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1 is of human immunodeficiency virus (HIV) and hepatitis C virus .
2 rapy, and, if applicable, elimination of the hepatitis C virus.
3 d protein are associated with changes in the hepatitis C virus.
4 er of patients undergoing reLT for recurrent hepatitis C virus.
5 logies were nonalcoholic steatohepatitis and hepatitis C virus.
6 proteins of human immunodeficiency virus and hepatitis C virus.
7 less than that of human immunodeficiency and hepatitis C viruses.
8 ridae family, including Zika, West Nile, and hepatitis C viruses.
9 due to hepatitis B virus (12.2 million) and hepatitis C virus (10.4 million), liver cancer due to he
11 SIV), irrespective of virus tropism, but not hepatitis C virus, adenovirus 5 (ADV5), Zika virus, and
13 f the mechanisms by which hepatitis B virus, hepatitis C virus, alcohol, fatty liver disease, and oth
14 f hepatitis C viral inhibitors and comparing hepatitis C virus and coronavirus replication, we previo
16 targets of interest (Plasmodium falciparum, Hepatitis C virus and T-cells) to demonstrate the value
19 e 1, Human Immunodeficiency Virus type 1 and Hepatitis C Virus as well as in the inflammatory conditi
20 ses, decompensated cirrhosis, cirrhosis, and hepatitis C virus compared to patients with chronic HBV.
21 re, we address this question by studying the hepatitis C virus core protein, a chaperone that promote
28 id agonist therapy (OAT) reduces the risk of hepatitis C virus (HCV) acquisition among people who inj
33 obtained from unrelated cases infected with hepatitis C virus (HCV) and compared its performance wit
36 eath and tumoral recurrence in patients with hepatitis C virus (HCV) and hepatocellular carcinoma (HC
38 cure for patients chronically infected with hepatitis C virus (HCV) and improved post-liver transpla
40 e who inject drugs have a high prevalence of hepatitis C virus (HCV) and significant disease associat
42 pendency is a hallmark of the human pathogen hepatitis C virus (HCV) and was also described for the r
45 ation step in the synthesis of simeprevir, a hepatitis C virus (HCV) antiviral drug, was studied.
50 who inject drugs (PWID) have had the highest hepatitis C virus (HCV) burden; however, young PWID now
51 care and treatment for persons infected with hepatitis C virus (HCV) can reduce HCV-related morbidity
57 years was 49.3 among hepatitis B virus (HBV)/hepatitis C virus (HCV) coinfected and 18.2 among HCV mo
58 mation in human immunodeficiency virus (HIV)/hepatitis C virus (HCV) coinfection increases cognitive
59 -associated substitutions (RAS) could hamper hepatitis C virus (HCV) cure rates and elimination effor
61 (OAT) and compared once-daily to twice-daily hepatitis C virus (HCV) direct-acting antiviral (DAA) th
64 the long-term outcomes in hepatitis B (HBV)/hepatitis C virus (HCV) dual-infected patients after ant
65 ose, human immunodeficiency virus (HIV), and hepatitis C virus (HCV) due to injection drug use (IDU)
66 iological function for the p7 viroporin from hepatitis C virus (HCV) during virus entry, but also ena
68 To achieve the World Health Organization hepatitis C virus (HCV) elimination targets, it is essen
75 y and safety in a phase IIa study in chronic hepatitis C virus (HCV) genotype (GT)-1-infected patient
76 th pibrentasvir is approved to treat chronic hepatitis C virus (HCV) genotype 1-6 infection in adults
79 of-life (HRQL) improvements in patients with hepatitis C virus (HCV) has been generally accepted.
