The many functions of ESCRTs

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351

Shedding light on the cell biology of extracellular vesicles

van Niel, G., D'Angelo, G., & Raposo, G. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.125 · Cited by 8,369

Syndecan–syntenin–ALIX regulates the biogenesis of exosomes

Baietti, M. F., Zhang, Z., Mortier, E., Melchior, A., Degeest, G., Geeraerts, A., Ivarsson, Y., Depoortere, F., Coomans, C., Vermeiren, E., et al. (2012) · Nature Cell Biology · doi:10.1038/ncb2502 · Cited by 1,899

Ubiquitin-Dependent Sorting into the Multivesicular Body Pathway Requires the Function of a Conserved Endosomal Protein Sorting Complex, ESCRT-I

Katzmann, D. J., Babst, M., & Emr, S. D. (2001) · Cell · doi:10.1016/s0092-8674(01)00434-2 · Cited by 1,473

The Hairpin-type Tail-Anchored SNARE Syntaxin 17 Targets to Autophagosomes for Fusion with Endosomes/Lysosomes

Itakura, E., Kishi‐Itakura, C., & Mizushima, N. (2012) · Cell · doi:10.1016/j.cell.2012.11.001 · Cited by 1,385

Tsg101 and the vacuolar protein sorting pathway are essential for HIV-1 budding

Garrus, J. E., von Schwedler, U. K., Pornillos, O. W., Morham, S. G., Zavitz, K. H., Wang, H. E., Wettstein, D. A., Stray, K. M., Côté, M., Rich, R. L., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00506-2 · Cited by 1,369

The ESCRT machinery in endosomal sorting of ubiquitylated membrane proteins

Raiborg, C., & Stenmark, H. (2009) · Nature · doi:10.1038/nature07961 · Cited by 1,359

Nuclear envelope rupture and repair during cancer cell migration

Denais, C. M., Gilbert, R. M., Isermann, P., McGregor, A. L., te Lindert, M., Weigelin, B., Davidson, P. M., Friedl, P., Wolf, K., & Lammerding, J. (2016) · Science · doi:10.1126/science.aad7297 · Cited by 1,318

DNA breaks and chromosome pulverization from errors in mitosis

Crasta, K., Ganem, N. J., Dagher, R., Lantermann, A. B., Ivanova, E. V., Pan, Y., Nezi, L., Protopopov, A., Chowdhury, D., & Pellman, D. (2012) · Nature · doi:10.1038/nature10802 · Cited by 1,227

Multivesicular bodies associate with components of miRNA effector complexes and modulate miRNA activity

Gibbings, D., Ciaudo, C., Erhardt, M., & Voinnet, O. (2009) · Nature Cell Biology · doi:10.1038/ncb1929 · Cited by 1,037

Conquering the Nuclear Envelope Barriers by EBV Lytic Replication

Lee, C., & Chen, M. (2021) · Viruses · doi:10.3390/v13040702 · Cited by 26

Novel Role for ESCRT-III Component CHMP4C in the Integrity of the Endocytic Network Utilized for Herpes Simplex Virus Envelopment

Russell, T., Samolej, J., Hollinshead, M. S., Smith, G. L., Kite, J., & Elliott, G. (2021) · mBio · doi:10.1128/mbio.02183-20 · Cited by 23

The ESCRT-III protein VPS4, but not CHMP4B or CHMP2B, is pathologically increased in familial and sporadic ALS neuronal nuclei

Coyne, A. N., & Rothstein, J. D. (2021) · Acta Neuropathologica Communications · doi:10.1186/s40478-021-01228-0 · Cited by 25

Lysosome-Targeting Strategy Using Polypeptides and Chimeric Molecules

Mondal, B., Dutta, T., Padhy, A., Das, S., & Gupta, S. S. (2021) · ACS Omega · doi:10.1021/acsomega.1c04771 · Cited by 23

The ESCRT machinery directs quality control over inner nuclear membrane architecture

Shankar, R., Lettman, M. M., Whisler, W., Frankel, E. B., & Audhya, A. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110263 · Cited by 25

The Role of Extracellular Vesicles in Osteoporosis: A Scoping Review

Zhang, W., Huang, P., Lin, J., & Zeng, H. (2022) · Membranes · doi:10.3390/membranes12030324 · Cited by 25

