Restricted expression of Epstein-Barr virus (EBV)-encoded, growth transformation-associated antigens in an EBV- and human herpesvirus type 8-carrying body cavity lymphoma line [published erratum appears in J Gen Virol 1998 Nov;79(Pt 11):2875]
L Szekely, F Chen, N Teramoto, B Ehlin-Henriksson, K Pokrovskaja, A Szeles, A Manneborg-Sandlund, M Lowbeer, ET Lennette and G Klein Microbiology and Tumour Biology Centre, Karolinska Institute, Stockholm, Sweden. lassze@ki.se A body cavity lymphoma-derived cell line (BC1), known to carry both Epste...
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| Veröffentlicht in: | Journal of general virology 1998-06, Vol.79 (6), p.1445-1452 |
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| creator | Szekely, L Chen, F Teramoto, N Ehlin-Henriksson, B Pokrovskaja, K Szeles, A Manneborg-Sandlund, A Lowbeer, M Lennette, ET Klein, G |
| description | L Szekely, F Chen, N Teramoto, B Ehlin-Henriksson, K Pokrovskaja, A Szeles, A Manneborg-Sandlund, M Lowbeer, ET Lennette and G Klein
Microbiology and Tumour Biology Centre, Karolinska Institute, Stockholm, Sweden. lassze@ki.se
A body cavity lymphoma-derived cell line (BC1), known to carry both
Epstein-Barr virus (EBV) and human herpes virus type 8 (HHV-8; or Kaposi's
sarcoma-associated herpesvirus, KSHV), was analysed for the expression of
EBV-encoded, growth transformation-associated antigens and cellular
phenotype by immunofluorescence staining, Western blotting, RT-PCR and flow
cytometry. A similar phenotypic analysis was also performed on another body
cavity lymphoma line, BCBL1, that is singly infected with HHV-8.
Phenotypically, the two lines were closely similar. Although both lines are
known to carry rearranged immunoglobulin genes, they were mostly negative
for B-cell surface markers. Both expressed the HHV-8-encoded nuclear
antigen (LNA1). Similarly to Epstein-Barr nuclear antigen type 1 (EBNA1),
LNA1 was associated with the chromatin in interphase nuclei and the mitotic
chromosomes in metaphase. It accumulated in a few well-circumscribed
nuclear bodies that did not co-localize with EBNA1. BC1 cells expressed
EBNA1, LMP2A and EBV-encoded small RNAs but not EBNA2-6, LMP1 and LMP2B.
They were thus similar to type I Burkitt's lymphoma cells and latently
infected peripheral B-cells. Analysis of the splicing pattern of the
EBNA1-encoding message by RT-PCR showed that BC1 cells used the QUK but not
the YUK splice, indicating that the mRNA was initiated from Qp and not from
Cp or Wp. |
| doi_str_mv | 10.1099/0022-1317-79-6-1445 |
| format | Article |
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Microbiology and Tumour Biology Centre, Karolinska Institute, Stockholm, Sweden. lassze@ki.se
A body cavity lymphoma-derived cell line (BC1), known to carry both
Epstein-Barr virus (EBV) and human herpes virus type 8 (HHV-8; or Kaposi's
sarcoma-associated herpesvirus, KSHV), was analysed for the expression of
EBV-encoded, growth transformation-associated antigens and cellular
phenotype by immunofluorescence staining, Western blotting, RT-PCR and flow
cytometry. A similar phenotypic analysis was also performed on another body
cavity lymphoma line, BCBL1, that is singly infected with HHV-8.
Phenotypically, the two lines were closely similar. Although both lines are
known to carry rearranged immunoglobulin genes, they were mostly negative
for B-cell surface markers. Both expressed the HHV-8-encoded nuclear
antigen (LNA1). Similarly to Epstein-Barr nuclear antigen type 1 (EBNA1),
LNA1 was associated with the chromatin in interphase nuclei and the mitotic
chromosomes in metaphase. It accumulated in a few well-circumscribed
nuclear bodies that did not co-localize with EBNA1. BC1 cells expressed
EBNA1, LMP2A and EBV-encoded small RNAs but not EBNA2-6, LMP1 and LMP2B.
