review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1048886796 |
P356 | DOI | 10.1007/BF00039382 |
P8608 | Fatcat ID | release_l2aafxflbvhdlmhqmv5v7vsoeu |
P932 | PMC publication ID | 7089402 |
P698 | PubMed publication ID | 8980479 |
P2093 | author name string | T Hohn | |
J Fütterer | |||
P2860 | cites work | A highly conserved eukaryotic protein family possessing properties of polypeptide chain release factor | Q24310622 |
A protein complex required for signal-sequence-specific sorting and translocation | Q24315826 | ||
Selection of AUG initiation codons differs in plants and animals | Q24556463 | ||
Downstream secondary structure facilitates recognition of initiator codons by eukaryotic ribosomes | Q24556622 | ||
Anti-peptidyl transferase leader peptides of attenuation-regulated chloramphenicol-resistance genes | Q24562850 | ||
Pseudoknot-dependent read-through of retroviral gag termination codons: importance of sequences in the spacer and loop 2 | Q24568287 | ||
The products of the SUP45 (eRF1) and SUP35 genes interact to mediate translation termination in Saccharomyces cerevisiae | Q24598514 | ||
Direct mapping of adeno-associated virus capsid proteins B and C: a possible ACG initiation codon | Q24610766 | ||
High molecular mass forms of basic fibroblast growth factor are initiated by alternative CUG codons | Q24621303 | ||
Cytoplasmic heat shock granules are formed from precursor particles and are associated with a specific set of mRNAs | Q24633797 | ||
Structural requirements for efficient translational frameshifting in the synthesis of the putative viral RNA-dependent RNA polymerase of potato leafroll virus | Q24633867 | ||
Mechanism and regulation of eukaryotic protein synthesis | Q24634693 | ||
Alternative translation of human fibroblast growth factor 2 mRNA occurs by internal entry of ribosomes | Q24647014 | ||
The scanning model for translation: an update | Q24679648 | ||
Position-dependent ATT initiation during plant pararetrovirus rice tungro bacilliform virus translation | Q24682796 | ||
The structure of an RNA pseudoknot that causes efficient frameshifting in mouse mammary tumor virus | Q27730190 | ||
Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes | Q27860600 | ||
Clustering of low usage codons and ribosome movement | Q72898260 | ||
Biphasic Stimulation of Translational Activity Correlates with Induction of Translation Elongation Factor 1 Subunit [alpha] upon Wounding in Potato Tubers | Q74790193 | ||
Heat Shock Gene Expression Is Controlled Primarily at the Translational Level in Carrot Cells and Somatic Embryos | Q77149438 | ||
Stress-Induced Translational Control in Potato Tubers May Be Mediated by Polysome-Associated Proteins | Q77222231 | ||
Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA | Q27861043 | ||
Suppression of ribosomal reinitiation at upstream open reading frames in amino acid-starved cells forms the basis for GCN4 translational control | Q27934439 | ||
Translation initiation at non-AUG triplets in mammalian cells | Q28251347 | ||
Nonlinear ribosome migration on cauliflower mosaic virus 35S RNA | Q28269505 | ||
Translational control in mammalian cells | Q28295830 | ||
The complete nucleotide sequence of tobacco rattle virus RNA-1 | Q28302595 | ||
Structural features in eukaryotic mRNAs that modulate the initiation of translation | Q29547921 | ||
The poly(A) binding protein is required for poly(A) shortening and 60S ribosomal subunit-dependent translation initiation | Q29614571 | ||
Construction and expression of nonsense suppressor tRNAs which function in plant cells. | Q30333938 | ||
Mutational analysis of the gag-pol junction of Moloney murine leukemia virus: requirements for expression of the gag-pol fusion protein | Q33191259 | ||
mRNAs encoding ribulose-1,5-bisphosphate carboxylase remain bound to polysomes but are not translated in amaranth seedlings transferred to darkness | Q33580371 | ||
A translational enhancer derived from tobacco mosaic virus is functionally equivalent to a Shine-Dalgarno sequence | Q33828240 | ||
tRNA-tRNA interactions within cellular ribosomes | Q33861143 | ||
Identification of amino acids inserted during suppression of UAA and UGA termination codons at the gag-pol junction of Moloney murine leukemia virus | Q33894696 | ||
Peptide inhibitors of peptidyltransferase alter the conformation of domains IV and V of large subunit rRNA: a model for nascent peptide control of translation | Q33915959 | ||
Expression of a plant viral polycistronic mRNA in yeast, Saccharomyces cerevisiae, mediated by a plant virus translational transactivator | Q33937319 | ||
Efficiency of reinitiation of translation on human immunodeficiency virus type 1 mRNAs is determined by the length of the upstream open reading frame and by intercistronic distance | Q34058977 | ||
The leading sequence of caulimovirus large RNA can be folded into a large stem-loop structure | Q34178505 | ||
Messenger RNA for the coat protein of tobacco mosaic virus | Q34184249 | ||
Translational termination efficiency in mammals is influenced by the base following the stop codon. | Q34222816 | ||
BinaryAgrobacteriumvectors for plant transformation | Q34245581 | ||
Initiation of protein synthesis by the eukaryotic translational apparatus on circular RNAs | Q34293657 | ||
Pararetroviruses and retroviruses: a comparative review of viral structure and gene expression strategies. | Q34315689 | ||
Gene VI of figwort mosaic virus (caulimovirus group) functions in posttranscriptional expression of genes on the full-length RNA transcript | Q34322424 | ||
High-level expression of sperm whale myoglobin in Escherichia coli | Q34377722 | ||
Adherence to the first-AUG rule when a second AUG codon follows closely upon the first | Q34489813 | ||
Translational control of photo-induced expression of the Cat2 catalase gene during leaf development in maize | Q34618071 | ||
The complete genome structure and synthesis of infectious RNA from clones of tomato bushy stunt virus. | Q34638255 | ||
When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells. | Q34693550 | ||
