Alpha-synuclein expression in substantia nigra and cortex in Parkinson's disease. (Q48198986)

9 February 2018

title

Alpha-synuclein expression in substantia nigra and cortex in Parkinson's disease. (English)

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9 February 2018

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Przedborski S

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9 February 2018

Neystat M

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9 February 2018

Lynch T

2

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9 February 2018

Kholodilov N

4

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9 February 2018

Rzhetskaya M

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9 February 2018

Burke RE

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language of work or name

English

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publication date

1 May 1999

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9 February 2018

published in

Movement Disorders

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9 February 2018

volume

14

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9 February 2018

issue

3

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9 February 2018

page(s)

417-422

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9 February 2018

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Mutations in RNA: a first example of molecular misreading in Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Molecular cloning of cDNA encoding an unrecognized component of amyloid in Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Tissue-dependent alternative splicing of mRNA for NACP, the precursor of non-A beta component of Alzheimer's disease amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Localization and dynamic regulation of biogenic amine transporters in the mammalian central nervous system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

The rat brain synucleins; family of proteins transiently associated with neuronal membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

The precursor protein of non-A beta component of Alzheimer's disease amyloid is a presynaptic protein of the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Characterization of a novel protein regulated during the critical period for song learning in the zebra finch.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Alpha-synuclein in Lewy bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Melanin, tyrosine hydroxylase, calbindin and substance P in the human midbrain and substantia nigra in relation to nigrostriatal projections and differential neuronal susceptibility in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

Identification of Spanish familial Parkinson's disease and screening for the Ala53Thr mutation of the α-synuclein gene in early onset patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28199905%2914%3A3%3C417%3A%3AAID-MDS1005%3E3.0.CO%3B2-X

10.1002/1531-8257(199905)14:3<417::AID-MDS1005>3.0.CO;2-X

21 January 2018

Identifiers

DOI

1 reference

9 February 2018

release_nxod5qcmjfdgxdjvxxa2dghzz4

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/nxod5qcmjfdgxdjvxxa2dghzz4

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

10348463

1 reference

9 February 2018