Last updated September 2023 - Medical Neurobiology
1.
Tal M, Minert A, Devor M. Resurgent neuropathic discharge: An obstacle to the therapeutic use of neuroma resection? Pain [Internet]. 2023;164(2):349–61. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146364114&doi=10.1097%252fj.pain.0000000000002704&partnerID=40&md5=1418afbeeb04bb4f4a2a8e4de177dff8
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Sharav Y, Haviv Y, Tal M. Placebo or Nocebo Interventions as Affected by Hypnotic Susceptibility. Applied Sciences (Switzerland) [Internet]. 2023;13(2). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146722765&doi=10.3390%252fapp13020931&partnerID=40&md5=f8544f5cdf7c90744b4ee209af5bf515
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Jahanbani S, Hansen PS, Blum LK, Bastounis EE, Ramadoss NS, Pandrala M, et al. Increased macrophage phagocytic activity with TLR9 agonist conjugation of an anti- Borrelia burgdorferi monoclonal antibody. Clinical Immunology [Internet]. 2023;246. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146222491&doi=10.1016%252fj.clim.2022.109180&partnerID=40&md5=d4dc99b82abb84d0b4111213e653f88a
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Muenkel M, Aparicio-Yuste R, Tal MC, Kraiczy P, Bastounis EE. Spatiotemporal characterization of endothelial cell motility and physical forces during exposure to Borrelia burgdorferi. STAR Protocols [Internet]. 2022;3(4). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85141486110&doi=10.1016%252fj.xpro.2022.101832&partnerID=40&md5=67a437442dbe5fef4baf6c1dea5ba696
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Ram-Mohan N, Rogers AJ, Blish CA, Nadeau KC, Zudock EJ, Kim D, et al. Using a 29-mRNA Host Response Classifier to Detect Bacterial Coinfections and Predict Outcomes in COVID-19 Patients Presenting to the Emergency Department. Microbiology Spectrum [Internet]. 2022;10(6). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85144637575&doi=10.1128%252fspectrum.02305-22&partnerID=40&md5=312348a3f98878d0852235bc99d3d6d9
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Yuste RA, Muenkel M, Axarlis K, Gómez Benito MJ, Reuss A, Blacker G, et al. Borrelia burgdorferi modulates the physical forces and immunity signaling in endothelial cells. iScience [Internet]. 2022;25(8). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85135954786&doi=10.1016%252fj.isci.2022.104793&partnerID=40&md5=04c24377d440950f057c3da88a4e2c54
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Sheikh-Mohamed S, Sanders EC, Gommerman JL, Tal MC. Guardians of the oral and nasopharyngeal galaxy: IgA and protection against SARS-CoV-2 infection*. Immunological Reviews [Internet]. 2022;309(1):75–85. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85133654921&doi=10.1111%252fimr.13118&partnerID=40&md5=a461e72b9e45e3e518160e2140a46ab0
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Sheikh-Mohamed S, Isho B, Chao GYC, Zuo M, Cohen C, Lustig Y, et al. Systemic and mucosal IgA responses are variably induced in response to SARS-CoV-2 mRNA vaccination and are associated with protection against subsequent infection. Mucosal Immunology [Internet]. 2022;15(5):799–808. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128807195&doi=10.1038%252fs41385-022-00511-0&partnerID=40&md5=d8ec5596f17f50f5103a219576d642b0
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Yiu YY, Hansen PS, Bear L, Dulgeroff T, Blacker G, Myers L, et al. CD47 Blockade Leads to Chemokine-Dependent Monocyte Infiltration and Loss of B Cells from the Splenic Marginal Zone. Journal of Immunology [Internet]. 2022;208(6):1371–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85126072813&doi=10.4049%252fjimmunol.2100352&partnerID=40&md5=671de2a0a5cefe3f3f35b524c65d526f
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Ram-Mohan N, Kim D, Zudock EJ, Hashemi MM, Tjandra KC, Rogers AJ, et al. SARS-CoV-2 RNAemia Predicts Clinical Deterioration and Extrapulmonary Complications from COVID-19. Clinical Infectious Diseases [Internet]. 2022;74(2):218–26. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85106527103&doi=10.1093%252fcid%252fciab394&partnerID=40&md5=a1ee80164a734c73932cceca8c53b68f
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Upton R, Banuelos A, Feng D, Biswas T, Kao K, McKenna K, et al. Combining CD47 blockade with trastuzumab eliminates HER2-positive breast cancer cells and overcomes trastuzumab tolerance. Proceedings of the National Academy of Sciences of the United States of America [Internet]. 2021;118(29). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85110542315&doi=10.1073%252fpnas.2026849118&partnerID=40&md5=5e969e0ef56bf5290e7a9f40c0f21da4
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Dulgeroff LBT, Oakley MS, Tal MC, Yiu YY, He JQ, Shoham M, et al. CD47 blockade reduces the pathologic features of experimental cerebral malaria and promotes survival of hosts with Plasmodium infection. Proceedings of the National Academy of Sciences of the United States of America [Internet]. 2021;118(11). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85102354152&doi=10.1073%252fpnas.1907653118&partnerID=40&md5=95f10c8360ba4ddf687fcff6d9ed527f
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Tal MC, Dulgeroff LBT, Myers L, Cham LB, Mayer-Barber KD, Bohrer AC, et al. Upregulation of CD47 is a host checkpoint response to pathogen recognition. mBio [Internet]. 2020;11(3):1–15. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85086858066&doi=10.1128%252fmBio.01293-20&partnerID=40&md5=fc483aa40c79d39aee8c72ae85feeabf
