ALIX and the multivesicular endosome: ALIX in Wonderland

Membrane vesicles as conveyors of immune responses

Théry, C., Ostrowski, M., & Segura, É. (2009) · Nature reviews. Immunology · doi:10.1038/nri2567 · Cited by 3,996

Ceramide Triggers Budding of Exosome Vesicles into Multivesicular Endosomes

Trajković, K., Hsu, C., Chiantia, S., Rajendran, L., Wenzel, D., Wieland, F., Schwille, P., Brügger, B., & Simons, M. (2008) · Science · doi:10.1126/science.1153124 · Cited by 3,760

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

The ESCRT Pathway

Henne, W. M., Buchkovich, N. J., & Emr, S. D. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.05.015 · Cited by 1,586

Ebola virus entry requires the cholesterol transporter Niemann–Pick C1

Carette, J. E., Raaben, M., Wong, A., Herbert, A. S., Obernosterer, G., Mulherkar, N., Kuehne, A. I., Kranzusch, P. J., Griffin, A. M., Ruthel, G. T., et al. (2011) · Nature · doi:10.1038/nature10348 · Cited by 1,327

Selective Enrichment of Tetraspan Proteins on the Internal Vesicles of Multivesicular Endosomes and on Exosomes Secreted by Human B-lymphocytes

Escola, J.-M., Kleijmeer, M. J., Stoorvogel, W., Griffith, J. M., Yoshie, O., & Geuze, H. J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.32.20121 · Cited by 1,228

Hydration forces between phospholipid bilayers

Rand, R. P., & Parsegian, V. A. (1989) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(89)90010-5 · Cited by 1,125

ExoCarta 2012: database of exosomal proteins, RNA and lipids

Mathivanan, S., Fahner, C. J., Reid, G. E., & Simpson, R. J. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr828 · Cited by 1,096

Localization of phosphatidylinositol 3-phosphate in yeast and mammalian cells

Gillooly, D. J., Morrow, I. C., Lindsay, M., Gould, R., Bryant, N. J., Gaullier, J., Parton, R. G., & Stenmark, H. (2000) · The EMBO Journal · doi:10.1093/emboj/19.17.4577 · Cited by 1,031

The Golgi apparatus (complex)-(1954-1981)-from artifact to center stage.

Farquhar, M. G., & Palade, G. E. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.91.3.77s · Cited by 999

The regulatory role of exosomes in venous thromboembolism

Ye, S., Li, W., Li, W.-X., Xiao, L., Ran, F., Chen, M., Li, X., & Sun, L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.956880 · Cited by 15

CIB1 depletion with docetaxel or TRAIL enhances triple-negative breast cancer cell death

Chung, A. H., Leisner, T. M., Dardis, G., Bivins, M. M., Keller, A. L., & Parise, L. V. (2019) · Cancer Cell International · doi:10.1186/s12935-019-0740-2 · Cited by 15

Distinct functions of dimeric and monomeric scaffold protein Alix in regulating F-actin assembly and loading of exosomal cargo

Qiu, X., Campos, Y., van de Vlekkert, D., Gomero, E. M., Tanwar, A. S., Kalathur, R., Weesner, J. A., Bongiovanni, A., Demmers, J., & d’Azzo, A. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102425 · Cited by 15

The pathological and therapeutically role of mesenchymal stem cell (MSC)-derived exosome in degenerative diseases; Particular focus on LncRNA and microRNA

Al‐Dhalimy, A. M. B., Salim, H. M., Shather, A. H., Naser, I. H., Hizam, M. M., & Alshujery, M. K. (2023) · Pathology - Research and Practice · doi:10.1016/j.prp.2023.154778 · Cited by 17

The Role of Cell Organelles in Rheumatoid Arthritis with Focus on Exosomes

Payandeh, Z., Tazehkand, A. P., Azargoonjahromi, A., Almasi, F., & Bahrami, A. A. (2021) · Biological Procedures Online · doi:10.1186/s12575-021-00158-4 · Cited by 14

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

Two-pore channels regulate endomembrane tension to enable remodeling and resolution of phagolysosomes