They were thus similar to type I Burkitt's lymphoma cells and latently
infected peripheral B-cells. Analysis of the splicing pattern of the
EBNA1-encoding message by RT-PCR showed that BC1 cells used the QUK but not
the YUK splice, indicating that the mRNA was initiated from Qp and not from
Cp or Wp.</description><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/0022-1317-79-6-1445</identifier><identifier>PMID: 9634087</identifier><language>eng</language><publisher>England: Soc General Microbiol</publisher><subject>AIDS/HIV ; Antigens, Viral - biosynthesis ; Antigens, Viral - genetics ; B-Lymphocytes - immunology ; B-Lymphocytes - virology ; Epstein-Barr Virus Nuclear Antigens - biosynthesis ; Epstein-Barr Virus Nuclear Antigens - genetics ; Fluorescent Antibody Technique, Indirect ; Gene Expression ; Gene Expression Regulation, Viral ; Herpesvirus 4, Human - genetics ; Herpesvirus 4, Human - immunology ; Herpesvirus 8, Human - genetics ; Herpesvirus 8, Human - immunology ; Humans ; Karyotyping ; Lymphoma - virology ; Nuclear Proteins - biosynthesis ; Nuclear Proteins - genetics ; Phenotype ; Polymerase Chain Reaction ; RNA Splicing ; Tumor Cells, Cultured ; Viral Matrix Proteins - biosynthesis ; Viral Matrix Proteins - genetics</subject><ispartof>Journal of general virology, 1998-06, Vol.79 (6), p.1445-1452</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-cb55c9c9be2ac3dd21ec31fa0521c2b115cdf9568a9071ab9a089b393b3aadeb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3733,3734,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9634087$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:1935191$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Szekely, L</creatorcontrib><creatorcontrib>Chen, F</creatorcontrib><creatorcontrib>Teramoto, N</creatorcontrib><creatorcontrib>Ehlin-Henriksson, B</creatorcontrib><creatorcontrib>Pokrovskaja, K</creatorcontrib><creatorcontrib>Szeles, A</creatorcontrib><creatorcontrib>Manneborg-Sandlund, A</creatorcontrib><creatorcontrib>Lowbeer, M</creatorcontrib><creatorcontrib>Lennette, ET</creatorcontrib><creatorcontrib>Klein, G</creatorcontrib><title>Restricted expression of Epstein-Barr virus (EBV)-encoded, growth transformation-associated antigens in an EBV- and human herpesvirus type 8-carrying body cavity lymphoma line [published erratum appears in J Gen Virol 1998 Nov;79(Pt 11):2875]</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>L Szekely, F Chen, N Teramoto, B Ehlin-Henriksson, K Pokrovskaja, A Szeles, A Manneborg-Sandlund, M Lowbeer, ET Lennette and G Klein
Microbiology and Tumour Biology Centre, Karolinska Institute, Stockholm, Sweden. lassze@ki.se
A body cavity lymphoma-derived cell line (BC1), known to carry both
Epstein-Barr virus (EBV) and human herpes virus type 8 (HHV-8; or Kaposi's
sarcoma-associated herpesvirus, KSHV), was analysed for the expression of
EBV-encoded, growth transformation-associated antigens and cellular
phenotype by immunofluorescence staining, Western blotting, RT-PCR and flow
cytometry. A similar phenotypic analysis was also performed on another body
cavity lymphoma line, BCBL1, that is singly infected with HHV-8.
Phenotypically, the two lines were closely similar. Although both lines are
known to carry rearranged immunoglobulin genes, they were mostly negative
for B-cell surface markers. Both expressed the HHV-8-encoded nuclear
antigen (LNA1). Similarly to Epstein-Barr nuclear antigen type 1 (EBNA1),
LNA1 was associated with the chromatin in interphase nuclei and the mitotic
chromosomes in metaphase. It accumulated in a few well-circumscribed
nuclear bodies that did not co-localize with EBNA1. BC1 cells expressed
EBNA1, LMP2A and EBV-encoded small RNAs but not EBNA2-6, LMP1 and LMP2B.
