Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles (exosomes)

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 316,394

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961

A SIMPLE METHOD FOR THE ISOLATION AND PURIFICATION OF TOTAL LIPIDES FROM ANIMAL TISSUES

Folch, J., Lees, M., & Stanley, G. H. S. (1957) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)64849-5 · Cited by 65,189

A new and rapid colorimetric determination of acetylcholinesterase activity

Ellman, G. L., Courtney, K. D., Andres, V., & Featherstone, R. M. (1961) · Biochemical Pharmacology · doi:10.1016/0006-2952(61)90145-9 · Cited by 27,221

The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes

Dodge, J. T., Mitchell, C. D., & Hanahan, D. J. (1963) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(63)90042-0 · Cited by 4,419

Fate of the transferrin receptor during maturation of sheep reticulocytes in vitro: Selective externalization of the receptor

Pan, B., & Johnstone, R. M. (1983) · Cell · doi:10.1016/0092-8674(83)90040-5 · Cited by 2,042

Receptor-mediated endocytosis of transferrin and recycling of the transferrin receptor in rat reticulocytes

Harding, C., Heuser, J., & Stahl, P. (1983) · The Journal of Cell Biology · doi:10.1083/jcb.97.2.329 · Cited by 1,775

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

Form and function of phospholipids

ANSELL, G. B., Hawthorne, J. N., & DAWSON, R. M. C. (1973) · Medical Entomology and Zoology · Cited by 1,069

Membrane Adenosine Triphosphatase as a Participant in the Active Transport of Sodium and Potassium in the Human Erythrocyte

Post, R. L., Merritt, C. R., Kinsolving, C. R., & Albright, C. D. (1960) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)76884-7 · Cited by 1,060

Potential Applications of Nanomaterials and Technology for Diabetic Wound Healing

Bai, Q., Han, K., Dong, K., Zheng, C., Zhang, Y., Long, Q., & Lu, T. (2020) · International Journal of Nanomedicine · doi:10.2147/ijn.s276001 · Cited by 266

Exosome-orchestrated hypoxic tumor microenvironment

Meng, W., Hao, Y., He, C., Li, L., & Zhu, G. (2019) · Molecular Cancer · doi:10.1186/s12943-019-0982-6 · Cited by 256

Exosome origin determines cell targeting and the transfer of therapeutic nanoparticles towards target cells

Sancho‐Albero, M., Navascués, N., Mendoza, G., Sebastián, V., Arruebo, M., Martín‐Duque, P., & Santamarı́a, J. (2019) · Journal of Nanobiotechnology · doi:10.1186/s12951-018-0437-z · Cited by 260

Exosomes and Their Therapeutic Potentials of Stem Cells

Han, C., Sun, X., Liu, L., Jiang, H., Shen, Y., Xu, X., Li, J., Zhang, G., Huang, J., Lin, Z., et al. (2015) · Stem Cells International · doi:10.1155/2016/7653489 · Cited by 248

Formation and role of exosomes in cancer

Brinton, L. T., Sloane, H. S., KESTER, M. A., & Kelly, K. A. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1764-3 · Cited by 254

Colorectal cancer-derived small extracellular vesicles establish an inflammatory premetastatic niche in liver metastasis

Shao, Y., Chen, T., Zheng, X. E., Yang, S., Xu, K., Chen, X., Xu, F., Wang, L., Shen, Y., Wang, T., et al. (2018) · Carcinogenesis · doi:10.1093/carcin/bgy115 · Cited by 252

Exosomes as new players in metabolic organ cross‐talk

Guay, C., & Regazzi, R. (2017) · Diabetes Obesity and Metabolism · doi:10.1111/dom.13027 · Cited by 251

Extracellular Vesicles under Oxidative Stress Conditions: Biological Properties and Physiological Roles

Chiaradia, E., Tancini, B., Emiliani, C., Delo, F., Pellegrino, R. M., Tognoloni, A., Urbanelli, L., & Buratta, S. (2021) · Cells · doi:10.3390/cells10071763 · Cited by 255

