Isolation and Characterization of Exosomes from Cell Culture Supernatants and Biological Fluids

B lymphocytes secrete antigen-presenting vesicles.

Raposo, G., Nijman, H. W., Stoorvogel, W., Liejendekker, R., Harding, C. V., Melief, C. J., & Geuze, H. J. (1996) · The Journal of experimental medicine · doi:10.1084/jem.183.3.1161 · Cited by 3,546

Eradication of established murine tumors using a novel cell-free vaccine: dendritic cell derived exosomes

Zitvogel, L., Régnault, A., Lozier, A., Wolfers, J., Flament, C., Tenza, D., Ricciardi‐Castagnoli, P., Raposo, G., & Amigorena, S. (1998) · Nature Medicine · doi:10.1038/nm0598-594 · Cited by 2,266

Identification and proteomic profiling of exosomes in human urine

Pisitkun, T., Shen, R., & Knepper, M. A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0403453101 · Cited by 2,162

Tumor-derived exosomes are a source of shared tumor rejection antigens for CTL cross-priming

Wolfers, J., Lozier, A., Raposo, G., Régnault, A., Théry, C., Masurier, C., Flament, C., Pouzieux, S., Faure, F., Tursz, T., et al. (2001) · Nature Medicine · doi:10.1038/85438 · Cited by 1,643

Proteomic Analysis of Dendritic Cell-Derived Exosomes: A Secreted Subcellular Compartment Distinct from Apoptotic Vesicles

Théry, C., Boussac, M., Véron, P., Ricciardi‐Castagnoli, P., Raposo, G., Garin, J., & Amigorena, S. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.12.7309 · Cited by 1,564

Activated Platelets Release Two Types of Membrane Vesicles: Microvesicles by Surface Shedding and Exosomes Derived From Exocytosis of Multivesicular Bodies and -Granules

Heijnen, H. F. G., Schiel, A. E., Fijnheer, R., Geuze, H. J., & Sixma, J. J. (1999) · Blood · doi:10.1182/blood.v94.11.3791 · Cited by 1,488

Exosomal-like vesicles are present in human blood plasma

Caby, M.-P., Lankar, D., Vincendeau-Scherrer, C., Raposo, G., & Bonnerot, C. (2005) · International Immunology · doi:10.1093/intimm/dxh267 · Cited by 1,348

Electron microscopic evidence for externalization of the transferrin receptor in vesicular form in sheep reticulocytes.

Pan, B., Teng, K., Wu, C., Adam, M., & Johnstone, R. M. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.101.3.942 · Cited by 1,242

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

Molecular Characterization of Dendritic Cell-Derived Exosomes

Théry, C., Régnault, A., Garin, J., Wolfers, J., Zitvogel, L., Ricciardi‐Castagnoli, P., Raposo, G., & Amigorena, S. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.3.599 · Cited by 1,065

Hypoxic Tumor-Derived Exosomal Long Noncoding RNA UCA1 Promotes Angiogenesis via miR-96-5p/AMOTL2 in Pancreatic Cancer

Guo, Z., Wang, X., Yang, Y., Chen, W., Zhang, K., Teng, B., Huang, C., Zhao, Q., & Qiu, Z. (2020) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2020.08.021 · Cited by 181

High-quality milk exosomes as oral drug delivery system

Zhong, J., Xia, B., Shan, S., Zheng, A., Zhang, S., Chen, J., & Liang, X. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121126 · Cited by 180

The Complete Exosome Workflow Solution: From Isolation to Characterization of RNA Cargo

Schageman, J. J., Zeringer, E., Li, M., Barta, T. J., Lea, K., Gu, J. H., Magdaleno, S. M., Setterquist, R. A., & Vlassov, A. V. (2013) · BioMed Research International · doi:10.1155/2013/253957 · Cited by 179

Small extracellular vesicles released by infused mesenchymal stromal cells target M2 macrophages and promote TGF‐β upregulation, microvascular stabilization and functional recovery in a rodent model of severe spinal cord injury

Nakazaki, M., Morita, T., Lankford, K. L., Askenase, P. W., & Kocsis, J. D. (2021) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12137 · Cited by 182

Residual matrix from different separation techniques impacts exosome biological activity

Paolini, L., Zendrini, A., Noto, G. D., Busatto, S., Lottini, E., Radeghieri, A., Dossi, A., Caneschi, A., Ricotta, D., & Bergese, P. (2016) · Scientific Reports · doi:10.1038/srep23550 · Cited by 185

