Deciphering the role of malin in the lafora progressive myoclonus epilepsy
about
Autophagy and neurodegenerationPolyglucosan body myopathy caused by defective ubiquitin ligase RBCK1Dimerization of the glucan phosphatase laforin requires the participation of cysteine 329.Quantitative and functional interrogation of parent-of-origin allelic expression biases in the brain.AMPKβ subunits: more than just a scaffold in the formation of AMPK complex.Homeostasis of the astrocytic glutamate transporter GLT-1 is altered in mouse models of Lafora disease.Suppression of leptin signaling reduces polyglucosan inclusions and seizure susceptibility in a mouse model for Lafora disease.Defective NHLRC1 does not ubiquitinate EPM2A (laforin) and PPP1R3C (PTG) (type 2B disease)
P2860
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P2860
Deciphering the role of malin in the lafora progressive myoclonus epilepsy
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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name
Deciphering the role of malin in the lafora progressive myoclonus epilepsy
@ast
Deciphering the role of malin in the lafora progressive myoclonus epilepsy
@en
type
label
Deciphering the role of malin in the lafora progressive myoclonus epilepsy
@ast
Deciphering the role of malin in the lafora progressive myoclonus epilepsy
@en
prefLabel
Deciphering the role of malin in the lafora progressive myoclonus epilepsy
@ast
Deciphering the role of malin in the lafora progressive myoclonus epilepsy
@en
P2860
P356
P1433
P1476
Deciphering the role of malin in the lafora progressive myoclonus epilepsy
@en
P2093
Matthew S Gentry
P2860
P304
P356
10.1002/IUB.1072
P577
2012-07-20T00:00:00Z