 Muscle, Skeletal
"Muscle, Skeletal" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A subtype of striated muscle, attached by TENDONS to the SKELETON. Skeletal muscles are innervated and their movement can be consciously controlled. They are also called voluntary muscles.
| Descriptor ID |
D018482
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| MeSH Number(s) |
A02.633.567 A10.690.552.500
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| Concept/Terms |
Muscle, Skeletal- Muscle, Skeletal
- Muscles, Skeletal
- Skeletal Muscles
- Skeletal Muscle
- Muscle, Voluntary
- Muscles, Voluntary
- Voluntary Muscle
- Voluntary Muscles
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Below are MeSH descriptors whose meaning is more general than "Muscle, Skeletal".
Below are MeSH descriptors whose meaning is more specific than "Muscle, Skeletal".
This graph shows the total number of publications written about "Muscle, Skeletal" by people in this website by year, and whether "Muscle, Skeletal" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 3 | 4 | | 2002 | 3 | 1 | 4 | | 2003 | 1 | 0 | 1 | | 2004 | 2 | 2 | 4 | | 2005 | 6 | 1 | 7 | | 2006 | 2 | 1 | 3 | | 2007 | 7 | 2 | 9 | | 2008 | 3 | 4 | 7 | | 2009 | 8 | 4 | 12 | | 2010 | 10 | 2 | 12 | | 2011 | 2 | 6 | 8 | | 2012 | 6 | 3 | 9 | | 2013 | 8 | 2 | 10 | | 2014 | 7 | 1 | 8 | | 2015 | 5 | 3 | 8 | | 2016 | 5 | 3 | 8 | | 2017 | 3 | 6 | 9 | | 2018 | 2 | 0 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Muscle, Skeletal" by people in Profiles.
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Gavin TP, Ernst JM, Kwak HB, Caudill SE, Reed MA, Garner RT, Nie Y, Weiss JA, Pories WJ, Dar M, Lin CT, Hubal MJ, Neufer PD, Kuang S, Dohm GL. High Incomplete Skeletal Muscle Fatty Acid Oxidation Explains Low Muscle Insulin Sensitivity in Poorly Controlled T2D. J Clin Endocrinol Metab. 2018 03 01; 103(3):882-889.
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Capogrosso RF, Mantuano P, Uaesoontrachoon K, Cozzoli A, Giustino A, Dow T, Srinivassane S, Filipovic M, Bell C, Vandermeulen J, Massari AM, De Bellis M, Conte E, Pierno S, Camerino GM, Liantonio A, Nagaraju K, De Luca A. Ryanodine channel complex stabilizer compound S48168/ARM210 as a disease modifier in dystrophin-deficient mdx mice: proof-of-concept study and independent validation of efficacy. FASEB J. 2018 02; 32(2):1025-1043.
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Liu D, Morales FE, IglayReger HB, Treutelaar MK, Rothberg AE, Hubal MJ, Nadler EP, Robidoux J, Barakat H, Horowitz JF, Hoffman EP, Burant CF, Gordon PM. Expression of macrophage genes within skeletal muscle correlates inversely with adiposity and insulin resistance in humans. Appl Physiol Nutr Metab. 2018 Feb; 43(2):187-193.
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Horn A, Van der Meulen JH, Defour A, Hogarth M, Sreetama SC, Reed A, Scheffer L, Chandel NS, Jaiswal JK. Mitochondrial redox signaling enables repair of injured skeletal muscle cells. Sci Signal. 2017 Sep 05; 10(495).
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Echigoya Y, Lim KRQ, Trieu N, Bao B, Miskew Nichols B, Vila MC, Novak JS, Hara Y, Lee J, Touznik A, Mamchaoui K, Aoki Y, Takeda S, Nagaraju K, Mouly V, Maruyama R, Duddy W, Yokota T. Quantitative Antisense Screening and Optimization for Exon 51 Skipping in Duchenne Muscular Dystrophy. Mol Ther. 2017 11 01; 25(11):2561-2572.
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Kesar TM, Belagaje SR, Pergami P, Haut MW, Hobbs G, Buetefisch CM. Effects of monoaminergic drugs on training-induced motor cortex plasticity in older adults. Brain Res. 2017 Sep 01; 1670:106-117.
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Defour A, Medikayala S, Van der Meulen JH, Hogarth MW, Holdreith N, Malatras A, Duddy W, Boehler J, Nagaraju K, Jaiswal JK. Annexin A2 links poor myofiber repair with inflammation and adipogenic replacement of the injured muscle. Hum Mol Genet. 2017 06 01; 26(11):1979-1991.
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Abath Neto O, Moreno CAM, Malfatti E, Donkervoort S, Böhm J, Guimarães JB, Foley AR, Mohassel P, Dastgir J, Bharucha-Goebel DX, Monges S, Lubieniecki F, Collins J, Medne L, Santi M, Yum S, Banwell B, Salort-Campana E, Rendu J, Fauré J, Yis U, Eymard B, Cheraud C, Schneider R, Thompson J, Lornage X, Mesrob L, Lechner D, Boland A, Deleuze JF, Reed UC, Oliveira ASB, Biancalana V, Romero NB, Bönnemann CG, Laporte J, Zanoteli E. Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients. Neuromuscul Disord. 2017 Nov; 27(11):975-985.
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Echigoya Y, Nakamura A, Nagata T, Urasawa N, Lim KRQ, Trieu N, Panesar D, Kuraoka M, Moulton HM, Saito T, Aoki Y, Iversen P, Sazani P, Kole R, Maruyama R, Partridge T, Takeda S, Yokota T. Effects of systemic multiexon skipping with peptide-conjugated morpholinos in the heart of a dog model of Duchenne muscular dystrophy. Proc Natl Acad Sci U S A. 2017 04 18; 114(16):4213-4218.
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Donkervoort S, Chan SHS, Hayes LH, Bradley N, Nguyen D, Leach ME, Mohassel P, Hu Y, Thangarajh M, Bharucha-Goebel D, Kan A, Ho RSL, Reyes CA, Nance J, Moore SA, Foley AR, Bönnemann CG. Cytoplasmic body pathology in severe ACTA1-related myopathy in the absence of typical nemaline rods. Neuromuscul Disord. 2017 Jun; 27(6):531-536.
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