scholarly article | Q13442814 |
P2093 | author name string | Berkhout B | |
Klaver B | |||
P2860 | cites work | Genes with promoters in retrovirus vectors can be independently suppressed by an epigenetic mechanism | Q72405316 |
Elements upstream of the AAUAAA within the human immunodeficiency virus polyadenylation signal are required for efficient polyadenylation in vitro | Q24601682 | ||
HIV-1 promotor insertion revealed by selective detection of chimeric provirus-host gene transcripts | Q24628751 | ||
Premature strand transfer by the HIV-1 reverse transcriptase during strong-stop DNA synthesis | Q28646822 | ||
A cDNA cloning vector that permits expression of cDNA inserts in mammalian cells | Q29614815 | ||
Identification and characterization of an enhancer in the coding region of the genome of human immunodeficiency virus type 1. | Q33649460 | ||
Differential transcription from the long terminal repeats of integrated avian leukosis virus DNA. | Q33927714 | ||
Activation of HIV-1 pre-mRNA 3' processing in vitro requires both an upstream element and TAR. | Q33938737 | ||
The trans-activator gene of HTLV-III is essential for virus replication | Q34161962 | ||
Promoter occlusion: Transcription through a promoter may inhibit its activity | Q34250774 | ||
Transcriptional interference in avian retroviruses—implications for the promoter insertion model of leukaemogenesis | Q34257238 | ||
Human immunodeficiency virus 1 tat protein binds trans-activation-responsive region (TAR) RNA in vitro | Q34303073 | ||
A promoterless retroviral vector indicates that there are sequences in U3 required for 3' RNA processing | Q34599447 | ||
In vivo selection of randomly mutated retroviral genomes | Q35019436 | ||
Comparison of promoter suppression in avian and murine retrovirus vectors | Q35058620 | ||
Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells | Q35604467 | ||
Efficient trans-activation by the HIV-2 Tat protein requires a duplicated TAR RNA structure | Q35835407 | ||
At least two regions of the viral genome determine the oncogenic potential of avian leukosis viruses | Q36282976 | ||
Poly(A) signals. | Q36485615 | ||
Unusually high frequency of reconstitution of long terminal repeats in U3-minus retrovirus vectors by DNA recombination or gene conversion | Q36691325 | ||
Transcriptional interaction between retroviral long terminal repeats (LTRs): mechanism of 5' LTR suppression and 3' LTR promoter activation of c-myc in avian B-cell lymphomas | Q36699989 | ||
DNase I-hypersensitive sites are associated with both long terminal repeats and with the intragenic enhancer of integrated human immunodeficiency virus type 1 | Q36828450 | ||
Polyadenylation at correct sites in genome RNA is not required for retrovirus replication or genome encapsidation | Q36829761 | ||
The NF-kappa B binding sites in the human immunodeficiency virus type 1 long terminal repeat are not required for virus infectivity. | Q36831819 | ||
trans activation of human immunodeficiency virus type 1 is sequence specific for both the single-stranded bulge and loop of the trans-acting-responsive hairpin: a quantitative analysis. | Q36832567 | ||
cis-acting regulatory elements within gag genes of avian retroviruses | Q36833805 | ||
Genetic evidence for promoter competition in Saccharomyces cerevisiae | Q36848316 | ||
Reverse transcription of retroviral genomes: mutations in the terminal repeat sequences. | Q36897673 | ||
Quantitative analysis of gene suppression in integrated retrovirus vectors | Q36910702 | ||
Effects of the position of the simian virus 40 enhancer on expression of multiple transcription units in a single plasmid | Q36917539 | ||
Sequence Comparison in the Crossover Region of an Oncogenic Avian Retrovirus Recombinant and Its Nononcogenic Parent: Genetic Regions That Control Growth Rate and Oncogenic Potential | Q36976026 | ||
The human immunodeficiency virus type 1 polyadenylylation signal: a 3' long terminal repeat element upstream of the AAUAAA necessary for efficient polyadenylylation | Q37426718 | ||
