(Q34194294)

English

Muscle-specific inositide phosphatase (MIP/MTMR14) is reduced with age and its loss accelerates skeletal muscle aging process by altering calcium homeostasis

scientific article published on August 1, 2010

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scholarly article

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31 July 2017

Muscle-specific inositide phosphatase (MIP/MTMR14) is reduced with age and its loss accelerates skeletal muscle aging process by altering calcium homeostasis (English)

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31 July 2017

Michael J Wacker

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Michael Wacker

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7 July 2024

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Sandra Romero-Suarez

1

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31 July 2017

Jinhua Shen

2

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31 July 2017

Leticia Brotto

3

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31 July 2017

Todd Hall

4

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31 July 2017

Chenglin Mo

5

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31 July 2017

Jon Andresen

7

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31 July 2017

Cheng-Kui Qu

10

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31 July 2017

Marco Brotto

11

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31 July 2017

Héctor H. Valdivia

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0000-0003-1231-6267

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20817957

7 July 2024

Thomas M. Nosek

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7 July 2024

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National Center for Biotechnology Information

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7 July 2024

publication date

1 August 2010

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31 July 2017

full work available at URL

https://doi.org/10.18632/aging.100190

online access status

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7 July 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20817957/?tool=EBI

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20817957

7 July 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20817957/pdf/?tool=EBI

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7 July 2024

https://europepmc.org/articles/PMC2954041

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Europe PubMed Central

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20817957

7 July 2024

https://europepmc.org/articles/PMC2954041?pdf=render

Portable Document Format

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content deliverer

Europe PubMed Central

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20817957

7 July 2024

https://www.aging-us.com/lookup/doi/10.18632/aging.100190

1 reference

10.18632/AGING.100190

https://api.crossref.org/works/10.18632/AGING.100190

7 July 2024

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Europe PubMed Central

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31 July 2017

2

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Europe PubMed Central

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31 July 2017

8

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31 July 2017

504-513

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Europe PubMed Central

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31 July 2017

Deficiency of MIP/MTMR14 phosphatase induces a muscle disorder by disrupting Ca(2+) homeostasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954041

5 July 2018

Proteomics of skeletal muscle aging

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Compromised store-operated Ca2+ entry in aged skeletal muscle

1 reference

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Oxidized phospholipids: emerging lipid mediators in pathophysiology

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5 July 2018

Skeletal muscle adaptation to fatty acid depends on coordinated actions of the PPARs and PGC1 alpha: implications for metabolic disease

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5 July 2018

Phosphoinositide-metabolizing enzymes at the interface between membrane traffic and cell signalling

1 reference

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5 July 2018

Phosphoinositides: regulators of membrane traffic and protein function

1 reference

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5 July 2018

Lipid signaling and synaptic plasticity

1 reference

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5 July 2018

Muscle aging is associated with compromised Ca2+ spark signaling and segregated intracellular Ca2+ release

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954041

5 July 2018

Myotubularin phosphatases: policing 3-phosphoinositides

1 reference

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5 July 2018

Transcriptional profiling of aging in human muscle reveals a common aging signature

1 reference

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5 July 2018

Phosphoinositide-derived messengers in endocrine signaling.

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5 July 2018

Enhanced resistance to fatigue and altered calcium handling properties of sarcalumenin knockout mice

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5 July 2018

Myofibrillar myosin ATPase activity in hindlimb muscles from young and aged rats

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5 July 2018

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma

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5 July 2018

Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15.

1 reference

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Molecular mechanisms and therapeutics of the deficit in specific force in ageing skeletal muscle

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Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2.

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A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast

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Identifiers

10.18632/AGING.100190

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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