. G., Gonzalez‐Lozano, M. A., Bresnahan, T., Niday, Z., del Camino, D., Fu, T., Paulo, J. A., Moran, M. M., Hélaine, S., et al. (2025) · Nature Structural & Molecular Biology · doi:10.1038/s41594-025-01581-x · Cited by 23

Cerenkov-Specific Contrast Agents for Detection of pH In Vivo

Czupryna, J., Kachur, A. V., Blankemeyer, E. R., Popov, A. V., Arroyo, A. D., Karp, J. S., & Delikatny, E. J. (2015) · Journal of Nuclear Medicine · doi:10.2967/jnumed.114.146605 · Cited by 23

Involvement of organelles and inter-organellar signaling in the pathogenesis of HIV-1 associated neurocognitive disorder and Alzheimer’s disease

Khan, N., Haughey, N. J., Nath, A., & Geiger, J. D. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146389 · Cited by 23

Adverse ocular events on miltefosine treatment for post-kala-azar dermal leishmaniasis in India

Saurabh, S., & Mahabir, M. (2019) · Tropical Doctor · doi:10.1177/0049475519877317 · Cited by 23

Phagocytosis of exogenous bacteria by gill epithelial cells in the deep-sea symbiotic mussel Bathymodiolus japonicus

Tame, A., Maruyama, T., & Yoshida, T. (2022) · Royal Society Open Science · doi:10.1098/rsos.211384 · Cited by 25

Drug-Loaded Polydopamine Nanoparticles for Chemo/Photothermal Therapy against Colorectal Cancer Cells

Carmignani, A., Battaglini, M., Marino, A., Pignatelli, F., & Ciofani, G. (2024) · ACS Applied Bio Materials · doi:10.1021/acsabm.3c01203 · Cited by 24

Acid-Tolerant Reversibly Switchable Green Fluorescent Protein for Super-resolution Imaging under Acidic Conditions

Shinoda, H., Lu, K., Nakashima, R., Wazawa, T., Noguchi, K., Matsuda, T., & Nagai, T. (2019) · Cell chemical biology · doi:10.1016/j.chembiol.2019.07.012 · Cited by 23

Cancer with low cathepsin D levels is susceptible to vacuolar (H+)‐ATPase inhibition

Kitazawa, S., Nishizawa, S., Nakagawa, H., Funata, M., Nishimura, K., Soga, T., & Hara, T. (2017) · Cancer Science · doi:10.1111/cas.13240 · Cited by 23

Lysosomes: guardians and healers within cells- multifaceted perspective and outlook from injury repair to disease treatment

Bi, J., Sun, Y., Guo, M., Sun, X., sun, J., Jiang, R., Wang, N., & Huang, G. (2025) · Cancer Cell International · doi:10.1186/s12935-025-03771-5 · Cited by 23

Cellular compartments challenged by membrane photo-oxidation

Tsubone, T. M., Martins, W. K., Franco, M. S. F., Silva, M. N., Itri, R., & Baptista, M. S. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108665 · Cited by 25

Reimagining dots and dashes: Visualizing structure and function of organelles for high-content imaging analysis

Chin, M. Y., Espinosa, J. A., Pohan, G., Markossian, S., & Arkin, M. R. (2021) · Cell chemical biology · doi:10.1016/j.chembiol.2021.01.016 · Cited by 21

Potential Treatment of Lysosomal Storage Disease through Modulation of the Mitochondrial—Lysosomal Axis

Kuk, M. U., Lee, Y. H., Kim, J., Hwang, S. Y., Park, J. T., & Park, S. C. (2021) · Cells · doi:10.3390/cells10020420 · Cited by 22

Ion Channels, Transporters, and Sensors Interact with the Acidic Tumor Microenvironment to Modify Cancer Progression

Boedtkjer, E. (2021) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/112_2021_63 · Cited by 22

Astragaloside IV enhances the sensibility of lung adenocarcinoma cells to bevacizumab by inhibiting autophagy