Extracellular vesicles as modulators of cell-to-cell communication in the healthy and diseased brain

Pegtel, D. M., Peferoen, L., & Amor, S. (2014) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2013.0516 · Cited by 232

Exosomes in gastric cancer: roles, mechanisms, and applications

Fu, M., Gu, J., Jiang, P., Qian, H., Xu, W., & Zhang, X. (2019) · Molecular Cancer · doi:10.1186/s12943-019-1001-7 · Cited by 238

Engineered Exosome for Drug Delivery: Recent Development and Clinical Applications

Tian, J., Han, Z., Song, D., Peng, Y., Xiong, M., Chen, Z., Duan, S., & Zhang, L. (2023) · International Journal of Nanomedicine · doi:10.2147/ijn.s444582 · Cited by 246

The role of exosomes in the processing of proteins associated with neurodegenerative diseases

Vella, L. J., Sharples, R. A., Nisbet, R. M., Cappai, R., & Hill, A. F. (2007) · European Biophysics Journal · doi:10.1007/s00249-007-0246-z · Cited by 242

A Ca2+-stimulated exosome release pathway in cancer cells is regulated by Munc13-4

Messenger, S. W., Woo, S. S., Sun, Z., & Martin, T. F. J. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201710132 · Cited by 236

Emerging roles of exosomal miRNAs in diabetes mellitus

He, X., Kuang, G., Wu, Y., & Ou, C. (2021) · Clinical and Translational Medicine · doi:10.1002/ctm2.468 · Cited by 234

The role of exosomal noncoding RNAs in cancer

Xie, Y., Dang, W., Zhang, S., Yue, W., Yang, L., Zhai, X., Yan, Q., & Lu, J. (2019) · Molecular Cancer · doi:10.1186/s12943-019-0984-4 · Cited by 230

Exosomes and Their Role in the Life Cycle and Pathogenesis of RNA Viruses

Chahar, H. S., Bao, X., & Casola, A. (2015) · Viruses · doi:10.3390/v7062770 · Cited by 231

Exosomes: an overview of biogenesis, composition and role in ovarian cancer

Beach, A., Zhang, H., Ratajczak, M. Z., & Kakar, S. S. (2014) · Journal of Ovarian Research · doi:10.1186/1757-2215-7-14 · Cited by 230

The role of extracellular vesicles in COVID-19 virus infection

Hassanpour, M., Rezaie, J., Nouri, M., & Panahi, Y. (2020) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2020.104422 · Cited by 235

The Pathophysiology of Sepsis-Associated AKI

Kuwabara, S., Goggins, E. S., & Okusa, M. D. (2022) · Clinical Journal of the American Society of Nephrology · doi:10.2215/cjn.00850122 · Cited by 236

Characterization of RNA in exosomes secreted by human breast cancer cell lines using next-generation sequencing

Jenjaroenpun, P., Kremenska, Y., Nair, V. M., Kremenskoy, M., Joseph, B., & Kurochkin, I. V. (2013) · PeerJ · doi:10.7717/peerj.201 · Cited by 232

Exosomal microRNAs (exomiRs): Small molecules with a big role in cancer

Bhome, R., Vecchio, F. D., Lee, G.-H., Bullock, M. D., Primrose, J. M., Sayan, E., & Mirnezami, A. H. (2018) · Cancer Letters · doi:10.1016/j.canlet.2018.02.002 · Cited by 235

Exosomes: Small vesicles with big roles in cancer, vaccine development, and therapeutics

Thakur, A., Parra, D. C., Motallebnejad, P., Brocchi, M., & Chen, H. J. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.08.029 · Cited by 224

Exosomes: The Messengers of Health and Disease

Isola, A. L., & Chen, S. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666160825160421 · Cited by 224

Methods and Technologies for Exosome Isolation and Characterization

Zhang, M., Jin, K., Gao, L., Zhang, Z., Li, F., Zhou, F., & Zhang, L. (2018) · Small Methods · doi:10.1002/smtd.201800021 · Cited by 234

