Prion diseases: from molecular biology to intervention strategies (Q35602374)

9 August 2017

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title

Prion diseases: from molecular biology to intervention strategies (English)

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9 August 2017

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3

Hermann M Schätzl

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9 August 2017

2

Sabine Gilch

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9 August 2017

Max Nunziante

1

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9 August 2017

language of work or name

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1 December 2003

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9 August 2017

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9 August 2017

volume

4

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9 August 2017

issue

12

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9 August 2017

page(s)

1268-1284

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https://api.crossref.org/works/10.1002%2FCBIC.200300704

9 August 2017

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Prion diseases of humans and animals: their causes and molecular basis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Structural clues to prion replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prions and the lymphoreticular system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Predictability of the UK variant Creutzfeldt-Jakob disease epidemic

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Transmission dynamics and epidemiology of BSE in British cattle

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-- Jakob disease: implications for human health

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The transmissible spongiform encephalopathies: disease risks for North America

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Synthesis and trafficking of prion proteins in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Sec61p mediates export of a misfolded secretory protein from the endoplasmic reticulum to the cytosol for degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

ER protein quality control and proteasome-mediated protein degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Retro-translocation of proteins from the endoplasmic reticulum into the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Endoplasmic reticulum degradation of a mutated ATP-binding cassette transporter Pdr5 proceeds in a concerted action of Sec61 and the proteasome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Novel aspects of degradation of T cell receptor subunits from the endoplasmic reticulum (ER) in T cells: importance of oligosaccharide processing, ubiquitination, and proteasome-dependent removal from ER membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

A transmembrane form of the prion protein contains an uncleaved signal peptide and is retained in the endoplasmic Reticulum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Proteasomes and ubiquitin are involved in the turnover of the wild-type prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Scrapie-like prion protein accumulates in aggresomes of cyclosporin A-treated cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Immunophilins: beyond immunosuppression

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Parkin accumulation in aggresomes due to proteasome impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Presenilin-binding protein forms aggresomes in monkey kidney COS-7 cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Aggresomes: a cellular response to misfolded proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Sulfated glycans stimulate endocytosis of the cellular isoform of the prion protein, PrPC, in cultured cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Cyclosporine: immunology, toxicity and pharmacology in experimental animals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Impairment of the ubiquitin-proteasome system by protein aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

New agents in cancer clinical trials

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

An inhibitor of HIV-1 protease modulates proteasome activity, antigen presentation, and T cell responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Mice devoid of PrP are resistant to scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Copper stimulates endocytosis of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Normal prion protein has an activity like that of superoxide dismutase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prion protein is necessary for normal synaptic function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Hippocampal slices from prion protein null mice: disrupted Ca(2+)-activated K+ currents.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Analysis of interaction sites in homo- and heteromeric complexes containing Bcl-2 family members and the cellular prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Signal transduction through prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

PrPC directly interacts with proteins involved in signaling pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Cloning from insulinoma cells of synapsin I associated with insulin secretory granules

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Interaction of Grb2 via its Src homology 3 domains with synaptic proteins including synapsin I

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

SH2 and SH3 domains: elements that control interactions of cytoplasmic signaling proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

A transmembrane form of the prion protein in neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

N-terminal truncation of prion protein affects both formation and conformation of abnormal protease-resistant prion protein generated in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

A dementing illness associated with a novel insertion in the prion protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The role of copper in neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Filipin prevents pathological prion protein accumulation by reducing endocytosis and inducing cellular PrP release

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Internalization of mammalian fluorescent cellular prion protein and N-terminal deletion mutants in living cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Ablation of the metal ion-induced endocytosis of the prion protein by disease-associated mutation of the octarepeat region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The mechanism of internalization of glycosylphosphatidylinositol-anchored prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Cell-free formation of protease-resistant prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Protease-resistant prion protein produced in vitro lacks detectable infectivity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prions in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Widespread PrPSc accumulation in muscles of hamsters orally infected with scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Inhibition of prion-protein conversion: a therapeutic tool?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Inhibition of protease-resistant prion protein formation by porphyrins and phthalocyanines