The Role of Exosomes and Exosomal Noncoding RNAs From Different Cell Sources in Spinal Cord Injury

Yang, Z., Rao, J., Lin, F., Liang, Z., Xu, X., Lin, Y., Chen, X., Wang, C., & Chen, C. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.882306 · Cited by 23

Tumor-derived extracellular vesicles in melanoma immune response and immunotherapy

Zhou, Q., Yan, Y., Li, Y., Fu, H., Lu, D., Li, Z., Wang, Y., Wang, J., Zhu, H., Ren, J., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113790 · Cited by 23

Role of Brain Derived Extracellular Vesicles in Decoding Sex Differences Associated with Nicotine Self-Administration

Koul, S., Schaal, V. L., Chand, S., Pittenger, S. T., Vellichirammal, N. N., Kumar, V., Guda, C., Bevins, R. A., Yelamanchili, S. V., & Pendyala, G. (2020) · Cells · doi:10.3390/cells9081883 · Cited by 23

A T‐Cell Inspired Sonoporation System Enhances Low‐Dose X‐Ray‐Mediated Pyroptosis and Radioimmunotherapy Efficacy by Restoring Gasdermin‐E Expression

Yin, H., Hu, X., Xie, C., Li, Y., Gao, Y., Zeng, H., Zhu, W., Xie, D., & Wang, Q. (2024) · Advanced Materials · doi:10.1002/adma.202401384 · Cited by 22

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

Bro1 stimulates Vps4 to promote intralumenal vesicle formation during multivesicular body biogenesis

Tseng, C., Dean, S., Davies, B. A., Azmi, I. F., Pashkova, N., Payne, J. A., Staffenhagen, J., West, M., Piper, R. C., Odorizzi, G., et al. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202102070 · Cited by 22

Keeping synapses in shape: degradation pathways in the healthy and aging brain

Kuijpers, M. (2022) · Neuronal Signaling · doi:10.1042/ns20210063 · Cited by 22

Nonlytic cellular release of hepatitis A virus requires dual capsid recruitment of the ESCRT-associated Bro1 domain proteins HD-PTP and ALIX

Shirasaki, T., Feng, H., Duyvesteyn, H. M. E., Fusco, W. G., McKnight, K. L., Xie, L., Boyce, M., Kumar, S., Barouch‐Bentov, R., González‐López, O., et al. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010543 · Cited by 22

Quality control mechanisms that protect nuclear envelope identity and function

Mannino, P. J., & Lusk, C. P. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202205123 · Cited by 22

Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes

Zhou, L., Xue, X., Yang, K. L., Feng, Z. J., Liu, M., & Pastor-Pareja, J. C. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202203045 · Cited by 22

ATG and ESCRT control multiple modes of microautophagy

Sakai, Y., & Oku, M. (2023) · FEBS Letters · doi:10.1002/1873-3468.14760 · Cited by 25

Ptpn23 Controls Cardiac T-Tubule Patterning by Promoting the Assembly of Dystrophin-Glycoprotein Complex

Chen, X., Zhang, G., Wang, X., Huang, X., Zhang, J., Han, S., Wang, J., Hall, D. D., Xu, R., He, F., et al. (2024) · Circulation · doi:10.1161/circulationaha.123.065767 · Cited by 22

Extracellular Vesicular miRNA in Pancreatic Cancer: From Lab to Therapy

Tiwari, P. K., Shanmugam, P., Karn, V., Gupta, S. K., Mishra, R., Rustagi, S., Chouhan, M., Verma, D., Jha, N. K., & Kumar, S. (2024) · Cancers · doi:10.3390/cancers16122179 · Cited by 24

Recent progress in type 1 classical dendritic cell cross-presentation - cytosolic, vacuolar, or both?

