Sarcoglycans
"Sarcoglycans" 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 family of transmembrane dystrophin-associated proteins that play a role in the membrane association of the DYSTROPHIN-ASSOCIATED PROTEIN COMPLEX.
Descriptor ID |
D049031
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MeSH Number(s) |
D12.776.210.500.410.750 D12.776.543.268.750 D12.776.543.550.712
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Concept/Terms |
beta-Sarcoglycan- beta-Sarcoglycan
- beta Sarcoglycan
- 43-kDa Dystrophin-Associated Glycoprotein
- 43 kDa Dystrophin Associated Glycoprotein
- Dystrophin-Associated Glycoprotein, 43-kDa
- Glycoprotein, 43-kDa Dystrophin-Associated
alpha-Sarcoglycan- alpha-Sarcoglycan
- alpha Sarcoglycan
- Adhalin
- 50-kDa Dystrophin-Associated glycoprotein
- 50 kDa Dystrophin Associated glycoprotein
- Dystrophin-Associated glycoprotein, 50-kDa
- glycoprotein, 50-kDa Dystrophin-Associated
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Below are MeSH descriptors whose meaning is more general than "Sarcoglycans".
Below are MeSH descriptors whose meaning is more specific than "Sarcoglycans".
This graph shows the total number of publications written about "Sarcoglycans" by people in this website by year, and whether "Sarcoglycans" 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 |
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2007 | 1 | 0 | 1 | 2010 | 0 | 1 | 1 | 2015 | 0 | 1 | 1 | 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Sarcoglycans" by people in Profiles.
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Khalil H, Kanisicak O, Vagnozzi RJ, Johansen AK, Maliken BD, Prasad V, Boyer JG, Brody MJ, Schips T, Kilian KK, Correll RN, Kawasaki K, Nagata K, Molkentin JD. Cell-specific ablation of Hsp47 defines the collagen-producing cells in the injured heart JCI Insight. 2019 08 08; 4(15):e128722.
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Peter AK, Miller G, Capote J, DiFranco M, Solares-P?rez A, Wang EL, Heighway J, Coral-V?zquez RM, Vergara J, Crosbie-Watson RH. Nanospan, an alternatively spliced isoform of sarcospan, localizes to the sarcoplasmic reticulum in skeletal muscle and is absent in limb girdle muscular dystrophy 2F. Skelet Muscle. 2017 06 06; 7(1):11.
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Hardin M, Cho MH, McDonald ML, Wan E, Lomas DA, Coxson HO, MacNee W, Vestbo J, Yates JC, Agusti A, Calverley PM, Celli B, Crim C, Rennard S, Wouters E, Bakke P, Bhatt SP, Kim V, Ramsdell J, Regan EA, Make BJ, Hokanson JE, Crapo JD, Beaty TH, Hersh CP. A genome-wide analysis of the response to inhaled ?2-agonists in chronic obstructive pulmonary disease. Pharmacogenomics J. 2016 08; 16(4):326-35.
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Hansel NN, Par? PD, Rafaels N, Sin DD, Sandford A, Daley D, Vergara C, Huang L, Elliott WM, Pascoe CD, Arsenault BA, Postma DS, Boezen HM, Boss? Y, van den Berge M, Hiemstra PS, Cho MH, Litonjua AA, Sparrow D, Ober C, Wise RA, Connett J, Neptune ER, Beaty TH, Ruczinski I, Mathias RA, Barnes KC. Genome-Wide Association Study Identification of Novel Loci Associated with Airway Responsiveness in Chronic Obstructive Pulmonary Disease. Am J Respir Cell Mol Biol. 2015 Aug; 53(2):226-34.
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Gazzerro E, Assereto S, Bonetto A, Sotgia F, Scarf? S, Pistorio A, Bonuccelli G, Cilli M, Bruno C, Zara F, Lisanti MP, Minetti C. Therapeutic potential of proteasome inhibition in Duchenne and Becker muscular dystrophies. Am J Pathol. 2010 Apr; 176(4):1863-77.
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Peter AK, Miller G, Crosbie RH. Disrupted mechanical stability of the dystrophin-glycoprotein complex causes severe muscular dystrophy in sarcospan transgenic mice. J Cell Sci. 2007 Mar 15; 120(Pt 6):996-1008.
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Hess CW, Raymond D, Aguiar Pde C, Frucht S, Shriberg J, Heiman GA, Kurlan R, Klein C, Bressman SB, Ozelius LJ, Saunders-Pullman R. Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers. Neurology. 2007 Feb 13; 68(7):522-4.
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Miller G, Wang EL, Nassar KL, Peter AK, Crosbie RH. Structural and functional analysis of the sarcoglycan-sarcospan subcomplex. Exp Cell Res. 2007 Feb 15; 313(4):639-51.
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Peter AK, Crosbie RH. Hypertrophic response of Duchenne and limb-girdle muscular dystrophies is associated with activation of Akt pathway. Exp Cell Res. 2006 Aug 01; 312(13):2580-91.
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