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

LTN1 promotes RLR degradation to inhibit immune response to RNA virus through the ESCRT pathway

Qin, F., Cai, B., Wang, P., Cao, R., Zhang, Y., Wen, H., Zheng, Y., Zhao, W., Gao, C., & Liu, B. (2023) · Autophagy · doi:10.1080/15548627.2023.2291939 · Cited by 15

Origin of eukaryotic-like Vps23 shapes an ancient functional interplay between ESCRT and ubiquitin system in Asgard archaea

Lu, Z., Zhang, S., Liu, Y., Xia, R., & Li, M. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113781 · Cited by 15

Nuclear and degradative functions of the ESCRT-III pathway: implications for neurodegenerative disease

Keeley, O., & Coyne, A. N. (2024) · Nucleus · doi:10.1080/19491034.2024.2349085 · Cited by 16

ESCRT-III: a versatile membrane remodeling machinery and its implications in cellular processes and diseases

Park, J., Kim, J., Park, H., Kim, T., & Lee, S. (2024) · Animal Cells and Systems · doi:10.1080/19768354.2024.2380294 · Cited by 18

Preserving Genome Integrity: Unveiling the Roles of ESCRT Machinery

Torre, M. L., Burla, R., & Saggio, I. (2024) · Cells · doi:10.3390/cells13151307 · Cited by 16

A relay race of ESCRT-III paralogs drives cell division in a hyperthermophilic archaeon

Liu, J., Lelek, M., Yang, Y., Salles, A., Zimmer, C., Shen, Y., & Krupovìč, M. (2024) · mBio · doi:10.1128/mbio.00991-24 · Cited by 13

Pre-treated mesenchymal stem cell-derived exosomes: A new perspective for accelerating spinal cord injury repair

Liao, Z., Zeng, J., Lin, A., Zou, Y., & Zhou, Z. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177349 · Cited by 19

Research progress of extracellular vesicles derived from mesenchymal stem cells in the treatment of neurodegenerative diseases

Shen, H., Chen, J., Liu, M., Zhao, M., Hu, D., Xie, F., Jin, Q., Xiao, D., Peng, Z., Qin, T., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1496304 · Cited by 17

The ESCRT-0 subcomplex component Hrs/Hgs is a master regulator of myogenesis via modulation of signaling and degradation pathways

Coudert, L., Osseni, A., Gangloff, Y., Schaeffer, L., & Leblanc, P. (2021) · BMC Biology · doi:10.1186/s12915-021-01091-4 · Cited by 15

A Review of APOE Genotype-Dependent Autophagic Flux Regulation in Alzheimer’s Disease

Chen, H., Chen, F., Zhang, M., Chen, Y., Cui, L., & Liang, C. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210602 · Cited by 15

The role and application of small extracellular vesicles in breast cancer

Yi, X.-K., Huang, D.-F., Li, Z., Wang, X.-X., Yang, T., Zhao, M.-H., Wu, J., & Zhong, T.-Y. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.980404 · Cited by 15

Listerin promotes α-synuclein degradation to alleviate Parkinson’s disease through the ESCRT pathway

Qin, F., Cao, R., Cui, W., Bai, X., Yuan, J., Zhang, Y., Liu, Y., Cao, N., Dong, N., Zhou, M., et al. (2025) · Science Advances · doi:10.1126/sciadv.adp3672 · Cited by 16

Small extracellular vesicles: messengers at the service of breast cancer agenda in the primary and distant microenvironments

Galardi, A., Fogazzi, V., Tottone, C., Giussani, M., Pupa, S. M., Cosentino, G., & Iorio, M. V. (2025) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-025-03471-y · Cited by 17

Mapping of endosomal proximity proteomes reveals Retromer as a hub for RAB GTPase regulation

Antón-Plágaro, C., Chen, K.-E., Guo, Q., Liu, M., Evans, A. J., Lewis, P. A., Heesom, K. J., Wilkinson, K. A., Collins, B. M., & Cullen, P. J. (2025) · Nature Communications · doi:10.1038/s41467-025-61802-1 · Cited by 14