Expression of mRNA electroporated into plant and animal cells | Q34694074 | ||
An inspection of the domain between putative TATA box and translation start site in 79 plant genes | Q34700594 | ||
A comparison of eukaryotic viral 5'-leader sequences as enhancers of mRNA expression in vivo | Q34718131 | ||
5' untranslated leader sequences of eukaryotic mRNAs encoding heat shock induced proteins | Q34737769 | ||
Post-Transcriptional Steps in the Expression of Chloroplast Genes | Q35161312 | ||
Translation initiation at a downstream AUG occurs with increased efficiency when the upstream AUG is located very close to the 5' cap. | Q36799975 | ||
Cap-independent enhancement of translation by a plant potyvirus 5' nontranslated region | Q36803474 | ||
Ribosomal pausing during translation of an RNA pseudoknot | Q36825631 | ||
Translational frameshifting mediated by a viral sequence in plant cells | Q36891579 | ||
Translational readthrough of an amber termination codon during synthesis of feline leukemia virus protease | Q36904990 | ||
Effects of intercistronic length on the efficiency of reinitiation by eucaryotic ribosomes | Q36922094 | ||
Towards a genetic dissection of the basis of triplet decoding, and its natural subversion: programmed reading frame shifts and hops | Q37041849 | ||
Regulation of protein synthesis at the elongation stage New insights into the control of gene expression in eukaryotes | Q37191842 | ||
Ribosomal movement impeded at a pseudoknot required for frameshifting | Q37203021 | ||
Binding of ribosomes to 5'-terminal leader sequences of eukaryotic messenger RNAs | Q37335345 | ||
Modification of the coding sequence enhances plant expression of insect control protein genes | Q37483639 | ||
Cauliflower mosaic virus gene VI produces a symptomatic phenotype in transgenic tobacco plants | Q37485103 | ||
The 5'-untranslated region of picornaviral genomes | Q37541012 | ||
Evidence that a downstream pseudoknot is required for translational read-through of the Moloney murine leukemia virus gag stop codon | Q37573972 | ||
Cap-independent translation of picornavirus RNAs: structure and function of the internal ribosomal entry site | Q37577378 | ||
Do the poly(A) tail and 3' untranslated region control mRNA translation? | Q37591951 | ||
Tales of poly(A): a review | Q37600123 | ||
Splicing of cauliflower mosaic virus 35S RNA is essential for viral infectivity | Q37620615 | ||
Positions +5 and +6 can be major determinants of the efficiency of non-AUG initiation codons for protein synthesis | Q37635118 | ||
Translation of bicistronic viral mRNA in transfected cells: regulation at the level of elongation | Q37665931 | ||
Mutations in GCD11, the structural gene for eIF-2 gamma in yeast, alter translational regulation of GCN4 and the selection of the start site for protein synthesis. | Q37697264 | ||
Picornavirus RNA translation continues to surprise | Q37778060 | ||
Recent advances in peptide chain termination | Q37966031 | ||
Eukaryotic protein elongation factors | Q38025213 | ||
Alternative Translation Initiation of the Moloney Murine Leukemia Virus mRNA Controlled by Internal Ribosome Entry Involving the p57/PTB Splicing Factor | Q38292035 | ||
Target-specific arrest of mRNA translation by antisense 2'-O-alkyloligoribonucleotides | Q38302506 | ||
Molecular dissection of the cauliflower mosaic virus translation transactivator | Q38317240 | ||
Multiple ribosome binding to the 5'-terminal leader sequence of tobacco mosaic virus RNA. Assembly of an 80S ribosome X mRNA complex at the AUU codon | Q38353787 | ||
The efficiency of translation termination is determined by a synergistic interplay between upstream and downstream sequences in Saccharomyces cerevisiae. | Q38531566 | ||
Stop making sense: or Regulation at the level of termination in eukaryotic protein synthesis | Q39514050 | ||
Translational inhibition by a human cytomegalovirus upstream open reading frame despite inefficient utilization of its AUG codon. | Q39868773 | ||
An internal ribosomal entry mechanism promotes translation of murine leukemia virus gag polyprotein precursors. | Q39869599 | ||
mRNAs containing the unstructured 5' leader sequence of alfalfa mosaic virus RNA 4 translate inefficiently in lysates from poliovirus-infected HeLa cells | Q39871245 | ||
Nascent peptide regulation of translation | Q39898726 | ||
The leader peptides of attenuation-regulated chloramphenicol resistance genes inhibit translational termination | Q39899137 | ||
Pulling the ribosome out of frame by +1 at a programmed frameshift site by cognate binding of aminoacyl-tRNA. | Q40021492 | ||
Contributions of the brome mosaic virus RNA-3 3'-nontranslated region to replication and translation | Q40045319 | ||
The signal for translational readthrough of a UGA codon in Sindbis virus RNA involves a single cytidine residue immediately downstream of the termination codon | Q40046708 | ||
Relative importance of 7-methylguanosine in ribosome binding and translation of vesicular stomatitis virus mRNA in wheat germ and reticulocyte cell-free systems | Q40050102 | ||
Cowpea mosaic virus middle component RNA contains a sequence that allows internal binding of ribosomes and that requires eukaryotic initiation factor 4F for optimal translation | Q40064715 | ||
The full-length transcript of a caulimovirus is a polycistronic mRNA whose genes are trans activated by the product of gene VI | Q40065489 | ||
Proteolytic cleavage of initiation factor eIF-4 gamma in the reticulocyte lysate inhibits translation of capped mRNAs but enhances that of uncapped mRNAs. | Q40392783 | ||
Autoregulation of poly(A)-binding protein synthesisin vitro | Q40394504 | ||
Differential codon usage: a safeguard against inappropriate expression of specialized genes? | Q40399226 | ||
The nucleic acid-binding zinc finger protein of potato virus M is translated by internal initiation as well as by ribosomal frameshifting involving a shifty stop codon and a novel mechanism of P-site slippage | Q40401371 | ||
Differential response to frameshift signals in eukaryotic and prokaryotic translational systems | Q40404909 | ||
