{"id":347,"date":"2016-01-04T20:38:55","date_gmt":"2016-01-04T20:38:55","guid":{"rendered":"https:\/\/nauka.meduniv.lviv.ua\/?page_id=347"},"modified":"2019-10-05T11:02:26","modified_gmt":"2019-10-05T08:02:26","slug":"top-10-najbilsh-tsytovanyh-statej-pratsiv","status":"publish","type":"page","link":"https:\/\/nauka.meduniv.lviv.ua\/?page_id=347","title":{"rendered":"\u0422\u041e\u041f-10 \u043d\u0430\u0439\u0431\u0456\u043b\u044c\u0448 \u0446\u0438\u0442\u043e\u0432\u0430\u043d\u0438\u0445 \u0441\u0442\u0430\u0442\u0435\u0439 \u043f\u0440\u0430\u0446\u0456\u0432\u043d\u0438\u043a\u0456\u0432 \u0423\u043d\u0456\u0432\u0435\u0440\u0441\u0438\u0442\u0435\u0442\u0443"},"content":{"rendered":"\n<style>\n      table, th, td {\nmargin-left: auto;\n    margin-right: auto;\n      padding: 10px;\n      border: 1px solid black; \n      border-collapse: collapse;\n      }\n<\/style>\n<table style=\"width: 900px; height: 1224px; blackmargin-left: auto; margin-right: auto;\">\n<tbody>\n<tr style=\"height: 64px;\">\n<td style=\"width: 35px; text-align: center; height: 64px;\"><strong>\u2116<\/strong><\/td>\n<td style=\"width: 474px; height: 64px;\">\n<p style=\"text-align: center;\"><strong>\u0421\u0442\u0430\u0442\u0442\u044f<\/strong><\/p>\n<\/td>\n<td style=\"width: 99px; text-align: center; height: 64px;\"><strong>\u041a\u0456\u043b\u044c\u043a\u0456\u0441\u0442\u044c \u0446\u0438\u0442\u0443\u0432\u0430\u043d\u044c<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 116px;\">\n<td style=\"width: 35px; text-align: center; height: 116px;\">1<\/td>\n<td style=\"width: 474px; height: 116px;\">Havrylyuk, Dmytro, et al. &#8220;Synthesis of novel thiazolone-based compounds containing pyrazoline moiety and&nbsp; valuation of their anticancer activity.&#8221; <em>European journal of medicinal chemistry<\/em>&nbsp;44.4 (2009): 1396-1404.<\/td>\n<td style=\"width: 99px; text-align: center; height: 116px;\"><strong>201<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 116px;\">\n<td style=\"width: 35px; text-align: center; height: 116px;\">2<\/td>\n<td style=\"width: 474px; height: 116px;\">Lesyk, R. B., and B. S. Zimenkovsky. &#8220;4-Thiazolidones: centenarian history, current status and perspectives for modern organic and medicinal chemistry.&#8221;&nbsp;<em>Current Organic Chemistry<\/em>&nbsp;8.16 (2004): 1547-1577.<\/td>\n<td style=\"width: 99px; text-align: center; height: 116px;\"><strong>186<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 116px;\">\n<td style=\"width: 35px; text-align: center; height: 116px;\">3<\/td>\n<td style=\"width: 474px; height: 116px;\">Havrylyuk, Dmytro, et al. &#8220;Synthesis and anticancer activity evaluation of 4-thiazolidinones containing benzothiazole moiety.&#8221;&nbsp;<em>European journal of medicinal chemistry<\/em>&nbsp;45.11 (2010): 5012-5021.<\/td>\n<td style=\"width: 99px; text-align: center; height: 116px;\"><strong>166<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 116px;\">\n<td style=\"width: 35px; text-align: center; height: 116px;\">4<\/td>\n<td style=\"width: 474px; height: 116px;\">Havrylyuk, Dmytro, et al. &#8220;Synthesis of new 4-thiazolidinone-, pyrazoline-, and isatin-based conjugates with promising antitumor activity.&#8221;&nbsp;<em>Journal of medicinal chemistry<\/em>&nbsp;55.20 (2012): 8630-8641.<\/td>\n<td style=\"width: 99px; text-align: center; height: 116px;\"><strong>134<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 116px;\">\n<td style=\"width: 35px; text-align: center; height: 116px;\">5<\/td>\n<td style=\"width: 474px; height: 116px;\">Lesyk, Roman, et al. &#8220;New 5-substituted thiazolo [3, 2-b][1, 2, 4] triazol-6-ones: synthesis and anticancer evaluation.&#8221;&nbsp;<em>European journal of medicinal chemistry<\/em>&nbsp;42.5 (2007): 641-648.<\/td>\n<td style=\"width: 99px; text-align: center; height: 116px;\"><strong>131<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 116px;\">\n<td style=\"width: 35px; text-align: center; height: 116px;\">6<\/td>\n<td style=\"width: 474px; height: 116px;\">Nadashkevich, O., et al. &#8220;A randomized unblinded trial of cyclophosphamide versus azathioprine in the treatment of systemic sclerosis.