Chadwick, S. R., Barreda, D., Wu, J., Ye, G., Yusuf, B., Ren, D., & Freeman, S. A. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2309465121 · Cited by 13

Alix-Mediated Rescue of Feline Immunodeficiency Virus Budding Differs from That Observed with Human Immunodeficiency Virus

Vecchio, C. D., Celestino, M., Celegato, M., Palù, G., Parolin, C., Bouamr, F., & Calistri, A. (2020) · Journal of Virology · doi:10.1128/jvi.02019-19 · Cited by 12

Proteome-Wide Covalent Targeting of Acidic Residues with Tunable N -Aryl Aziridines

Qiu, N., Tan, H., Pechalrieu, D., Abegg, D., Fnu, D., Mukherjee, P., Rentería‐Gómez, Á., Gutiérrez, O., Powers, D. C., & Adibekian, A. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c04685 · Cited by 12

Roles of Bile‐Derived Exosomes in Hepatobiliary Disease

Yao, Y., Dechao, J., Li, Z., Zhou, X., Li, J., Liu, Z., & Han, X. (2021) · BioMed Research International · doi:10.1155/2021/8743409 · Cited by 14

Failure to detect functional transfer of active K-Ras protein from extracellular vesicles into recipient cells in culture

Luhtala, N., & Hunter, T. R. (2018) · PLoS ONE · doi:10.1371/journal.pone.0203290 · 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

Exosomes: Methods for Isolation and Characterization in Biological Samples

Singh, S., Dansby, C., Agarwal, D., Bhat, P. D., Dubey, P. K., & Krishnamurthy, P. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-3995-5_17 · Cited by 16

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

Identification of proteins associated with Aha1 in HeLa cells by quantitative proteomics

Sun, L., Hartson, S. D., & Matts, R. L. (2015) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2015.01.002 · Cited by 11

ALIX promotes cell migration and invasion of head and neck squamous cell carcinoma by regulating the expression of MMP9, MMP14, VEGF-C

Xie, Q., Wang, W., Yang, J., Xia, H.-F., Xiao, B.-L., Chen, G., Huang, J., Li, R., & Chen, G. (2023) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2023.105696 · Cited by 11

ESCRT-III on endosomes: new functions, new activation pathway

Woodman, P. G. (2016) · Biochemical Journal · doi:10.1042/bj20151115 · Cited by 13

Lysosomal N-acetyltransferase interacts with ALIX and is detected in extracellular vesicles

Fedele, A. O., Isenmann, S., Kamei, M., Snel, M. F., Trim, P. J., Proud, C. G., & Hopwood, J. J. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.07.001 · Cited by 10

Exosomes: Biological Couriers with Transformative Messages

Yousef, M. H., & Abdelnaser, A. (2019) · Journal of Biomedicine · doi:10.7150/jbm.34611 · Cited by 10

Checkpoints Under Traffic Control: From and to Organelles

Deng, S., Zhou, X., & Xu, J. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-3266-5_18 · Cited by 10

Extracellular Vesicles in Cardiovascular Pathophysiology: Communications, Biomarkers, and Therapeutic Potential

Cui, Z., Zhang, L., Hu, G., & Zhang, F. (2024) · Cardiovascular Toxicology · doi:10.1007/s12012-024-09875-0 · Cited by 9

The HIV-1 late domain-2 S40A polymorphism in antiretroviral (or ART)-exposed individuals influences protease inhibitor susceptibility

Watanabe, S. M., Simon, V. R., Durham, N. D., Kemp, B., Machihara, S., Kemal, K. S., Shi, B., Foley, B. T., Li, H., Chen, B. K., et al. (2016) · Retrovirology · doi:10.1186/s12977-016-0298-1 · Cited by 9

Cell-Secreted Vesicles: Novel Opportunities in Cancer Diagnosis, Monitoring and Treatment

Catoni, C., Paolo, V. D., Rossi, E. M. C., Quintieri, L., & Zamarchi, R. (2021) · Diagnostics · doi:10.3390/diagnostics11061118 · Cited by 9

