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Person
ISNI: 
0000 0000 2757 4216
Name: 
Lindquist, S.
Lindquist, Susan
Lindquist, Susan L.
Susan Lindquist (American geneticist)
Susan Lindquist (Amerikaans biologe)
Susan Lindquist (US-amerikanische Molekularbiologin und Hochschullehrerin)
سوزان ليندكويست
سوزان لیندکوئست
スーザン・リンドキスト
苏珊·林德奎斯特
Dates: 
born 1949-06-05
Creation class: 
article
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Related names: 
Feramisco, James
Heat Shock Meeting (1990 : Ravello, Italy)
Maresca, B. (1950-)
Maresca, Bruno (1950-)
Pardue, Mary Lou
UCLA Symposium on Stress-Induced Proteins (1988 : Keystone, Colo.)
Titles: 
Aggregation of huntingtin in yeast varies with the length of the polyglutamine expansion and the expression of chaperone proteins
Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models.
[alpha]-Synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity
Amyloid deposits: protection against toxic protein species?
Amyloid fibres of Sup35 support a prion-like mechanism of inheritance in yeast.
Analysis of prion factors in yeast.
Antagonistic interactions between yeast chaperones Hsp104 and Hsp70 in prion curing.
Asymmetric deceleration of ClpB or Hsp104 ATPase activity unleashes protein-remodeling activity
Atypical AAA+ subunit packing creates an expanded cavity for disaggregation by the protein-remodeling factor Hsp104.
BETASCAN: probable beta-amyloids identified by pairwise probabilistic analysis.
Bridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicity
Cdc37 is a molecular chaperone with specific functions in signal transduction
Changes in the middle region of Sup35 profoundly alter the nature of epigenetic inheritance for the yeast prion [PSI+].
Chaperone-dependent amyloid assembly protects cells from prion toxicity
Chaperone Pathway in Protein Disaggregation: Hsp26 alters the nature of protein aggregates to facilitate reactivation by Hsp104, A
Compounds from an unbiased chemical screen reverse both ER-to-Golgi trafficking defects and mitochondrial dysfunction in Parkinson's disease models.
Conducting nanowires built by controlled self-assembly of amyloid fibers and selective metal deposition.
Context dependent neuroprotective properties of prion protein (PrP).
Context-dependent perturbation of neural systems in transgenic mice expressing a cytosolic prion protein
Conversion of a yeast prion protein to an infectious form in bacteria
Conversion of PrP to a Self-Perpetuating PrP super(Sc)-like Conformation in the Cytosol
Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol.
Cooperative kinetics of both Hsp104 ATPase domains and interdomain communication revealed by AAA sensor-1 mutants
Creating a protein-based element of inheritance
Defining a pathway of communication from the C-terminal peptide binding domain to the N-terminal ATPase domain in a AAA protein.
Destruction or potentiation of different prions catalyzed by similar Hsp104 remodeling activities.
Detection of compounds that rescue Rab1-synuclein toxicity.
Diminishing apoptosis by deletion of Bax or overexpression of Bcl-2 does not protect against infectious prion toxicity in vivo.
Direct and selective elimination of specific prions and amyloids by 4,5-dianilinophthalimide and analogs
Dominant Gain-of-Function Mutations in Hsp104p Reveal Crucial Roles for the Middle Region
Effects of Q/N-rich, polyQ, and non-polyQ amyloids on the de novo formation of the [PSI super(+)] prion in yeast and aggregation of Sup35 in vitro
Effects of Q/N-rich, polyQ, and non-polyQ amyloids on the de novo formation of the [PSI+] prion in yeast and aggregation of Sup35 in vitro.
elongated of yeast prion fibers involves separable steps of association and conversion, The
elongation of yeast prion fibers involves separable steps of association and conversion, The
Epigenetic regulation of translation reveals hidden genetic variation to produce complex traits
Epigenetics in the Extreme: Prions and the Inheritance of Environmentally Acquired Traits
Evidence that alpha-synuclein does not inhibit phospholipase D.
