The Faculty of Medicine - Biochemistry and Molecular Biology: Rones Zichria

1.

Alfi O, Hamdan M, Wald O, Yakirevitch A, Wandel O, Oiknine-Djian E, et al. SARS-CoV-2 Omicron Induces Enhanced Mucosal Interferon Response Compared to other Variants of Concern, Associated with Restricted Replication in Human Lung Tissues. Viruses [Internet]. 2022;14(7). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85135106041&doi=10.3390%252fv14071583&partnerID=40&md5=bb381b9463bad39cc4c4de2bd64ac310

2.

Vorontsov O, Levitt L, Lilleri D, Vainer GW, Kaplan O, Schreiber L, et al. Amniotic fluid biomarkers predict the severity of congenital cytomegalovirus infection. Journal of Clinical Investigation [Internet]. 2022;132(11). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85131220591&doi=10.1172%252fJCI157415&partnerID=40&md5=ce84dcd7638626d6a20ff13b8afac02e

3.

Alfi O, Yakirevitch A, Wald O, Wandel O, Izhar U, Oiknine-Djian E, et al. Human nasal and lung tissues infected ex vivo with SARS-CoV-2 provide insights into differential tissue-specific and virus-specific innate immune responses in the upper and lower respiratory tract. Journal of Virology [Internet]. 2021;95(14). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85108880122&doi=10.1128%252fJVI.00130-21&partnerID=40&md5=c6f9b9b4b4525ee1f289b2c456340d23

4.

Alfi O, From I, Yakirevitch A, Drendel M, Wolf M, Meir K, et al. Human nasal turbinate tissues in organ culture as a model for human cytomegalovirus infection at the mucosal entry site. Journal of Virology [Internet]. 2020;94(19). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85091127238&doi=10.1128%252fJVI.01258-20&partnerID=40&md5=83ad8786372eb31f4d73299acdc3c11b

5.

Weisblum Y, Oiknine-Djian E, Vorontsov OM, Haimov-Kochman R, Zakay-Rones Z, Meir K, et al. Erratum: Correction for Weisblum et al., "zika virus infects early-and midgestation human maternal decidual tissues, inducing distinct innate tissue responses in the maternal-fetal interface(Journal of Virology (2017) 91:4 (e01905-e01916) DOI: 10.1128/JVI.01905-16). Journal of Virology [Internet]. 2019;93(22). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85074290844&doi=10.1128%252fJVI.01451-19&partnerID=40&md5=43c4a21345d237630db5a25c86c1ca99

6.

Neto CC, Penndorf KA, Feldman M, Meron-Sudai S, Zakay-Rones Z, Steinberg D, et al. Characterization of non-dialyzable constituents from cranberry juice that inhibit adhesion, co-aggregation and biofilm formation by oral bacteria. Food and Function [Internet]. 2017;8(5):1955–65. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021833565&doi=10.1039%252fc7fo00109f&partnerID=40&md5=471b2ae1a1be8429ccdf2fa1f363c174

7.

Weisblum Y, Oiknine-Djian E, Vorontsov OM, Haimov-Kochman R, Zakay-Rones Z, Meir K, et al. Zika virus infects early- and midgestation human maternal decidual tissues, inducing distinct innate tissue responses in the maternal-fetal interface. Journal of Virology [Internet]. 2017;91(4). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85012024098&doi=10.1128%252fJVI.01905-16&partnerID=40&md5=94de66da08aae059f6ad20e6f754f8c7

8.

Weisblum Y, Panet A, Zakay-Rones Z, Vitenshtein A, Haimov-Kochman R, Goldman-Wohl D, et al. Human cytomegalovirus induces a distinct innate immune response in the maternal-fetal interface. Virology [Internet]. 2015;485:289–96. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84940027690&doi=10.1016%252fj.virol.2015.06.023&partnerID=40&md5=d6486c3e4d0d9286aa0c20f45bc3aad5

9.

Yaacov B, Lazar I, Tayeb S, Frank S, Izhar U, Lotem M, et al. Extracellular matrix constituents interfere with Newcastle disease virus spread in solid tissue and diminish its potential oncolytic activity. Journal of General Virology [Internet]. 2012;93(8):1664–72. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84864045413&doi=10.1099%252fvir.0.043281-0&partnerID=40&md5=f8dd233f40d64b45d9946125a5bd37d1

10.

Oiknine-Djian E, Houri-Haddad Y, Weiss E, Ofek I, Greenbaum E, Hartshorn K, et al. High molecular weight constituents of cranberry interfere with influenza virus neuraminidase activity in vitro. Planta Medica [Internet]. 2012;78(10):962–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84863572275&doi=10.1055%252fs-0031-1298579&partnerID=40&md5=12bc2586a25ea85ee372132b04fd74dc

11.

Shmuely H, Ofek I, Weiss EI, Rones Z, Houri-Haddad Y. Cranberry components for the therapy of infectious disease. Current Opinion in Biotechnology [Internet]. 2012;23(2):148–52. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84859163259&doi=10.1016%252fj.copbio.2011.10.009&partnerID=40&md5=c582deb5700c2d24a90c3b759d81e1c8

12.

Hojsak I, Avitzur Y, Mor E, Shamir R, Haimi-Cohen Y, Zakay-Rones Z, et al. Antibody response to influenza vaccine in pediatric liver transplant recipients. Pediatric Infectious Disease Journal [Internet]. 2011;30(6):491–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-79957990137&doi=10.1097%252fINF.0b013e31820b7c22&partnerID=40&md5=3627fc70cfc965e9759987699658ba77

13.

Engelhard D, Zakay-Rones Z, Shapira MY, Resnick I, Averbuch D, Grisariu S, et al. The humoral immune response of hematopoietic stem cell transplantation recipients to AS03-adjuvanted A/California/7/2009 (H1N1)v-like virus vaccine during the 2009 pandemic. Vaccine [Internet]. 2011;29(9):1777–82. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-79952703352&doi=10.1016%252fj.vaccine.2010.12.113&partnerID=40&md5=f258df3931f2a43bb454f3fd9733c9a4

14.

