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1) Boulant S, Targett-Adams P, McLauchlan J. Disrupting the association of hepatitis C virus core protein with lipid droplets correlates with a loss in production of infectious virus. J Gen Virol. 2007; 88(Pt 8): 2204-13
PubMed CrossRef
医中誌リンクサービス
2) Shavinskaya A, Boulant S, Penin F, et al. The lipid droplet binding domain of hepatitis C virus core protein is a major determinant for efficient virus assembly. J Biol Chem. 2007; 282: 37158-69
PubMed CrossRef
医中誌リンクサービス
3) Miyanari Y, Atsuzawa K, Usuda N, et al. The lipid droplet is an important organelle for hepatitis C virus production. Nat Cell Biol. 2007; 9: 1089-97
PubMed CrossRef
医中誌リンクサービス
4) Tellinghuisen TL, Foss KL, Treadaway J. Regulation of hepatitis C virion production via phosphorylation of the NS5A protein. PLoS Pathog. 2008; 4: e1000032
PubMed CrossRef
医中誌リンクサービス
5) Masaki T, Suzuki R, Murakami K, et al. Interaction of hepatitis C virus nonstructural protein 5A with core protein is critical for the production of infectious virus particles. J Virol. 2008; 82: 7964-76
PubMed CrossRef
医中誌リンクサービス
6) Jones CT, Murray CL, Eastman DK, et al. Hepatitis C virus p7 and NS2 proteins are essential for production of infectious virus. J Virol. 2007; 81: 8374-83
PubMed CrossRef
医中誌リンクサービス
7) Pietschmann T, Kaul A, Koutsoudakis G, et al. Construction and characterization of infectious intragenotypic and intergenotypic hepatitis C virus chimeras. Proc Natl Acad Sci U S A. 2006; 103: 7408-13
PubMed CrossRef
医中誌リンクサービス
8) Phan T, Beran RK, Peters C, et al. Hepatitis C virus NS2 protein contributes to virus particle assembly via opposing epistatic interactions with the E1-E2 glycoprotein and NS3-NS4A enzyme complexes. J Virol. 2009; 83: 8379-95
PubMed CrossRef
医中誌リンクサービス
9) Jirasko V, Montserret R, Lee JY, et al. Structural and functional studies of nonstructural protein 2 of the hepatitis C virus reveal its key role as organizer of virion assembly. PLoS Pathog. 2010; 6: e1001233
PubMed CrossRef
医中誌リンクサービス
10) Ma Y, Anantpadma M, Timpe JM, et al. Hepatitis C virus NS2 protein serves as a scaffold for virus assembly by interacting with both structural and nonstructural proteins. J Virol. 2011; 85: 86-97
PubMed CrossRef
医中誌リンクサービス
11) Stapleford KA, Lindenbach BD. Hepatitis C virus NS2 coordinates virus particle assembly through physical interactions with the E1-E2 glycoprotein and NS3-NS4A enzyme complexes. J Virol. 2011; 85: 1706-17
PubMed CrossRef
医中誌リンクサービス
12) Tedbury P, Welbourn S, Pause A, et al. The subcellular localization of the hepatitis C virus non-structural protein NS2 is regulated by an ion channel-independent function of the p7 protein. J Gen Virol. 2011; 92(Pt 4): 819-30
PubMed CrossRef
医中誌リンクサービス
13) Popescu CI, Callens N, Trinel D, et al. NS2 protein of hepatitis C virus interacts with structural and non-structural proteins towards virus assembly. PLoS Pathog. 2011; 7: e1001278
PubMed CrossRef
医中誌リンクサービス
14) Ma Y, Yates J, Liang Y, et al. NS3 helicase domains involved in infectious intracellular hepatitis C virus particle assembly. J Virol. 2008; 82: 7624-39
PubMed CrossRef
医中誌リンクサービス
15) Mousseau G, Kota S, Takahashi V, et al. Dimerization-driven interaction of hepatitis C virus core protein with NS3 helicase. J Gen Virol. 2011; 92(Pt 1): 101-11
PubMed CrossRef
医中誌リンクサービス
16) Phan T, Kohlway A, Dimberu P, et al. The acidic domain of hepatitis C virus NS4A contributes to RNA replication and virus particle assembly. J Virol. 2011; 85: 1193-204
PubMed CrossRef
医中誌リンクサービス
17) Jones DM, Patel AH, Targett-Adams P, et al. The hepatitis C virus NS4B protein can trans-complement viral RNA replication and modulates production of infectious virus. J Virol. 2009; 83: 2163-77
PubMed CrossRef
医中誌リンクサービス
