Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora disease. (Q36127081)

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3 February 2020

title

Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora disease (English)

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3 February 2020

4

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author name string

Erica Tiberia

1

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3 February 2020

Julie Turnbull

2

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3 February 2020

Tony Wang

3

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3 February 2020

Xiao-Chu Zhao

5

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3 February 2020

Nela Pencea

6

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3 February 2020

Johan Israelian

7

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3 February 2020

Yin Wang

8

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3 February 2020

Cameron A Ackerley

9

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3 February 2020

Peixiang Wang

10

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3 February 2020

Yan Liu

11

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3 February 2020

Berge A Minassian

12

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language of work or name

English

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publication date

5 June 2012

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Journal of Biological Chemistry

3 February 2020

published in

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volume

287

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issue

30

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3 February 2020

page(s)

25650-25659

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describes a project that uses

3 February 2020

ImageJ

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11 June 2022

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inferred from PubMed Central ID database lookup

cites work

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

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Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism

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

2 October 2017

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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

2 October 2017

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Modulation of functional properties of laforin phosphatase by alternative splicing reveals a novel mechanism for the EPM2A gene in Lafora progressive myoclonus epilepsy

2 October 2017

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

2 October 2017

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

2 October 2017

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Relationship between glycogen accumulation and the laforin dual specificity phosphatase

2 October 2017

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Laforin, a dual specificity phosphatase that dephosphorylates complex carbohydrates

2 October 2017

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

2 October 2017

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

2 October 2017

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2 October 2017

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Functional diversity of protein phosphatase-1, a cellular economizer and reset button

2 October 2017

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Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulation

2 October 2017

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Familial cirrhosis of the liver with storage of abnormal glycogen

2 October 2017

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Mutations in NHLRC1 cause progressive myoclonus epilepsy

2 October 2017

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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

2 October 2017

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2 October 2017

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

2 October 2017

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2 October 2017

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

2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 July 2018

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23 September 2018

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The carbohydrate-binding domain of Lafora disease protein targets Lafora polyglucosan bodies.

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23 September 2018

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Crossref

https://api.crossref.org/works/10.1074%2FJBC.M111.331611

Type IV glycogenosis (amylopectinosis). Light and electron microscopic observations

21 January 2018

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12 December 2020

[Production of monoclonal antibody that recognizes glycogen and its application for immunohistochemistry]

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A method for the colorimetric estimation of glycogen with lodine

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Identifiers

DOI

10.1074/JBC.M111.331611

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22669944%20AND%20SRC:MED&resulttype=core&format=json

3 February 2020

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3 February 2020

PubMed publication ID

22669944

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22669944%20AND%20SRC:MED&resulttype=core&format=json