Extracellular Vesicles and Infection: From Hijacked Machinery to Therapeutic Tools

Gonçalves, D., Pinto, S. N., & Fernandes, F. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15061738 · Cited by 16

HRS mediates tumor immune evasion by regulating proteostasis-associated interferon pathway activation

Zhang, W., Yang, J.-G., Wang, B.-K., Lu, Y.-T., Yang, J.-B., Zhong, W.-Q., Yu, Z.-Y., Qin, Z., Xiao, B., Wang, K.-M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113352 · Cited by 15

Therapeutic potential of microglia-derived extracellular vesicles in ischemic stroke

Yan, B., Liao, P., Liu, Y., Han, Z., Wang, C., Chen, F., & Lei, P. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112712 · Cited by 14

Intercellular Transmission of Naked Viruses through Extracellular Vesicles: Focus on Polyomaviruses

Helle, F., Handala, L., Bentz, M., Duverlie, G., & Brochot, É. (2020) · Viruses · doi:10.3390/v12101086 · Cited by 14

Egress of archaeal viruses

Baquero, D. P., Liu, J., & Prangishvili, D. A. (2021) · Cellular Microbiology · doi:10.1111/cmi.13394 · Cited by 12

Extracellular vesicles: General features and usefulness in diagnosis and therapeutic management of colorectal cancer

Mammes, A., Pasquier, J., Mammes, O., Conti, M., Douard, R., & Loric, S. (2021) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v13.i11.1561 · Cited by 16

Virus Hijacks Host Proteins and Machinery for Assembly and Budding, with HIV-1 as an Example

Lin, C. C., Urbina, A. N., Wang, W., Thitithanyanont, A., & Wang, S. (2022) · Viruses · doi:10.3390/v14071528 · Cited by 14

Adipose-Secreted Exosomes and Their Pathophysiologic Effects on Skeletal Muscle

Yue, B., Wang, H., Cai, X. M., Wang, J., Chai, Z., Peng, W., Shu, S., Fu, C., & Zhong, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012411 · Cited by 14

Crosstalk between exosomes and autophagy in spinal cord injury: fresh positive target for therapeutic application

Li, R., Hu, Q., Shi, X., Luo, Z., & Dong-hua, S. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03699-6 · Cited by 15

TOR complex 2 (TORC2) signaling and the ESCRT machinery cooperate in the protection of plasma membrane integrity in yeast

Schmidt, O., Weyer, Y., Sprenger, S., Widerin, M. A., Eising, S., Baumann, V., Angelova, M., Loewith, R., Stefan, C. J., Hess, M. W., et al. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.013222 · Cited by 14

Elucidating the Role of Extracellular Vesicles in Pancreatic Cancer

Marzan, A. L., & Stewart, S. E. (2021) · Cancers · doi:10.3390/cancers13225669 · Cited by 16

Proteomic insights uncover enhanced neurotherapeutic potential in conditioned mesenchymal stem cell-derived extracellular vesicles

Xi, J., Wang, T., Xian, P., Liu, X., Du, M., Yang, H., Palanisamy, C. P., Lin, W., & Long, Q. (2024) · Extracellular Vesicle · doi:10.1016/j.vesic.2024.100037 · Cited by 14

Endosomal trafficking in schizophrenia

Plooster, M., Brennwald, P., & Gupton, S. L. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102539 · Cited by 12

Protein palmitoylation regulates extracellular vesicle production and function in sepsis

Yang, X., Zheng, E., Chatterjee, V., Ma, Y., Reynolds, A., Villalba, N., Wu, M. H., & Yuan, S. Y. (2022) · Journal of Extracellular Biology · doi:10.1002/jex2.50 · Cited by 14

Advances in Drug Discovery Targeting Lysosomal Membrane Proteins

Wang, H., Zhu, Y., Liu, H., Liang, T., & Wei, Y. (2023) · Pharmaceuticals · doi:10.3390/ph16040601 · Cited by 13