Characterizing Extracellular Vesicles and Their Diverse RNA Contents

Veziroglu, E. M., & Mias, G. I. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00700 · Cited by 229

Exosomes and the kidney: prospects for diagnosis and therapy of renal diseases

van Balkom, B. W. M., Pisitkun, T., Verhaar, M. C., & Knepper, M. A. (2011) · Kidney International · doi:10.1038/ki.2011.292 · Cited by 229

B cell–derived exosomes can present allergen peptides and activate allergen-specific T cells to proliferate and produce TH2-like cytokines

Admyre, C., Bohle, B., Johansson, S. M., Focke‐Tejkl, M., Valenta, R., Scheynius, A., & Gabrielsson, S. (2007) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2007.06.040 · Cited by 222

A novel strategy for facile serum exosome isolation based on specific interactions between phospholipid bilayers and TiO 2

Gao, F., Jiao, F., Xia, C., Zhao, Y. C., Ying, W., Xie, Y., Guan, X., Tao, M., Zhang, Y., Qin, W., et al. (2018) · Chemical Science · doi:10.1039/c8sc04197k · Cited by 226

Plant extracellular vesicles

Cui, Y., Gao, J., He, Y., & Jiang, L. (2019) · PROTOPLASMA · doi:10.1007/s00709-019-01435-6 · Cited by 218

Exosomes as drug carriers for cancer therapy and challenges regarding exosome uptake

Zhao, X., Wu, D., Ma, X., Wang, J., Hou, W., & Zhang, W. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110237 · Cited by 197

Degradation of AP2 During Reticulocyte Maturation Enhances Binding of Hsc70 and Alix to a Common Site on TfR for Sorting into Exosomes

Géminard, C., Gassart, A. D., Blanc, L., & Vidal, M. (2004) · Traffic · doi:10.1111/j.1600-0854.2004.0167.x · Cited by 217

REVIEW ARTICLE: The Role of Placental Exosomes in Reproduction

Mincheva‐Nilsson, L., & Baranov, V. I. (2010) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.2010.00822.x · Cited by 219

Exosomes Derived from Genetically Modified DC Expressing FasL Are Anti-inflammatory and Immunosuppressive

Kim, S. H., Bianco, N. R., Menon, R., Lechman, E. R., Shufesky, W. J., Morelli, A. E., & Robbins, P. D. (2005) · Molecular Therapy · doi:10.1016/j.ymthe.2005.09.015 · Cited by 225

Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis

Pang, B., Zhu, Y., Ni, J., Thompson, J. E., Malouf, D. J., Bucci, J. A., Graham, P., & Li, Y. (2020) · Theranostics · doi:10.7150/thno.39486 · Cited by 221

Isolation of extracellular vesicles with combined enrichment methods

Stam, J., Bartel, S., Bischoff, R., & Wolters, J. C. (2021) · Journal of Chromatography B · doi:10.1016/j.jchromb.2021.122604 · Cited by 224

Exosomes in inflammation and role as biomarkers

Console, L., Scalise, M., & Indiveri, C. (2018) · Clinica Chimica Acta · doi:10.1016/j.cca.2018.11.009 · Cited by 225

Caveolin-1 selectively regulates microRNA sorting into microvesicles after noxious stimuli

Lee, H., Li, C., Zhang, Y., Zhang, D., Otterbein, L. E., & Jin, Y. (2019) · Journal of Experimental Medicine · doi:10.1084/jem.20182313 · Cited by 219

Current Progresses of Exosomes as Cancer Diagnostic and Prognostic Biomarkers

Huang, T., & Deng, C.-X. (2019) · International Journal of Biological Sciences · doi:10.7150/ijbs.27796 · Cited by 228

Association of hepatitis C virus envelope proteins with exosomes

Masciopinto, F., Giovani, C., Campagnoli, S., Galli‐Stampino, L., Colombatto, P., Brunetto, M. R., Yen, T. S. B., Houghton, M., Pileri, P., & Abrignani, S. (2004) · European Journal of Immunology · doi:10.1002/eji.200424887 · Cited by 214

Serum transferrin receptor is a truncated form of tissue receptor.