The translational termination signal database | Q40408267 | ||
Elongation factor 1α, translation and the cytoskeleton | Q40443868 | ||
Cytoplasmic mRNA-protein interactions in eukaryotic gene expression | Q40443890 | ||
Pea early browning virus RNA1 encodes four polypeptides including a putative zinc-finger protein. | Q40448174 | ||
Sequence of a 21 kd zein gene from maize containing an in-frame stop codon. | Q40448216 | ||
Infectious TYMV RNA from cloned cDNA: effects in vitro and in vivo of point substitutions in the initiation codons of two extensively overlapping ORFs. | Q40450654 | ||
Diversity of cytoplasmic functions for the 3' untranslated region of eukaryotic transcripts. | Q40475495 | ||
Binding of ribosomes to the 5′ leader sequence (N = 258) of RNA 3 from alfalfa mosaic virus | Q40495773 | ||
An analysis of the sequence of an infectious clone of rice tungro bacilliform virus, a plant pararetrovirus | Q40503856 | ||
Eukaryotic start and stop translation sites. | Q40504517 | ||
Functional analysis of the tobacco mosaic virus tRNA-like structure in cytoplasmic gene regulation | Q40507051 | ||
Translatability of a plant-mRNA strongly influences its accumulation in transgenic plants | Q40516582 | ||
Role of an upstream open reading frame in the translation of polycistronic mRNAs in plant cells | Q40533336 | ||
Identification of the motifs within the tobacco mosaic virus 5'-leader responsible for enhancing translation | Q40534058 | ||
Internal initiation of mRNA translation in eukaryotes. | Q40535148 | ||
Pseudouridine in the anticodon G psi A of plant cytoplasmic tRNA(Tyr) is required for UAG and UAA suppression in the TMV-specific context | Q40535542 | ||
The 5'-leader sequence of tobacco mosaic virus RNA enhances the expression of foreign gene transcripts in vitro and in vivo | Q40566200 | ||
Studies on the mechanism of translational enhancement by the 5'-leader sequence of tobacco mosaic virus RNA. | Q41968149 | ||
Rice dwarf phytoreovirus segment S12 transcript is tricistronic in vitro | Q42028190 | ||
Insect resistant rice generated by introduction of a modified delta-endotoxin gene of Bacillus thuringiensis. | Q42069567 | ||
A phylogenetically conserved sequence within viral 3' untranslated RNA pseudoknots regulates translation | Q42221538 | ||
Complete nucleotide sequence of peanut clump virus RNA 1 and relationships with other fungus-transmitted rod-shaped viruses | Q42594545 | ||
In vivo expression and mutational analysis of the barley yellow dwarf virus readthrough gene | Q42595004 | ||
A plant plasma membrane proton-ATPase gene is regulated by development and environment and shows signs of a translational regulation | Q42596034 | ||
Rice tungro bacilliform virus: transcription and translation in protoplasts | Q42601255 | ||
Nucleotide sequence of carnation ringspot dianthovirus RNA-1. | Q42602390 | ||
Analysis of a translational enhancer upstream from the coat protein open reading frame of potato virus S. | Q42603244 | ||
Expression of a downstream gene from a bicistronic transcription unit in transgenic tobacco plants | Q42603588 | ||
Identification and analysis of the site of -1 ribosomal frameshifting in red clover necrotic mosaic virus | Q42605487 | ||
Beet yellows closterovirus: complete genome structure and identification of a leader papain-like thiol protease | Q42610419 | ||
Splicing in a plant pararetrovirus | Q42611891 | ||
Control of start codon choice on a plant viral RNA encoding overlapping genes | Q42613381 | ||
Translational frameshifting by barley yellow dwarf virus RNA (PAV serotype) in Escherichia coli and in eukaryotic cell-free extracts | Q42617361 | ||
Synthesis of full-length transcripts of beet western yellows virus RNA: Messenger properties and biological activity in protoplasts | Q42617453 | ||
The beet western yellows virus ST9-associated RNA shares structural and nucleotide sequence homology with carmo-like viruses | Q42618584 | ||
Synthesis of the putative red clover necrotic mosaic virus RNA polymerase by ribosomal frameshifting in vitro | Q42619559 | ||
Translation of the mRNA of the maize transcriptional activator Opaque-2 is inhibited by upstream open reading frames present in the leader sequence | Q42619691 | ||
The complete nucleotide sequence of tobacco necrosis virus strain D | Q42622333 | ||
The nucleotide sequence and luteovirus-like nature of RNA 1 of an aphid non-transmissible strain of pea enation mosaic virus | Q42622853 | ||
Mutational analysis of the RNA pseudoknot component of a coronavirus ribosomal frameshifting signal | Q42623053 | ||
Effect of eukaryotic initiation factor 4F on AUG selection in a bicistronic mRNA. | Q42626886 | ||
Infectious transcripts from cloned cucumber necrosis virus cDNA: evidence for a bifunctional subgenomic mRNA. | Q42627506 | ||
Characterization of a potato leafroll luteovirus subgenomic RNA: differential expression by internal translation initiation and UAG suppression | Q42634399 | ||
Posttranscriptional trans-activation in cauliflower mosaic virus | Q42643433 | ||
Sequences that surround the stop codons of upstream open reading frames in GCN4 mRNA determine their distinct functions in translational control | Q42645039 | ||
Nucleotide sequence and translation of satellite tobacco mosaic virus RNA. | Q42645947 | ||
Translation of the second gene of peanut clump virus RNA 2 occurs by leaky scanning in vitro | Q42669428 | ||
Genes and cis-Acting Sequences Involved in Replication of Barley Yellow Dwarf Virus-PAV RNA | Q42682082 | ||
Complete sequence of the citrus tristeza virus RNA genome | Q42684039 | ||
The putative replicase of the cocksfoot mottle sobemovirus is translated as a part of the polyprotein by -1 ribosomal frameshift | Q42691542 | ||
The role of the 3'-untranslated region of non-polyadenylated plant viral mRNAs in regulating translational efficiency | Q43490448 | ||
Translation efficiency of the human T-cell leukemia virus (HTLV-2) gag gene modulates the frequency of ribosomal frameshifting | Q43583563 | ||
The cap and poly(A) tail function synergistically to regulate mRNA translational efficiency | Q43620210 | ||