Ohara, R. A., & MURPHY, K. M. M. (2023) · Current Opinion in Immunology · doi:10.1016/j.coi.2023.102350 · Cited by 21

Mechanism and cellular function of direct membrane binding by the ESCRT and ERES-associated Ca 2+ -sensor ALG-2

Shukla, S., Chen, W., Rao, S., Yang, S., Ou, C., Larsen, K. P., Hummer, G., Hanson, P. I., & Hurley, J. H. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2318046121 · Cited by 21

The Pyroptosis-Related Gene Signature Predicts the Prognosis of Hepatocellular Carcinoma

Zhang, S., Li, X., Zhang, X., Zhang, S., Tang, C., & Kuang, W. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.781427 · Cited by 21

Tumor Susceptibility Gene 101 (TSG101) Contributes to Virion Formation of Porcine Reproductive and Respiratory Syndrome Virus via Interaction with the Nucleocapsid (N) Protein along with the Early Secretory Pathway

Zhang, L., Li, R., Geng, R., Wang, L., Chen, X., Qiao, S., & Zhang, G. (2022) · Journal of Virology · doi:10.1128/jvi.00005-22 · Cited by 21

Molecular insights into endolysosomal microcompartment formation and maintenance

Kümmel, D., Herrmann, E., Langemeyer, L., & Ungermann, C. (2022) · Biological Chemistry · doi:10.1515/hsz-2022-0294 · Cited by 21

Epstein-Barr virus LMP1 enhances levels of large extracellular vesicle-associated PD-L1

Harb, M. A., Sun, L., & Meckes, D. G. (2023) · Journal of Virology · doi:10.1128/jvi.00219-23 · Cited by 21

An ESCRT grommet cooperates with a diffusion barrier to maintain nuclear integrity

Ader, N. R., Chen, L., Surovtsev, I. V., Chadwick, W. L., Rodriguez, E. C., King, M. C., & Lusk, C. P. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01235-4 · Cited by 23

Vitis vinifera Kyoho-derived exosome-like nanoparticles-based drug delivery and therapeutic modalities for breast cancer therapy

Farheen, J., Iqbal, M. Z., Lu, Y., Tang, Z., & Kong, X. (2023) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2023.105332 · Cited by 23

Small Extracellular Vesicles and Metastasis—Blame the Messenger

Seibold, T., Waldenmaier, M., Seufferlein, T. T. W., & Eiseler, T. (2021) · Cancers · doi:10.3390/cancers13174380 · Cited by 20

Selective microautophagy of proteasomes is initiated by ESCRT-0 and is promoted by proteasome ubiquitylation

Li, J., & Hochstrasser, M. (2022) · Journal of Cell Science · doi:10.1242/jcs.259393 · Cited by 21

Exosomes: A promising therapeutic strategy for intervertebral disc degeneration

Wang, C., Guo, S., Gu, Q., Wang, X., Long, L., Xiao, C., Xie, M., Shen, H., & Li, S. (2022) · Experimental Gerontology · doi:10.1016/j.exger.2022.111806 · Cited by 22

Stress‐induced Rab11a‐exosomes induce amphiregulin‐mediated cetuximab resistance in colorectal cancer

Mason, J. D., Marks, E., Fan, S., McCormick, K., WILSON, C. G., Harris, A. L., Hamdy, F. C., Cunningham, C., & Goberdhan, D. C. I. (2024) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12465 · Cited by 20

Macrophage-driven exosomes regulate the progression of cardiovascular disease

Qi, L., Luo, D.-Z., Li, H., Yan, J., & He, W. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1563800 · Cited by 20

ESCRT-III function in membrane fission and repair

Burigotto, M., & Carlton, J. G. (2025) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-025-00909-1 · Cited by 20

Human Cytomegalovirus Egress: Overcoming Barriers and Co-Opting Cellular Functions

Sánchez, V., & Britt, W. J. (2021) · Viruses · doi:10.3390/v14010015 · Cited by 20

Exosomes in urological diseases - Biological functions and clinical applications

Song, Q., Yu, H., Han, J., Lv, J., Lv, Q., & Yang, H. (2022) · Cancer Letters · doi:10.1016/j.canlet.2022.215809 · Cited by 21

Nucleoporins are degraded via upregulation of ESCRT-III/Vps4 complex in Drosophila models of C9-ALS/FTD

Dubey, S. K., Maulding, K., Sung, H., & Lloyd, T. E. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111379 · Cited by 20

Modelling membrane reshaping by staged polymerization of ESCRT-III filaments

Jiang, X., Harker-Kirschneck, L., Vanhille-Campos, C., Pfitzner, A.-K., Lominadze, E., Roux, A., Baum, B., & Šarić, A. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010586 · Cited by 20

Selective cargo sorting in stem cell‐derived small extracellular vesicles: impact on therapeutic efficacy for intervertebral disc degeneration