Shih, Y. J., Baynes, R. D., Hudson, B. G., Flowers, C. H., SKIKNE, B. S., & Cook, J. D. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)30627-0 · Cited by 211

The how and why of exocytic vesicles

Greenwalt, T. J. (2005) · Transfusion · doi:10.1111/j.1537-2995.2006.00692.x · Cited by 210

Circulating exosomes and exosomal microRNAs as biomarkers in gastrointestinal cancer

Nedaeinia, R., Manian, M., Jazayeri, M. H., Ranjbar, M., Salehi, R., Sharifi, M., Mohaghegh, F., Goli, M., Jahednia, S. H., Avan, A., et al. (2016) · Cancer Gene Therapy · doi:10.1038/cgt.2016.77 · Cited by 214

Exosomes – Structure, Biogenesis and Biological Role in Non‐Small‐Cell Lung Cancer

Frydrychowicz, M., Kolecka-Bednarczyk, A., Madejczyk, M., Yasar, S. J., & Dworacki, G. (2014) · Scandinavian Journal of Immunology · doi:10.1111/sji.12247 · Cited by 211

Exosomes in developmental signalling

McGough, I. J., & Vincent, J. (2016) · Development · doi:10.1242/dev.126516 · Cited by 217

Message in a Bubble: Shuttling Small RNAs and Proteins Between Cells and Interacting Organisms Using Extracellular Vesicles

Cai, Q., He, B., Wang, S., Fletcher, S. J., Niu, D., Mitter, N., Birch, P. R. J., & Jin, H. (2021) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-081720-010616 · Cited by 208

Exosome-Based Vaccines: History, Current State, and Clinical Trials

dos Santos, P. W. D. S., & Almeida, F. B. D. R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.711565 · Cited by 213

Exosomes from Human Adipose Tissue-Derived Mesenchymal Stem Cells Promote Epidermal Barrier Repair by Inducing de Novo Synthesis of Ceramides in Atopic Dermatitis

Shin, K., Ha, D. H., Kim, J. O., Crumrine, D. A., Meyer, J. M., Wakefield, J. S., Lee, Y., Kim, B., Kim, S., Kim, H.-K., et al. (2020) · Cells · doi:10.3390/cells9030680 · Cited by 208

Advances in Circular RNA and Its Applications

Zhao, X., Zhong, Y., Wang, X., Shen, J., & An, W. (2022) · International Journal of Medical Sciences · doi:10.7150/ijms.71840 · Cited by 217

Exosomes for repair, regeneration and rejuvenation

Basu, J., & Ludlow, J. W. (2015) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2016.1131976 · Cited by 204

Extracellular vesicles are integral and functional components of the extracellular matrix

Rilla, K. J., Mustonen, A., Arasu, U. T., Härkönen, K., Matilainen, J., & Nieminen, P. (2017) · Matrix Biology · doi:10.1016/j.matbio.2017.10.003 · Cited by 207

The emerging role of exosome-derived non-coding RNAs in cancer biology

Fan, Q., Yang, L., Zhang, X., Peng, X., Wei, S., Su, D., Zhai, Z., Hua, X., & Li, H. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.10.040 · Cited by 209

The crosstalk: exosomes and lipid metabolism

Wang, W., Zhu, N., Yan, T., Shi, Y.-N., Chen, J., Zhang, C.-J., Xie, X.-J., Liao, D.-F., & Qin, L. (2020) · Cell Communication and Signaling · doi:10.1186/s12964-020-00581-2 · Cited by 203

Exosomes from Plasmodium yoelii-Infected Reticulocytes Protect Mice from Lethal Infections

Jaular, L. M., Nakayasu, E. S., Ferrer, M., de Almeida, I. C., & Portillo, H. A. D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026588 · Cited by 203