Endocytic trafficking of connexins in cancer pathogenesis

Totland, M. Z., Omori, Y., Sørensen, V., Kryeziu, K., Aasen, T., Brech, A., & Leithe, E. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166812 · Cited by 13

Rab41-mediated ESCRT machinery repairs membrane rupture by a bacterial toxin in xenophagy

Nozawa, T., Toh, H., Iibushi, J., Kogai, K., Minowa‐Nozawa, A., Satoh, J., Ito, S., Murase, K., & Nakagawa, I. (2023) · Nature Communications · doi:10.1038/s41467-023-42039-2 · Cited by 13

The landscape of extracellular vesicles combined with intranasal delivery towards brain diseases

Li, J., Zhang, H., Jiang, Y., Li, N., Zhu, A., Zhang, Y., Feng, K., Zeng, W., Di, L., & Wang, R. (2024) · Nano Today · doi:10.1016/j.nantod.2024.102169 · Cited by 15

ALIX and TSG101 are essential for cellular entry and replication of two porcine alphacoronaviruses

Chen, X., Liang, Y., Weng, Z., Hu, C., Peng, Y.-Z., Sun, Y., Gao, Q., Huang, Z., Tang, S.-Q., Gong, L., et al. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012103 · Cited by 15

A Current Synopsis of the Emerging Role of Extracellular Vesicles and Micro-RNAs in Pancreatic Cancer: A Forward-Looking Plan for Diagnosis and Treatment

Trifylli, E.-M., Kriebardis, A. G., Koustas, E., Papadopoulos, N., Fortis, S. P., Tzounakas, V. L., Anastasiadi, A. T., Sarantis, P., Vasileiadi, S., Tsagarakis, A., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063406 · Cited by 14

Neurons dispose of hyperactive kinesin into glial cells for clearance

Xie, C., Chen, G., Li, M., Huang, P., Chen, Z., Lei, K., Li, D., Wang, Y., Cleetus, A., Mohamed, M. A., et al. (2024) · The EMBO Journal · doi:10.1038/s44318-024-00118-0 · Cited by 14

USP8 promotes intracellular infection by enhancing ESCRT-mediated membrane repair, limiting xenophagy, and reducing oxidative stress

Chandra, P., & Philips, J. A. (2024) · Autophagy · doi:10.1080/15548627.2024.2395134 · Cited by 13

Insights into tumor-derived exosome inhibition in cancer therapy

Tang, Z., Chen, C., Zhou, C., Li, T., Li, T., Zhang, Y., Feng, Y., Gu, C., Li, S., & Chen, J. (2025) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2025.117278 · Cited by 13

His domain protein tyrosine phosphatase and Rabaptin-5 couple endo-lysosomal sorting of EGFR with endosomal maturation

Parkinson, G. T., Roboti, P., Zhang, L., Taylor, S., & Woodman, P. G. (2021) · Journal of Cell Science · doi:10.1242/jcs.259192 · Cited by 13

Natural Occurring Polymorphisms in HIV-1 Integrase and RNase H Regulate Viral Release and Autoprocessing

Imamichi, T., Bernbaum, J. G., Laverdure, S., Yang, J., Chen, Q., Highbarger, H., Hao, M., Sui, H., Dewar, R. L., Chang, W., et al. (2021) · Journal of Virology · doi:10.1128/jvi.01323-21 · Cited by 12

Cellular abundance of sodium phosphate cotransporter SLC20A1/PiT1 and phosphate uptake are controlled post-transcriptionally by ESCRT

Zechner, C., Henne, W. M., Sathe, A. A., Xing, C., Hernandez, G., Sun, S., & Cheong, M. C. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.101945 · Cited by 13

The challenges of interrogating adipose tissue extracellular vesicle functions in physiology

Crewe, C. (2022) · Communications Biology · doi:10.1038/s42003-022-03511-9 · Cited by 14

Structure and dynamics of ESCRT-III membrane remodeling proteins by high-speed atomic force microscopy

