Protein degradation and quality control in cells from laforin and malin knockout mice (Q33947038)

30 July 2017

title

Protein degradation and quality control in cells from laforin and malin knockout mice (English)

1 reference

30 July 2017

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NHL repeat containing 1

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Epilepsy, progressive myoclonic epilepsy, type 2 gene alpha

GOA release 2020-03-11

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GOA release 2020-03-11

author name string

Punitee Garyali

1

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30 July 2017

Dyann M Segvich

2

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30 July 2017

Anna A DePaoli-Roach

3

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30 July 2017

Peter J Roach

4

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30 July 2017

language of work or name

English

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publication date

1 July 2014

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Journal of Biological Chemistry

30 July 2017

published in

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30 July 2017

volume

289

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30 July 2017

issue

30

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30 July 2017

page(s)

20606-20614

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Inhibiting glycogen synthesis prevents Lafora disease in a mouse model

30 July 2017

cites work

1 reference

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Malin knockout mice support a primary role of autophagy in the pathogenesis of Lafora disease

5 July 2018

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Glycogen and its metabolism: some new developments and old themes

5 July 2018

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Starch-binding domain-containing protein 1 (Stbd1) and glycogen metabolism: Identification of the Atg8 family interacting motif (AIM) in Stbd1 required for interaction with GABARAPL1

5 July 2018

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

5 July 2018

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Starch Binding Domain-containing Protein 1/Genethonin 1 Is a Novel Participant in Glycogen Metabolism

5 July 2018

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Genetic depletion of the malin E3 ubiquitin ligase in mice leads to lafora bodies and the accumulation of insoluble laforin

5 July 2018

1 reference

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Laforin, the most common protein mutated in Lafora disease, regulates autophagy

5 July 2018

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Increased endoplasmic reticulum stress and decreased proteasomal function in lafora disease models lacking the phosphatase laforin

5 July 2018

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RING domain E3 ubiquitin ligases

5 July 2018

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5 July 2018

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AMP-activated protein kinase phosphorylates R5/PTG, the glycogen targeting subunit of the R5/PTG-protein phosphatase 1 holoenzyme, and accelerates its down-regulation by the laforin-malin complex

5 July 2018

1 reference

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Abnormal metabolism of glycogen phosphate as a cause for Lafora disease

5 July 2018

1 reference

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Malin decreases glycogen accumulation by promoting the degradation of protein targeting to glycogen (PTG)

5 July 2018

1 reference

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Laforin is a glycogen phosphatase, deficiency of which leads to elevated phosphorylation of glycogen in vivo.

5 July 2018

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A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori's disease

5 July 2018

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Glycogen storage disease: clinical, biochemical, and molecular heterogeneity

5 July 2018

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Relationship between glycogen accumulation and the laforin dual specificity phosphatase

5 July 2018

1 reference

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Lysosomal turnover, but not a cellular level, of endogenous LC3 is a marker for autophagy

5 July 2018

1 reference

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Ubiquitylation and cell signaling

5 July 2018

1 reference

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Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy

5 July 2018

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

5 July 2018

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Role and regulation of starvation-induced autophagy in the Drosophila fat body

5 July 2018

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Mutations in NHLRC1 cause progressive myoclonus epilepsy

5 July 2018

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

5 July 2018

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5 July 2018

Glycogen storage disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110273

Glycogen and its Metabolism

5 July 2018

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Lafora's disease: towards a clinical, pathologic, and molecular synthesis

5 July 2018

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Insulin control of glycogen metabolism in knockout mice lacking the muscle-specific protein phosphatase PP1G/RGL.

5 July 2018

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Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

5 July 2018

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CHOP is implicated in programmed cell death in response to impaired function of the endoplasmic reticulum

5 July 2018

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Tor, a phosphatidylinositol kinase homologue, controls autophagy in yeast

5 July 2018

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Studies in myoclonus epilepsy (Lafora body form). I. Isolation and preliminary characterization of Lafora bodies in two cases

5 July 2018

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5 July 2018

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

5 July 2018

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Progressive familial myoclonic epilepsy in three families: its clinical features and pathological basis.

5 July 2018

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Glycogen accumulation underlies neurodegeneration and autophagy impairment in Lafora disease

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M114.580167

The malin-laforin complex suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin-proteasome system

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.580167

Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.580167

Laforin and malin knockout mice have normal glucose disposal and insulin sensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.580167

Fanconi anemia type C and p53 cooperate in apoptosis and tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.580167

Lafora disease ubiquitin ligase malin promotes proteasomal degradation of neuronatin and regulates glycogen synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.580167

Dysfunctions in endosomal-lysosomal and autophagy pathways underlie neuropathology in a mouse model for Lafora disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.580167

PTG protein depletion rescues malin-deficient Lafora disease in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.580167

Beitrag zur Histopathologie der myoklonischen Epilepsie

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.580167

21 January 2018

Identifiers

DOI

10.1074/JBC.M114.580167

1 reference

30 July 2017

1 reference

30 July 2017

1 reference