Zakay-Rones Z. Human influenza vaccines and assessment of immunogenicity. Expert Review of Vaccines [Internet]. 2010;9(12):1423–39. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-78649527527&doi=10.1586%252ferv.10.144&partnerID=40&md5=9ff439625b2b3a023f1beb499602c214

15.

Lazar I, Yaacov B, Shiloach T, Eliahoo E, Kadouri L, Lotem M, et al. The oncolytic activity of Newcastle disease virus NDV-HUJ on chemoresistant primary melanoma cells is dependent on the proapoptotic activity of the inhibitor of apoptosis protein livin. Journal of Virology [Internet]. 2010;84(1):639–46. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-72849135966&doi=10.1128%252fJVI.00401-09&partnerID=40&md5=553be87c46f84ae422406142998a19a5

16.

Cohen-Daniel L, Zakay-Rones Z, Resnick IB, Shapira MY, Dorozhko M, Mador N, et al. Emergence of oseltamivir-resistant influenza A/H3N2 virus with altered hemagglutination pattern in a hematopoietic stem cell transplant recipient. Journal of Clinical Virology [Internet]. 2009;44(2):138–40. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-59849099415&doi=10.1016%252fj.jcv.2008.11.014&partnerID=40&md5=b6aba1ad522eb374a66f838faeff07f6

17.

Yaacov B, Elihaoo E, Lazar I, Ben-Shlomo M, Greenbaum I, Panet A, et al. Selective oncolytic effect of an attenuated Newcastle disease virus (NDV-HUJ) in lung tumors (Cancer Gene Therapy (2008) 15, (795-807) DOI: 10.1038/cgt.2008.31). Cancer Gene Therapy [Internet]. 2008;15(12):832. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-56049091766&doi=10.1038%252fcgt.2008.56&partnerID=40&md5=410fd7bd0e2d7be28291486ed123fa13

18.

Yaacov B, Elihaoo E, Lazar I, Ben-Shlomo M, Greenbaum I, Panet A, et al. Selective oncolytic effect of an attenuated Newcastle disease virus (NDV-HUJ) in lung tumors. Cancer Gene Therapy [Internet]. 2008;15(12):795–807. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-56049097651&doi=10.1038%252fcgt.2008.31&partnerID=40&md5=fc4ca84ca01bc246bd5fd8196b4a5149

19.

Gazit R, Gruda R, Elboim M, Arnon TI, Katz G, Achdout H, et al. Lethal influenza infection in the absence of the natural killer cell receptor gene Ncr1. Nature Immunology [Internet]. 2006;7(5):517–23. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645964977&doi=10.1038%252fni1322&partnerID=40&md5=1e67d0589c465728dbbf5e569532d109

20.

Muhamed G, Greenbaum E, Zakay-Rones Z. Neuraminidase antibody response to inactivated influenza virus vaccine following intranasal and intramuscular vaccination. Israel Medical Association Journal [Internet]. 2006;8(3):155–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645469069&partnerID=40&md5=817199d0095f6a70f4f3170f0af36de0

21.

Freeman AI, Zakay-Rones Z, Gomori JM, Linetsky E, Rasooly L, Greenbaum E, et al. Phase I/II trial of intravenous NDV-HUJ oncolytic virus in recurrent glioblastoma multiforme. Molecular Therapy [Internet]. 2006;13(1):221–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-28844468988&doi=10.1016%252fj.ymthe.2005.08.016&partnerID=40&md5=072f61e82dfb510bd32670dabfc72a90

22.

Paritsky M, Raz R, Zakay-Rones Z, Flatau E. Incidence of influenza among patients admitted to the Department of Internal Medicine during the winter season. Harefuah [Internet]. 2005;144(10):689–91. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-28444439555&partnerID=40&md5=d3b8787ddb28638e66db47dfde737fa8

23.

Weiss EI, Houri-Haddad Y, Greenbaum E, Hochman N, Ofek I, Zakay-Rones Z. Cranberry juice constituents affect influenza virus adhesion and infectivity. Antiviral Research [Internet]. 2005;66(1):9–12. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-15244349259&doi=10.1016%252fj.antiviral.2004.12.011&partnerID=40&md5=e2ef1c095320cfa70899a3ef97f6193b

24.

Wolf DG, Rekhtman D, Kerem E, Hay A, Mador N, Greenbaum E, et al. A summer outbreak of influenza A virus infection among young children. Clinical Infectious Diseases [Internet]. 2004;39(4):595–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-4344641324&doi=10.1086%252f422457&partnerID=40&md5=371e4f713f4a620b9358e5568620c736

25.

Greenbaum E, Engelhard D, Levy R, Schlezinger M, Morag A, Zakay-Rones Z. Mucosal (SIgA) and serum (IgG) immunologic responses in young adults following intranasal administration of one or two doses of inactivated, trivalent anti-influenza vaccine. Vaccine [Internet]. 2004;22(20):2566–77. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-2942558585&doi=10.1016%252fj.vaccine.2003.12.018&partnerID=40&md5=4d9063bbe64edf5297ffce99b13424ec

26.

Zakay-Rones Z, Thom E, Wollan T, Wadstein J. Randomized study of the efficacy and safety of oral elderberry extract in the treatment of influenza A and B virus infections. Journal of International Medical Research [Internet]. 2004;32(2):132–40. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-1642569220&doi=10.1177%252f147323000403200205&partnerID=40&md5=37b62fd87eb05219ebc631973f590a4b

27.