Jukic, N., Perrino, A. P., Redondo‐Morata, L., & Scheuring, S. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104575 · Cited by 13

Regulation of the phosphoinositide code by phosphorylation of membrane readers

Kervin, T. A., & Overduin, M. (2021) · Cells · doi:10.3390/cells10051205 · Cited by 13

Identification of RNA content of CHO-derived extracellular vesicles from a production process

Busch, D. J., Zhang, Y., Kumar, A., Huhn, S. C., Du, Z., & Liu, R. (2022) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2022.03.004 · Cited by 11

Vps68 cooperates with ESCRT-III in intraluminal vesicle formation

Alsleben, S., & Kölling, R. (2022) · Journal of Cell Science · doi:10.1242/jcs.259743 · Cited by 12

Exosomal Long Noncoding RNAs in NSCLC: Dysfunctions and Clinical Potential

Lin, H., Li, J., Wang, M., Zhang, X., & Zhu, T. (2023) · Journal of Cancer · doi:10.7150/jca.84506 · Cited by 15

Regulatory mechanism and promising clinical application of exosomal circular RNA in gastric cancer

Han, M., Zhang, M., Qi, M., Zhou, Y., Li, F., & Fang, S.-Q. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1236679 · Cited by 12

A specific module of ESCRT regulates STING activity termination by controlling STING degradation

Zhao, Y., Zhou, C., Tian, W., Chen, Y., Zhao, C., Li, Y., Wang, S., & Rong, Y. (2024) · 中国科学通报：英文版 · doi:10.1016/j.scib.2024.01.005 · Cited by 12

Identification of membrane curvature sensing motifs essential for VPS37A phagophore recruitment and autophagosome closure

Ye, Y., Liang, X., Wang, G., Bewley, M. C., Hamamoto, K., Liu, X., Flanagan, J. M., Wang, H., Takahashi, Y., & Tian, F. (2024) · Communications Biology · doi:10.1038/s42003-024-06026-7 · Cited by 12

The GTPase activating protein Gyp7 regulates Rab7/Ypt7 activity on late endosomes

Füllbrunn, N., Nicastro, R., Mari, M. C., Griffith, J. M., Herrmann, E., Rasche, R., Borchers, A.-C., Auffarth, K., Kümmel, D., Reggiori, F., et al. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202305038 · Cited by 13

RNA binding protein RALY facilitates colorectal cancer metastasis via enhancing exosome biogenesis in m6A dependent manner

Zhou, J., Li, L., Han, Y., Ge, G., Ji, Q., & Li, H. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.133112 · Cited by 12

Intervention strategies targeting virus and host factors against porcine reproductive and respiratory syndrome virus: A systematic review

Zhang, X., Chen, Y., Liu, M., Long, X., & Guo, C. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.135403 · Cited by 12

Emerging roles of small extracellular vesicles in metabolic reprogramming and drug resistance in cancers

Shi, J., Shen, Y. H., & Zhang, J. (2024) · Cancer Drug Resistance · doi:10.20517/cdr.2024.81 · Cited by 13

The impact of exosomes on bone health: A focus on osteoporosis

Mehrvar, A., Akbari, M., Khosroshahi, E. M., Nekavand, M., Mokhtari, K., Baniasadi, M., Aghababaian, M., Karimi, M., Amiri, S., Moazen, A., et al. (2024) · Pathology - Research and Practice · doi:10.1016/j.prp.2024.155618 · Cited by 13

Unlocking the Potential of Extracellular Vesicles in Cardiovascular Disease

Li, H., Wang, L., Cheng, H., Zhang, Q. H., Wang, S., Zhong, W., He, C., & Wei, Q. (2025) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70407 · Cited by 12

Unveiling exosomal biomarkers in neurodegenerative diseases: LC-MS-based profiling

Bi, Y.-L., Wang, L., Li, C., Shan, Z. J., & Bi, L. (2025) · Extracellular Vesicle · doi:10.1016/j.vesic.2025.100071 · Cited by 13