The HTLV-I rex response element mediates a novel form of mRNA polyadenylation | Q38336494 | ||
The role of avian retroviral LTRs in the regulation of gene expression and viral replication | Q39500835 | ||
Human immunodeficiency virus vectors for inducible expression of foreign genes | Q40065232 | ||
Identification of a U5-specific sequence required for efficient polyadenylation within the human immunodeficiency virus long terminal repeat. | Q40100135 | ||
Secondary structure of the human T-cell leukemia virus type 1 rex-responsive element is essential for rex regulation of RNA processing and transport of unspliced RNAs | Q40109255 | ||
Involvement of long terminal repeat U3 sequences overlapping the transcription control region in human immunodeficiency virus type 1 mRNA 3' end formation | Q40677805 | ||
Interaction in vivo between strong closely spaced constitutive promoters | Q41022421 | ||
TAR independent activation of the human immunodeficiency virus in phorbol ester stimulated T lymphocytes | Q41238682 | ||
Regulation of polyadenylation in human immunodeficiency virus (HIV): contributions of promoter proximity and upstream sequences | Q41521560 | ||
Changes in growth properties on passage in tissue culture of viruses derived from infectious molecular clones of HIV-1LAI, HIV-1MAL, and HIV-1ELI. | Q41655443 | ||
SPT15, the gene encoding the yeast TATA binding factor TFIID, is required for normal transcription initiation in vivo. | Q43498350 | ||
HIV-1 tat trans-activation requires the loop sequence within tar. | Q44349676 | ||
The trans-activator gene of the human T cell lymphotropic virus type III is required for replication | Q44579665 | ||
Tat trans-activates the human immunodeficiency virus through a nascent RNA target | Q45847022 | ||
Location and function of retroviral and SV40 sequences that enhance biochemical transformation after microinjection of DNA | Q53558937 | ||
Natural variants of the HIV-1 long terminal repeat: analysis of promoters with duplicated DNA regulatory motifs | Q67591586 | ||
Occlusion of the HIV poly(A) site | Q68198316 | ||
In vitro dimerization of HIV-2 leader RNA in the absence of PuGGAPuA motifs | Q70535959 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | virology | Q7215 |
P304 | page(s) | 3830-3840 | |
P577 | publication date | 1994-06-01 | |
P1433 | published in | Journal of Virology | Q1251128 |
P1476 | title | Comparison of 5' and 3' long terminal repeat promoter function in human immunodeficiency virus | |
P478 | volume | 68 |
Q28608107 | A Novel Terminal-Repeat Retrotransposon in Miniature (TRIM) Is Massively Expressed in Echinococcus multilocularis Stem Cells |
Q35674509 | A Simple Retroelement Based Knock-Down System in Dictyostelium: Further Insights into RNA Interference Mechanisms |
Q39548579 | A hairpin structure in the R region of the human immunodeficiency virus type 1 RNA genome is instrumental in polyadenylation site selection |
Q38315663 | A structured RNA motif is involved in correct placement of the tRNA(3)(Lys) primer onto the human immunodeficiency virus genome |
Q37088793 | BCL11B is a general transcriptional repressor of the HIV-1 long terminal repeat in T lymphocytes through recruitment of the NuRD complex |
Q36250079 | CRISPR/gRNA-directed synergistic activation mediator (SAM) induces specific, persistent and robust reactivation of the HIV-1 latent reservoirs |
Q36883462 | Cell-cell contact viral transfer contributes to HIV infection and persistence in astrocytes |
Q35129108 | Chemokine CXCL8 promotes HIV-1 replication in human monocyte-derived macrophages and primary microglia via nuclear factor-κB pathway. |
Q44692673 | Curcumin inhibits ultraviolet light induced human immunodeficiency virus gene expression |
Q89669108 | Epigenetic crosstalk in chronic infection with HIV-1 |