Greenbaum E, Nir-Paz R, Linton DM, Ben-Hur T, Meirovitz A, Zakay-Rones Z. Severe influenza infection in a chronic hepatitis C carrier: Failure of protective serum HI antibodies after IM vaccination. Journal of Clinical Virology [Internet]. 2004;29(1):23–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0348111361&doi=10.1016%2fS1386-6532%2803%2900194-X&partnerID=40&md5=5e1bcc7df6e55dd1cbeb162865500554

28.

Wolf DG, Zakay-Rones Z, Fadeela A, Greenberg D, Dagan R. High Seroprevalence of Human Metapneumovirus among Young Children in Israel. Journal of Infectious Diseases [Internet]. 2003;188(12):1865–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0347950956&doi=10.1086%252f380100&partnerID=40&md5=34dadb8e01ee67fb045a2e940d6bdb73

29.

Bronstein-Sitton N, Cohen-Daniel L, Vaknin I, Ezernitchi AV, Leshem B, Halabi A, et al. Sustained exposure to bacterial antigen induces interferon-γ-dependent T cell receptor ζ down-regulation and impaired T cell function. Nature Immunology [Internet]. 2003;4(10):957–64. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0142070778&doi=10.1038%252fni975&partnerID=40&md5=502c0360839ee5ac30106de6d32f49c0

30.

Ben-Yehuda A, Joseph A, Barenholz Y, Zeira E, Even-Chen S, Louria-Hayon I, et al. Immunogenicity and safety of a novel IL-2-supplemented liposomal influenza vaccine (INFLUSOME-VAC) in nursing-home residents. Vaccine [Internet]. 2003;21(23):3169–78. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-12444343718&doi=10.1016%2fS0264-410X%2803%2900251-2&partnerID=40&md5=f71050868fd07b0d7ca35671ae3276f9

31.

Ben-Yehuda A, Joseph A, Zeira E, Even-Chen S, Louria-Hayon I, Babai I, et al. Immunogenicity and safety of a novel liposomal influenza subunit vaccine (INFLUSOME-VAC) in young adults. Journal of Medical Virology [Internet]. 2003;69(4):560–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037399598&doi=10.1002%252fjmv.10345&partnerID=40&md5=00af83cd528f828f175a97ded69ecfc0

32.

Muszkat M, Greenbaum E, Ben-Yehuda A, Oster M, Yeu’l E, Heimann S, et al. Local and systemic immune response in nursing-home elderly following intranasal or intramuscular immunization with inactivated influenza vaccine. Vaccine [Internet]. 2003;21(11–12):1180–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037424106&doi=10.1016%2fS0264-410X%2802%2900481-4&partnerID=40&md5=a9ab76b8d9220e946306494895cfdad3

33.

Muszkat M, Friedman G, Dannenberg HD, Greenbaum E, Lipo M, Heymann Y, et al. Response to influenza vaccination in community and in nursing home residing elderly: Relation to clinical factors. Experimental Gerontology [Internet]. 2003;38(10):1199–203. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0142217355&doi=10.1016%252fj.exger.2003.07.004&partnerID=40&md5=233a60ad09538a2daab8f44fbd496bb6

34.

Joseph A, Louria-Hayon I, Plis-Finarov A, Zeira E, Zakay-Rones Z, Raz E, et al. Liposomal immunostimulatory DNA sequence (ISS-ODN): An efficient parenteral and mucosal adjuvant for influenza and hepatitis B vaccines. Vaccine [Internet]. 2002;20(27–28):3342–54. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037056027&doi=10.1016%2fS0264-410X%2802%2900295-5&partnerID=40&md5=255f7637aef4f2fbeed63f5dbc9be14d

35.

Kiderman A, Furst AL, Miller T, Schmidt-Afek N, Morag A, Zakay-Rones Z. How successfully do general practitioners diagnose herpetic gingivo-stomatitis clinically? British Journal of General Practice [Internet]. 2002;52(479):481–2. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036264717&partnerID=40&md5=57cd1e10b7c6f6c88ba63816a917392d

36.

Greenbaum E, Furst A, Kiderman A, Stewart B, Levy R, Schlesinger M, et al. Mucosal [SIgA] and serum [IgG] immunologic responses in the community after a single intra-nasal immunization with a new inactivated trivalent influenza vaccine. Vaccine [Internet]. 2002;20(7–8):1232–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0037081380&doi=10.1016%2fS0264-410X%2801%2900396-6&partnerID=40&md5=a13759083676c46427805d5461ab4484

37.

Isacsohn M, Smetana Z, Rones ZZ, Raveh D, Diamant Y, Samueloff A, et al. A sero-epidemiological study of herpes virus type 1 and 2 infection in Israel. Journal of Clinical Virology [Internet]. 2002;24(1–2):85–92. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036137305&doi=10.1016%2fS1386-6532%2801%2900233-5&partnerID=40&md5=340006bb96e80584a172e0d2e778ceab

38.

Babai I, Barenholz Y, Zakay-Rones Z, Greenbaum E, Samira S, Hayon I, et al. A novel liposomal influenza vaccine (INFLUSOME-VAC) containing hemagglutinin-neuraminidase and IL-2 or GM-CSF induces protective anti-neuraminidase antibodies cross-reacting with a wide spectrum of influenza A viral strains. Vaccine [Internet]. 2001;20(3–4):505–15. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035851359&doi=10.1016%2fS0264-410X%2801%2900326-7&partnerID=40&md5=e1349eb55a0ab5e43387000c292551e7

39.

Greenbaum E, Furst A, Kiderman A, Stewart B, Levy R, Schlesinger M, et al. Area under the viraemia curve versus absolute viral load: Utility for predicting symptomatic cytomegalovirus infections in kidney transplant patients. Journal of Medical Virology [Internet]. 2001;65(1):85–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034906280&doi=10.1002%252fjmv.2005&partnerID=40&md5=dbdae6df7045247245719eeaafd3f58e

40.