Non-coding RNAs in adipose-derived stem cell exosomes: Mechanisms, therapeutic potential, and challenges in wound healing

Rong, J., Li, Y., Wang, X., Wang, J., & Song, M. L. (2025) · World Journal of Stem Cells · doi:10.4252/wjsc.v17.i4.102917 · Cited by 12

Transcriptional landscape of the cell cycle in a model thermoacidophilic archaeon reveals similarities to eukaryotes

Gomez-Raya-Vilanova, M. V., Teulière, J., Medvedeva, S., Dai, Y., Corel, E., Lopez, P., Lapointe, F., Bhattacharya, D., Haraoui, L., Turc, É., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60613-8 · Cited by 11

LRRK2 to the rescue of damaged endomembranes

Radulovic, M., & Stenmark, H. (2020) · The EMBO Journal · doi:10.15252/embj.2020106162 · Cited by 12

The PI3 Kinase Complex II–PI3P–Vps27 Axis on Vacuolar Membranes is Critical for Microautophagy Induction and Nutrient Stress Adaptation

Tasnin, M. N., Ito, K., Katsuta, H., Takuma, T., Sharmin, T., & Ushimaru, T. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167360 · Cited by 12

Regulation of Blos1 by IRE1 prevents the accumulation of Huntingtin protein aggregates

Bae, D., Jones, R., Piscopo, K. M., Tyagi, M., Shepherd, J. D., & Hollien, J. (2022) · Molecular Biology of the Cell · doi:10.1091/mbc.e22-07-0281 · Cited by 17

Cruciferous vegetable-derived indole-3-carbinol prevents coronavirus cell egression mechanisms in tracheal and intestinal 3D in vitro models.

Pennarossa, G., Arcuri, S., Pasquariello, R., Gandolfi, F., Maranesi, M., & Brevini, T. A. L. (2023) · Phytochemistry · doi:10.1016/j.phytochem.2023.113713 · Cited by 12

NSF/αSNAP2-mediated cis-SNARE complex disassembly precedes vesicle fusion in Arabidopsis cytokinesis

Park, M., Mayer, U., Richter, S., & Jürgens, G. (2023) · Nature Plants · doi:10.1038/s41477-023-01427-8 · Cited by 12

PAG1 directs SRC-family kinase intracellular localization to mediate receptor tyrosine kinase-induced differentiation

Foltz, L., Palacios-Moreno, J., Mayfield, M. E., Kinch, S., Dillon, J., Syrenne, J. T., Levy, T. M., & Grimes, M. L. (2020) · Molecular Biology of the Cell · doi:10.1091/mbc.e20-02-0135 · Cited by 12

TORC2 inhibition of α-arrestin Aly3 mediates cell surface persistence of S. pombe Ght5 glucose transporter in low glucose.

Toyoda, Y., Soejima, S., Masuda, F., & Saitoh, S. (2021) · Journal of Cell Science · doi:10.1242/jcs.257485 · Cited by 10

A novel synaptopathy‐defective synaptic vesicle protein trafficking in the mutant CHMP2B mouse model of frontotemporal dementia

Clayton, E. L., Bonnycastle, K., Isaacs, A. M., Cousin, M. A., & Schorge, S. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15551 · Cited by 12

Autophagy and Bacterial infections

Cadwell, K., Abraham, C., Bel, S., Chauhan, S., Coers, J., Colombo, M. I., Davis, J. R., Hofius, D., Nguyen, H. T. T., Ogawa, M., et al. (2025) · Autophagy Reports · doi:10.1080/27694127.2025.2542904 · Cited by 12

Endocytic evasion confers resistance to antibody-drug conjugates therapy in cancer

Wang, Y., Chen, Z., Wang, W., Jiang, L., Liang, X., Liu, Z., & Ma, Z. (2026) · Cancer Cell · doi:10.1016/j.ccell.2026.04.010 · Cited by 11

Current and prospective applications of exosomal microRNAs in pulmonary fibrosis (Review)