Liao, Z., Tong, B., Zhang, X., Zhang, W., Ke, W., Liang, H., Lei, M., Hua, W., Li, S., Song, Y., et al. (2023) · Clinical and Translational Medicine · doi:10.1002/ctm2.1494 · Cited by 20

Human Induced Pluripotent Stem Cell Models of Neurodegenerative Disorders for Studying the Biomedical Implications of Autophagy

Seranova, E., Palhegyi, A. M., Verma, S., Dimova, S., Lasry, R., Naama, M., Sun, C., Barrett, T. G., Rosenstock, T. R., Kumar, D., et al. (2020) · Journal of Molecular Biology · doi:10.1016/j.jmb.2020.01.024 · Cited by 20

Metabolic engineering of HEK293 cells to improve transient transfection and cell budding of HIV‐1 virus‐like particles

Lavado‐García, J., Díaz‐Maneh, A., Canal‐Paulí, N., Pérez‐Rubio, P., Gòdia, F., & Cervera, L. (2021) · Biotechnology and Bioengineering · doi:10.1002/bit.27679 · Cited by 20

miRNA packaging into small extracellular vesicles and implications in pain

DaCunza, J., Wickman, J. R., & Ajit, S. K. (2024) · PAIN Reports · doi:10.1097/pr9.0000000000001198 · Cited by 21

Exosome: an overview on enhanced biogenesis by small molecules

Bavafa, A., Izadpanahi, M., Hosseini, E., Hajinejad, M., Abedi, M., Forouzanfar, F., & Negah, S. S. (2025) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-024-03762-9 · Cited by 20

Structuring of the endolysosomal system by HOPS and CORVET tethering complexes

Ungermann, C., & Moeller, A. (2025) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2025.102504 · Cited by 19

Pathological Contribution of Extracellular Vesicles and Their MicroRNAs to Progression of Chronic Liver Disease

Lee, C., Han, J., & Jung, Y. (2022) · Biology · doi:10.3390/biology11050637 · Cited by 19

Recruitment of Tetraspanin TSP-15 Regulates Plasma Membrane Repair in C. elegans Epidermis

Wang, Y., Yang, Q., Meng, X., Wijaya, C. S., Ren, X., & Xu, S. (2021) · Developmental Cell · doi:10.1016/j.devcel.2022.06.004 · Cited by 20

SMSCs-derived sEV overexpressing miR-433-3p inhibits angiogenesis induced by sEV released from synoviocytes under triggering of ferroptosis

Lin, Z., Li, W., Wang, Y., Lang, X., Sun, W., Zhu, X., Bian, R., Ma, Y., Wei, X., Zhang, J., et al. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109875 · Cited by 19

Attachment, Entry, and Intracellular Trafficking of Classical Swine Fever Virus

Guo, X., Zhang, M., Liu, X., Zhang, Y., Wang, C., & Guo, Y. (2023) · Viruses · doi:10.3390/v15091870 · Cited by 22

Rab27a GTPase and its effector Myosin Va are host factors required for efficient Oropouche virus cell egress

Concha, J. O., Manchay, K. I. G., Barbosa, N. S., Rodrigues, R. L., de Carvalho, A. N., Tavares, L., Rudd, J. S., Costa, C. S., Andrade, B. Y. G., Espreáfico, E. M., et al. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012504 · Cited by 19

Functions of Wnt and Hedgehog-containing extracellular vesicles in development and disease

Matusek, T., Marcetteau, J., & Thérond, P. P. (2020) · Journal of Cell Science · doi:10.1242/jcs.209742 · Cited by 19

Rab11FIP1 maintains Rab35 at the intercellular bridge to promote actin removal and abscission

Iannantuono, N., & Emery, G. (2021) · Journal of Cell Science · doi:10.1242/jcs.244384 · Cited by 19

Linking glycosphingolipids to Alzheimer’s amyloid-ß: extracellular vesicles and functional plant materials

Yuyama, K., & Igarashi, Y. (2022) · Glycoconjugate Journal · doi:10.1007/s10719-022-10066-8 · Cited by 21

Extracellular Vesicles as Unique Signaling Messengers: Role in Lung Diseases

Gao, Y., & Raj, J. U. (2020) · Comprehensive physiology · doi:10.1002/cphy.c200006 · Cited by 21

Lysosome-associated CASM: from upstream triggers to downstream effector mechanisms

Kaur, N., Carlsson, S. R., & Lystad, A. H. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1559125 · Cited by 19

