"Cerebellum" 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.
The part of brain that lies behind the BRAIN STEM in the posterior base of skull (CRANIAL FOSSA, POSTERIOR). It is also known as the "little brain" with convolutions similar to those of CEREBRAL CORTEX, inner white matter, and deep cerebellar nuclei. Its function is to coordinate voluntary movements, maintain balance, and learn motor skills.
Descriptor ID |
D002531
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MeSH Number(s) |
A08.186.211.132.810.428.200
|
Concept/Terms |
Cerebellum- Cerebellum
- Cerebellums
- Corpus Cerebelli
- Cerebelli, Corpus
- Cerebellus, Corpus
- Corpus Cerebellus
- Parencephalon
- Parencephalons
|
Below are MeSH descriptors whose meaning is more general than "Cerebellum".
Below are MeSH descriptors whose meaning is more specific than "Cerebellum".
This graph shows the total number of publications written about "Cerebellum" by people in this website by year, and whether "Cerebellum" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2007 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2014 | 0 | 1 | 1 |
2015 | 2 | 4 | 6 |
2017 | 1 | 0 | 1 |
2018 | 2 | 1 | 3 |
2019 | 0 | 1 | 1 |
2020 | 0 | 1 | 1 |
2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cerebellum" by people in Profiles.
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A Novel SCA3 Knock-in Mouse Model Mimics the Human SCA3 Disease Phenotype Including Neuropathological, Behavioral, and Transcriptional Abnormalities Especially in Oligodendrocytes. Mol Neurobiol. 2022 Jan; 59(1):495-522.
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Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. Brain. 2020 01 01; 143(1):94-111.
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Novel EXOSC3 pathogenic variant results in a mild course of neurologic disease with cerebellum involvement. Eur J Med Genet. 2020 Feb; 63(2):103649.
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Aberrant ERBB4-SRC Signaling as a Hallmark of Group 4 Medulloblastoma Revealed by Integrative Phosphoproteomic Profiling. Cancer Cell. 2018 09 10; 34(3):379-395.e7.
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Homozygosity for the c.428delG variant in KIAA0586 in a healthy individual: implications for molecular testing in patients with Joubert syndrome. J Med Genet. 2019 04; 56(4):261-264.
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Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling. Eur J Hum Genet. 2018 02; 26(2):197-209.
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Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation. Eur Radiol. 2017 Dec; 27(12):5080-5092.
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"Acquired" Dandy-Walker malformation and cerebellar hemorrhage: Usefulness of serial MRI. Eur J Paediatr Neurol. 2016 Jan; 20(1):188-91.
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TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23). Elife. 2015 Sep 19; 4.
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In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11. PLoS Genet. 2015 Aug; 11(8):e1005454.