School of Pharmacy : Lazarovici Philip

1.

Klazas M, Naamneh MS, Zheng W, Lazarovici P. Gabapentin Increases Intra-Epidermal and Peptidergic Nerve Fibers Density and Alleviates Allodynia and Thermal Hyperalgesia in a Mouse Model of Acute Taxol-Induced Peripheral Neuropathy. Biomedicines [Internet]. 2022;10(12). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85144676064&doi=10.3390%252fbiomedicines10123190&partnerID=40&md5=5d692f1b7c9f4d399a41c76386b952db

2.

Jiang Y, Rubin L, Zhou Z, Zhang H, Su Q, Hou ST, et al. Pharmacological therapies and drug development targeting SARS-CoV-2 infection. Cytokine and Growth Factor Reviews [Internet]. 2022;68:13–24. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85140727841&doi=10.1016%252fj.cytogfr.2022.10.003&partnerID=40&md5=ec1e87d9bceb0ebba6ce02735840d9f5

3.

Naamneh MS, Lazarovici P, Katzhendler J. Ring-Opening Polymerization (ROP) of Phenylalanine Derived O-Carboxyanhydride (OCA) Using Different Mono- and Bimolecular Conjugated Catalysts and Amino or Alcohol Initiators. ACS Applied Polymer Materials [Internet]. 2022;4(10):7699–709. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85139362977&doi=10.1021%252facsapm.2c01256&partnerID=40&md5=bd652e362f456edd6e48960645aaec29

4.

Ge L, Liu S, Rubin L, Lazarovici P, Zheng W. Research Progress on Neuroprotection of Insulin-Like Growth Factor-1 towards Glutamate-Induced Neurotoxicity. Cells [Internet]. 2022;11(4). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124424026&doi=10.3390%252fcells11040666&partnerID=40&md5=1521fa07eafde61b8d83d3f20be97a82

5.

Li Q, Rubin L, Silva M, Li S, Yang C, Lazarovici P, et al. Current Progress on Neuroprotection Induced by Artemisia, Ginseng, Astragalus, and Ginkgo Traditional Chinese Medicines for the Therapy of Alzheimer’s Disease. Oxidative Medicine and Cellular Longevity [Internet]. 2022;2022. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85132920314&doi=10.1155%252f2022%252f3777021&partnerID=40&md5=56ff34cde71dc4d92c5b02315f78e52a

6.

Jiang Y, Rubin L, Peng T, Liu L, Xing X, Lazarovici P, et al. Cytokine storm in COVID-19: from viral infection to immune responses, diagnosis and therapy. International Journal of Biological Sciences [Internet]. 2022;18(2):459–72. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85123342163&doi=10.7150%252fijbs.59272&partnerID=40&md5=d03353d41c0e764cc9744feeb5931f75

7.

Gilon C, Klazas M, Lahiani A, Schumacher-Klinger A, Merzbach S, Naoum JN, et al. Synthesis and Pharmacological Characterization of Visabron, a Backbone Cyclic Peptide Dual Antagonist of α4β1 (VLA-4)/α9β1 Integrin for Therapy of Multiple Sclerosis. JACS Au [Internet]. 2021;1(12):2361–76. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85137361519&doi=10.1021%252fjacsau.1c00496&partnerID=40&md5=f7aff69de508db1d77f25c9984d87429

8.

Rubin L, Stabler CT, Schumacher-Klinger A, Marcinkiewicz C, Lelkes PI, Lazarovici P. Neurotrophic factors and their receptors in lung development and implications in lung diseases. Cytokine and Growth Factor Reviews [Internet]. 2021;59:84–94. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85100975327&doi=10.1016%252fj.cytogfr.2021.01.008&partnerID=40&md5=a4aaadf3626130bc67852744b6fff594

9.

Gilon C, Gitlin-Domagalska A, Lahiani A, Yehoshua-Alshanski S, Shumacher-Klinger A, Gilon D, et al. Novel humanin analogs confer neuroprotection and myoprotection to neuronal and myoblast cell cultures exposed to ischemia-like and doxorubicin-induced cell death insults. Peptides [Internet]. 2020;134. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090566097&doi=10.1016%252fj.peptides.2020.170399&partnerID=40&md5=eda8033762cdb1af0b96f4d664161db0

10.

Talhami A, Swed A, Hess S, Ovadia O, Greenberg S, Schumacher-Klinger A, et al. Cyclizing Painkillers: Development of Backbone-Cyclic TAPS Analogs. Frontiers in Chemistry [Internet]. 2020;8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85096668052&doi=10.3389%252ffchem.2020.532577&partnerID=40&md5=8a89663d707adc88a9f97f1be09f9796

11.

Fluksman A, Steinberg E, Orehov N, Shai E, Lahiani A, Katzhendler J, et al. Integrin α2β1-Targeted Self-Assembled Nanocarriers for Tumor Bioimaging. ACS Applied Bio Materials [Internet]. 2020;3(9):6059–70. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85093682481&doi=10.1021%252facsabm.0c00662&partnerID=40&md5=678a8fbd3c0e053d249f6e18320fbed0

12.

Yan F, Liao R, Silva M, Li S, Jiang Y, Peng T, et al. Pristimerin-induced uveal melanoma cell death via inhibiting PI3K/Akt/FoxO3a signalling pathway. Journal of Cellular and Molecular Medicine [Internet]. 2020;24(11):6208–19. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85084007566&doi=10.1111%252fjcmm.15249&partnerID=40&md5=c84d46b721b9665f0f5e2341b2e5b34f

13.

Jiang Y, Yan F, Feng Z, Lazarovici P, Zheng W. Signaling network of forkhead family of transcription factors (FOXO) in dietary restriction. Cells [Internet]. 2020;9(1). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128283830&doi=10.3390%252fcells9010100&partnerID=40&md5=85e86204532342f055f5bc4c0aa2b46b

14.

Yan F, Wang R, Li S, Zhao X, Jiang Y, Liu L, et al. Foxo3a suppresses neuropeptide w expression in neuronal cells and in rat hypothalamus and its implication in hypothalamic-pituitary-adrenal (HPA) axis. International Journal of Biological Sciences [Internet]. 2020;16(15):2775–87. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090593994&doi=10.7150%252fijbs.45619&partnerID=40&md5=c45c0e6bcb6f50ae73d62a37b38d2e11

15.

Lahiani A, Haham-Geula D, Lankri D, Cornell-Kennon S, Schaefer EM, Tsvelikhovsky D, et al. Neurotropic activity and safety of methylene-cycloalkylacetate (MCA) derivative 3-(3-allyl-2-methylenecyclohexyl) propanoic acid. ACS Chemical Neuroscience [Internet]. 2020;11(17):2577–89. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090252366&doi=10.1021%252facschemneuro.0c00255&partnerID=40&md5=b471d258a291652a121e9d14832646cd

16.

Lazarovici P. Snake- and spider-venom-derived toxins as lead compounds for drug development. Methods in Molecular Biology [Internet]. 2020;2068:3–26. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85072847595&doi=10.1007%252f978-1-4939-9845-6_1&partnerID=40&md5=8d92ec1dbaa121a602c10f2174811c1d

17.

Maatuf Y, Priel A, Lazarovici P. Measurements of cell death induced by snake and spider’s venoms and derived toxins. Methods in Molecular Biology [Internet]. 2020;2068:239–68. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85072847497&doi=10.1007%252f978-1-4939-9845-6_13&partnerID=40&md5=41a94874caf75bb9c0fe4744e901741a

18.

Lazarovici P, Marcinkiewicz C, Lelkes PI. Cell-based adhesion assays for isolation of snake venom’s integrin antagonists. Methods in Molecular Biology [Internet]. 2020;2068:205–23. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85072847378&doi=10.1007%252f978-1-4939-9845-6_11&partnerID=40&md5=bceb00bfd781db6f4dfbcf364d66bcc4

19.

