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Tunneling nanotubes: A new route for the exchange of components between animal cells
Abstract
Recently, highly sensitive nanotubular structures mediating membrane continuity between mammalian cells have been discovered. With respect to their peculiar architecture, these membrane channels were termed tunneling nanotubes (TNTs). TNTs could form de novo between animal cells leading to the generation of complex cellular networks. They have been shown to facilitate the intercellular transfer of organelles as well as, on a limited scale, of membrane components and cytoplasmic molecules. It has been proposed that TNTs represent a novel and general biological principle of cell‐to‐cell communication and it becomes increasingly apparent that they fulfill important functions in the physiological processes of multicellular organisms.
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“Later, HIV-1 and HTLV-1 cell-to-cell transmission via TNT was reported.”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [107]
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Cites
Südhof, T. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131412 · Cited by 2,491
Nanotubular Highways for Intercellular Organelle Transport
Rustom, A., Saffrich, R., Markovic, I., Walther, P., & Gerdes, H.-H. (2004) · Science · doi:10.1126/science.1093133 · Cited by 2,038
Self-citationThe Gap Junction Communication Channel
Kumar, N. M., & Gilula, N. B. (1996) · Cell · doi:10.1016/s0092-8674(00)81282-9 · Cited by 1,929
Cholesterol Modification of Hedgehog Signaling Proteins in Animal Development
Porter, J. A., Young, K. E., & Beachy, P. A. (1996) · Science · doi:10.1126/science.274.5285.255 · Cited by 1,360
The Biogenesis and Functions of Exosomes
Stoorvogel, W., Kleijmeer, M. J., Geuze, H. J., & Raposo, G. (2002) · Traffic · doi:10.1034/j.1600-0854.2002.30502.x · Cited by 848
Identification of a Palmitic Acid-modified Form of Human Sonic hedgehog
Pepinsky, R. B., Zeng, C., Wen, D., Rayhorn, P., Baker, D. P., Williams, K. P., Bixler, S. A., Ambrose, C. M., Garber, E. A., Miatkowski, K., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.22.14037 · Cited by 754
Ramı́rez-Weber, F.-A., & Kornberg, T. B. (1999) · Cell · doi:10.1016/s0092-8674(00)80771-0 · Cited by 614
The origin of the cancer stem cell: current controversies and new insights
Bjerkvig, R., Tysnes, B. B., Aboody, K. S., Najbauer, J., & Terzis, A. J. A. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1740 · Cited by 604
STUDIES ON THE FINE STRUCTURE OF THE MAMMALIAN TESTIS
Burgos, M. H., & Fawcett, D. W. (1955) · The Journal of Cell Biology · doi:10.1083/jcb.1.4.287 · Cited by 561
Önfelt, B., Nedvetzki, S., Benninger, R. K. P., Purbhoo, M. A., Sowinski, S., Hume, A. N., Seabra, M. C., Neil, M. A. A., French, P. M. W., & Davis, D. M. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.12.8476 · Cited by 503
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Ülger, Ö., & Kubat, G. B. (2022) · Biochimie · doi:10.1016/j.biochi.2022.01.002 · Cited by 56
On the role of membrane anisotropy and BAR proteins in the stability of tubular membrane structures
Kabaso, D., Bobrovska, N., Góźdź, W. T., Gov, N. S., Kralj‐Iglič, V., Veranič, P., & Iglič, A. (2011) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2011.10.039 · Cited by 55
Tetraspanins and cell membrane tubular structures
Zhang, X. A., & Huang, C. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0954-0 · Cited by 56
Kabaso, D., Lokar, M., Kralj‐Iglič, V., Veranič, P., & Iglic, A. (2011) · International Journal of Nanomedicine · doi:10.2147/ijn.s16982 · Cited by 54
Brain clearance of protein aggregates: a close-up on astrocytes
Giusti, V., Kaur, G., Giusto, E., & Civiero, L. (2024) · Molecular Neurodegeneration · doi:10.1186/s13024-024-00703-1 · Cited by 54
Zani, B. G., & Edelman, E. R. (2010) · Communicative & Integrative Biology · doi:10.4161/cib.3.3.11659 · Cited by 52
Dendritic cell altered states: what role for calcium?