Cytokinetic Abscission Regulation in Neural Stem Cells and Tissue Development

McNeely, K. C., & Dwyer, N. D. (2021) · Current Stem Cell Reports · doi:10.1007/s40778-021-00193-7 · Cited by 19

Caspases help to spread the message via extracellular vesicles

Hill, C., Dellar, E. R., & Baena-López, L. A. (2022) · FEBS Journal · doi:10.1111/febs.16418 · Cited by 17

Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy

Brügger, M., Lauri, A., Zhen, Y., Gramegna, L. L., Zott, B., Sekulić, N., Fasano, G., Kopajtich, R., Cordeddu, V., Radio, F. C., et al. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2024.02.005 · Cited by 17

Ik2/TBK1 and Hook/Dynein, an adaptor complex for early endosome transport, are genetic modifiers of FTD-associated mutant CHMP2B toxicity in Drosophila

Lu, Y., West, R. J. H., Pons, M., Sweeney, S. T., & Gao, F. (2020) · Scientific Reports · doi:10.1038/s41598-020-71097-5 · Cited by 19

Remodeling of organelles and microtubules during spermiogenesis in the liverwort Marchantia polymorpha

Minamino, N., Norizuki, T., Mano, S., Ebine, K., & Ueda, T. (2022) · Development · doi:10.1242/dev.200951 · Cited by 19

ESCRT recruitment by the S. cerevisiae inner nuclear membrane protein Heh1 is regulated by Hub1-mediated alternative splicing

Capella, M., Caballero, L. M., Pfander, B., Braun, S. J., & Jentsch, S. (2020) · Journal of Cell Science · doi:10.1242/jcs.250688 · Cited by 18

α-Synuclein aggregates inhibit ESCRT-III through sequestration and collateral degradation

Sitron, C. S., Trinkaus, V. A., Galesic, A., Garhammer, M., Yuste‐Checa, P., Dransfeld, U., Feigenbutz, D., Zhang, J., Ivashko, L., Dudanova, I., et al. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.08.022 · Cited by 19

Prazoles Targeting Tsg101 Inhibit Release of Epstein-Barr Virus following Reactivation from Latency

Mannemuddhu, S. S., Xu, H., Bleck, C. K. E., Tjandra, N., Carter, C., & Bhaduri‐McIntosh, S. (2021) · Journal of Virology · doi:10.1128/jvi.02466-20 · Cited by 17

Endofin is required for HD-PTP and ESCRT-0 interdependent endosomal sorting of ubiquitinated transmembrane cargoes

Kazan, J. M., Desrochers, G., Martin, C. E., Jeong, H., Kharitidi, D., Apaja, P. M., Roldán, A., St‐Denis, N., Gingras, A., Lukács, G. L., et al. (2021) · iScience · doi:10.1016/j.isci.2021.103274 · Cited by 17

Exosomal MiRNAs in Osteosarcoma: Biogenesis and Biological Functions

Tang, J., He, J., Feng, C., & Tu, C. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.902049 · Cited by 17

Reversible phase separation of ESCRT protein ALIX through tyrosine phosphorylation

Elias, R. D., Zhu, Y., Su, Q., Ghirlando, R., Zhang, J., & Deshmukh, L. (2023) · Science Advances · doi:10.1126/sciadv.adg3913 · Cited by 17

Exosomal non-coding RNAs: Blueprint in colorectal cancer metastasis and therapeutic targets

Hussen, B. M., Abdullah, S. T., Abdullah, S. R., Younis, Y. M., Hidayat, H. J., Rasul, M. F., & Mohamadtahr, S. (2023) · Non-coding RNA Research · doi:10.1016/j.ncrna.2023.09.001 · Cited by 17

Removal of hypersignaling endosomes by simaphagy

Migliano, S. M., Schultz, S. W., Wenzel, E. M., Takáts, S., Liu, D., Mørk, S., Tan, K. W., Rusten, T. E., Raiborg, C., & Stenmark, H. (2023) · Autophagy · doi:10.1080/15548627.2023.2267958 · Cited by 17

Listerin promotes cGAS protein degradation through the ESCRT pathway to negatively regulate cGAS-mediated immune response

Qin, F., Cai, B., Cao, R., Bai, X., Yuan, J., Zhang, Y., Liu, Y., Chen, T., Liu, F., Sun, W., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2308853120 · Cited by 18