Fang J, Zhao X, Li S, Xing X, Wang H, Lazarovici P, et al. Protective mechanism of artemisinin on rat bone marrow-derived mesenchymal stem cells against apoptosis induced by hydrogen peroxide via activation of c-Raf-Erk1/2-p90rsk-CREB pathway. Stem Cell Research and Therapy [Internet]. 2019;10(1). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85074155490&doi=10.1186%252fs13287-019-1419-2&partnerID=40&md5=891efef6b7d80b365151dc1af86c4602

20.

Lazarovici P, Marcinkiewicz C, Lelkes PI. From snake venom’s disintegrins and C-type lectins to anti-platelet drugs. Toxins [Internet]. 2019;11(5). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85067312566&doi=10.3390%252ftoxins11050303&partnerID=40&md5=86459a62842e8fb7763b8f5311cd92f4

21.

Shilo D, Cohen G, Blumenfeld A, Goren K, Hanhan S, Sharon S, et al. Tuftelin Is Required for NGF-Induced Differentiation of PC12 Cells. Journal of molecular neuroscience : MN [Internet]. 2019;68(1):135–43. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85064577349&doi=10.1007%252fs12031-019-01292-1&partnerID=40&md5=11e03ae9de4b03c4537ce722205d5ff9

22.

Li S, Zhao X, Lazarovici P, Zheng W. Artemether Activation of AMPK/GSK3 β (ser9)/Nrf2 Signaling Confers Neuroprotection towards β- Amyloid-Induced Neurotoxicity in 3xTg Alzheimer’s Mouse Model. Oxidative Medicine and Cellular Longevity [Internet]. 2019;2019. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85075996050&doi=10.1155%252f2019%252f1862437&partnerID=40&md5=c1b6d2b62ebeecf6f0b06d1b32ed15f3

23.

Peng T, Jiang Y, Farhan M, Lazarovici P, Chen L, Zheng W. Anti-inflammatory effects of traditional Chinese medicines on preclinical in vivo models of brain ischemia-reperfusion-injury: Prospects for neuroprotective drug discovery and therapy. Frontiers in Pharmacology [Internet]. 2019;10(MAR). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85066630497&doi=10.3389%252ffphar.2019.00204&partnerID=40&md5=8197d8454c1fb67cba75b3eff73c45fd

24.

Tiram G, Ferber S, Ofek P, Eldar-Boock A, Ben-Shushan D, Yeini E, et al. Reverting the molecular fingerprint of tumor dormancy as a therapeutic strategy for glioblastoma. FASEB Journal [Internet]. 2018;32(11):5835–50. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85055792111&doi=10.1096%252ffj.201701568R&partnerID=40&md5=0f587b27a8e53dd67ef899704cb03ca5

25.

Wang H, Xu J, Lazarovici P, Quirion R, Zheng W. cAMP Response Element-Binding Protein (CREB): A Possible Signaling Molecule Link in the Pathophysiology of Schizophrenia. Frontiers in Molecular Neuroscience [Internet]. 2018;11. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054866136&doi=10.3389%252ffnmol.2018.00255&partnerID=40&md5=467060996bd24b5f70c0fda01aed9d72

26.

Lankri D, Haham D, Lahiani A, Lazarovici P, Tsvelikhovsky D. Methylene-Cycloalkylacetate (MCA) Scaffold-Based Compounds as Novel Neurotropic Agents. ACS Chemical Neuroscience [Internet]. 2018;9(4):691–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045566570&doi=10.1021%252facschemneuro.7b00473&partnerID=40&md5=d4d4f8ee191b45bb29c3236bf3974e23

27.

Lahiani A, Brand-Yavin A, Yavin E, Lazarovici P. Neuroprotective effects of bioactive compounds and mapk pathway modulation in “ischemia”—stressed PC12 pheochromocytoma cells. Brain Sciences [Internet]. 2018;8(2). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042297646&doi=10.3390%252fbrainsci8020032&partnerID=40&md5=d4d9a2684d452191fab27181ce9376d0

28.

Gincberg G, Shohami E, Trembovler V, Alexandrovich AG, Lazarovici P, Elchalal U. Nerve growth factor plays a role in the neurotherapeutic effect of a CD45 + pan-hematopoietic subpopulation derived from human umbilical cord blood in a traumatic brain injury model. Cytotherapy [Internet]. 2018;20(2):245–61. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85038890770&doi=10.1016%252fj.jcyt.2017.11.008&partnerID=40&md5=8487686386e72fa0867be96b746f8187

29.

Gincberg G, Shohami E, Lazarovici P, Elchalal U. Human Umbilical Cord Blood CD45+ Pan-Hematopoietic Cells Induced a Neurotherapeutic Effect in Mice with Traumatic Brain Injury: Immunophenotyping, Comparison of Maternal and Neonatal Parameters, and Immunomodulation. Journal of Molecular Neuroscience [Internet]. 2018;64(2):185–99. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85038090921&doi=10.1007%252fs12031-017-1008-8&partnerID=40&md5=010d05de8b23e618a9a3668994e6e7dd

30.

Lazarovici P, Lahiani A, Gincberg G, Haham D, Fluksman A, Benny O, et al. Nerve growth factor-induced angiogenesis: 1. Endothelial cell tube formation assay. Methods in Molecular Biology [Internet]. 2018;1727:239–50. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85037689136&doi=10.1007%252f978-1-4939-7571-6_18&partnerID=40&md5=323c73a742e993bccfe786d649935a39

31.

Lazarovici P, Lahiani A, Gincberg G, Haham D, Marcinkiewicz C, Lelkes PI. Nerve growth factor-induced angiogenesis: 2. The quail chorioallantoic membrane assay. Methods in Molecular Biology [Internet]. 2018;1727:251–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85037680267&doi=10.1007%252f978-1-4939-7571-6_19&partnerID=40&md5=703c7490209d794b443ae45750d31d55

32.

Wang H, Xu J, Lazarovici P, Zheng W. Dysbindin-1 involvement in the etiology of schizophrenia. International Journal of Molecular Sciences [Internet]. 2017;18(10). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85030102154&doi=10.3390%252fijms18102044&partnerID=40&md5=4b2202034c8811e411e40f23fbdc1005

33.

Amsalem O, Nassar T, Benhamron S, Lazarovici P, Benita S, Yavin E. Solid nano-in-nanoparticles for potential delivery of siRNA. Journal of Controlled Release [Internet]. 2017;257:144–55. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85006940809&doi=10.1016%252fj.jconrel.2016.05.043&partnerID=40&md5=e61e6a7cc759ba481be1e67227c420d1

34.

Wang H, Farhan M, Xu J, Lazarovici P, Zheng W. The involvement of DARPP-32 in the pathophysiology of schizophrenia. Oncotarget [Internet]. 2017;8(32):53791–803. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85030117190&doi=10.18632%252foncotarget.17339&partnerID=40&md5=397bd8216cbaa48ddacf3dcd3c6a5341

35.

Lahiani A, Yavin E, Lazarovici P. The molecular basis of toxins’ interactions with intracellular signaling via discrete portals. Toxins [Internet]. 2017;9(3). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015789215&doi=10.3390%252ftoxins9030107&partnerID=40&md5=efb7f1c5bf3adcba8df6d5e9f2e70c3c

36.

Geron M, Kumar R, Matzner H, Lahiani A, Gincberg G, Cohen G, et al. Protein toxins of the Echis coloratus viper venom directly activate TRPV1. Biochimica et Biophysica Acta - General Subjects [Internet]. 2017;1861(3):615–23. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85008952006&doi=10.1016%252fj.bbagen.2017.01.004&partnerID=40&md5=f4bcb8574ec502a393b165365271188e

37.

Lahiani A, Hidmi A, Katzhendler J, Yavin E, Lazarovici P. Novel Synthetic PEGylated Conjugate of α-Lipoic Acid and Tempol Reduces Cell Death in a Neuronal PC12 Clonal Line Subjected to Ischemia. ACS Chemical Neuroscience [Internet]. 2016;7(10):1452–62. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84992221791&doi=10.1021%252facschemneuro.6b00211&partnerID=40&md5=3a40fa468ebc3c45dd214dd4b9a8a42a

38.

