| Q36686185 | 3' RNA Processing Efficiency Plays a Primary Role in Generating Termination-Competent RNA Polymerase II Elongation Complexes |
| Q44925931 | A 40 kDa isoform of the type 5 adenovirus IVa2 protein is sufficient for virus viability |
| Q36636868 | A late adenovirus factor induces eIF-4E dephosphorylation and inhibition of cell protein synthesis. |
| Q42163295 | A model for the initiation of translation at the late stage after infection by adenoviruses |
| Q34369553 | A poly(A) addition site and a downstream termination region are required for efficient cessation of transcription by RNA polymerase II in the mouse beta maj-globin gene |
| Q36886728 | Abundant expression of polyomavirus middle T antigen and dihydrofolate reductase in an adenovirus recombinant. |
| Q40594994 | Activation of the early-late switch in adenovirus type 5 major late transcription unit expression by L4 gene products. |
| Q36179657 | Adenoviral vectors: development and application |
| Q57158379 | Adenoviromics: Mining the Human Adenovirus Species D Genome |
| Q41388647 | Adenovirus VA RNAI mediates a translational stimulation which is not restricted to the viral mRNAs |
| Q33785452 | Adenovirus induction of an interferon-regulatory factor during entry into the late phase of infection. |
| Q41687251 | Adenovirus inhibition of cellular protein synthesis involves inactivation of cap-binding protein |
| Q36919365 | Adenovirus proteins associated with mRNA and hnRNA in infected HeLa cells |
| Q36873615 | Adenovirus vector expressing functional herpes simplex virus ICP0. |
| Q35228887 | Adenovirus-Based Expression Vectors and Recombinant Vaccines |
| Q45881297 | Adenovirus-mediated in vivo gene transfer rapidly protects ornithine transcarbamylase-deficient mice from an ammonium challenge |
| Q22254379 | Adenovirus-specific translation by displacement of kinase Mnk1 from cap-initiation complex eIF4F |
| Q39657553 | An adenoviral vector expressing human adenovirus 5 and 3 fiber proteins for targeting heterogeneous cell populations |
| Q37679093 | An adenovirus vector system used to express polyoma virus tumor antigens |
| Q36868882 | Analysis of the transcript of the herpes simplex virus DNA polymerase gene provides evidence that polymerase expression is inefficient at the level of translation |
| Q33881292 | At least two nuclear gene products are specifically required for translation of a single yeast mitochondrial mRNA |
| Q24648355 | Cap-binding protein (eukaryotic initiation factor 4E) and 4E-inactivating protein BP-1 independently regulate cap-dependent translation |
| Q40934358 | Cell-biological assessment of human glucokinase mutants causing maturity-onset diabetes of the young type 2 (MODY-2) or glucokinase-linked hyperinsulinaemia (GK-HI). |
| Q36870618 | Cellular mRNA translation is blocked at both initiation and elongation after infection by influenza virus or adenovirus |
| Q36899070 | Cellular promoters incorporated into the adenovirus genome: cell specificity of albumin and immunoglobulin expression |
| Q41817304 | Characterization of the mouse beta maj globin transcription termination region: a spacing sequence is required between the poly(A) signal sequence and multiple downstream termination elements |
| Q36831171 | Characterization of the translational defect to fiber synthesis in monkey cells abortively infected with human adenovirus: role of ancillary leaders. |
| Q36144119 | Cis and trans activation of adenovirus IVa2 gene transcription |
| Q35977284 | Cis-acting regions sufficient for spermatocyte-specific transcriptional and spermatid-specific translational control of the Drosophila melanogaster gene mst(3)gl-9. |
| Q41704828 | Co-expression of hepatitis B virus antigens by a non-defective adenovirus vaccine vector |
| Q40640181 | Codon optimization of the adenoviral fiber negatively impacts structural protein expression and viral fitness |
| Q33872445 | Construction and immunogenicity of replication-competent adenovirus 5 host range mutant recombinants expressing HIV-1 gp160 of SF162 and TV1 strains |
| Q36918636 | Construction of a helper-free recombinant adenovirus that expresses polyomavirus large T antigen |
| Q40242166 | Contributions of CD8 T cells to the pathogenesis of mouse adenovirus type 1 respiratory infection |
| Q36765595 | Control of the Saccharomyces cerevisiae regulatory gene PET494: transcriptional repression by glucose and translational induction by oxygen |
| Q35609040 | Core labeling of adenovirus with EGFP. |