Li, L., Gao, L., Chen, M., & Cai, R. (2021) · Drug Development Research · doi:10.1002/ddr.21878 · Cited by 22

The Regulation of MiTF/TFE Transcription Factors Across Model Organisms: from Brain Physiology to Implication for Neurodegeneration

Agostini, F., Agostinis, R., Medina, D. L., Bisaglia, M., Greggio, E., & Plotegher, N. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02895-3 · Cited by 22

Single Fluorescent Probe for Multiple Tasks: Illuminating Lipid Droplets and Lysosomes in Dual Channels and Distinguishing Autophagy and Apoptosis

Dai, C., Ge, W., Li, T., Kong, X., Tian, M., & Niu, J. (2024) · Analytical Chemistry · doi:10.1021/acs.analchem.3c03653 · Cited by 22

Multiassay analysis of the toxic potential of hydrogen peroxide on cultured neurons

Hohnholt, M. C., Blumrich, E. M., & Dringen, R. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23502 · Cited by 22

Molecular Structure and Regulation of P2X Receptors With a Special Emphasis on the Role of P2X2in the Auditory System

Mittal, R., Chan, B., Grati, M., Mittal, J., Patel, K., Debs, L. H., Patel, A. P., Yan, D. L. S., Chapagain, P. P., & Liu, X. Z. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25274 · Cited by 21

Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia

Stapf, M., Pömpner, N., Teichgräber, U. K.-M., & Hilger, I. (2016) · International Journal of Nanomedicine · doi:10.2147/ijn.s94384 · Cited by 22

Analysis of Lysosomal pH by Flow Cytometry Using FITC-Dextran Loaded Cells

Eriksson, I., Öllinger, K. M., & Appelqvist, H. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6934-0_11 · Cited by 28

Spermine modified starch-based carrier for gene delivery: Structure-transfection activity relationships

Huang, X., Li, X., Chen, L., & Li, L. (2017) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2017.05.099 · Cited by 22

Effective Labeling of Primary Somatic Stem Cells with BaTiO3Nanocrystals for Second Harmonic Generation Imaging

Sugiyama, N., Sonay, A. Y., Tussiwand, R., Cohen, B. E., & Pantazis, P. (2018) · Small · doi:10.1002/smll.201703386 · Cited by 27

Different localization of lysosomal-associated membrane protein 1 (LAMP1) in mammalian cultured cell lines

Baba, K., Kuwada, S., Nakao, A., Li, X., Okuda, N., Nishida, A., Mitsuda, S., Fukuoka, N., Kakeya, H., & Kataoka, T. (2020) · Histochemistry and Cell Biology · doi:10.1007/s00418-019-01842-z · Cited by 22

Deciphering interior polarity of lysosome in live cancer and normal cells using spectral scanning microscopy

Pal, K., Kumar, P., & Koner, A. L. (2020) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2020.111848 · Cited by 22

Transcriptional regulation, stabilization, and subcellular redistribution of multidrug resistance-associated protein 1 (MRP1) by glycogen synthase kinase 3αβ: novel insights on modes of cadmium-induced cell death stimulated by MRP1

Kim, H.-R., Lee, K.-Y., Ahn, S., Lee, B.-H., Jung, K. T., Yoon, J., Yoon, H., & Oh, S. (2014) · Archives of Toxicology · doi:10.1007/s00204-014-1381-9 · Cited by 22

Manganese-Driven Plasmid Nanofibers Formed In Situ for Cancer Gene Delivery and Metalloimmunotherapy

Li, J., Yang, R., Zhang, C., Lovell, J. F., & Zhang, Y. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.4c18511 · Cited by 21

N - and S -donor leaving groups in triazole-based ruthena( ii )cycles: potent anticancer activity, selective activation, and mode of action studies

Riedl, C. A., Hejl, M., Klose, M. H. M., Roller, A., Jakupec, M. A., Kandioller, W., & Keppler, B. K. (2018) · Dalton Transactions · doi:10.1039/c8dt00449h · Cited by 21