Extracellular Vesicle Isolation and Analysis by Western Blotting

Kowal, E. J. K., Ter‐Ovanesyan, D., Regev, A., & Church, G. M. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7253-1_12 · Cited by 175

In Situ Detection of Plasma Exosomal MicroRNA-1246 for Breast Cancer Diagnostics by a Au Nanoflare Probe

Zhai, L.-Y., Li, M., Pan, W., Chen, Y., Li, M., Jian-xin, P., Zheng, L., Chen, J.-X., & Duan, W. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b12725 · Cited by 182

Secretion of tau via an unconventional non-vesicular mechanism

Merezhko, M., Brunello, C. A., Yan, X., Vihinen, H., Jokitalo, E., Uronen, R.-L., & Huttunen, H. J. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.078 · Cited by 166

Inhibiting membrane rupture with NINJ1 antibodies limits tissue injury

Kayagaki, N., Stowe, I. B., Alegre, K. O., Deshpande, I., Wu, S., Lin, Z., Kornfeld, O. S., Lee, B. L., Zhang, J., Liu, J., et al. (2023) · Nature · doi:10.1038/s41586-023-06191-5 · Cited by 195

Exosome-like vesicles released from lipid-induced insulin-resistant muscles modulate gene expression and proliferation of beta recipient cells in mice

Jalabert, A., Vial, G., Guay, C., Wiklander, O. P. B., Nordin, J. Z., Aswad, H., Forterre, A., Meugnier, E., Pesenti, S., Regazzi, R., et al. (2016) · Diabetologia · doi:10.1007/s00125-016-3882-y · Cited by 177

Drosophila S2 Cells Secrete Wingless on Exosome‐Like Vesicles but the Wingless Gradient Forms Independently of Exosomes

Beckett, K., Monier, S., Palmer, L., Alexandre, C., Green, H., Bonneil, É., Raposo, G., Thibault, P., Borgne, R. L., & Vincent, J. (2012) · Traffic · doi:10.1111/tra.12016 · Cited by 177

Quantitative proteomics of fractionated membrane and lumen exosome proteins from isogenic metastatic and nonmetastatic bladder cancer cells reveal differential expression of EMT factors

Jeppesen, D. K., Nawrocki, A., Jensen, S. G., Thorsen, K., Whitehead, B. J., Howard, K. A., Dyrskjøt, L., Orntoft, T. F., Larsen, M. R., & Ostenfeld, M. S. (2013) · PROTEOMICS · doi:10.1002/pmic.201300452 · Cited by 182

Reversible HuR‐microRNA binding controls extracellular export of miR‐122 and augments stress response

Mukherjee, K., Ghoshal, B., Ghosh, S., Chakrabarty, Y., Shwetha, S., Das, S., & Bhattacharyya, S. N. (2016) · The EMBO Reports · doi:10.15252/embr.201541930 · Cited by 184

Lung cancer exosomes as drivers of epithelial mesenchymal transition

Rahman, M. A., Barger, J. F., Lovat, F., Gao, M., Otterson, G. A., & Nana-Sinkam, P. S. (2016) · Oncotarget · doi:10.18632/oncotarget.10243 · Cited by 177

Mesenchymal stem cell-derived exosomes have altered microRNA profiles and induce osteogenic differentiation depending on the stage of differentiation

Wang, X., Omar, O., Vazirisani, F., Thomsen, P., & Ekström, K. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193059 · Cited by 176

Rapid Detection of Exosomal MicroRNAs Using Virus‐Mimicking Fusogenic Vesicles

Gao, X., Li, S., Ding, F., Fan, H.-J., Shi, L., Zhu, L., Li, J., Feng, J., Zhu, X., & Zhang, C. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201901997 · Cited by 177

Scaffolds with controlled release of pro-mineralization exosomes to promote craniofacial bone healing without cell transplantation

Swanson, W. B., Zhang, Z., Xiu, K., Gong, T., Eberle, M., Wang, Z., & Ma, P. X. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.09.052 · Cited by 180

Plant‐derived exosome‐like nanoparticles: A concise review on its extraction methods, content, bioactivities, and potential as functional food ingredient

