| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1146/ANNUREV.CELLBIO.15.1.661 |
| P698 | PubMed publication ID | 10611975 |
| P2093 | author name string | Lindquist SL | |
| Serio TR | |||
| P921 | main subject | regulation of molecular function | Q22260622 |
| P304 | page(s) | 661-703 | |
| P577 | publication date | 1999-01-01 | |
| P1433 | published in | Annual Review of Cell and Developmental Biology | Q4497277 |
| P1476 | title | [PSI+]: an epigenetic modulator of translation termination efficiency | |
| P478 | volume | 15 |
| Q41199178 | A Size Threshold Limits Prion Transmission and Establishes Phenotypic Diversity |
| Q24671061 | A census of glutamine/asparagine-rich regions: implications for their conserved function and the prediction of novel prions |
| Q24796241 | A method to assess compositional bias in biological sequences and its application to prion-like glutamine/asparagine-rich domains in eukaryotic proteomes |
| Q33319303 | A novel mutant of the Sup35 protein of Saccharomyces cerevisiae defective in translation termination and in GTPase activity still supports cell viability |
| Q28140932 | A yeast prion provides a mechanism for genetic variation and phenotypic diversity |
| Q35764299 | Amyloid formation of a yeast prion determinant. |
| Q28243882 | Amyloid-associated activity contributes to the severity and toxicity of a prion phenotype |
| Q37184755 | Amyloidogenesis of natively unfolded proteins |
| Q39051223 | Analysis of [SWI+ ] formation and propagation events. |
| Q34694904 | Analysis of prion factors in yeast |
| Q41775107 | Analysis of the Generation and Segregation of Propagons: Entities That Propagate the [PSI+] Prion in Yeast |
| Q33966829 | Analysis of the [RNQ+] prion reveals stability of amyloid fibers as the key determinant of yeast prion variant propagation |
| Q41995900 | Asparagine and glutamine ladders promote cross-species prion conversion |
| Q43553476 | Bidirectional amyloid fiber growth for a yeast prion determinant. |
| Q50725851 | Biochemical and genetic methods for characterization of [PIN+] prions in yeast. |
| Q21563345 | Complex adaptations can drive the evolution of the capacitor [PSI], even with realistic rates of yeast sex |
| Q46425975 | Conformational diversity in a yeast prion dictates its seeding specificity |
| Q27644061 | Crystal structure of a conserved N-terminal domain of histone deacetylase 4 reveals functional insights into glutamine-rich domains |
| Q30849388 | De novo [PSI +] prion formation involves multiple pathways to form infectious oligomers |
| Q36182814 | Distinct Prion Domain Sequences Ensure Efficient Amyloid Propagation by Promoting Chaperone Binding or Processing In Vivo |
| Q34389862 | Does the central dogma still stand? |
| Q39643430 | Dom34 rescues ribosomes in 3' untranslated regions |
| Q35212560 | Functional diversification of hsp40: distinct j-protein functional requirements for two prions allow for chaperone-dependent prion selection |
| Q39675179 | Guanidine hydrochloride inhibits the generation of prion "seeds" but not prion protein aggregation in yeast. |
| Q40869564 | Heterogeneous expression of the virulence-related adhesin Epa1 between individual cells and strains of the pathogen Candida glabrata |
| Q39354530 | Heterologous stop codon readthrough of metazoan readthrough candidates in yeast |
| Q30415108 | High pressure, a tool to switch between soluble and fibrillar prion protein structures. |
| Q55191686 | Hsf1 Phosphorylation Generates Cell-to-Cell Variation in Hsp90 Levels and Promotes Phenotypic Plasticity. |
| Q33766780 | Hsp104 overexpression cures Saccharomyces cerevisiae [PSI+] by causing dissolution of the prion seeds |
| Q46149440 | Increased -1 ribosomal frameshifting efficiency by yeast prion-like phenotype [PSI+]. |
| Q35194908 | Insights into prion biology: integrating a protein misfolding pathway with its cellular environment |
| Q34443841 | Interactions among prions and prion "strains" in yeast |
| Q34092913 | Leaky termination at premature stop codons antagonizes nonsense-mediated mRNA decay in S. cerevisiae |
| Q48251902 | Mammalian amyloidogenic proteins promote prion nucleation in yeast. |
| Q90379922 | More than Just a Phase: Prions at the Crossroads of Epigenetic Inheritance and Evolutionary Change |
| Q34152266 | Mouse GSPT2, but not GSPT1, can substitute for yeast eRF3 in vivo |
| Q43711735 | Multiple Gln/Asn-rich prion domains confer susceptibility to induction of the yeast [PSI(+)] prion. |
| Q35162895 | Newly identified prions in budding yeast, and their possible functions |
| Q35370931 | Nonsense codon suppression in fission yeast due to mutations of tRNA(Ser.11) and translation release factor Sup35 (eRF3). |
| Q52559873 | Nonsense mutations in the essential gene SUP35 of Saccharomyces cerevisiae are non-lethal. |
| Q35189946 | Nonsense suppression by near-cognate tRNAs employs alternative base pairing at codon positions 1 and 3. |
| Q35805382 | Origins of variation in the fungal cell surface |
| Q26823798 | Physicochemical properties of cells and their effects on intrinsically disordered proteins (IDPs) |
| Q34278926 | Poly(A)-binding protein acts in translation termination via eukaryotic release factor 3 interaction and does not influence [PSI(+)] propagation |
| Q26825056 | Potential roles for prions and protein-only inheritance in cancer |
| Q33325657 | Prion protein insertional mutations increase aggregation propensity but not fiber stability |
| Q53658117 | Prion protein remodelling confers an immediate phenotypic switch. |
| Q33965774 | Prion-dependent switching between respiratory competence and deficiency in the yeast nam9-1 mutant. |
| Q99209252 | Prion-like proteins as epigenetic devices of stress adaptation |
| Q24657467 | Probing the role of PrP repeats in conformational conversion and amyloid assembly of chimeric yeast prions |
| Q33838279 | Protein-only inheritance in yeast: something to get [PSI+]-ched about |
| Q73456437 | Rnq1: an epigenetic modifier of protein function in yeast |
| Q42073173 | Septin-containing barriers control the differential inheritance of cytoplasmic elements |
| Q27324147 | Spreading of a prion domain from cell-to-cell by vesicular transport in Caenorhabditis elegans |
| Q39646125 | Strains of [PSI(+)] are distinguished by their efficiencies of prion-mediated conformational conversion |
| Q36498591 | Structural variants of yeast prions show conformer-specific requirements for chaperone activity. |
| Q35942095 | Testing the faux-UTR model for NMD: analysis of Upf1p and Pab1p competition for binding to eRF3/Sup35p. |
| Q28303621 | The NatA acetyltransferase couples Sup35 prion complexes to the [PSI+] phenotype |
| Q34046537 | The protein kingdom extended: ordered and intrinsically disordered proteins, their folding, supramolecular complex formation, and aggregation. |
| Q42467404 | The role of DNA polymerase alpha in the control of mutagenesis in Saccharomyces cerevisiae cells starved for nutrients |
| Q36287669 | The role of Sse1 in the de novo formation and variant determination of the [PSI+] prion |
| Q34520452 | The utility of prions |
| Q34545641 | The yeast prion [PSI+]: molecular insights and functional consequences |
| Q27934115 | Tpa1p is part of an mRNP complex that influences translation termination, mRNA deadenylation, and mRNA turnover in Saccharomyces cerevisiae |
| Q44071728 | Transmissible spongiform encephalopathies: the story of a pathogenic protein |
| Q34305018 | [PSI+], SUP35, and chaperones |
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