They were thus similar to type I Burkitt's lymphoma cells and latently
infected peripheral B-cells. Analysis of the splicing pattern of the
EBNA1-encoding message by RT-PCR showed that BC1 cells used the QUK but not
the YUK splice, indicating that the mRNA was initiated from Qp and not from
Cp or Wp.</description><subject>AIDS/HIV</subject><subject>Antigens, Viral - biosynthesis</subject><subject>Antigens, Viral - genetics</subject><subject>B-Lymphocytes - immunology</subject><subject>B-Lymphocytes - virology</subject><subject>Epstein-Barr Virus Nuclear Antigens - biosynthesis</subject><subject>Epstein-Barr Virus Nuclear Antigens - genetics</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Gene Expression</subject><subject>Gene Expression Regulation, Viral</subject><subject>Herpesvirus 4, Human - genetics</subject><subject>Herpesvirus 4, Human - immunology</subject><subject>Herpesvirus 8, Human - genetics</subject><subject>Herpesvirus 8, Human - immunology</subject><subject>Humans</subject><subject>Karyotyping</subject><subject>Lymphoma - virology</subject><subject>Nuclear Proteins - biosynthesis</subject><subject>Nuclear Proteins - genetics</subject><subject>Phenotype</subject><subject>Polymerase Chain Reaction</subject><subject>RNA Splicing</subject><subject>Tumor Cells, Cultured</subject><subject>Viral Matrix Proteins - biosynthesis</subject><subject>Viral Matrix Proteins - genetics</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUl2L1DAULaKs4-gvECFPMgtGk35Hn9xlXJVFRXRfREKS3k7jtk1N0hn7t_0FpnYYH4XAvTf3nHMv3BNFjyl5TgljLwiJY0wTWuCC4RzTNM3uRCua5hmOQ_9utDoh7kcPnPtByIwpzqIzlicpKYtV9PszOG-18lAh-DVYcE6bHpkabQfnQff4QliL9tqODm22FzfnGHplKqieoZ01B98gb0XvamM74QMVC-eM0mIWFL3XO-gd0n3IUWDjECvUjF0oG7ADuEXZTwOgEqswa9L9DklTTUiJvfYTaqduaEwnUKt7QN-GUbbaNfO-1go_dkgMAwj7d8p7dAU9utHWtIgyVqIPZv-qYJtPHlF6_jIui-z7w-heLVoHj45xHX19s_1y-RZff7x6d_n6GquMZh4rmWWKKSYhFiqpqpiCSmgtSBZTFUtKM1XVLMtLwUhBhWSClEwmLJGJEBXIZB3hRdcdICzNB6s7YSduhObHr9uQAU-TNEvTgH-64Adrfo7hLLzTTkHbih7M6HjBWEpSVv4XSPM0zpPw1lGyAJU1zlmoTztQwmcL8dkgfDZIUOc5n-0RWE-O8qPsoDpxjp4J_c3Sb_SuOWgLPNy402GG1IaHe_6T-gNc2NN0</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>Szekely, L</creator><creator>Chen, F</creator><creator>Teramoto, N</creator><creator>Ehlin-Henriksson, B</creator><creator>Pokrovskaja, K</creator><creator>Szeles, A</creator><creator>Manneborg-Sandlund, A</creator><creator>Lowbeer, M</creator><creator>Lennette, ET</creator><creator>Klein, G</creator><general>Soc General Microbiol</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>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>19980601</creationdate><title>Restricted expression of Epstein-Barr virus (EBV)-encoded, growth transformation-associated antigens in an EBV- and human herpesvirus type 8-carrying body cavity lymphoma line [published erratum appears in J Gen Virol 1998 Nov;79(Pt 11):2875]</title><author>Szekely, L ; Chen, F ; Teramoto, N ; Ehlin-Henriksson, B ; Pokrovskaja, K ; Szeles, A ; Manneborg-Sandlund, A ; Lowbeer, M ; Lennette, ET ; Klein, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-cb55c9c9be2ac3dd21ec31fa0521c2b115cdf9568a9071ab9a089b393b3aadeb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>AIDS/HIV</topic><topic>Antigens, Viral - biosynthesis</topic><topic>Antigens, Viral - genetics</topic><topic>B-Lymphocytes - immunology</topic><topic>B-Lymphocytes - virology</topic><topic>Epstein-Barr Virus Nuclear Antigens - biosynthesis</topic><topic>Epstein-Barr Virus Nuclear Antigens - genetics</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Gene Expression</topic><topic>Gene Expression Regulation, Viral</topic><topic>Herpesvirus 4, Human - genetics</topic><topic>Herpesvirus 4, Human - immunology</topic><topic>Herpesvirus 8, Human - genetics</topic><topic>Herpesvirus 8, Human - immunology</topic><topic>Humans</topic><topic>Karyotyping</topic><topic>Lymphoma - virology</topic><topic>Nuclear Proteins - biosynthesis</topic><topic>Nuclear Proteins - genetics</topic><topic>Phenotype</topic><topic>Polymerase Chain Reaction</topic><topic>RNA Splicing</topic><topic>Tumor Cells, Cultured</topic><topic>Viral Matrix Proteins - biosynthesis</topic><topic>Viral Matrix