Neural Cell Adhesion Molecules
"Neural Cell Adhesion Molecules" 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.
Cell adhesion molecule involved in a diverse range of contact-mediated interactions among neurons, astrocytes, oligodendrocytes, and myotubes. It is widely but transiently expressed in many tissues early in embryogenesis. Four main isoforms exist, including CD56; (CD56 ANTIGEN); but there are many other variants resulting from alternative splicing and post-translational modifications. (From Pigott & Power, The Adhesion Molecule FactsBook, 1993, pp115-119)
| Descriptor ID |
D019006
|
| MeSH Number(s) |
D12.776.395.550.200.250.520 D12.776.543.550.200.250.520 D23.050.301.350.250.520
|
| Concept/Terms |
Neural Cell Adhesion Molecules- Neural Cell Adhesion Molecules
- NCAM
- Neural Cell Adhesion Molecule
- Cell Adhesion Molecules, Neural
- Cell Adhesion Molecule, Neural
|
Below are MeSH descriptors whose meaning is more general than "Neural Cell Adhesion Molecules".
Below are MeSH descriptors whose meaning is more specific than "Neural Cell Adhesion Molecules".
This graph shows the total number of publications written about "Neural Cell Adhesion Molecules" by people in this website by year, and whether "Neural Cell Adhesion Molecules" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 4 | 0 | 4 |
| 1998 | 2 | 0 | 2 |
| 1999 | 1 | 0 | 1 |
| 2000 | 2 | 1 | 3 |
| 2001 | 1 | 1 | 2 |
| 2002 | 2 | 0 | 2 |
| 2003 | 2 | 0 | 2 |
| 2004 | 1 | 0 | 1 |
| 2005 | 0 | 3 | 3 |
| 2006 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 1 | 1 | 2 |
| 2012 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Neural Cell Adhesion Molecules" by people in Profiles.
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Highly Conserved Molecular Features in IgLONs Contrast Their Distinct Structural and Biological Outcomes. J Mol Biol. 2020 09 04; 432(19):5287-5303.
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Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants. Genet Med. 2019 04; 21(4):816-825.
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Neuronal degeneration and regeneration induced by axotomy in the olfactory epithelium of Xenopus laevis. Dev Neurobiol. 2017 11; 77(11):1308-1320.
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Identification of Rare Variants in Metabolites of the Carnitine Pathway by Whole Genome Sequencing Analysis. Genet Epidemiol. 2016 09; 40(6):486-91.
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Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM. Transl Psychiatry. 2015 Oct 13; 5:e658.
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Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects. Cell Stem Cell. 2015 Dec 03; 17(6):705-718.
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NeuroD1 regulates survival and migration of neuroendocrine lung carcinomas via signaling molecules TrkB and NCAM. Proc Natl Acad Sci U S A. 2013 Apr 16; 110(16):6524-9.
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Investigation of NRXN1 deletions: clinical and molecular characterization. Am J Med Genet A. 2013 Apr; 161A(4):717-31.
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Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions. Eur J Hum Genet. 2012 Dec; 20(12):1240-7.
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Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 2011 Jun 09; 70(5):863-85.