Suharta, S., Barlian, A., Hidajah, A. C., Notobroto, H. B., Ana, I. D., Indariani, S., Wungu, T. D. K., & Wijaya, C. H. (2021) · Journal of Food Science · doi:10.1111/1750-3841.15787 · Cited by 178

Human Breast Milk: From Food to Active Immune Response With Disease Protection in Infants and Mothers

Lokossou, A. G., Kouakanou, L., Schumacher, A., & Zenclussen, A. C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.849012 · Cited by 201

Exosomes from Bronchoalveolar Fluid of Tolerized Mice Prevent Allergic Reaction

Prado, N., Marazuela, E. G., Segura, É., Fernández‐García, H., Villalba, M., Théry, C., Rodrı́guez, R., & Batanero, E. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.2.1519 · Cited by 176

Proteomic Analysis of C2C12 Myoblast and Myotube Exosome-Like Vesicles: A New Paradigm for Myoblast-Myotube Cross Talk?

Forterre, A. V., Jalabert, A., Berger, E., Baudet, M., Chikh, K., Errazuriz-Cerda, E., Larichaudy, J. D., Chanon, S., Weiss‐Gayet, M., Hesse, A.-M., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084153 · Cited by 176

Molecular mechanisms of biogenesis of apoptotic exosome-like vesicles and their roles as damage-associated molecular patterns

Park, S.-J., Kim, J. M., Kim, J., Hur, J., Park, S., Kim, K. H., Shin, H., & Chwae, Y. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1811432115 · Cited by 182

Exosomal therapy—a new frontier in regenerative medicine

Muthu, S., Bapat, A., Jain, R., Jeyaraman, N., & Jeyaraman, M. (2021) · Stem Cell Investigation · doi:10.21037/sci-2020-037 · Cited by 185

Long non-coding RNAs harboring miRNA seed regions are enriched in prostate cancer exosomes

Ahadi, A., Brennan, S. E., Kennedy, P. J., Hutvágner, G., & Tran, N. (2016) · Scientific Reports · doi:10.1038/srep24922 · Cited by 175

Monocyte exosomes induce adhesion molecules and cytokines via activation of NF‐κB in endothelial cells

Tang, N., Sun, B., Gupta, A. A., Rempel, H. C., & Pulliam, L. (2016) · The FASEB Journal · doi:10.1096/fj.201600368rr · Cited by 172

Liver governs adipose remodelling via extracellular vesicles in response to lipid overload

Zhao, Y., Zhao, M., Jiang, S., Wu, J., Liu, J., Yuan, X., Shen, D., Zhang, J., Zhou, N., He, J., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14450-6 · Cited by 181

Extracellular Tau Levels Are Influenced by Variability in Tau That Is Associated with Tauopathies

Karch, C. M. M., Jeng, A. T., & Goate, A. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.380642 · Cited by 185

Good things come in small packages: Overcoming challenges to harness extracellular vesicles for therapeutic delivery

Ingato, D., Lee, J. U., Sim, S. J., & Kwon, Y. J. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.09.016 · Cited by 177

Methods for the identification and characterization of extracellular vesicles in cardiovascular studies: from exosomes to microvesicles

Davidson, S. M., Boulanger, C. M., Aïkawa, E., Badimón, L., Barile, L., Binder, C. J., Brisson, A. R., Buzás, E. I., Emanueli, C., Jansen, F., et al. (2022) · Cardiovascular Research · doi:10.1093/cvr/cvac031 · Cited by 178

Immunotherapeutic Potential of Extracellular Vesicles

Zhang, B., Yin, Y., Lai, R. C., & Lim, S. K. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00518 · Cited by 172

Effect of bovine oviductal extracellular vesicles on embryo development and quality in vitro

Lopera-Vásquez, R., Hamdi, M., Maillo, V., Gutiérrez‐Adán, A., Bermejo‐Álvarez, P., Ramírez, M. Á., Yáñez‐Mó, M., & Rizos, D. V. (2017) · Reproduction · doi:10.1530/rep-16-0384 · Cited by 182

Beta cell extracellular vesicle miR-21-5p cargo is increased in response to inflammatory cytokines and serves as a biomarker of type 1 diabetes

Lakhter, A. J., Pratt, R. E., Moore, R. E., Doucette, K. K., Maier, B. F., DiMeglio, L. A., & Sims, E. K. (2018) · Diabetologia · doi:10.1007/s00125-018-4559-5 · Cited by 169