Mechanistic roles of tyrosine phosphorylation in reversible amyloids, autoinhibition, and endosomal membrane association of ALIX

Elias, R. D., Ramaraju, B., & Deshmukh, L. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.101328 · Cited by 10

Brain Delivery of Therapeutics via Transcytosis: Types and Mechanisms of Vesicle-Mediated Transport Across the BBB

Haqqani, A. S., & Stanimirovic, D. B. (2022) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-030-88773-5_3 · Cited by 9

Tracking matricellular protein SPARC in extracellular vesicles as a non-destructive method to evaluate lipid-based antifibrotic treatments

Zivko, C., Fuhrmann, K., Fuhrmann, G., & Luciani, P. (2022) · Communications Biology · doi:10.1038/s42003-022-04123-z · Cited by 9

Tubular microdomains of Rab7-positive endosomes retrieve TrkA, a mechanism disrupted in Charcot–Marie–Tooth disease 2B

Markworth, R., Dambeck, V., Steinbeck, L. M., Koufali, A., Bues, B., Dankovich, T. M., Wichmann, C., & Burk, K. (2021) · Journal of Cell Science · doi:10.1242/jcs.258559 · Cited by 9

Distinct Trafficking of Cell Surface and Endosomal TIM ‐1 to the Immune Synapse

Echbarthi, M., Zonca, M., Santarella‐Mellwig, R., Schwab, Y., Kaplan, G. G., DeKruyff, R. H., Roda‐Navarro, P., & Casasnovas, J. M. (2015) · Traffic · doi:10.1111/tra.12329 · Cited by 8

Conserved Mode of Interaction between Yeast Bro1 Family V Domains and YP(X) n L Motif-Containing Target Proteins

Kimura, Y., Tanigawa, M., Kawawaki, J., Takagi, K., Mizushima, T., Maeda, T., & Tanaka, K. (2015) · Eukaryotic Cell · doi:10.1128/ec.00091-15 · Cited by 9

Alpha-synuclein is strategically positioned for afferent modulation of midbrain dopamine neurons and is essential for cocaine preference

Trubetckaia, O., Lane, A. E., Qian, L., Zhou, P., & Lane, D. (2019) · Communications Biology · doi:10.1038/s42003-019-0651-8 · Cited by 8

The Late Endosome

Vacca, F., Scott, C. C., & Grüenberg, J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.20017-5 · Cited by 13

Food-derived exosomes as the future of drug delivery

Yang, B., Zhang, M., Yue, L., Zhang, N., Wei, H., Zhang, H., Wang, B., & Liu, P. (2024) · Nano Research · doi:10.1007/s12274-024-6961-2 · Cited by 8

PTPN23-dependent ESCRT machinery functions as a cell death checkpoint

Song, D., Cen, Y., Qian, Z., Wu, X., Rivera, K. D., Wee, T.-L., Demerdash, O. E., Chang, K., Pappin, D., Vakoc, C. R., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-54749-2 · Cited by 9

Adaptor Protein Complexes in HIV-1 Pathogenesis: Mechanisms and Therapeutic Potential

Barone, M. E., Lim, A., Woody, M., Taklifi, P., Yeasmin, F., Wang, K., Lewinski, M. K., Singh, R., Stoneham, C. A., Jia, X., et al. (2025) · Viruses · doi:10.3390/v17050715 · Cited by 8

Harnessing the Therapeutic Potential of Cell Secretomes and Extracellular Vesicles for Craniofacial Regenerative Applications

Shanbhag, S., Mayol, M., Domic, D., Bobbili, M. R., Grillari, J., Sanz, M., & Gruber, R. (2025) · Journal of Periodontal Research · doi:10.1111/jre.70007 · Cited by 7

Mechanism of exercise-derived circulating exosomes as a target for sarcopenia management

Wang, X., Huang, H., Chen, J., Zhang, Q., Yuan, Z., Yin, M., Peng, C., & liu, S. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2025.1680485 · Cited by 7

Interactions of ubiquitin and CHMP5 with the V domain of HD-PTP reveals role for regulation of Vps4 ATPase