Salter, R. D., & Watkins, S. C. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2009.00806.x · Cited by 53
Ma, Z., Yang, H., Liu, H., Xu, M., Runyan, R. B., Eisenberg, C. A., Markwald, R. R., Borg, T. K., & Gao, B. Z. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056554 · Cited by 51
Proteins Regulating Microvesicle Biogenesis and Multidrug Resistance in Cancer
Taylor, J., & Bebawy, M. (2018) · PROTEOMICS · doi:10.1002/pmic.201800165 · Cited by 53
Cell polarity during motile processes: keeping on track with the exocyst complex
Hertzog, M., & Chavrier, P. (2011) · Biochemical Journal · doi:10.1042/bj20101214 · Cited by 48
Guo, R., Davis, D. L., & Fāng, Y. (2018) · Virology · doi:10.1016/j.virol.2017.12.018 · Cited by 48
Imaging Tunneling Membrane Tubes Elucidates Cell Communication in Tumors
Lou, E., Gholami, S., Romin, Y., Thayanithy, V., Fujisawa, S., Desir, S., Steer, C. J., Subramanian, S., Fong, Y., Manova-Todorova, K. O., et al. (2017) · Trends in cancer · doi:10.1016/j.trecan.2017.08.001 · Cited by 50
Formicola, B., D’Aloia, A., Magro, R. D., Stucchi, S., Rigolio, R., Ceriani, M., & Re, F. (2019) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2019.00403 · Cited by 48
Caicedo, A., Zambrano, K., Sanon, S., Luis Vélez, J., Montalvo, M., Jara, F., Moscoso, S. A., Vélez, P., Maldonado, A., & Velarde, G. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.02.014 · Cited by 48
Meraz, I. M., Melendez, B., Gu, J., Wong, S. T. C., Liu, X., Andersson, H. A., & Serda, R. E. (2012) · Molecular Pharmaceutics · doi:10.1021/mp3001292 · Cited by 46
Tao, X., Li, W., Su, J., Jin, C., Wang, X., Li, J., Hu, J., Xiang, Z.-H., Lau, J. T. Y., & Hu, Y. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22306 · Cited by 46
Controlling Chemistry by Geometry in Nanoscale Systems
Lizana, L., Konkoli, Z., Bauer, B., Jesorka, A., & Orwar, O. (2008) · Annual Review of Physical Chemistry · doi:10.1146/annurev.physchem.040808.090255 · Cited by 45
The secret life of extracellular vesicles in metal homeostasis and neurodegeneration
Bellingham, S. A., Guo, B. B., & Hill, A. F. (2015) · Biology of the Cell · doi:10.1111/boc.201500030 · Cited by 45
A role for RASSF1A in tunneling nanotube formation between cells through GEFH1/Rab11 pathway control
Dubois, F., Jean‐Jacques, B., Roberge, H., Bénard, M., Galas, L., Schapman, D., Elie, N., Goux, D., Keller, M., Maille, E., et al. (2018) · Cell Communication and Signaling · doi:10.1186/s12964-018-0276-4 · Cited by 45
Molecular events underlying the cell‐to‐cell transmission of α‐synuclein
Choi, Y. R., Park, S., & Park, S. M. (2020) · FEBS Journal · doi:10.1111/febs.15674 · Cited by 47
Non‐classical membrane trafficking processes galore
Chua, C. E. L., Lim, Y. S., Lee, M. G., & Tang, B. L. (2012) · Journal of Cellular Physiology · doi:10.1002/jcp.24082 · Cited by 44
Melcher, M., Danhauser, K., Seibt, A., Degistirici, Ö., Baertling, F., Kondadi, A. K., Reichert, A. S., Koopman, W. J. H., Willems, P. H. G. M., Rodenburg, R. J., et al. (2017) · Stem Cell Research & Therapy · doi:10.1186/s13287-017-0601-7 · Cited by 47
Formigli, L., Francini, F., Nistri, S., Margheri, M., Luciani, G., Naro, F., Silvertown, J. D., Orlandini, S. Z., Meacci, E., & Bani, D. (2009) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2009.05.008 · Cited by 43
Lokar, M., Iglič, A., & Veranič, P. (2010) · PROTOPLASMA · doi:10.1007/s00709-010-0143-7 · Cited by 43
Keratinocytes Share Gene Expression Fingerprint with Epidermal Langerhans Cells via mRNA Transfer
Su, Q., & Igyártó, B. Z. (2019) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2019.05.006 · Cited by 42
The Novel Roles of Connexin Channels and Tunneling Nanotubes in Cancer Pathogenesis
Valdebenito, S., Lou, E., Baldoni, J., Okafo, G. N., & Eugenín, E. A. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051270 · Cited by 41
Oxidative stress and mitochondrial transfer: A new dimension towards ocular diseases
