| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Yury O Chernoff | |
| Sergey G Inge-Vechtomov | |||
| Galina A Zhouravleva | |||
| P2860 | cites work | Evolutionary conservation of prion-forming abilities of the yeast Sup35 protein | Q73486816 |
| [A possible role of genetic translation ambiguity in evolution ] | Q77989504 | ||
| Functional amyloid formation within mammalian tissue | Q21092782 | ||
| Prion Protein Biology | Q21972822 | ||
| THE EVOLUTION OF THE EVOLVABILITY PROPERTIES OF THE YEAST PRION [PSI + ] | Q22065711 | ||
| The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription | Q22254119 | ||
| An abundant erythroid protein that stabilizes free alpha-haemoglobin | Q24299833 | ||
| Eukaryotic release factors (eRFs) history | Q24309050 | ||
| Yeast prions [URE3] and [PSI+] are diseases | Q24532887 | ||
| Genetic and environmental factors affecting the de novo appearance of the [PSI+] prion in Saccharomyces cerevisiae | Q24533260 | ||
| Enzyme evolution. I. The importance of untranslatable intermediates | Q24533393 | ||
| Structure of the cross-beta spine of amyloid-like fibrils | Q24548308 | ||
| Stress granule assembly is mediated by prion-like aggregation of TIA-1 | Q24559953 | ||
| Propagation of the yeast prion-like [psi+] determinant is mediated by oligomerization of the SUP35-encoded polypeptide chain release factor | Q24562896 | ||
| The protein product of the het-s heterokaryon incompatibility gene of the fungus Podospora anserina behaves as a prion analog | Q24643343 | ||
| A census of glutamine/asparagine-rich regions: implications for their conserved function and the prediction of novel prions | Q24671061 | ||
| Prions affect the appearance of other prions: the story of [PIN(+)]. | Q27937880 | ||
| A caspase-related protease regulates apoptosis in yeast | Q27938405 | ||
| A yeast prion provides a mechanism for genetic variation and phenotypic diversity | Q28140932 | ||
| Protein misfolding, evolution and disease | Q28143452 | ||
| On protein synthesis | Q28183644 | ||
| Mutation processes at the protein level: is Lamarck back? | Q28202414 | ||
| The evolution of the evolvability properties of the yeast prion [PSI+] | Q28203689 | ||
| Protein folding and misfolding | Q28235199 | ||
| Mice devoid of PrP are resistant to scrapie | Q28249108 | ||
| Prions as adaptive conduits of memory and inheritance | Q28254236 | ||
| Polyglycine expansions in eRF3/GSPT1 are associated with gastric cancer susceptibility | Q28259039 | ||
| The psi factor of yeast: a problem in inheritance | Q28289388 | ||
| Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila | Q29616737 | ||
| Why genes in pieces? | Q29618207 | ||
| Self-seeded fibers formed by Sup35, the protein determinant of [PSI+], a heritable prion-like factor of S. cerevisiae. | Q30427504 | ||
| The relationship between visible intracellular aggregates that appear after overexpression of Sup35 and the yeast prion-like elements [PSI(+)] and [PIN(+)]. | Q31727422 | ||
| The Saccharomyces cerevisiae ESU1 gene, which is responsible for enhancement of termination suppression, corresponds to the 3'-terminal half of GAL11. | Q33222623 | ||
| Functional insights from the distribution and role of homopeptide repeat-containing proteins | Q33736258 | ||
| Primary sequence independence for prion formation | Q33943998 | ||
| A neuronal isoform of the aplysia CPEB has prion-like properties | Q33974852 | ||
| Spontaneous assembly of a self-complementary oligopeptide to form a stable macroscopic membrane | Q34058519 | ||
| Internal initiation drives the synthesis of Ure2 protein lacking the prion domain and affects [URE3] propagation in yeast cells. | Q34179953 | ||
| Protein aggregation and aggregate toxicity: new insights into protein folding, misfolding diseases and biological evolution | Q34225700 | ||
| Beyond the Qs in the polyglutamine diseases | Q34228238 | ||
| Human lysozyme gene mutations cause hereditary systemic amyloidosis | Q34362632 | ||
| Structural insights into a yeast prion illuminate nucleation and strain diversity | Q34425023 | ||
| Interactions among prions and prion "strains" in yeast | Q34443841 | ||