Van Slooten ML, Hayon I, Babai I, Zakay-Rones Z, Wagner E, Storm G, et al. Immunoadjuvant activity of interferon-γ-liposomes co-administered with influenza vaccines. Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids [Internet]. 2001;1531(1–2):99–110. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035970710&doi=10.1016%2fS1388-1981%2801%2900092-0&partnerID=40&md5=1731dd0e36b39d319471527d0d4259f3

41.

Heling I, Morag-Hezroni M, Marva E, Hochman N, Zakay-Rones Z, Morag A. Is herpes simplex virus associated with pulp/periapical inflammation? Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics [Internet]. 2001;91(3):359–61. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035289910&doi=10.1067%252fmoe.2001.113162&partnerID=40&md5=0b11f97e7c2b704c3aaa0d58889790cd

42.

Kiderman A, Furst A, Stewart B, Greenbaum E, Morag A, Zakay-Rones Z. A double-blind trial of a new inactivated, trivalent, intra-nasal anti-influenza vaccine in general practice: Relationship between immunogenicity and respiratory morbidity over the winter of 1997-98. Journal of Clinical Virology [Internet]. 2001;20(3):155–61. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035141627&doi=10.1016%2fS1386-6532%2800%2900175-X&partnerID=40&md5=548b1746095a4b299eee15d463b7db37

43.

Muszkat M, Ben Yehuda A, Schein MH, Friedlander Y, Naveh P, Greenbaum E, et al. Local and systemic immune response in community-dwelling elderly after intranasal or intramuscular immunization with inactivated influenza vaccine. Journal of Medical Virology [Internet]. 2000;61(1):100–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034085917&doi=10.1002%2f%28SICI%291096-9071%28200005%2961%3a1%3c100%3a%3aAID-JMV16%3e3.0.CO%3b2-5&partnerID=40&md5=55cb2499ae772947dc05de246fd11d23

44.

Muszkat M, Friedman G, Schein MH, Naveh P, Greenbaum E, Schlesinger M, et al. Local SIgA response following administration of a novel intranasal inactivated influenza virus vaccine in community residing elderly. Vaccine [Internet]. 2000;18(16):1696–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033951397&doi=10.1016%2fS0264-410X%2899%2900509-5&partnerID=40&md5=365811ca866f235ce0404317feb3c051

45.

Babai I, Samira S, Barenholz Y, Zakay-Rones Z, Kedar E. A novel influenza subunit vaccine composed of liposome-encapsulated haemagglutinin/neuraminidase and IL-2 or GM-CSF. II. Induction of TH1 and TH2 responses in mice. Vaccine [Internet]. 1999;17(9–10):1239–50. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033525805&doi=10.1016%2fS0264-410X%2898%2900347-8&partnerID=40&md5=d47d6b26c2618022295c6c8c2f811ccb

46.

Babai I, Samira S, Barenholz Y, Zakay-Rones Z, Kedar E. A novel influenza subunit vaccine composed of liposome-encapsulated haemagglutinin/neuraminidase and IL-2 or GM-CSF. I. Vaccine characterization and efficacy studies in mice. Vaccine [Internet]. 1999;17(9–10):1223–38. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033525602&doi=10.1016%2fS0264-410X%2898%2900346-6&partnerID=40&md5=e093a0377aa139bd4483fe34d9b938d3

47.

Morecki S, Nagler A, Zakay-Rones Z, Schlesinger M, Lubina-Salomon A, Pugatsch T, et al. Tumorigenicity and immunogenicity in a murine model of B-cell leukemia/lymphoma (BCL1). Leukemia Research [Internet]. 1998;22(9):831–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032171597&doi=10.1016%2fS0145-2126%2898%2900080-0&partnerID=40&md5=8265b927d878ff40135493c5335ed53f

48.

Ben-Yehuda A, Danenberg HD, Zakay-Rones Z, Gross DJ, Friedman G. The influence of sequential annual vaccination and of DHEA administration on the efficacy of the immune response to influenza vaccine in the elderly. Mechanisms of Ageing and Development [Internet]. 1998;102(2–3):299–306. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032524998&doi=10.1016%2fS0047-6374%2898%2900017-7&partnerID=40&md5=650ed0b020fb5e484f47f737a78b851b

49.

Samina I, Zakay-Rones Z, Peleg BA. Homologous and heterologous antibody response of cattle and sheep after vaccination with foot and mouth disease and influenza viruses. Vaccine [Internet]. 1998;16(6):551–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032053987&doi=10.1016%2fS0264-410X%2897%2900243-0&partnerID=40&md5=7480a00b789b8be9b73fd3d44d6dc3e2

50.

Hochman N, Zakay-Rones Z, Shohat H, Ever-Hadani P, Ehrlich J, Schlesinger M, et al. Antibodies to cytomegalo and Epstein-Barr viruses in human saliva and gingival fluid. New Microbiologica [Internet]. 1998;21(2):131–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032044399&partnerID=40&md5=5d48c54e0a870e5af52b9aeb46faf554

51.

Samina I, Zakay-Rones Z, Weller JI, Peleg BA. Host factors affecting the homologous and heterologous immune response of cattle to FMDV: Genetic background, age, virus strains and route of administration. Vaccine [Internet]. 1998;16(4):335–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032008091&doi=10.1016%2fS0264-410X%2897%2900212-0&partnerID=40&md5=bd77cded0f960214fb3d3abc4057a0f7

52.

Greenbaum E, Morag A, Zakay-Rones Z. Isolation of influenza C virus during an outbreak of influenza A and B viruses. Journal of Clinical Microbiology [Internet]. 1998;36(5):1441–2. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0031978379&doi=10.1128%252fjcm.36.5.1441-1442.1998&partnerID=40&md5=f04cb0a6b3cb47bad2754231aafeb99b

53.

