scholarly article | Q13442814 |
P50 | author | Reed Wickner | Q7306711 |
P2093 | author name string | R. B. Wickner | |
S. S. Sommer | |||
S. P. Ridley | |||
P2860 | cites work | Yeast Killer Mutants with Altered Double-Stranded Ribonucleic Acid | Q33793363 |
[HOK], a new yeast non-Mendelian trait, enables a replication-defective killer plasmid to be maintained | Q33948471 | ||
Genetic analysis of mutations affecting growth of Saccharomyces cerevisiae at low temperature | Q33989810 | ||
A mutant killer plasmid whose replication depends on a chromosomal "superkiller" mutation | Q34000634 | ||
Selection of lys2 Mutants of the Yeast SACCHAROMYCES CEREVISIAE by the Utilization of alpha-AMINOADIPATE. | Q34002073 | ||
Twenty-six chromosomal genes needed to maintain the killer double-stranded RNA plasmid of Saccharomyces cerevisiae | Q34015682 | ||
Genetic mapping in yeast | Q34058219 | ||
A comparison of the killer character in different yeasts and its classification | Q34263534 | ||
A mutant of Saccharomyces cerevisiae defective for nuclear fusion | Q35031157 | ||
Electron microscopic heteroduplex analysis of "killer" double-stranded RNA species from yeast | Q35989744 | ||
Ribosomal protein L3 is involved in replication or maintenance of the killer double-stranded RNA genome of Saccharomyces cerevisiae | Q36306758 | ||
Co-curing of plasmids affecting killer double-stranded RNAs of Saccharomyces cerevisiae: [HOK], [NEX], and the abundance of L are related and further evidence that M1 requires L | Q36309952 | ||
Chromosomal superkiller mutants of Saccharomyces cerevisiae | Q36342332 | ||
"Superkiller" mutations suppress chromosomal mutations affecting double-stranded RNA killer plasmid replication in saccharomyces cerevisiae | Q36353194 | ||
"Killer character" of Saccharomyces cerevisiae: curing by growth at elevated temperature. | Q36770005 | ||
Defective Interference in the Killer System of Saccharomyces cerevisiae | Q36930560 | ||
Killer systems in Saccharomyces cerevisiae: three distinct modes of exclusion of M2 double-stranded RNA by three species of double-stranded RNA, M1, L-A-E, and L-A-HN. | Q36938202 | ||
Two New Double-Stranded RNA Molecules Showing Non-Mendelian Inheritance and Heat Inducibility in Saccharomyces cerevisiae | Q36940801 | ||
Virus-like particles from killer, neutral, and sensitive strains of Saccharomyces cerevisiae | Q37499374 | ||
Yeast Killer Toxin: Purification and Characterisation of the Protein Toxin from Saccharomyces cerevisiae | Q39238032 | ||
Genetic control of replication of the double-stranded RNA segments of the killer systems in Saccharomyces cerevisiae | Q40147316 | ||
Physiology of killer factor in yeast. | Q40324938 | ||
Sequences at the 3' ends of yeast viral dsRNAs: proposed transcriptase and replicase initiation sites. | Q40499573 | ||
Translation of the L-species dsRNA genome of the killer-associated virus-like particles of Saccharomyces cerevisiae | Q40829329 | ||
Virus-like particles and double stranded RNA from killer and non-killer strains of Saccharomyces cerevisiae | Q41052584 | ||
Preliminary Characterization of Two Species of dsRNA in Yeast and their Relationship to the “Killer” Character | Q44092718 | ||
Virus-like Particles Associated with the Double-stranded RNA Species Found in Killer and Sensitive Strains of the Yeast Saccharomyces cerevisiae | Q44990276 | ||
Translational analysis of the killer-associated virus-like particle dsRNA genome of S. cerevisiae: M dsRNA encodes toxin | Q45793377 | ||
Chromosomal genes essential for replication of a double-stranded RNA plasmid of Saccharomyces cerevisiae: the killer character of yeast | Q67491031 | ||
Yeast L dsRNA consists of at least three distinct RNAs; evidence that the non-Mendelian genes [HOK], [NEX] and [EXL] are on one of these dsRNAs | Q71642297 | ||