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Cham LB, Torrez Dulgeroff LB, Tal MC, Adomati T, Li F, Bhat H, et al. Immunotherapeutic Blockade of CD47 Inhibitory Signaling Enhances Innate and Adaptive Immune Responses to Viral Infection. Cell Reports [Internet]. 2020;31(2). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85083004040&doi=10.1016%252fj.celrep.2020.03.058&partnerID=40&md5=ff54b5d4f7a72a2fd5be3731c66f34c9
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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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Cohen A, Troib S, Dotan S, Najmuldeen H, Yesilkaya H, Kushnir T, et al. Streptococcus pneumoniae Cell Wall-Localized Trigger Factor Elicits a Protective Immune Response and Contributes to Bacterial Adhesion to the Host. Scientific Reports [Internet]. 2019;9(1). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85062837371&doi=10.1038%252fs41598-019-40779-0&partnerID=40&md5=75d74b224e67f5971ff8b1ccb320051a
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Myers LM, Tal MC, Torrez Dulgeroff LB, Carmody AB, Messer RJ, Gulati G, et al. A functional subset of CD8 + T cells during chronic exhaustion is defined by SIRPα expression. Nature Communications [Internet]. 2019;10(1). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85061613835&doi=10.1038%252fs41467-019-08637-9&partnerID=40&md5=7c4743f3d4c7477f62aa5833fb1f0d1f
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Morozov GI, Porat N, Kushnir T, Najmuldeen H, Adawi A, Chalifa-Caspi V, et al. Flavin Reductase Contributes to Pneumococcal Virulence by Protecting from Oxidative Stress and Mediating Adhesion and Elicits Protection Against Pneumococcal Challenge. Scientific Reports [Internet]. 2018;8(1). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040458386&doi=10.1038%252fs41598-017-18645-8&partnerID=40&md5=7583602131fbaa2a9ed49169136d95cd
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Goldman SE, Dotan S, Talias A, Lilo A, Azriel S, Malka I, et al. Streptococcus pneumoniae fructose-1,6-bisphosphate aldolase, a protein vaccine candidate, elicits Th1/Th2/Th17-type cytokine responses in mice. International Journal of Molecular Medicine [Internet]. 2016;37(4):1127–38. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960532269&doi=10.3892%252fijmm.2016.2512&partnerID=40&md5=c3c54e7ee74188b0208c7454a8e611e5
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Nebenzahl YM, Blau K, Kushnir T, Shagan M, Portnoi M, Cohen A, et al. Streptococcus pneumoniae cell-wall-localized phosphoenolpyruvate protein phosphotransferase can function as an adhesin: Identification of its host target molecules and evaluation of its potential as a vaccine. PLoS ONE [Internet]. 2016;11(3). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962144484&doi=10.1371%252fjournal.pone.0150320&partnerID=40&md5=abdb47c76a603f379cf1ea330048cc2c
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Ziv NY, Tal M, Shavit Y. The transition from naïve to primed nociceptive state: A novel wind-up protocol in mice. Experimental Neurology [Internet]. 2016;275:133–42. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84946882272&doi=10.1016%252fj.expneurol.2015.09.020&partnerID=40&md5=37fa6d62f11079fa51ee7cd30bcd49d9
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Devor M, Tal M. Nerve resection for the treatment of chronic neuropathic pain. Pain [Internet]. 2014;155(6):1053–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84899940947&doi=10.1016%252fj.pain.2014.02.015&partnerID=40&md5=24443a1a94d91dae557aa73d6f008724
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Nitzan-Luques A, Minert A, Devor M, Tal M. Dynamic genotype-selective “phenotypic switching” of CGRP expression contributes to differential neuropathic pain phenotype. Experimental Neurology [Internet]. 2013;250:194–204. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84886064678&doi=10.1016%252fj.expneurol.2013.09.011&partnerID=40&md5=50f03ef03e297e1e59a96a6a3d971c7a
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Muchnik L, Adawi A, Ohayon A, Dotan S, Malka I, Azriel S, et al. NADH Oxidase Functions as an Adhesin in Streptococcus pneumoniae and Elicits a Protective Immune Response in Mice. PLoS ONE [Internet]. 2013;8(4). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84875984604&doi=10.1371%252fjournal.pone.0061128&partnerID=40&md5=43e9c6d613959a9627f95d7c2295b2f4
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Ringkamp M, Tal M, Hartke TV, Wooten M, McKelvy A, Turnquist BP, et al. Local loperamide injection reduces mechanosensitivity of rat cutaneous, nociceptive C-fibers. PLoS ONE [Internet]. 2012;7(7). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84864442234&doi=10.1371%252fjournal.pone.0042105&partnerID=40&md5=fdcfa4cf89aa79b9831d937a42ed0145
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Nitzan-Luques A, Devor M, Tal M. Genotype-selective phenotypic switch in primary afferent neurons contributes to neuropathic pain. Pain [Internet]. 2011;152(10):2413–26. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-80053212575&doi=10.1016%252fj.pain.2011.07.012&partnerID=40&md5=439053a4250ba6a5599f91113c304641
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Gabay E, Wolf G, Shavit Y, Yirmiya R, Tal M. Chronic blockade of interleukin-1 (IL-1) prevents and attenuates neuropathic pain behavior and spontaneous ectopic neuronal activity following nerve injury. European Journal of Pain [Internet]. 2011;15(3):242–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-79952447647&doi=10.1016%252fj.ejpain.2010.07.012&partnerID=40&md5=2c6863bba9c5619328bae702eb9f815b
