Discovery of a hepatitis C target and its pharmacological inhibitors by microfluidic affinity analysis.
about
Hepatitis C virus NS4B protein targets STING and abrogates RIG-I-mediated type I interferon-dependent innate immunityIdentification and targeting of an interaction between a tyrosine motif within hepatitis C virus core protein and AP2M1 essential for viral assemblyChronic Hepatitis C Infection in Children: Current Treatment and New TherapiesStructures of hepatitis C virus nonstructural proteins required for replicase assembly and functionDirect acting antivirals for the treatment of chronic viral hepatitisThe Hepatitis C Virus NS4B Protein Can trans-Complement Viral RNA Replication and Modulates Production of Infectious VirusIdentification of a Novel Determinant for Membrane Association in Hepatitis C Virus Nonstructural Protein 4BHepatitis C virus NS4B carboxy terminal domain is a membrane binding domainFormation and function of hepatitis C virus replication complexes require residues in the carboxy-terminal domain of NS4B proteinAn Amphipathic -Helix at the C Terminus of Hepatitis C Virus Nonstructural Protein 4B Mediates Membrane AssociationHepatitis C: recent successes and continuing challenges in the development of improved treatment modalitiesMutations in Classical Swine Fever Virus NS4B Affect Virulence in SwineMassively parallel measurements of molecular interaction kinetics on a microfluidic platform.Using chimeric mice with humanized livers to predict human drug metabolism and a drug-drug interaction.Identification of PTC725, an orally bioavailable small molecule that selectively targets the hepatitis C Virus NS4B proteinChip in a lab: Microfluidics for next generation life science research.Examining the interactions of the splicing factor MBNL1 with target RNA sequences via a label-free, multiplex methodRNA-protein binding kinetics in an automated microfluidic reactorAn in vitro microfluidic approach to generating protein-interaction networksCurrent and future therapies for hepatitis C virus infection.A 1536-well fluorescence polarization assay to screen for modulators of the MUSASHI family of RNA-binding proteins.New antiviral therapies for chronic hepatitis CARF1 and GBF1 generate a PI4P-enriched environment supportive of hepatitis C virus replication.Hepatitis C virus experimental model systems and antiviral drug research.Particles and microfluidics merged: perspectives of highly sensitive diagnostic detection.Repurposing of the antihistamine chlorcyclizine and related compounds for treatment of hepatitis C virus infection.Targeting the non-structural proteins of hepatitis C virus: beyond hepatitis C virus protease and polymerase.Programmable and automated bead-based microfluidics for versatile DNA microarrays under isothermal conditions.Experimental strategies for studying transcription factor-DNA binding specificities.Computational modeling of mammalian signaling networks.New strategies for the treatment of hepatitis C virus infection and implications of resistance to new direct-acting antiviral agentsGenetic complementation of hepatitis C virus nonstructural protein functions associated with replication exhibits requirements that differ from those for virion assembly.Conserved GXXXG- and S/T-like motifs in the transmembrane domains of NS4B protein are required for hepatitis C virus replicationCharged residues in hepatitis C virus NS4B are critical for multiple NS4B functions in RNA replication.Identification of AP80978, a novel small-molecule inhibitor of hepatitis C virus replication that targets NS4B.A microfluidic platform for systems pathology: multiparameter single-cell signaling measurements of clinical brain tumor specimens.A microfluidic platform for high-throughput multiplexed protein quantitation.The interaction between the hepatitis C proteins NS4B and NS5A is involved in viral replicationHepatitis C Viral Kinetics in the Era of Direct Acting Antiviral Agents and IL28B.Rapid, automated, parallel quantitative immunoassays using highly integrated microfluidics and AlphaLISA.
P2860
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P2860
Discovery of a hepatitis C target and its pharmacological inhibitors by microfluidic affinity analysis.
description
2008 nî lūn-bûn
@nan
2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Discovery of a hepatitis C tar ...... icrofluidic affinity analysis.
@ast
Discovery of a hepatitis C tar ...... icrofluidic affinity analysis.
@en
type
label
Discovery of a hepatitis C tar ...... icrofluidic affinity analysis.
@ast
Discovery of a hepatitis C tar ...... icrofluidic affinity analysis.
@en
prefLabel
Discovery of a hepatitis C tar ...... icrofluidic affinity analysis.
@ast
Discovery of a hepatitis C tar ...... icrofluidic affinity analysis.
@en
P2093
P2860
P356
P1433
P1476
Discovery of a hepatitis C tar ...... icrofluidic affinity analysis.
@en
P2093
Doron Gerber
Ella H Sklan
Jeffrey S Glenn
Menashe Elazar
Paul D Bryson
Shirit Einav
Stephen R Quake
P2860
P2888
P304
P356
10.1038/NBT.1490
P577
2008-09-01T00:00:00Z
P5875
P6179
1051305415