Q39549399 | Evolution of the human immunodeficiency virus type 1 long terminal repeat promoter by conversion of an NF-kappaB enhancer element into a GABP binding site. |
Q35161813 | Focus formation: a cell-based assay to determine the oncogenic potential of a gene |
Q39991696 | Forced selection of a human immunodeficiency virus type 1 variant that uses a non-self tRNA primer for reverse transcription: involvement of viral RNA sequences and the reverse transcriptase enzyme |
Q39590547 | Functional differences between the long terminal repeat transcriptional promoters of human immunodeficiency virus type 1 subtypes A through G. |
Q39549272 | Genetic instability of live, attenuated human immunodeficiency virus type 1 vaccine strains |
Q37490454 | HIV Tat Impairs Neurogenesis through Functioning As a Notch Ligand and Activation of Notch Signaling Pathway |
Q41172672 | HIV-1 Rev downregulates Tat expression and viral replication via modulation of NAD(P)H:quinine oxidoreductase 1 (NQO1). |
Q38747519 | HIV-1 Tat Promotes Lysosomal Exocytosis in Astrocytes and Contributes to Astrocyte-mediated Tat Neurotoxicity |
Q36320721 | HIV-1 Tat protein enhances the intracellular growth of Leishmania amazonensis via the ds-RNA induced protein PKR. |
Q24802185 | HIV-1 can escape from RNA interference by evolving an alternative structure in its RNA genome |
Q40058710 | HIV-1 tolerates changes in A-count in a small segment of the pol gene |
Q40284337 | Hairpin-induced tRNA-mediated (HITME) recombination in HIV-1. |
Q37378812 | Hepatitis B Virus Protein X Induces Degradation of Talin-1. |
Q36858891 | In search of a function for the most frequent naturally-occurring length polymorphism (MFNLP) of the HIV-1 LTR: retaining functional coupling, of Nef and RBF-2, at RBEIII? |
Q36515063 | Molecular mechanisms of HIV latency |
Q36645526 | NF45 and NF90 Bind HIV-1 RNA and Modulate HIV Gene Expression |
Q33783417 | Naturally Occurring Human Immunodeficiency Virus Type 1 Long Terminal Repeats Have a Frequently Observed Duplication That Binds RBF-2 and Represses Transcription |
Q60907385 | Noninvasive optical activation of Flp recombinase for genetic manipulation in deep mouse brain regions |
Q36939741 | Novel RNA Duplex Locks HIV-1 in a Latent State via Chromatin-mediated Transcriptional Silencing. |
Q28262840 | RNA structure modulates splicing efficiency at the human immunodeficiency virus type 1 major splice donor |
Q37115966 | Regulation of host gene expression by HIV-1 TAR microRNAs. |
Q39597535 | Stabilization of the U5-leader stem in the HIV-1 RNA genome affects initiation and elongation of reverse transcription |
Q33835795 | Strict control of human immunodeficiency virus type 1 replication by a genetic switch: Tet for Tat. |
Q39582195 | The 5′ and 3′ TAR Elements of Human Immunodeficiency Virus Exert Effects at Several Points in the Virus Life Cycle |
Q36813536 | The BARE-1 retrotransposon is transcribed in barley from an LTR promoter active in transient assays. |
Q33312534 | The Ixodes scapularis salivary protein, salp15, prevents the association of HIV-1 gp120 and CD4 |
Q39736726 | The leader of human immunodeficiency virus type 1 genomic RNA harbors an internal ribosome entry segment that is active during the G2/M phase of the cell cycle |
Q35870272 | The simian foamy virus type 1 transcriptional transactivator (Tas) binds and activates an enhancer element in the gag gene. |
Q34969808 | The tRNA primer activation signal in the human immunodeficiency virus type 1 genome is important for initiation and processive elongation of reverse transcription |
Q35126347 | Transcription regulatory complexes bind the human T-cell leukemia virus 5' and 3' long terminal repeats to control gene expression |
Q55296960 | Transposable elements generate regulatory novelty in a tissue-specific fashion. |
Q33400343 | Yeast genetic analysis reveals the involvement of chromatin reassembly factors in repressing HIV-1 basal transcription |
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