Localization of in vivo ribosome pause sites | Q43661243 | ||
A nascent peptide is required for ribosomal bypass of the coding gap in bacteriophage T4 gene 60. | Q43672520 | ||
Translation enhancing properties of the 5'-leader of potato virus X genomic RNA | Q43746812 | ||
Characterization of the cell-free translation products of carnation mottle virus genomic and subgenomic RNAs | Q43782117 | ||
Coevolution of codon usage and transfer RNA abundance | Q43851327 | ||
Leaky UAG termination codon in tobacco mosaic virus RNA | Q44134735 | ||
The signal for a leaky UAG stop codon in several plant viruses includes the two downstream codons | Q44362876 | ||
Enhancing effect of the 3′‐untranslated region of tobacco mosaic virus RNA on protein synthesis in vitro | Q44416209 | ||
Translation of tobacco rattle virus RNAs in vitro: four proteins from three RNAs | Q44839075 | ||
The 5'-leader sequence of tobacco mosaic virus RNA mediates initiation-factor-4E-independent, but still initiation-factor-4A-dependent translation in yeast extracts | Q44973916 | ||
Poly(A) binds to initiation factors and increases cap-dependent translation in vitro | Q44985687 | ||
Translation controls the expression level of a chimaeric reporter gene | Q45078680 | ||
Coding density of the turnip yellow mosaic virus genome: roles of the overlapping coat protein and p206-readthrough coding regions | Q45082661 | ||
Role of the Leader Sequence during Thermal Repression of Translation in Maize, Tobacco, and Carrot Protoplasts | Q45151540 | ||
Sequence of the 3' untranslated region of brome mosaic virus coat protein messenger RNA. | Q45393446 | ||
Translational control of GCN4: an in vivo barometer of initiation-factor activity | Q40566888 | ||
The remarkable variety of plant RNA virus genomes | Q40585020 | ||
Codon context and protein synthesis: enhancements of the genetic code | Q40587970 | ||
Determinants of translational fidelity and efficiency in vertebrate mRNAs | Q40606822 | ||
Eukaryotic protein synthesis: an in vitro analysis | Q40606827 | ||
Regulation of translation by specific protein/mRNA interactions | Q40606863 | ||
Regulation and function of non-AUG-initiated proto-oncogenes | Q40606869 | ||
Translational control during amino acid starvation | Q40614287 | ||
Basepairing with 18S ribosomal RNA in internal initiation of translation | Q40632640 | ||
Efficiency of translation initiation by non-AUG codons in Saccharomyces cerevisiae | Q40660561 | ||
Initiation codons within 5'-leaders of mRNAs as regulators of translation | Q40664332 | ||
Codon replacement in the PGK1 gene of Saccharomyces cerevisiae: experimental approach to study the role of biased codon usage in gene expression | Q40670961 | ||
Plant viruses as model systems for the study of non-canonical translation mechanisms in higher plants | Q40698395 | ||
Termination of translation in eukaryotes is governed by two interacting polypeptide chain release factors, eRF1 and eRF3 | Q40789153 | ||
The second to last amino acid in the nascent peptide as a codon context determinant. | Q40790501 | ||
The immediate downstream codon strongly influences the efficiency of utilization of eukaryotic translation initiation codons. | Q40792763 | ||
The identity of the base following the stop codon determines the efficiency of in vivo translational termination in Escherichia coli | Q40805404 | ||
Structural and functional studies of retroviral RNA pseudoknots involved in ribosomal frameshifting: nucleotides at the junction of the two stems are important for efficient ribosomal frameshifting. | Q40805858 | ||
Post-transcriptional regulation of nuclear-encoded genes in higher plants: the roles of mRNA stability and translation | Q40806927 | ||
Alternative readings of the genetic code | Q40839200 | ||
Regulation of eukaryotic protein synthesis by initiation factors. | Q40873679 | ||
The end in sight: terminating translation in eukaryotes | Q40951525 | ||
Translation of a polycistronic mRNA in the presence of the cauliflower mosaic virus transactivator protein | Q41083475 | ||
In vitro expression of cauliflower mosaic virus genes | Q41091118 | ||
Scanning independent ribosomal initiation of the Sendai virus X protein | Q41106902 | ||
Ribosomal frameshifting in plants: a novel signal directs the -1 frameshift in the synthesis of the putative viral replicase of potato leafroll luteovirus | Q41113896 | ||
The 5' untranslated region from pea seedborne mosaic potyvirus RNA as a translational enhancer in pea and tobacco protoplasts | Q41115999 | ||
The reverse transcriptase gene of cauliflower mosaic virus is translated separately from the capsid gene | Q41136555 | ||
Identification of the initiation codon of plum pox potyvirus genomic RNA. | Q41172841 | ||
Positive and negative control of translation by the leader sequence of cauliflower mosaic virus pregenomic 35S RNA. | Q41211910 | ||
Structure and function of the selenium translation element in the 3'-untranslated region of human cellular glutathione peroxidase mRNA. | Q41333165 | ||
Studies on the translocation of the amino terminus of apolipoprotein B into the endoplasmic reticulum | Q41357823 | ||
Cap accessibility correlates with the initiation efficiency of alfalfa mosaic virus RNAs | Q41360555 | ||
Coding from a distance: dissection of the mRNA determinants required for the incorporation of selenocysteine into protein | Q41534158 | ||
The leaky UGA termination codon of tobacco rattle virus RNA is suppressed by tobacco chloroplast and cytoplasmic tRNAs(Trp) with CmCA anticodon | Q41540748 | ||
A difference in the rate of ribosomal elongation balances the synthesis of eukaryotic translation initiation factor (eIF)-2 alpha and eIF-2 beta | Q41546788 | ||
UAG readthrough during TMV RNA translation: isolation and sequence of two tRNAs with suppressor activity from tobacco plants. | Q41562776 | ||
The molecular basis for the differential translation of TMV RNA in tobacco protoplasts and wheat germ extracts. | Q41571454 | ||
Initiation of translation of the cauliflower mosaic virus genome from a polycistronic mRNA: evidence from deletion mutagenesis. | Q41584804 | ||