FedExosomes: Engineering Therapeutic Biological Nanoparticles that Truly Deliver

Marcus, M., & Leonard, J. N. (2013) · Pharmaceuticals · doi:10.3390/ph6050659 · Cited by 204

Tumor-Associated Macrophages in Pancreatic Ductal Adenocarcinoma: Origin, Polarization, Function, and Reprogramming

Yang, S., Liu, Q., & Liao, Q. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.607209 · Cited by 212

miR-212 and miR-132 Are Downregulated in Neurally Derived Plasma Exosomes of Alzheimer’s Patients

Cha, D. J., Mengel, D., Mustapic, M., Liu, W., Selkoe, D. J., Kapogiannis, D., Galasko, D., Rissman, R. A., Bennett, D. A., & Walsh, D. M. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01208 · Cited by 204

Enrichment of prion protein in exosomes derived from ovine cerebral spinal fluid

Vella, L. J., Greenwood, D. L. V., Cappai, R., Scheerlinck, J. Y., & Hill, A. F. (2008) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2008.04.002 · Cited by 200

Advanced liquid biopsy technologies for circulating biomarker detection

Soda, N., Rehm, B. H. A., Sonar, P. M., Nguyen, N., & Shiddiky, M. J. A. (2019) · Journal of Materials Chemistry B · doi:10.1039/c9tb01490j · Cited by 205

Physiologic relevance of the membrane attack complex inhibitory protein CD59 in human seminal plasma: CD59 is present on extracellular organelles (prostasomes), binds cell membranes, and inhibits complement-mediated lysis.

Rooney, I. A., Atkinson, J. P., Krul, E. S., Schonfeld, G., Polakoski, K. L., Saffitz, J. E., & Morgan, B. P. (1993) · The Journal of Experimental Medicine · doi:10.1084/jem.177.5.1409 · Cited by 201

The role of extracellular vesicles in neurodegenerative diseases

Quek, C., & Hill, A. F. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.09.090 · Cited by 213

Proteomics characterization of exosome cargo

Schey, K. L., Luther, J. M., & Rose, K. L. (2015) · Methods · doi:10.1016/j.ymeth.2015.03.018 · Cited by 207

Exosomes in Pathogen Infections: A Bridge to Deliver Molecules and Link Functions

Zhang, W., Jiang, X., Bao, J., Wang, Y., Liu, H., & Tang, L. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00090 · Cited by 203

Exosomal miRNA-mediated intercellular communications and immunomodulatory effects in tumor microenvironments

Nail, H. M., Chiu, C., Leung, C., Ahmed, M. M. M., & Wang, H. (2023) · Journal of Biomedical Science · doi:10.1186/s12929-023-00964-w · Cited by 203

Inclusion Biogenesis, Methods of Isolation and Clinical Application of Human Cellular Exosomes

Tschuschke, M., Kocherova, I., Bryja, A., Mozdziak, P. E., Volponi, A. A., Janowicz, K., Sibiak, R., Piotrowska‐Kempisty, H., Iżycki, D., Bukowska, D., et al. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9020436 · Cited by 205

Proteomic Analysis of Exosomes from Human Neural Stem Cells by Flow Field-Flow Fractionation and Nanoflow Liquid Chromatography−Tandem Mass Spectrometry

Kang, D., Oh, S., Ahn, S., Lee, B.-H., & Moon, M. H. (2008) · Journal of Proteome Research · doi:10.1021/pr800225z · Cited by 195

Microfluidics‐based on‐a‐chip systems for isolating and analysing extracellular vesicles

Guo, S., Tao, S., & Dawn, H. (2018) · Journal of Extracellular Vesicles · doi:10.1080/20013078.2018.1508271 · Cited by 206

Exosomes and their role in tumorigenesis and anticancer drug resistance

Milman, N., Ginini, L., & Gil, Z. (2019) · Drug Resistance Updates · doi:10.1016/j.drup.2019.07.003 · Cited by 193

Therapeutic Potential of Multipotent Mesenchymal Stromal Cells and Their Extracellular Vesicles

