The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII). (Q36223972)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22595755%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

title

The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII) (English)

1 reference

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1 February 2020

main subject

autophagy

0 references

glycogen storage disease

1 reference

4

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1 February 2020

author name string

A C Nascimbeni

1

1 reference

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1 February 2020

M Fanin

2

1 reference

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1 February 2020

E Masiero

3

1 reference

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1 February 2020

M Sandri

5

1 reference

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1 February 2020

publication date

18 May 2012

1 reference

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Cell Death & Differentiation

1 February 2020

published in

1 reference

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1 February 2020

volume

19

1 reference

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1 February 2020

page(s)

1698-1708

1 reference

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1 February 2020

issue

10

1 reference

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describes a project that uses

1 February 2020

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3438501/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

exact match

https://scigraph.springernature.com/pub.10.1038/cdd.2012.52

0 references

cites work

Fiber type conversion by PGC-1α activates lysosomal and autophagosomal biogenesis in both unaffected and Pompe skeletal muscle

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Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder--murine Pompe disease

1 October 2017

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The values and limits of an in vitro model of Pompe disease: the best laid schemes o' mice an' men..

1 October 2017

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Regulation of the aging process by autophagy

1 October 2017

1 reference

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RETRACTED: VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification

1 October 2017

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When more is less: excess and deficiency of autophagy coexist in skeletal muscle in Pompe disease

1 October 2017

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Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease

1 October 2017

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Autophagy fights disease through cellular self-digestion

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3438501

FoxO3 controls autophagy in skeletal muscle in vivo

1 October 2017

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Deconstructing Pompe disease by analyzing single muscle fibers: to see a world in a grain of sand...

1 October 2017

1 reference

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Human skeletal muscle atrophy in amyotrophic lateral sclerosis reveals a reduction in Akt and an increase in atrogin-1.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3438501

Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3438501

Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression

1 October 2017

1 reference

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Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

1 October 2017

1 reference

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Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

1 October 2017

1 reference

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Inhibition of lysosomal function in red and white skeletal muscles by chloroquine

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3438501

X-linked myopathy with excessive autophagy: a new hereditary muscle disease

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3438501

Autophagy is required to maintain muscle mass.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3438501

Molecular pathology and enzyme processing in various phenotypes of acid maltase deficiency

22 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22595755

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/CDD.2012.52

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22595755%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

1 reference

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1 February 2020

1 reference

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