Last updated September 2023 - Medical Neurobiology
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Zohar K, Lezmi E, Reichert F, Eliyahu T, Rotshenker S, Weinstock M, et al. Coordinated Transcriptional Waves Define the Inflammatory Response of Primary Microglial Culture. International Journal of Molecular Sciences [Internet]. 2023;24(13). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85164845929&doi=10.3390%252fijms241310928&partnerID=40&md5=5dad29380a4666eee4962c58c283a501
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Rotshenker S. Galectin-3 (MAC-2) controls phagocytosis and macropinocytosis through intracellular and extracellular mechanisms. Frontiers in Cellular Neuroscience [Internet]. 2022;16. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85140232811&doi=10.3389%252ffncel.2022.949079&partnerID=40&md5=f5748cf69fc6609e5ba5cac6cea5b476
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Elberg G, Liraz-Zaltsman S, Reichert F, Matozaki T, Tal M, Rotshenker S. Deletion of SIRPα (signal regulatory protein-α) promotes phagocytic clearance of myelin debris in Wallerian degeneration, axon regeneration, and recovery from nerve injury. Journal of Neuroinflammation [Internet]. 2019;16(1). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85077317321&doi=10.1186%252fs12974-019-1679-x&partnerID=40&md5=b0ceb7dbf3149795fe0300104db43cc4
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Reichert F, Rotshenker S. Galectin-3 (MAC-2) controls microglia phenotype whether amoeboid and phagocytic or branched and non-phagocytic by regulating the cytoskeleton. Frontiers in Cellular Neuroscience [Internet]. 2019;13. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85064207165&doi=10.3389%252ffncel.2019.00090&partnerID=40&md5=17fcc82b5648680dabbcdb3c29564278
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Menzfeld C, John M, van Rossum D, Regen T, Scheffel J, Janova H, et al. Tyrphostin AG126 exerts neuroprotection in CNS inflammation by a dual mechanism. GLIA [Internet]. 2015;63(6):1083–99. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84927970668&doi=10.1002%252fglia.22803&partnerID=40&md5=d30edb4662a183f41276bcd7c5870893
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Rotshenker S. Traumatic Injury to Peripheral Nerves [Internet]. Vol. 2, Nerves and Nerve Injuries. 2015. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84940010516&doi=10.1016%252fB978-0-12-802653-3.00088-9&partnerID=40&md5=72c3658965c2f3532c28c499b5347990
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Gitik M, Kleinhaus R, Hadas S, Reichert F, Rotshenker S. Phagocytic receptors activate and immune inhibitory receptor SIRPα inhibits phagocytosis through paxillin and cofilin. Frontiers in Cellular Neuroscience [Internet]. 2014;8(1 APR). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84898841614&doi=10.3389%252ffncel.2014.00104&partnerID=40&md5=e507c5b07b9a63a18539a37f02a727c3
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Hadas S, Spira M, Hanisch UK, Reichert F, Rotshenker S. Complement receptor-3 negatively regulates the phagocytosis of degenerated myelin through tyrosine kinase Syk and cofilin. Journal of Neuroinflammation [Internet]. 2012;9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84863511515&doi=10.1186%252f1742-2094-9-166&partnerID=40&md5=785cf01f0486a2098aba177bc815a60f
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Rotshenker S. Wallerian degeneration: The innate-immune response to traumatic nerve injury. Journal of Neuroinflammation [Internet]. 2011;8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-80052104308&doi=10.1186%252f1742-2094-8-109&partnerID=40&md5=3b39d670c14d8f75c33dcb696fedb20a
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Gitik M, Liraz-Zaltsman S, Oldenborg PA, Reichert F, Rotshenker S. Myelin down-regulates myelin phagocytosis by microglia and macrophages through interactions between CD47 on myelin and SIRPα (signal regulatory protein-α) on phagocytes. Journal of Neuroinflammation [Internet]. 2011;8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-79952545687&doi=10.1186%252f1742-2094-8-24&partnerID=40&md5=bda360f70fba275b11f96937204088f6
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Gitik M, Reichert F, Rotshenker S. Cytoskeleton plays a dual role of activation and inhibition in myelin and zymosan phagocytosis by microglia. FASEB Journal [Internet]. 2010;24(7):2211–21. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-77954447521&doi=10.1096%252ffj.09-146118&partnerID=40&md5=c2ac3c6c7356427325ff027d73b2038a
