References
- Théry C, Witwer KW, Aikawa E, et al. Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines. J Extracell Vesicles. 2018;7(1):1535750. Available from: https://www.tandfonline.com/doi/full/10.1080/20013078.2018.1535750
- Lötvall J, Hill AF, Hochberg F, et al. Minimal experimental requirements for definition of extracellular vesicles and their functions: a position statement from the International Society for Extracellular Vesicles. J Extracell Vesicles. 2014;3(1):26913.
- Fox AS, Duggleby WF, Gelbart WM, et al. DNA-induced transformation in Drosophila: evidence for transmission without integration. Proc Natl Acad Sci U S A. 1970;67(4):1834–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/5275381
- Fox AS, Yoon SB. DNA-induced transformation in Drosophila: locus-specificity and the establishment of transformed stocks. Proc Natl Acad Sci U S A. 1970;67(3):1608–1615. Available from: http://www.ncbi.nlm.nih.gov/pubmed/5274483
- Fox AS, Yoon SB, Gelbart WM. DNA-induced transformation in Drosophila: genetic analysis of transformed stocks. Proc Natl Acad Sci U S A. 1971;68(2):342–346. Available from: http://www.ncbi.nlm.nih.gov/pubmed/5277082
- Mishra NC, Tatum EL. Non-Mendelian inheritance of DNA-induced inositol independence in Neurospora. Proc Natl Acad Sci U S A. 1973;70(12):3875–3879. Available from: http://www.ncbi.nlm.nih.gov/pubmed/4521213
- Aaronson S, Behrens U, Orner R, et al. Ultrastructure of intracellular and extracellular vesicles, membranes, and myelin figures produced by Ochromonas danica. J Ultrastruct Res. 1971;35(5):418–430. Available from: http://www.ncbi.nlm.nih.gov/pubmed/4111037
- Chargaff E, West R. The biological significance of the thromboplastic protein of blood. J Biol Chem. 1946 Nov 1;166(1):189–197. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20273687
- Wolf P. The nature and significance of platelet products in human plasma. Br J Haematol. 1967 May 1;13(3):269–288. Available from: http://www.ncbi.nlm.nih.gov/pubmed/6025241
- Anderson HC. Vesicles associated with calcification in the matrix of epiphyseal cartilage. J Cell Biol. 1969 Apr 1;41(1):59–72. Available from: http://www.ncbi.nlm.nih.gov/pubmed/5775794
- Anderson HC. Electron microscopic studies of induced cartilage development and calcification. J Cell Biol. 1967;35(1):81–101. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2107116&tool=pmcentrez&rendertype=abstract
- Bonucci E. Fine structure of early cartilage calcification. J Ultrastruct Res. 1967;20(1):33–50. Available from: http://www.ncbi.nlm.nih.gov/pubmed/4195919
- Sun CN. Lattice structures and osmiophilic bodies in the developing respiratory tissue of rats. J Ultrastruct Res. 1966;15(3):380–388. Available from: http://www.ncbi.nlm.nih.gov/pubmed/5943006
- Mercer EH, Shaffer BM. Electron microscopy of solitary and aggregated slime mould cells. J Biophys Biochem Cytol. 1960;7(2):353–356. Available from: http://www.jcb.org/cgi/doi/10.1083/jcb.7.2.353
- VICKERMAN K. Patterns of cellular organisation in Limax amoebae. An electron microscope study. Exp Cell Res. 1962;26:497–519. Available from: http://www.ncbi.nlm.nih.gov/pubmed/13925773
- Nunez EA, Wallis J, Gershon MD. Secretory processes in follicular cells of the bat thyroid. III. The occurrence of extracellular vesicles and colloid droplets during arousal from hibernation. Am J Anat. 1974;141(2):179–201. Available from: http://www.ncbi.nlm.nih.gov/pubmed/4415703
- Kahn SE, Jafri AM, Lewis NJ, et al. Purification of alkaline phosphatase from extracellular vesicles of fracture callus cartilage. Calcif Tissue Res. 1978;25(1):85–92. Available from: http://www.ncbi.nlm.nih.gov/pubmed/647441