Plasmids controlled exclusion of the K2 killer double-stranded RNA plasmid of yeast | Q72148034 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Saccharomyces cerevisiae | Q719725 |
cell biology | Q7141 | ||
P304 | page(s) | 761-770 | |
P577 | publication date | 1984-04-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Superkiller Mutations in Saccharomyces cerevisiae Suppress Exclusion of M2 Double-Stranded RNA by L-A-HN and Confer Cold Sensitivity in the Presence of M and L-A-HN | |
P478 | volume | 4 |
Q40420151 | 20S RNA narnavirus defies the antiviral activity of SKI1/XRN1 in Saccharomyces cerevisiae. |
Q27938357 | 3' poly(A) is dispensable for translation |
Q36866145 | A deletion mutant of L-A double-stranded RNA replicates like M1 double-stranded RNA. |
Q27937973 | A novel Rtg2p activity regulates nitrogen catabolism in yeast |
Q27934140 | A nuclear 3'-5' exonuclease involved in mRNA degradation interacts with Poly(A) polymerase and the hnRNA protein Npl3p |
Q40731576 | A population study of killer viruses reveals different evolutionary histories of two closely related Saccharomyces sensu stricto yeasts |
Q37425038 | A promiscuous prion: efficient induction of [URE3] prion formation by heterologous prion domains |
Q35791051 | A protein required for prion generation: [URE3] induction requires the Ras-regulated Mks1 protein |
Q54402482 | A short splicing isoform of HBS1L links the cytoplasmic exosome and SKI complexes in humans. |
Q39443387 | A whole genome screen for HIV restriction factors |
Q48138559 | A yeast antiviral protein, SKI8, shares a repeated amino acid sequence pattern with beta-subunits of G proteins and several other proteins |
Q44283235 | A yeast assay for high throughput screening of natural anti-viral agents |
Q93078425 | An RNA Metabolism and Surveillance Quartet in the Major Histocompatibility Complex |
Q27931005 | Antiviral protein Ski8 is a direct partner of Spo11 in meiotic DNA break formation, independent of its cytoplasmic role in RNA metabolism |
Q28260762 | Cell and molecular biology of the exosome: how to make or break an RNA |
Q33823326 | Circular single-stranded RNA replicon in Saccharomyces cerevisiae |
Q58450814 | Cloning and characterization of the SKI3 gene of Saccharomyces cerevisiae demonstrates allelism to SKI5 |
Q42715521 | Conserved functions of yeast genes support the duplication, degeneration and complementation model for gene duplication |
Q48234144 | Cytoplasmic N-terminal protein acetylation is required for efficient photosynthesis in Arabidopsis |
Q36551077 | Decoying the cap- mRNA degradation system by a double-stranded RNA virus and poly(A)- mRNA surveillance by a yeast antiviral system |
Q36802258 | Degradation of mRNAs that lack a stop codon: a decade of nonstop progress |
Q35922438 | Discovering protein-based inheritance through yeast genetics |
Q37039276 | Diverse aberrancies target yeast mRNAs to cytoplasmic mRNA surveillance pathways |
Q24537457 | Domain interactions within the Ski2/3/8 complex and between the Ski complex and Ski7p |
Q36670977 | Double-stranded RNA viruses of Saccharomyces cerevisiae. |
Q36947302 | Double-stranded RNAs that encode killer toxins in Saccharomyces cerevisiae: unstable size of M double-stranded RNA and inhibition of M2 replication by M1. |
Q24634261 | Double-stranded ribonucleic acid killer systems in yeasts |
Q36645641 | Elimination of L-A double-stranded RNA virus of Saccharomyces cerevisiae by expression of gag and gag-pol from an L-A cDNA clone |
Q27936790 | Evidence that the SKI antiviral system of Saccharomyces cerevisiae acts by blocking expression of viral mRNA. |
Q36687857 | Expression of yeast L-A double-stranded RNA virus proteins produces derepressed replication: a ski- phenocopy |
Q53331688 | Functional interactions among members of the meiotic initiation complex in fission yeast. |