Heldring, N., Mäger, I., Wood, M. J. A., Blanc, K. L., & Andaloussi, S. E. (2015) · Human Gene Therapy · doi:10.1089/hum.2015.072 · Cited by 191

Exosomes Isolated from Mycobacteria-Infected Mice or Cultured Macrophages Can Recruit and Activate Immune Cells In Vitro and In Vivo

Singh, P., Smith, V. L., Karakousis, P. C., & Schorey, J. S. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1103638 · Cited by 191

Nanocarriers as a powerful vehicle to overcome blood-brain barrier in treating neurodegenerative diseases: Focus on recent advances

Niu, X., Chen, J., & Gao, J. (2018) · Asian Journal of Pharmaceutical Sciences · doi:10.1016/j.ajps.2018.09.005 · Cited by 191

Extracellular vesicles – Their role in the packaging and spread of misfolded proteins associated with neurodegenerative diseases

Coleman, B. M., & Hill, A. F. (2015) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2015.02.007 · Cited by 208

Revisiting the road to the discovery of exosomes

Johnstone, R. M. (2005) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2005.03.002 · Cited by 190

Cushioned–Density Gradient Ultracentrifugation (C-DGUC): A Refined and High Performance Method for the Isolation, Characterization, and Use of Exosomes

Li, K., Wong, D., Hong, K. Y., & Raffaı̈, R. L. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7652-2_7 · Cited by 191

Advances in Analysis of Biodistribution of Exosomes by Molecular Imaging

Yi, Y. W., Lee, J. H., Kim, S., Pack, C., Ha, D. H., Park, S. R., Youn, J., & Cho, B. S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020665 · Cited by 194

“Exosomics”—A Review of Biophysics, Biology and Biochemistry of Exosomes With a Focus on Human Breast Milk

de la Torre, C., Goreham, R. V., Bech‐Serra, J. J., Nann, T., & Kussmann, M. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00092 · Cited by 196

Characterization of brain‐derived extracellular vesicle lipids in Alzheimer's disease

Su, H., Rustam, Y. H., Masters, C. L., Makalic, E., McLean, C., Hill, A. F., Barnham, K. J., Reid, G. E., & Vella, L. J. (2021) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12089 · Cited by 194

Therapeutic and diagnostic applications of extracellular vesicles

Stremersch, S., Smedt, S. C. D., & Raemdonck, K. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.07.054 · Cited by 189

The Yin and Yang of exosome isolation methods: conventional practice, microfluidics, and commercial kits

Shirejini, S. Z., & İnci, F. (2021) · Biotechnology Advances · doi:10.1016/j.biotechadv.2021.107814 · Cited by 194

Exosomes serve as novel modes of tick-borne flavivirus transmission from arthropod to human cells and facilitates dissemination of viral RNA and proteins to the vertebrate neuronal cells

Zhou, W., Woodson, M., Neupane, B., Bai, F., Sherman, M. B., Choi, K. H., Neelakanta, G., & Sultana, H. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1006764 · Cited by 185

Extracellular Vesicles and Exosomes: Insights From Exercise Science

Nederveen, J. P., Warnier, G., Carlo, A. D., Nilsson, M. I., & Tarnopolsky, M. A. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2020.604274 · Cited by 200

Exosomes released during reticulocyte maturation bind to fibronectin via integrin α4β1

Rieu, S., Géminard, C., Rabesandratana, H., Sainte‐Marie, J., & Vidal, M. (2000) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2000.01036.x · Cited by 184

The biology and function of extracellular vesicles in immune response and immunity

Kalluri, R. (2024) · Immunity · doi:10.1016/j.immuni.2024.07.009 · Cited by 202

Exosome‐encapsulated microRNAs as circulating biomarkers for breast cancer

Joyce, D. P., Kerin, M. J., & Dwyer, R. M. (2016) · International Journal of Cancer · doi:10.1002/ijc.30179 · Cited by 187

Aggregation reroutes molecules from a recycling to a vesicle-mediated secretion pathway during reticulocyte maturation

