Cell Adhesion Molecules, Neuronal
"Cell Adhesion Molecules, Neuronal" 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.
Surface ligands that mediate cell-to-cell adhesion and function in the assembly and interconnection of the vertebrate nervous system. These molecules promote cell adhesion via a homophilic mechanism. These are not to be confused with NEURAL CELL ADHESION MOLECULES, now known to be expressed in a variety of tissues and cell types in addition to nervous tissue.
Descriptor ID |
D015816
|
MeSH Number(s) |
D12.776.395.550.200.250 D12.776.543.550.200.250 D23.050.301.350.250
|
Concept/Terms |
Axon-Associated Adhesion Molecules- Axon-Associated Adhesion Molecules
- Adhesion Molecules, Axon-Associated
- Axon Associated Adhesion Molecules
- Molecules, Axon-Associated Adhesion
|
Below are MeSH descriptors whose meaning is more general than "Cell Adhesion Molecules, Neuronal".
Below are MeSH descriptors whose meaning is more specific than "Cell Adhesion Molecules, Neuronal".
This graph shows the total number of publications written about "Cell Adhesion Molecules, Neuronal" by people in this website by year, and whether "Cell Adhesion Molecules, Neuronal" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1995 | 0 | 1 | 1 |
1996 | 1 | 0 | 1 |
1998 | 3 | 0 | 3 |
1999 | 3 | 0 | 3 |
2000 | 0 | 1 | 1 |
2001 | 3 | 2 | 5 |
2002 | 0 | 2 | 2 |
2003 | 2 | 2 | 4 |
2004 | 1 | 2 | 3 |
2006 | 0 | 2 | 2 |
2007 | 3 | 1 | 4 |
2008 | 3 | 5 | 8 |
2009 | 2 | 1 | 3 |
2010 | 1 | 2 | 3 |
2011 | 1 | 2 | 3 |
2012 | 5 | 2 | 7 |
2013 | 0 | 2 | 2 |
2014 | 2 | 0 | 2 |
2016 | 1 | 2 | 3 |
2017 | 1 | 2 | 3 |
2018 | 1 | 1 | 2 |
2019 | 1 | 2 | 3 |
2020 | 2 | 0 | 2 |
2021 | 1 | 1 | 2 |
2023 | 0 | 2 | 2 |
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Below are the most recent publications written about "Cell Adhesion Molecules, Neuronal" by people in Profiles.
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Targeting PD-L2-RGMb overcomes microbiome-related immunotherapy resistance. Nature. 2023 05; 617(7960):377-385.
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A neurodevelopmental epigenetic programme mediated by SMARCD3-DAB1-Reelin signalling is hijacked to promote medulloblastoma metastasis. Nat Cell Biol. 2023 03; 25(3):493-507.
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The Role of Hyperexcitability in Gliomagenesis. Int J Mol Sci. 2023 Jan 01; 24(1).
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Urine ALCAM, PF4 and VCAM-1 Surpass Conventional Metrics in Identifying Nephritis Disease Activity in Childhood-Onset Systemic Lupus Erythematosus. Front Immunol. 2022; 13:885307.
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The CD6/ALCAM pathway promotes lupus nephritis via T cell-mediated responses. J Clin Invest. 2022 01 04; 132(1).
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Genetic targeting of Card19 is linked to disrupted NINJ1 expression, impaired cell lysis, and increased susceptibility to Yersinia infection. PLoS Pathog. 2021 10; 17(10):e1009967.
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Downregulation of glial genes involved in synaptic function mitigates Huntington's disease pathogenesis. Elife. 2021 04 19; 10.
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ALCAM and VCAM-1 as urine biomarkers of activity and long-term renal outcome in systemic lupus erythematosus. Rheumatology (Oxford). 2020 09 01; 59(9):2237-2249.
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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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Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancer. BMC Med Genet. 2020 05 06; 21(1):92.