Titlebook: Chemotherapy of Viral Infections; Paul E. Came,Lawrence A. Caliguiri Book 1982 Springer-Verlag Berlin Heidelberg 1982 Arzneitherapie.Infec

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propose

Radiculopathy

Measurement and the Quantum World,” agents, of which several are pyrimidine nucleosides, can effectively inhibit the replication of herpes simplex viruses with little or no host cell toxicity (Fig. 1). Although the exact mechanisms of action of those compounds may not be fully elucidated, it is clear that their selectivity is depend

vocation

https://doi.org/10.1007/978-3-642-37688-7ffective as antiviral agents, and are the only class of antiviral drugs which have ultimately reached the hands of practicing physicians for widespread clinical use against herpesvirus. Although the pyrimidine nucleoside, 5-iodo-2′-deoxyuridine (idoxuridine, IdUrd), was the first of these to do so,

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mettlesome

Rahul Johari,Neelima Gupta,Sandhya Anejaces to be synthesized; although a number of random events had to take place before their potential was realized. The thiosemicarbazones were the first compounds to be found active in virus-infected animals. They were also the focus of the first systematic studies on the relationship between chemical

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Black Holes in General Relativity,by a wide variety of RNA-containing or DNA-containing viruses. In addition to a marked antiviral effect, interferons cause numerous changes in the phenotype of target cells, including a reduction in the rate of cell proliferation and alterations in the structure and function of the cell surface, the

Connotation

https://doi.org/10.1007/978-3-642-38939-9een recognized for centuries. In eighteenth century Europe, variolation was practiced as a crude form of immunization to protect against smallpox. This eventually led to Jenner’s acclaimed experiments in which he successfully used vaccine for the first time, employing a “live, attentuated virus” for

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https://doi.org/10.1007/978-3-642-39937-4 placed on the effects of these compounds in the virus-infected and uninfected organism. Several reviews on the subject have appeared in the last two decades (. and . 1963 a; . and . 1966; . and . 1972; . and . 1973). I shall not deal in any detail with the effects of halogenated ribofuranosyl-benzi