Pashkova, N., Yu, L., Schnicker, N., Tseng, C.-C., Gakhar, L., Katzmann, D. J., & Piper, R. C. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e21-04-0219 · Cited by 7

A new paradigm for epidermal growth factor receptor expression exists in PTC and NIFTP regulated by microRNAs

Al-Abdallah, A., Jahanbani, I., Ali, R. H., Al-Brahim, N., Prasanth, J., Al-Shammary, B., & Al‐Bader, M. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1080008 · Cited by 6

Extracellular Vesicle-Derived Non-Coding RNAs: Key Mediators in Remodelling Heart Failure

Zhao, J., & Huang, H. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46090559 · Cited by 7

Advances and challenges in clinical applications of tumor cell-derived extracellular vesicles

Li, Y., Zeng, X., Hu, X., Wen, Q., & Chen, P. (2023) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2023.113704 · Cited by 7

KRS: A cut away from release in exosomes

Rabouille, C. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201706039 · Cited by 6

Heparanase‐Loaded CAR T Extracellular Vesicles Remodel the Colorectal Tumour Microenvironment and Boost T Cell Antitumor Immunity

Zhu, S., Yin, J., Yang, W., Fu, X., Zeng, Y., Huang, N., Zhang, L., Yu, C., Ouyang, P., Huang, K., et al. (2026) · Journal of Extracellular Vesicles · doi:10.1002/jev2.70310 · Cited by 5

Emerging role and translational potential of small extracellular vesicles in neuroscience

Shanmugam, I., Radhakrishnan, S., Santosh, S., Ramnath, A., Anil, M., Devarajan, Y., Maheswaran, S., Narayanan, V., & Pitchaimani, A. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122987 · Cited by 6

Common Energetic and Mechanical Features of Membrane Fusion and Fission Machineries

Tareste, D. C., & Roux, A. (2018) · Springer eBooks · doi:10.1007/978-3-030-00630-3_16 · Cited by 6

Primary cilia as architects of the neocortex: Roles in brain development, function, and microcephaly

Thomsen, O. K., Fialová, J. L., Doğanlı, C., Herrera-Cid, C., Møllgård, K., Benmerah, A., Larsen, L. A., & Christensen, S. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.11.002 · Cited by 6

Exosomes: the future of acellular nanotherapeutics in regenerative vascularization

Dawes, J. D. K., Abdelaal, M., Landmesser, M. E., Asgardoon, M. H., Waldron, O., Park, J., Jikaria, N. R., & Ravnic, D. J. (2025) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2025.1607605 · Cited by 4

A Novel HTNV Budding Inhibitor Interferes the Interaction Between Viral Glycoprotein and Host ESCRT Accessory Protein ALIX

Ying, Q., Zhang, X., Wang, S., Gu, T., Zhang, J., Feng, W., Li, D., Dong, Y., Wu, X., & Wang, F. (2025) · Journal of Medical Virology · doi:10.1002/jmv.70182 · Cited by 4

Advances in Exosome Research: Multifaceted Roles in Myeloid Leukemia Progression and Therapy

Zheng, J., Wang, H., & Ge, L. (2025) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70315 · Cited by 4

ESCRTs and associated proteins in lysosomal fusion with endosomes and autophagosomes

Majumder, P., & Chakrabarti, O. (2016) · Biochemistry and Cell Biology · doi:10.1139/bcb-2016-0099 · Cited by 4

The interplay between phosphoinositides and ESCRT proteins

Giannini, C., Ponzone, L., Barroero, N., & Hirsch, E. (2025) · Advances in Biological Regulation · doi:10.1016/j.jbior.2025.101126 · Cited by 4

The profiling of extracellular vesicle subtypes in Huntington’s disease brains identifies Alix as a novel marker of neuropathology

Pérez‐González, R., Vázquez‐Oliver, A., Salvat‐Rovira, N., Martínez‐Horta, S., Rivas‐Asensio, E., Borràs, E., Ortuño‐Miquel, S., Sánchez-Carcelén, M., García-Forn, M., Sampedro, F., et al. (2025) · Acta Neuropathologica Communications · doi:10.1186/s40478-025-02187-6 · Cited by 3

