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Titlebook: HIV Protocols; Nelson L. Michael,Jerome H. Kim Book 19991st edition Humana Press 1999

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書目名稱HIV Protocols
編輯Nelson L. Michael,Jerome H. Kim
視頻videohttp://file.papertrans.cn/421/420198/420198.mp4
叢書名稱Methods in Molecular Medicine
圖書封面Titlebook: HIV Protocols;  Nelson L. Michael,Jerome H. Kim Book 19991st edition Humana Press 1999
描述The worldwide impact of infection with human immunodeficiency virus type 1 (HIV- is reflected in the cumulative number ofHIV- 1 infections, which is now predicted to exceed 40 million by the year 2000---equivalent to the n- ber of humans who perished in World War II. The medical and scientific - sponse to the HIV-1 pandemic has steadily grown since its recognition in 1981. The outlay by the United States alone for HIV research funded by the National Institutes of Health in 1997 was $1. 4 billion. Laboratory-based HIV research has brought together academic clinicians, retrovirologists, molecular biologists, and immunologists in the formation of research teams attempting to dissect the viral and host factors contributing to disease pathogenesis. Increasing focus is being placed on those aspects of viral biology and host immune responses that bear on the development of vaccines to prevent HIV infection. HIVProtocols reflects the state of HIV research in several ways. First, chapters are organized into four sections: Virology, Molecular Biology, Humoral Immunology, and Cellular Immunology. This organization is a natural consequence of the diverse scientific disciplines that have been a
出版日期Book 19991st edition
版次1
doihttps://doi.org/10.1385/0896033694
isbn_ebook978-1-59259-601-0Series ISSN 1543-1894 Series E-ISSN 1940-6037
issn_series 1543-1894
copyrightHumana Press 1999
The information of publication is updating

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Rapid Identification of Cloned HIV-1 Fragmentsntification, vectors containing the lacZ promoter and a partial . gene encoding the α-fragment of β-galactosidase were developed (pUC vectors) (.,.). Upon induction by IPTG (isopropyl-β-.-thio-galactopyranoside), the expressed β-galactosidase could cleave X-gal (5-bromo-4-choloro-3-indoyl-β-.-galact
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Diagnosis and Direct Automated Sequencing of HIV-1 From Dried Blood Spots (DBS) Collected on Filter esignated A through H, have been identified (.,.). More recently, a ninth subtype, I, has been detected (.), as well as several highly divergent, or “outlying” variants of HIV-1 that have been tentatively classified as group O (.,.). This subtyping is based on a relatively small number of specimens
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Book 19991st editionIV infection. HIVProtocols reflects the state of HIV research in several ways. First, chapters are organized into four sections: Virology, Molecular Biology, Humoral Immunology, and Cellular Immunology. This organization is a natural consequence of the diverse scientific disciplines that have been a
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https://doi.org/10.1007/978-3-030-57473-4ted “R5,” whereas syncytium-inducing viruses preferentially utilize CXCR4, but may be dual tropic and are designated either “X4” or X4R5, respectively (.,.). Some viruses also appear to be able to utilize chemokine receptors CCR2B and CCR3 (.–.). In addition, the role of chemokine coreceptors in the
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https://doi.org/10.1007/978-94-6300-654-5ntification, vectors containing the lacZ promoter and a partial . gene encoding the α-fragment of β-galactosidase were developed (pUC vectors) (.,.). Upon induction by IPTG (isopropyl-β-.-thio-galactopyranoside), the expressed β-galactosidase could cleave X-gal (5-bromo-4-choloro-3-indoyl-β-.-galact
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Gagari Chakrabarti,Chitrakalpa Senesignated A through H, have been identified (.,.). More recently, a ninth subtype, I, has been detected (.), as well as several highly divergent, or “outlying” variants of HIV-1 that have been tentatively classified as group O (.,.). This subtyping is based on a relatively small number of specimens
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