Mitochondrial fission and remodelling contributes to muscle atrophy. (Q39713513)

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31 January 2020

title

Mitochondrial fission and remodelling contributes to muscle atrophy (English)

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31 January 2020

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mitochondrial fission

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31 January 2020

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31 January 2020

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31 January 2020

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31 January 2020

Vanina Romanello

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31 January 2020

Ligia Gomes

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31 January 2020

Ira Roder

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31 January 2020

Claudia Sandri

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31 January 2020

Yvonne Petersen

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31 January 2020

Giulia Milan

1 reference

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31 January 2020

Eva Masiero

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31 January 2020

Paola Del Piccolo

1 reference

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31 January 2020

Marco Sandri

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31 January 2020

language of work or name

English

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publication date

16 April 2010

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31 January 2020

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volume

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issue

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31 January 2020

page(s)

1774-1785

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describes a project that uses

31 January 2020

ImageJ

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11 June 2022

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Signaling in muscle atrophy and hypertrophy

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FoxO3 coordinately activates protein degradation by the autophagic/lysosomal and proteasomal pathways in atrophying muscle cells

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The muscle-specific ubiquitin ligase atrogin-1/MAFbx mediates statin-induced muscle toxicity

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PGC-1alpha protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription

14 September 2017

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The mitochondrial fission protein hFis1 requires the endoplasmic reticulum gateway to induce apoptosis

14 September 2017

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(De)constructing mitochondria: what for?

14 September 2017

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Protein degradation by the ubiquitin-proteasome pathway in normal and disease states

14 September 2017

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Response to myocardial ischemia/reperfusion injury involves Bnip3 and autophagy

14 September 2017

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Direct in vivo monitoring of sarcoplasmic reticulum Ca2+ and cytosolic cAMP dynamics in mouse skeletal muscle

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Burn injury causes mitochondrial dysfunction in skeletal muscle

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In vivo monitoring of Ca(2+) uptake into mitochondria of mouse skeletal muscle during contraction

14 September 2017

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

14 September 2017

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

14 September 2017

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14 September 2017

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14 September 2017

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14 September 2017

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14 September 2017

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14 September 2017

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14 September 2017

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17 June 2018

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Rapid disuse and denervation atrophy involve transcriptional changes similar to those of muscle wasting during systemic diseases

17 June 2018

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17 June 2018

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S6 kinase deletion suppresses muscle growth adaptations to nutrient availability by activating AMP kinase

20 August 2018

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Bnip3 mediates mitochondrial dysfunction and cell death through Bax and Bak.

20 August 2018

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20 August 2018

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Denervation in murine fast-twitch muscle: short-term physiological changes and temporal expression profiling

20 August 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/20400940

inferred from PubMed ID database lookup

12 December 2020

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Evidence for a mitochondrial regulatory pathway defined by peroxisome proliferator-activated receptor-gamma coactivator-1 alpha, estrogen-related receptor-alpha, and mitofusin 2

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20400940

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EMBOJ.2010.60

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20400940%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference

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31 January 2020

PubMed publication ID

20400940

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20400940%20AND%20SRC:MED&resulttype=core&format=json