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Nissenbaum J, Devor M, Seltzer Z, Gebauer M, Michaelis M, Tal M, et al. Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2. Genome Research [Internet]. 2010;20(9):1180–90. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-77956272138&doi=10.1101%252fgr.104976.110&partnerID=40&md5=a8f6f12f2cd8da8c134e0e79101c67b6
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Eliav E, Benoliel R, Herzberg U, Kalladka M, Tal M. The role of IL-6 and IL-1β in painful perineural inflammatory neuritis. Brain, Behavior, and Immunity [Internet]. 2009;23(4):474–84. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-63549116683&doi=10.1016%252fj.bbi.2009.01.012&partnerID=40&md5=3fff695baa72862f957616408d72ac73
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Devor M, Tal M. What causes low back pain? Pain [Internet]. 2009;142(1–2):11–2. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-60249097122&doi=10.1016%252fj.pain.2009.01.002&partnerID=40&md5=d1b6e75fbb4a2a33c91fccd54f32b000
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Kaufmann D, Yagen B, Minert A, Tal M, Devor M, Bialer M. Evaluation of the enantioselective antiallodynic and pharmacokinetic profile of propylisopropylacetamide, a chiral isomer of valproic acid amide. Neuropharmacology [Internet]. 2008;54(4):699–707. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-39049159090&doi=10.1016%252fj.neuropharm.2007.11.020&partnerID=40&md5=6fc67121b39df6d08ca376cb495c11f6
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Kleibeuker W, Gabay E, Kavelaars A, Zijlstra J, Wolf G, Ziv N, et al. IL-1β signaling is required for mechanical allodynia induced by nerve injury and for the ensuing reduction in spinal cord neuronal GRK2. Brain, Behavior, and Immunity [Internet]. 2008;22(2):200–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-37349018685&doi=10.1016%252fj.bbi.2007.07.009&partnerID=40&md5=87ba5418e78c5680d2f42c7f901dd3c9
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Tal M, Devor M. Anatomy and neurophysiology of orofacial pain [Internet]. Orofacial Pain and Headache. 2008. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-60149110257&doi=10.1016%252fB978-0-7234-3412-2.10002-1&partnerID=40&md5=41867acf41bc26c491bf9f9cd5010730
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Sharav Y, Tal M. Response to Editorial on Sharav and Tal (2006). Pain [Internet]. 2007;127(1–2):195. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33845650917&doi=10.1016%252fj.pain.2006.07.018&partnerID=40&md5=63e94551c21dd1771d6535697987e4fb
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Benoliel R, Tal M, Eliav E. Effects of Topiramate on the Chronic Constriction Injury Model in the Rat. Journal of Pain [Internet]. 2006;7(12):878–83. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33845197528&doi=10.1016%252fj.jpain.2006.04.008&partnerID=40&md5=4009f6b24dea54d2fb5ffa432f662c7f
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Sharav Y, Tal M. Focused hypnotic analgesia: Local and remote effects. Pain [Internet]. 2006;124(3):280–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33748703835&doi=10.1016%252fj.pain.2006.04.016&partnerID=40&md5=1017c62d49474397e485b4430e136f4e
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Wolf G, Gabay E, Tal M, Yirmiya R, Shavit Y. Genetic impairment of interleukin-1 signaling attenuates neuropathic pain, autotomy, and spontaneous ectopic neuronal activity, following nerve injury in mice. Pain [Internet]. 2006;120(3):315–24. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-31644436766&doi=10.1016%252fj.pain.2005.11.011&partnerID=40&md5=e10665348bf88da5130b3a57d20f98df
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Tal M, Sharav Y. Jaw clenching modulates sensory perception in high- but not in low-hypnotizable subjects. Journal of Orofacial Pain [Internet]. 2005;19(1):76–81. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-13544260666&partnerID=40&md5=13384033a44d712f86c88462ef388247
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Eliav E, Tal M, Benoliel R. Experimental malignancy in the rat induces early hypersensitivity indicative of neuritis. Pain [Internet]. 2004;110(3):727–37. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-3843097470&doi=10.1016%252fj.pain.2004.05.013&partnerID=40&md5=f81ad6bbb8413f836c65d90a0b0af3d3
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Gabay E, Tal M. Pain behavior and nerve electrophysiology in the CCI model of neuropathic pain. Pain [Internet]. 2004;110(1–2):354–60. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-3242668887&doi=10.1016%252fj.pain.2004.04.021&partnerID=40&md5=9d60a1a62958d78be97e42419403740f
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Cherkas PS, Huang TY, Pannicke T, Tal M, Reichenbach A, Hanani M. The effects of axotomy on neurons and satellite glial cells in mouse trigeminal ganglion. Pain [Internet]. 2004;110(1–2):290–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-3242660930&doi=10.1016%252fj.pain.2004.04.007&partnerID=40&md5=6492ff340c780307447f346c4b4e1e2c
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Sharav Y, Tal M. Focused analgesia and generalized relaxation produce differential hypnotic analgesia in response to ascending stimulus intensity. International Journal of Psychophysiology [Internet]. 2004;52(2):187–96. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-1642503863&doi=10.1016%252fj.ijpsycho.2003.10.001&partnerID=40&md5=152cf73fd3fdcdf57b918082fd1bdf7b