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Hadas S, Reichert F, Rotshenker S. Dissimilar and similar functional properties of complement receptor-3 in microglia and macrophages in combating yeast pathogens by phagocytosis. GLIA [Internet]. 2010;58(7):823–30. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-77952567454&doi=10.1002%252fglia.20966&partnerID=40&md5=4343486a3eb2ac59c3931d0b76c57fe2
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Rotshenker S. The role of Galectin-3/MAC-2 in the activation of the innate-immune function of phagocytosis in microglia in injury and disease. Journal of Molecular Neuroscience [Internet]. 2009;39(1–2):99–103. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-74149092361&doi=10.1007%252fs12031-009-9186-7&partnerID=40&md5=2556092fb7bc5abf5c40f2cf56acb592
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Rotshenker S, Reichert F, Gitik M, Haklai R, Elad-Sfadia G, Kloog Y. Galectin-3/MAC-2, ras and PI3K activate complement receptor-3 and scavenger receptor-AI/II mediated myelin phagocytosis in microglia. GLIA [Internet]. 2008;56(15):1607–13. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-58149343875&doi=10.1002%252fglia.20713&partnerID=40&md5=f7398d82aaf3eafe87ea461fb90d10e1
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Cohen G, Makranz C, Spira M, Kodama T, Reichert F, Rotshenker S. Non-PKC DAG/phorbol-ester receptor(s) inhibit complement receptor-3 and nPKC inhibit scavenger receptor-AI/II-mediated myelin phagocytosis but cPKC, PI3K, and PLCγ activate myelin phagocytosis by both. GLIA [Internet]. 2006;53(5):538–50. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645387750&doi=10.1002%252fglia.20304&partnerID=40&md5=e7eaa672de7098458c20e8df1fd5b034
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Makranz C, Cohen G, Reichert F, Kodama T, Rotshenker S. cAMP cascade (PKA, Epac, adenylyl cyclase, Gi, and phosphodiesterases) regulates myelin phagocytosis mediated by complement receptor-3 and scavenger receptor-AI/II in microglia and macrophages. GLIA [Internet]. 2006;53(4):441–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33644512079&doi=10.1002%252fglia.20303&partnerID=40&md5=1e4ade543953fa92a41268ccb7a2a3bf
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Makranz C, Cohen G, Baron A, Levidor L, Kodama T, Reichert F, et al. Erratum: Phosphatidylinositol 3-kinase, phosphoinositide-specific phospholipase-Cγ and protein kinase-C signal myelin phagocytosis mediated by complement receptor-3 alone and combined with scavenger receptor-AI/II in macrophages (Neurobiology Disease (2004) 15 (279-286) DOI: 10.1016/j.nbd.2003. 11.007. Neurobiology of Disease [Internet]. 2004;16(3):659. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-3242735939&doi=10.1016%252fj.nbd.2004.04.005&partnerID=40&md5=8ba9928952938147f9cfc60a4e3f3801
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Makranz C, Cohen G, Baron A, Levidor L, Kodama T, Reichert F, et al. Phosphatidylinositol 3-kinase, phosphoinositide-specific phospholipase-Cγ and protein kinase-C signal myelin phagocytosis mediated by complement receptor-3 alone and combined with scavenger receptor-AI/II in macrophages. Neurobiology of Disease [Internet]. 2004;15(2):279–86. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-1542270757&doi=10.1016%252fj.nbd.2003.11.007&partnerID=40&md5=1e2a39d680c6c8e478ccf86a820ef300
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Rotshenker S. Microglia and macrophage activation and the regulation of complement-receptor-3 (CR3/MAC-1)-mediated myelin phagocytosis in injury and disease. Journal of Molecular Neuroscience [Internet]. 2003;21(1):65–72. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0141450468&doi=10.1385%252fJMN%253a21%253a1%253a65&partnerID=40&md5=f2e370279d92040b6b8760c6da7342fc
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Mirski R, Reichert F, Klar A, Rotshenker S. Granulocyte macrophage colony stimulating factor (GM-CSF) activity is regulated by a GM-CSF binding molecule in Wallerian degeneration following injury to peripheral nerve axons. Journal of Neuroimmunology [Internet]. 2003;140(1–2):88–96. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037629298&doi=10.1016%2fS0165-5728%2803%2900179-6&partnerID=40&md5=d892c139c9a7e998981f5d2eaa93d64f
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Reichert F, Rotshenker S. Complement-receptor-3 and scavenger-receptor-AI/II mediated myelin phagocytosis in microglia and macrophages. Neurobiology of Disease [Internet]. 2003;12(1):65–72. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037327741&doi=10.1016%2fS0969-9961%2802%2900008-6&partnerID=40&md5=3fe55c1366e8b7ad46cea8a4752e991f