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Porphyrin and phthalocyanine antiscrapie compounds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Elimination of prions by branched polyamines and implications for therapeutics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prion protein gene variation among primates

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Eight prion strains have PrP(Sc) molecules with different conformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Mimicking dominant negative inhibition of prion replication through structure-based drug design

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

A kinetic model for amyloid formation in the prion diseases: importance of seeding

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prion-protein-specific aptamer reduces PrPSc formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Intracellular re-routing of prion protein prevents propagation of PrP(Sc) and delays onset of prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Potent inhibition of scrapie prion replication in cultured cells by bis-acridines

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Dominant-negative inhibition of prion replication in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

PrP genotype and agent effects in scrapie: change in allelic interaction with different isolates of agent in sheep, a natural host of scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Complement facilitates early prion pathogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Temporary depletion of complement component C3 or genetic deficiency of C1q significantly delays onset of scrapie.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Distinct roles of lymphotoxin alpha and the type I tumor necrosis factor (TNF) receptor in the establishment of follicular dendritic cells from non-bone marrow-derived cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Impaired prion replication in spleens of mice lacking functional follicular dendritic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Postexposure prophylaxis against prion disease with a stimulator of innate immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Interactions between bacterial CpG-DNA and TLR9 bridge innate and adaptive immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Complete Freund's adjuvant immunization prolongs survival in experimental prion disease in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Prevention of scrapie pathogenesis by transgenic expression of anti-prion protein antibodies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Antibodies inhibit prion propagation and clear cell cultures of prion infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Vaccine development for Alzheimer's disease: a shot of good news.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Immunotherapy for Alzheimer's disease: will vaccination work?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Nerve inflammation halts trial for Alzheimer's drug.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Neuropathology of human Alzheimer disease after immunization with amyloid-beta peptide: a case report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Induction of antibodies against murine full-length prion protein in wild-type mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Modulation of proteinase-K resistant prion protein by prion peptide immunization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Immunization delays the onset of prion disease in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Polyclonal anti-PrP auto-antibodies induced with dimeric PrP interfere efficiently with PrPSc propagation in prion-infected cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

A prion protein epitope selective for the pathologically misfolded conformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The same prion strain causes vCJD and BSE

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Post-exposure prophylaxis after accidental prion inoculation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Cationic Lipopolyamines Induce Degradation of PrPSc in Scrapie-Infected Mouse Neuroblastoma Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Quinacrine does not prolong survival in a murine Creutzfeldt-Jakob disease model

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Altered circadian activity rhythms and sleep in mice devoid of prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Monoclonal antibodies inhibit prion replication and delay the development of prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Transmissible spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Blockade of glycosylation promotes acquisition of scrapie-like properties by the prion protein in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

B lymphocytes and neuroinvasion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Mannosidase action, independent of glucose trimming, is essential for proteasome-mediated degradation of unassembled glycosylated Ig light chains

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Proteasomal Degradation and N-terminal Protease Resistance of the Codon 145 Mutant Prion Protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The Chaperone Protein BiP Binds to a Mutant Prion Protein and Mediates Its Degradation by the Proteasome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Ubiquitin and the control of protein fate in the secretory and endocytic pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Ultrastructural localization of cellular prion protein (PrPc) at the neuromuscular junction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Copper binding to the N-terminal tandem repeat region of mammalian and avian prion protein: structural studies using synthetic peptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

The N-terminal domain of a glycolipid-anchored prion protein is essential for its endocytosis via clathrin-coated pits

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Predicting the CJD epidemic in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Scrapie replication in lymphoid tissues depends on prion protein-expressing follicular dendritic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

Role of spleen macrophages in the clearance of scrapie agent early in pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200300704

21 January 2018

Identifiers

DOI

10.1002/CBIC.200300704

1 reference

9 August 2017

1 reference