81 k of immunocompetent small animal models for hepatitis C virus (HCV) has greatly hindered the develop
82 e and safe direct-acting antivirals to treat hepatitis C virus (HCV) has resulted in greater ease and
83 y effective direct-acting antivirals against Hepatitis C virus (HCV) have created an opportunity to t
84 Direct-acting antivirals (DAAs) targeting hepatitis C virus (HCV) have revolutionized outcomes in
85 Limited treatment data are available for hepatitis C virus (HCV) in sub-Saharan Africa, especiall
86 cting antiviral therapy is expected to abate hepatitis C virus (HCV) incidence among human immunodefi
90 g for human immunodeficiency virus (HIV) and hepatitis C virus (HCV) infection among persons who inje
91 requent complication associated with chronic hepatitis C virus (HCV) infection and is a key prognosti
93 lth Organization has set a goal to eliminate hepatitis C virus (HCV) infection as public health threa
94 al natural killer (NK) cell responses during hepatitis C virus (HCV) infection can be restored after
96 of direct-acting antiviral (DAA) therapy for hepatitis C virus (HCV) infection for patients with a hi
98 t of direct-acting antiviral agents to treat hepatitis C virus (HCV) infection has raised the possibi
99 Although adaptive immune responses against hepatitis C virus (HCV) infection have been studied in g
101 ion, diagnosis, evaluation, and treatment of hepatitis C virus (HCV) infection in chronic kidney dise
104 though curative therapy is now available for hepatitis C virus (HCV) infection in the United States,
105 resulted in an increase in organ donors with hepatitis C virus (HCV) infection in the United States.
106 an safely prevent the development of chronic hepatitis C virus (HCV) infection in uninfected recipien
107 liver-related mortality among patients with hepatitis C virus (HCV) infection increased from 2007 th
121 croglobulin and CD40 antigen and presence of hepatitis C virus (HCV) infection predicted early (year
125 erum aspartate aminotransferase (AST) value, Hepatitis C virus (HCV) infection, alcohol abuse, CD4/CD
126 abase was used to identify adults with NASH, hepatitis C virus (HCV) infection, and alcohol-related l
127 important role in immune-mediated control of hepatitis C virus (HCV) infection, but the relative cont
128 inject drugs (PWID) are denied treatment for hepatitis C virus (HCV) infection, even if they are rece
129 ldren under 12 years of age who have chronic hepatitis C virus (HCV) infection, there are currently n
131 Despite recent breakthroughs in treatment of hepatitis C virus (HCV) infection, we have limited under
132 s associated with hepatitis B virus (HBV) or hepatitis C virus (HCV) infection, with or without a sus
133 Africa has a large population of people with hepatitis C virus (HCV) infection, yet little is known a
147 Current guidelines for the management of hepatitis C virus (HCV) infections provide varying recom
148 FDA-approved drug used for the treatment of hepatitis C virus (HCV) infections, is a potent antivira
149 elaprevir-an FDA-approved drug used to treat hepatitis C virus (HCV) infections-as a potent antiviral
151 ations and scale-up scenarios of combination hepatitis C virus (HCV) interventions for exhaustive tes
156 tions for HCV vaccine development.IMPORTANCE Hepatitis C virus (HCV) is a leading cause of liver-rela
157 e assembly.IMPORTANCE Chronic infection with hepatitis C virus (HCV) is a major cause of severe liver
164 o drive ongoing viral replication.IMPORTANCE Hepatitis C virus (HCV) is known for its ability to modu
170 REV-ERBalpha influence several steps in the hepatitis C virus (HCV) life cycle, including particle e
177 mapping of the specificity landscape of the hepatitis C virus (HCV) NS3/4A protease, whose function-
179 We conducted a retrospective cohort study of hepatitis C virus (HCV) patients who achieved SVR with D
180 pment of successful commercial drugs against hepatitis C virus (HCV) polymerase and HIV-1 reverse tra
182 rom high-income countries suggest increasing hepatitis C virus (HCV) prevalence/incidence among human
183 cost of direct-acting antivirals (DAAs) for hepatitis C virus (HCV) prompted many payers to restrict
184 ersible-covalent inhibitor that binds to the hepatitis C virus (HCV) protease active site is conjugat
185 ors, and social determinants associated with hepatitis C virus (HCV) reinfection following DAA therap
187 he development of a prophylactic vaccine for hepatitis C virus (HCV) remains a global health challeng
188 .IMPORTANCE The development of a vaccine for hepatitis C virus (HCV) remains a global health challeng
192 been reported to be necessary for efficient hepatitis C virus (HCV) replication, but the specific me
199 S Preventive Services Task Force (USPSTF) of hepatitis C virus (HCV) screening found interferon-based