| Q45863164 | Correction of ureagenesis after gene transfer in an animal model and after liver transplantation in humans with ornithine transcarbamylase deficiency. |
| Q51743112 | Deep sequencing reveals different compositions of mRNA transcribed from the F8 gene in a panel of FVIII-producing CHO cell lines. |
| Q40324469 | Dependence of the encapsidation function of the adenovirus L1 52/55-kilodalton protein on its ability to bind the packaging sequence. |
| Q33929346 | Differential splicing yields novel adenovirus 5 E1A mRNAs that encode 30 kd and 35 kd proteins |
| Q36826782 | Distinctive properties of the hepatitis B virus envelope proteins |
| Q36917834 | Downstream sequences affect transcription initiation from the adenovirus major late promoter |
| Q64377203 | Effect of adenovirus infection on transgene expression under the adenoviral MLP/TPL and the CMVie promoter/enhancer in CHO cells |
| Q36135138 | Effect of the tripartite leader on synthesis of a non-viral protein in an adenovirus 5 recombinant. |
| Q55003335 | Effects of long 5' leader sequences on initiation by eukaryotic ribosomes in vitro |
| Q36866698 | Efficient transcription, not translation, is dependent on adenovirus tripartite leader sequences at late times of infection |
| Q39580980 | Encapsidation of viral DNA requires the adenovirus L1 52/55-kilodalton protein |
| Q36881555 | Expression of bicistronic measles virus P/C mRNA by using hybrid adenoviruses: levels of C protein synthesized in vivo are unaffected by the presence or absence of the upstream P initiator codon |
| Q37554507 | Expression of hepatitis B surface antigen with a recombinant adenovirus |
| Q45843578 | Functional mapping of the activity of the R region in the human T-cell leukemia virus type I long terminal repeat to increase gene expression |
| Q40130193 | High-level eucaryotic in vivo expression of biologically active measles virus hemagglutinin by using an adenovirus type 5 helper-free vector system |
| Q40131194 | Identification and mapping of Epstein-Barr virus early antigens and demonstration of a viral gene activator that functions in trans |
| Q37676332 | Identification of the components necessary for adenovirus translational control and their utilization in cDNA expression vectors |
| Q41333213 | Identification of two distinct elements in the long terminal repeat of HTLV-I responsible for maximum gene expression |
| Q40417989 | In vivo identification of sequence elements required for normal function of the adenovirus major late transcriptional control region |
| Q43535009 | Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis. |
| Q45856291 | Intratracheal injection of adenovirus containing the human MnSOD transgene protects athymic nude mice from irradiation-induced organizing alveolitis. |
| Q24632213 | Iron regulates ferritin mRNA translation through a segment of its 5' untranslated region |
| Q36685587 | Large-scale transfection of mammalian cells for the fast production of recombinant protein |
| Q40041334 | Late transcripts of adenovirus type 12 DNA are not translated in hamster cells expressing the E1 region of adenovirus type 5. |
| Q36791411 | Leader length and secondary structure modulate mRNA function under conditions of stress |
| Q36830512 | Leader-encoded open reading frames modulate both the absolute and relative rates of synthesis of the virion proteins of simian virus 40 |
| Q47579448 | Mouse adenovirus type 1 infection of adipose tissue |
| Q40658747 | Mutations in the adenovirus major late promoter: effects on viability and transcription during infection |
| Q37448942 | Oncolytic adenoviral gene therapy in ovarian cancer: why we are not wasting our time |
| Q40390175 | Optimizing gene expression in BPV-transformed cells: effects of cell type on enhancer/promoter interaction |
| Q36886766 | Overproduction of polyomavirus middle T antigen in mammalian cells through the use of an adenovirus vector. |
| Q37689369 | Overproduction of the protein product of a nonselected foreign gene carried by an adenovirus vector |
| Q36862385 | Polyomavirus late leader region serves an essential spacer function necessary for viability and late gene expression |
| Q34161762 | Post-transcriptional regulation accounts for the trans-activation of the human T-lymphotropic virus type III. |
| Q67965743 | Post-transcriptional regulation in higher eukaryotes: the role of the reporter gene in controlling expression |
