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1 ding a self-cleaving ribozyme from hepatitis delta virus.
2 fic entry of hepatitis B virus and hepatitis delta virus.
3 rum titers were lower against the B.1.617.2 (Delta) virus.
4 supported the replication of hepatitis B and delta viruses.
5 n host cell entry factor for hepatitis B and delta viruses.
6 cases poorly neutralizes early pandemic and Delta viruses.
7 viruses related to coronaviruses, hepatitis delta virus and huge phages, respectively, and analysed
8 rus, human immunodeficiency virus, hepatitis delta virus, and alanine aminotransferase levels were li
9 Self-cleaving hammerhead, hairpin, hepatitis delta virus, and glmS ribozymes comprise a family of sma
10 ing RNAs: the hammerhead, hairpin, hepatitis delta virus, and in vitro-selected lead-dependent ribozy
12 mosaic virus 35S promoter and the hepatitis delta virus antigenomic ribozyme with a downstream nopal
15 Hepatitis D virus (also known as hepatitis delta virus) can establish a persistent infection in peo
20 iety of catalysts that include the hepatitis delta virus, hammerhead, X motif and Tetrahymena group I
23 /W site) in the antigenomic RNA of hepatitis delta virus (HDV) allows two essential forms of the vira
25 formation on the early kinetics of hepatitis delta virus (HDV) and hepatitis B surface antigen (HBsAg
26 small, 195-amino-acid form of the hepatitis delta virus (HDV) antigen (deltaAg-S) is essential for g
29 is delta antigen (HDAg-L) mediates hepatitis delta virus (HDV) assembly and inhibits HDV RNA replicat
30 ty of data regarding the extent of hepatitis delta virus (HDV) associated health care burden in the U
32 omic and antigenomic RNAs of human hepatitis delta virus (HDV) can fold into a rod-like structure wit
44 -S and deltaAg-L, respectively) of hepatitis delta virus (HDV) differ only in the 19-aa C-terminal ex
49 ize self-cleaving ribozymes of the hepatitis delta virus (HDV) family for processing their 5' termini
50 ular genome and antigenome RNAs of hepatitis delta virus (HDV) form characteristic unbranched, quasi-
51 as 5 days after DNA copies of the hepatitis delta virus (HDV) genome or even in vitro-transcribed HD
53 d with a cDNA expressing a mutated hepatitis delta virus (HDV) genome that could only replicate by us
54 ng sequences or ribozymes from the hepatitis delta virus (HDV) genomic RNA and its complement form si
65 of chronic liver disease caused by hepatitis delta virus (HDV) infection superimposed on chronic hepa
66 f 46 Italian patients with chronic hepatitis delta virus (HDV) infection were analyzed for HDV RNA by
69 e replication of the RNA genome of hepatitis delta virus (HDV) involves redirection of RNA polymerase
81 similarity between them.IMPORTANCE Hepatitis delta virus (HDV) is a satellite of hepatitis B virus th
95 Intrinsic to the life cycle of hepatitis delta virus (HDV) is the fact that its RNAs undergo diff
97 The self-cleaving ribozyme of the hepatitis delta virus (HDV) is the only catalytic RNA known to be
99 ations of genetic variations among hepatitis delta virus (HDV) isolates have focused principally on p
109 mic and antigenomic ribozymes from hepatitis delta virus (HDV) requires divalent cation for optimal a
113 goribonucleotide substrate for the hepatitis delta virus (HDV) ribozyme and investigated the pH depen
114 RNA transcripts: one encodes a 3'- hepatitis delta virus (HDV) ribozyme and the other, used in combin
115 d magnesium hydrate in crystals of hepatitis delta virus (HDV) ribozyme and to follow the effects of
120 bozyme related in structure to the hepatitis delta virus (HDV) ribozyme occurs in a number of mammals
123 forms of the cis-cleaving genomic hepatitis delta virus (HDV) ribozyme show a divalent metal ion bou
127 Well-ordered crystals of a genomic hepatitis delta virus (HDV) ribozyme, a large, globular RNA, were
132 ctures proposed for the cis-acting hepatitis delta virus (HDV) ribozymes contain four duplex regions,
136 ation for the ribozyme activity of hepatitis delta virus (HDV) RNA in infected cells is unknown.