Q45865212 | Genetic analysis of maintenance and expression of L and M double-stranded RNAs from yeast killer virus K28. |
Q27930309 | Genetic architecture of ethanol-responsive transcriptome variation in Saccharomyces cerevisiae strains |
Q35970856 | Heritable activity: a prion that propagates by covalent autoactivation |
Q36650814 | His-154 is involved in the linkage of the Saccharomyces cerevisiae L-A double-stranded RNA virus Gag protein to the cap structure of mRNAs and is essential for M1 satellite virus expression |
Q33967514 | Identification of novel genes required for yeast pre-mRNA splicing by means of cold-sensitive mutations |
Q35611714 | In vitro L-A double-stranded RNA synthesis in virus-like particles from Saccharomyces cerevisiae |
Q34366941 | Inhibition of 5' to 3' mRNA degradation under stress conditions in Saccharomyces cerevisiae: from GCN4 to MET16. |
Q37187943 | Interfaces of the yeast killer phenomenon |
Q36724713 | K28, a unique double-stranded RNA killer virus of Saccharomyces cerevisiae |
Q33965012 | KRB1, a suppressor of mak7-1 (a mutant RPL4A), is RPL4B, a second ribosomal protein L4 gene, on a fragment of Saccharomyces chromosome XII |
Q36833912 | L-A double-stranded RNA viruslike particle replication cycle in Saccharomyces cerevisiae: particle maturation in vitro and effects of mak10 and pet18 mutations |
Q36689865 | Localization and roles of Ski8p protein in Sordaria meiosis and delineation of three mechanistically distinct steps of meiotic homolog juxtaposition |
Q33959884 | MAK10, a glucose-repressible gene necessary for replication of a dsRNA virus of Saccharomyces cerevisiae, has T cell receptor alpha-subunit motifs |
Q36270620 | MKT1, a nonessential Saccharomyces cerevisiae gene with a temperature-dependent effect on replication of M2 double-stranded RNA |
Q27933062 | Mak21p of Saccharomyces cerevisiae, a homolog of human CAATT-binding protein, is essential for 60 S ribosomal subunit biogenesis |
Q27933744 | Mak5p, which is required for the maintenance of the M1 dsRNA virus, is encoded by the yeast ORF YBR142w and is involved in the biogenesis of the 60S subunit of the ribosome |
Q38042403 | Mechanism of the initiation of mRNA decay: role of eRF3 family G proteins |
Q36448739 | Molecular cloning of chromosome I DNA from Saccharomyces cerevisiae: isolation of the MAK16 gene and analysis of an adjacent gene essential for growth at low temperatures |
Q40666049 | Mutations in the G-domain of Ski7 cause specific dysfunction in non-stop decay. |
Q40756496 | New developments in fungal virology |
Q54445090 | On the mechanism of exclusion of M2 double-stranded RNA by L-A-E double-stranded RNA in Saccharomyces cerevisiae. |
Q36758757 | Overproduction of yeast viruslike particles by strains deficient in a mitochondrial nuclease |
Q60321615 | Persistent Yeast Single-stranded RNA Viruses Existin Vivoas Genomic RNA·RNA Polymerase Complexes in 1:1 Stoichiometry |
Q46021819 | RNA and protein interactions modulated by protein arginine methylation. |
Q49912881 | RNA helicases in RNA decay |
Q28251052 | RNA-quality control by the exosome |
Q27930255 | RRP1, a Saccharomyces cerevisiae gene affecting rRNA processing and production of mature ribosomal subunits |
Q39111714 | Relationships and Evolution of Double-Stranded RNA Totiviruses of Yeasts Inferred from Analysis of L-A-2 and L-BC Variants in Wine Yeast Strain Populations |
Q36698153 | Ribosomal frameshifting efficiency and gag/gag-pol ratio are critical for yeast M1 double-stranded RNA virus propagation |
Q33957131 | Ribosomal protein L3 mutants alter translational fidelity and promote rapid loss of the yeast killer virus |
Q36701036 | Scrambled prion domains form prions and amyloid |
