Enhanced Tumor Homografts Following Pretreatment of Donor Mice.
Conclusion In 3 series of experiments employing 675 BALB/c, 108 C57BR/cd and 50 C57BL/6 mice, the first of double isografts of EO771 mammary carcinoma acquired an altered enhanced status comparable with that of the second of double isografts and each of the double isografts had 9 times the homotrans...
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| Veröffentlicht in: | Experimental biology and medicine (Maywood, N.J.) N.J.), 1959-04, Vol.100 (4), p.762-763 |
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| container_title | Experimental biology and medicine (Maywood, N.J.) |
| container_volume | 100 |
| creator | Casey, A. E. Casey, J. G. Hathaway, C. O. Dowling, E. A. |
| description | Conclusion
In 3 series of experiments employing 675 BALB/c, 108 C57BR/cd and 50 C57BL/6 mice, the first of double isografts of EO771 mammary carcinoma acquired an altered enhanced status comparable with that of the second of double isografts and each of the double isografts had 9 times the homotransplantability (24%) of single control isografts (2.7%). Within the conditions of the experiment neither size, nor age of the isograft was of importance. The altered enhanced status was abiding as determined by serial homotransplantability without further treatment. |
| doi_str_mv | 10.3181/00379727-100-24770 |
| format | Article |
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In 3 series of experiments employing 675 BALB/c, 108 C57BR/cd and 50 C57BL/6 mice, the first of double isografts of EO771 mammary carcinoma acquired an altered enhanced status comparable with that of the second of double isografts and each of the double isografts had 9 times the homotransplantability (24%) of single control isografts (2.7%). Within the conditions of the experiment neither size, nor age of the isograft was of importance. The altered enhanced status was abiding as determined by serial homotransplantability without further treatment.</description><identifier>ISSN: 0037-9727</identifier><identifier>ISSN: 1535-3702</identifier><identifier>EISSN: 1535-3699</identifier><identifier>DOI: 10.3181/00379727-100-24770</identifier><identifier>PMID: 13645711</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Allografts ; Animals ; Mice ; Neoplasms ; Neoplasms, Experimental ; Old Medline ; Transplantation, Homologous</subject><ispartof>Experimental biology and medicine (Maywood, N.J.), 1959-04, Vol.100 (4), p.762-763</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/13645711$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Casey, A. E.</creatorcontrib><creatorcontrib>Casey, J. G.</creatorcontrib><creatorcontrib>Hathaway, C. O.</creatorcontrib><creatorcontrib>Dowling, E. A.</creatorcontrib><title>Enhanced Tumor Homografts Following Pretreatment of Donor Mice.</title><title>Experimental biology and medicine (Maywood, N.J.)</title><addtitle>Proc Soc Exp Biol Med</addtitle><description>Conclusion
In 3 series of experiments employing 675 BALB/c, 108 C57BR/cd and 50 C57BL/6 mice, the first of double isografts of EO771 mammary carcinoma acquired an altered enhanced status comparable with that of the second of double isografts and each of the double isografts had 9 times the homotransplantability (24%) of single control isografts (2.7%). Within the conditions of the experiment neither size, nor age of the isograft was of importance. The altered enhanced status was abiding as determined by serial homotransplantability without further treatment.</description><subject>Allografts</subject><subject>Animals</subject><subject>Mice</subject><subject>Neoplasms</subject><subject>Neoplasms, Experimental</subject><subject>Old Medline</subject><subject>Transplantation, Homologous</subject><issn>0037-9727</issn><issn>1535-3702</issn><issn>1535-3699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1959</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAURS0EoqXwBxhQJra0_ojteEKotBSpCIYyW3byXFolcbETIf49KS1iY3rS1blXegeha4LHjORkgjGTSlKZEoxTmkmJT9CQcMZTJpQ6RcM9kO6JAbqIcYsx4ZKKczQgTGRcEjJEd7Pm3TQFlMmqq31IFr7262BcG5O5ryr_uWnWyWuANoBpa2jaxLvkwTc9-rwpYHyJzpypIlwd7wi9zWer6SJdvjw-Te-XaUEVbVMhrCBU2RwocZxhY01GgZecmNxBrjJOmGOikNxiC2CkzZUqTUFtxm0mHBuh28PuLviPDmKr600soKpMA76LOqeMCIZpD9IDWAQfYwCnd2FTm_ClCdZ7bfpXWx9g_aOtL90c1ztbQ_lXOXrqgckBiGYNeuu70PTf_jf5DdLpdPQ</recordid><startdate>195904</startdate><enddate>195904</enddate><creator>Casey, A. E.</creator><creator>Casey, J. G.</creator><creator>Hathaway, C. O.</creator><creator>Dowling, E. A.</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>195904</creationdate><title>Enhanced Tumor Homografts Following Pretreatment of Donor Mice.</title><author>Casey, A. E. ; Casey, J. G. ; Hathaway, C. O. ; Dowling, E. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c292t-66b6129b8e21f530aba42e5d51a8fe894513f36c75b0beea7b899dac2b45b46f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1959</creationdate><topic>Allografts</topic><topic>Animals</topic><topic>Mice</topic><topic>Neoplasms</topic><topic>Neoplasms, Experimental</topic><topic>Old Medline</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Casey, A. E.</creatorcontrib><creatorcontrib>Casey, J. G.</creatorcontrib><creatorcontrib>Hathaway, C. O.</creatorcontrib><creatorcontrib>Dowling, E. A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Casey, A. E.</au><au>Casey, J. G.</au><au>Hathaway, C. O.</au><au>Dowling, E. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhanced Tumor Homografts Following Pretreatment of Donor Mice.</atitle><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle><addtitle>Proc Soc Exp Biol Med</addtitle><date>1959-04</date><risdate>1959</risdate><volume>100</volume><issue>4</issue><spage>762</spage><epage>763</epage><pages>762-763</pages><issn>0037-9727</issn><issn>1535-3702</issn><eissn>1535-3699</eissn><abstract>Conclusion
In 3 series of experiments employing 675 BALB/c, 108 C57BR/cd and 50 C57BL/6 mice, the first of double isografts of EO771 mammary carcinoma acquired an altered enhanced status comparable with that of the second of double isografts and each of the double isografts had 9 times the homotransplantability (24%) of single control isografts (2.7%). Within the conditions of the experiment neither size, nor age of the isograft was of importance. The altered enhanced status was abiding as determined by serial homotransplantability without further treatment.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>13645711</pmid><doi>10.3181/00379727-100-24770</doi><tpages>2</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0037-9727 |
| ispartof | Experimental biology and medicine (Maywood, N.J.), 1959-04, Vol.100 (4), p.762-763 |
| issn | 0037-9727 1535-3702 1535-3699 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_82316302 |
| source | MEDLINE; Alma/SFX Local Collection |
| subjects | Allografts Animals Mice Neoplasms Neoplasms, Experimental Old Medline Transplantation, Homologous |
| title | Enhanced Tumor Homografts Following Pretreatment of Donor Mice. |
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