- Ketenjian AY, Arsenis C. Morphological and biochemical studies during differentiation and calcification of fracture callus cartilage. Clin Orthop Relat Res. 1975;107(107):266–273. Available from: http://www.ncbi.nlm.nih.gov/pubmed/48443
- Chigaleĭchik AG, Belova LA, Grishchenko VM, et al. Several properties of the extracellular vesicles of Candida tropicalis yeasts grown on n-alkanes. Mikrobiologiia. 1977;46(3):467–471. Available from: http://www.ncbi.nlm.nih.gov/pubmed/895555
- Vysotskiĭ VV, Mazurova IK, Shmeleva EA. Extracellular material of some representatives of the genus Corynebacterium (the electron microscopic aspect). Zh Mikrobiol Epidemiol Immunobiol. 1977;(8):90–95. Available from: http://www.ncbi.nlm.nih.gov/pubmed/411293
- Käppeli O, Finnerty WR. Partition of alkane by an extracellular vesicle derived from hexadecane-grown Acinetobacter. J Bacteriol. 1979;140(2):707–712. Available from: http://www.ncbi.nlm.nih.gov/pubmed/500568
- Palay SL, Palade GE. The fine structure of neurons. J Cell Biol. 1955;1(1):69–88. Available from: http://www.ncbi.nlm.nih.gov/pubmed/,14381429
- Haguenau F. “Viruslike” particles as observed with the electron microscope. In: Dalton A, Hauguenau F, editors. Ultrastructure of animal viruses and bacteriophages an Atlas. New York: Academic Press; 1973. p. 391–397.
- De Tkaczevski LZ. “Pequenas particulas” observadas en algunos seuros animales. Rev Soc Argent Biol. 1968;44(1):19–27. Available from: http://www.ncbi.nlm.nih.gov/pubmed/4902747
- Benz EW, Moses HL. Brief communication: small, virus-like particles detected in bovine sera by electron microscopy2. J Natl Cancer Inst. 1974;52(6):1931–1934. Available from: http://www.ncbi.nlm.nih.gov/pubmed/4834422
- Feller WF, Chopra HC. A small virus-like particle observed in human breast cancer by means of electron microscopy. J Natl Cancer Inst. 1968;40(6):1359–1373. Available from: https://academic.oup.com/jnci/article-lookup/doi/10.1093/jnci/40.6.1359
- Dalton AJ. Microvesicles and vesicles of multivesicular bodies versus “virus-like” particles. J Natl Cancer Inst. 1975;54(5):1137–1148. Available from: http://www.ncbi.nlm.nih.gov/pubmed/165305
- van Blitterswijk WJ, Emmelot P, Hilkmann HA, et al. Rigid plasma-membrane-derived vesicles, enriched in tumour-associated surface antigens (MLr), occurring in the ascites fluid of a murine leukaemia (GRSL). Int J Cancer. 1979;23(1):62–70. Available from: http://www.ncbi.nlm.nih.gov/pubmed/83306
- Trams EG, Lauter CJ, Salem N, et al. Exfoliation of membrane ecto-enzymes in the form of micro-vesicles. Biochim Biophys Acta. 1981;645(1):63–70. Available from: http://www.ncbi.nlm.nih.gov/pubmed/6266476
- Kassis S, Lauter CJ, Stojanov M, et al. Exfoliation of the beta-adrenergic receptor and the regulatory components of adenylate cyclase by cultured rat glioma C6 cells. Biochim Biophys Acta. 1986;886(3):474–482. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2871868
- Johnstone RM, Adam M, Hammond JR, et al. Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles (exosomes). J Biol Chem. 1987;262(19):9412–9420. Available from: http://www.ncbi.nlm.nih.gov/pubmed/3597417
- Mitchell P, Petfalski E, Shevchenko A, et al. The exosome: a conserved eukaryotic RNA processing complex containing multiple 3ʹ–>5ʹ exoribonucleases. Cell. 1997;91(4):457–466. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9390555
- Johnstone RM, Bianchini A, Teng K. Reticulocyte maturation and exosome release: transferrin receptor containing exosomes shows multiple plasma membrane functions. Blood. 1989;74(5):1844–1851. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2790208
