(Q42503942)

1 November 2017

title

Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues (English)

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1 November 2017

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8

Collins FS

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1 November 2017

Strong TV

1

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1 November 2017

Tagle DA

2

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1 November 2017

Valdes JM

3

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1 November 2017

Elmer LW

4

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1 November 2017

Boehm K

5

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1 November 2017

Swaroop M

6

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1 November 2017

Kaatz KW

7

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1 November 2017

Albin RL

9

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1 November 2017

language of work or name

English

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publication date

1 November 1993

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1 November 2017

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1 November 2017

volume

5

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1 November 2017

issue

3

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1 November 2017

page(s)

259-265

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https://scigraph.springernature.com/pub.10.1038/ng1193-259

1 November 2017

exact match

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cites work

Excitotoxic injury of the neostriatum: a model for Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

Homozygotes for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

Survival of basal ganglia neuropeptide Y-somatostatin neurones in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

Sparing of acetylcholinesterase-containing striatal neurons in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

Striosomes and extrastriosomal matrix contain different amounts of immunoreactive choline acetyltransferase in the human striatum

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

Abnormalities of striatal projection neurons and N-methyl-D-aspartate receptors in presymptomatic Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

7 January 2021

Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

7 January 2021

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

7 January 2021

Differential loss of striatal projection neurons in Huntington disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

7 January 2021

A comprehensive set of sequence analysis programs for the VAX

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-259

7 January 2021

Identifiers

DOI

10.1038/NG1193-259

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Dimensions Publication ID

1 November 2017

1046494495

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1 reference