"Corpus Callosum" 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.
Broad plate of dense myelinated fibers that reciprocally interconnect regions of the cortex in all lobes with corresponding regions of the opposite hemisphere. The corpus callosum is located deep in the longitudinal fissure.
| Descriptor ID |
D003337
|
| MeSH Number(s) |
A08.186.211.730.885.390.750
|
| Concept/Terms |
Corpus Callosum- Corpus Callosum
- Callosum, Corpus
- Callosums, Corpus
- Corpus Callosums
- Neocortical Commissure
- Commissure, Neocortical
- Commissures, Neocortical
- Neocortical Commissures
- Interhemispheric Commissure
- Commissure, Interhemispheric
- Commissures, Interhemispheric
- Interhemispheric Commissures
|
Below are MeSH descriptors whose meaning is more general than "Corpus Callosum".
Below are MeSH descriptors whose meaning is more specific than "Corpus Callosum".
This graph shows the total number of publications written about "Corpus Callosum" by people in this website by year, and whether "Corpus Callosum" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2013 | 1 | 1 | 2 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Corpus Callosum" by people in Profiles.
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Mutations in SMARCB1 and in other Coffin-Siris syndrome genes lead to various brain midline defects. Nat Commun. 2019 07 04; 10(1):2966.
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A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system. PLoS Genet. 2013; 9(12):e1003988.
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Biallelic SZT2 mutations cause infantile encephalopathy with epilepsy and dysmorphic corpus callosum. Am J Hum Genet. 2013 Sep 05; 93(3):524-9.
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Myelin debris regulates inflammatory responses in an experimental demyelination animal model and multiple sclerosis lesions. Glia. 2012 Oct; 60(10):1468-80.
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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. J Med Genet. 2011 Jun; 48(6):396-406.
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Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literature. Neuropediatrics. 2002 Dec; 33(6):309-13.
MeSH information