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Weick M, Cherkas PS, Härtig W, Pannicke T, Uckermann O, Bringmann A, et al. P2 receptors in satellite glial cells in trigeminal ganglia of mice. Neuroscience [Internet]. 2003;120(4):969–77. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0043135215&doi=10.1016%2fS0306-4522%2803%2900388-9&partnerID=40&md5=f06441c5d297f146c5f54b3f9657fb1d
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Benoliel R, Sharav Y, Tal M, Eliav E. Management of chronic orofacial pain: today and tomorrow. Compendium of continuing education in dentistry (Jamesburg, NJ : 1995) [Internet]. 2003;24(12):909–20, 922–4, 926-928 passim; quiz 932. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-1342263841&partnerID=40&md5=784a77ad15d31393cf66e7662eae367d
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Zubare-Samuelov M, Peri I, Tal M, Tarshish M, Spielman AI, Naim M. Some sweet and bitter tastants stimulate inhibitory pathway of adenylyl cyclase via melatonin and α2-adrenergic receptors in Xenopus laevis melanophores. American Journal of Physiology - Cell Physiology [Internet]. 2003;285(5 54-5):C1255–62. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0142116212&doi=10.1152%252fajpcell.00149.2003&partnerID=40&md5=d90038bccf60c99ebfbce8b0b21a7b76
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Eliav E, Teich S, Nitzan D, El Raziq DA, Nahlieli O, Tal M, et al. Facial arthralgia and myalgia: Can they be differentiated by trigeminal sensory assessment? Pain [Internet]. 2003;104(3):481–90. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0141990651&doi=10.1016%2fS0304-3959%2803%2900077-0&partnerID=40&md5=4443790158daa86411147abf8a2581eb
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Guo W, Zou S, Tal M, Ren K. Activation of spinal kainate receptors after inflammation: Behavioral hyperalgesia and subunit gene expression. European Journal of Pharmacology [Internet]. 2002;452(3):309–18. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037064249&doi=10.1016%2fS0014-2999%2802%2902333-6&partnerID=40&md5=6c83ff29b65dca8f11034f93fb572d25
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Benoliel R, Wilensky A, Tal M, Eliav E. Application of a pro-inflammatory agent to the orbital portion of the rat infraorbital nerve induces changes indicative of ongoing trigeminal pain. Pain [Internet]. 2002;99(3):567–78. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036804983&doi=10.1016%2fS0304-3959%2802%2900272-5&partnerID=40&md5=5d9ebe384faf65b54637b3ee294eff90
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Guo W, Zou S, Guan Y, Ikeda T, Tal M, Dubner R, et al. Tyrosine phosphorylation of the NR2B subunit of the NMDA receptor in the spinal cord during the development and maintenance of inflammatory hyperalgesia. Journal of Neuroscience [Internet]. 2002;22(14):6208–17. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037101627&doi=10.1523%252fjneurosci.22-14-06208.2002&partnerID=40&md5=6d8520902fb5721b8fe62a4c26512876
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Benoliel R, Eliav E, Tal M. Strain-dependent modification of neuropathic pain behaviour in the rat hindpaw by a priming painful trigeminal nerve injury. Pain [Internet]. 2002;97(3):203–12. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036284271&doi=10.1016%2fS0304-3959%2801%2900428-6&partnerID=40&md5=de9e8e0dab2f62cae781633eb4d313af
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Eliav E, Benoliel R, Tal M. Inflammation with no axonal damage of the rat saphenous nerve trunk induces ectopic discharge and mechanosensitivity in myelinated axons. Neuroscience Letters [Internet]. 2001;311(1):49–52. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035929485&doi=10.1016%2fS0304-3940%2801%2902143-7&partnerID=40&md5=95d2e880502a814ab29323be4e6c2f13
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Benoliel R, Eliav E, Tal M. No sympathetic nerve sprouting in rat trigeminal ganglion following painful and non-painful infraorbital nerve neuropathy. Neuroscience Letters [Internet]. 2001;297(3):151–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035910627&doi=10.1016%2fS0304-3940%2800%2901681-5&partnerID=40&md5=342c0c4aa7a806c98aa2862dd1983d7c
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Levy D, Tal M, Höke A, Zochodne DW. Transient action of the endothelial constitutive nitric oxide synthase (ecNOS) mediates the development of thermal hypersensitivity following peripheral nerve injury. European Journal of Neuroscience [Internet]. 2000;12(7):2323–32. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033931905&doi=10.1046%252fj.1460-9568.2000.00129.x&partnerID=40&md5=38bffc7836aaa8424ce6ebc5e8b5f3fe
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Tal M, Wall PD, Devor M. Myelinated afferent fiber types that become spontaneously active and mechanosensitive following nerve transection in the rat. Brain Research [Internet]. 1999;824(2):218–23. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033541510&doi=10.1016%2fS0006-8993%2899%2901190-7&partnerID=40&md5=ba89b1048f329dc3a00fdf16afedf1f1
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Yagil G, Shimron F, Tal M. DNA unwinding in the CYC1 and DED1 yeast promoters. Gene [Internet]. 1998;225(1–2):153–62. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032576530&doi=10.1016%2fS0378-1119%2898%2900525-3&partnerID=40&md5=69e6dbd664ee48a586fc1014a1a84a46
56.