Non-bone-derived exosomes: a new perspective on regulators of bone homeostasis

Wang, P., Shao, W., Li, Z., Wang, B., Lv, X., Huang, Y., & Feng, Y. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-023-01431-7 · Cited by 19

Integration of JAK/STAT receptor-ligand trafficking, signalling and gene expression in Drosophila melanogaster cells

Moore, R. K., Vogt, K. L., Acosta‐Martin, A. E., Shire, P., Zeidler, M. P., & Smythe, E. (2020) · Journal of Cell Science · doi:10.1242/jcs.246199 · Cited by 17

PTPN9-mediated dephosphorylation of VTI1B promotes ATG16L1 precursor fusion and autophagosome formation

Chou, H.-Y., Lee, Y.-T., Lin, Y. J., Wen, J., Peng, W.-H., Hsieh, P.-L., Lin, S., Hung, C.-C., & Chen, G. (2020) · Autophagy · doi:10.1080/15548627.2020.1838117 · Cited by 16

Small but mighty: Atg8s and Rabs in membrane dynamics during autophagy

Barz, S., Kriegenburg, F., Sánchez‐Martín, P., & Kraft, C. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2021.119064 · Cited by 17

Emerging function and clinical significance of extracellular vesicle noncoding RNAs in lung cancer

Shan, C., Liang, Y., Cai, H., Wang, F., Chen, X., Yin, Q., Wang, K., & Wang, Y. (2022) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2022.02.016 · Cited by 16

Membrane remodeling via ubiquitin-mediated pathways

Jacomin, A., & Đikić, I. (2024) · Cell chemical biology · doi:10.1016/j.chembiol.2024.08.007 · Cited by 19

Oral natural extracellular vesicles for biomedical applications: Advances and clinical perspectives

Guan, X., Zhu, M., Zhu, H., Wang, Q., Chen, J., Chen, Y., Mou, X., & Si, J. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.08.003 · Cited by 17

Extracellular Vesicles: An Emerging Regenerative Treatment for Oral Disease

He, F., Li, L., Fan, R., Wang, X., Chen, X., & Xu, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.669011 · Cited by 17

Ectosomes and exosomes modulate neuronal spontaneous activity

Brás, I. C., Khani, M. H., Riedel, D., Parfentev, I., Gerhardt, E., van Riesen, C., Urlaub, H., Gollisch, T., & Outeiro, T. F. (2022) · Journal of Proteomics · doi:10.1016/j.jprot.2022.104721 · Cited by 22

Mechanochemical Rules for Shape-Shifting Filaments that Remodel Membranes

Meadowcroft, B., Palaia, I., Pfitzner, A.-K., Roux, A., Baum, B., & Šarić, A. (2022) · Physical Review Letters · doi:10.1103/physrevlett.129.268101 · Cited by 16

Non-muscle MYH10/myosin IIB recruits ESCRT-III to participate in autophagosome closure to maintain neuronal homeostasis

Jun, Y., Lee, S., Ban, B.-K., Lee, J., & Gao, F. (2023) · Autophagy · doi:10.1080/15548627.2023.2169309 · Cited by 16

Vps60 initiates alternative ESCRT-III filaments

Pfitzner, A.-K., Zivkovic, H., Bernat-Silvestre, C., West, M., Peltier, T., Humbert, F., Odorizzi, G., & Roux, A. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202206028 · Cited by 18

The Arising Role of Extracellular Vesicles in Cholangiocarcinoma: A Rundown of the Current Knowledge Regarding Diagnostic and Therapeutic Approaches

Trifylli, E.-M., Kriebardis, A. G., Koustas, E., Papadopoulos, N., Vasileiadi, S., Fortis, S. P., Tzounakas, V. L., Anastasiadi, A. T., Sarantis, P., Papageorgiou, E. G., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115563 · Cited by 18

ESCRT disruption provides evidence against trans-synaptic signaling via extracellular vesicles

Dresselhaus, E. C., Harris, K. P., Blanchette, C. R., Koles, K., Signore, S. J. D., Pescosolido, M. F., Ermanoska, B., Rozencwaig, M., Soslowsky, R. C., Parisi, M. J., et al. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202405025 · Cited by 16

EndoMAP.v1 charts the structural landscape of human early endosome complexes

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