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Shamash S, Reichert F, Rotshenker S. The cytokine network of wallerian degeneration: Tumor necrosis factor-α, interleukin-1α, and interleukin-1β. Journal of Neuroscience [Internet]. 2002;22(8):3052–60. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037092441&doi=10.1523%252fjneurosci.22-08-03052.2002&partnerID=40&md5=9acc7257e23896b47c920074bebc5704
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Slobodov U, Reichert F, Mirski R, Rotshenker S. Distinct inflammatory stimuli induce different patterns of myelin phagocytosis and degradation in recruited macrophages. Experimental Neurology [Internet]. 2001;167(2):401–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035134433&doi=10.1006%252fexnr.2000.7559&partnerID=40&md5=8aa90ca8d434ef35216182552151b9ca
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Reichert F, Slobodov U, Makranz C, Rotshenker S. Modulation (inhibition and augmentation) of complement receptor-3-mediated myelin phagocytosis. Neurobiology of Disease [Internet]. 2001;8(3):504–12. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034984592&doi=10.1006%252fnbdi.2001.0383&partnerID=40&md5=b7d42f9731016491ccdc98aefc92ffa4
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Reichert F, Rotshenker S. Galectin-3/MAC-2 in experimental allergic encephalomyelitis. Experimental Neurology [Internet]. 1999;160(2):508–14. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032763663&doi=10.1006%252fexnr.1999.7229&partnerID=40&md5=7225d4f57caa3c0322ad0190bf22a8d0
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Be’eri H, Reichert F, Saada A, Rotshenker S. The cytokine network of Wallerian degeneration: IL-10 and GM-CSF. European Journal of Neuroscience [Internet]. 1998;10(8):2707–13. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0031901842&doi=10.1046%252fj.1460-9568.1998.00277.x&partnerID=40&md5=baf5c52abf57560d5477fde57db9f777
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Rand N, Reichert F, Floman Y, Rotshenker S. Murine nucleus pulposus-derived cells secrete interleukins-1-β, -6, and -10 and granulocyte-macrophage colony-stimulating factor in cell culture. Spine [Internet]. 1997;22(22):2598–602. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0031409005&doi=10.1097%252f00007632-199711150-00002&partnerID=40&md5=e52f7e7275dc384f556d875bfbcf6864
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Saada A, Reichert F, Rotshenker S. Granulocyte macrophage colony stimulating factor produced in lesioned peripheral nerves induces the up-regulation of cell surface expression of MAC-2 by macrophages and Schwann cells. Journal of Cell Biology [Internet]. 1996;133(1):159–67. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029929404&doi=10.1083%252fjcb.133.1.159&partnerID=40&md5=f74c3009f9d70d8bac5bc40c9d089b6f
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Reichert F, Levitzky R, Rotshenker S. Interleukin 6 in intact and injured mouse peripheral nerves. European Journal of Neuroscience [Internet]. 1996;8(3):530–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029875871&doi=10.1111%252fj.1460-9568.1996.tb01237.x&partnerID=40&md5=9702a4381c784c75f128d0c04b35d8dc
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Reichert F, Rotshenker S. Deficient activation of microglia during optic nerve degeneration. Journal of Neuroimmunology [Internet]. 1996;70(2):153–61. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0030298442&doi=10.1016%2fS0165-5728%2896%2900112-9&partnerID=40&md5=5990c4f3bc273c5b84a627d533f3b8ab
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Saada A, Dunaevsky‐Hutt A, Aamar A, Reichert F, Rotshenker S. Fibroblasts that Reside in Mouse and Frog Injured Peripheral Nerves Produce Apolipoproteins. Journal of Neurochemistry [Internet]. 1995;64(5):1996–2003. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028930810&doi=10.1046%252fj.1471-4159.1995.64051996.x&partnerID=40&md5=359eba21bf1e1de72456466a03344f5e
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Groner Y, Elroy-Sterol O, Avraham KB, Schickler M, Knobler H, Minc-Golomb D, et al. Cell damage by excess CuZnSOD and down’s syndrome. Biomedicine and Pharmacotherapy [Internet]. 1994;48(5–6):231-237,240. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028365043&doi=10.1016%2f0753-3322%2894%2990138-4&partnerID=40&md5=a2781c5fc3893c0e3e2bb51232f8457a