- Vidal M, Sainte-Marie J, Philippot JR, et al. Asymmetric distribution of phospholipids in the membrane of vesicles released during in vitro maturation of guinea pig reticulocytes: evidence precluding a role for “aminophospholipid translocase”. J Cell Physiol. 1989;140(3):455–462. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2777884
- Raposo G, Nijman HW, Stoorvogel W, et al. B lymphocytes secrete antigen-presenting vesicles. J Exp Med. 1996 Mar 1;183(3):1161–1172. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8642258
- Vidal MJ, Stahl PD. The small GTP-binding proteins Rab4 and ARF are associated with released exosomes during reticulocyte maturation. Eur J Cell Biol. 1993;60(2):261–267. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8330623
- Johnstone RM. The Jeanne Manery-fisher memorial lecture 1991. Maturation of reticulocytes: formation of exosomes as a mechanism for shedding membrane proteins. Biochem Cell Biol. 1992;70(3–4):179–190. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1515120
- Harding C, Heuser J, Stahl P. Receptor-mediated endocytosis of transferrin and recycling of the transferrin receptor in rat reticulocytes. J Cell Biol. 1983;97(2):329–339. Available from: http://www.ncbi.nlm.nih.gov/pubmed/6309857
- Harding C, Heuser J, Stahl P. Endocytosis and intracellular processing of transferrin and colloidal gold-transferrin in rat reticulocytes: demonstration of a pathway for receptor shedding. Eur J Cell Biol. 1984;35(2):256–263. Available from: http://www.ncbi.nlm.nih.gov/pubmed/6151502
- Pan BT, Teng K, Wu C, et al. Electron microscopic evidence for externalization of the transferrin receptor in vesicular form in sheep reticulocytes. J Cell Biol. 1985;101(3):942–948. Available from: http://www.jcb.org/cgi/doi/10.1083/jcb.101.3.942
- Bretting H, Königsmann K. Investigations on the lectin-producing cells in the sponge Axinella polypoides (Schmidt). Cell Tissue Res. 1979;201(3):487–497. Available from: http://www.ncbi.nlm.nih.gov/pubmed/509491
- Roth LM, LUSE SA. Fine structure of the neurohypophysis of the opossum (Didelphis virginiana). J Cell Biol. 1964;20(3):459–472. Available from: http://www.ncbi.nlm.nih.gov/pubmed/14128048
- Astner S, Cheung AC, Rius-Díaz F, et al. Non-invasive evaluation of the kinetics of allergic and irritant contact dermatitis. J Invest Dermatol. 2005;124(2):351–359. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15675954
- Van Deun J, Mestdagh P, Agostinis P, et al. EV-TRACK: transparent reporting and centralizing knowledge in extracellular vesicle research. Nat Methods. 2017;14(3):228–232. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28245209
- György B, Szabó TG, Pásztói M, et al. Membrane vesicles, current state-of-the-art: emerging role of extracellular vesicles. Cell Mol Life Sci. 2011;68(16):2667–2688.
- Witwer KW, Buzás EI, Bemis LT, et al. Standardization of sample collection, isolation and analysis methods in extracellular vesicle research. J Extracell Vesicles. 2013;2:1–25.
- Hill AF, Pegtel DM, Lambertz U, et al. ISEV position paper: extracellular vesicle RNA analysis and bioinformatics. J Extracell Vesicles. 2013;2. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24376909
- Roy S, Hochberg FH, Jones PS. Extracellular vesicles: the growth as diagnostics and therapeutics; a survey. J Extracell Vesicles. 2018;7(1):1438720. Available from: http://www.ncbi.nlm.nih.gov/pubmed/29511461
- Gould SJ, Raposo G As we wait: coping with an imperfect nomenclature for extracellular vesicles. J Extracell Vesicles. 2013 Sep 7;2. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24009890