A. Clayton, Human Tumor-Derived Exosomes Selectively Impair Lymphocyte Responses to Interleukin-2, Cancer Research, vol.67, issue.15, p.31, 2007.
DOI : 10.1158/0008-5472.can-06-3456

URL : http://cancerres.aacrjournals.org/content/canres/67/15/7458.full.pdf

C. Liu, Murine Mammary Carcinoma Exosomes Promote Tumor Growth by Suppression of NK Cell Function, The Journal of Immunology, vol.176, issue.3, p.31, 2006.
DOI : 10.4049/jimmunol.176.3.1375

URL : http://www.jimmunol.org/content/176/3/1375.full.pdf

A. Clayton, Human Tumor-Derived Exosomes Down-Modulate NKG2D Expression, The Journal of Immunology, vol.180, issue.11, p.31, 2008.
DOI : 10.4049/jimmunol.180.11.7249

URL : http://www.jimmunol.org/content/180/11/7249.full.pdf

S. Yu, Tumor Exosomes Inhibit Differentiation of Bone Marrow Dendritic Cells, The Journal of Immunology, vol.178, issue.11, p.31, 2007.
DOI : 10.4049/jimmunol.178.11.6867

X. Xiang, Induction of myeloid-derived suppressor cells by tumor exosomes, International journal of cancer. Journal international du cancer, vol.124, issue.11, p.31, 2009.
DOI : 10.1002/ijc.24249

URL : http://europepmc.org/articles/pmc2757307?pdf=render

H. Pêche, Presentation of donor major histocompatibility complex antigens by bone marrow dendritic cell-derived exosomes modulates allograft rejection1, Transplantation, vol.76, issue.10, p.31, 2003.

S. Kim, Effective Treatment of Inflammatory Disease Models with Exosomes Derived from Dendritic Cells Genetically Modified to Express IL-4, The Journal of Immunology, vol.179, issue.4, p.31, 2007.
DOI : 10.4049/jimmunol.179.4.2242

URL : http://www.jimmunol.org/content/179/4/2242.full.pdf

N. Prado, Exosomes from Bronchoalveolar Fluid of Tolerized Mice Prevent Allergic Reaction, The Journal of Immunology, vol.181, issue.2, p.31, 2008.
DOI : 10.4049/jimmunol.181.2.1519

URL : http://www.jimmunol.org/content/181/2/1519.full.pdf

A. G. Thompson, Extracellular vesicles in neurodegenerative disease-pathogenesis to biomarkers, Nature Reviews Neurology, vol.12, issue.6, p.31, 2016.
DOI : 10.1038/nrneurol.2016.68

J. Fauré, Exosomes are released by cultured cortical neurones, Molecular and Cellular Neuroscience, vol.31, issue.4, p.31, 2006.

M. Chivet, Emerging role of neuronal exosomes in the central nervous system, Frontiers in Physiology, vol.3, p.31, 2012.
URL : https://hal.archives-ouvertes.fr/inserm-00733770

A. M. Janas, Exosomes and other extracellular vesicles in neural cells and neurodegenerative diseases, Biochimica et Biophysica Acta-Biomembranes, vol.1858, issue.6, p.31, 2016.
DOI : 10.1016/j.bbamem.2016.02.011

URL : https://doi.org/10.1016/j.bbamem.2016.02.011

B. Zhang, Synaptic Vesicle Size and Number Are Regulated by a Clathrin Adaptor Protein Required for Endocytosis, Neuron, vol.21, issue.6, p.31, 1998.
DOI : 10.1016/s0896-6273(00)80664-9

URL : https://doi.org/10.1016/s0896-6273(00)80664-9

R. Jahn, Molecular machines governing exocytosis of synaptic vesicles, Nature, vol.490, issue.7419, p.31, 2012.
DOI : 10.1038/nature11320

URL : http://europepmc.org/articles/pmc4461657?pdf=render

V. Budnik, Extracellular vesicles round off communication in the nervous system, Nature reviews. Neuroscience, vol.17, issue.3, p.31, 2016.

E. Krämer-albers, Oligodendrocytes secrete exosomes containing major myelin and stress-protective proteins: Trophic support for axons?, PROTEOMICS-Clinical Applications, vol.1, issue.11, p.31, 2007.

F. Antonucci, Microvesicles released from microglia stimulate synaptic activity via enhanced sphingolipid metabolism, The EMBO Journal, vol.31, issue.5, p.31, 2012.
DOI : 10.1038/emboj.2011.489

URL : http://emboj.embopress.org/content/31/5/1231.full.pdf

L. Morel, Neuronal Exosomal miRNA-dependent Translational Regulation of Astroglial Glutamate Transporter GLT1, Journal of Biological Chemistry, vol.288, issue.10, p.31, 2013.
DOI : 10.1074/jbc.m112.410944

URL : http://www.jbc.org/content/288/10/7105.full.pdf

C. A. Escudero, The p75 neurotrophin receptor evades the endolysosomal route in neuronal cells, favouring multivesicular bodies specialised for exosomal release, Journal of Cell Science, vol.127, issue.9, p.31, 2014.

