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A bioassay for Lafora disease and laforin glucan phosphatase activity.

A bioassay for Lafora disease and laforin glucan phosphatase activity.

http://www.wikidata.org/entity/Q37394687

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Assessing the Biological Activity of the Glucan Phosphatase Laforin Identification and analysis of OsttaDSP, a phosphoglucan phosphatase from Ostreococcus tauri.

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P2860

A bioassay for Lafora disease and laforin glucan phosphatase activity.

http://www.wikidata.org/entity/Q37394687

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 06 September 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

A bioassay for Lafora disease and laforin glucan phosphatase activity.

@en

A bioassay for Lafora disease and laforin glucan phosphatase activity.

@nl

type

label

A bioassay for Lafora disease and laforin glucan phosphatase activity.

@en

A bioassay for Lafora disease and laforin glucan phosphatase activity.

@nl

prefLabel

A bioassay for Lafora disease and laforin glucan phosphatase activity.

@en

A bioassay for Lafora disease and laforin glucan phosphatase activity.

@nl

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P356

J.CLINBIOCHEM.2013.08.016

P1433

Clinical Biochemistry

P1476

A bioassay for Lafora disease and laforin glucan phosphatase activity

@en

P2093

Amanda R Sherwood

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Mary Beth Johnson

http://www.w3.org/2001/XMLSchema#string

Matthew S Gentry

http://www.w3.org/2001/XMLSchema#string

P2860

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)

Insights into Lafora disease: malin is an E3 ubiquitin ligase that ubiquitinates and promotes the degradation of laforin.

The purification and characterization of a human dual-specific protein tyrosine phosphatase

Structural basis for the glucan phosphatase activity of Starch Excess4

Laforin, a dual specificity phosphatase that dephosphorylates complex carbohydrates

Phosphate incorporation during glycogen synthesis and Lafora disease

PTG depletion removes Lafora bodies and rescues the fatal epilepsy of Lafora disease

Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice

Conservation of the glucan phosphatase laforin is linked to rates of molecular evolution and the glucan metabolism of the organism

A unique carbohydrate binding domain targets the lafora disease phosphatase to glycogen.

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1869-1876

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scholarly article

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10.1016/J.CLINBIOCHEM.2013.08.016

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18

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46

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Antonio V Delgado-Escueta

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2013-09-06T00:00:00Z

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24012855

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3864130

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