"Cytoskeletal Proteins" 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.
Major constituent of the cytoskeleton found in the cytoplasm of eukaryotic cells. They form a flexible framework for the cell, provide attachment points for organelles and formed bodies, and make communication between parts of the cell possible.
| Descriptor ID |
D003598
|
| MeSH Number(s) |
D12.776.220
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Cytoskeletal Proteins".
Below are MeSH descriptors whose meaning is more specific than "Cytoskeletal Proteins".
This graph shows the total number of publications written about "Cytoskeletal Proteins" by people in this website by year, and whether "Cytoskeletal Proteins" 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 |
|---|
| 2000 | 0 | 2 | 2 |
| 2001 | 0 | 2 | 2 |
| 2003 | 0 | 1 | 1 |
| 2007 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 2 | 2 |
| 2014 | 1 | 1 | 2 |
| 2015 | 1 | 0 | 1 |
| 2016 | 0 | 2 | 2 |
| 2019 | 0 | 1 | 1 |
| 2020 | 2 | 2 | 4 |
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Below are the most recent publications written about "Cytoskeletal Proteins" by people in Profiles.
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Two novel heteropolymer-forming proteins maintain the multicellular shape of the cyanobacterium Anabaena sp. PCC 7120. FEBS J. 2021 05; 288(10):3197-3216.
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DNA Methylation-Mediated Modulation of Endocytosis as Potential Mechanism for Synaptic Function Regulation in Murine Inhibitory Cortical Interneurons. Cereb Cortex. 2020 06 01; 30(7):3921-3937.
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A novel septal protein of multicellular heterocystous cyanobacteria is associated with the divisome. Mol Microbiol. 2020 06; 113(6):1140-1154.
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Identification and characterization of novel filament-forming proteins in cyanobacteria. Sci Rep. 2020 02 05; 10(1):1894.
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Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature. Eur J Hum Genet. 2019 07; 27(7):1061-1071.
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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat Genet. 2016 09; 48(9):1043-8.
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Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: Expanding the mutational spectrum. Am J Med Genet A. 2016 May; 170A(5):1295-301.
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The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS. PLoS One. 2015; 10(3):e0119066.
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Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina. Hum Mol Genet. 2015 Mar 15; 24(6):1584-601.
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Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndrome. Am J Hum Genet. 2014 Nov 06; 95(5):622-32.
MeSH information
