(Q48750988)

15 February 2018

title

Scrapie infection alters the membrane and synaptic properties of mouse hippocampal CA1 pyramidal neurones. (English)

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15 February 2018

author name string

Johnston AR

1

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15 February 2018

Black C

2

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15 February 2018

Fraser J

3

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15 February 2018

MacLeod N

4

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15 February 2018

language of work or name

English

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publication date

1 April 1997

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15 February 2018

published in

Journal of Physiology

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15 February 2018

volume

500 ( Pt 1)

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15 February 2018

page(s)

1-15

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15 February 2018

Quantal analysis of excitatory synaptic action and depression in hippocampal slices

cites work

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Synaptic integration in hippocampal CA1 pyramids.

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Exposure to high-pH medium increases the incidence and extent of dye coupling between rat hippocampal CA1 pyramidal neurons in vitro.

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

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Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells

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Synaptic degeneration is the primary neuropathological feature in prion disease: a preliminary study.

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Occurrence and three-dimensional structure of multiple synapses between individual radiatum axons and their target pyramidal cells in hippocampal area CA1

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Scrapie prions alter receptor-mediated calcium responses in cultured cells

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

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Prion protein is necessary for normal synaptic function

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Glutamate receptors and the induction of excitotoxic neuronal death

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Ionic conductances contributing to spike repolarization and after-potentials in rat medial vestibular nucleus neurones

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Excitotoxicity and the NMDA receptor--still lethal after eight years

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12 December 2020

Ultrastructural localization of cellular prion protein (PrPc) in synaptic boutons of normal hamster hippocampus

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PrP gene dosage and long term potentiation

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Conformational transitions in peptides containing two putative alpha-helices of the prion protein.

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Dendritic morphology of CA1 pyramidal neurones from the rat hippocampus: II. Spine distributions

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Human prion diseases and neurodegeneration

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

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Regulation of intracellular free calcium levels by the cellular prion protein

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Motor neurone disease and animal models

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Creutzfeldt-Jakob disease. An electroencephalographic study.

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Periodic lateralized epileptiform complexes (PLEDs) in Creutzfeldt-Jakob disease

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Golgi and electronmicroscopic studies of spongifom encephalopathy

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Decreased High-Affinity Binding of [3H]Muscimol to Cerebral Synaptic Membranes of Scrapie-Infected Mice

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Experimental scrapie in rats: First electrophysiological observations

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Degenerative hippocampal pathology in mice infected with scrapie

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Electroencephalogram and evoked potentials in naturally occurring scrapie in sheep.

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Impairment of the cortical and thalamic electrical activity in scrapie-infected rats

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Involvement of N-methyl-D-aspartate receptors in epileptiform bursting in the rat hippocampal slice

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Neuronal alterations in experimental Creutzfeldt-Jakob disease: a Golgi study

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Calcium-mediated neurotoxicity: relationship to specific channel types and role in ischemic damage

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Precise targeting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapie

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Potassium currents in hippocampal pyramidal cells

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12 December 2020

Bursting response to current-evoked depolarization in rat CA1 pyramidal neurons is correlated with lucifer yellow dye coupling but not with the presence of calbindin-D28k

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12 December 2020

10.1113/JPHYSIOL.1997.SP021994

Identifiers

DOI

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15 February 2018

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15 February 2018