| Document Date: 2014-12-16 13:44:06
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City Worcester / / Company Qiagen / Creative Commons / / / Event FDA Phase / / Facility University of Alabama / University of Massachusetts Medical School / / IndustryTerm treatment for advanced liver disease / treatment of HCV / HCV treatment / internal ribosome entry site / exosome isolation protocol / / MedicalCondition human hepatoma cell line / productive infection / free HCV virus infection / retroviral infection / active infection / lysosomal dysfunction / cirrhosis / Hepatitis C / subsequent infection / liver disease / Introduction Hepatitis C / infections / tumor / active HCV infection / hepatoma cells / disease / post infection / infectious virus / hepatocellular carcinoma / caused significant disease / chronic HCV / liver allograft infection / HCV1 infection / HCV / HCV infection / virus infection / infection / infectious prion protein / advanced liver disease / fibrosis / HCV RNA / Infected Patients Transmit HCV Infection / / MedicalTreatment immunotherapies / antibody therapy / / Organization Gyongyi Szabo* Department of Medicine / University of Massachusetts Medical School / University of Alabama at Birmingham / / Person Karen Kodys / Shashi Bala / Terence N. Bukong / Fatemeh Momen-Heravi / / Position original author / Editor / Author / representative / / Product Exoquick / ribavirin / Lansoprazole / CD9 / / ProvinceOrState Alabama / Massachusetts / / PublishedMedium PLOS Pathogens / / Technology alpha / siRNA / Antibodies / transplantation / using RNA ChIP / simulation / exosome isolation protocol / / URL www.plospathogens.org / /
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Exosomes from Hepatitis C Infected Patients Transmit HCV Infection and Contain Replication Competent Viral RNA in Complex with Ago2-miR122-HSP90 Terence N. Bukong., Fatemeh Momen-Heravi., Karen Kodys, Shashi Bala, Gyongy