Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease. (Q50674960)

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1 January 2020

title

Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease (English)

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Emma Colucci-Guyon

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1 January 2020

author name string

Cyril Mignot

1

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1 January 2020

Séverine Escaich

3

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1 January 2020

Bruno Della Gaspera

4

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1 January 2020

Eric Noé

5

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1 January 2020

Charles Babinet

7

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1 January 2020

Milos Pekny

8

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1 January 2020

Patrick Vicart

9

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1 January 2020

Odile Boespflug-Tanguy

10

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1 January 2020

André Dautigny

11

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1 January 2020

Diana Rodriguez

12

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1 January 2020

Danielle Pham-Dinh

13

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language of work or name

English

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publication date

24 May 2007

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Experimental Cell Research

1 January 2020

published in

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1 January 2020

volume

313

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issue

13

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1 January 2020

page(s)

2766-2779

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Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant.

1 January 2020

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Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

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Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation

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Mutations associated with a childhood leukodystrophy, Alexander disease, cause deficiency in dimerization of the cytoskeletal protein GFAP

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