(Q48431743)

11 February 2018

title

Context-dependent perturbation of neural systems in transgenic mice expressing a cytosolic prion protein. (English)

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11 February 2018

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6

Susan Lindquist

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11 February 2018

7

Alan Jasanoff

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11 February 2018

author name string

Henryk Faas

1

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11 February 2018

Walker S Jackson

2

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11 February 2018

Andrew W Borkowski

3

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11 February 2018

Xinhe Wang

4

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11 February 2018

Jiyan Ma

5

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11 February 2018

language of work or name

English

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publication date

14 October 2009

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11 February 2018

number of pages

11

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inferred from page(s)

published in

NeuroImage

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11 February 2018

volume

49

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11 February 2018

issue

3

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11 February 2018

page(s)

2607-2617

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11 February 2018

Synapse loss associated with abnormal PrP precedes neuronal degeneration in the scrapie-infected murine hippocampus

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Conditions of endoplasmic reticulum stress favor the accumulation of cytosolic prion protein

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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

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Synaptic changes characterize early behavioural signs in the ME7 model of murine prion disease

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Neuropathology and treatment of Alzheimer disease: did we lose the forest for the trees?

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An integrated, temporal study of the behavioural, electrophysiological and neuropathological consequences of murine prion disease.

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Spontaneous neurodegeneration in transgenic mice with mutant prion protein

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Positron emission tomography with [(18)F]FDG in the diagnosis of Creutzfeldt-Jakob disease (CJD).

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In vivo neuronal tract tracing using manganese-enhanced magnetic resonance imaging.

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Perturbation of endoplasmic reticulum homeostasis facilitates prion replication.

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Enhancement of brain activation during trial-and-error sequence learning in early PD.

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Cytosolic prion protein is not toxic and protects against Bax-mediated cell death in human primary neurons

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Trinucleotide Repeat Disorders

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The interaction between cytoplasmic prion protein and the hydrophobic lipid core of membrane correlates with neurotoxicity

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Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study

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Segmentation of skull and scalp in 3-D human MRI using mathematical morphology

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

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Manganese ion enhances T1-weighted MRI during brain activation: an approach to direct imaging of brain function

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

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

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Manganese-enhanced magnetic resonance imaging (MEMRI): methodological and practical considerations

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Cytoplasmic prion protein induces forebrain neurotoxicity

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Cytosolic prion protein (PrP) is not toxic in N2a cells and primary neurons expressing pathogenic PrP mutations

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MRI of mouse models of neurological disorders

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Role of hyperactive cerebellum and motor cortex in Parkinson's disease

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Novel proteinaceous infectious particles cause scrapie

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Environmental enrichment slows disease progression in R6/2 Huntington's disease mice

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A network dysfunction perspective on neurodegenerative diseases

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The genomic action potential

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Recovery of locomotor function in cats after localized cerebellar lesions.

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A vector for expressing foreign genes in the brains and hearts of transgenic mice

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10.1016/J.NEUROIMAGE.2009.10.009

Identifiers

DOI

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11 February 2018

journals/neuroimage/FaasJBWMLJ10

DBLP publication ID

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DBLP Dataset 2021-01-02

28 January 2021

PMC publication ID

7605312

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11 February 2018