(Q48581887)

13 February 2018

title

Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein (English)

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13 February 2018

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5

John Q Trojanowski

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13 February 2018

author name string

Benoit I Giasson

1

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13 February 2018

John E Duda

2

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13 February 2018

Shawn M Quinn

3

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13 February 2018

Bin Zhang

4

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13 February 2018

Virginia M-Y Lee

6

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13 February 2018

language of work or name

English

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publication date

1 May 2002

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13 February 2018

published in

Neuron

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13 February 2018

volume

34

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13 February 2018

issue

4

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13 February 2018

page(s)

521-533

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13 February 2018

Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system

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Immunohistochemical and biochemical studies demonstrate a distinct profile of alpha-synuclein permutations in multiple system atrophy

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Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathology

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Mutant and wild type human alpha-synucleins assemble into elongated filaments with distinct morphologies in vitro

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A panel of epitope-specific antibodies detects protein domains distributed throughout human alpha-synuclein in Lewy bodies of Parkinson's disease

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Age-Dependent Emergence and Progression of a Tauopathy in Transgenic Mice Overexpressing the Shortest Human Tau Isoform

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Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disorders

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beta-amyloid peptides enhance alpha-synuclein accumulation and neuronal deficits in a transgenic mouse model linking Alzheimer's disease and Parkinson's disease

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7 January 2021

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Identifiers

DOI

1 reference

13 February 2018

1 reference

13 February 2018