Zheng W, Chong CM, Wang H, Zhou X, Zhang L, Wang R, et al. Artemisinin conferred ERK mediated neuroprotection to PC12 cells and cortical neurons exposed to sodium nitroprusside-induced oxidative insult. Free Radical Biology and Medicine [Internet]. 2016;97:158–67. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84973883730&doi=10.1016%252fj.freeradbiomed.2016.05.023&partnerID=40&md5=17be8ceeec8fcd83884c93c993277b6c

39.

Stabler CT, Caires LC, Mondrinos MJ, Marcinkiewicz C, Lazarovici P, Wolfson MR, et al. Enhanced Re-Endothelialization of Decellularized Rat Lungs. Tissue Engineering - Part C: Methods [Internet]. 2016;22(5):439–50. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84969262224&doi=10.1089%252ften.tec.2016.0012&partnerID=40&md5=f158d891cc10b36a6e9f3e40a26f3699

40.

Stabler CT, Lecht S, Lazarovici P, Lelkes PI. Mesenchymal stem cells for therapeutic applications in pulmonary medicine. British Medical Bulletin [Internet]. 2015;115(1):45–56. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84941254661&doi=10.1093%252fbmb%252fldv026&partnerID=40&md5=e565bb9844f46b3865200c4b46b9e290

41.

Cohen G, Natsheh H, Sunny Y, Bawiec CR, Touitou E, Lerman MA, et al. Enhanced Therapeutic Anti-Inflammatory Effect of Betamethasone on Topical Administration with Low-Frequency, Low-Intensity (20 kHz, 100 mW/cm2) Ultrasound Exposure on Carrageenan-Induced Arthritis in a Mouse Model. Ultrasound in Medicine and Biology [Internet]. 2015;41(9):2449–57. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84938199600&doi=10.1016%252fj.ultrasmedbio.2015.04.009&partnerID=40&md5=bd311bebe25e00ccefd9ad136d959c41

42.

Ettinger K, Nevo Y, Marcinkiewicz C, Lazarovici P. Nerve growth factor-induced myoprotection in C2C12 muscle cells is mediated by α9β1 integrin via release of PGE2. Journal of Basic and Clinical Physiology and Pharmacology [Internet]. 2015;26(4):411–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84934283350&doi=10.1515%252fjbcpp-2014-0111&partnerID=40&md5=5b9577be3af190d4ddc9c035bc3654f0

43.

Ventresca EM, Lecht S, Jakubowski P, Chiaverelli RA, Weaver M, Del Valle L, et al. Association of p75NTR and α9β1 integrin modulates NGF-dependent cellular responses. Cellular Signalling [Internet]. 2015;27(6):1225–36. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84939972347&doi=10.1016%252fj.cellsig.2015.02.029&partnerID=40&md5=939d7e2f7d2904dc521661eb57435100

44.

Wang H, Liao S, Geng R, Zheng Y, Liao R, Yan F, et al. IGF-1 Signaling via the PI3K/Akt Pathway Confers Neuroprotection in Human Retinal Pigment Epithelial Cells Exposed to Sodium Nitroprusside Insult. Journal of Molecular Neuroscience [Internet]. 2015;55(4):931–40. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84925505883&doi=10.1007%252fs12031-014-0448-7&partnerID=40&md5=7e03da968dad292519261ff68097d307

45.

Wang R, Yang J, Peng L, Zhao J, Mu N, Huang J, et al. Gardenamide A attenuated cell apoptosis induced by serum deprivation insult via the ERK1/2 and PI3K/AKT signaling pathways. Neuroscience [Internet]. 2015;286:242–50. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84918767986&doi=10.1016%252fj.neuroscience.2014.11.056&partnerID=40&md5=793fce8db3afb91b96a5cccfe354310d

46.

Lahiani A, Zahavi E, Netzer N, Ofir R, Pinzur L, Raveh S, et al. Human PLacental eXpanded (PLX) mesenchymal-like adherent stromal cells confer neuroprotection to nerve growth factor (NGF)-differentiated PC12 cells exposed to ischemia by secretion of IL-6 and VEGF. Biochimica et Biophysica Acta - Molecular Cell Research [Internet]. 2015;1853(2):422–30. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84916898576&doi=10.1016%252fj.bbamcr.2014.11.009&partnerID=40&md5=737b317018c13ff798c3027049a27b30

47.

Momic T, Katzhendler J, Shai E, Noy E, Senderowitz H, Aeble J, et al. Vipegitide: A folded peptidomimetic partial antagonist of α2β1 integrin with antiplatelet aggregation activity. Drug Design, Development and Therapy [Internet]. 2015;9:291–303. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84920527818&doi=10.2147%252fDDDT.S72844&partnerID=40&md5=fdfa745924346dd0c0bcdffd2baeeca0

48.

Stabler CT, Lecht S, Mondrinos MJ, Goulart E, Lazarovici P, Lelkes PI. Revascularization of decellularized lung scaffolds: Principles and progress. American Journal of Physiology - Lung Cellular and Molecular Physiology [Internet]. 2015;309(11):L1273–85. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84949493515&doi=10.1152%252fajplung.00237.2015&partnerID=40&md5=2093677fcf92bdf60bc9d8b6178129fc

49.

Lecht S, Chiaverelli RA, Gerstenhaber J, Calvete JJ, Lazarovici P, Casewell NR, et al. Anti-angiogenic activities of snake venom CRISP isolated from Echis carinatus sochureki. Biochimica et Biophysica Acta - General Subjects [Internet]. 2015;1850(6):1169–79. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84923296277&doi=10.1016%252fj.bbagen.2015.02.002&partnerID=40&md5=cac54b8d5f8dbe8f3735496d7219a8c6

50.

Galski H, Oved-Gelber T, Simanovsky M, Lazarovici P, Gottesman MM, Nagler A. Corrigendum to “P-glycoprotein-dependent resistance of cancer cells toward the extrinsic TRAIL apoptosis signaling pathway” [Biochem. Pharmacol. 86 (2013) 584-596]. Biochemical Pharmacology [Internet]. 2014;92(3):518. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84910666991&doi=10.1016%252fj.bcp.2014.08.020&partnerID=40&md5=4278f26df2ff80050f2ba4378af9efd0

51.

Cohen G, Ettinger K, Lecht S, Lelkes PI, Lazarovici P. Transcriptional Down-regulation of Epidermal Growth Factor (EGF) Receptors by Nerve Growth Factor (NGF) in PC12 Cells. Journal of Molecular Neuroscience [Internet]. 2014;54(3):574–85. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84939885232&doi=10.1007%252fs12031-014-0388-2&partnerID=40&md5=7bf7d4ff5a0a7680999a1067ea00931b

52.

Arien-Zakay H, Gincberg G, Nagler A, Cohen G, Liraz-Zaltsman S, Trembovler V, et al. Neurotherapeutic effect of cord blood derived CD45+ hematopoietic cells in mice after traumatic brain injury. Journal of Neurotrauma [Internet]. 2014;31(16):1405–16. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84907417598&doi=10.1089%252fneu.2013.3270&partnerID=40&md5=dacb45519a0e47b796cee8cb35e4ba69

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Lazarovici P, Li M, Perets A, Mondrinos MJ, Lecht S, Koharski CD, et al. Intelligent Biomatrices and Engineered Tissue Constructs: In-Vitro Models for Drug Discovery and Toxicity Testing [Internet]. Drug Testing in vitro: Breakthroughs and Trends in Cell Culture Technology. 2006. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84889459222&doi=10.1002%252f9783527609611.ch1&partnerID=40&md5=df1ce3bc8486dd9c60f2a9edc37334c1

105.