Q33786495 | Ski6p is a homolog of RNA-processing enzymes that affects translation of non-poly(A) mRNAs and 60S ribosomal subunit biogenesis |
Q35555143 | Structure and expression of the M2 genomic segment of a type 2 killer virus of yeast. |
Q36693068 | Structure, function, and amyloidogenesis of fungal prions: filament polymorphism and prion variants |
Q36784058 | Suppression of chromosomal mutations affecting M1 virus replication in Saccharomyces cerevisiae by a variant of a viral RNA segment (L-A) that encodes coat protein |
Q40016255 | Synthetic lethality of sep1 (xrn1) ski2 and sep1 (xrn1) ski3 mutants of Saccharomyces cerevisiae is independent of killer virus and suggests a general role for these genes in translation control |
Q37661690 | Targeting RNA for processing or destruction by the eukaryotic RNA exosome and its cofactors |
Q27934144 | The 3' to 5' degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3' to 5' exonucleases of the exosome complex |
Q36820913 | The coat protein of the yeast double-stranded RNA virus L-A attaches covalently to the cap structure of eukaryotic mRNA. |
Q27675788 | The crystal structure of S. cerevisiae Ski2, a DExH helicase associated with the cytoplasmic functions of the exosome |
Q27930922 | The exosome: a conserved eukaryotic RNA processing complex containing multiple 3'-->5' exoribonucleases |
Q47289620 | The exosome: a versatile RNA processing machine |
Q24307917 | The human PAF complex coordinates transcription with events downstream of RNA synthesis |
Q39751720 | The killer phenomenon in yeasts |
Q36819760 | The prion model for [URE3] of yeast: spontaneous generation and requirements for propagation |
Q33643644 | The ski7 antiviral protein is an EF1-alpha homolog that blocks expression of non-Poly(A) mRNA in Saccharomyces cerevisiae. |
Q45186189 | The structural basis of recognition and removal of cellular mRNA 7-methyl G 'caps' by a viral capsid protein: a unique viral response to host defense |
Q30341567 | The structure of Ski8p, a protein regulating mRNA degradation: Implications for WD protein structure |
Q58760688 | The viral killer system in yeast: from molecular biology to application |
Q36711315 | The yeast KRE5 gene encodes a probable endoplasmic reticulum protein required for (1----6)-beta-D-glucan synthesis and normal cell growth |
Q27931202 | The yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo |
Q36909420 | Thermolabile L-A virus-like particles from pet18 mutants of Saccharomyces cerevisiae |
Q36913649 | Three different M1 RNA-containing viruslike particle types in Saccharomyces cerevisiae: in vitro M1 double-stranded RNA synthesis |
Q35586102 | Translation and M1 double-stranded RNA propagation: MAK18 = RPL41B and cycloheximide curing |
Q33962265 | Translational maintenance of frame: mutants of Saccharomyces cerevisiae with altered -1 ribosomal frameshifting efficiencies |
Q36955579 | Virus-like particle capsid proteins encoded by different L double-stranded RNAs of Saccharomyces cerevisiae: their roles in maintenance of M double-stranded killer plasmids |
Q34077960 | Viruses and prions of Saccharomyces cerevisiae |
Q41813616 | Yeast KRE genes provide evidence for a pathway of cell wall beta-glucan assembly |
Q47605842 | Yeast Killer Toxin K28: Biology and Unique Strategy of Host Cell Intoxication and Killing |
Q42724712 | Yeast double-stranded RNA virus L-A deliberately synthesizes RNA transcripts with 5'-diphosphate |
Q36465377 | Yeast dsRNA viruses: replication and killer phenotypes |
Q35606863 | Yeast killer elements hold their hosts hostage |
Q24532887 | Yeast prions [URE3] and [PSI+] are diseases |
Q24548790 | Yeast transcripts cleaved by an internal ribozyme provide new insight into the role of the cap and poly(A) tail in translation and mRNA decay |
Q27936971 | Yeast virus propagation depends critically on free 60S ribosomal subunit concentration |