Desmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desmin (Q24291234)

GOA release 2020-03-11

author name string

Y Mizuno

1

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T G Thompson

2

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J R Guyon

3

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H G Lidov

4

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M Brosius

5

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M Imamura

6

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E Ozawa

7

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S C Watkins

8

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L M Kunkel

Proceedings of the National Academy of Sciences of the United States of America

9

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language of work or name

English

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publication date

22 May 2001

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published in

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volume

98

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issue

11

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page(s)

6156-61

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cites work

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Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene

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Molecular characteristics and interactions of the intermediate filament protein synemin. Interactions with alpha-actinin may anchor synemin-containing heterofilaments

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Molecular characteristics of the novel intermediate filament protein paranemin. Sequence reveals EAP-300 and IFAPa-400 are highly homologous to paranemin

27 September 2017

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Mammalian alpha 1- and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus

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Dystrophin-associated protein A0 is a homologue of the Torpedo 87K protein

27 September 2017

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The 87K postsynaptic membrane protein from Torpedo is a protein-tyrosine kinase substrate homologous to dystrophin.

27 September 2017

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A protein expressed in the growth cones of embryonic vertebrate neurons defines a new class of intermediate filament protein

30 May 2018

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Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution.

30 May 2018

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Crossref

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A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation.

21 January 2018

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