Homeotic gene Antennapedia mRNA contains 5'-noncoding sequences that confer translational initiation by internal ribosome binding | Q41606264 | ||
Analysis of unstable RNA transcripts of insecticidal crystal protein genes of Bacillus thuringiensis in transgenic plants and electroporated protoplasts | Q41681910 | ||
Electron microscopic evidence for the circular form of RNA in the cytoplasm of eukaryotic cells | Q41700525 | ||
Initiation of translation at CUG, GUG, and ACG codons in mammalian cells | Q41727844 | ||
RNA pseudoknot domain of tobacco mosaic virus can functionally substitute for a poly(A) tail in plant and animal cells | Q41729789 | ||
Subcellular fate of the int-2 oncoprotein is determined by choice of initiation codon | Q41743775 | ||
The 3' untranslated region of satellite tobacco necrosis virus RNA stimulates translation in vitro | Q41763167 | ||
Expression of the genome of potato leafroll virus: readthrough of the coat protein termination codon in vivo | Q41837054 | ||
Precise mapping and in vitro translation of a trifunctional subgenomic RNA of barley yellow dwarf virus | Q41854874 | ||
Analysis of the role of the pseudoknot component in the SRV-1 gag-pro ribosomal frameshift signal: loop lengths and stability of the stem regions | Q41864618 | ||
Special peptidyl-tRNA molecules can promote translational frameshifting without slippage. | Q41945785 | ||
Regulation of translation in eukaryotic systems | Q35237445 | ||
Specific binding of eukaryotic initiation factor 2 to satellite tobacco necrosis virus RNA at a 5'-terminal sequence comprising the ribosome binding site | Q35323957 | ||
Influences of mRNA secondary structure on initiation by eukaryotic ribosomes | Q35602187 | ||
A consideration of alternative models for the initiation of translation in eukaryotes | Q35815713 | ||
Codon usage in plant genes | Q35862195 | ||
Sequence analysis suggests that tetra-nucleotides signal the termination of protein synthesis in eukaryotes | Q35885214 | ||
Ribosome pausing and stacking during translation of a eukaryotic mRNA. | Q35993850 | ||
In vitro transcription and translational efficiency of chimeric SP6 messenger RNAs devoid of 5' vector nucleotides | Q36005483 | ||
Overlapping open reading frames revealed by complete nucleotide sequencing of turnip yellow mosaic virus genomic RNA | Q36012120 | ||
Translational suppression in retroviral gene expression | Q36063387 | ||
Transcriptional and translational control of gene expression in cauliflower mosaic virus | Q36333803 | ||
Polyribosome targeting to microtubules: enrichment of specific mRNAs in a reconstituted microtubule preparation from sea urchin embryos | Q36382948 | ||
Tissue specific expression of the retinoic acid receptor-beta 2: regulation by short open reading frames in the 5'-noncoding region | Q36382977 | ||
An upstream open reading frame represses expression of Lc, a member of the R/B family of maize transcriptional activators | Q36519257 | ||
Selection of CUG and AUG initiator codons for Drosophila E74A translation depends on downstream sequences | Q36576099 | ||
Translation of equine infectious anemia virus bicistronic tat-rev mRNA requires leaky ribosome scanning of the tat CTG initiation codon | Q36643523 | ||
Effect of sequence context at stop codons on efficiency of reinitiation in GCN4 translational control | Q36644113 | ||
Translational inhibition mediated by a short upstream open reading frame in the human cytomegalovirus gpUL4 (gp48) transcript | Q36652154 | ||
RNA sequence of astrovirus: distinctive genomic organization and a putative retrovirus-like ribosomal frameshifting signal that directs the viral replicase synthesis | Q36659951 | ||
Cap-dependent and cap-independent translation by internal initiation of mRNAs in cell extracts prepared from Saccharomyces cerevisiae | Q36669457 | ||
Alternative initiation of translation determines cytoplasmic or nuclear localization of basic fibroblast growth factor | Q36682049 | ||
Subgenomic RNAs mediate expression of cistrons located internally on the genomic RNA of tobacco necrosis virus strain A | Q36685045 | ||
Ribosomal frameshifting requires a pseudoknot in the Saccharomyces cerevisiae double-stranded RNA virus | Q36690615 | ||
Bipartite signal for read-through suppression in murine leukemia virus mRNA: an eight-nucleotide purine-rich sequence immediately downstream of the gag termination codon followed by an RNA pseudoknot | Q36701300 | ||
mRNA poly(A) tail, a 3' enhancer of translational initiation | Q36715215 | ||
The AAPT1 gene of soybean complements a cholinephosphotransferase-deficient mutant of yeast | Q36730141 | ||
Cap recap: The involvement of eIF-4F in regulating gene expression | Q36749974 | ||
mRNA structures influencing translation in the yeast Saccharomyces cerevisiae | Q36786647 | ||
Leader length and secondary structure modulate mRNA function under conditions of stress | Q36791411 | ||
Context effects and inefficient initiation at non-AUG codons in eucaryotic cell-free translation systems | Q36795895 | ||
An RNA pseudoknot and an optimal heptameric shift site are required for highly efficient ribosomal frameshifting on a retroviral messenger RNA | Q36795944 | ||
Circumstances and mechanisms of inhibition of translation by secondary structure in eucaryotic mRNAs | Q36796132 | ||
Expression of dicistronic transcriptional units in transgenic tobacco | Q36798169 | ||
Successful expression in pollen of various plant species of in vitro synthesized mRNA introduced by particle bombardment. | Q52208773 | ||
The computer simulation of RNA folding pathways using a genetic algorithm. | Q52338286 | ||
Selenocysteyl-tRNAs recognize UGA in Beta vulgaris, a higher plant, and in Gliocladium virens, a filamentous fungus. | Q53490849 | ||
Control of mRNA Stability in Higher Plants. | Q53995510 | ||
Multiple elements in the 5' untranslated region down-regulate c-sis messenger RNA translation. | Q54003496 | ||
Elongation and Folding of Nascent Ricin Chains a Peptidyl-tRNA on Ribosomes: The Effect of Amino Acid Deletion on these Processes | Q54603803 | ||