Danenberg HD, Ben-Yehuda A, Zakay-Rones Z, Gross DJ, Friedman G. Dehydroepiandrosterone treatment is not beneficial to the immune response to influenza in elderly subjects. Journal of Clinical Endocrinology and Metabolism [Internet]. 1997;82(9):2911–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0030986512&doi=10.1210%252fjc.82.9.2911&partnerID=40&md5=da97b37e8df2407401c2fc89108008ff

54.

Abdul-Hai A, Ben-Yehuda A, Weiss L, Friedman G, Zakay-Rones Z, Slavin S, et al. Interleukin-7-enhanced cytotoxic T lymphocyte activity after viral infection in marrow transplanted mice. Bone Marrow Transplantation [Internet]. 1997;19(6):539–43. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0030894382&doi=10.1038%252fsj.bmt.1700706&partnerID=40&md5=b182e742a9eda39d2532282b4dd2c3cc

55.

Admon D, Engelhard D, Strauss N, Goldman N, Zakay-Rones Z. Antibody response to influenza immunization in patients after heart transplantation. Vaccine [Internet]. 1997;15(14):1518–22. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0030803740&doi=10.1016%2fS0264-410X%2897%2900193-X&partnerID=40&md5=fd9eb1b1065b22e51317f38d8a1a5287

56.

Magdassi S, Toledano O, Zakay-Rones Z. Solubilization in colloidal immunoclusters. Journal of Colloid and Interface Science [Internet]. 1996;184(2):360–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0030602303&doi=10.1006%252fjcis.1996.0630&partnerID=40&md5=2a2c7e2b4ca46facb0eac91a112e7464

57.

Mumcuoglu M, Zakay-Rones Z, Weiss L, Slavin S. Enhancement of primary and secondary responses to sheep red blood cells and influenza virus in BALB/c mice by recombinant human interleukin-2. Experimental Hematology [Internet]. 1996;24(13):1516–20. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029955504&partnerID=40&md5=992d06f6d084e035b221dd578530fd82

58.

Bar-Eli N, Giloh H, Schlesinger M, Zakay-Rones Z. Preferential cytotoxic effect of Newcastle disease virus on lymphoma cells. Journal of Cancer Research and Clinical Oncology [Internet]. 1996;122(7):409–15. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029927813&doi=10.1007%252fBF01212880&partnerID=40&md5=3332e92f00129d399965e87a5d18cce7

59.

Zakay-Rones Z, Varsano N, Zlotnik M, Manor O, Regev L, Schlesinger M, et al. Inhibition of Several Strains of Influenza Virus in Vitro and Reduction of Symptoms by an Elderberry Extract (Sambucus nigra L.) during an Outbreak of Influenza B Panama. Journal of Alternative and Complementary Medicine [Internet]. 1995;1(4):361–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029420438&doi=10.1089%252facm.1995.1.361&partnerID=40&md5=80c12ba97ba13179698ab1cf1a73f6c6

60.

Tzadok-David Y, Metzkin-Eizenberg M, Zakay-Rones Z. The effect of a mesogenic and a lentogenic Newcastle disease virus strain on Burkitt lymphoma Daudi cells. Journal of Cancer Research and Clinical Oncology [Internet]. 1995;121(3):169–74. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028948716&doi=10.1007%252fBF01198099&partnerID=40&md5=1e4c81e9b0139e2e79ee40c2550e4c1f

61.

DANENBERG HD, BEN‐YEHUDA A, ZAKAY‐RONES Z, FRIEDMAN G. Dehydroepiandrosterone Enhances Influenza Immunization in Aged Mice. Annals of the New York Academy of Sciences [Internet]. 1995;774(1):297–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029551971&doi=10.1111%252fj.1749-6632.1995.tb17391.x-i1&partnerID=40&md5=7c68b55c5dafe60da459c8b5def02775

62.

Morag A, Abed Y, Schoub BD, Lifshitz A, Zakay-Rones Z. Enteric viral infections in Gaza children - Incidence and associated factors and phenomena. Israel Journal of Medical Sciences [Internet]. 1995;31(1):49–53. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028896882&partnerID=40&md5=d2490df9c6cc80a5a372d586c14add1b

63.

Danenberg HD, Ben-Yehuda A, Zakay-Rones Z, Friedman G. Dehydroepiandrosterone (DHEA) treatment reverses the impaired immune response of old mice to influenza vaccination and protects from influenza infection. Vaccine [Internet]. 1995;13(15):1445–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028804990&doi=10.1016%2f0264-410X%2895%2900063-7&partnerID=40&md5=52855e48179f0ef497cf227b0e3b824b

64.

Magdassi S, Toledano O, Zakay-Rhones Z. Formation of novel colloidal immunoclusters by surface active antibodies. Journal of Colloid And Interface Science [Internet]. 1995;175(2):435–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0001310127&doi=10.1006%252fjcis.1995.1473&partnerID=40&md5=e8a6c58d75c6c0a9d46e19195673cecd

65.

Hochman N, Mizrachi E, Ehrlich J, Morag A, Schlesinger M, Ever-Hadani P, et al. Prevalence of viral antibodies in gingival crevicular fluid. The new microbiologica : official journal of the Italian Society for Medical, Odontoiatric, and Clinical Microbiology (SIMMOC) [Internet]. 1994;17(2):75–84. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028414295&partnerID=40&md5=0b19ca3769acffe69c6805f03131ec2f

66.

Engelhard D, Nagler A, Hardan I, Morag A, Aker M, Baciu H, et al. Antibody response to a two-dose regimen of influenza vaccine in allogeneic T cell-depleted and autologous BMT recipients. Bone Marrow Transplantation [Internet]. 1993;11(1):1–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0027465332&partnerID=40&md5=aa9682d2fc3eacce3216c3ad2bc0c5fa

67.