137 ite in the antigenomic sequence of hepatitis delta virus (HDV) RNA is 33-nt downstream of the poly(A)
140 A replication and transcription of hepatitis delta virus (HDV) RNA, generating a full-length (1.7-kb)
141 models of the replication of human hepatitis delta virus (HDV) RNA, it is generally assumed that circ
142 1,679-nucleotide (nt) unit-length hepatitis delta virus (HDV) RNAs in the livers of two HDV-infected
147 -mediated RNA-editing event allows hepatitis delta virus (HDV) to express two essential proteins, the
150 d changes in hepatitis B virus and hepatitis delta virus (HDV) viral loads (VL) during tenofovir-cont
152 study assessed the epidemiology of hepatitis delta virus (HDV) within the University of Utah UHealth
153 gs are currently available against hepatitis delta virus (HDV), a defective virus leading to the most
155 ication of the RNA genome of human hepatitis delta virus (HDV), a series of linear RNAs containing HD
157 rimary human hepatocytes either by hepatitis delta virus (HDV), a subviral agent that uses HBV envelo
158 role in the replication scheme of hepatitis delta virus (HDV), allowing the virus to produce two fun
159 Interestingly, a human pathogen, hepatitis delta virus (HDV), also replicates via a rolling circle
163 of human hepatitis B virus (HBV), hepatitis delta virus (HDV), requires only the envelope proteins f
164 tigenomic RNA strands of the human hepatitis delta virus (HDV), where they serve a crucial role in pa
165 No specific therapy exists for hepatitis delta virus (HDV), which can cause severe liver disease.
166 g an RNA-dependent RNA polymerase, hepatitis delta virus (HDV), which contains a circular RNA of 1.7
167 ficulties can be circumvented with hepatitis delta virus (HDV), which needs the HBV large envelope pr
168 ilar to those observed for HBV and hepatitis delta virus (HDV), which shares the same L, M, and S.
171 the breadth and specificity of the hepatitis delta virus (HDV)-specific T-cell response in patients a
174 Two classes of pathogenic RNAs (hepatitis delta virus in animals and viroids in plants) are copied
175 Activity of the two ribozymes from hepatitis delta virus in monovalent salts was examined and compare
178 Replication was similar for Omicron and Delta virus isolates in human nasal epithelial cultures.
185 (18)O kinetic isotope effects for hepatitis delta virus ribozyme catalysis that reveal a dissociativ
187 promoter and upstream of the human hepatitis delta virus ribozyme domain, we inserted a complete cDNA
189 ecular dynamics simulations on the hepatitis delta virus ribozyme in the product form and assessed co
191 ase promoter and the autocatalytic hepatitis delta virus ribozyme of a transcription plasmid, pBR 322
193 f the plasmid, a cDNA encoding the hepatitis delta virus ribozyme was added to the 3' end of the FMDV
194 seP and an artificial trans-acting hepatitis delta virus ribozyme were expressed as the exon portion
195 om the antigenomic sequence of the hepatitis delta virus ribozyme with the P2 and P3 stems from the r
196 RNAs, the hairpin ribozyme and the hepatitis delta virus ribozyme, and that the shifts are likely to
197 n yellows virus pseudoknot and the hepatitis delta virus ribozyme, despite distinct structural contex
201 normal; after several years, both hepatitis delta virus RNA and serum HBsAg became undetectable.
205 ein complexes (RNPs) formed by the hepatitis delta virus RNAs and protein, HDAg, perform critical rol
207 and consider situations where the B1.617.2 (delta) virus strain is dominant and parts of the populat
208 pe proteins, hepatitis B virus and hepatitis delta virus use the sodium/taurocholate cotransporting p