18) Steinmann E, Penin F, Kallis S, et al. Hepatitis C virus p7 protein is crucial for assembly and release of infectious virions. PLoS Pathog. 2007; 3: e103
PubMed CrossRef
医中誌リンクサービス
19) Wozniak AL, Griffin S, Rowlands D, et al. Intracellular proton conductance of the hepatitis C virus p7 protein and its contribution to infectious virus production. PLoS Pathog. 2010; 6: e1001087
PubMed CrossRef
医中誌リンクサービス
20) Andréo U, Maillard P, Kalinina O, et al. Lipoprotein lipase mediates hepatitis C virus (HCV) cell entry and inhibits HCV infection. Cell Microbiol. 2007; 9: 2445-56
PubMed CrossRef
医中誌リンクサービス
21) Shimizu Y, Hishiki T, Sugiyama K, et al. Lipoprotein lipase and hepatic triglyceride lipase reduce the infectivity of hepatitis C virus (HCV) through their catalytic activities on HCV-associated lipoproteins. Virology. 2010; 407: 152-9
PubMed CrossRef
医中誌リンクサービス
22) Huang H, Sun F, Owen DM, et al. Hepatitis C virus production by human hepatocytes dependent on assembly and secretion of very low-density lipoproteins. Proc Natl Acad Sci U S A. 2007; 104: 5848-53
PubMed CrossRef
医中誌リンクサービス
23) Icard V, Diaz O, Scholtes C, et al. Secretion of hepatitis C virus envelope glycoproteins depends on assembly of apolipoprotein B positive lipoproteins. PLoS One. 2009; 4: e4233
CrossRef
医中誌リンクサービス
24) Chang KS, Jiang J, Cai Z, et al. Human apolipoprotein e is required for infectivity and production of hepatitis C virus in cell culture. J Virol. 2007; 81: 13783-93
PubMed CrossRef
医中誌リンクサービス
25) Hishiki T, Shimizu Y, Tobita R, et al. Infectivity of hepatitis C virus is influenced by association with apolipoprotein E isoforms. J Virol. 2010; 84: 12048-57
PubMed CrossRef
医中誌リンクサービス
26) Benga WJ, Krieger SE, Dimitrova M, et al. Apolipoprotein E interacts with hepatitis C virus nonstructural protein 5A and determines assembly of infectious particles. Hepatology. 2010; 51: 43-53
PubMed CrossRef
医中誌リンクサービス
27) Cun W, Jiang J, Luo G. The C-terminal alpha-helix domain of apolipoprotein E is required for interaction with nonstructural protein 5A and assembly of hepatitis C virus. J Virol. 2010; 84: 11532-41
PubMed CrossRef
医中誌リンクサービス
28) Jiang J, Luo G. Apolipoprotein E but not B is required for the formation of infectious hepatitis C virus particles. J Virol. 2009; 83: 12680-91
PubMed CrossRef
医中誌リンクサービス
29) Herker E, Harris C, Hernandez C, et al. Efficient hepatitis C virus particle formation requires diacylglycerol acyltransferase-1. Nat Med. 2010; 16: 1295-8
PubMed CrossRef
医中誌リンクサービス
30) Parent R, Qu X, Petit MA, et al. The heat shock cognate protein 70 is associated with hepatitis C virus particles and modulates virus infectivity. Hepatology. 2009; 49: 1798-809
PubMed CrossRef
医中誌リンクサービス
31) Backes P, Quinkert D, Reiss S, et al. Role of annexin A2 in the production of infectious hepatitis C virus particles. J Virol. 2010; 84: 5775-89
PubMed CrossRef
医中誌リンクサービス
32) Corless L, Crump CM, Griffin SD, et al. Vps4 and the ESCRT-III complex are required for the release of infectious hepatitis C virus particles. J Gen Virol. 2010; 91(Pt 2): 362-72
PubMed CrossRef
医中誌リンクサービス
33) Dreux M, Dao Thi VL, Fresquet J, et al. Receptor complementation and mutagenesis reveal SR-BI as an essential HCV entry factor and functionally imply its intra- and extra-cellular domains. PLoS Pathog. 2009; 5: e1000310
PubMed CrossRef
医中誌リンクサービス
34) Catanese MT, Ansuini H, Graziani R, et al. Role of scavenger receptor class B type I in hepatitis C virus entry: kinetics and molecular determinants. J Virol. 2010; 84: 34-43
PubMed CrossRef
医中誌リンクサービス
35) Harris HJ, Davis C, Mullins JG, et al. Claudin association with CD81 defines hepatitis C virus entry. J Biol Chem. 2010; 285: 21092-102
PubMed CrossRef
医中誌リンクサービス