A second putative mRNA binding site on the Escherichia coli ribosome. | Q54608686 | ||
Consecutive low-usage leucine codons block translation only when near the 5' end of a message in Escherichia coli. | Q54617430 | ||
Codon bias in Escherichia coli may modulate translation initiation. | Q54618011 | ||
Translation. Knowing when to stop. | Q54622300 | ||
Effects of long 5' leader sequences on initiation by eukaryotic ribosomes in vitro | Q55003335 | ||
Transfer RNA-mediated suppression of stop codons in protoplasts and transgenic plants | Q58065541 | ||
Recognition of UGA as a selenocysteine codon in Type I deiodinase requires sequences in the 3′ untranslated region | Q59064314 | ||
Enhanced translation of chimaeric messenger RNAs containing a plant viral untranslated leader sequence | Q59067188 | ||
Selection of the 5'-proximal translation initiation site is influenced by mRNA and eIF-2 concentrations | Q59661286 | ||
Development of a heat shock inducible expression cassette for plants: characterization of parameters for its use in transient expression assays | Q67258721 | ||
Analysis of leaky viral translation termination codons in vivo by transient expression of improved beta-glucuronidase vectors | Q67260890 | ||
Efficient initiation of translation at non-AUG triplets in plant cells | Q67482533 | ||
Effect of two consensus sequences preceding the translation initiator codon on gene expression in plant protoplasts | Q67533890 | ||
Ribosomes pause at specific sites during synthesis of membrane-bound chloroplast reaction center protein D1 | Q67941202 | ||
Post-transcriptional regulation in higher eukaryotes: the role of the reporter gene in controlling expression | Q67965743 | ||
Translation inhibition by an mRNA coding region secondary structure is determined by its proximity to the AUG initiation codon | Q68021134 | ||
Evidence for the translational control of storage protein gene expression in oat seeds | Q68027485 | ||
Regulation of caulimovirus gene expression and the involvement of cis-acting elements on both viral transcripts | Q68050478 | ||
Cap recognition and the entry of mRNA into the protein synthesis initiation cycle | Q68054422 | ||
Hypothesis: is eukaryotic initiation factor 2 the scanning factor? | Q68192533 | ||
Role of the 3'-poly(A) sequence in translational regulation of mRNAs in Xenopus laevis oocytes | Q68311775 | ||
Light-mediated control of translational initiation of ribulose-1, 5-bisphosphate carboxylase in amaranth cotyledons | Q68445175 | ||
Ribosomal frameshifting in the yeast retrotransposon Ty: tRNAs induce slippage on a 7 nucleotide minimal site | Q68468601 | ||
RNA pseudoknots: translational frameshifting and readthrough on viral RNAs | Q68924260 | ||
A tunnel in the large ribosomal subunit revealed by three-dimensional image reconstruction | Q69004129 | ||
E. coli ribosomes re-phase on retroviral frameshift signals at rates ranging from 2 to 50 percent | Q69366217 | ||
The function of plant heat shock promoter elements in the regulated expression of chimaeric genes in transgenic tobacco | Q69705862 | ||
Circular polysomes predominate on the rough endoplasmic reticulum of somatotropes and mammotropes in the rat anterior pituitary | Q69772873 | ||
Destabilization of messenger RNA/complementary DNA duplexes by the elongating 80 S ribosome | Q70154102 | ||
Electron microscopic evidence of circular molecules in 9-S globin mRNA from rabbit reticulocytes | Q70162281 | ||
Frameshifting in the expression of the E. coli trpR gene occurs by the bypassing of a segment of its coding sequence | Q70535266 | ||
UGA: a split personality in the universal genetic code | Q70703365 | ||
The signal sequence moves through a ribosomal tunnel into a noncytoplasmic aqueous environment at the ER membrane early in translocation | Q70766402 | ||
Analysis of action of the wobble adenine on codon reading within the ribosome | Q71751571 | ||
mRNA binding properties of wheat germ protein synthesis initiation factor 2 | Q71780666 | ||
Synthesis of ribosomal proteins from stored mRNAs early in seed germination | Q71841328 | ||
Ribosomal Decoding Processes at Codons in the A or P Sites Depend Differently on 2′-OH Groups | Q71941938 | ||
Translational arrest in hypoxic potato tubers is correlated with the aberrant association of elongation factor EF-1? with polysomes | Q71989432 | ||
The 5' untranslated region of PVY RNA, even located in an internal position, enables initiation of translation | Q72279089 | ||
Plant viral leaders influence expression of a reporter gene in tobacco | Q72553610 | ||
Role of the AGA/AGG codons, the rarest codons in global gene expression in Escherichia coli | Q72801102 | ||
Evidence for an internal ribosome entry site within the 5' non-translated region of turnip mosaic potyvirus RNA | Q72815514 | ||
Bacterial gene inserted in an engineered RNA virus: efficient expression in monocotyledonous plant cells | Q45400241 | ||
Cauliflower Mosaic Virus Gene VI Controls Translation from Dicistronic Expression Units in Transgenic Arabidopsis Plants | Q45730710 | ||
The tomato bushy stunt virus replicase proteins are coordinately expressed and membrane associated | Q45733828 | ||
The 5' and 3' untranslated regions of satellite tobacco necrosis virus RNA affect translational efficiency and dependence on a 5' cap structure | Q45773296 | ||
The 3'-terminal untranslated region of alfalfa mosaic virus RNA 4 facilitates the RNA entry into translation in a cell-free system | Q45776435 | ||
Complete nucleotide sequence and organization of the bipartite RNA genome of soil-borne wheat mosaic virus | Q45776514 | ||
The 3'-untranslated region of brome mosaic virus RNA does not enhance translation of capped mRNAs in vitro | Q45783730 | ||
A sequence located 4.5 to 5 kilobases from the 5' end of the barley yellow dwarf virus (PAV) genome strongly stimulates translation of uncapped mRNA. | Q45785409 | ||
A new tobacco mosaic virus vector and its use for the systemic production of angiotensin-I-converting enzyme inhibitor in transgenic tobacco and tomato | Q45785478 | ||