Amit R, Morag A, Ravid Z, Hochman N, Ehrlich J, Zakay-Rones Z. Detection of herpes simplex virus in gingival tissue. Journal of periodontology [Internet]. 1992;63(6):502–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026876930&doi=10.1902%252fjop.1992.63.6.502&partnerID=40&md5=f1e897ee206ae94ff1c099f4d4ffe5eb

68.

Leshem B, Dekel R, Bercovier H, Tchakirov R, Polacheck I, Zakay-Rones Z, et al. Cytokine-induced resistance to microbial infections in normal, immunosuppressed and bone marrow transplanted mice. Bone Marrow Transplantation [Internet]. 1992;9(6):471–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026747764&partnerID=40&md5=e6fc3f8d6f6a9c8e7fe6e5cfb291e281

69.

Grunwald-Beard L, Gamliel H, Parag G, Vedantham S, Zakay-Rones Z. Killing of burkitt-lymphoma-derived daudi cells by ultraviolet-inactivated vaccinia virus. Journal of Cancer Research and Clinical Oncology [Internet]. 1991;117(6):561–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025933244&doi=10.1007%252fBF01613289&partnerID=40&md5=eaed5ffe7aa4e4b4278199f768390f01

70.

Huminer D, Pitlik SD, Katz A, Metzker A, David M, Zimran A, et al. Untoward effects of gas masks during Persian Gulf war. New England Journal of Medicine [Internet]. 1991;325(8):582–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025777097&doi=10.1056%252fNEJM199108223250812&partnerID=40&md5=875775b3a303de3d6d6470399d60a243

71.

Weil-Hillman G, Levi R, Zakay-Rones Z. Increase in concanavalin A cap formation on lymphoma cells following interaction with inactive influenza viruses. Acta virologica [Internet]. 1991;35(3):238–46. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026161640&partnerID=40&md5=fb349b67eb5d96eb25aa2961d95e36ce

72.

Mumcuoglu M, Zakay-Rones Z, Weiss L, Slavin S. The effect of total or partial T lymphocyte depletion on susceptibility to influenza virus infection and development of antiviral immunity in lethally irradiated mice reconstituted with immune syngeneic bone marrow grafts. Bone Marrow Transplantation [Internet]. 1991;7(3):217–20. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0026026037&partnerID=40&md5=dce9890680a0b6f7a3e834f2be2207e3

73.

Shoham J, Hirsch R, Zakay-Rones Z, Osband ME, Brennert HJ. Augmentation of tumor cell immunogenicity by viruses - an approach to specific immunotherapy of cancer1. Natural Immunity and Cell Growth Regulation [Internet]. 1990;9(3):165–72. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0025076694&partnerID=40&md5=99d0b563639878b30c8a8141b9804278

74.

Shlomi Y, Zakay-Rones Z. Sensitivity of Burkitt lymphoma Daudi cells to inactive influenza virus. Journal of Cancer Research and Clinical Oncology [Internet]. 1989;115(3):308. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-34249967651&doi=10.1007%252fBF00391708&partnerID=40&md5=7a93d6a4e798ee790127c538f51c36fd

75.

Shlomi Y, Zakay-Rones Z. Sensitivity of Burkitt lymphoma Daudi cells to inactive influenza virus. Journal of Cancer Research and Clinical Oncology [Internet]. 1989;115(1):61–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024602731&doi=10.1007%252fBF00391601&partnerID=40&md5=8ea642d24e5e5381b80fb6cd28b43fd5

76.

Zakay‐Rones Z, Meijer A, Morag A. Prevalence of antibody to current influenza virus strains in adolescents. Journal of Medical Virology [Internet]. 1989;29(4):308–10. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024841382&doi=10.1002%252fjmv.1890290416&partnerID=40&md5=b4df681e046430db2fc08af3a12dea60

77.

Hochman N, Ehrlich J, Zakay-Rones Z. Oral cavity herpes simplex virus–a risk factor to dental personnel and patients. An overview. Israel journal of dental sciences [Internet]. 1989;2(3):158–61. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024751171&partnerID=40&md5=1d25ddd0c4546cda3ae1271a120decca

78.

Slosaris M, Levy B, Katz E, Levy R, Zakay-Rones Z. Elevated virulence of Newcastle disease virus strains following serial passages in kidney cells in vitro. Avian diseases [Internet]. 1989;33(2):248–53. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0024651643&doi=10.2307%252f1590839&partnerID=40&md5=211eeb65784416178b0f765b646d7494

79.

Keren G, Segev S, Morag A, Zakay‐Rones Z, Barzilai A, Rubinstein E. Failure of influenza vaccination in the aged. Journal of Medical Virology [Internet]. 1988;25(1):85–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023924299&doi=10.1002%252fjmv.1890250112&partnerID=40&md5=c9872171d16ad07a4b3a76d2501a840c

80.

Meijer A, Zakay‐Rones Z, Morag A. Post‐influenzal psychiatric disorder in adolescents. Acta Psychiatrica Scandinavica [Internet]. 1988;78(2):176–81. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023688644&doi=10.1111%252fj.1600-0447.1988.tb06319.x&partnerID=40&md5=4864c6336a4c0092e8df6ca0355a14a3

81.

Mumcuoglu M, Zakay-Rones Z, Parag G, Weiss L, Slavin S. The effect of T lymphocyte depletion on susceptibility to influenza virus infection and development of anti-viral immunity in lethally irradiated mice reconstituted with syngeneic bone marrow grafts. Bone Marrow Transplantation [Internet]. 1987;2(4):403–12. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023578541&partnerID=40&md5=16ebc136c15490068b13611f9f21d02c

82.

Weil-Hillman G, Zakay-Rones Z. Inhibition of Daudi tumor formation by inactive influenza virus in a nude mouse model. Cancer Journal [Internet]. 1987;1(5):208–13. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023119287&partnerID=40&md5=6330a5135b91eb4866d12cc024fd9edc

83.