36) Krieger SE, Zeisel MB, Davis C, et al. Inhibition of hepatitis C virus infection by anti-claudin-1 antibodies is mediated by neutralization of E2-CD81-claudin-1 associations. Hepatology. 2010; 51: 1144-57
PubMed CrossRef
医中誌リンクサービス
37) Ploss A, Evans MJ, Gaysinskaya VA, et al. Human occludin is a hepatitis C virus entry factor required for infection of mouse cells. Nature. 2009; 457: 882-6
PubMed
医中誌リンクサービス
38) Brazzoli M, Bianchi A, Filippini S, et al. CD81 is a central regulator of cellular events required for hepatitis C virus infection of human hepatocytes. J Virol. 2008; 82: 8316-29
PubMed CrossRef
医中誌リンクサービス
39) Lupberger J, Zeisel MB, Xiao F, et al. EGFR and EphA2 are host factors for hepatitis C virus entry and possible targets for antiviral therapy. Nat Med. 2011; 17: 589-95
PubMed CrossRef
医中誌リンクサービス
40) Syder AJ, Lee H, Zeisel MB, et al. Small molecule scavenger receptor BI antagonists are potent HCV entry inhibitors. J Hepatol. 2011; 54: 48-55
PubMed CrossRef
医中誌リンクサービス
41) Moradpour D, Penin F, Rice CM. Replication of hepatitis C virus. Nat Rev Microbiol. 2007; 5: 453-63
PubMed CrossRef
医中誌リンクサービス
42) Suzuki T. A Hepatitis C virus-host interaction involved in viral replication: toward the identification of antiviral targets. Jpn J Infect Dis. 2010; 63: 307-11
医学中央雑誌刊行会  PubMed
医中誌リンクサービス
43) ENCODE Project Consortium, Birney E, Stamatoyannopoulos JA, Dutta A, et al. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature. 2007; 447: 799-816
医中誌リンクサービス
44) Jopling CL, Yi M, Lancaster AM, et al. Modulation of hepatitis C virus RNA abundance by a liver-specific MicroRNA. Science. 2005; 309: 1577-81
PubMed
医中誌リンクサービス
45) Henke JI, Goergen D, Zheng J, et al. micro RNA-122 stimulates translation of hepatitis C virus RNA. EMBO J. 2008; 27: 3300-10
PubMed CrossRef
医中誌リンクサービス
46) Jopling CL, Schütz S, Sarnow P. Position-dependent function for a tandem microRNA miR-122-binding site located in the hepatitis C virus RNA genome. Cell Host Microbe. 2008; 4: 77-85
PubMed CrossRef
医中誌リンクサービス
47) Wilson JA, Zhang C, Huys A, et al. Human Ago2 is required for efficient microRNA 122 regulation of hepatitis C virus RNA accumulation and translation. J Virol. 2011; 85: 2342-50
PubMed CrossRef
医中誌リンクサービス
48) Roberts AP, Lewis AP, Jopling CL. miR-122 activates hepatitis C virus translation by a specialized mechanism requiring particular RNA components. Nucleic Acids Res. 2011: 39(17): 7716-29
PubMed CrossRef
医中誌リンクサービス
49) Machlin ES, Sarnow P, Sagan SM. Masking the 5' terminal nucleotides of the hepatitis C virus genome by an unconventional microRNA-target RNA complex. Proc Natl Acad Sci U S A. 2011; 108: 3193-8
PubMed CrossRef
医中誌リンクサービス
50) Villanueva RA, Jangra RK, Yi M, et al. miR-122 does not modulate the elongation phase of hepatitis C virus RNA synthesis in isolated replicase complexes. Antiviral Res. 2010; 88: 119-23
PubMed CrossRef
医中誌リンクサービス
51) Chang J, Guo JT, Jiang D, et al. Liver-specific microRNA miR-122 enhances the replication of hepatitis C virus in nonhepatic cells. J Virol. 2008; 82: 8215-23
PubMed CrossRef
医中誌リンクサービス
52) Pedersen IM, Cheng G, Wieland S, et al. Interferon modulation of cellular microRNAs as an antiviral mechanism. Nature. 2007; 449: 919-22
PubMed
医中誌リンクサービス
53) Sarasin-Filipowicz M, Krol J, Markiewicz I, et al. Decreased levels of microRNA miR-122 in individuals with hepatitis C responding poorly to interferon therapy. Nat Med. 2009; 15: 31-3
PubMed CrossRef
医中誌リンクサービス
54) Elmén J, Lindow M, Schütz S, et al. LNA-mediated microRNA silencing in non-human primates. Nature. 2008; 452: 896-9
PubMed
医中誌リンクサービス
55) Lanford RE, Hildebrandt-Eriksen ES, Petri A, et al. Therapeutic silencing of microRNA-122 in primates with chronic hepatitis C virus infection. Science. 2010; 327: 198-201
PubMed
医中誌リンクサービス
