(Q45294402)

English

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

scientific article published in July 1997

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scholarly article

1 reference

Europe PubMed Central

11 December 2017

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

1 reference

Europe PubMed Central

11 December 2017

Huntington's disease

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1 reference

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inferred from title

Emmanuel Brouillet

6

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Europe PubMed Central

11 December 2017

author name string

Guyot MC

1

1 reference

Europe PubMed Central

11 December 2017

Hantraye P

2

1 reference

Europe PubMed Central

11 December 2017

Dolan R

3

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Europe PubMed Central

11 December 2017

Palfi S

4

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Europe PubMed Central

11 December 2017

Maziére M

5

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Europe PubMed Central

11 December 2017

language of work or name

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publication date

1 July 1997

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Europe PubMed Central

11 December 2017

number of pages

12

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inferred from page(s)

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Europe PubMed Central

11 December 2017

79

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Europe PubMed Central

11 December 2017

45-56

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Europe PubMed Central

11 December 2017

1

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Europe PubMed Central

11 December 2017

Alternative excitotoxic hypotheses

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https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

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Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses?

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

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Age-dependent striatal excitotoxic lesions produced by the endogenous mitochondrial inhibitor malonate

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Chronic quinolinic acid lesions in rats closely resemble Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

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Aminooxyacetic Acid Results in Excitotoxin Lesions by a Novel Indirect Mechanism

1 reference

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7 January 2021

based on heuristic

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Systemic 3-nitropropionic acid: behavioral deficits and striatal damage in adult rats

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

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Systemic or local administration of azide produces striatal lesions by an energy impairment-induced excitotoxic mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Age-dependent vulnerability of the striatum to the mitochondrial toxin 3-nitropropionic acid.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Manganese injection into the rat striatum produces excitotoxic lesions by impairing energy metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatotopic organization in rat striatum: evidence for a combinational map.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Lesion of striatal neurons with kainic acid provides a model for Huntington's chorea

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Selective sparing of a class of striatal neurons in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Proliferative and degenerative changes in striatal spiny neurons in Huntington's disease: a combined study using the section-Golgi method and calbindin D28k immunocytochemistry

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Brain enzyme and clinical alterations induced in rats and mice by nitroaliphatic toxicants.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Inhibition of succinate dehydrogenase by malonic acid produces an "excitotoxic" lesion in rat striatum

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Correlation of morphologic brain lesions with physiologic alterations and blood-brain barrier impairment in 3-nitropropionic acid toxicity in rats.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

A primate model of Huntington's disease: behavioral and anatomical studies of unilateral excitotoxic lesions of the caudate-putamen in the baboon

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Intrastriatal transplantation of cross-species fetal striatal cells reduces abnormal movements in a primate model of Huntington disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Trinucleotide repeat length and rate of progression of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

'Choreic' movement induced by unilateral kainate lesion of the striatum and L-DOPA administration in monkey

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

The gait abnormality of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Systemic 3-nitropropionic acid: long-term effects on locomotor behavior.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

New insights into the clinical features, pathogenesis and molecular genetics of Huntington disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Huntington's disease gene (IT15) is widely expressed in human and rat tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

3-Nitropropionic acid-exogenous animal neurotoxin and possible human striatal toxin.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Duplication of biochemical changes of Huntington's chorea by intrastriatal injections of glutamic and kainic acids

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical and neuropathologic assessment of severity in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Chronically administered 3-nitropropionic acid induces striatal lesions attributed to dysfunction of the blood-brain barrier

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Chronic 3-nitropropionic acid treatment in baboons replicates the cognitive and motor deficits of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Increase of ATP levels by glutamate antagonists is unrelated to neuroprotection

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

3-Acetylpyridine produces age-dependent excitotoxic lesions in rat striatum.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial impairment reduces the threshold for in vivo NMDA-mediated neuronal death in the striatum.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

The coexistence of bradykinesia and chorea in Huntington's disease and its implications for theories of basal ganglia control of movement

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Neuropathological classification of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

3-Nitropropionic acid toxicity in the striatum

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

NMDA receptor involvement in toxicity to dopamine neurons in vitro caused by the succinate dehydrogenase inhibitor 3-nitropropionic acid.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2896%2900602-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0306-4522(96)00602-1

1 reference

Europe PubMed Central

11 December 2017

1 reference

Europe PubMed Central

11 December 2017

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