Vidal, M., Mangeat, P. H., & Hoekstra, D. (1997) · Journal of Cell Science · doi:10.1242/jcs.110.16.1867 · Cited by 184

Detection of Aggregation-Competent Tau in Neuron-Derived Extracellular Vesicles

Guix, F. X., Corbett, G. T., Cha, D., Mustapić, M., Liu, W., Mengel, D., Chen, Z., Aïkawa, E., Young‐Pearse, T. L., Kapogiannis, D., et al. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19030663 · Cited by 186

Maturing reticulocytes internalize plasma membrane in glycophorin A–containing vesicles that fuse with autophagosomes before exocytosis

Griffiths, R. E., Kupzig, S., Cogan, N. M., Mankelow, T. J., Betin, V. M. S., Trakarnsanga, K., Massey, E., Lane, J. D., Parsons, S. F., & Anstee, D. J. (2012) · Blood · doi:10.1182/blood-2011-09-376475 · Cited by 182

The Role of Extracellular Vesicles in Viral Infection and Transmission

Urbanelli, L., Buratta, S., Tancini, B., Sagini, K., Delo, F., Porcellati, S., & Emiliani, C. (2019) · Vaccines · doi:10.3390/vaccines7030102 · Cited by 181

Mesenchymal stem cell and derived exosome as small RNA carrier and Immunomodulator to improve islet transplantation

Wen, D., Peng, Y., Liu, D., Weizmann, Y., & Mahato, R. I. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.07.044 · Cited by 186

Exosomes and Their MicroRNA Cargo: New Players in Peripheral Nerve Regeneration

Qing, L., Chen, H. A., Tang, J., & Jia, X. (2018) · Neurorehabilitation and neural repair · doi:10.1177/1545968318798955 · Cited by 182

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

Organelle proteomics: looking at less to see more

Brunet, S. (2003) · Trends in Cell Biology · doi:10.1016/j.tcb.2003.10.006 · Cited by 180

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Henderson, M. C., & Azorsa, D. O. (2012) · Frontiers in Oncology · doi:10.3389/fonc.2012.00038 · Cited by 184

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Zou, W., Lai, M., Zhang, Y., Zheng, L., Xing, Z., Li, T., Zou, Z., Song, Q., Zhao, X., Xia, L., et al. (2018) · Advanced Science · doi:10.1002/advs.201801313 · Cited by 174

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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

Horizontal transfer of RNAs: exosomes as mediators of intercellular communication

Ramachandran, S., & Palanisamy, V. (2011) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.115 · Cited by 178

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Utsugi-Kobukai, S., Fujimaki, H., Hotta, C., Nakazawa, M., & Minami, M. (2003) · Immunology Letters · doi:10.1016/s0165-2478(03)00128-7 · Cited by 176

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Shinohara, H., Kuranaga, Y., Kumazaki, M., Sugito, N., Yoshikawa, Y., Takai, T., Taniguchi, K., Ito, Y., & Akao, Y. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700167 · Cited by 182

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Madison, M. N., & Okeoma, C. M. (2015) · Viruses · doi:10.3390/v7072810 · Cited by 175

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Hargett, L. A., & Bauer, N. N. (2013) · Pulmonary Circulation · doi:10.4103/2045-8932.114760 · Cited by 187

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Desdín-Micó, G., & Mittelbrunn, M. (2016) · Cell Adhesion & Migration · doi:10.1080/19336918.2016.1251000 · Cited by 183

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Cass, C. E., & King, K. M. (2008) · Current Cancer Therapy Reviews · doi:10.2174/157339408783565501 · Cited by 2

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Mangravite, L. M., Badagnani, I., & Giacomini, K. M. (2003) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2003.08.076 · Cited by 84

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Li, X., Zhou, M., & Wang, J. (2006) · doi:10.1002/9780470140505.ch8 · Cited by 1

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Hanson, S., & Ullman, B. (1988) · Pediatric Research · doi:10.1203/00006450-198807000-00072