Separation and properties of cellular and scrapie prion proteins.
about
Glypican-1 mediates both prion protein lipid raft association and disease isoform formationPUF60: a novel U2AF65-related splicing activityPropagation of the yeast prion-like [psi+] determinant is mediated by oligomerization of the SUP35-encoded polypeptide chain release factorConversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteinsAssignment of the human and mouse prion protein genes to homologous chromosomesPrionsMicrodissection: a method developed to investigate mechanisms involved in transmissible spongiform encephalopathy pathogenesisInsoluble cellular prion protein and its association with prion and Alzheimer diseasesIntraperitoneal Infection of Wild-Type Mice with Synthetically Generated Mammalian PrionNMR solution structure of the human prion proteinSolution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseasesInteraction between yeast Sup45p (eRF1) and Sup35p (eRF3) polypeptide chain release factors: implications for prion-dependent regulation.Rapid folding of the prion protein captured by pressure-jumpProteasomes and ubiquitin are involved in the turnover of the wild-type prion proteinDistinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.Considering protonation as a posttranslational modification regulating protein structure and function.Biophysical insights into how surfaces, including lipid membranes, modulate protein aggregation related to neurodegeneration.Live imaging of prions reveals nascent PrPSc in cell-surface, raft-associated amyloid strings and websPrion removal capacity of plasma protein manufacturing processes: a data collection from PPTA member companies.Glycosylation differences between the normal and pathogenic prion protein isoformsCopper(II)-induced conformational changes and protease resistance in recombinant and cellular PrP. Effect of protein age and deamidation.Spectroscopic and Theoretical Study of Cu(I) Binding to His111 in the Human Prion Protein Fragment 106-115.The role of disulfide bridge in the folding and stability of the recombinant human prion protein.High yield purification and physico-chemical properties of full-length recombinant allelic variants of sheep prion protein linked to scrapie susceptibility.Prions, amyloids, and RNA: Pieces of a puzzle.Methionine sulfoxides on prion protein Helix-3 switch on the alpha-fold destabilization required for conversion.Protease-sensitive synthetic prions.Glycosylphosphatidylinositol anchoring directs the assembly of Sup35NM protein into non-fibrillar, membrane-bound aggregatesNeurodegeneration in humans caused by prionsIn vitro expression in eukaryotic cells of a prion protein gene cloned from scrapie-infected mouse brain.Nerve growth factor increases mRNA levels for the prion protein and the beta-amyloid protein precursor in developing hamster brainA new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrPSc.Attempts to convert the cellular prion protein into the scrapie isoform in cell-free systems.Molecular mass, biochemical composition, and physicochemical behavior of the infectious form of the scrapie precursor protein monomerPrion dynamics and the quest for the genetic determinant in protein-only inheritancePrion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoformChemical induction of misfolded prion protein conformers in cell culture.Amphotericin B inhibits the generation of the scrapie isoform of the prion protein in infected cultures.Deletion of beta-strand and alpha-helix secondary structure in normal prion protein inhibits formation of its protease-resistant isoform.Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation
P2860
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P2860
Separation and properties of cellular and scrapie prion proteins.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Separation and properties of cellular and scrapie prion proteins.
@ast
Separation and properties of cellular and scrapie prion proteins.
@en
type
label
Separation and properties of cellular and scrapie prion proteins.
@ast
Separation and properties of cellular and scrapie prion proteins.
@en
prefLabel
Separation and properties of cellular and scrapie prion proteins.
@ast
Separation and properties of cellular and scrapie prion proteins.
@en
P2093
P2860
P356
P1476
Separation and properties of cellular and scrapie prion proteins.
@en
P2093
K A Bowman
M B Braunfeld
M P McKinley
P2860
P304
P356
10.1073/PNAS.83.8.2310
P407
P577
1986-04-01T00:00:00Z