Cerebellar pathology and motor deficits in the palmitoyl protein thioesterase 1-deficient mouse (Q37186176)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19416667%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

title

Cerebellar pathology and motor deficits in the palmitoyl protein thioesterase 1-deficient mouse (English)

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27 January 2020

0 references

1

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27 January 2020

Jonathan D. Cooper

5

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27 January 2020

Mark S Sands

6

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27 January 2020

author name string

David F Wozniak

2

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27 January 2020

Catherine Kielar

3

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27 January 2020

Yun Tan

4

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language of work or name

English

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publication date

10 February 2009

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27 January 2020

published in

Experimental Neurology

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27 January 2020

volume

217

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27 January 2020

page(s)

124-135

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27 January 2020

issue

1

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Treatment of late infantile neuronal ceroid lipofuscinosis by CNS administration of a serotype 2 adeno-associated virus expressing CLN2 cDNA.

27 January 2020

cites work

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6 September 2017

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6 September 2017

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A mouse model of classical late-infantile neuronal ceroid lipofuscinosis based on targeted disruption of the CLN2 gene results in a loss of tripeptidyl-peptidase I activity and progressive neurodegeneration

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Why do Purkinje cells die so easily after global brain ischemia? Aldolase C, EAAT4, and the cerebellar contribution to posthypoxic myoclonus.

6 September 2017

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The role of activated astrocytes and of the neurotrophic cytokine S100B in the pathogenesis of Alzheimer's disease

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Disruption of PPT1 or PPT2 causes neuronal ceroid lipofuscinosis in knockout mice

6 September 2017

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6 September 2017

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6 September 2017

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Tissue expression and subcellular localization of CLN3, the Batten disease protein

6 September 2017

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Overexpression of the neurotrophic cytokine S100 beta in human temporal lobe epilepsy

6 September 2017

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Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

6 September 2017

1 reference

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Infantile type of so-called neuronal ceroid-lipofuscinosis. 1. A clinical study of 15 patients

6 September 2017

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Infantile type of so-called neuronal ceroid-lipofuscinosis

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Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies

6 September 2017

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6 September 2017

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Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies

28 September 2017

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Neuropathology of the acid sphingomyelinase knockout mouse model of Niemann-Pick A disease including structure-function studies associated with cerebellar Purkinje cell degeneration.

26 June 2018

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Intraventricular enzyme replacement improves disease phenotypes in a mouse model of late infantile neuronal ceroid lipofuscinosis

3 September 2018

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CNS-directed AAV2-mediated gene therapy ameliorates functional deficits in a murine model of infantile neuronal ceroid lipofuscinosis.

3 September 2018

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3 September 2018

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3 September 2018

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3 September 2018

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Adeno-associated virus 2-mediated gene therapy decreases autofluorescent storage material and increases brain mass in a murine model of infantile neuronal ceroid lipofuscinosis

3 September 2018

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3 September 2018

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3 September 2018

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Constitutive expression of heat shock protein HSP25 in the central nervous system of the developing and adult mouse.

3 September 2018

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Lysosomal ceroid depletion by drugs: therapeutic implications for a hereditary neurodegenerative disease of childhood

3 September 2018

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Aldolase C-positive cerebellar Purkinje cells are resistant to delayed death after cerebral trauma and AMPA-mediated excitotoxicity

3 September 2018

1 reference

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Constitutive expression of the 25-kDa heat shock protein Hsp25 reveals novel parasagittal bands of purkinje cells in the adult mouse cerebellar cortex

20 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19416667

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

EEG and evoked potentials in infantile neuronal ceroid-lipofuscinosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19416667

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/19416667

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.EXPNEUROL.2009.01.022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19416667%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19416667%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

1 reference