Polymerase Chain Reaction Facilitates Archival Autopsy Studies of Sickle Cell Disease
Archival autopsy studies of sickle cell disease have often been hampered by inadequate documentation of the genotype. Although the polymerase chain reaction (PCR) has been applied to the prenatal diagnosis of sickle cell disease, its use has not been reported in archival studies of sickle cell disea...
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Veröffentlicht in: | Fetal and pediatric pathology 1993, Vol.13 (1), p.75-81 |
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creator | Manci, Elizabeth A. Culberson, Donald E. Chen, Guey-Jen Lee Mankad, Vipul Joshi, Vijay V. Fujimura, F. K. |
description | Archival autopsy studies of sickle cell disease have often been hampered by inadequate documentation of the genotype. Although the polymerase chain reaction (PCR) has been applied to the prenatal diagnosis of sickle cell disease, its use has not been reported in archival studies of sickle cell disease. In this study, DNAs from formalin-fixed, paraffin-embedded archival tissues were amplified by PCR and analyzed by dot-blot hybridization using allele-specific oligonucleotides. These S and C genotypes for 9 of 10 archival specimens studied blindly were correctly identified by PCR. The tenth specimen consistently failed to amplify by PCR, yielding no result. These data demonstrate the utility of PCR for retrospective identification of the genotype of sickle cell disease. This application of PCR will significantly expand the number of autopsy cases suitable for retrospective studies of the morbidity and mortality of sickle cell disease. |
doi_str_mv | 10.3109/15513819309048195 |
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K.</creatorcontrib><title>Polymerase Chain Reaction Facilitates Archival Autopsy Studies of Sickle Cell Disease</title><title>Fetal and pediatric pathology</title><addtitle>Pediatr Pathol</addtitle><description>Archival autopsy studies of sickle cell disease have often been hampered by inadequate documentation of the genotype. Although the polymerase chain reaction (PCR) has been applied to the prenatal diagnosis of sickle cell disease, its use has not been reported in archival studies of sickle cell disease. In this study, DNAs from formalin-fixed, paraffin-embedded archival tissues were amplified by PCR and analyzed by dot-blot hybridization using allele-specific oligonucleotides. These S and C genotypes for 9 of 10 archival specimens studied blindly were correctly identified by PCR. The tenth specimen consistently failed to amplify by PCR, yielding no result. These data demonstrate the utility of PCR for retrospective identification of the genotype of sickle cell disease. This application of PCR will significantly expand the number of autopsy cases suitable for retrospective studies of the morbidity and mortality of sickle cell disease.</description><subject>Anemia, Sickle Cell - blood</subject><subject>Anemia, Sickle Cell - diagnosis</subject><subject>Anemia, Sickle Cell - genetics</subject><subject>archival studies</subject><subject>Autopsy</subject><subject>Child</subject><subject>DNA - genetics</subject><subject>Evaluation Studies as Topic</subject><subject>Genotype</subject><subject>Hemoglobins - genetics</subject><subject>Humans</subject><subject>polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Retrospective Studies</subject><subject>sickle cell disease</subject><subject>Tissue Preservation</subject><issn>1551-3815</issn><issn>0277-0938</issn><issn>1551-3823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLAzEUhYMotT5-gAthVu6qyWQyk0E3pT6hoFi7HtLMDU3NTGqSUfrvTWkRRNTVDTnnfNx7EDoh-JwSXF4QxgjlpKS4xFmcbAf1138DylO6-_UmbB8deL_AmBacFz3U41mRlSzro-mTNasGnPCQjOZCt8kzCBm0bZNbIbXRQQTwydDJuX4XJhl2wS79KpmErtZRsCqZaPlqYhqMSa61h4g6QntKGA_H23mIprc3L6P7wfjx7mE0HA9kRtMwkJjlKTCmcg4FkBrDjPA8l_VM8TpepPK05DUFzLHKyhnjmGWlZAAMcso5oYfobMNdOvvWgQ9Vo72Mi4gWbOerguVFgUn6r5HknJKCs2gkG6N01nsHqlo63Qi3qgiu1p1XPzqPmdMtvJs1UH8ltiVH_Wqj61ZZ14gP60xdBbEy1iknWqn9Gv07_vJbfA7ChLkUDqqF7VwbC_5juU9jb6DB</recordid><startdate>1993</startdate><enddate>1993</enddate><creator>Manci, Elizabeth A.