&#8221;&nbsp;<em>Clinical rheumatology<\/em>&nbsp;25.2 (2006): 205-212.<\/td>\n<td style=\"width: 99px; text-align: center; height: 116px;\"><strong>113<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 88px;\">\n<td style=\"width: 35px; text-align: center; height: 88px;\">7<\/td>\n<td style=\"width: 474px; height: 88px;\">Zayachkivska, O. S., et al. &#8220;Gastroprotective effects of flavonoids in plant extracts.&#8221;&nbsp;<em>Journal of Physiology and Pharmacology. Supplement<\/em>&nbsp;56.1 (2005): 219-231.<\/td>\n<td style=\"width: 99px; text-align: center; height: 88px;\"><strong>107<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 172px;\">\n<td style=\"width: 35px; text-align: center; height: 172px;\">8<\/td>\n<td style=\"width: 474px; height: 172px;\">O&#8217;Brien, Mary ER, et al. &#8220;Randomized phase III trial comparing single-agent paclitaxel Poliglumex (CT-2103, PPX) with single-agent gemcitabine or vinorelbine for the treatment of PS 2 patients with chemotherapy-naive advanced non-small cell lung cancer.&#8221;&nbsp;<em>Journal of Thoracic Oncology<\/em>&nbsp;3.7 (2008): 728-734.<\/td>\n<td style=\"width: 99px; text-align: center; height: 172px;\"><strong>106<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 88px;\">\n<td style=\"width: 35px; text-align: center; height: 88px;\">9<\/td>\n<td style=\"width: 474px; height: 88px;\">Feagan, Brian G., et al. &#8220;The role of centralized reading of endoscopy in a randomized controlled trial of mesalamine for ulcerative colitis.&#8221;&nbsp;<em>Gastroenterology<\/em>&nbsp;145.1 (2013): 149-157.<\/td>\n<td style=\"width: 99px; text-align: center; height: 88px;\"><strong>105<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 116px;\">\n<td style=\"width: 35px; text-align: center; height: 116px;\">10<\/td>\n<td style=\"width: 474px; height: 116px;\">Vynograd, N., I. Vynograd, and Z. Sosnowski. &#8220;A comparative multi-centre study of the efficacy of propolis, acyclovir and placebo in the treatment of genital herpes (HSV).&#8221;&nbsp;<em>Phytomedicine<\/em>&nbsp;7.1 (2000): 1-6.<\/td>\n<td style=\"width: 99px; text-align: center; height: 116px;\"><strong>96<\/strong><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n\n","protected":false},"excerpt":{"rendered":"<p>\u2116 \u0421\u0442\u0430\u0442\u0442\u044f \u041a\u0456\u043b\u044c\u043a\u0456\u0441\u0442\u044c \u0446\u0438\u0442\u0443\u0432\u0430\u043d\u044c 1 Havrylyuk, Dmytro, et al. &#8220;Synthesis of novel thiazolone-based compounds containing pyrazoline moiety and&nbsp; valuation of their anticancer activity.&#8221; European journal of medicinal chemistry&nbsp;44.4 (2009): 1396-1404. 201 2 Lesyk, R. B., and B. S. Zimenkovsky. &#8220;4-Thiazolidones:&hellip;&nbsp;<a href=\"https:\/\/nauka.meduniv.lviv.ua\/?page_id=347\" class=\"more-link\">Read More<\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"templates\/full-width.php","meta":{"footnotes":""},"featured_image_src":null,"_links":{"self":[{"href":"https:\/\/nauka.meduniv.lviv.ua\/index.php?rest_route=\/wp\/v2\/pages\/347"}],"collection":[{"href":"https:\/\/nauka.meduniv.lviv.ua\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/nauka.meduniv.lviv.ua\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/nauka.meduniv.lviv.ua\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/nauka.meduniv.lviv.ua\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=347"}],"version-history":[{"count":34,"href":"https:\/\/nauka.meduniv.lviv.ua\/index.php?rest_route=\/wp\/v2\/pages\/347\/revisions"}],"predecessor-version":[{"id":25296,"href":"https:\/\/nauka.meduniv.lviv.ua\/index.php?rest_route=\/wp\/v2\/pages\/347\/revisions\/25296"}],"wp:attachment":[{"href":"https:\/\/nauka.meduniv.lviv.ua\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=347"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}