Cryo-electron microscopy of extracellular vesicles from cerebrospinal fluid

Emelyanov, A., Shtam, T. A., Kamyshinsky, R. A., Garaeva, L. A., Верлов, Н. А., Miliukhina, I. V., Kudrevatykh, A., Владимирович, Г. Г., Zabrodskaya, Y., Pchelina, S., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0227949 · Cited by 175

A rapid, automated surface protein profiling of single circulating exosomes in human blood

Kibria, G., Ramos, E. K., Lee, K. E., Bedoyan, S., Huang, S., Samaeekia, R., Athman, J. J., Harding, C. V., Lötvall, J. O., Harris, L. N., et al. (2016) · Scientific Reports · doi:10.1038/srep36502 · Cited by 170

Intranasal administration of exosomes derived from mesenchymal stem cells ameliorates autistic-like behaviors of BTBR mice

Perets, N., Hertz, S., London, M., & Offen, D. (2018) · Molecular Autism · doi:10.1186/s13229-018-0240-6 · Cited by 172

Free and hydrogel encapsulated exosome-based therapies in regenerative medicine

Akbari, A., Jabbari, N., Sharifi, R., Ahmadi, M., Vahhabi, A., Seyedzadeh, S. J., Nawaz, M., Szafert, S., Mahmoodi, M., Jabbari, E., et al. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.117447 · Cited by 174

The RNA binding protein FMR1 controls selective exosomal miRNA cargo loading during inflammation

Wozniak, A. L., Adams, A., King, K. E., Dunn, W., Christenson, L. K., Hung, W., & Weinman, S. A. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201912074 · Cited by 180

MicroRNAs in extracellular vesicles: Sorting mechanisms, diagnostic value, isolation, and detection technology

Xu, D., Di, K., Fan, B., Wu, J., Gu, X., Sun, Y., Khan, A., Li, P., & Li, Z. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.948959 · Cited by 181

Exosomes and Microvesicles: Identification and Targeting By Particle Size and Lipid Chemical Probes

Kastelowitz, N., & Yin, H. H. (2014) · ChemBioChem · doi:10.1002/cbic.201400043 · Cited by 174

Improvement of Cloned Embryos Development by Co-Culturing with Parthenotes: A Possible Role of Exosomes/Microvesicles for Embryos Paracrine Communication

Saadeldin, I. M., Kim, S. J., Choi, Y. B., & Lee, B. C. (2014) · Cellular Reprogramming · doi:10.1089/cell.2014.0003 · Cited by 173

Therapeutic Effect of Camel Milk and Its Exosomes on MCF7 Cells In Vitro and In Vivo

Badawy, A. A., El‐Magd, M. A., & AlSadrah, S. A. (2018) · Integrative Cancer Therapies · doi:10.1177/1534735418786000 · Cited by 177

Myeloid-Derived Suppressive Cells Promote B cell–Mediated Immunosuppression via Transfer of PD-L1 in Glioblastoma

Lee-Chang, C., Rashidi, A., Miska, J. M., Zhang, P., Pituch, K. C., Hou, D., Xiao, T., Fischietti, M., Kang, S. J., Appin, C., et al. (2019) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-19-0240 · Cited by 174

Clinical safety and efficacy of allogenic human adipose mesenchymal stromal cells‐derived exosomes in patients with mild to moderate Alzheimer’s disease: a phase I/II clinical trial

Xie, X., Song, Q., Dai, C., Cui, S., Tang, R., Li, S., Chang, J. K., Li, P., Wang, J., Li, J., et al. (2023) · General Psychiatry · doi:10.1136/gpsych-2023-101143 · Cited by 171

Cytomegalovirus-Infected Human Endothelial Cells Can Stimulate Allogeneic CD4+ Memory T Cells by Releasing Antigenic Exosomes

Walker, J. D., Maier, C. L., & Pober, J. S. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.3.1548 · Cited by 170

A review of exosome separation techniques and characterization of B16-F10 mouse melanoma exosomes with AF4-UV-MALS-DLS-TEM

Petersen, K. E., Manangón, E., Hood, J. L., Wickline, S. A., Fernández, D. P., Johnson, W. P., & Gale, B. K. (2014) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-014-8040-0 · Cited by 176

Extracellular vesicle mediated intercellular communication at the porcine maternal-fetal interface: A new paradigm for conceptus-endometrial cross-talk

