Data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin

Skeletal muscle apoptosis and autophagy are catabolic processes that contribute to muscle atrophy during aging, disease, and following muscle injury. In this article, we present data on skeletal muscle apoptosis, autophagy, and morphology in C57BL/6 mice following doxorubicin administration. More sp...

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Detalles Bibliográficos
Autores principales: Campbell, Troy L., Quadrilatero, Joe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Data Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816877/
https://www.ncbi.nlm.nih.gov/pubmed/27077080
http://dx.doi.org/10.1016/j.dib.2016.03.009
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author Campbell, Troy L.
Quadrilatero, Joe
author_facet Campbell, Troy L.
Quadrilatero, Joe
author_sort Campbell, Troy L.
collection PubMed
description Skeletal muscle apoptosis and autophagy are catabolic processes that contribute to muscle atrophy during aging, disease, and following muscle injury. In this article, we present data on skeletal muscle apoptosis, autophagy, and morphology in C57BL/6 mice following doxorubicin administration. More specifically, time-course data on caspase-3, caspase-8, caspase-9, calpain, and cathepsin activity are presented, along with data on ATG7, p62, LC3-I, and LC3-II protein expression. Data on skeletal muscle reactive oxygen species (ROS) production, muscle morphology, as well as body and muscle weights are also presented.
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spelling pubmed-48168772016-04-13 Data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin Campbell, Troy L. Quadrilatero, Joe Data Brief Data Article Skeletal muscle apoptosis and autophagy are catabolic processes that contribute to muscle atrophy during aging, disease, and following muscle injury. In this article, we present data on skeletal muscle apoptosis, autophagy, and morphology in C57BL/6 mice following doxorubicin administration. More specifically, time-course data on caspase-3, caspase-8, caspase-9, calpain, and cathepsin activity are presented, along with data on ATG7, p62, LC3-I, and LC3-II protein expression. Data on skeletal muscle reactive oxygen species (ROS) production, muscle morphology, as well as body and muscle weights are also presented. Elsevier 2016-03-10 /pmc/articles/PMC4816877/ /pubmed/27077080 http://dx.doi.org/10.1016/j.dib.2016.03.009 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Campbell, Troy L.
Quadrilatero, Joe
Data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin
title Data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin
title_full Data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin
title_fullStr Data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin
title_full_unstemmed Data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin
title_short Data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin
title_sort data on skeletal muscle apoptosis, autophagy, and morphology in mice treated with doxorubicin
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816877/
https://www.ncbi.nlm.nih.gov/pubmed/27077080
http://dx.doi.org/10.1016/j.dib.2016.03.009
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