Innovative applications of exosomes in precision medicine: From diagnostic biomarkers to engineered therapeutics

Duan, L., Tan, X., Li, J. J., Wang, Z., Zhou, Q., & Ding, X. (2026) · Nano Biomedicine and Engineering · doi:10.1016/j.nbe.2025.100039 · Cited by 3

Insights into the function of ESCRT complex and LBPA in ASFV infection

Barrado-Gil, L., García-Dorival, I., Galindo, I., Alonso, C., & Cuesta-Geijo, M. Á. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1163569 · Cited by 3

The roles of extracellular vesicles in gliomas: Challenge or opportunity?

Huang, L., Zhan, J., Li, Y., Huang, K., Zhu, X., & Li, J. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.123150 · Cited by 3

Methodological Assessment of ExoGAG for Isolation of Cerebrospinal Fluid Extracellular Vesicles as a Source of Biomarkers

Salvat‐Rovira, N., Vázquez‐Oliver, A., Rivas‐Asensio, E., Herrero‐Lorenzo, M., Gámez‐Valero, A., Pérez‐Pérez, J., Izquierdo, C., Campolongo, A., Martı́, E., Kulisevsky, J., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413705 · 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

Structural Determinants of Small Extracellular Vesicles (Exosomes) and Their Role in Biological Functions

Turchinets, A., & Yakovlev, A. A. (2023) · Neurochemical Journal · doi:10.1134/s1819712423040220 · Cited by 3

Entamoeba histolytica: EhADH, an Alix Protein, Participates in Several Virulence Events through Its Different Domains

Zanatta, D., Betanzos, A., Azuara-Liceaga, E. I., Montaño, S., & Orozco, E. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147609 · Cited by 3

Scalable isolation of high-purity milk extracellular vesicles via synergistic casein removal and membrane concentration strategy: from process optimization to functional validation

Ye, Y., Ge, J., Hu, X., Zhao, Y., Zhao, Z., Feng, H., Sun, L., He, J., & Liu, X. (2025) · Journal of Future Foods · doi:10.1016/j.jfutfo.2025.09.007 · Cited by 2

Seminal fluid extracellular vesicles restore human sperm osmoregulation after cystic fibrosis transmembrane conductance regulator inhibition

Pereira, S., Fomichova, O., Damião, I., Oliveira, S., Almeida, V., Monteiro, M. P., Sousa, M., & Bernardino, R. L. (2025) · Scientific Reports · doi:10.1038/s41598-025-27409-8 · Cited by 2

The Endosomal Sorting Complex, ESCRT, has diverse roles in blood progenitor maintenance, lineage choice and immune response

Ray, A., Rai, Y., & Inamdar, M. S. (2024) · Biology Open · doi:10.1242/bio.060412 · Cited by 2

Mapping the landscape of allele-specific expression in porcine genomes

Yao, W.-Y., Gòdia, M., Fang, L., Groenen, M., Bai, L.-J., Li, K., & Madsen, O. (2025) · bioRxiv · doi:10.1186/s13059-026-04174-z · Cited by 3

Exosome Secretion — More Than Simple Waste Disposal? Implications for Physiology, Diagnostics and Therapeutics

Nagarajah, S. (2016) · Journal of Circulating Biomarkers · doi:10.33393/jcb.2016.2075 · Cited by 2

Role of Horizontal Gene Transfer in Cancer Progression

Abril, A. G., & Notario, V. (2019) · Springer eBooks · doi:10.1007/978-3-030-21862-1_17 · Cited by 3

The endocytosis, trafficking, sorting and signaling of neurotrophic receptors

Burk, K. (2022) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2022.06.033 · Cited by 2

CARM1-mediated methylation controls interactions of ALIX with key partners important for cytokinesisPreprint

Huard, S., Suresh, S., Vayr, J., Ruggiero, S., Dakroub, R., Masson, V., Petrović, A., Dibsy, R., Thomsen, J. H., Younes, Y. H., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.06.663356 · Cited by 2

