Neurofibromatosis 2 tumour suppressor schwannomin interacts with betaII-spectrin (Q24323104)

Spectrin beta, non-erythrocytic 1

GOA release 2020-03-11

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neurofibromatosis type II

GOA release 2020-03-11

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D R Scoles

1

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D P Huynh

2

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P A Morcos

3

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E R Coulsell

4

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N G Robinson

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F Tamanoi

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S M Pulst

https://scigraph.springernature.com/pub.10.1038/ng0498-354

7

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language of work or name

English

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publication date

April 1998

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published in

Nature Genetics

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volume

18

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issue

4

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page(s)

354-9

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exact match

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cites work

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Ankyrin binds to the 15th repetitive unit of erythroid and nonerythroid beta-spectrin

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Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.

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Alternative transcripts in the mouse neurofibromatosis type 2 (NF2) gene are conserved and code for schwannomins with distinct C-terminal domains

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A missense mutation in the NF2 gene results in moderate and mild clinical phenotypes of neurofibromatosis type 2.

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Ezrin has a COOH-terminal actin-binding site that is conserved in the ezrin protein family

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7 January 2021

Interdomain binding mediates tumor growth suppression by the NF2 gene product

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Soluble ezrin purified from placenta exists as stable monomers and elongated dimers with masked C-terminal ezrin-radixin-moesin association domains

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Calcium ionophore induced proteolysis and cataract: inhibition by cell permeable calpain antagonists

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Congenital hypertrophy of the retinal pigment epithelium associated with familial adenomatous polyposis.

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Human cardiac and skeletal muscle spectrins: differential expression and localization

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Impaired interaction of naturally occurring mutant NF2 protein with actin-based cytoskeleton and membrane

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