{"title":"[体外培养牙组织中基底膜重构的超微结构方面]。","authors":"J M Meyer, V Karcher-Djuricic, M Osman, J V Ruch","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Separation of the enamel organ and pulp of mice tooth germs by trypsin removed the basal lamina. Within 18 hours in cultivated reassociations of enamel organ and pulp, a new lamina was deposited. When the epithelial component was cultivated alone, no basal lamina formed.</p>","PeriodicalId":10544,"journal":{"name":"Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles","volume":"287 4","pages":"329-31"},"PeriodicalIF":0.0000,"publicationDate":"1978-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Ultrastructural aspects of reconstitution of the basal membrane in associations of dental components cultured in vitro].\",\"authors\":\"J M Meyer, V Karcher-Djuricic, M Osman, J V Ruch\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Separation of the enamel organ and pulp of mice tooth germs by trypsin removed the basal lamina. Within 18 hours in cultivated reassociations of enamel organ and pulp, a new lamina was deposited. When the epithelial component was cultivated alone, no basal lamina formed.</p>\",\"PeriodicalId\":10544,\"journal\":{\"name\":\"Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles\",\"volume\":\"287 4\",\"pages\":\"329-31\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1978-09-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Ultrastructural aspects of reconstitution of the basal membrane in associations of dental components cultured in vitro].
Separation of the enamel organ and pulp of mice tooth germs by trypsin removed the basal lamina. Within 18 hours in cultivated reassociations of enamel organ and pulp, a new lamina was deposited. When the epithelial component was cultivated alone, no basal lamina formed.