Context dependent neuroprotective properties of prion protein (PrP). (Q33595425)

28 July 2017

title

Context dependent neuroprotective properties of prion protein (PrP). (English)

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28 July 2017

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8

Susan Lindquist

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Marie-Françoise Chesselet

28 July 2017

Walker S Jackson

3

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7

object named as

Marie-Francoise Chesselet

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28 July 2017

Andrew D Steele

1

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28 July 2017

Zhipeng Zhou

2

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28 July 2017

Chunni Zhu

4

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28 July 2017

Pavan Auluck

5

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28 July 2017

Michael A Moskowitz

6

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28 July 2017

publication date

16 October 2009

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28 July 2017

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28 July 2017

volume

3

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28 July 2017

issue

4

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28 July 2017

page(s)

240-249

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Cellular prion protein mediates impairment of synaptic plasticity by amyloid-beta oligomers

28 July 2017

cites work

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Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities.

21 June 2018

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Opposing roles of prion protein in oxidative stress- and ER stress-induced apoptotic signaling

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Heat shock factor 1 regulates lifespan as distinct from disease onset in prion disease

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Prion protein attenuates excitotoxicity by inhibiting NMDA receptors

21 June 2018

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Human tau protein forms complex with PrP and some GSS- and fCJD-related PrP mutants possess stronger binding activities with tau in vitro

21 June 2018

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Diminishing apoptosis by deletion of Bax or overexpression of Bcl-2 does not protect against infectious prion toxicity in vivo

21 June 2018

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Cellular prion protein (PrPC) protects neuronal cells from the effect of huntingtin aggregation

21 June 2018

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Insights into prion strains and neurotoxicity

21 June 2018

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Cellular prion protein regulates beta-secretase cleavage of the Alzheimer's amyloid precursor protein

21 June 2018

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The prion protein family: diversity, rivalry, and dysfunction

21 June 2018

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Normal cellular prion protein protects against manganese-induced oxidative stress and apoptotic cell death

21 June 2018

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Disease-associated prion protein oligomers inhibit the 26S proteasome

21 June 2018

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The cellular prion protein (PrP(C)): its physiological function and role in disease

21 June 2018

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The power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases

21 June 2018

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Lethal recessive myelin toxicity of prion protein lacking its central domain

21 June 2018

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Deletion of cellular prion protein results in reduced Akt activation, enhanced postischemic caspase-3 activation, and exacerbation of ischemic brain injury

21 June 2018

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Prion protein (PrPc) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis

21 June 2018

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21 June 2018

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Anchorless prion protein results in infectious amyloid disease without clinical scrapie

21 June 2018

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21 June 2018

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Genetic mapping of activity determinants within cellular prion proteins: N-terminal modules in PrPC offset pro-apoptotic activity of the Doppel helix B/B' region

21 June 2018

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Prion protein accumulation and neuroprotection in hypoxic brain damage

21 June 2018

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Mammalian prion biology: one century of evolving concepts

21 June 2018

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Neuroprotective functions of prion protein

21 June 2018

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Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis.

21 June 2018

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Games played by rogue proteins in prion disorders and Alzheimer's disease

21 June 2018

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Neurodegenerative disorders of protein aggregation

21 June 2018

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Human alpha-synuclein-harboring familial Parkinson's disease-linked Ala-53 --> Thr mutation causes neurodegenerative disease with alpha-synuclein aggregation in transgenic mice

21 June 2018

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Huntington disease phenocopy is a familial prion disease

21 June 2018

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Shattuck lecture--neurodegenerative diseases and prions

21 June 2018

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Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein

21 June 2018

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Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disorders

21 June 2018

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

21 June 2018

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21 June 2018

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2807698

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

21 June 2018

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

21 June 2018

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Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene

21 June 2018

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Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features

21 June 2018

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All quiet on the neuronal front: NMDA receptor inhibition by prion protein

21 June 2018

1 reference

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Neonatal lethality in transgenic mice expressing prion protein with a deletion of residues 105-125.

30 October 2018

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Early behavioral deficits in R6/2 mice suitable for use in preclinical drug testing

30 October 2018

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Prion protein (PrPc) promotes beta-amyloid plaque formation.

30 October 2018

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Aggravation of ischemic brain injury by prion protein deficiency: role of ERK-1/-2 and STAT-1.

30 October 2018

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MCP-1 and murine prion disease: separation of early behavioural dysfunction from overt clinical disease

30 October 2018

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Early and progressive sensorimotor anomalies in mice overexpressing wild-type human alpha-synuclein.

30 October 2018

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Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol

30 October 2018

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Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia

30 October 2018

1 reference

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Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin

30 October 2018

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

30 October 2018

1 reference

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2807698

Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17

30 October 2018

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12 December 2020

Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family

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12 December 2020

A note on a simple apparatus for detecting neurological deficit in rats and mice

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12 December 2020

Mouse Models of Triplet Repeat Diseases

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12 December 2020

Identifiers

DOI

10.4161/PRI.3.4.10135

1 reference

28 July 2017

1 reference

28 July 2017

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