(Q40684026)

22 September 2017

title

Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease (English)

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22 September 2017

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4

Zbigniew Wszolek

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22 September 2017

11

Nobutaka Hattori

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22 September 2017

10

Yoshikuni Mizuno

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22 September 2017

9

Olaf Riess

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22 September 2017

2

Rejko Krüger

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22 September 2017

8

Kimie Murayama

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22 September 2017

Hirokazu Kobayashi

1

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22 September 2017

Katerina Markopoulou

3

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22 September 2017

Bruce Chase

5

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22 September 2017

Hikaru Taka

6

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22 September 2017

Reiko Mineki

7

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22 September 2017

language of work or name

English

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publication date

1 January 2003

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22 September 2017

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22 September 2017

volume

126

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22 September 2017

issue

Pt 1

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22 September 2017

page(s)

32-42

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Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein

22 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Fibrils formed in vitro from alpha-synuclein and two mutant forms linked to Parkinson's disease are typical amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Acceleration of oligomerization, not fibrillization, is a shared property of both alpha-synuclein mutations linked to early-onset Parkinson's disease: implications for pathogenesis and therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Modeling stochastic gene expression: implications for haploinsufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Synthetic filaments assembled from C-terminally truncated alpha-synuclein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

A Drosophila model of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Real time quantitative PCR

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Haploinsufficiency of MSX1: a mechanism for selective tooth agenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Myotonic dystrophy: molecular windows on a complex etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

Alpha-synuclein in Lewy bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

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/10.1093%2FBRAIN%2FAWG010

The molecular basis of genetic dominance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWG010

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWG010

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22 September 2017

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