Cantitate/Preț
Produs

Pathogenicity of Human Herpesviruses due to Specific Pathogenicity Genes: Frontiers of Virology, cartea 3

Editat de Yechiel Becker, Gholamreza Darai
en Limba Engleză Paperback – 15 dec 2011
Six members of the Herpesviridae family are human pathogens, including herpes and 2 (HSV-I and 2), Epstein-Barr virus (EBV), varicella zoster simplex virus I virus (VZV), human cytomegalovirus (HCMV), and human herpesvirus 6 (HHV 6). Each of these viruses is capable of causing distinct diseases of varying severity in children, young adults, and the aged. The diseases range from infection of epithelial tissue to the infection of internal organs and white blood cells. A common feature of the six pathogenic human herpesviruses is their ability to latently infect different cell types in which the viral DNA is not integrated and is unable to express its pathogenicity. Reactivation of the herpesviruses is a result of cellular processes which reactivate viral genes, leading to virus progeny and to signs of infection. Due to their ability to become latent after initial infection, once the pathogenic herpesviruses infect children they are maintained throughout life, having the potential of cause various diseases upon reactivation.
Citește tot Restrânge

Din seria Frontiers of Virology

Preț: 63273 lei

Preț vechi: 74439 lei
-15% Nou

Puncte Express: 949

Preț estimativ în valută:
12109 12578$ 10058£

Carte tipărită la comandă

Livrare economică 03-17 februarie 25

Preluare comenzi: 021 569.72.76

Specificații

ISBN-13: 9783642850066
ISBN-10: 3642850065
Pagini: 408
Ilustrații: XVI, 387 p.
Dimensiuni: 155 x 235 x 21 mm
Greutate: 0.57 kg
Ediția:Softcover reprint of the original 1st ed. 1994
Editura: Springer Berlin, Heidelberg
Colecția Springer
Seria Frontiers of Virology

Locul publicării:Berlin, Heidelberg, Germany

Public țintă

Research

Cuprins

A. Herpes Simplex Virus.- I. Genes Involved in Entry.- 1 Entry of Herpes Simplex Virus Type 1 into Cells — Early Steps in Virus Pathogenicity.- 2 Neomycin and Herpes Simplex Virus Receptor Binding: The Role of Glycoprotein C.- 3 Pathogenicity of Glycoprotein C-Negative Herpes Simplex Virus Type 1 in Herpetic Keratitis.- 4 Structure and Function of Glycoprotein D of Herpes Simplex Virus.- II. Genes Coding for Enzymes.- 5 The Role of Herpes Simplex Virus Thymidine Kinase Expression in Pathogenesis and Latency.- 6 Herpes Simplex Virus Type 1 DNA Polymerase: Eukaryotic Model Enzyme and Principal Target of Antiviral Therapy.- 7 Ribonucleotide Reductase and the Ocular Virulence of Herpes Simplex Virus Type 1.- 8 Ribonucleotide Reductase Gene in Herpes Simplex Virus Type 2 and Virus Pathogenicity.- III. Genes Related to Intraperitoneal Pathogenicity.- 9 Effect of Herpes Simplex Virus Type 1 UL41 Gene Product on mdr-1 Gene-mRNA in Infected Adrenal Glands.- 10 Pathogenicity and Latency of Herpes Simplex Virus in the Animal Model System Tree Shrew.- 11 Computer Analysis of the Protein Coded by Herpes Simplex Virus Type 1 UL56 Gene.- IV. Genes and Latency and Intracerebral Pathogenicity.- 12 The Herpes Simplex Type 1 Virus Latency Gene.- 13 Neurovirulence of Herpes Simplex Virus Type 1 Accessory Gene Mutants.- 14 Herpes Simplex Virus Latency and Immediate Early Gene Repression by the Cellular Octamer-Binding Protein Oct-2.- 15 The Cell Fusion Protein Gene (UL53) of Herpes Simplex Virus Type 1—A Pathogenicity Gene.- V. Effect of Cellular Defenses on Virus Pathogenicity.- 16 Role of Langerhans Cells and Other Dendritic Cells in the Pathogenesis of Herpes Simplex Virus Type 1 Infection.- B. Epstein Barr Virus.- 17 Gene Expression in Burkitt’s Lymphoma Cells.- 18 MolecularMechanisms of the Development of EBV-Related B Lymphomas: Functional Cooperation of EBV with IL-6 and HIV-1.- C. Human Cytomegalovirus.- 19 Murine Cytomegalovirus Genes Influencing Virus Growth and Tropism for Salivary Gland.- D. Human Herpesvirus 6.- 20 Pathogenicity of Human Herpesvirus-6.- E. Trends.- 21 Herpes Simplex Virus Type 1 Genes Involved in Virus Pathogenicity: A Review.- 22 Live Herpesvirus Vaccines: Serendipity or Engineering of the Virus Genome.