Effects of sequence elements in the potato virus X RNA 5' non-translated alpha beta-leader on its translation enhancing activity. | Q45790087 | ||
Binding of ribosomes to linear and circular forms of the 5'-terminal leader fragment of tobacco-mosaic-virus RNA. | Q45794353 | ||
Evidence that the requirements for ATP and wheat germ initiation factors 4A and 4F are affected by a region of satellite tobacco necrosis virus RNA that is 3' to the ribosomal binding site. | Q45832131 | ||
Cauliflower mosaic virus 35 S RNA leader region inhibits translation of downstream genes | Q45833413 | ||
Signals for ribosomal frameshifting in the Rous sarcoma virus gag-pol region | Q45840877 | ||
Characterisation of the 5'-leader sequence of tobacco mosaic virus RNA as a general enhancer of translation in vitro | Q45841808 | ||
Differential inhibition of downstream gene expression by the cauliflower mosaic virus 35S RNA leader | Q45842765 | ||
The absence of a m7G cap on beta-globin mRNA and alfalfa mosaic virus RNA 4 increases the amounts of initiation factor 4F required for translation | Q45849906 | ||
Requirement of gene VII in cis for the expression of downstream genes on the major transcript of figwort mosaic virus | Q45853850 | ||
The sequence between nucleotides 161 and 512 of cowpea mosaic virus M RNA is able to support internal initiation of translation in vitro | Q45854198 | ||
Evidence that the 75K readthrough protein of beet necrotic yellow vein virus RNA-2 is essential for transmission by the fungus Polymyxa betae | Q45854697 | ||
The mechanism of translation of cowpea mosaic virus middle component RNA: no evidence for internal initiation from experiments in an animal cell transient expression system | Q45857335 | ||
Translational efficiency and competitive ability of mRNAs with 5'-untranslated alpha beta-leader of potato virus X RNA. | Q45857380 | ||
The 5'-untranslated leader sequence of potato virus X RNA enhances the expression of a heterologous gene in vivo | Q45877850 | ||
Codon context effect in virus translational readthrough. A study in vitro of the determinants of TMV and Mo-MuLV amber suppression | Q45878463 | ||
Two-step binding of eukaryotic ribosomes to brome mosaic virus RNA3 | Q45890675 | ||
Amber codon suppression: the in vivo and in vitro analysis of two C-hordein genes from barley. | Q45909328 | ||
Heat Shock Disrupts Cap and Poly(A) Tail Function during Translation and Increases mRNA Stability of Introduced Reporter mRNA. | Q45943321 | ||
The regulation of gene expression in transformed maize aleurone and endosperm protoplasts. Analysis of promoter activity, intron enhancement, and mRNA untranslated regions on expression. | Q46016159 | ||
Synthesis and turnover of the light-harvesting chlorophylla/b-protein inLemna gibba grown with intermittent red light: possible translational control. | Q46048093 | ||
Elongation and termination reactions of protein synthesis on maize root tip polyribosomes studied in a homologous cell-free system | Q46126520 | ||
Visualizing mRNA expression in plant protoplasts: factors influencing efficient mRNA uptake and translation | Q46231009 | ||
Hypoxic stress-induced changes in ribosomes of maize seedling roots. | Q46370403 | ||
Characterization of ribosomal frameshifting in HIV-1 gag-pol expression | Q46573916 | ||
Regulation of mRNA entry into polysomes. Parameters affecting polysome size and the fraction of mRNA in polysomes | Q47192614 | ||
Partial resistance of nascent polypeptide chains to proteolytic digestion due to ribosomal shielding | Q47708573 | ||
Continuously coupled transcription-translation system for the production of rice cytoplasmic aldolase | Q47865224 | ||
Codon usage in higher plants, green algae, and cyanobacteria. | Q47922895 | ||
Identification of Selenocysteine in the Proteins of Selenate-grown Vigna radiata | Q47937892 | ||
Structure of globin mRNA and mRNA-protein particles. Use of dark-field electron microscopy | Q47962205 | ||
The homeobox gene ATH1 of Arabidopsis is derepressed in the photomorphogenic mutants cop1 and det1 | Q48076516 | ||
Transcriptional characterization of an alpha-zein gene cluster in maize | Q48121202 | ||
Translational activation of the non-AUG-initiated c-myc 1 protein at high cell densities due to methionine deprivation | Q48166624 | ||
The AU-rich sequences present in the introns of plant nuclear pre-mRNAs are required for splicing. | Q48289953 | ||
Mutations at a Zn(II) finger motif in the yeast eIF-2 beta gene alter ribosomal start-site selection during the scanning process | Q48317024 | ||
A persistent untranslated sequence within bacteriophage T4 DNA topoisomerase gene 60. | Q48328742 | ||
The leader peptide of yeast gene CPA1 is essential for the translational repression of its expression | Q48343035 | ||
Analysis of the stop codon context in plant nuclear genes | Q49170471 | ||
Different 3' end regions strongly influence the level of gene expression in plant cells | Q49171614 | ||
The relationship between eukaryotic translation and mRNA stability. A short upstream open reading frame strongly inhibits translational initiation and greatly accelerates mRNA degradation in the yeast Saccharomyces cerevisiae | Q50113260 | ||
P433 | issue | 1-2 | |
P1104 | number of pages | 31 | |
P304 | page(s) | 159-189 | |
P577 | publication date | 1996-10-01 | |
P1433 | published in | Plant Molecular Biology | Q15761850 |
P1476 | title | Translation in plants--rules and exceptions | |
P478 | volume | 32 |
Q33869122 | 'Green revolution' genes encode mutant gibberellin response modulators. |
Q44083058 | A KAS2 cDNA complements the phenotypes of the Arabidopsis fab1 mutant that differs in a single residue bordering the substrate binding pocket |
Q31075913 | A long leader intron of the Ostub16 rice beta-tubulin gene is required for high-level gene expression and can autonomously promote transcription both in vivo and in vitro |
Q42675889 | A maize r1 gene is regulated post-transcriptionally by differential splicing of its leader |
Q30651072 | A novel strategy for the expression of foreign genes from plant virus vectors |
