(Q33857802)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10191337%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

title

Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation (English)

1 reference

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3 December 2019

0 references

7

1 reference

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3 December 2019

8

A J Morton

1 reference

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3 December 2019

author name string

R J Carter

1

1 reference

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3 December 2019

L A Lione

2

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3 December 2019

T Humby

3

1 reference

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3 December 2019

L Mangiarini

4

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3 December 2019

A Mahal

5

1 reference

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3 December 2019

G P Bates

6

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3 December 2019

language of work or name

English

0 references

publication date

1 April 1999

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3 December 2019

published in

Journal of Neuroscience

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3 December 2019

volume

19

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3 December 2019

page(s)

3248-3257

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3 December 2019

issue

8

1 reference

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Behavioral pathology induced by repeated systemic injections of 3-nitropropionic acid mimics the motoric symptoms of Huntington's disease

3 December 2019

cites work

1 reference

12 December 2020

Huntington's disease: translating a CAG repeat into a pathogenic mechanism

1 reference

12 December 2020

Quantifiable bradykinesia, gait abnormalities and Huntington's disease-like striatal lesions in rats chronically treated with 3-nitropropionic acid

1 reference

12 December 2020

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

1 reference

12 December 2020

Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid

1 reference

12 December 2020

The quinolinic acid model of Huntington's disease: locomotor abnormalities

1 reference

12 December 2020

Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid

1 reference

12 December 2020

Striatal transplantation in a transgenic mouse model of Huntington's disease

1 reference

12 December 2020

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

1 reference

12 December 2020

Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates

1 reference

12 December 2020

Mitochondrial toxin 3-nitropropionic acid produces startle reflex abnormalities and striatal damage in rats that model some features of Huntington's disease

1 reference

12 December 2020

Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human huntington disease gene

1 reference

12 December 2020

Trinucleotide repeats in neurogenetic disorders

1 reference

12 December 2020

Mouse models of human CAG repeat disorders

1 reference

12 December 2020

Prepulse inhibition in the rat is regulated by ventral and caudodorsal striato-pallidal circuitry

1 reference

12 December 2020

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

12 December 2020

Impaired prepulse inhibition of acoustic and tactile startle response in patients with Huntington's disease

1 reference

12 December 2020

The gait abnormality of Huntington's disease

1 reference

12 December 2020

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

1 reference

12 December 2020

10.1523/JNEUROSCI.19-08-03248.1999

Identifiers

DOI

1 reference

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3 December 2019

1 reference

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3 December 2019

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