</creator><creator>Culberson, Donald E.</creator><creator>Chen, Guey-Jen Lee</creator><creator>Mankad, Vipul</creator><creator>Joshi, Vijay V.</creator><creator>Fujimura, F. K.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>1993</creationdate><title>Polymerase Chain Reaction Facilitates Archival Autopsy Studies of Sickle Cell Disease</title><author>Manci, Elizabeth A. ; Culberson, Donald E. ; Chen, Guey-Jen Lee ; Mankad, Vipul ; Joshi, Vijay V. ; Fujimura, F. K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-c0562e55f68e7e1d0eb1866cdbf8d904f6298d3e080f49b580549c5ee5e638813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Anemia, Sickle Cell - blood</topic><topic>Anemia, Sickle Cell - diagnosis</topic><topic>Anemia, Sickle Cell - genetics</topic><topic>archival studies</topic><topic>Autopsy</topic><topic>Child</topic><topic>DNA - genetics</topic><topic>Evaluation Studies as Topic</topic><topic>Genotype</topic><topic>Hemoglobins - genetics</topic><topic>Humans</topic><topic>polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Retrospective Studies</topic><topic>sickle cell disease</topic><topic>Tissue Preservation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Manci, Elizabeth A.</creatorcontrib><creatorcontrib>Culberson, Donald E.</creatorcontrib><creatorcontrib>Chen, Guey-Jen Lee</creatorcontrib><creatorcontrib>Mankad, Vipul</creatorcontrib><creatorcontrib>Joshi, Vijay V.</creatorcontrib><creatorcontrib>Fujimura, F. K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Fetal and pediatric pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Manci, Elizabeth A.</au><au>Culberson, Donald E.</au><au>Chen, Guey-Jen Lee</au><au>Mankad, Vipul</au><au>Joshi, Vijay V.</au><au>Fujimura, F. K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymerase Chain Reaction Facilitates Archival Autopsy Studies of Sickle Cell Disease</atitle><jtitle>Fetal and pediatric pathology</jtitle><addtitle>Pediatr Pathol</addtitle><date>1993</date><risdate>1993</risdate><volume>13</volume><issue>1</issue><spage>75</spage><epage>81</epage><pages>75-81</pages><issn>1551-3815</issn><issn>0277-0938</issn><eissn>1551-3823</eissn><abstract>Archival autopsy studies of sickle cell disease have often been hampered by inadequate documentation of the genotype. Although the polymerase chain reaction (PCR) has been applied to the prenatal diagnosis of sickle cell disease, its use has not been reported in archival studies of sickle cell disease. In this study, DNAs from formalin-fixed, paraffin-embedded archival tissues were amplified by PCR and analyzed by dot-blot hybridization using allele-specific oligonucleotides. These S and C genotypes for 9 of 10 archival specimens studied blindly were correctly identified by PCR. The tenth specimen consistently failed to amplify by PCR, yielding no result. These data demonstrate the utility of PCR for retrospective identification of the genotype of sickle cell disease. This application of PCR will significantly expand the number of autopsy cases suitable for retrospective studies of the morbidity and mortality of sickle cell disease.</abstract><cop>United States</cop><pub>Informa UK Ltd</pub><pmid>8474954</pmid><doi>10.3109/15513819309048195</doi><tpages>7</tpages></addata></record> |
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subjects | Anemia, Sickle Cell - blood Anemia, Sickle Cell - diagnosis Anemia, Sickle Cell - genetics archival studies Autopsy Child DNA - genetics Evaluation Studies as Topic Genotype Hemoglobins - genetics Humans polymerase chain reaction Polymerase Chain Reaction - methods Retrospective Studies sickle cell disease Tissue Preservation |
title | Polymerase Chain Reaction Facilitates Archival Autopsy Studies of Sickle Cell Disease |
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