α-Glucosidase inhibitors as potential broad based anti-viral agents
about
Alpha-glucosidase inhibitors reduce dengue virus production by affecting the initial steps of virion morphogenesis in the endoplasmic reticulumStudy of the mechanism of antiviral action of iminosugar derivatives against bovine viral diarrhea virusAssembly and Maturation of the Flavivirus Kunjin Virus Appear To Occur in the Rough Endoplasmic Reticulum and along the Secretory Pathway, RespectivelyAntiviral effects of an iminosugar derivative on flavivirus infectionsDetection of Inhibition of Bovine Viral Diarrhea Virus by Aromatic Cationic MoleculesImino sugars inhibit the formation and secretion of bovine viral diarrhea virus, a pestivirus model of hepatitis C virus: implications for the development of broad spectrum anti-hepatitis virus agentsReplication-Competent Recombinant Vesicular Stomatitis Virus Encoding Hepatitis C Virus Envelope ProteinsSpecificity of Processing -Glucosidase I Is Guided by the Substrate Conformation: CRYSTALLOGRAPHIC AND IN SILICO STUDIESThe heterodimeric structure of glucosidase II is required for its activity, solubility, and localization in vivoGlycosidase inhibitors: a patent review (2008-2013).Analysis of the pre-S2 N- and O-linked glycans of the M surface protein from human hepatitis B virus.Mass spectrometric characterization of proteins from the SARS virus: a preliminary report.Transcriptome analysis of the whitefly, Bemisia tabaci MEAM1 during feeding on tomato infected with the crinivirus, Tomato chlorosis virus, identifies a temporal shift in gene expression and differential regulation of novel orphan genes.Use of targeted glycoproteomics to identify serum glycoproteins that correlate with liver cancer in woodchucks and humans.Resistance of human immunodeficiency virus type 1 to the high-mannose binding agents cyanovirin N and concanavalin A.Alkaloidal sugar mimetics: biological activities and therapeutic applications.Identification of the genes involved in 1-deoxynojirimycin synthesis in Bacillus subtilis MORI 3K-85.Hepatitis B virus large and middle glycoproteins are degraded by a proteasome pathway in glucosidase-inhibited cells but not in cells with functional glucosidase enzyme.Folding of viral envelope glycoproteins in the endoplasmic reticulum.Strategies to eliminate HBV infection.Evolving therapies for the treatment of chronic hepatitis B virus infection.Iminosugars as possible broad spectrum anti hepatitis virus agents: the glucovirs and alkovirs.Hepatitis C virus therapies: current treatments, targets and future perspectives.Effects of interferon, ribavirin, and iminosugar derivatives on cells persistently infected with noncytopathic bovine viral diarrhea virus.Possible FDA-approved drugs to treat Ebola virus infectionA Novel Iminosugar UV-12 with Activity against the Diverse Viruses Influenza and Dengue (Novel Iminosugar Antiviral for Influenza and Dengue)Characterization of different crystal forms of the alpha-glucosidase MalA from Sulfolobus solfataricusRNA Interference based Approach to Down Regulate Osmoregulators of Whitefly (Bemisia tabaci): Potential Technology for the Control of Whitefly.Versatility of the endoplasmic reticulum protein folding factory.Monitoring of S protein maturation in the endoplasmic reticulum by calnexin is important for the infectivity of severe acute respiratory syndrome coronavirus.Inhibition of endoplasmic reticulum glucosidases is required for in vitro and in vivo dengue antiviral activity by the iminosugar UV-4.Glycosidase inhibition: assessing mimicry of the transition state.Alternative approaches to antiviral treatments: focusing on glycosylation as a target for antiviral therapy.Bitter-sweet symphony: glycan-lectin interactions in virus biology.Computer-aided molecular design of novel glucosidase inhibitors for AIDS treatment.Emerging structural insights into glycoprotein quality control coupled with N-glycan processing in the endoplasmic reticulum.Treatment of hepatitis B virus: an update.Investigational drugs in early development for treating dengue infection.alpha-Glucosidase inhibitors have a prolonged antiviral effect against hepatitis B virus through the sustained inhibition of the large and middle envelope glycoproteins.The use of calnexin and calreticulin by cellular and viral glycoproteins.
P2860
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P2860
α-Glucosidase inhibitors as potential broad based anti-viral agents
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
α-Glucosidase inhibitors as potential broad based anti-viral agents
@ast
α-Glucosidase inhibitors as potential broad based anti-viral agents
@en
type
label
α-Glucosidase inhibitors as potential broad based anti-viral agents
@ast
α-Glucosidase inhibitors as potential broad based anti-viral agents
@en
prefLabel
α-Glucosidase inhibitors as potential broad based anti-viral agents
@ast
α-Glucosidase inhibitors as potential broad based anti-viral agents
@en
P2093
P2860
P3181
P1433
P1476
α-Glucosidase inhibitors as potential broad based anti-viral agents
@en
P2093
Anand Mehta
Nicole Zitzmann
Pauline M Rudd
Raymond A Dwek
Timothy M Block
P2860
P3181
P356
10.1016/S0014-5793(98)00525-0
P407
P577
1998-06-23T00:00:00Z