201 r demographic characteristics, behavior, and hepatitis C virus (HCV) seropositivity assessed the rela
211 he effects of interferon-based therapies for hepatitis C virus (HCV) upon the risk of diabetes are co
216 rary 2019, 532 individuals were screened for hepatitis C virus (HCV), 180 tested HCV antibody positiv
217 V.IMPORTANCE Development of vaccines against hepatitis C virus (HCV), a major cause of cirrhosis and
219 ion to its known benefits on preventing HIV, hepatitis C virus (HCV), and overdose among PWID, our mo
220 an immunodeficiency virus type 1 (HIV-1) and hepatitis C virus (HCV), as a paradigm to model control
221 mark of a protective immune response against hepatitis C virus (HCV), associated with spontaneous vir
222 ses represent promising surrogate models for hepatitis C virus (HCV), for which there are no efficien
223 on-nucleoside polymerase (NS5B) inhibitor of hepatitis C virus (HCV), in which an N-benzyl boronic ac
224 the existence of established treatments for hepatitis C virus (HCV), more effective means of prevent
229 h men (MSMs), intravenous drug users (IDUs), hepatitis C virus (HCV)-infected and patients with diabe
231 milarity to eIF3 recognizing motifs found in hepatitis C virus (HCV)-like IRESs, suggesting mechanist
251 e activation of CD81 [the portal of entry of hepatitis C virus (HCV)] by agonistic antibody results i
252 to develop an effective vaccine against the hepatitis C virus (HCV; human hepacivirus) have been sty
254 responding to chronic viral infections (HIV, hepatitis C virus [HCV], Epstein-Barr virus [EBV], and c
255 LT registration, by disease etiology (NASH, hepatitis C virus [HCV], other liver disease etiologies
258 lar carcinoma (HCC) in patients with chronic hepatitis C virus; however, their impact in patients wit
259 munodeficiency virus-1/2, hepatitis B virus, hepatitis C virus, human T-cell lymphotropic virus-1/2,
261 ce of viral hepatitis (hepatitis B virus and hepatitis C virus) in migrants is higher than among the
262 viral agents, there has been a rapid rise in hepatitis C virus-infected (HCV+) heart transplantation.
263 ent hepatocellular carcinoma (HCC) in 15,059 hepatitis C virus-infected patients with advanced liver
264 njection drug use (4.89; 1.95-12.26), active hepatitis C virus infection (3.39; 1.10-12.26), and iden
266 ansfusions throughout her life, leading to a hepatitis C virus infection (which was treated, achievin
267 sting for race/ethnicity, age, HIV load, and hepatitis C virus infection and controlling for multipli
268 tus of direct-acting antiviral therapies for hepatitis C virus infection and discuss remaining challe
270 Eliminating the burden of disease caused by hepatitis C virus infection is proving difficult, despit
274 e II diabetes (T2D) may worsen the course of hepatitis C virus infection with a greater risk of liver
275 g sofosbuvir, approved for the management of hepatitis C virus infection, and the broad-acting antivi
276 atorvastatin or rosuvastatin or simvastatin, hepatitis C virus infection, prior treatment with busulf
279 emic has been associated with an increase in hepatitis C virus infections among women of childbearing
280 of treating human immunodeficiency virus and hepatitis C virus infections, ID physicians have unique
281 e to an effective vaccine for HCV.IMPORTANCE Hepatitis C virus infects approximately 1% of the world'
282 identification of compounds that target the hepatitis C virus internal ribosome entry site (IRES) an
283 substitutions in the NS3-4A protease of the hepatitis C virus lead to protease inhibitor (PI) resist
284 st common etiology of liver disease (LD) was hepatitis C virus (N = 48) and nonalcoholic steatohepati
285 es by diagnosis of hepatocellular carcinoma, hepatitis C virus, nonalcoholic steatohepatitis, or Medi
286 HCC) development in alcohol Western diet-fed hepatitis C virus NS5A Tg mice with hepatocyte-specific
287 even when under antiretroviral therapy), and hepatitis C virus or those of mice with lymphocytic chor
290 ration of median wait times, availability of hepatitis C virus-positive organs, and degree of liver d
291 stem is based on the interaction between the hepatitis C virus protease (HCVp) NS3a and a genetically
292 allosteric inhibitors have been reported for hepatitis C virus RdRp, few have been described for DENV
294 ound kidney disease, dialysis vintage, donor hepatitis C virus status, cardiovascular diseases, panel
297 % of diagnosed cases) were initiated on anti-hepatitis C virus treatment in the Veterans Affairs heal
298 effect of sustained virological response to hepatitis C virus treatment on the progression of liver
300 or in patients undergoing reLT for recurrent hepatitis C virus who achieved SVR after reLT compared w