Lipman T, Tabakman R, Lazarovici P. Neuroprotective effects of the stable nitroxide compound Tempol on 1-methyl-4-phenylpyridinium ion-induced neurotoxicity in the Nerve Growth Factor-differentiated model of pheochromocytoma PC12 cells. European Journal of Pharmacology [Internet]. 2006;549(1–3):50–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33749154294&doi=10.1016%252fj.ejphar.2006.08.022&partnerID=40&md5=8e025819de1d1d2223364e32f3c057d1

106.

Galski H, Sivan H, Lazarovici P, Nagler A. In vitro and in vivo reversal of MDR1-mediated multidrug resistance by KT-5720: Implications on hematological malignancies. Leukemia Research [Internet]. 2006;30(9):1151–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33745836868&doi=10.1016%252fj.leukres.2006.02.016&partnerID=40&md5=4f260910fcda6da6a05df7d16ca6e48e

107.

Lazarovici P, Marcinkiewicz C, Lelkes PI. Cross talk between the cardiovascular and nervous systems: Neurotrophic effects of vascular endothelial growth factor (VEGF) and angiogenic effects of nerve growth factor (NGF)-implications in drug development. Current Pharmaceutical Design [Internet]. 2006;12(21):2609–22. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33745740520&doi=10.2174%252f138161206777698738&partnerID=40&md5=405179e31a3d5edf67531997ddc44c33

108.

Rocha AS, Risberg B, Magalhães J, Trovisco V, de Castro IV, Lazarovici P, et al. The p75 neurotrophin receptor is widely expressed in conventional papillary thyroid carcinoma. Human Pathology [Internet]. 2006;37(5):562–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33646486717&doi=10.1016%252fj.humpath.2005.12.016&partnerID=40&md5=fc513c0e59ce01a9859fa7c737e38bdf

109.

Lazarovici P, Gazit A, Staniszewska I, Marcinkiewicz C, Lelkes PI. Nerve Growth Factor (NGF) promotes angiogenesis in the quail chorioallantoic membrane. Endothelium: Journal of Endothelial Cell Research [Internet]. 2006;13(1):51–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33646505056&doi=10.1080%252f10623320600669053&partnerID=40&md5=1460b727dab8df9b03eafdf8d9707e5d

110.

Dollé JP, Rezvan A, Allen FD, Lazarovici P, Lelkes PI. Nerve growth factor-induced migration of endothelial cells. Journal of Pharmacology and Experimental Therapeutics [Internet]. 2005;315(3):1220–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-27844605447&doi=10.1124%252fjpet.105.093252&partnerID=40&md5=b8db0d4be74ff51a4d67754c58d2451b

111.

Jiang H, Zhang L, Koubi D, Kuo J, Groc L, Rodriguez AI, et al. Roles of Ras-Erk in apoptosis of PC12 cells induced by trophic factor withdrawal or oxidative stress. Journal of Molecular Neuroscience [Internet]. 2005;25(2):133–40. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-22244459847&doi=10.1385%252fJMN%253a25%253a2%253a133&partnerID=40&md5=a2ea2ec6a2e518f5dc7834b989832b70

112.

Hoke A, Lazarovici P, Youdim M, Banik N, Faden A, Doré S, et al. Questions and answers: Session X: Novel approaches to neuroprotection. Annals of the New York Academy of Sciences [Internet]. 2005;1053:502–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-29744470168&doi=10.1196%252fannals.1344.069&partnerID=40&md5=e8dd1d3a312c0e1da7a2707cb36ea29a

113.

Wiklund L, Fiskum G, Chuang DM, Slikker Jr. W, Xi X, Banik N, et al. Questions and answers: Session V: Neuroprotective approaches and models. Annals of the New York Academy of Sciences [Internet]. 2005;1053:233–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-29744464871&doi=10.1196%252fannals.1344.064&partnerID=40&md5=2183ef4d16dfa4fe6238e5b8c6d51e14

114.

Banik N, Slikker Jr. W, Sharma H, Qi X, Lazarovici P, Chuang DM, et al. Questions and answers: Session II: Mechanisms of neuroprotection (1). Annals of the New York Academy of Sciences [Internet]. 2005;1053:99–106. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-29744448895&doi=10.1196%252fannals.1344.061&partnerID=40&md5=200501051d885046169ef6298b98c1db

115.

Skaper S, Kuan CY, Lazarovici P, Mandel S, Weinreb O, Ali S. Questions and answers: Session VIII: Mechanisms of neuroprotection (2). Annals of the New York Academy of Sciences [Internet]. 2005;1053:405–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-29744448894&doi=10.1196%252fannals.1344.067&partnerID=40&md5=ceec36f1ac3c7f7d82d5627e72198c5e

116.

Tabakman R, Jiang H, Shahar I, Arien-Zakay H, Levine RA, Lazarovici P. Neuroprotection by NGF in the PC12 in vitro OGD model: Involvement of mitogen-activated protein kinases and gene expression. Annals of the New York Academy of Sciences [Internet]. 2005;1053:84–96. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-29744447230&doi=10.1196%252fannals.1344.008&partnerID=40&md5=867d3e8202e0de87afa9b760cd438fcf

117.

Jevtovic-Todorovic V, Sharma HS, Lazarovici P, Kuan CY, Sanzenbacher K, Wiklund L, et al. Questions and answers: Session VII: The NMDA receptor as a target for neurotoxicity and neuroprotection. Annals of the New York Academy of Sciences [Internet]. 2005;1053:330–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-29744442890&doi=10.1196%252fannals.1344.066&partnerID=40&md5=60c7f8638872a98989957493e1d8febc

118.

Qi X, Hoke A, Turski L, Youdim M, Lazarovici P, Mocchetti I. Questions and answers: Session VI: Neuroprotective agents and mechanisms. Annals of the New York Academy of Sciences [Internet]. 2005;1053:287–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-29744439672&doi=10.1196%252fannals.1344.065&partnerID=40&md5=c00efb53afe8b2118eb6cbe52a686109

119.

Fiskum G, Slikker Jr. W, Lazarovici P, Maynard K, Binienda Z, Sharma H, et al. Questions and answers: Session IV: Role of carnitines and other agents in neuroprotection. Annals of the New York Academy of Sciences [Internet]. 2005;1053:192–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-29744436091&doi=10.1196%252fannals.1344.063&partnerID=40&md5=47e03de8713d2f665f0080350c118cde

120.

Kisiel DG, Calvete JJ, Katzhendler J, Fertala A, Lazarovici P, Marcinkiewicz C. Structural determinants of the selectivity of KTS-disintegrins for the α1β1 integrin. FEBS Letters [Internet]. 2004;577(3):478–82. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-8844224111&doi=10.1016%252fj.febslet.2004.10.050&partnerID=40&md5=996b9793d02388bce8488a8cb6d28a5a

121.

Davidson B, Reich R, Lazarovici P, Flørenes VA, Risberg B, Nielsen S, et al. Expression of the nerve growth factor receptors TrkA and p75 in malignant mesothelioma. Lung Cancer [Internet]. 2004;44(2):159–65. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-1842634536&doi=10.1016%252fj.lungcan.2003.11.014&partnerID=40&md5=fcd7f4981e5e8d0b426a9962c57e301d

122.

Tabakman R, Jiang H, Schaefer E, Levine RA, Lazarovici P. Nerve growth factor pretreatment attenuates oxygen and glucose deprivation-induced c-Jun amino-terminal kinase 1 and stress-activated kinases p38α and p38β activation and confers neuroprotection in the pheochromocytoma PC12 model. Journal of Molecular Neuroscience [Internet]. 2004;22(3):237–49. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-2942514365&doi=10.1385%252fJMN%253a22%253a3%253a237&partnerID=40&md5=64f11617421e52f581be33d7e1029e6e

123.

Tabakman R, Jiang H, Levine RA, Kohen R, Lazarovici P. Apoptotic Characteristics of Cell Death and the Neuroprotective Effect of Homocarnosine on Pheochromocytoma PC12 Cells Exposed to Ischemia. Journal of Neuroscience Research [Internet]. 2004;75(4):499–507. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0742270427&doi=10.1002%252fjnr.20008&partnerID=40&md5=266b72c0065999527ba2fba1be4519b5

124.

