Replication of hepatitis C virus.
By Ralf Bartenschlager, V. Lohmann. Journal of General Virology, 2000
1,278 citations recorded by the source corpus.
Subfields: Animal Science and Zoology, Epidemiology, Hepatology
View Paper: https://www.semanticscholar.org/paper/80d3e2aa369550d841c67f7d122882bfaec4b7d7
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In Animal Science and Zoology
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Citations in the corpus
- iArc monogrAphs on the evAluAtion oF cArcinogenic risks to humAns (2012, background): “This includes the lipoprotein receptors scavenger receptor B1 (SR-B1), and the low-density lipoprotein receptor (LDLr), which may mediate indirect uptake of HCV via HCV-associated lipoproteins (Moradpour et al., 2007).”
- Phosphoinositides: tiny lipids with giant impact on cell regulation. (2013, background): “viral protein NS5A (13), which by itself can generate membrane structures resembling the “membranous web” (1082).”
- Endoplasmic Reticulum Stress in Liver Disease (2010, background): “Thus, HCV viral replication is intimately linked to the ER [93].”
- Interferon-Stimulated Genes: A Complex Web of Host Defenses (2014, background): “Within these droplets viperin interacts with both the host [vesicle-associated membrane protein–associated protein A (VAP-A, also known as VAP-33)] and the HCV non-structural protein 5A (NS5A), a key protein required for viral replication, assembly, and egress (202).”
- Modification of intracellular membrane structures for virus replication (2008, background): “HCV infection is a major cause of chronic hepatitis, liver cirrhosis and hepatocellular carcinoma, and affects 170 million people worldwide 4 .”
- Infectious Hepatitis C Virus Pseudo-particles Containing Functional E1–E2 Envelope Protein Complexes (2003, background): “Our data indicate that the E1 and E2 glycoproteins represent the envelope glycoproteins of wild-type HCV and are both required for infection; each glycoprotein is potentially involved in separate steps of cell entry (9, 17).”