Yang, T., Wang, J., Zhao, J., & Liu, Y. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5092 · Cited by 12

Safeguarding Lysosomal Homeostasis by DNAJC5/CSPα-Mediated Unconventional Protein Secretion and Endosomal Microautophagy

Lee, J., Xu, Y., & Ye, Y. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.906453 · Cited by 11

Plasma membrane repair empowers the necrotic survivors as innate immune modulators

Xu, S., Yang, T. J., Xu, S., & Gong, Y. (2023) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2023.08.001 · Cited by 13

Methylation of ESCRT-III components regulates the timing of cytokinetic abscission

Richard, A., Berthelet, J., Judith, D., Advedissian, T., Espadas, J., Jannot, G., Amo, A., Loew, D., Lombard, B., Casanova, A. G., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-47717-3 · Cited by 11

NEDD4 family ubiquitin ligase AIP4 interacts with Alix to enable HBV naked capsid egress in an Alix ubiquitination-independent manner

Shen, S., Cai, D., Liang, H., Zeng, G., Liu, W., Yan, R., Yu, X., Zhang, H., Liu, S., Li, W., et al. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012485 · Cited by 11

SARS-CoV-2 Assembly: Gaining Infectivity and Beyond

Katiyar, H., Arduini, A., Li, Y., & Liang, C. (2024) · Viruses · doi:10.3390/v16111648 · Cited by 12

Hypoxia regulates small extracellular vesicle biogenesis and cargo sorting through HIF-1α/HRS signaling pathway in head and neck squamous cell carcinoma

Wang, Y., Xiao, B.-L., Li, J., Zhang, M., Zhang, L., Chen, L., Zhang, J., Chen, G., & Zhang, W. (2024) · Cellular Signalling · doi:10.1016/j.cellsig.2024.111546 · Cited by 12

CHMP2B promotes CHMP7 mediated nuclear pore complex injury in sporadic ALS

Keeley, O., Mendoza, E., Menon, D., & Coyne, A. N. (2024) · Acta Neuropathologica Communications · doi:10.1186/s40478-024-01916-7 · Cited by 11

Biogenesis of DNA-carrying extracellular vesicles by the dominant human gut methanogenic archaeon

Baquero, D. P., Borrel, G., Gazi, A. D., Martin‐Gallausiaux, C., Cvirkaitė‐Krupovič, V., Commère, P., Pende, N., Tachon, S., Sartori-Rupp, A., Douché, T., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60272-9 · Cited by 11

ESCRT-I fuels lysosomal degradation to restrict TFEB/TFE3 signaling via the Rag-mTORC1 pathway

Wróbel, M., Cendrowski, J., Szymańska, E., Grębowicz-Maciukiewicz, M., Budick-Harmelin, N., Macias, M., Szybińska, A., Mazur, M., Kolmus, K., Goryca, K., et al. (2022) · Life Science Alliance · doi:10.26508/lsa.202101239 · Cited by 11

Coatomer in the universe of cellular complexity

Field, M. C., & Rout, M. (2022) · Molecular Biology of the Cell · doi:10.1091/mbc.e19-01-0012 · Cited by 7

The promising roles of exosomal microRNAs in osteosarcoma: A new insight into the clinical therapy

Tian, W., Niu, X., Feng, F., Wang, X., Wang, J., Yao, W., & Zhang, P. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114771 · Cited by 12

Late ESCRT machinery mediates the recycling and Rescue of Invariant Surface Glycoprotein 65 in Trypanosoma brucei

Umaer, K., & Bangs, J. D. (2020) · Cellular Microbiology · doi:10.1111/cmi.13244 · Cited by 11

Evolution and diversification of the nuclear envelope

Padilla-Mejía, N. E., Makarov, A. A., Barlow, L. D., Butterfield, E. R., & Field, M. C. (2021) · Nucleus · doi:10.1080/19491034.2021.1874135 · Cited by 12

Novel Tsg101 Binding Partners Regulate Viral L Domain Trafficking

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