Subramaniam, M. D., Iyer, M., Nair, A. P., Venkatesan, D., Mathavan, S., Eruppakotte, N., Kizhakkillach, S., Chandran, M. K., Roy, A., Gopalakrishnan, A. V., et al. (2020) · Genes & Diseases · doi:10.1016/j.gendis.2020.11.020 · Cited by 41
Chen, Y., Yang, F., Chu, Y., Yun, Z., Yan, Y., & Jin, J. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03693-0 · Cited by 41
Eugenín, E. A., Camporesi, E. M., & Peracchia, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23116133 · Cited by 40
Zhu, C., Shi, Y., & You, J. (2021) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.0c01248 · Cited by 39
Long filopodia and tunneling nanotubes define new phenotypes of breast cancer cells in 3D cultures
Franchi, M., Piperigkou, Z., Riti, E., Masola, V., Onisto, M., & Karamanos, N. (2020) · Matrix Biology Plus · doi:10.1016/j.mbplus.2020.100026 · Cited by 39
Direct Transfer of Mesoporous Silica Nanoparticles between Macrophages and Cancer Cells
Franco, S., Noureddine, A., Guo, J., Keth, J., Paffett, M. L., Brinker, C. J., & Serda, R. E. (2020) · Cancers · doi:10.3390/cancers12102892 · Cited by 39
Tunneling nanotubes: A bridge for heterogeneity in glioblastoma and a new therapeutic target?
Venkatesh, V. S., & Lou, E. (2019) · Cancer Reports · doi:10.1002/cnr2.1185 · Cited by 37
Asencio-Barría, C. A., Defamie, N., Sáez, J. C., Mesnil, M., & Godoy, A. (2019) · Cancers · doi:10.3390/cancers11091370 · Cited by 37
Tetraspanin-enriched microdomains regulate digitation junctions
Huang, C., Fu, C., Wren, J. D., Wang, X., Zhang, F., Zhang, Y. H., Connell, S. A., Chen, T., & Zhang, X. A. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2803-2 · Cited by 36
Exosomes Are Unlikely Involved in Intercellular Nef Transfer
Luo, X., Fan, Y., Park, I.-W., & He, J. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124436 · Cited by 35
Linked in: immunologic membrane nanotube networks
Zaccard, C. R., Rinaldo, C. R., & Mailliard, R. B. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.4vmr0915-395r · Cited by 36
Hu, J., Deng, G., Tian, Y. E., Pu, Y., Cao, P., & Yuan, W. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4139 · Cited by 35
Intercellular Transport of Oct4 in Mammalian Cells: A Basic Principle to Expand a Stem Cell Niche?
Rolf, H., Niebert, S., Niebert, M., Gaus, L., Schliephake, H., & Wiese, K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032287 · Cited by 28
Walsh, F. C., Balasubramaniam, S., Botvich, D., Suda, T., Nakano, T., Bush, S. F., & Foghlú, M. Ó. (2009) · Lecture notes of the Institute for Computer Sciences, Social Informatics and Telecommunications Engineering · doi:10.1007/978-3-642-02427-6_7 · Cited by 34
Güngör‐Ordueri, N. E., Tang, E. I., Çelik-Özenci, Ç., & Cheng, C. Y. (2014) · Endocrinology · doi:10.1210/en.2014-1163 · Cited by 33
Cytomixis in plants: facts and doubts
Mursalimov, S. R., & Дейнеко, Е. В. (2017) · PROTOPLASMA · doi:10.1007/s00709-017-1188-7 · Cited by 33
Zhang, Y. (2011) · Communicative & Integrative Biology · doi:10.4161/cib.4.3.14855 · Cited by 33
Intercellular transfer of mitochondria
Plotnikov, E. Y., Babenko, V. А., Silachev, D. N., Zorova, L. D., Khryapenkova, T. G., Savchenko, E. S., Pevzner, I. B., & Zorov, D. B. (2015) · Biochemistry (Moscow) · doi:10.1134/s0006297915050041 · Cited by 33
Inter‐endothelial Transport of Microvectors using Cellular Shuttles and Tunneling Nanotubes
Ferrati, S., Shamsudeen, S., Summers, H. D., Rees, P. C. T., Abbey, J. V. A., Schmulen, J., Liu, X., Wong, S. T. C., Bean, A. J., Mauro Ferrari, B., et al. (2012) · Small · doi:10.1002/smll.201200472 · Cited by 32
Sánchez, V., Villalba, N., Fiore, L., Luzzani, C., Miriuka, S., Boveris, A., Gelpi, R. J., Brusco, A., & Poderoso, J. J. (2017) · Stem Cell Reviews and Reports · doi:10.1007/s12015-017-9730-8 · Cited by 31
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Polyakova, N., Kalashnikova, M., & Belyavsky, A. V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076455 · Cited by 34
