(Q36914449)

17 August 2017

title

Prion protein and the transmissible spongiform encephalopathies (English)

1 reference

17 August 2017

0 references

Caughey B

1

1 reference

17 August 2017

Chesebro B

series ordinal

2

1 reference

17 August 2017

publication date

1 February 1997

1 reference

17 August 2017

published in

Trends in Cell Biology

1 reference

17 August 2017

volume

7

1 reference

17 August 2017

issue

2

1 reference

17 August 2017

page(s)

56-62

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

17 August 2017

1 reference

7 January 2021

Self-replication and scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Novel proteinaceous infectious particles cause scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Abnormal fibrils from scrapie-infected brain

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Identification of a protein that purifies with the scrapie prion.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Scrapie infectivity, fibrils and low molecular weight protein

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Natural scrapie in a closed flock of Cheviot sheep occurs only in specific PrP genotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Identification of five allelic variants of the sheep PrP gene and their association with natural scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Mice devoid of PrP are resistant to scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Molecular biology of prion diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Scrapie associated PrP accumulation and its prevention: insights from cell culture

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Truncated forms of the human prion protein in normal brain and in prion diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Regulation of intracellular free calcium levels by the cellular prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Prion protein is necessary for normal synaptic function

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

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%2FS0962-8924%2896%2910054-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Normal and scrapie-associated forms of prion protein differ in their sensitivities to phospholipase and proteases in intact neuroblastoma cells

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase C.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Mouse T cell membrane proteins Rt6-1 and Rt6-2 are arginine/protein mono(ADPribosyl)transferases and share secondary structure motifs with ADP-ribosylating bacterial toxins

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

A 60-kDa prion protein (PrP) with properties of both the normal and scrapie-associated forms of PrP.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Chimeric prion protein expression in cultured cells and transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Biochemical differences among scrapie-associated fibrils support the biological diversity of scrapie agents

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Aggregates of scrapie-associated prion protein induce the cell-free conversion of protease-sensitive prion protein to the protease-resistant state

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Partial unfolding and refolding of scrapie-associated prion protein: evidence for a critical 16-kDa C-terminal domain.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Transmissible and non-transmissible amyloidoses: autocatalytic post-translational conversion of host precursor proteins to beta-pleated sheet configurations

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Normal host prion protein necessary for scrapie-induced neurotoxicity.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Mouse cortical cells lacking cellular PrP survive in culture with a neurotoxic PrP fragment

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Cytoprotective effect of NMDA receptor antagonists on prion protein (PrionSc)-induced toxicity in rat cortical cell cultures

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Neurotoxicity of a prion protein fragment

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Cytotoxicity of prion protein peptide (PrP106-126) differs in mechanism from the cytotoxic activity of the Alzheimer's disease amyloid peptide, A beta 25-35.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Detection of apoptosis in murine scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Altered GABA distribution in hamster brain is an early molecular consequence of infection by scrapie prions.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Alterations in neurotransmitter-related enzyme activity in scrapie-infected PC12 cells

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Scrapie prions alter receptor-mediated calcium responses in cultured cells

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Activation of cerebral cytokine gene expression and its correlation with onset of reactive astrocyte and acute-phase response gene expression in scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Cytokines, prostaglandins and lipocortin-1 are present in the brains of scrapie-infected mice

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

7 January 2021

Evidence for an early inflammatory response in the central nervous system of mice with scrapie.

1 reference

https://api.crossref.org/works/10.1016%2FS0962-8924%2896%2910054-4

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%2FS0962-8924%2896%2910054-4

7 January 2021

10.1016/S0962-8924(96)10054-4

Identifiers

DOI

1 reference

17 August 2017

1 reference