56) Young DD, Connelly CM, Grohmann C, et al. Small molecule modifiers of microRNA miR-122 function for the treatment of hepatitis C virus infection and hepatocellular carcinoma. J Am Chem Soc. 2010; 132: 7976-81
PubMed CrossRef
医中誌リンクサービス
57) Lohmann V, Körner F, Koch J, et al. Replication of subgenomic hepatitis C virus RNAs in a hepatoma cell line. Science. 1999; 285: 110-3
PubMed
医中誌リンクサービス
58) Bartosch B, Dubuisson J, Cosset FL. Infectious hepatitis C virus pseudo-particles containing functional E1-E2 envelope protein complexes. J Exp Med. 2003; 197: 633-42
PubMed CrossRef
医中誌リンクサービス
59) Wakita T, Pietschmann T, Kato T, et al. Production of infectious hepatitis C virus in tissue culture from a cloned viral genome. Nat Med. 2005; 11: 791-6
PubMed CrossRef
医中誌リンクサービス
60) Murayama A, Weng L, Date T, et al. RNA polymerase activity and specific RNA structure are required for efficient HCV replication in cultured cells. PLoS Pathog. 2010; 6: e1000885
PubMed CrossRef
医中誌リンクサービス
61) Mercer DF, Schiller DE, Elliott JF, et al. Hepatitis C virus replication in mice with chimeric human livers. Nat Med. 2001; 7: 927-33
PubMed CrossRef
医中誌リンクサービス
62) Suemizu H, Hasegawa M, Kawai K, et al. Establishment of a humanized model of liver using NOD/Shi-scid IL2Rgnull mice. Biochem Biophys Res Commun. 2008; 377: 248-52
PubMed CrossRef
医中誌リンクサービス
63) Song X, Guo Y, Duo S, et al. A mouse model of inducible liver injury caused by tet-on regulated urokinase for studies of hepatocyte transplantation. Am J Pathol. 2009; 175: 1975-83
PubMed CrossRef
医中誌リンクサービス
64) Bissig KD, Wieland SF, Tran P, et al. Human liver chimeric mice provide a model for hepatitis B and C virus infection and treatment. J Clin Invest. 2010; 120: 924-30
PubMed CrossRef
医中誌リンクサービス
65) Robinet E, Baumert TF. A first step towards a mouse model for hepatitis C virus infection containing a human immune system. J Hepatol. 2011: 55(3): 718-20
PubMed CrossRef
医中誌リンクサービス
66) Dorner M, Horwitz JA, Robbins JB, et al. A genetically humanized mouse model for hepatitis C virus infection. Nature. 2011; 474: 208-11
PubMed
医中誌リンクサービス
67) Washburn ML, Bility MT, Zhang L, et al. A humanized mouse model to study hepatitis C virus infection, immune response, and liver disease. Gastroenterology. 2011; 140: 1334-44
医中誌リンクサービス
68) Youn JW, Hu YW, Tricoche N, et al. Evidence for protection against chronic hepatitis C virus infection in chimpanzees by immunization with replicating recombinant vaccinia virus. J Virol. 2008; 82: 10896-905
PubMed CrossRef
医中誌リンクサービス
69) Ge D, Fellay J, Thompson AJ, et al. Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. Nature. 2009; 461: 399-401
医中誌リンクサービス
70) Tanaka Y, Nishida N, Sugiyama M, et al. Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. Nat Genet. 2009; 41: 1105-9
CrossRef
医中誌リンクサービス
71) Suppiah V, Moldovan M, Ahlenstiel G, et al. IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy. Nat Genet. 2009; 41: 1100-4
CrossRef
医中誌リンクサービス
72) Fellay J, Thompson AJ, Ge D, et al. ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C. Nature. 2010; 464: 405-8
PubMed
医中誌リンクサービス
73) Kumar V, Kato N, Urabe Y, et al. Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma. Nat Genet. 2011; 43: 455-8
PubMed CrossRef
医中誌リンクサービス
74) Ashfaq UA, Javed T, Rehman S, et al. An overview of HCV molecular biology, replication and immune responses. Virol J. 2011; 8: 161
PubMed
医中誌リンクサービス
75) Neumann AU, Lam NP, Dahari H, et al. Hepatitis C viral dynamics in vivo and the antiviral efficacy of interferon-alpha therapy. Science. 1998; 282: 103-7
PubMed
医中誌リンクサービス
76) Ogata N, Alter HJ, Miller RH, et al. Nucleotide sequence and mutation rate of the H strain of hepatitis C virus. Proc Natl Acad Sci U S A. 1991; 88: 3392-6
PubMed CrossRef
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