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GenomicsCoxsackievirus B3
Coxsackievirus B3 Genome sequencing and assembly
PRJNA329169 | ENA
ModelsLopacinski2021 - Coxsackievirus B3 (CVB3) complete kinetics ODE model
Encoded model contains complete kinetics of infection for coxsackievirus B3 (CVB3), a compact and fast-acting RNA virus. The model consists of separable, detailed modules describing viral binding-delivery, translation-replication, and encapsidation. Specific module activities are dampened by the typ...
2021-10-26 | MODEL2110250001 | BioModels
GenomicsCoxsackievirus B3
Coxsackievirus B3 Raw sequence reads
PRJNA345651 | ENA
GenomicsCoxsackievirus B3 strain:Nancy
Coxsackievirus B3 strain:Nancy Variation
PRJNA670075 | ENA
ProteomicsAssessing Customized Multivalent Chemokine-Binding Peptide Treatment in a Murine Model of Coxsackievirus B3 Infection
This study investigates the therapeutic potential of BK1.3, a synthetic Evasin-derived peptide, in a murine model of Coxsackievirus B3 (CVB3)-induced viral myocarditis. Myocarditis, an inflammatory disease of the heart muscle, is often triggered by viral infections and driven by excessive immune cel...
ORGANISM(S): Mus musculus (Mouse) Coxsackievirus 
2025-05-07 | PXD060461 | Pride
Infection Inflammation Liver metabolism Evasin Chemokines Coxsackievirus b3 
TranscriptomicsHuman Induced Pluripotent Stem Cell-Derived Cardiomyocytes as an In Vitro Model for Coxsackievirus B3-Induced Myocarditis and Antiviral Drug Screening Platform
ABSTRACT Background: Viral myocarditis is a life-threatening illness that may lead to heart failure or cardiac arrhythmias. This study examined whether human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) could be used to model the pathogenic processes of coxsackievirus-induced vi...
ORGANISM(S): Homo sapiens 
2014-05-19 | E-GEOD-57781 | biostudies-arrayexpress
TranscriptomicsCoxsackievirus B3 (CVB3) infection of AJ, B10.A, CSS3 and B6.chr3AJ (heart tissue day 4)
The pathogenesis of viral myocarditis is a multifactorial process involving host genetics, viral genetics and the environment in which they interact. Here, we used a model of infection with Coxsackievirus B3 to characterize the contribution of host genetics to viral myocarditis. We determined heart ...
ORGANISM(S): Mus musculus 
2011-05-01 | E-GEOD-19496 | biostudies-arrayexpress
TranscriptomicsCoxsackievirus B3 (CVB3) infection of 129S1 and 129X1 (heart tissue day 6)
We infected two strains of mice, 129S1/SvImJ and 129X1/SvJ, with coxsackievirus type b3 (CVB3) at a dose of 500 pfu/g. 129S1 mice developed increased cardiopathology despite equal viral replication. We hypothesized that the increased cardiopathology might result from an ongoing pathologic host respo...
ORGANISM(S): Mus musculus 
2013-04-01 | GSE44706 | GEO
GenomicsTranscriptomic analysis of coxsackievirus B3 infection in induced pluripotent stem cell-derived brain-like endothelial cells
Transcriptomic analysis of coxsackievirus B3 infection in induced pluripotent stem cell-derived brain-like endothelial cells
PRJNA1121408 | ENA
TranscriptomicsCoxsackievirus B3 (CVB3) infection of 129S1 and 129X1 (heart tissue day 6)
We infected two strains of mice, 129S1/SvImJ and 129X1/SvJ, with coxsackievirus type b3 (CVB3) at a dose of 500 pfu/g. 129S1 mice developed increased cardiopathology despite equal viral replication. We hypothesized that the increased cardiopathology might result from an ongoing pathologic host res...
ORGANISM(S): Mus musculus 
2013-04-01 | E-GEOD-44706 | biostudies-arrayexpress
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