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EPM2A gene

Known as: LD, LDE, EPM2A, ISOFORM B 
National Institutes of Health

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2 relations
EPM2A protein, humanLafora Disease

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Bovine papillomavirus E5 oncoprotein upregulates parkin-dependent mitophagy in urothelial cells of cattle with spontaneous papillomavirus infection: A mechanistic study.
2016
2016
Incorporation of phosphate into glycogen by glycogen synthase.
2014
2014
A Fast Image Encryption Algorithm Based on Chaotic Maps and the Linear Diophantine Equation
: In recent years, chaos-based encryption has suggested a new and efficient way to deal with the intractable problem of fast and… 
2012
2012
Expression of efflux pump gene lde in ciprofloxacin‐resistant foodborne isolates of Listeria monocytogenes
The expression of efflux pump gene lde in ciprofloxacin resistant (CipR) and susceptible strains of Listeria monocytogenes… 
2010
2010
Effects of caloric restriction with varying energy density and aerobic exercise on weight change and satiety in young female adults
This study examines the combined effects of caloric restriction on body composition, blood lipid, and satiety in slightly… 
2006
2006
Molecular characterization of laforin, a dual-specificity protein phosphatase implicated in Lafora disease.
Highly Cited
2004
Highly Cited
2004
Glycogen and related polysaccharides inhibit the laforin dual-specificity protein phosphatase.
2003
2003
The Lafora disease gene product laforin interacts with HIRIP5, a phylogenetically conserved protein containing a NifU-like domain.
Lafora disease is an autosomal recessive type of progressive myoclonus epilepsy caused by mutations in the EPM2A gene. The EPM2A… 
2001
2001
In vitro cytotoxicity of the LDE: daunorubicin complex in acute myelogenous leukemia blast cells.
Acute myelogenous leukemia (AML) blast cells show high-affinity degradation of low-density lipoprotein (LDL), suggesting an… 
2000
2000
Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions
Progressive myoclonus epilepsy of the Lafora type (Lafora disease) is an autosomal recessive disease characterised by epilepsy… 
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