HRS Facilitates Newcastle Disease Virus Replication in Tumor Cells by Promoting Viral Budding

Chen, Y., Wang, C., Hu, S., & Liu, X. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251810060 · Cited by 1

A Further Case Supporting PDCD6IP as the Gene Responsible for a Neurodevelopmental Disorder With Microcephaly

D’Alessio, A. M., Torella, A., Morleo, M., Nigro, V., TUDP Study Group, & Brunetti‐Pierri, N. (2025) · Clinical Genetics · doi:10.1111/cge.70025 · Cited by 1

Hepatoviruses, Extracellular Vesicles, and the Concept of Enveloped Versus Nonenveloped Viruses

Lemon, S. M. (2025) · Annual Review of Virology · doi:10.1146/annurev-virology-093022-013811 · Cited by 1

Centrosomal P4.1-associated protein is a novel regulator of ESCRT pathway function during endosome maturation

Gudi, R. R., & Vasu, C. (2026) · iScience · doi:10.1016/j.isci.2026.114659 · Cited by 1

Exosomal MicroRNAs in Cancer: Bridging Mechanistic Insights with Biomarker Potential

Kumar, S. K., Thalakanti, S., Patnam, S., Kanaparthi, N., & Venkata, S. M. (2026) · Advances in biochemistry in health and disease · doi:10.1007/978-3-032-08824-6_24 · Cited by 1

RAB4A acts as a negative feedback regulator of extracellular vesicle secretion during TGF ‐β signaling

Rodrigues‐Junior, D. M., Doumani, M. A., Fu, H., van den Bor, J., Idevall‐Hagren, O., & Moustakas, A. (2026) · FEBS Journal · doi:10.1111/febs.70520 · Cited by 1

The Roles of Alix and VPS4A in Autophagy and Endosomal Pathways and Their Relation to HBV Replication

Li, J., Kemper, T., Tong, S., Wang, X., Lin, Y. Y., & Lu, M. (2026) · The FASEB Journal · doi:10.1096/fj.202504742r · Cited by 1

Hit the bull's eye: Engineered extracellular vesicles for targeted therapy

Cai, Y., Zhang, H., Fan, X., Fu, H., Li, H., Fu, X., Wang, X., Yuan, C., Lin, K., & Zhuang, Y. (2026) · Bioactive Materials · doi:10.1016/j.bioactmat.2026.04.035 · Cited by 1

Cell Biology: ESCRTing Trouble Out!

McNeil, P. L. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.044 · Cited by 1

Burning cellular bridges: Two pathways to the big breakup

Frankel, E. B., & Audhya, A. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201602003 · Cited by 1

Biogenesis and Functions of Extracellular Vesicles

Zou, W., Zhang, K., Lai, M., Jiang, Y., Zhang, Y., & Bai, X. (2024) · Springer eBooks · doi:10.1007/978-981-99-8365-0_2 · Cited by 1

Ensamblaje y liberación del virus dengue: controversia sobre la participación de la proteína Alix

Angarita, C. L. B., Morales, L., Velandia-Romero, M. L., Calderón-Peláez, M.-A., & Chaparro‐Olaya, J. (2019) · Acta Biológica Colombiana · doi:10.15446/abc.v24n3.79321 · Cited by 1

Measuring capture, internalization and cytosolic delivery of extracellular vesicle-embedded synteninPreprint

Hyka, L., Jaafar, E., Meeussen, S., Joliot, A., David, G., & Zimmermann, P. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.05.704011 · Cited by 1

Development of a Novel Super Resolution Microscopy Technique using an Electron Beam for High Resolution Imaging

Dennison, C. L. (2014) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)

THE PATHWAY OF VSV ENTRY INTO CELLS

Johnson, S., & Grüenberg, J. (2014) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789814635349_0003

Necrobiology of Liver Cancer: Other Forms of Cell Death Related or not Related to Apoptosis

Zimmermann, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-26587-2_177-1

The Liquid Biopsies: A New Important Step in Cancer Research

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