(Q34382758)

1 August 2017

1 reference

title

The prion gene complex encoding PrP(C) and Doppel: insights from mutational analysis (English)

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1 August 2017

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Mastrangelo P

1

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1 August 2017

Westaway D

series ordinal

2

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1 August 2017

language of work or name

English

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publication date

1 September 2001

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1 August 2017

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1 August 2017

volume

275

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1 August 2017

issue

1

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1 August 2017

page(s)

1-18

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Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Characterisation of two promoters for prion protein (PrP) gene expression in neuronal cells

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Identification of two biologically distinct strains of transmissible mink encephalopathy in hamsters

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Non-genetic propagation of strain-specific properties of scrapie prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

DNA methylation and the frequency of CpG in animal DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

B lymphocytes and neuroinvasion

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Effects of copper on survival of prion protein knockout neurons and glia.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Consequences of manganese replacement of copper for prion protein function and proteinase resistance

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Mice devoid of PrP are resistant to scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Linkage of prion protein and scrapie incubation time genes

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Genetics and polymorphism of the mouse prion gene complex: control of scrapie incubation time

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Role of the chaperone protein Hsp104 in propagation of the yeast prion-like factor [psi+]

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Prion protein is necessary for normal synaptic function

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Molecular basis of base substitution hotspots in Escherichia coli

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

The protein product of the het-s heterokaryon incompatibility gene of the fungus Podospora anserina behaves as a prion analog

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Two alleles of a neural protein gene linked to scrapie in sheep

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

A transmembrane form of the prion protein in neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Patch-clamp analysis of synaptic transmission to cerebellar purkinje cells of prion protein knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Evidence of presynaptic location and function of the prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Prion protein binds copper within the physiological concentration range

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

The cellular prion protein (PrP) selectively binds to Bcl-2 in the yeast two-hybrid system

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Prions prevent neuronal cell-line death.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresis.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Complete genomic sequence and analysis of the prion protein gene region from three mammalian species

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Identification of a novel gene encoding a PrP-like protein expressed as chimeric transcripts fused to PrP exon 1/2 in ataxic mouse line with a disrupted PrP gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Physiological expression of the gene for PrP-like protein, PrPLP/Dpl, by brain endothelial cells and its ectopic expression in neurons of PrP-deficient mice ataxic due to Purkinje cell degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Characterization of a prion protein (PrP) gene from rabbit; a species with apparent resistance to infection by prions

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

NMR structure of the bovine prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

De novo generation of a PrPSc-like conformation in living cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Complementary hydropathy identifies a cellular prion protein receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Cleavage of the amino terminus of the prion protein by reactive oxygen species.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Selectivity at the cleavage/attachment site of phosphatidylinositol-glycan anchored membrane proteins is enzymatically determined

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Two different neurodegenerative diseases caused by proteins with similar structures

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Mice with gene targetted prion protein alterations show that Prnp, Sinc and Prni are congruent

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Signal transduction through prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Demyelinating peripheral neuropathy in Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Identification of cellular proteins binding to the scrapie prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

PrP genotypes and experimental scrapie in orally inoculated Suffolk sheep in the United States

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Copper stimulates endocytosis of the prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Long-range disruption of gene expression by a selectable marker cassette

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Copper(II)-induced conformational changes and protease resistance in recombinant and cellular PrP. Effect of protein age and deamidation

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Neuron-specific expression of a hamster prion protein minigene in transgenic mice induces susceptibility to hamster scrapie agent

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

NMR structure of the mouse prion protein domain PrP(121-231)

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Prion protein NMR structure and familial human spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Familial neurological disease associated with spongiform encephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

No propagation of prions in mice devoid of PrP.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Chimeric prion protein expression in cultured cells and transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

A C-terminal-truncated PrP Isoform Is Present in Mature Sperm

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

A glycolipid-anchored prion protein is endocytosed via clathrin-coated pits.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Assignment of the human and mouse prion protein genes to homologous chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Scrapie prion protein contains a phosphatidylinositol glycolipid

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

First experimental transmission of fatal familial insomnia

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

The PrP-like protein Doppel gene in sheep and cattle: cDNA sequence and expression

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Doxycycline control of prion protein transgene expression modulates prion disease in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Copper binding to the prion protein: structural implications of four identical cooperative binding sites

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Brain copper content and cuproenzyme activity do not vary with prion protein expression level

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

1 reference

7 January 2021

NEUROBIOLOGY:PrP's Double Causes Trouble

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Distinct prion proteins in short and long scrapie incubation period mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Unraveling prion diseases through molecular genetics

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Paradoxical shortening of scrapie incubation times by expression of prion protein transgenes derived from long incubation period mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Structure and polymorphism of the mouse prion protein gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Prion protein-deficient neurons reveal lower glutathione reductase activity and increased susceptibility to hydrogen peroxide toxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Copper binding to octarepeat peptides of the prion protein monitored by mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

[URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel function.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Glycosylation of prions and its effects on protein conformation relevant to amino acid mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Identification of candidate proteins binding to prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

NMR solution structure of the human prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

Solution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900627-8

7 January 2021

10.1016/S0378-1119(01)00627-8

Identifiers

DOI

1 reference

1 August 2017

1 reference