Burt, R. K., Chen, Y.-H., Verda, L., Lucena, C., Navale, S., Johnson, J., Han, X., Lomasney, J. W., Baker, J. M., Ngai, K.-L., et al. (2012) · Circulation Research · doi:10.1161/circresaha.111.262584 · Cited by 30
Zhang, C., & Schekman, R. W. (2023) · eLife · doi:10.7554/elife.84391 · Cited by 30
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Pienaar, I. S., Burn, D. J., Morris, C. M., & Dexter, D. T. (2011) · Molecular Neurobiology · doi:10.1007/s12035-011-8226-9 · Cited by 28
Valdebenito, S., Damico, D. C. S., & Eugenín, E. A. (2019) · Cancer Reports · doi:10.1002/cnr2.1220 · Cited by 29
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Shinn-Thomas, J. H., & Mohler, W. A. (2011) · International review of cytology · doi:10.1016/b978-0-12-386039-2.00005-5 · Cited by 29
Mitochondrial donation in translational medicine; from imagination to reality
Bagheri, H. S., Bani, F., Taşoğlu, S., Zarebkohan, A., Rahbarghazi, R., & Sokullu, E. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02529-z · Cited by 28
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Nordengen, K., & Morland, C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25020986 · Cited by 30
Halász, H., Ghadaksaz, A., Madarász, T., Huber, K., Harami, G. M., Tóth, E. A., Osteikoetxea-Molnár, A., Kovács, M., Balogi, Z., Nyitrai, M., et al. (2018) · Methods and Applications in Fluorescence · doi:10.1088/2050-6120/aad57d · Cited by 27
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Hurtig, J., & Orwar, O. (2008) · Soft Matter · doi:10.1039/b800333e · Cited by 27
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Ben‐Shachar, D., & Ene, H. M. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.08.007 · Cited by 27
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Dols-Pérez, A., Marin, V., Amador, G. J., Kieffer, R., Tam, D. S. W., & Aubin‐Tam, M. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b09983 · Cited by 25
Huda, F., Fan, Y., Suzuki, M., Konno, A., Matsuzaki, Y., Takahashi, N., Chan, J. K. Y., & Hirai, H. (2016) · PLoS ONE · doi:10.1371/journal.pone.0164202 · Cited by 24
Shear flow-induced nanotubulation of surface-immobilized liposomes
Sekine, Y., Abe, K., Shimizu, A., Sasaki, Y., Sawada, S., & Akiyoshi, K. (2012) · RSC Advances · doi:10.1039/c2ra00629d · Cited by 24
Pascoal, P., Kosanic, D., Gjoni, M., & Vogel, H. (2010) · Lab on a Chip · doi:10.1039/c004659k · Cited by 23
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Delage, E., & Zurzolo, C. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00504 · Cited by 23
Miyazawa, K., Emmerling, K., & Manuelidis, L. (2010) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22723 · Cited by 24
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Zalepa-King, L., & Citovsky, V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058025 · Cited by 22
Ghezeldasht, S. A., Blackbourn, D. J., Mosavat, A., & Rezaee, S. A. (2023) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408363.2022.2157791 · Cited by 20
Class I myosins: Highly versatile proteins with specific functions in the immune system
Girón‐Pérez, D. A., Piedra-Quintero, Z. L., & Santos‐Argumedo, L. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.1mr0918-350rrr · Cited by 21
Labudová, M., Tomášková, J., Škultéty, Ľ., Pastorek, J., & Pastoreková, S. (2009) · Journal of Virology · doi:10.1128/jvi.00309-09 · Cited by 22
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Ryskalin, L., Biagioni, F., Lenzi, P., Frati, A., & Fornai, F. (2020) · Cancers · doi:10.3390/cancers12092486 · Cited by 19
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A note on testing hypotheses for stationary processes in the frequency domain
Holger Dette, A., & Hildebrandt, T. (2011) · Journal of Multivariate Analysis · doi:10.1016/j.jmva.2011.07.002 · Cited by 19