| Q36898661 | Product of Saccharomyces cerevisiae nuclear gene PET494 activates translation of a specific mitochondrial mRNA. |
| Q45876696 | Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors |
| Q36567679 | Promoter-proximal poly(A) sites are processed efficiently, but the RNA products are unstable in the nucleus |
| Q44776939 | Protein synthesis in Giardia lamblia may involve interaction between a downstream box (DB) in mRNA and an anti-DB in the 16S-like ribosomal RNA. |
| Q40045524 | RNA-binding properties of a translational activator, the adenovirus L4 100-kilodalton protein |
| Q64381455 | Recombinant adenovirus vector mediated expression of lipoprotein (a) [Lp(a)] in rabbit plasma |
| Q39742705 | Regulation of adenovirus mRNA formation |
| Q35882839 | Regulation of p53-dependent apoptosis, transcriptional repression, and cell transformation by phosphorylation of the 55-kilodalton E1B protein of human adenovirus type 5. |
| Q40100264 | Regulation of poly(A) site selection in adenovirus. |
| Q39504602 | Regulation of protein synthesis in virus-infected animal cells. |
| Q40435988 | Regulation of translation by ribosome shunting through phosphotyrosine-dependent coupling of adenovirus protein 100k to viral mRNAs |
| Q36892208 | Replication and supercoiling of simian virus 40 DNA in cell extracts from human cells |
| Q36677188 | Selective destabilization of short-lived mRNAs with the granulocyte-macrophage colony-stimulating factor AU-rich 3' noncoding region is mediated by a cotranslational mechanism |
| Q33931644 | Selective translation of heat shock mRNA in Drosophila melanogaster depends on sequence information in the leader |
| Q35857024 | Sequences regulating poly(A) site selection within the adenovirus major late transcription unit influence the interaction of constitutive processing factors with the pre-mRNA. |
| Q40642300 | Sequences regulating temporal poly(A) site switching in the adenovirus major late transcription unit |
| Q36884926 | Structural requirements of adenovirus VAI RNA for its translation enhancement function |
| Q36639281 | TAR-independent transactivation of the murine cytomegalovirus major immediate-early promoter by the Tat protein |
| Q33683962 | Tetracycline-controlled transgene activation using the ROSA26-iM2-GFP knock-in mouse strain permits GFP monitoring of DOX-regulated transgene-expression |
| Q36698120 | The 11,600-MW protein encoded by region E3 of adenovirus is expressed early but is greatly amplified at late stages of infection |
| Q37541012 | The 5'-untranslated region of picornaviral genomes |
| Q37355995 | The adenovirus E1B 55-kilodalton and E4 open reading frame 6 proteins limit phosphorylation of eIF2alpha during the late phase of infection |
| Q36807155 | The adenovirus L4 100-kilodalton protein is necessary for efficient translation of viral late mRNA species. |
| Q30415541 | The adenovirus L4-22K protein has distinct functions in the posttranscriptional regulation of gene expression and encapsidation of the viral genome |
| Q36055639 | The adenovirus tripartite leader sequence can alter nuclear and cytoplasmic metabolism of a non-adenovirus mRNA within infected cells |
| Q36800343 | The adenovirus type 5 i-leader open reading frame functions in cis to reduce the half-life of L1 mRNAs |
| Q64082124 | The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism |
| Q24679648 | The scanning model for translation: an update |
| Q33781940 | The tripartite leader sequence of subgroup C adenovirus major late mRNAs can increase the efficiency of mRNA export. |
| Q27939777 | The yeast nuclear gene CBS1 is required for translation of mitochondrial mRNAs bearing the cob 5' untranslated leader |
| Q45862470 | Tissue-specific consequences of the anti-adenoviral immune response: implications for cardiac transplants |
| Q24609345 | Translation by ribosome shunting on adenovirus and hsp70 mRNAs facilitated by complementarity to 18S rRNA |
| Q36806954 | Translation by the adenovirus tripartite leader: elements which determine independence from cap-binding protein complex |
| Q41411842 | Translation efficiency of zein mRNA is reduced by hybrid formation between the 5'- and 3'-untranslated region. |
| Q33935121 | Translational control of viral gene expression in eukaryotes |
| Q35862192 | mRNA export correlates with activation of transcription in human subgroup C adenovirus-infected cells |
| Q33814900 | p53-Independent and -dependent requirements for E1B-55K in adenovirus type 5 replication |