Naim M, Striem BJ, Tal M. Cellular Signal Transduction of Sweetener-Induced Taste. Advances in Food and Nutrition Research [Internet]. 1998;42(C):211–43. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0031628467&doi=10.1016%2fS1043-4526%2808%2960096-0&partnerID=40&md5=c161b71b71e65016e8747ee301fff61e
57.
Tal M, Liberman R. Local injection of nerve growth factor (NGF) triggers degranulation of mast cells in rat paw. Neuroscience Letters [Internet]. 1997;221(2–3):129–32. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0343052745&doi=10.1016%2fS0304-3940%2896%2913318-8&partnerID=40&md5=4c1cfc42a4200ff1de7c6596d3bf8c4b
58.
Tal M, Eliav E. Abnormal discharge originates at the site of nerve injury in experimental constriction neuropathy (CCI) in the rat. Pain [Internet]. 1996;64(3):511–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029893712&doi=10.1016%2f0304-3959%2895%2900175-1&partnerID=40&md5=a2beffdbb9412990a570c35589435ff7
59.
Tal M. A novel antioxidant alleviates heat hyperalgesia in rats with an experimental painful peripheral neuropathy. NeuroReport [Internet]. 1996;7(8):1382–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029742740&doi=10.1097%252f00001756-199605310-00010&partnerID=40&md5=4a8156799b9bf92eb9c07665ccab1f51
60.
Ben-Aharon U, Gutman M, Shani E, Chatsubi I, Pfefferman R, Shiloh Y, et al. Amplification of protooncogenes and expression of the HER2/NEU oncogene in invasive breast cancer. Harefuah [Internet]. 1996;130(1):4–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029685325&partnerID=40&md5=999d0aa90709a53da4604f2492faff5e
61.
Guthmann MD, Tal M, Pecht I. A secretion inhibitory signal transduction molecule on mast cells is another C-type lectin. Proceedings of the National Academy of Sciences of the United States of America [Internet]. 1995;92(20):9397–401. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029026024&doi=10.1073%252fpnas.92.20.9397&partnerID=40&md5=926ba032be95c704ac871cdc4db93c1b
62.
Guthmann MD, Tal M, Pecht I. A new member of the C-type lectin family is a modulator of the mast cell secretory response. International Archives of Allergy and Immunology [Internet]. 1995;107(1–3):82–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029059042&doi=10.1159%252f000236938&partnerID=40&md5=a7ddd7dde7bc51aa3c0f390ffed41811
63.
Tal M, Ammar DA, Karpuj M, Krizhanovsky V, Naim M, Thompson DA. A Novel Putative Neuropeptide Receptor Expressed in Neural Tissue, Including Sensory Epithelia. Biochemical and Biophysical Research Communications [Internet]. 1995;209(2):752–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028943373&doi=10.1006%252fbbrc.1995.1563&partnerID=40&md5=430a0342bc2a3bb2ab37934f1bf03737
64.
Sharav Y, Tal M. Hypnotic analgesia and reflex activity. Pain [Internet]. 1995;63(3):391. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028856683&doi=10.1016%2f0304-3959%2895%2900122-0&partnerID=40&md5=62ae6ae4ad6fc3b06ff951b071988f5f
65.
Tal M, Shimron F, Yagil G. Unwound regions in yeast centromere IV DNA. Journal of Molecular Biology [Internet]. 1994;243(2):179–89. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0027971482&doi=10.1006%252fjmbi.1994.1645&partnerID=40&md5=1cd55f6b594c6ec77925605896186a6b
66.
Tal M, Bennett GJ. Extra-territorial pain in rats with a peripheral mononeuropathy: mechano-hyperalgesia and mechano-allodynia in the territory of an uninjured nerve. Pain [Internet]. 1994;57(3):375–82. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028233550&doi=10.1016%2f0304-3959%2894%2990013-2&partnerID=40&md5=62d029e6b868ba9be2d31060d8c97757
67.