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Ghezeldasht, S. A., Shamsian, S. A. A., Navashenaq, J. G., Miri, R., Ashrafi, F., Mosavat, A., & Rezaee, S. A. (2021) · Reviews in Medical Virology · doi:10.1002/rmv.2235 · Cited by 17
Hu, C., Shi, Z., Liu, X., & Sun, C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021175 · Cited by 18
Jhala, D., Rather, H., & Vasita, R. (2020) · Biomedical Materials · doi:10.1088/1748-605x/ab772e · Cited by 18
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Silverman, A. A., Olszewski, J. D., Siadat, S. M., & Ruberti, J. W. (2024) · Matter · doi:10.1016/j.matt.2024.01.023 · Cited by 17
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Zhang, X., Yu, H., & Feng, J. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1411104 · Cited by 17
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Li, S. C., Acevedo, J., Wang, L., Jiang, H., Luo, J., Pestell, R. G., Loudon, W. G., & Chang, A. C. (2012) · Current Stem Cell Research & Therapy · doi:10.2174/157488812798483449 · Cited by 17
Agnati, L. F., Fuxé, K., Baluška, F., & Guidolin, D. (2009) · Journal of Neural Transmission · doi:10.1007/s00702-009-0193-1 · Cited by 17
Chu, P. P., Bari, S., Fan, X., Gay, F. P. H., Ang, J. M. L., Chiu, G. N. C., Lim, S. K., & Hwang, W. Y. K. (2012) · Cytotherapy · doi:10.3109/14653249.2012.697146 · Cited by 17
Mentor, S., & Fisher, D. W. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.661065 · Cited by 15
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Matozo, T., Kogachi, L., & de Alencar, B. C. (2022) · Cytoskeleton · doi:10.1002/cm.21718 · Cited by 15
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Morin, A., Cordelières, F. P., Cherfils, J., & Olofsson, B. (2010) · Small GTPases · doi:10.4161/sgtp.1.3.15112 · Cited by 15
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Wang, C., Shen, Z., Chen, Y., Wang, Y., Zhou, X., Chen, X., Li, Y., Zhang, P., & Zhang, Q. (2024) · International Journal of Nanomedicine · doi:10.2147/ijn.s487303 · Cited by 13
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Talianová, M., & Janoušek, B. (2011) · American Journal of Botany · doi:10.3732/ajb.1000370 · Cited by 13
Novel drug-delivery approaches to the blood-brain barrier
Wang, X., Yu, X., Vaughan, W., Liu, M., & Guan, Y. (2015) · Neuroscience Bulletin · doi:10.1007/s12264-014-1498-0 · Cited by 13
Cellular parabiosis and the latency of age-related diseases
Radman, M. (2019) · Open Biology · doi:10.1098/rsob.180250 · Cited by 13
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Salazar, J. J., Gallego‐Pinazo, R., de Hoz, R., Pinazo-Duran, M. D., Rojas, B., Ramirez, A. I., Serrano, M., & Ramirez, J. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065446 · Cited by 12
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Aufderklamm, S., Aicher, W. K., Amend, B., & Stenzl, A. (2019) · Current Opinion in Urology · doi:10.1097/mou.0000000000000624 · Cited by 12
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Metadata
- Authors
- Gerdes, H.-H., Bukoreshtliev, N. V., & Barroso, J. F. V.
- Affiliations
- University of Bergen (NO)
- Corresponding author
- Gerdes, Hans-Hermann
- Venue
- FEBS Letters
- Publisher
- Wiley
- Published
- 2007-04-04
- Volume
- 581
- Issue
- 11
- Pages
- 2194-2201
- ISSN
- 0014-5793 (ISSN-L)
- 1873-3468
- OpenAlex
- W2044320361
- Cited by
- 304
- References
- 61
- Citations by year
- 2026: 9 · 2025: 6 · 2024: 18 · 2023: 11 · 2022: 18 · 2021: 20 · 2020: 18 · 2019: 18 · 2018: 21 · 2017: 16 · 2016: 14 · 2015: 13 · 2014: 11 · 2013: 14 · 2012: 22
- FWCI
- 1.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- FEBS Letters (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Caveolin-1 and cellular processes
- Keywords
- tunneling nanotubes, intercellular communication, membrane continuity, organelle transfer, multicellular organisms
- MeSH terms
- Animals, Biological Transport, Cell Communication, Cell Membrane, Humans, Plasmodesmata, Nanotubes
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