B. Kumar, Acute myeloid leukemia transforms the bone marrow niche into a leukemiapermissive microenvironment through exosome secretion, Leukemia, p.31, 2017.
DOI : 10.1038/leu.2017.259

URL : https://www.nature.com/articles/leu2017259.pdf

Y. Lee, Oligodendroglia metabolically support axons and contribute to neurodegeneration, Nature, vol.487, issue.7408, p.31, 2012.
DOI : 10.1038/nature11314

URL : http://europepmc.org/articles/pmc3408792?pdf=render

H. K. Lee, Mesenchymal Stem Cells Deliver Exogenous miRNAs to Neural Cells and Induce Their Differentiation and Glutamate Transporter Expression, Stem Cells and Development, vol.23, issue.23, p.31, 2014.
DOI : 10.1089/scd.2014.0146

S. A. Bellingham, Exosomes: Vehicles for the transfer of toxic proteins associated with neurodegenerative diseases?, Membrane Physiology and Membrane Biophysics, vol.3, p.31, 2012.

X. Cao, MicroRNA biomarkers of Parkinson's disease in serum exosome-like microvesicles, Neuroscience Letters, vol.644, p.31, 2017.

A. M. Miranda, Neuronal lysosomal dysfunction releases exosomes harboring APP C-terminal fragments and unique lipid signatures, Nature Communications, vol.9, issue.1, p.31, 2018.
DOI : 10.1038/s41467-017-02533-w

URL : https://www.nature.com/articles/s41467-017-02533-w.pdf

F. Fenizia, EGFR mutations in lung cancer: From tissue testing to liquid biopsy, Future Oncology, vol.11, issue.11, p.32, 2015.
DOI : 10.2217/fon.15.23

A. Lewis, Pancreatic cancer: Are "liquid biopsies" ready for prime-time?, World Journal of Gastroenterology, vol.22, issue.32, p.32, 2016.
DOI : 10.3748/wjg.v22.i32.7175

URL : https://doi.org/10.3748/wjg.v22.i32.7175

M. Gerlinger, Intratumor heterogeneity and branched evolution revealed by multiregion sequencing, The New England Journal of Medicine, vol.366, issue.10, p.32, 2012.

A. Panagiotara, Exosomes: A Cancer Theranostics Road Map, Public Health Genomics, vol.20, issue.2, p.32, 2017.
DOI : 10.1159/000478253

URL : https://www.karger.com/Article/Pdf/478253

T. Steuber, Serum markers for prostate cancer: A rational approach to the literature, European Urology, vol.54, issue.1, pp.31-40, 1932.
DOI : 10.1016/j.eururo.2008.01.034

M. R. Fernando, New evidence that a large proportion of human blood plasma cell-free DNA is localized in exosomes, PLoS ONE, vol.12, issue.8, p.32, 2017.

H. W. Hou, Isolation and retrieval of circulating tumor cells using centrifugal forces, Scientific Reports, vol.3, p.32, 2013.
DOI : 10.1038/srep01259

URL : https://www.nature.com/articles/srep01259.pdf

L. Guo, Extracellular vesicles and their diagnostic and prognostic potential in cancer, Translational Cancer Research, vol.6, issue.3, p.32, 2017.
DOI : 10.21037/tcr.2017.06.32

M. Tkach, Communication by Extracellular Vesicles: Where We Are and Where We Need to Go, Cell, vol.164, issue.6, p.32, 2016.
DOI : 10.1016/j.cell.2016.01.043

URL : https://doi.org/10.1016/j.cell.2016.01.043

M. Kanada, Signaling by Extracellular Vesicles Advances Cancer Hallmarks, Trends in Cancer, vol.2, issue.2, p.32, 2016.
DOI : 10.1016/j.trecan.2015.12.005

O. Lorraine and . Driscoll, Expanding on Exosomes and Ectosomes in Cancer, New England Journal of Medicine, vol.372, issue.24, p.32, 2015.

M. Wiktoria and . Suchorska, The role of exosomes in tumor progression and metastasis (Review), Oncology Reports, vol.35, issue.3, p.32, 2016.

C. Honorary, Research Director, Founder of RevInterCell, a et al. Cell-derived Extracellular Vesicles Open New Perspectives for Cancer Research, ) and UPMC, vol.1, p.32, 2015.

K. Al-nedawi, Intercellular transfer of the oncogenic receptor EGFRvIII by microvesicles derived from tumour cells, Nature Cell Biology, vol.10, issue.5, pp.619-624, 1932.
DOI : 10.1038/ncb1725

H. Peinado, Melanoma exosomes educate bone marrow progenitor cells toward a prometastatic phenotype through MET, Nature Medicine, vol.18, issue.6, p.32, 2012.
DOI : 10.1038/nm.2753

URL : http://europepmc.org/articles/pmc3645291?pdf=render