Flørenes VA, Mælandsmo GM, Holm R, Reich R, Lazarovici P, Davidson B. Expression of activated TrkA protein in melanocytic tumors: Relationship to cell profileration and clinical outcome. American Journal of Clinical Pathology [Internet]. 2004;122(3):412–20. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-4344645086&doi=10.1309%252fCHFHEYAT44WWP7J3&partnerID=40&md5=002a4c87d6ee3bd2b65402cf15089e1f

125.

Davidson B, Reich R, Lazarovici P, Flørenes VA, Nielsen S, Nesland JM. Altered expression and activation of the nerve growth factor receptors TrkA and p75 provide the first evidence of tumor progression to effusion in breast carcinoma. Breast Cancer Research and Treatment [Internet]. 2004;83(2):119–28. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0742304068&doi=10.1023%252fB%253aBREA.0000010704.17479.8a&partnerID=40&md5=3e050e66974e785889c29db41ab10147

126.

Tabakman R, Lecht S, Lazarovici P. Neuroprotection by monoamine oxidase B inhibitors: A therapeutic strategy for Parkinson’s disease? BioEssays [Internet]. 2004;26(1):80–90. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0347635418&doi=10.1002%252fbies.10378&partnerID=40&md5=2b4fa8d26d06304b3bc4feaa577d22ee

127.

Tabakman R, Lecht S, Sephanova S, Arien-Zakay H, Lazarovici P. Interactions between the cells of the immune and nervous system: Neurotrophins as neuroprotection mediators in CNS injury. Progress in Brain Research [Internet]. 2004;146:385–401. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0346219194&doi=10.1016%2fs0079-6123%2803%2946024-x&partnerID=40&md5=db91fb9cfd7090db91eaba99caf41e8f

128.

Davidson B, Givant-Horwitz V, Lazarovici P, Risberg B, Nesland JM, Trope CG, et al. Matrix metalloproteinases (MMP), EMMPRIN (extracellular matrix metalloproteinase inducer) and mitogen-activated protein kinases (MAPK): Co-expression in metastatic serous ovarian carcinoma. Clinical and Experimental Metastasis [Internet]. 2003;20(7):621–31. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0344441770&doi=10.1023%252fA%253a1027347932543&partnerID=40&md5=3da0bee9fbd0838bbd61e3606ed0194a

129.

Katzir I, Shani J, Shabashov D, Dagan J, Lazarovici P. Establishment and characterization of pheochromocytoma tumor models expressing different levels of trkA receptors. Cancer Letters [Internet]. 2003;200(2):177–85. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0642273298&doi=10.1016%2fS0304-3835%2803%2900414-2&partnerID=40&md5=970fe33ed1b89dfcef4aff71cf868847

130.

Katzir I, Shani J, Goshen G, Sela J, Ninary E, Dogonovski AM, et al. Characterization of nerve growth factors (NGFs) from snake venoms by use of a novel, quantitative bioassay utilizing pheochromocytoma (PC12) cells overexpressing human trkA receptors. Toxicon [Internet]. 2003;42(5):481–90. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-12144287587&doi=10.1016%2fS0041-0101%2803%2900225-3&partnerID=40&md5=33a97cefc08eefda12c5a4328701ae0e

131.

Givant-Horwitz V, Davidson B, Lazarovici P, Schaefer E, Nesland JM, Tropé CG, et al. Mitogen-activated protein kinases (MAPK) as predictors of clinical outcome in serous ovarian carcinoma in effusions. Gynecologic Oncology [Internet]. 2003;91(1):160–72. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0141534435&doi=10.1016%2fS0090-8258%2803%2900434-7&partnerID=40&md5=0ec84f057c6bf31de5597e265f13a796

132.

Davidson B, Reich R, Lazarovici P, Nesland JM, Skrede M, Risberg B, et al. Expression and activation of the nerve growth factor receptor TrkA in serous ovarian carcinoma. Clinical Cancer Research [Internet]. 2003;9(6):2248–59. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037500963&partnerID=40&md5=e45c3670d710f2af453260a0927c857c

133.

Lazarovici P. The structure and function of pardaxin. Journal of Toxicology - Toxin Reviews [Internet]. 2002;21(4):391–421. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036449590&doi=10.1081%252fTXR-120014410&partnerID=40&md5=ee55c0c57f3ba7c928b667b61a31934d

134.

Bloch-Shilderman E, Abu-Raya S, Trembovler V, Boschwitz H, Gruzman A, Linial M, et al. Pardaxin stimulation of phospholipases A2 and their involvement in exocytosis in PC-12 cells. Journal of Pharmacology and Experimental Therapeutics [Internet]. 2002;301(3):953–62. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036264462&doi=10.1124%252fjpet.301.3.953&partnerID=40&md5=9ffe5bc12d8ac4fb0b4edc37e507a5d1

135.

Vaudry D, Stork PJS, Lazarovici P, Eiden LE. Signaling pathways for PC12 cell differentiation: Making the right connections. Science [Internet]. 2002;296(5573):1648–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037205044&doi=10.1126%252fscience.1071552&partnerID=40&md5=98734a449b9b761cd5b69f39a318bdaa

136.

Tabakman R, Lazarovici P, Kohen R. Neuroprotective effects of carnosine and homocarnosine on pheochromocytoma PC12 cells exposed to ischemia. Journal of Neuroscience Research [Internet]. 2002;68(4):463–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037093669&doi=10.1002%252fjnr.10228&partnerID=40&md5=f5886b7725bdeed49c4bccdf62ceafaa

137.

Abu-Raya S, Tabakman R, Blaugrund E, Trembovler V, Lazarovici P. Neuroprotective and neurotoxic effects of monoamine oxidase-B inhibitors and derived metabolites under ischemia in PC12 cells. European Journal of Pharmacology [Internet]. 2002;434(3):109–16. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037059430&doi=10.1016%2fS0014-2999%2801%2901548-5&partnerID=40&md5=07b58686f9c344845150330305207aed

138.

Cantarella G, Lempereur L, Presta M, Ribatti D, Lombardo G, Lazarovici P, et al. Nerve growth factor-endothelial cell interaction leads to angiogenesis in vitro and in vivo. The FASEB journal : official publication of the Federation of American Societies for Experimental Biology [Internet]. 2002;16(10):1307–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036674499&doi=10.1096%252ffj.01-1000fje&partnerID=40&md5=c3a958692626b9032a6144f82152de98

139.

Katzir I, Shani J, Regev K, Shabashov D, Lazarovici P. A quantitative bioassay for nerve growth factor, using PC12 clones expressing different levels of trkA receptors. Journal of Molecular Neuroscience [Internet]. 2002;18(3):251–64. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036014123&doi=10.1385%252fJMN%253a18%253a3%253a251&partnerID=40&md5=c7190c141b35ed7119a3fbe5ae11cd03

140.

Bloch-Shilderman E, Jiang H, Dingel JD, Lazarovici P. Pardaxin, an ionophore neurotoxin, induces PC12 cell death: Activation of stress kinases and production of reactive oxygen species. Journal of Natural Toxins [Internet]. 2002;11(2):71–85. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035985030&partnerID=40&md5=9d23709b6ca571c79f8d1a273886f082

141.

Chiarenza A, Lazarovici P, Lempereur L, Cantarella G, Bianchi A, Bernardini R. Tamoxifen inhibits nerve growth factor-induced proliferation of the human breast cancerous cell line MCF-7. Cancer Research [Internet]. 2001;61(7):3002–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035300597&partnerID=40&md5=c0ce3ad6607c674d5d36f31eb06bebf0

142.

Bloch-Shilderman E, Jiang H, Abu-Raya S, Linial M, Lazarovici P. Involvement of extracellular signal-regulated kinase (ERK) in pardaxin-induced dopamine release from PC12 cells. Journal of Pharmacology and Experimental Therapeutics [Internet]. 2001;296(3):704–11. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035127213&partnerID=40&md5=cffeeeb6bacfc0f0f4c8bedf5f54e5e7

143.