Bidarimath, M., Khalaj, K., Kridli, R. T., Kan, F. W. K., Koti, M., & Tayade, C. (2017) · Scientific Reports · doi:10.1038/srep40476 · Cited by 170

Metalloproteinases in extracellular vesicles

Shimoda, M., & Khokha, R. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.05.027 · Cited by 171

Extracellular vesicles as modulators of wound healing

Cabral, J., Ryan, A. E., Griffin, M. D., & Ritter, T. (2018) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2018.01.018 · Cited by 171

Systematic characterization of extracellular vesicle sorting domains and quantification at the single molecule – single vesicle level by fluorescence correlation spectroscopy and single particle imaging

Corso, G., Heusermann, W., Trojer, D., Görgens, A., Steib, E., Voshol, J., Graff, A., Genoud, C., Lee, Y., Hean, J., et al. (2019) · Journal of Extracellular Vesicles · doi:10.1080/20013078.2019.1663043 · Cited by 180

Characterization of Human NK Cell-Derived Exosomes: Role of DNAM1 Receptor in Exosome-Mediated Cytotoxicity against Tumor

Pace, A. L. D., Tumino, N., Besi, F., Alicata, C., Conti, L. A., Munari, E., Maggi, E., Vacca, P., & Moretta, L. (2020) · Cancers · doi:10.3390/cancers12030661 · Cited by 171

Human fibrocyte-derived exosomes accelerate wound healing in genetically diabetic mice

Geiger, A., Walker, A., & Nissen, E. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.09.166 · Cited by 171

Exosomes Released from Breast Cancer Carcinomas Stimulate Cell Movement

Harris, D. A., Patel, S., Guček, M., Hendrix, A., Westbroek, W., & Taraska, J. W. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117495 · Cited by 174

Exosomes Derived from Squamous Head and Neck Cancer Promote Cell Survival after Ionizing Radiation

Mutschelknaus, L., Peters, C., Winkler, K., Yentrapalli, R., Heider, T., Atkinson, M. J., & Moertl, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152213 · Cited by 176

Real time and label free profiling of clinically relevant exosomes

Sina, A. A. I., Vaidyanathan, R., Dey, S., Carrascosa, L. G., Shiddiky, M. J. A., & Trau, M. (2016) · Scientific Reports · doi:10.1038/srep30460 · Cited by 170

Passion fruit-like exosome-PMA/Au-BSA@Ce6 nanovehicles for real-time fluorescence imaging and enhanced targeted photodynamic therapy with deep penetration and superior retention behavior in tumor

Pan, S., Pei, L., Zhang, A., Zhang, Y., Zhang, C., Huang, M., Huang, Z., Liu, B., Wang, L., Ma, L., et al. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.119606 · Cited by 172

Therapeutic Effects of Transplanted Exosomes Containing miR-29b to a Rat Model of Alzheimer’s Disease

Jahangard, Y., Monfared, H., Moradi, A., Zare, M., Mirnajafi-Zadeh, J., & Mowla, S. J. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00564 · Cited by 162

Mesenchymal stem cells‐derived exosomes ameliorate intervertebral disc degeneration through inhibiting pyroptosis

Zhang, J., Zhang, J., Zhang, Y., Liu, W., Ni, W., Huang, X., Yuan, J., Zhao, B., Xiao, H., & Xue, F. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15784 · Cited by 169

Exosomes Are Involved in Mediating Radiation Induced Bystander Signaling in Human Keratinocyte Cells

Jella, K. K., Rani, S., O’Driscoll, L., McClean, B., Byrne, H. J., & Lyng, F. M. (2014) · Radiation Research · doi:10.1667/rr13337.1 · Cited by 169

The αvβ6 Integrin Is Transferred Intercellularly via Exosomes

Fedele, C., Singh, A., Zerlanko, B. J., Iozzo, R. V., & Languino, L. R. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.c114.617662 · Cited by 167

Preservation of small extracellular vesicles for functional analysis and therapeutic applications: a comparative evaluation of storage conditions

Wu, J., Li, Y., Hu, X.-B., Huang, S. Q., & Xiang, D. (2021) · Drug Delivery · doi:10.1080/10717544.2020.1869866 · Cited by 168

Cancer‐associated fibroblast‐derived exosomal microRNA‐20a suppresses the PTEN/PI3K‐AKT pathway to promote the progression and chemoresistance of non‐small cell lung cancer