Efrat S, Tal M, Lodish HF. The pancreatic β-cell glucose sensor. Trends in Biochemical Sciences [Internet]. 1994;19(12):535–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028173313&doi=10.1016%2f0968-0004%2894%2990056-6&partnerID=40&md5=10ffad33f6a359caddfe15aae9442af0
68.
Tal M, Bennett GJ. Neuropathic pain sensations are differentially sensitive to dextrorphan. NeuroReport [Internet]. 1994;5(12):1438–40. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028064408&doi=10.1097%252f00001756-199407000-00008&partnerID=40&md5=619211b5feb229c31e82049daaa3db0e
69.
Rapaport D, Greenberg DS, Tal M, Yaffe D, Nudel U. Dp71, the nonmuscle product of the Duchenne muscular dystrophy gene is associated with the cell membrane. FEBS Letters [Internet]. 1993;328(1–2):197–202. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0027178851&doi=10.1016%2f0014-5793%2893%2980992-4&partnerID=40&md5=cac0df6a0a65edaec71366ee6ddbab6c
70.
Tal M, Bennett GJ. Dextrorphan relieves neuropathic heat-evoked hyperalgesia in the rat. Neuroscience Letters [Internet]. 1993;151(1):107–10. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0027210790&doi=10.1016%2f0304-3940%2893%2990058-S&partnerID=40&md5=fd4697b231d4680b7d0dfae654e47ed8
71.
Lev-Tov A, Tal M, Lavy R. Diverse firing properties of single motor units in the inner and outer portions of the guinea pig anterior digastric muscle. Archives of Oral Biology [Internet]. 1993;38(2):169–78. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0027550666&doi=10.1016%2f0003-9969%2893%2990203-X&partnerID=40&md5=ad931eda5a69a275f75e34c64af07f7f
72.
Efrat S, Leiser M, Surana M, Tal M, Fusco-Demane D, Fleischer N. Murine insulinoma cell line with normal glucose-regulated insulin secretion. Diabetes [Internet]. 1993;42(6):901–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0027233478&doi=10.2337%252fdiab.42.6.901&partnerID=40&md5=107620d850990c579309be66b51fe78a
73.
Tal M, Wu YJ, Leiser M, Surana M, Lodish H, Fleischer N, et al. [Val12]HRAS downregulates GLUT2 in β cells of transgenic mice without affecting glucose homeostasis. Proceedings of the National Academy of Sciences of the United States of America [Internet]. 1992;89(13):5744–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026611169&doi=10.1073%252fpnas.89.13.5744&partnerID=40&md5=1fcd9899bcdc34d0364f43b7137e06d6
74.
Tal M, Devor M. Ectopic discharge in injured nerves: comparison of trigeminal and somatic afferent. Brain Research [Internet]. 1992;579(1):148–51. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026562103&doi=10.1016%2f0006-8993%2892%2990753-V&partnerID=40&md5=fa2d388005eecf38a9ea3af56bd83ea1
75.
Tal M, Liang Y, Najafi H, Lodish HF, Matschinsky FM. Expression and function of GLUT-1 and GLUT-2 glucose transporter isoforms in cells of cultured rat pancreatic islets. Journal of Biological Chemistry [Internet]. 1992;267(24):17241–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026788504&partnerID=40&md5=0fe6795f3d9dbc565d47f8bd0ab3413c
76.
Liang Y, Najafi H, Smith RM, Zimmerman EC, Magnuson MA, Tal M, et al. Concordant glucose induction of glucokinase, glucose usage, and glucose-stimulated insulin release in pancreatic islets maintained in organ culture. Diabetes [Internet]. 1992;41(7):792–806. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026625602&doi=10.2337%252fdiab.41.7.792&partnerID=40&md5=648ce390fea664f2de1e8e268a8d6119
77.
Tal M, Thorens B, Surana M, Fleischer N, Lodish HF, Hanahan D, et al. Glucose transporter isotypes switch in T-antigen-transformed pancreatic β cells growing in culture and in mice. Molecular and Cellular Biology [Internet]. 1992;12(1):422–32. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026569910&doi=10.1128%252fmcb.12.1.422&partnerID=40&md5=4525041081d813b1f39bf2e72423e898
78.
Tal M, Kahn BB, Lodish HF. Expression of the low Km GLUT-1 glucose transporter is turned on in perivenous hepatocytes of insulin-deficient diabetic rats. Endocrinology [Internet]. 1991;129(4):1933–41. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85003186469&doi=10.1210%252fendo-129-4-1933&partnerID=40&md5=d77ec82b0de4b4263ee357b72307e81c
79.
YAFFE A, TAL M, EHRLICH J. Effect of occlusal bite‐raising splint on electromyogram, motor unit histochemistry and myoneuronal dimensions in rats. Journal of Oral Rehabilitation [Internet]. 1991;18(4):343–51. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026199555&doi=10.1111%252fj.1365-2842.1991.tb00066.x&partnerID=40&md5=416b124c7455abe3db1319de1727bab5
80.