Proteins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Szekely, L</creatorcontrib><creatorcontrib>Chen, F</creatorcontrib><creatorcontrib>Teramoto, N</creatorcontrib><creatorcontrib>Ehlin-Henriksson, B</creatorcontrib><creatorcontrib>Pokrovskaja, K</creatorcontrib><creatorcontrib>Szeles, A</creatorcontrib><creatorcontrib>Manneborg-Sandlund, A</creatorcontrib><creatorcontrib>Lowbeer, M</creatorcontrib><creatorcontrib>Lennette, ET</creatorcontrib><creatorcontrib>Klein, G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Szekely, L</au><au>Chen, F</au><au>Teramoto, N</au><au>Ehlin-Henriksson, B</au><au>Pokrovskaja, K</au><au>Szeles, A</au><au>Manneborg-Sandlund, A</au><au>Lowbeer, M</au><au>Lennette, ET</au><au>Klein, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Restricted expression of Epstein-Barr virus (EBV)-encoded, growth transformation-associated antigens in an EBV- and human herpesvirus type 8-carrying body cavity lymphoma line [published erratum appears in J Gen Virol 1998 Nov;79(Pt 11):2875]</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>1998-06-01</date><risdate>1998</risdate><volume>79</volume><issue>6</issue><spage>1445</spage><epage>1452</epage><pages>1445-1452</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><abstract>L Szekely, F Chen, N Teramoto, B Ehlin-Henriksson, K Pokrovskaja, A Szeles, A Manneborg-Sandlund, M Lowbeer, ET Lennette and G Klein
Microbiology and Tumour Biology Centre, Karolinska Institute, Stockholm, Sweden. lassze@ki.se
A body cavity lymphoma-derived cell line (BC1), known to carry both
Epstein-Barr virus (EBV) and human herpes virus type 8 (HHV-8; or Kaposi's
sarcoma-associated herpesvirus, KSHV), was analysed for the expression of
EBV-encoded, growth transformation-associated antigens and cellular
phenotype by immunofluorescence staining, Western blotting, RT-PCR and flow
cytometry. A similar phenotypic analysis was also performed on another body
cavity lymphoma line, BCBL1, that is singly infected with HHV-8.
Phenotypically, the two lines were closely similar. Although both lines are
known to carry rearranged immunoglobulin genes, they were mostly negative
for B-cell surface markers. Both expressed the HHV-8-encoded nuclear
antigen (LNA1). Similarly to Epstein-Barr nuclear antigen type 1 (EBNA1),
LNA1 was associated with the chromatin in interphase nuclei and the mitotic
chromosomes in metaphase. It accumulated in a few well-circumscribed
nuclear bodies that did not co-localize with EBNA1. BC1 cells expressed
EBNA1, LMP2A and EBV-encoded small RNAs but not EBNA2-6, LMP1 and LMP2B.
They were thus similar to type I Burkitt's lymphoma cells and latently
infected peripheral B-cells. Analysis of the splicing pattern of the
EBNA1-encoding message by RT-PCR showed that BC1 cells used the QUK but not
the YUK splice, indicating that the mRNA was initiated from Qp and not from
Cp or Wp.</abstract><cop>England</cop><pub>Soc General Microbiol</pub><pmid>9634087</pmid><doi>10.1099/0022-1317-79-6-1445</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0022-1317 |
| ispartof | Journal of general virology, 1998-06, Vol.79 (6), p.1445-1452 |
| issn | 0022-1317 1465-2099 |
| language | eng |
| recordid | cdi_swepub_primary_oai_swepub_ki_se_434544 |
| source | MEDLINE; Microbiology Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
| subjects | AIDS/HIV Antigens, Viral - biosynthesis Antigens, Viral - genetics B-Lymphocytes - immunology B-Lymphocytes - virology Epstein-Barr Virus Nuclear Antigens - biosynthesis Epstein-Barr Virus Nuclear Antigens - genetics Fluorescent Antibody Technique, Indirect Gene Expression Gene Expression Regulation, Viral Herpesvirus 4, Human - genetics Herpesvirus 4, Human - immunology Herpesvirus 8, Human - genetics Herpesvirus 8, Human - immunology Humans Karyotyping Lymphoma - virology Nuclear Proteins - biosynthesis Nuclear Proteins - genetics Phenotype Polymerase Chain Reaction RNA Splicing Tumor Cells, Cultured Viral Matrix Proteins - biosynthesis Viral Matrix Proteins - genetics |
| title | Restricted expression of Epstein-Barr virus (EBV)-encoded, growth transformation-associated antigens in an EBV- and human herpesvirus type 8-carrying body cavity lymphoma line [published erratum appears in J Gen Virol 1998 Nov;79(Pt 11):2875] |
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