"Microtubule-Associated 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.
High molecular weight proteins found in the MICROTUBULES of the cytoskeletal system. Under certain conditions they are required for TUBULIN assembly into the microtubules and stabilize the assembled microtubules.
Descriptor ID |
D008869
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MeSH Number(s) |
D12.776.220.600.450 D12.776.631.560
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Concept/Terms |
Microtubule-Associated Protein 2- Microtubule-Associated Protein 2
- Microtubule Associated Protein 2
- MAP2 Microtubule-Associated Protein
- MAP2 Microtubule Associated Protein
- Microtubule-Associated Protein, MAP2
Microtubule-Associated Protein 3- Microtubule-Associated Protein 3
- Microtubule Associated Protein 3
- MAP3 Microtubule-Associated Protein
- MAP3 Microtubule Associated Protein
- Microtubule-Associated Protein, MAP3
Microtubule-Associated Protein 1- Microtubule-Associated Protein 1
- Microtubule Associated Protein 1
- MAP1 Microtubule-Associated Protein
- MAP1 Microtubule Associated Protein
- Microtubule-Associated Protein, MAP1
|
Below are MeSH descriptors whose meaning is more general than "Microtubule-Associated Proteins".
Below are MeSH descriptors whose meaning is more specific than "Microtubule-Associated Proteins".
This graph shows the total number of publications written about "Microtubule-Associated Proteins" by people in this website by year, and whether "Microtubule-Associated Proteins" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2008 | 2 | 0 | 2 |
2010 | 1 | 0 | 1 |
2013 | 0 | 2 | 2 |
2014 | 0 | 2 | 2 |
2015 | 2 | 1 | 3 |
2016 | 2 | 0 | 2 |
2020 | 0 | 1 | 1 |
2021 | 1 | 0 | 1 |
2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Microtubule-Associated Proteins" by people in Profiles.
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Blood transcriptome sequencing identifies biomarkers able to track disease stages in spinocerebellar ataxia type 3. Brain. 2023 10 03; 146(10):4132-4143.
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Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ. Genes (Basel). 2021 05 13; 12(5).
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Critical Interaction Between Telomerase and Autophagy in Mediating Flow-Induced Human Arteriolar Vasodilation. Arterioscler Thromb Vasc Biol. 2021 01; 41(1):446-457.
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Interrogating the degradation pathways of unstable mRNAs with XRN1-resistant sequences. Nat Commun. 2016 12 05; 7:13691.
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Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations. Muscle Nerve. 2016 09; 54(3):496-500.
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A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family. Hum Genet. 2016 Feb; 135(2):157-70.
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Regulation of Insulin Receptor Trafficking by Bardet Biedl Syndrome Proteins. PLoS Genet. 2015 Jun; 11(6):e1005311.
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Regulation of endoplasmic reticulum turnover by selective autophagy. Nature. 2015 Jun 18; 522(7556):354-8.
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Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy. Nat Genet. 2014 Dec; 46(12):1283-1292.
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The Vip1 inositol polyphosphate kinase family regulates polarized growth and modulates the microtubule cytoskeleton in fungi. PLoS Genet. 2014 Sep; 10(9):e1004586.