Tal M, Kahn BB, Lodish HF. Expression of the low KmGLUT-1 glucose transporter is turned on in perivenous hepatocytes of insulin-deficient diabetic rats. Endocrinology [Internet]. 1991;129(4):193–1941. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025925275&doi=10.1210%252fendo-129-4-1933&partnerID=40&md5=a13ade8c9b1aa9a1c1c5ba137c24304e
81.
Tal M, Schneider DL, Thorens B, Lodish HF. Restricted expression of the erythroid/brain glucose transporter isoform to perivenous hepatocytes in rats: Modulation by glucose. Journal of Clinical Investigation [Internet]. 1990;86(3):986–92. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025027463&doi=10.1172%252fJCI114801&partnerID=40&md5=3e2aee1d1b25a28f46d00d21104b8e9f
82.
Tal M, Sharav Y. Masseter inhibitory periods and sensations upon electrical tooth-pulp stimulation in children and adults. Brain Research [Internet]. 1989;497(1):138–41. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024455867&doi=10.1016%2f0006-8993%2889%2990979-7&partnerID=40&md5=019a7ce1ce0618d2e508dbfa8cfecddd
83.
Sharav Y, Tal M. Masseter inhibitory periods and sensations evoked by electrical tooth-pulp stimulation in subjects under hypnotic anesthesia. Brain Research [Internet]. 1989;479(2):247–54. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024597403&doi=10.1016%2f0006-8993%2889%2991625-9&partnerID=40&md5=17ad345fca733975f7cf5c08c2a3a4c2
84.
Seltzer Z, Tal M, Sharav Y. Autotomy behavior in rats following peripheral deafferentation is suppressed by daily injections of amitriptyline, diazepam and saline. Pain [Internet]. 1989;37(2):245–50. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024333520&doi=10.1016%2f0304-3959%2889%2990136-X&partnerID=40&md5=aad822c1c1eced137c2e2e1d457e2ffc
85.
Tal M, Josefberg Z, Wetzler M, Deutch A, Gutman M, Assaf D, et al. Sporadic Amplification of the HER2/neu Protooncogene in Adenocarcinomas of Various Tissues. Cancer Research [Internet]. 1988;48(6):1517–20. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023906224&partnerID=40&md5=97cdb26659c47310b81721f7c2c12968
86.
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
87.
Tal M. Neural basis for initiation of rhythmic digastric activity upon midbrain stimulation in the guinea pig. Brain Research [Internet]. 1987;411(1):58–64. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023187164&doi=10.1016%2f0006-8993%2887%2990680-9&partnerID=40&md5=e5e1cb5d349296dc08635e6856387365
88.
Tal M, King CR, Kraus MH, Ullrich A, Schlessinger J, Givol D. Human HER2 (neu) promoter: evidence for multiple mechanisms for transcriptional initiation. Molecular and cellular biology [Internet]. 1987;7(7):2597–601. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023371106&doi=10.1128%252fMCB.7.7.2597&partnerID=40&md5=44ed911f4075027282412007777ab547
89.
Lev-Tov A, Tal M. The organization and activity patterns of the anterior and posterior heads of the guinea pig digastric muscle. Journal of Neurophysiology [Internet]. 1987;58(3):496–509. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023241941&doi=10.1152%252fjn.1987.58.3.496&partnerID=40&md5=5b6a635517871d1143d18d67b1ec20e7
90.
Chandler SH, Tal M. Brain-stem perturbations during cortically evoked rhythmical jaw movements: Effects of activation of brain-stem loci on jaw muscle cycle characteristics. Journal of Neuroscience [Internet]. 1987;7(2):463–72. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023119037&doi=10.1523%252fjneurosci.07-02-00463.1987&partnerID=40&md5=c23963ec1c9659b7a334a052eb961bcc
91.
Chandler SH, Tal M. The effects of brain stem transections on the neuronal networks responsible for rhythmical jaw muscle activity in the guinea pig. Journal of Neuroscience [Internet]. 1986;6(6):1831–42. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0022545854&doi=10.1523%252fjneurosci.06-06-01831.1986&partnerID=40&md5=49b6eca844c431365e991118ea2e97c6
92.
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
93.
Tal M, Sharav Y. Development of sensory and reflex responses to tooth-pulp stimulation in children. Archives of Oral Biology [Internet]. 1985;30(6):467–70. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021782378&doi=10.1016%2f0003-9969%2885%2990091-3&partnerID=40&md5=88485445ac45a344233ad7a65b8c192f
94.
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
95.
Tal M. The threshold for eliciting the jaw opening reflex in rats is not increased by neonatal capsaicin. Behavioural Brain Research [Internet]. 1984;13(2):197–200. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021205836&doi=10.1016%2f0166-4328%2884%2990150-5&partnerID=40&md5=ee1daa41c85d04d77cf6aeca5648b65c
96.
RAJSTEIN J, TAL M. The effect of ultrasonic scaling on the surface of Class V amalgam restorations—a scanning electron microscopy study. Journal of Oral Rehabilitation [Internet]. 1984;11(3):299–305. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021174775&doi=10.1111%252fj.1365-2842.1984.tb00580.x&partnerID=40&md5=2bce37d3a5fcfe4a755bce2f34fedb82
97.