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Reichert F, Saada A, Rotshenker S. Peripheral nerve injury induces Schwann cells to express two macrophage phenotypes: Phagocytosis and the galactose-specific lectin MAC-2. Journal of Neuroscience [Internet]. 1994;14(5 II):3231–45. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028334842&doi=10.1523%252fjneurosci.14-05-03231.1994&partnerID=40&md5=8550db01ebe1f44b787cb40443766a3f
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Aamar S, Saada A, Rotshenker S. Lesion‐Induced Changes in the Production of Newly Synthesized and Secreted Apo‐E and Other Molecules Are Independent of the Concomitant Recruitment of Blood‐Borne Macrophages into Injured Peripheral Nerves. Journal of Neurochemistry [Internet]. 1992;59(4):1287–92. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026761485&doi=10.1111%252fj.1471-4159.1992.tb08439.x&partnerID=40&md5=7db44e1f7d6aea3acf7ad0c627988d89
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Rotshenker S, Aamar S, Barak V. Interleukin-1 activity in lesioned peripheral nerve. Journal of Neuroimmunology [Internet]. 1992;39(1–2):75–80. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026753607&doi=10.1016%2f0165-5728%2892%2990176-L&partnerID=40&md5=a2a832b33ee820eb5185b605dc851802
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Sugarman H, Dunaevsky-Hutt A, Rotshenker S. The roles of the synaptic basal lamina and of innervation in directing the accumulation of a synaptic molecule, mAb 3B6 antigen, in regenerating skeletal muscles. Journal of Neurocytology [Internet]. 1991;20(10):810–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025916712&doi=10.1007%252fBF01191732&partnerID=40&md5=1ee8a77cf40ca8a2940b6ce8b859510d
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Connor EA, Sugarman H, Rotshenker S. Molecular alterations in the perijunctional region of frog skeletal muscle fibres following denervation. Journal of Neurocytology [Internet]. 1991;20(4):323–31. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026021043&doi=10.1007%252fBF01235549&partnerID=40&md5=499ca013eefac316f19b521460dc6e09
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Avraham KB, Sugarman H, Rotshenker S, Groner Y. Down’s syndrome: morphological remodelling and increased complexity in the neuromuscular junction of transgenic CuZn-superoxide dismutase mice. Journal of Neurocytology [Internet]. 1991;20(3):208–15. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026096819&doi=10.1007%252fBF01186993&partnerID=40&md5=76ba1cc0930dbea7841655dc7eef05f1
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Rotshenker S. Multiple modes and sites for the induction of axonal growth. Trends in Neurosciences [Internet]. 1988;11(8):363–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023801605&doi=10.1016%2f0166-2236%2888%2990059-8&partnerID=40&md5=a3ee425dddf47dec764548d5950f44cd
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Rotshenker S, Ring G, Tal M, Sugarman H, Reichert F. Regulation of motor axon sprouting. Israel Journal of Medical Sciences [Internet]. 1987;23(1–2):89–94. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023253971&partnerID=40&md5=967132be795d43e95df1f5119fc0cb05
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Rotshenker S, Tal M. The transneuronal induction of sprouting and synapse formation in intact mouse muscles. The Journal of Physiology [Internet]. 1985;360(1):387–96. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021895471&doi=10.1113%252fjphysiol.1985.sp015623&partnerID=40&md5=6e1796526269ebbad9ec4338ccec025a
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Tal M, Rotshenker S. Sprouting and synapse formation produced by carbocaine. Journal of Neuroscience [Internet]. 1984;4(2):458–63. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021276815&doi=10.1523%252fjneurosci.04-02-00458.1984&partnerID=40&md5=bd5d54b8c93a414066e477a683f96e8b
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Tal M, Rotshenker S. Recycling of synaptic vesicles in motor nerve endings separated from their target muscle fibers. Brain Research [Internet]. 1983;270(1):131–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020563448&doi=10.1016%2f0006-8993%2883%2990799-0&partnerID=40&md5=8cf34d3a40cb322c9f32ce9b8df023a4
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Ring G, Reichert F, Rotshenker S. Sprouting in intact sartorius muscles of the frog following contralateral axotomy. Brain Research [Internet]. 1983;260(2):313–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020684369&doi=10.1016%2f0006-8993%2883%2990687-X&partnerID=40&md5=0c3dc663c407b71db2f6449e78eb5b4e