Shi, L., Zhu, W., Huang, Y., Zhuo, L., Wang, S., Chen, S., Zhang, B., & Ke, B. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.989 · Cited by 169

Human T-lymphotropic Virus Type 1-infected Cells Secrete Exosomes That Contain Tax Protein*

Jaworski, E., Narayanan, A., Duyne, R. V., Shabbeer-Meyering, S., Iordanskiy, S., Saifuddin, M., Das, R., Afonso, P. V., Sampey, G., Chung, M., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.549659 · Cited by 167

Quantification of Exosomes

Koritzinsky, E. H., Street, J. M., Star, R. A., & Yuen, P. S. T. (2016) · Journal of Cellular Physiology · doi:10.1002/jcp.25387 · Cited by 165

Exosome Therapy for Stroke

Chen, J., & Chopp, M. (2018) · Stroke · doi:10.1161/strokeaha.117.018292 · Cited by 152

APC-activated long noncoding RNA inhibits colorectal carcinoma pathogenesis through reduction of exosome production

Wang, F., Cao, C., Han, K., Zhao, Y.-X., Cai, M.-Y., Xiang, Z., Zhang, J., Chen, J.-W., Zhong, L.-P., Huang, Y., et al. (2018) · Journal of Clinical Investigation · doi:10.1172/jci122478 · Cited by 162

The generation and use of recombinant extracellular vesicles as biological reference material

Geeurickx, E., Tulkens, J., Dhondt, B., Deun, J. V., Lippens, L., Vergauwen, G., Heyrman, E., Sutter, D. D., Gevaert, K., Impens, F., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11182-0 · Cited by 165

Knowledge Mapping of Exosomes in Autoimmune Diseases: A Bibliometric Analysis (2002–2021)

Wu, F., Gao, J., Kang, J., Wang, X., Niu, Q., Liu, J., & Zhang, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.939433 · Cited by 163

Exosomes as New Generation Vehicles for Drug Delivery: Biomedical Applications and Future Perspectives

Rajput, A., Varshney, A., Bajaj, R., & Pokharkar, V. (2022) · Molecules · doi:10.3390/molecules27217289 · Cited by 172

Therapeutic potential of extracellular vesicles derived from human mesenchymal stem cells in a model of progressive multiple sclerosis

Laso-García, F., Ramos‐Cejudo, J., Carrillo-Salinas, F. J., Otero‐Ortega, L., Feliú, A., Frutos, M. G.-D., Mecha, M., Díez‐Tejedor, E., Guaza, C., & Gutiérrez‐Fernández, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0202590 · Cited by 169

C-Terminally Truncated Forms of Tau, But Not Full-Length Tau or Its C-Terminal Fragments, Are Released from Neurons Independently of Cell Death

Kanmert, D., Cantlon, A., Muratore, C., Jin, M., O’Malley, T. T., Lee, G. S., Young‐Pearse, T. L., Selkoe, D. J., & Walsh, D. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0387-15.2015 · Cited by 169

3D plasmonic nanobowl platform for the study of exosomes in solution

Lee, C., Carney, R. P., Hazari, S., Smith, Z. J., Knudson, A., Robertson, C. S., Lam, K. S., & Wachsmann‐Hogiu, S. (2015) · Nanoscale · doi:10.1039/c5nr01333j · Cited by 163

Extracellular miRNA: A Collision of Two Paradigms

Turchinovich, A. A., Tonevitsky, A., & Burwinkel, B. (2016) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2016.08.004 · Cited by 168

Exosomes as a liquid biopsy for lung cancer

Cui, S., Cheng, Z., Qin, W., & Jiang, L. (2017) · Lung Cancer · doi:10.1016/j.lungcan.2017.12.012 · Cited by 167

Natural-Killer-Derived Extracellular Vesicles: Immune Sensors and Interactors

Federici, C., Shahaj, E., Cecchetti, S., Camerini, S., Casella, M., Iessi, E., Camisaschi, C., Paolino, G., Calvieri, S., Ferro, S., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00262 · Cited by 166

Isolation and analysis methods of extracellular vesicles (EVs)

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Exosomes from hyperglycemia-stimulated vascular endothelial cells contain versican that regulate calcification/senescence in vascular smooth muscle cells

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Proteome Profiling of Neuroblastoma-Derived Exosomes Reveal the Expression of Proteins Potentially Involved in Tumor Progression

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