Flanking sequences profoundly alter polyglutamine toxicity in yeast
flurry of folding problems: an interview with Susan Lindquist by Jane Gitschier, A
function of heat-shock proteins in stress tolerance: degradation and reactivation of damaged proteins., The
Genetic Architecture of Hsp90-Dependent Drug Resistance
Genetic evidence for a functional relationship between Hsp104 and Hsp70.
Green tea (-)-epigallocatechin-gallate modulates early events in huntingtin misfolding and reduces toxicity in Huntington's disease models
Harnessing Hsp90 function as a powerful, broadly effective therapeutic strategy for fungal infectious disease
Harnessing natural diversity to probe metabolic pathways.
Heat shock, c1991:
Heat shock factor 1 is a powerful multifaceted modifier of carcinogenesis.
Heat shock factor 1 regulates lifespan as distinct from disease onset in prion disease
Heat-shock protein hsp90 governs the activity of pp60v-src kinase.
Heat shock proteins affect RNA processing during the heat shock response of Saccharomyces cerevisiae.
Heat-shock proteins and stress tolerance in microorganisms.
heritable switch in carbon source utilization driven by an unusual yeast prion., A
HSP100/Clp proteins: A common mechanism explains diverse functions
Hsp104 antagonizes [alpha]-synuclein aggregation and reduces dopaminergic degeneration in a rat model of Parkinson disease
Hsp104 Catalyzes Formation and Elimination of Self-Replicating Sup35 Prion Conformers
Hsp104, Hsp70, and Hsp40: A Novel Chaperone System that Rescues Previously Aggregated Proteins
Hsp104, Hsp70 and Hsp40 interplay regulates formation, growth and elimination of Sup35 prions
Hsp110 chaperones regulate prion formation and propagation in S. cerevisiae by two discrete activities.
HSP90 affects the expression of genetic variation and developmental stability in quantitative traits
Hsp90 and Environmental Stress Transform the Adaptive Value of Natural Genetic Variation
HSP90 and the chaperoning of cancer
Hsp90 as a capacitor for morphological evolution.
Hsp90 as a capacitor of phenotypic variation
HSP90 at the hub of protein homeostasis: emerging mechanistic insights.
HSP90-buffered genetic variation is common in Arabidopsis thaliana
Hsp90 Potentiates the Rapid Evolution of New Traits: Drug Resistance in Diverse Fungi
Impaired ERAD and ER stress are early and specific events in polyglutamine toxicity
Increase in Activity During Calorie Restriction Requires Sirt1
Inhibiting the transcription factor HSF1 as an anticancer strategy.
Interactions Among alpha -Synuclein, Dopamine, and Biomembranes: Some Clues for Understanding Neurodegeneration in Parkinson's Disease
Investigating protein conformation-based inheritance and disease in yeast.
Loss of Hsp70 exacerbates pathogenesis but not levels of fibrillar aggregates in a mouse model of Huntington's disease.
Lymphotoxin-dependent prion replication in inflammatory stromal cells of granulomas.
Mad cow meets psi-chotic yeast, 1998:
Mad cows meet psi-chotic yeast: The expansion of the prion hypothesis
Maturation of the tyrosine kinase c-src as a kinase and as a substrate depends on the molecular chaperone Hsp90.
Methods of identifying agents that diminish cellular toxicity associated with an .alpha.-synuclein polypeptide of Parkinson's disease in yeast
Modelling neurodegeneration in Saccharomyces cerevisiae: why cook with baker's yeast?
Molecular population genetics and evolution of a prion-like protein in Saccharomyces cerevisiae.
Motor Mechanism for Protein Threading through Hsp104
Mutational analysis of Hsp90 function: Interactions with a steroid receptor and a protein kinase
natively unfolded yeast prion monomer adopts an ensemble of collapsed and rapidly fluctuating structures, A
Navigating the ClpB channel to solution
network of protein interactions determines polyglutamine toxicity, A
neuronal isoform of the aplysia CPEB has prion-like properties., A
Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol.
Nucleated conformational conversion and the replication of conformational information by a prion determinant.
nucleolar protein allows viability in the absence of the essential ER-residing molecular chaperone calnexin., A
Parkinson's disease protein alpha -synuclein disrupts cellular Rab homeostasis, The
Phenotypic diversity and altered environmental plasticity in Arabidopsis thaliana with reduced Hsp90 levels.