Davidson B, Nesland JM, Berner A, Risberg B, Goscinski M, Tropé CG, et al. Expression levels of the nerve growth factor receptors TrkA and p75 in effusions and solid tumors of serous ovarian carcinoma patients. Clinical Cancer Research [Internet]. 2001;7(11):3457–64. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035191001&partnerID=40&md5=f017ab99b58be780b7b8662e5d5d69f1

144.

Weinstock M, Kirschbaum-Slager N, Lazarovici P, Bejar C, Youdim MBH, Shoham S. Neuroprotective effects of novel cholinesterase inhibitors derived from rasagiline as potential anti-Alzheimer drugs. Annals of the New York Academy of Sciences [Internet]. 2001;939:148–61. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034932067&doi=10.1111%252fj.1749-6632.2001.tb03622.x&partnerID=40&md5=217c971833fd87c4ecc6ec8ceab7e6e5

145.

Desai R, Peretz A, Idelson H, Lazarovici P, Attali B. Ca2+-activated K+ channels in human leukemic Jurkat T cells. Journal of Biological Chemistry [Internet]. 2000;275(51):39954–63. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034704075&doi=10.1074%252fjbc.M001562200&partnerID=40&md5=778c13263a081441e8758d8181c75752

146.

Monshipouri M, Jiang H, Lazarovici P. NGF stimulation of erk phosphorylation is impaired by a point mutation in the transmembrane domain of trkA receptor. Journal of Molecular Neuroscience [Internet]. 2000;14(1–2):69–76. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034039955&doi=10.1385%252fjmn%253a14%253a1-2%253a069&partnerID=40&md5=135ea902392d335f7e9495a81a14eb36

147.

Abu-Raya S, Blaugrund E, Trembovler V, Lazarovici P. Rasagiline, a novel monoamine oxidase-B inhibitor with neuroprotective effects under ischemic conditions in PC12 cells. Drug Development Research [Internet]. 2000;50(3–4):285–90. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033814711&doi=10.1002%2f1098-2299%28200007%2f08%2950%3a3%2f4%3c285%3a%3aAID-DDR11%3e3.0.CO%3b2-8&partnerID=40&md5=490f15f77fc071f310ca1bace810caed

148.

Moalem G, Gdalyahu A, Shani Y, Otten U, Lazarovici P, Cohen IR, et al. Production of neurotrophins by activated T cells: Implications for neuroprotective autoimmunity. Journal of Autoimmunity [Internet]. 2000;15(3):331–45. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033712614&doi=10.1006%252fjaut.2000.0441&partnerID=40&md5=c9e3452fd477826abef222654ec87701

149.

Abu-Raya S, Blaugrund E, Trembovler V, Shilderman-Bloch E, Shohami E, Lazarovici P. Rasagiline, a monoamine oxidase-B inhibitor, protects NGF-differentiated PC12 cells against oxygen-glucose deprivation. Journal of Neuroscience Research [Internet]. 1999;58(3):456–63. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033231244&doi=10.1002%2f%28SICI%291097-4547%2819991101%2958%3a3%3c456%3a%3aAID-JNR12%3e3.0.CO%3b2-S&partnerID=40&md5=f2e5651e639ac4a2328e054378c2e471

150.

Stein S, Weiss A, Adermann K, Lazarovici P, Hochman J, Wellhöner H. A disulfide conjugate between anti-tetanus antibodies and HIV (37-72)Tat neutralizes tetanus toxin inside chromaffin cells. FEBS Letters [Internet]. 1999;458(3):383–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032883128&doi=10.1016%2fS0014-5793%2899%2901186-2&partnerID=40&md5=08debad1dfb858f25e8d0efa09acf90a

151.

Jiang H, Takeda K, Lazarovici P, Katagiri Y, Yu ZX, Dickens G, et al. Nerve growth factor (NGF)-induced calcium influx and intracellular calcium mobilization in 3T3 cells expressing NGF receptors. Journal of Biological Chemistry [Internet]. 1999;274(37):26209–16. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033543580&doi=10.1074%252fjbc.274.37.26209&partnerID=40&md5=65dce959e63568b5ba18972018719c68

152.

Brodie C, Bogi K, Acs P, Lazarovici P, Petrovics G, Anderson WB, et al. Protein kinase C-ε plays a role in neurite outgrowth in response to epidermal growth factor and nerve growth factor in PC12 cells. Cell Growth and Differentiation [Internet]. 1999;10(3):183–91. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032989245&partnerID=40&md5=a62b3625295781ff4d2be204c0e4d345

153.

Abu-Raya S, Bloch-Shilderman E, Lelkes PI, Trembovler V, Shohami E, Gutman Y, et al. Characterization of pardaxin-induced dopamine release from pheochromocytoma cells: Role of calcium and eicosanoids. Journal of Pharmacology and Experimental Therapeutics [Internet]. 1999;288(2):399–406. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033036808&partnerID=40&md5=e15726950da0a4c1729b1f283c3d289c

154.

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Lazarovici P, Jiang H, Fink Jr. D. The 38-amino-acid form of pituitary adenylate cyclase-activating polypeptide induces neurite outgrowth in PC12 cells that is dependent on protein kinase C and extracellular signal-regulated kinase but not on protein kinase A, nerve growth factor receptor tyrosine kinase, p21(ras) G protein, and pp60(c-src) cytoplasmic tyrosine kinase. Molecular Pharmacology [Internet]. 1998;54(3):547–58. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0031664979&doi=10.1124%252fmol.54.3.547&partnerID=40&md5=39d889fd4f2dc17f9a9d9dec28470d3b

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Galski H, Lazarovici P, Gottesman MM, Murakata C, Matsuda Y, Hochman J. Kt-5720 reverses multidrug resistance in variant S49 mouse lymphoma cells transduced with the human MDR1 cDNA and in human multidrug-resistant carcinoma cells. European Journal of Cancer [Internet]. 1995;31(3):380–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028915160&doi=10.1016%2f0959-8049%2894%2900511-3&partnerID=40&md5=fa5b3f89149959a17c59d863d2c55818

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Rasouly D, Lazarovici P. Staurosporine induces tyrosine phosphorylation of a 145 kDa protein but does not activate gp140trk in PC12 cells. European Journal of Pharmacology: Molecular Pharmacology [Internet]. 1994;269(2):255–64. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028172015&doi=10.1016%2f0922-4106%2894%2990094-9&partnerID=40&md5=712daa7abb2aab520cbbeaeba93b04e2

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Rasouly D, Lazarovici P. Staurosporine, a streptomyces alkaloid toxin as a neurotropic tool. Toxin Reviews [Internet]. 1994;13(1):11–23. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028216943&doi=10.3109%252f15569549409006478&partnerID=40&md5=848e6d67254236f07340c70641ff520a

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Arribas M, Blasi J, Lazarovici P, Marsal J. Calcium‐Dependent and ‐Independent Acetylcholine Release from Electric Organ Synaptosomes by Pardaxin: Evidence of a Biphasic Action of an Excitatory Neurotoxin. Journal of Neurochemistry [Internet]. 1993;60(2):552–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0027465996&doi=10.1111%252fj.1471-4159.1993.tb03184.x&partnerID=40&md5=38bcb3eab072897fc7956d53f6f5b0bf

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Rasouly D, Rahamim E, Lester D, Matsuda Y, Lazarovici P. Staurosporine-induced neurite outgrowth in PC12 cells is independent of protein kinase C inhibition. Molecular Pharmacology [Internet]. 1992;42(1):35–43. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0027093254&partnerID=40&md5=52ffdf7768f58ddb47b46a462f2b51db