| Progressive disruption of cellular protein folding in models of polyglutamine diseases. | Q34493281 | ||
| Identification of the genes encoding the cytosolic translation release factors from Podospora anserina and analysis of their role during the life cycle | Q34604908 | ||
| Genetic study of interactions between the cytoskeletal assembly protein sla1 and prion-forming domain of the release factor Sup35 (eRF3) in Saccharomyces cerevisiae | Q34607678 | ||
| A role for cytosolic hsp70 in yeast [PSI(+)] prion propagation and [PSI(+)] as a cellular stress. | Q34610589 | ||
| Molecular population genetics and evolution of a prion-like protein in Saccharomyces cerevisiae. | Q34613582 | ||
| Prion properties of the Sup35 protein of yeast Pichia methanolica | Q34661848 | ||
| Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology | Q35134776 | ||
| Sexual transmission of the [Het-s] prion leads to meiotic drive in Podospora anserina | Q35143742 | ||
| Mitochondrial dysfunction and reactive oxygen species in excitotoxicity and apoptosis: implications for the pathogenesis of neurodegenerative diseases | Q35564763 | ||
| Mammalian prion biology: one century of evolving concepts | Q35639302 | ||
| Prion species barrier between the closely related yeast proteins is detected despite coaggregation. | Q35669744 | ||
| Polyglutamine aggregates alter protein folding homeostasis in Caenorhabditis elegans | Q35746858 | ||
| Pathology and pathogenesis of bovine spongiform encephalopathy and scrapie. | Q35776122 | ||
| Neuronal cell death in transmissible spongiform encephalopathies (prion diseases) revisited: from apoptosis to autophagy. | Q35869394 | ||
| Prion genetics: new rules for a new kind of gene | Q35881769 | ||
| Amyloidogenic domains, prions and structural inheritance: rudiments of early life or recent acquisition? | Q35958560 | ||
| Cellular prion protein neuroprotective function: implications in prion diseases | Q36006619 | ||
| The role of apoptotic pathways in Alzheimer's disease neurodegeneration and cell death | Q36296817 | ||
| Superoxide is a mediator of an altruistic aging program in Saccharomyces cerevisiae | Q36321871 | ||
| Huntington toxicity in yeast model depends on polyglutamine aggregation mediated by a prion-like protein Rnq1 | Q36325681 | ||
| Prion domains: sequences, structures and interactions | Q36356816 | ||
| The efficiency of translation termination is determined by a synergistic interplay between upstream and downstream sequences in Saccharomyces cerevisiae. | Q38531566 | ||
| Role of Escherichia coli curli operons in directing amyloid fiber formation | Q39620298 | ||
| The behaviour of polyamino acids reveals an inverse side chain effect in amyloid structure formation | Q39665703 | ||
| A novel class of secreted hydrophobic proteins is involved in aerial hyphae formation in Streptomyces coelicolor by forming amyloid-like fibrils | Q39895836 | ||
| Aggregation of expanded polyglutamine domain in yeast leads to defects in endocytosis | Q39940570 | ||
| Freezing of a fish antifreeze protein results in amyloid fibril formation | Q40227486 | ||
| Stressful initiations | Q40715443 | ||
| Strong aggregation and increased toxicity of polyleucine over polyglutamine stretches in mammalian cells | Q40727766 | ||
| Deadly conformations--protein misfolding in prion disease | Q41478736 | ||
| Molecular basis of a yeast prion species barrier | Q41717715 | ||
| Genesis and variability of [PSI] prion factors in Saccharomyces cerevisiae. | Q41815189 | ||
| Translation termination efficiency can be regulated in Saccharomyces cerevisiae by environmental stress through a prion-mediated mechanism | Q41874945 | ||
| Modulation of prion formation, aggregation, and toxicity by the actin cytoskeleton in yeast | Q42119762 | ||
| Chronological aging leads to apoptosis in yeast | Q42774835 | ||
| Interaction of the yeast omnipotent suppressors SUP1(SUP45) and SUP2(SUP35) with non-mendelian factors | Q42962392 | ||
| Multiple Gln/Asn-rich prion domains confer susceptibility to induction of the yeast [PSI(+)] prion. | Q43711735 | ||
| Conformational variations in an infectious protein determine prion strain differences | Q44187524 | ||