Q40695194 | ARC-1, a sequence element complementary to an internal 18S rRNA segment, enhances translation efficiency in plants when present in the leader or intercistronic region of mRNAs |
Q33983301 | An internal ribosome entry site directs translation of the 3'-gene from Pelargonium flower break virus genomic RNA: implications for infectivity. |
Q35171250 | An unusual internal ribosomal entry site of inverted symmetry directs expression of a potato leafroll polerovirus replication-associated protein |
Q84587612 | Availability of Rubisco small subunit up-regulates the transcript levels of large subunit for stoichiometric assembly of its holoenzyme in rice |
Q34366200 | Bicistronic and fused monocistronic transcripts are derived from adjacent loci in the Arabidopsis genome |
Q42674684 | Characterisation and promoter analysis of the Arabidopsis gene encoding high-mobility-group protein HMG-I/Y. |
Q30940475 | Characterization and translational regulation of the arginine decarboxylase gene in carnation (Dianthus caryophyllus L.). |
Q33187723 | Characterization of a PttRPS18 promoter active in the vascular cambium region of hybrid aspen. |
Q48041170 | Cloning and characterisation of MEK1, an Arabidopsis gene encoding a homologue of MAP kinase kinase |
Q56879450 | Computational analyses and annotations of theArabidopsisperoxidase gene family |
Q39528287 | Contribution of downstream promoter elements to transcriptional regulation of the rice tungro bacilliform virus promoter |
Q41299727 | Coupled termination/reinitiation for translation of the downstream open reading frame B of the prototypic hypovirus CHV1-EP713 |
Q48328873 | DEX1, a novel plant protein, is required for exine pattern formation during pollen development in Arabidopsis |
Q24817119 | Evolutionary conservation suggests a regulatory function of AUG triplets in 5'-UTRs of eukaryotic genes |
Q46055002 | Eyes off transcription! The wonderful world of post-transcriptional regulation. |
Q38971780 | Hahb-4, a sunflower homeobox-leucine zipper gene, is a developmental regulator and confers drought tolerance to Arabidopsis thaliana plants |
Q52105529 | In silico identification of putative regulatory sequence elements in the 5'-untranslated region of genes that are expressed during male gametogenesis. |
Q39581475 | In vivo translation of the triple gene block of potato virus X requires two subgenomic mRNAs |
Q46611150 | Microspore separation in the quartet 3 mutants of Arabidopsis is impaired by a defect in a developmentally regulated polygalacturonase required for pollen mother cell wall degradation |
Q42681812 | Molecular analysis of PHYA in wild-type and phytochrome A-deficient mutants of tomato |
Q33960869 | Non-AUG initiation of AGAMOUS mRNA translation in Arabidopsis thaliana |
Q48273417 | Non-AUG translation initiation of mRNA encoding plastid-targeted phage-type RNA polymerase in Nicotiana sylvestris. |
Q45091407 | Overexpression of constitutive differential growth 1 gene, which encodes a RLCKVII-subfamily protein kinase, causes abnormal differential and elongation growth after organ differentiation in Arabidopsis |
Q36323796 | Programmed ribosomal frameshifting in HIV-1 and the SARS-CoV. |
Q39804672 | Prokaryotic-style frameshifting in a plant translation system: conservation of an unusual single-tRNA slippage event. |
Q33947680 | Prospecting sugarcane resistance to Sugarcane yellow leaf virus by genome-wide association |
Q24794842 | Recombination every day: abundant recombination in a virus during a single multi-cellular host infection |
Q40442630 | Ribosome shunting in the cauliflower mosaic virus 35S RNA leader is a special case of reinitiation of translation functioning in plant and animal systems |
Q39881626 | Rice tungro bacilliform virus open reading frames II and III are translated from polycistronic pregenomic RNA by leaky scanning. |
Q41664118 | Selective translation of cytoplasmic mRNAs in plants |
Q42681169 | Signs of translational regulation within the transcript leader of a plant plasma membrane H(+)-ATPase gene |
Q48298595 | Six active phage-type RNA polymerase genes in Nicotiana tabacum |
Q24534818 | Soybean ENOD40 encodes two peptides that bind to sucrose synthase |
Q43628353 | The 5' untranslated region of the At-P5R gene is involved in both transcriptional and post-transcriptional regulation |
Q43264739 | The 5' untranslated region of the VR-ACS1 mRNA acts as a strong translational enhancer in plants |
Q74099671 | The 5'-untranslated region of the ntp303 gene strongly enhances translation during pollen tube growth, but not during pollen maturation |
Q38326140 | The bean pod mottle virus RNA2-encoded 58-kilodalton protein P58 is required in cis for RNA2 accumulation |
Q38928252 | The intron of the Arabidopsis thaliana COX5c gene is able to improve the drought tolerance conferred by the sunflower Hahb-4 transcription factor |
Q42619806 | The large intergenic region of Rice tungro bacilliform virus evolved differentially among geographically distinguished isolates |
Q28360007 | The salt stress-inducible protein kinase gene, Esi47, from the salt-tolerant wheatgrass Lophopyrum elongatum is involved in plant hormone signaling |
Q47930520 | Transcript accumulation and utilization of alternate and non-consensus splice sites in rice granule-bound starch synthase are temperature-sensitive and controlled by a single-nucleotide polymorphism |
Q28284997 | Translation reinitiation and leaky scanning in plant viruses |
Q24550749 | Translational and structural requirements of the early nodulin gene enod40, a short-open reading frame-containing RNA, for elicitation of a cell-specific growth response in the alfalfa root cortex |
Q33785638 | Uncoupled expression of p33 and p92 permits amplification of tomato bushy stunt virus RNAs. |
Q38333118 | Use of alternate splice sites in granule-bound starch synthase mRNA from low-amylose rice varieties |
Q91901589 | V, 2.Ribosomal frameshifting in astroviruses |
Q34806611 | Viral strategies of translation initiation: ribosomal shunt and reinitiation |
Q37583114 | Virus versus host cell translation love and hate stories |
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