Polyamine pathway contributes to the pathogenesis of Parkinson disease
Polyglutamine aggregates alter protein folding homeostasis in Caenorhabditis elegans
power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases, The
Prion formation and polyglutamine aggregation are controlled by two classes of genes.
Prion induction involves an ancient system for the sequestration of aggregated proteins and heritable changes in prion fragmentation
Prion pathogenesis is independent of caspase-12.
Prion protein gene polymorphisms in Saccharomyces cerevisiae
Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal
prion protein knockout mouse: a phenotype under challenge., The
Prion protein (PrP super(c)) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis
Prion protein (PrPc) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis.
Prion recognition elements govern nucleation, strain specificity and species barriers
Prion switching in response to environmental stress
Prions As Adaptive Conduits of Memory and Inheritance
Prions as protein-based genetic elements.
Prions, protein homeostasis, and phenotypic diversity.
Probing the Role of PrP Repeats in Conformational Conversion and Amyloid Assembly of Chimeric Yeast Prions
Protein folding sculpting evolutionary change.
Protein-only inheritance in yeast: something to get [PSI+]-ched about.
Protein-only mechanism induces self-perpetuating changes in the activity of neuronal Aplysia cytoplasmic polyadenylation element binding protein (CPEB)
Rapid selection of cyclic peptides that reduce alpha-synuclein toxicity in yeast and animal models.
Regulation of Protein Synthesis During Heat Shock.
RNA metabolism: strategies for regulation in the heat shock response.
RNA splicing is interrupted by heat shock and is rescued by heat shock protein synthesis.
Rnq1: an epigenetic modifier of protein function in yeast.
role of calorie restriction and SIRT1 in prion-mediated neurodegeneration, The
role of Sis1 in the maintenance of the [RNQ+] prion., The
Role of the chaperone protein Hsp104 in propagation of the yeast prion-like factor [psi+].
Role of the chaperone protein Hsp104 in propagation of the yeast prion-like factor (psipositive)
Schizosaccharomyces pombe Hsp104 disaggregase is unable to propagate the [PSI] prion., The
Screening for amyloid aggregation by Semi-Denaturing Detergent-Agarose Gel Electrophoresis.
Self-perpetuating structural states in biology, disease, and genetics.
Spontaneous Generation of Prion Infectivity in Fatal Familial Insomnia Knockin Mice
Strains of [PSI(+)] are distinguished by their efficiencies of prion-mediated conformational conversion.
Stress-induced proteins, 1988:
Structural insights into a yeast prion illuminate nucleation and strain diversity
Subunit interactions influence the biochemical and biological properties of Hsp 104
Subunit interactions influence the biochemical and biological properties of Hsp104
suite of Gateway(r) cloning vectors for high-throughput genetic analysis in Saccharomyces cerevisiae, A
suite of Gateway® cloning vectors for high-throughput genetic analysis in Saccharomyces cerevisiae, A
Support for the prion hypothesis for inheritance of a phenotypic trait in yeast
Susan L. Lindquist.
systematic survey identifies prions and illuminates sequence features of prionogenic proteins., A
Thermotolerance in Saccharomyces cerevisiae: the Yin and Yang of trehalose
Three quite different things that matter to me.
Translation of unspliced transcripts after heat shock.
Under cover: causes, effects and implications of Hsp90-mediated genetic capacitance.
Unraveling infectious structures, strain variants and species barriers for the yeast prion [PSI+]
Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation
Yeast Cells Provide Insight into Alpha-Synuclein Biology and Pathobiology
Yeast Genes That Enhance the Toxicity of a Mutant Huntingtin Fragment or [alpha]-Synuclein
yeast non-Mendelian factor [ETA super(+)] is a variant of [PSI super(+)], a prion-like form of release factor eRF3, The
yeast non-Mendelian factor [ETA+] is a variant of [PSI+], a prion-like form of release factor eRF3, The
yeast prion provides a mechanism for genetic variation and phenotypic diversity, A
yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity, A
α-Synuclein: membrane interactions and toxicity in Parkinson's disease.
Contributed to or performed: 
CURRENT OPINION IN GENETICS AND DEVELOPMENT
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