| An antiprion effect of the anticytoskeletal drug latrunculin A in yeast. | Q45021453 | ||
| Dosage-dependent translational suppression in yeast Saccharomyces cerevisiae | Q45189931 | ||
| Mechanism of cross-species prion transmission: an infectious conformation compatible with two highly divergent yeast prion proteins | Q46476432 | ||
| Heat shock prevents alpha-synuclein-induced apoptosis in a yeast model of Parkinson's disease | Q46624111 | ||
| Prion variant maintained only at high levels of the Hsp104 disaggregase | Q46819506 | ||
| Cross-beta order and diversity in nanocrystals of an amyloid-forming peptide | Q47761131 | ||
| Protein-only transmission of three yeast prion strains | Q47929764 | ||
| Intracellular localization of homopolymeric amino acid-containing proteins expressed in mammalian cells | Q48016847 | ||
| Prion protein gene polymorphisms in Saccharomyces cerevisiae | Q48234799 | ||
| Yeast [PSI+] "prions" that are crosstransmissible and susceptible beyond a species barrier through a quasi-prion state | Q48356057 | ||
| Survival of water stress in annual fish embryos: dehydration avoidance and egg envelope amyloid fibers. | Q50668782 | ||
| Modulation of prion-dependent polyglutamine aggregation and toxicity by chaperone proteins in the yeast model. | Q50771820 | ||
| A small reservoir of disabled ORFs in the yeast genome and its implications for the dynamics of proteome evolution. | Q53878162 | ||
| The formation of Escherichia coli curli amyloid fibrils is mediated by prion-like peptide repeats. | Q54481174 | ||
| Amyloidogenic nature of spider silk | Q57220923 | ||
| Absence of structural homology between sup1 and sup2 genes of yeast Saccharomyces cerevisiae and identification of their transcripts | Q70147857 | ||
| [Prionization of the Pichia methanolica SUP35 gene product in the yeast Saccharomyces cerevisiae] | Q73232237 | ||
| P433 | issue | 4 | |
| P921 | main subject | prion protein family | Q24724413 |
| P304 | page(s) | 228-235 | |
| P577 | publication date | 2007-10-01 | |
| P1433 | published in | Prion | Q26842757 |
| P1476 | title | Biological roles of prion domains | |
| P478 | volume | 1 |
| Q45356010 | A putative role of the Sup35p C-terminal domain in the cytoskeleton organization during yeast mitosis |
| Q34985224 | Destabilization and recovery of a yeast prion after mild heat shock. |
| Q26796603 | Disaggregases, molecular chaperones that resolubilize protein aggregates |
| Q34714516 | Discovering putative prion sequences in complete proteomes using probabilistic representations of Q/N-rich domains |
| Q34389862 | Does the central dogma still stand? |
| Q42133943 | Genetic and epigenetic control of the efficiency and fidelity of cross-species prion transmission. |
| Q50490011 | Hsp104 as a key modulator of prion-mediated oxidative stress in Saccharomyces cerevisiae. |
| Q34814695 | In Sup35p filaments (the [PSI+] prion), the globular C-terminal domains are widely offset from the amyloid fibril backbone |
| Q33772936 | Interdependence of amyloid formation in yeast: implications for polyglutamine disorders and biological functions |
| Q34829539 | Looked at life from both sides now |
| Q21266674 | Origins of amyloid-β |
| Q34246922 | Polyglutamine toxicity is controlled by prion composition and gene dosage in yeast |
| Q26825056 | Potential roles for prions and protein-only inheritance in cancer |
| Q39315112 | Prion: disease or relief? |
| Q36154362 | Prions in yeast |
| Q37162363 | Prions: Beyond a Single Protein |
| Q27008857 | Quantum dots and prion proteins: is this a new challenge for neurodegenerative diseases imaging? |
| Q40561872 | Strain conformation controls the specificity of cross-species prion transmission in the yeast model |
| Q36825349 | Stress and prions: lessons from the yeast model |
| Q42467404 | The role of DNA polymerase alpha in the control of mutagenesis in Saccharomyces cerevisiae cells starved for nutrients |
| Q33575482 | Yeast prions assembly and propagation: contributions of the prion and non-prion moieties and the nature of assemblies |
| Q83011244 | [Cutaneous amyloidosis] |
Search more.