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Rotshenker S. Transneuronal and peripheral mechanisms for the induction of motor neuron sprouting. Journal of Neuroscience [Internet]. 1982;2(10):1359–68. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020470184&doi=10.1523%252fjneurosci.02-10-01359.1982&partnerID=40&md5=639db3178167482250f086714df47ed3
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Rotshenker S. Sprouting and synapse formation by motor axons separated from their cell bodies. Brain Research [Internet]. 1981;223(1):141–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019453622&doi=10.1016%2f0006-8993%2881%2990813-1&partnerID=40&md5=5ddf9bd5c88b04caac845e599d969bb4
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Rotshenker S, Reichert F. Motor axon sprouting and site of synapse formation in intact innervated skeletal muscle of the frog. Journal of Comparative Neurology [Internet]. 1980;193(2):413–22. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019135628&doi=10.1002%252fcne.901930208&partnerID=40&md5=d46388138f1685935493df35a88183a2
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Rotshenker S. Colchicine induces sprouting and synapse formation. Israel Journal of Medical Sciences [Internet]. 1980;16(8):614. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018819797&partnerID=40&md5=e687ed8a2c35a960aa5f416a5a93b2bf
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Reichert F, Rotshenker S. Motor axon terminal sprouting in intact muscles. Brain Research [Internet]. 1979;170(1):187–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018358830&doi=10.1016%2f0006-8993%2879%2990952-1&partnerID=40&md5=c628ac89ed84df06802f3204d3f2d152
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Rotshenker S. Synapse formation in intact innervated cutaneous‐pectoris muscles of the frog following denervation of the opposite muscle. The Journal of Physiology [Internet]. 1979;292(1):535–47. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018657178&doi=10.1113%252fjphysiol.1979.sp012870&partnerID=40&md5=86cbf75ee17fa25228c6eb85d8871687
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Rotshenker S. Sprouting of intact motor neurons induced by neuronal lesion in the absence of denervated muscle fibers and degenerating axons. Brain Research [Internet]. 1978;155(2):354–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018091609&doi=10.1016%2f0006-8993%2878%2991029-6&partnerID=40&md5=3f3f21c66f5cb6b341b187b59ab2cf7e
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Erulkar SD, Rahamimoff R, Rotshenker S. Quelling of spontaneous transmitter release by nerve impulses in low extracellular calcium solutions. The Journal of Physiology [Internet]. 1978;278(1):491–500. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018199181&doi=10.1113%252fjphysiol.1978.sp012319&partnerID=40&md5=0fa71e1a4272962ebd78e6b60849b501
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Rotshenker S, McMahan UJ. Altered patterns of innervation in frog muscle after denervation. Journal of Neurocytology [Internet]. 1976;5(6):719–30. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017144891&doi=10.1007%252fBF01181583&partnerID=40&md5=22fa6bde1aac43b10d1b0fdbff3ba136
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Rotshenker S, Palti Y. The latent period of anode break excitation in myelinated and giant axons. Journal of Theoretical Biology [Internet]. 1976;59(2):293–302. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017069149&doi=10.1016%2f0022-5193%2876%2990171-5&partnerID=40&md5=69adfaafc34390f3e1882b5de87034e6
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Rotshenker S, Erulkar SD, Rahamimoff R. Reduction in the frequency of miniature end-plate potentials by nerve stimulation in low calcium solutions. Brain Research [Internet]. 1976;101(2):362–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0016809202&doi=10.1016%2f0006-8993%2876%2990277-8&partnerID=40&md5=4047cd18f335ad72940fa360c64ef0c6
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Rahamimoff R, Erulkar SD, Alnaes E, Meiri H, Rotshenker S, Rahamimoff H. Modulation of transmitter release by calcium ions and nerve impulses. Cold Spring Harbor symposia on quantitative biology [Internet]. 1976;40:107–16. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0016910106&doi=10.1101%252fSQB.1976.040.01.012&partnerID=40&md5=6003d396be29406297a004a09283b73c
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