Zakay-Rones Z, Ehrlich J, Hochman N, Levy R. Hypothesis: the gingival tissue as a reservoir for herpes simplex virus. Microbiologica [Internet]. 1986;9(3):367–71. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0022749865&partnerID=40&md5=8208faf54d0948ae29f0cbe06347d0e0

84.

Weil-Hillman G, Zakay-Rones Z. ARREST OF DAUDI CELL GROWTH BY INACTIVE INFLUENZA VIRUS IN-VITRO. Scanning Electron Microscopy [Internet]. 1985;v:1679–86. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0022270456&partnerID=40&md5=d5b6c5e354c80a477664477df430a010

85.

Weil-Hillman G, Gamliel H, Friedmann A, Zakay-Rones Z. VISUALIZATION OF THE FATE OF INACTIVE INFLUENZA VIRUSES IN DAUDI CELLS BY ELECTRON MICROSCOPY. Scanning Electron Microscopy [Internet]. 1985;v:1687–93. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0022270451&partnerID=40&md5=ffe59fe671335de76cf64220b8a4681a

86.

Shapira‐Nahor O, Zakay‐Rones Z. Local and peripheral cell‐mediated immune response to influenza virus in mice. Journal of Medical Virology [Internet]. 1985;15(1):81–91. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021930736&doi=10.1002%252fjmv.1890150111&partnerID=40&md5=956a38fe51fc7dfa2a5560f4bc85f869

87.

Taya M, Morag A, Abramowitz A, Goldblum N, Zakay-Rones Z. Prevalence of antibodies to respiratory syncytial virus in various populations in Israel. Israel Journal of Medical Sciences [Internet]. 1984;20(12):1146–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0021715129&partnerID=40&md5=bae00fedf90c6fce549dea0072d33a75

88.

Morag A, Levy R, Weil G, Zakay‐Rones Z. Clinical and serological response in humans following immunization with gripax influenza vaccine. Journal of Medical Virology [Internet]. 1983;11(1):67–75. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020698395&doi=10.1002%252fjmv.1890110109&partnerID=40&md5=f28c6270f35009a3c16aaac7fd0b1027

89.

Rones Y, Hochman N, Ehrlich J, Zakay Rones Z. Sensitivity of oral tissues to herpes simplex virus in vitro. Journal of Periodontology [Internet]. 1983;54(2):91–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020629009&doi=10.1902%252fjop.1983.54.2.91&partnerID=40&md5=e473531fc6f26c678b8bacaae14aae2e

90.

Levy R, Zakay‐Rones Z. Preparation and evaluation of a zonal purified influenza vaccine gripax. Journal of Medical Virology [Internet]. 1982;10(4):265–72. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020410744&doi=10.1002%252fjmv.1890100406&partnerID=40&md5=13b7989215b97412833dd5064594c75d

91.

Zakay Rones Z, Hochman N, Rones Y. Immunological response to herpes simplex virus in human gingival fluid. Journal of Periodontology [Internet]. 1982;53(1):42–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0020038548&doi=10.1902%252fjop.1982.53.1.42&partnerID=40&md5=f628f569bfd06783bcf791165bc7eadf

92.

Shapira‐Nahor O, Morag A, Levy R, Zakay‐Rones Z. Cellular response in humans following vaccination with gripax influenza virus. Journal of Medical Virology [Internet]. 1982;10(1):75–80. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019915423&doi=10.1002%252fjmv.1890100110&partnerID=40&md5=44616f0abe98c24b34b008b0bf5736ff

93.

Hochman N, Rones Y, Ehrlich J, Levy R, Zakay-Rones Z. Antibodies to herpes simplex virus in human gingival fluid. Journal of Periodontology [Internet]. 1981;52(6):324–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019862888&doi=10.1902%252fjop.1981.52.6.324&partnerID=40&md5=aeb8524beb2fde6f22e3cb8c877656e1

94.

Zakay-Rones Z, Margalith E, Levy R, Katz E. A sensitive plaque inhibition technique for assay of antibodies to influenza virus: Use to detect previous antigenic priming with influenza viruses. Journal of Virological Methods [Internet]. 1980;1(6):355–60. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0019192279&doi=10.1016%2f0166-0934%2880%2990053-1&partnerID=40&md5=69ba041796cfb6ef237be20f800a2a76

95.

Zakay-Rones Z, Hadas O, Levy R. Modulation of the lung local immune response by systemic immunization. Medical Microbiology and Immunology [Internet]. 1978;166(1–4):43–50. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0018161582&doi=10.1007%252fBF02121133&partnerID=40&md5=ff7fdbabc6fac1111e391689b16da9d3

96.

Spira G, Silvian I, Zakay Rones Z. Iodination of Newcastle disease virus envelope proteins with lactoperoxidase. Israel Journal of Medical Sciences [Internet]. 1977;13(1):76–80. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017367943&partnerID=40&md5=63acacdc9ed090f7efff934f33652d6f

97.

Spira G, Silvian I, Zakay Rones Z. Radioimmunoassay for detection of antigen and antibodies to Newcastle disease virus. JIMMUNOL [Internet]. 1976;116(4):1089–92. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0017105502&partnerID=40&md5=b628d0c9fc2626bdc05d46de425bdcd4

98.

Levy R, Spira G, Zakay-Rones Z. Newcastle disease virus pathogenesis in the respiratory tract of local or systemic immunized chickens. Avian diseases [Internet]. 1975;19(4):700–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0016566239&doi=10.2307%252f1589183&partnerID=40&md5=2639c8ac40f7fe9f44772147e46b8ffe

99.

Zakay-Rones Z, Spira G, Levy R. Local antibody formation in the brain of chickens. Archiv für die gesamte Virusforschung [Internet]. 1974;45(3):290–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-34250414393&doi=10.1007%252fBF01249693&partnerID=40&md5=409e32a5959647b895bf03d780a54990

100.