Temozolomide-Perillyl alcohol conjugate impairs Mitophagy flux by inducing lysosomal dysfunction in non-small cell lung Cancer cells and sensitizes them to irradiation

Chang, M., Song, X., Geng, X., Wang, X., Wang, W., Chen, T. C., Xie, L., & Song, X. (2018) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-018-0905-1 · Cited by 21

Bioimaging of Lysosomes with a BODIPY pH-Dependent Fluorescent Probe

Gonçalves, R. C. R., Belmonte‐Reche, E., Pina, J., da Silva, M. C., Pinto, S. C. S., Gallo, J., Costa, S. P. G., & Raposo, M. M. M. (2022) · Molecules · doi:10.3390/molecules27228065 · Cited by 21

No energy, no autophagy—Mechanisms and therapeutic implications of autophagic response energy requirements

Mandić, M., Paunović, V., Vucicevic, L. M., Kosić, M., Mijatović, S., Trajković, V., & Harhaji-Trajkovic, L. M. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31366 · Cited by 22

V-type ATPase proton pump expression during enamel formation

Sarkar, J., Wen, X., Simanian, E. J., & Paine, M. L. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.11.004 · Cited by 21

A pH-sensitive methenamine mandelate-loaded nanoparticle induces DNA damage and apoptosis of cancer cells

Zhang, L., Hao, W., Xu, L. S., Gao, Y., Wang, X., Zhu, D., Chen, Z., Zhang, X., Chen, H., & Mei, L. (2017) · Acta Biomaterialia · doi:10.1016/j.actbio.2017.08.019 · Cited by 21

Bulk pH-Responsive DNA Quadruplex Hydrogels Prepared by Liquid-Phase, Large-Scale DNA Synthesis

Tanaka, S., Yukami, S., Fukushima, K., Wakabayashi, K., Ohya, Y., & Kuzuya, A. (2018) · ACS Macro Letters · doi:10.1021/acsmacrolett.8b00063 · Cited by 22

Solid lipid nanoparticles release DNA upon endosomal acidification in human embryonic kidney cells

Radaic, A., & de Jesus, M. B. (2018) · Nanotechnology · doi:10.1088/1361-6528/aac447 · Cited by 21

DNA Delivery Systems Based on Peptide-Mimicking Cationic Lipids─The Effect of the Co-Lipid on the Structure and DNA Binding Capacity

Taßler, S., Dobner, B., Lampp, L., Ziółkowski, R., Malinowska, E., Wölk, C., & Brezesinski, G. (2019) · Langmuir · doi:10.1021/acs.langmuir.8b04139 · Cited by 21

Lysosome activates AKT inducing cancer and metastasis

Radisavljevic, Z. M. (2019) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28752 · Cited by 21

UVA-induced photoaging inhibits autophagic degradation by impairing lysosomal function in dermal fibroblasts

Huang, Y., Li, Y., Qu, Y., Zheng, Y., Ouyang, M., Zhang, Y., Lai, W., & Xu, Q. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.08.103 · Cited by 21

Serum- and glucocorticoid- inducible kinase 2, SGK2, is a novel autophagy regulator and modulates platinum drugs response in cancer cells

Ranzuglia, V., Lorenzon, I., Pellarin, I., Sonego, M., Dall’Acqua, A., D’Andrea, S., Lovisa, S., Segatto, I., Coan, M., Polesel, J., et al. (2020) · Oncogene · doi:10.1038/s41388-020-01433-6 · Cited by 21

Fluorescent Chiral Quantum Dots to Unveil Origin-Dependent Exosome Uptake and Cargo Release

Kim, G., Zhu, R., Zhang, Y., Jeon, H., Shirinichi, F., & Wang, Y. (2024) · ACS Applied Bio Materials · doi:10.1021/acsabm.4c00296 · Cited by 22

The “click-on-tube” approach for the production of efficient drug carriers based on oxidized multi-walled carbon nanotubes

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