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Lazarovici P, Lelkes PI. Pardaxin induces exocytosis in bovine adrenal medullary chromaffin cells independent of calcium. Journal of Pharmacology and Experimental Therapeutics [Internet]. 1992;263(3):1317–26. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026996702&partnerID=40&md5=742947ba6d59c25d55ee0718c4c04faf

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Nikodijevic B, Nikodijevic D, Lazarovici P. Pardaxin-stimulated calcium uptake in pc12 cells is blocked by cadmium and is not mediated by l-type calcium channels. Journal of Basic and Clinical Physiology and Pharmacology [Internet]. 1992;3(4):359–70. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026997568&doi=10.1515%252fJBCPP.1992.3.4.359&partnerID=40&md5=5fe6b2491ef7d734376c4f7c52545bf1

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Lazarovici P, Bergel M, Hasson T, Rahamim E, Hochman J. Immunomagnetic separation and analysis of non‐malignant variants and parental malignant mouse lymphoma cells. Journal of Molecular Recognition [Internet]. 1991;4(4):143–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026185478&doi=10.1002%252fjmr.300040406&partnerID=40&md5=e5ef03b2200b11660a6721a0559a213d

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Hochman J, Park SS, Lazarovici P, Bergel M, Gottesman MM. Monoclonal antibodies to immunogenic lymphoma cell variants displaying impaired neoplastic properties: Characterization and applications. Journal of the National Cancer Institute [Internet]. 1990;82(23):1821–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025683115&doi=10.1093%252fjnci%252f82.23.1821&partnerID=40&md5=2cbf97a3d351c50bce6d1cca8c1a349e

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Lazarovici P. Characterization and visualization of tetanus toxin acceptors on adrenal chromaffin granules. Journal de Physiologie [Internet]. 1990;84(3):197–205. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025666745&partnerID=40&md5=16d6977b91215bc9f889b212c92187ea

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Fujita K, Guroff G, Yavin E, Goping G, Orenberg R, Lazarovici P. Preparation of affinity-purified, biotinylated tetanus toxin, and characterization and localization of cell surface binding sites on nerve growth factor-treated PC12 cells. Neurochemical Research [Internet]. 1990;15(4):373–83. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025282505&doi=10.1007%252fBF00969922&partnerID=40&md5=a0fc27aa4274ac197c42b001c3bf4f79

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Lazarovici P, Fujita K, Contreras ML, DiOrio JP, Lelkes PI. Affinity purified tetanus toxin binds to isolated chromaffin granules and inhibits catecholamine release in digitonin-permeabilized chromaffin cells. FEBS Letters [Internet]. 1989;253(1–2):121–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024375930&doi=10.1016%2f0014-5793%2889%2980943-3&partnerID=40&md5=aa54261e49d9ef8cee75433f04bf25cd

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Fujita K, Lazarovici P, Guroff G. Regulation of the differentiation of PC12 pheochromocytoma cells. Environmental Health Perspectives [Internet]. 1989;80:127–42. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024550673&doi=10.1289%252fehp.8980127&partnerID=40&md5=4b2898632fa1f1d211e881ea60ad09f3

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Rudkin BB, Lazarovici P, Levi BZ, Abe Y, Fujita K, Guroff G. Cell cycle-specific action of nerve growth factor in PC12 cells: Differentiation without proliferation. EMBO Journal [Internet]. 1989;8(11):3319–25. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024465402&doi=10.1002%252fj.1460-2075.1989.tb08493.x&partnerID=40&md5=3a7bad922dd10240209a394ef77d9620

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Fink D, Contreras ML, Lelkes PI, Lazarovici P. Staphylococcus aureus α-toxin activates phospholipases and induces a Ca2+ influx in PC12 cells. Cellular Signalling [Internet]. 1989;1(4):387–93. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024360840&doi=10.1016%2f0898-6568%2889%2990057-0&partnerID=40&md5=58afdaf6ed29ccb42bbc2b99b409a125

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Lazarovici P, Levi B ‐Z., Lelkes PI, Koizumi S, Fujita K, Matsuda Y, et al. K‐252a inhibits the increase in c‐fos transcription and the increase in intracellular calcium produced by nerve growth factor in PC12 cells. Journal of Neuroscience Research [Internet]. 1989;23(1):1–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024359945&doi=10.1002%252fjnr.490230102&partnerID=40&md5=be31ff060e30758f5544c647e1c59b04

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Shai Y, Fox J, Caratsch C, Shih YL, Edwards C, Lazarovici P. Sequencing and synthesis of pardaxin, a polypeptide from the Red Sea Moses sole with ionophore activity. FEBS Letters [Internet]. 1988;242(1):161–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024292077&doi=10.1016%2f0014-5793%2888%2981007-X&partnerID=40&md5=7fe62a12b075af99fc13a1219be0bc65

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Lelkes PI, Lazarovici P. Pardaxin induces aggregation but not fusion of phosphatidylserine vesicles. FEBS Letters [Internet]. 1988;230(1–2):131–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023851691&doi=10.1016%2f0014-5793%2888%2980656-2&partnerID=40&md5=a79f54127789d0a8a79112908ca9af07

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Koizumi S, Contreras ML, Matsuda Y, Hama T, Lazarovici P, Guroff G. K-252a: A specific inhibitor of the action of nerve growth factor on PC 12 cells. Journal of Neuroscience [Internet]. 1988;8(2):715–21. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023864240&doi=10.1523%252fjneurosci.08-02-00715.1988&partnerID=40&md5=fe693a2bde7a42d9676abb7b2d6a3015

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Lazarovici P, Yanai P, Yavin E. Molecular interactions between micellar polysialogangliosides and affinity-purified tetanotoxins in aqueous solution. Journal of Biological Chemistry [Internet]. 1987;262(6):2645–51. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023664026&partnerID=40&md5=dacea9cef9eb886029320b0826b9e682

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Renner P, Caratsch CG, Waser PG, Lazarovici P, Primor N. Presynaptic effects of the Pardaxins, polypeptides isolated from the gland secretion of the flatfish Pardachirus marmoratus. Neuroscience [Internet]. 1987;23(1):319–25. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023629686&doi=10.1016%2f0306-4522%2887%2990292-2&partnerID=40&md5=dd651ed70076f4cbf4689eea0c1057eb

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Lazarovici P, Chan KFJ. Staphylococcus aureus α-toxin. 2. Reduction of epidermal growth factor receptor affinity in PC12 cells. Toxicon [Internet]. 1987;25(6):637–47. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023605429&doi=10.1016%2f0041-0101%2887%2990110-3&partnerID=40&md5=961b5f30936eb083bc4b9baa48f7f76c

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Chan KFJ, Lazarovici P. Staphylococcus aureus α-toxin. 1. Effect on protein phosphorylation in myelin. Toxicon [Internet]. 1987;25(6):631–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023525829&doi=10.1016%2f0041-0101%2887%2990109-7&partnerID=40&md5=e582945dd95743757ea9424bf30351c8

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Lazarovici P, Dickens G, Kuzuya H, Guroff G. Long-term, heterologous down-regulation of the epidermal growth factor receptor in PC12 cells by nerve growth factor. Journal of Cell Biology [Internet]. 1987;104(6):1611–21. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023267658&doi=10.1083%252fjcb.104.6.1611&partnerID=40&md5=579121fe0523712d66c94b42fc7e6c36

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Wan YY, Orrison BM, Lieberman R, Lazarovici P, Ozato K. Induction of major histocompatibility class I antigens by interferons in undifferentiated F9 cells. Journal of Cellular Physiology [Internet]. 1987;130(2):276–83. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023117629&doi=10.1002%252fjcp.1041300214&partnerID=40&md5=a6898141aa4270df8f8fedae487f7da0

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Lazarovici P, Primor N, Loew LM. Purification and pore-forming activity of two hydrophobic polypeptides from the secretion of the Red Sea Moses sole (Pardachirus marmoratus). Journal of Biological Chemistry [Internet]. 1986;261(35):16704–13. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0022869696&partnerID=40&md5=626c4fd39d73f0af8aa483ab4940c643