Zakay Rones Z, Levy R. Immunologic response of chicks to inactivated Newcastle disease virus. Avian Diseases [Internet]. 1973;17(2):450–2. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015875027&doi=10.2307%252f1589231&partnerID=40&md5=6440a6e89e1e24f24fbc324ab03f1fa7

101.

Levy R, Zakay Rones Z. Immunization of chickens with an inactivated oil adjuvant Newcastle disease virus vaccine. Avian Diseases [Internet]. 1973;17(3):598–604. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015792160&doi=10.2307%252f1589160&partnerID=40&md5=2f7e1f8900f37899d338d1d50f8a8f3a

102.

Zakay Rones Z, Ehrlich J, Hochman N, Levy R. The sulcular epithelium as a reservoir for Herpes Simplex Virus in man. Journal of Periodontology [Internet]. 1973;44(12):779–81. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015748430&doi=10.1902%252fjop.1973.44.12.779&partnerID=40&md5=d714bfe4327c61c655236254ef7c5bd4

103.

Maythar B, Zakay-Rones Z. Local and humoral chlamydial antibodies in trachoma patients of different age groups. Investigative ophthalmology [Internet]. 1972;11(8):651–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015384973&partnerID=40&md5=dbd1082a6619ae8296ce65e343b2c61c

104.

Zakay-Rones Z, Levy R, Spira G. Secretory Newcastle disease virus antibodies from chicken respiratory tract. Journal of Immunology [Internet]. 1972;109(2):311–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015384140&partnerID=40&md5=0c7d4fc31c84d137a45f8c1041a525cb

105.

Zakay-Rones Z, Levy R, Maythar B. Local antibodies to trachoma agent. Israel Journal of Medical Sciences [Internet]. 1972;8(8):1130–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015377389&partnerID=40&md5=0d755de1e1677c2a39edcfc188e39f91

106.

Becker Y, Asher Y, Zakay-Rones Z. Congocidine and distamycin A, antipoxvirus antibiotics. Antimicrobial agents and chemotherapy [Internet]. 1972;1(6):483–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015347434&doi=10.1128%252fAAC.1.6.483&partnerID=40&md5=30c7f56ef063ac456a5b163d8cfc6b9e

107.

Zakay-Rones Z, Spira G, Levy R. Local immunologic response to immunization with inactivated Newcastle disease virus. Journal of Immunology [Internet]. 1971;107(4):1180–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0015141529&partnerID=40&md5=734fb7e2c358e5182da2e9ff1ec93c12

108.

Becker Y, Asher Y, Himmel N, Zakay-Rones Z. Anti-trachoma activity of rifampicin and rifamycin SV derivatives. Nature [Internet]. 1970;225(5231):454–5. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0014968934&doi=10.1038%252f225454a0&partnerID=40&md5=73ba07d369da84bfb9840540e09ab4df

109.

Zakay-Rones Z, Becker Y. Anti-poxvirus activity of rifampicin associated with hydrazone side chain. Nature [Internet]. 1970;226(5251):1162–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0014956242&doi=10.1038%252f2261162a0&partnerID=40&md5=57de5c89e86766b6bb4114bbb7d66c6a

110.

Becker Y, Zakay-Rones Z. Rifampicin - A new antitrachoma drug. Nature [Internet]. 1969;222(5196):851–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0014697108&doi=10.1038%252f222851a0&partnerID=40&md5=d1b512dca960b8d2985d7a8af0be0688

111.

Becker Y, Asher Y, Himmel N, Zakay-Rones Z, Maythar B. Rifampicin poxvirus and trachoma agent: Rifampicin Inhibition of trachoma agent in vivo. Nature [Internet]. 1969;224(5214):33–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0014663881&doi=10.1038%252f224033a0&partnerID=40&md5=645dc378fcf93606327c33f8dff1fd36

112.

Zakay-Rones Z, Levi R, Maythar B, Becker Y. The antibody response of guinea pigs to topical and intramuscular administration of trachoma antigens. Journal of Immunology [Internet]. 1969;102(5):1290–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0014511060&partnerID=40&md5=4d0188fa126659a5a27724330da3bdcd

113.

Becker Y, Hochberg E, Zakay-Rones Z. Interaction of trachoma elementary bodies with host cells. Israel Journal of Medical Sciences [Internet]. 1969;5(1):121–4. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0014462348&partnerID=40&md5=e769bf46d4a61929421f640ad9bea0f1

114.

Zakay-Rones Z, Katzenelson E, Levy R. Hemagglutinin of trachoma agent. Israel Journal of Medical Sciences [Internet]. 1968;4(2):305–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0014263054&partnerID=40&md5=a97f0972647e5bb4b776d6889d917a35

115.

Barron AL, Zakay-Roness Z, Bernkopf H. Hemagglutination of Chicken Erythrocytes by the Agent of Psittacosis. Proceedings of the Society for Experimental Biology and Medicine [Internet]. 1965;119(2):377–81. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-78651172554&doi=10.3181%252f00379727-119-30186&partnerID=40&md5=86e73a5201bdba926b911e3f7c54c53b

116.

Zakay-Roness Z, Bernkopf H. Effect of Active and Ultraviolet-irradiated Inactive Vaccinia Virus on the Development of Shay Leukemia in Rats. Cancer Research [Internet]. 1964;24:373–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-8944257838&partnerID=40&md5=a393b9770a6ec3ab8ce57573a37e5488

117.

ZAKAY-RONESS Z, ROSIN A, BERNKOFF H. A study on toxic effect of vaccinia virus in mice with special reference to hematological changes. Journal of immunology (Baltimore, Md : 1950) [Internet]. 1962;88:184–90. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84936414732&partnerID=40&md5=741c0ea7a1679f58a4721badc7329819