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
98.
Goldberg LJ, Chandler SH, Tal M. Relationship between jaw movements and trigeminal motoneuron membrane-potential fluctuations during cortically induced rhythmical jaw movements in the guinea pig. Journal of Neurophysiology [Internet]. 1982;48(1):110–25. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020319368&doi=10.1152%252fjn.1982.48.1.110&partnerID=40&md5=5f12ac8c567eb16d6228b796c2c670f5
99.
Tal M. The effect of a long-acting local anaesthetic agent (Marcaine®) on the masticatory muscle in rats. International Journal of Oral Surgery [Internet]. 1982;11(2):101–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019994885&doi=10.1016%2fS0300-9785%2882%2980017-3&partnerID=40&md5=3493a57927555798ae5388bf65e692dd
100.
Tal M, Sharav Y, Devor M. Modulation of the jaw-opening reflex by peripheral electrical stimulation. Experimental Neurology [Internet]. 1981;74(3):907–19. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019787085&doi=10.1016%2f0014-4886%2881%2990262-4&partnerID=40&md5=695c08707faba42df4907d06ed46b6c6
101.
Tal M, Goldberg LJ. Masticatory muscle activity during rhythmic jaw movements in the anaesthetized guinea-pig. Archives of Oral Biology [Internet]. 1981;26(10):803–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019786954&doi=10.1016%2f0003-9969%2881%2990176-X&partnerID=40&md5=37bede686f0c0dcc1ad43b1833cfeb8c
102.
Laufer B, Mayer I, Gedalia I, Deutsch D, Kaufman HW, Tal M. Fluoride-uptake and fluoride-residual of fluoride-treated human root dentine in vitro determined by chemical, scanning electron microscopy and X-ray diffraction analyses. Archives of Oral Biology [Internet]. 1981;26(3):159–63. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019458757&doi=10.1016%2f0003-9969%2881%2990125-4&partnerID=40&md5=067b7b7eee0d899ea0d7a8f948348492
103.
Tal M. Representation of some masticatory muscles in the trigeminal motor nucleus of the guinea pig: Horseradish peroxidase study. Experimental Neurology [Internet]. 1980;70(3):726–30. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019212353&doi=10.1016%2f0014-4886%2880%2990200-9&partnerID=40&md5=6422e377f6029ad878a447e31ed90ea4
104.
RAJSTEIN J, TAL M. A study of the contour and external surface of Class V composite resin fillings. Journal of Oral Rehabilitation [Internet]. 1979;6(1):21–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018348681&doi=10.1111%252fj.1365-2842.1979.tb00400.x&partnerID=40&md5=9981d46041bc724239b8fd7c57e976cd
105.
TAL M, KAUFMAN AY, BUCHNER A. Bone necrosis and dentine resorption caused by Toxavit: a case report. International Endodontic Journal [Internet]. 1978;11(2):77–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84987317285&doi=10.1111%252fj.1365-2591.1978.tb00665.x&partnerID=40&md5=2129b63f330f33be0cd20629a70e898b
106.
Goldberg LJ, Tal M. Intracellular recording in trigeminal motoneurons of the anesthetized guinea pig during rhythmic jaw movements. Experimental Neurology [Internet]. 1978;58(1):102–10. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017913239&doi=10.1016%2f0014-4886%2878%2990125-5&partnerID=40&md5=c127e78e4543cb22c607b3a4b8dd2596
107.
Kaufman AY, Binderman I, Tal M, Gedalia I, Peretz G. New chemotherapeutic agent for root canal treatment. A preliminary electron microscopic study on an in vivo and in vitro endodontically treated tooth. Oral Surgery, Oral Medicine, Oral Pathology [Internet]. 1978;46(2):283–95. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017897663&doi=10.1016%2f0030-4220%2878%2990204-9&partnerID=40&md5=085993d0f5a3669432d05e882c60ed67
108.
Kaufman AY, Tal M, Binderman I. Internal root resorption: Report of case with scanning electron microscopic study. Journal of Endodontics [Internet]. 1977;3(6):236–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017497110&doi=10.1016%2fS0099-2399%2877%2980138-6&partnerID=40&md5=f9fc5804545e8d86bddf647054a6364c
109.
Tal M, Oron M, Gedalia I, Ehrlich J. X-ray diffraction and scanning electron microscope investigations of fluoride-treated dentine in man. Archives of Oral Biology [Internet]. 1976;21(5):285–90. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017099224&doi=10.1016%2f0003-9969%2876%2990050-9&partnerID=40&md5=dea206710a519e40c40d6f28d8dcfea3
110.
Ehrlich J, Hochman N, Gedalia I, Tal M. Residual Fluoride Concentrations and Scanning Electron Microscopic Examination of Root Surfaces of Human Teeth After Topical Application of Fluoride In Vivo. Journal of Dental Research [Internet]. 1975;54(4):897–900. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0016591343&doi=10.1177%252f00220345750540043101&partnerID=40&md5=2e9e368db0b1b39f63d65f2ade0c03eb