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Lazarovici P, Yavin E. Affinity-Purified Tetanus Neurotoxin Interaction with Synaptic Membranes: Properties of a Protease-Sensitive Receptor Component. Biochemistry [Internet]. 1986;25(22):7047–54. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0022993108&doi=10.1021%252fbi00370a044&partnerID=40&md5=0bd2049e1cf31069bfa35a7d54c709e4

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Loew LM, Benson L, Lazarovici P, Rosenberg I. Fluorometric Analysis of Transferable Membrane Pores. Biochemistry [Internet]. 1985;24(9):2101–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021854712&doi=10.1021%252fbi00330a001&partnerID=40&md5=ac9965bbd731a57dbe02f285df1e6ff7

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Lazarovici P, Yavin E. Tetanus toxin interaction with human erythrocytes. II. Kinetic properties of toxin association and evidence for a ganglioside-toxin macromolecular complex formation. BBA - Biomembranes [Internet]. 1985;812(2):532–42. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021978808&doi=10.1016%2f0005-2736%2885%2990328-1&partnerID=40&md5=4fc3a63b2445abfe40c182609c39b7ee

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Lazarovici P, Yavin E. Tetanus toxin interaction with human erythrocytes. I. Properties of polysialoganglioside association with the cell surface. BBA - Biomembranes [Internet]. 1985;812(2):523–31. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021953447&doi=10.1016%2f0005-2736%2885%2990327-X&partnerID=40&md5=6f1ec1a8a990ae60d67d5fec257dee2a

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Lazarovici P, Menashe M, Zlotkin E. Toxicity to crustacea due to polypeptide-phospholipase interaction in the venom of a chactoid scorpion. Archives of Biochemistry and Biophysics [Internet]. 1984;229(1):270–86. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021345384&doi=10.1016%2f0003-9861%2884%2990153-X&partnerID=40&md5=4db4ca59a6a6793a2cc51cd21a4aa8d2

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Lazarovici P, Shapira D, Pisarev V, Shaaya E. Ecdysteroid level and the change in sensitivity to a juvenile hormone analogue in Ephestia cautella larvae (Lepidoptera, Phycitidae). Archives of Insect Biochemistry and Physiology [Internet]. 1984;1(4):409–15. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84990424030&doi=10.1002%252farch.940010410&partnerID=40&md5=eb1693aa1d36feac9ca00da5d39b6941

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Lazarovici P, Tayot JL, Yavin E. Affinity chromatographic purification and characterization of two iodinated tetanus toxin fractions exhibiting different binding properties. Toxicon [Internet]. 1984;22(3):401–13. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021159786&doi=10.1016%2f0041-0101%2884%2990084-9&partnerID=40&md5=fd52b0568108d998bb4ef1ccc8335ef7

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Lazarovici P, Shapira D, Shaaya E. Determination of ecdysteroid titers by a double-antibody precipitation in the tropical warehouse moth, Ephestia cautella (Lepidoptera, phycitidae). Comparative Biochemistry and Physiology – Part A: Physiology [Internet]. 1983;74(3):525–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-49049127185&doi=10.1016%2f0300-9629%2883%2990542-X&partnerID=40&md5=67c51fe0404e9f001314168ea505f7a5

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Lazarovici P, Hochman J, Menashe M, Primor N, Zlotkin E. The cytotoxicity of a cobra venom phospholipase to mouse lymphoma cells. Archives of Toxicology [Internet]. 1982;51(2):167–73. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020446357&doi=10.1007%252fBF00302757&partnerID=40&md5=9f8cc1d8c77ba9e6e259ffadb333eade

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Lester D, Lazarovici P, Pelhate M, Zlotkin E. Purification, characterization and action of two insect toxins from the venom of the scorpion buthotus judaicus. Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular [Internet]. 1982;701(3):370–81. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020073253&doi=10.1016%2f0167-4838%2882%2990240-0&partnerID=40&md5=4fc9d7c9cd186d0089f77ecf23dd3b18

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Breuer E, Deutsch J, Lazarovici P. A practical synthesis of the aggregation pheromone of Tribolium castaneum and Tribolium confusum. Chemistry and Industry (London) [Internet]. 1982;No. 22:907–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020460360&partnerID=40&md5=6e74c953a57a442389ce85aed24f98c2

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Lazarovici P, Yanai P, Pelhate M, Zlotkin E. Insect toxic components from the venom of a chactoid scorpion, Scorpio maurus palmatus (Scorpionidae). Journal of Biological Chemistry [Internet]. 1982;257(14):8397–404. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020336076&partnerID=40&md5=e30f51b75db4d83cefa77a8c34bdd88a

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Zlotkin E, Lester D, Lazarovici P, Pelhate M. The chemistry and axonal action of two insect toxins derived from the venom of the scorpion Buthotus judaicus. Toxicon [Internet]. 1982;20(1):323–31. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020029002&doi=10.1016%2f0041-0101%2882%2990235-5&partnerID=40&md5=62111c64bf2794a5d0ca3cf86208c396

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Lazarovici P, Zlotkin E. A mammal toxin derived from the venom of a chactoid scorpion. Comparative Biochemistry and Physiology Part C, Comparative [Internet]. 1982;71(2):177–81. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019988152&doi=10.1016%2f0306-4492%2882%2990033-8&partnerID=40&md5=03e2a2e312e8ed9a2bd02fce2d9d4a6e

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Primor N, Lazarovici P. Pardachirus marmoratus (Red Sea flatfish) secretion and its isolated toxic fraction pardaxin: The relationship between hemolysis and ATPase inhibition. Toxicon [Internet]. 1981;19(4):573–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019488265&doi=10.1016%2f0041-0101%2881%2990018-0&partnerID=40&md5=493cae7791b9cd80fdf1e62def2f19fc

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PENER MP, LAZAROVICI P. Effect of exogenous juvenile hormones on mating behaviour and yellow colour in allatectomized adult male desert locusts. Physiological Entomology [Internet]. 1979;4(3):251–61. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84981606475&doi=10.1111%252fj.1365-3032.1979.tb00202.x&partnerID=40&md5=d492a01755c5af2036525f06f7574012

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Lazarovici P, Lester D, Menashá M, Hochman Y, Zlotkin E. Phospholipases and direct lytic factors (DLFs) derived from the venom of the scorpion Scorpio maurus palmatus (Scorpionidae). Toxicon [Internet]. 1979;17(Suppl 1):97. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018690618&doi=10.1016%2f0041-0101%2879%2990098-9&partnerID=40&md5=a453e4269a7bfc2158c1f2a666760318

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Lazarovici P, Zlotkin E. Toxins specifically active to arthropods and mammals from the venom of the scorpion Scorpio maurus palmatus (Scorpionidae). Toxicon [Internet]. 1979;17(Suppl 1):98. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018675603&doi=10.1016%2f0041-0101%2879%2990099-0&partnerID=40&md5=78ab544aeb53c585d12bd6d70d92c394

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Zlotkin E, Teitelbaum Z, Lester D, Lazarovici P. Toxins selective to insects derived from scorpion venoms. Toxicon [Internet]. 1979;17(Suppl 1):208. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018667766&doi=10.1016%2f0041-0101%2879%2990207-1&partnerID=40&md5=8420e76e276d6b51f8422c836714d942

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Teitelbaum Z, Lazarovici P, Zlotkin E. Selective binding of the scorpion venom insect toxin to insect nervous tissue. Insect Biochemistry [Internet]. 1979;9(4):343–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0007312820&doi=10.1016%2f0020-1790%2879%2990080-5&partnerID=40&md5=1d011d53e1140ed15a8b73ea3a5cce24

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Lazaroviçi P, Pener MP. Juvenile hormones (JHs) and completion of oöcyte development in the African migratory locust: A comparative and quantitative study. General and Comparative Endocrinology [Internet]. 1977;33(3):434–52. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017665467&doi=10.1016%2f0016-6480%2877%2990060-0&partnerID=40&md5=2b912fb09f008f488745262ade9c0818