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Titlebook: Epstein-Barr Virus and Human Disease • 1988; Dharam V. Ablashi,Alberto Faggioni,Gary R. Pearson Book 1989 The Humana Press Inc. 1989 DNA.P

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书目名称Epstein-Barr Virus and Human Disease • 1988
编辑Dharam V. Ablashi,Alberto Faggioni,Gary R. Pearson
视频video
丛书名称Experimental Biology and Medicine
图书封面Titlebook: Epstein-Barr Virus and Human Disease • 1988;  Dharam V. Ablashi,Alberto Faggioni,Gary R. Pearson Book 1989 The Humana Press Inc. 1989 DNA.P
描述Epstein-Barr virus (EBV) is one of the most widespread human viruses, with over 80% of the general population exposed by young adulthood, as determined by antibody studies. Initial infection usu­ ally occurs during childhood or the teenage years. It is clear that, de­ pending on the age of the recipient, clinical manifestations of the primary infection can vary. It has been known for 20 years that EBV is the etiologic agent of acute infectious mononucleosis (IM) and is also closely associated with African Burkitt‘s lymphoma (BL) and naso­ it is a pharyngeal carcinoma (NPC). There is increasing evidence that factor in the etiology of B-celllymphomas, which arise at a high fre­ quency in immunodeficient populations. EBV may also contribute to the development of autoimmune disease. Thus, this virus continues to attract world-wide attention. The major target cell for EBV infection has now been conclusively identified as the complement receptor-type 2 (CR2), the Cd/Cdg 3 3 receptor on B lymphocyte. It is apparent, however, that other cells also can become infected by EBV, such as epithelial cells in the parotid gland and other epithelial cells in the upper respiratory tract. This might
出版日期Book 1989
关键词DNA; Promoter; cell lines; gene expression; genes; molecular biology; phorbol ester; transcription
版次1
doihttps://doi.org/10.1007/978-1-4612-4508-7
isbn_softcover978-1-4612-8852-7
isbn_ebook978-1-4612-4508-7
copyrightThe Humana Press Inc. 1989
The information of publication is updating

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Zielsetzung, Fragestellungen und Hypothesen,). The duplicated left (DL) promoter is almost a perfect copy of the DR promoter region (Figure 1F) (1) and directs the expression of early mRNAs containing short tandem repeats, the IR2 repeats which are partially homologous to the IR4 repeats (4, 5, 6).
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https://doi.org/10.1007/978-3-662-26693-9re than 100 kbp (1). After induction of EBV very abundant transcripts are started from DL and DR leftward. These RNAs can be detected in the polyribosomal fraction. They are polyadenylated and contain open reading frames (ORFs). These ORFs include partially homologous clusters of short tandem repeat
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Dritte Hauptgruppe (B, Al, Ga, In, Tl3+),embrane protein (LMP).. We have investigated these “latent” proteins in a nude mouse propagated NPC tumour, C15., in EBV associated transplant lymphomas. and in a newly established Burkitt’s lymphoma (BL) cell line (D.K, unpublished) by western-immunoblotting. The transplant tumours appear to have a
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https://doi.org/10.1007/978-3-7091-3207-4lls already carrying EBV genomes and expressing latent gene products. We used BJA-B and BL02 cells for infection experiments with P3HR1 virus, which has no immortalizing capacity for umbilical cord blood lymphocytes, and B95–8, which is able to immortalize. We investigated the transcription and prot
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