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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 0 | 1 |
| 2017 | 4 | 1 | 5 |
| 2018 | 5 | 0 | 5 |
To return to the timeline, click here.
Below are the most recent publications written about "Cell Adhesion Molecules, Neuronal" by people in Profiles.
-
Macrophagic Stabilin-1 Restored Disruption of Vascular Integrity Caused by Sepsis. Thromb Haemost. 2018 Oct; 118(10):1776-1789.
-
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.
-
T cell and monocyte/macrophage activation markers associate with adverse outcome, but give limited prognostic value in anemic patients with heart failure: results from RED-HF. Clin Res Cardiol. 2019 Feb; 108(2):133-141.
-
Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China. Behav Brain Res. 2018 09 17; 350:1-5.
-
The impact of body mass index in gene expression of reelin pathway mediators in individuals with schizophrenia and mood disorders: A post-mortem study. J Psychiatr Res. 2018 07; 102:186-191.
-
The neurobiological bases of autism spectrum disorders: the R451C-neuroligin 3 mutation hampers the expression of long-term synaptic depression in the dorsal striatum. Eur J Neurosci. 2018 03; 47(6):701-708.
-
Potential contribution of the neurodegenerative disorders risk loci to cognitive performance in an elderly male gout population. Medicine (Baltimore). 2017 Sep; 96(39):e8195.
-
Genetic variants and clinical relevance associated with gestational diabetes mellitus in Chinese women: a case-control study. J Matern Fetal Neonatal Med. 2018 Aug; 31(16):2115-2121.
-
Meta-analyses of RELN variants in neuropsychiatric disorders. Behav Brain Res. 2017 08 14; 332:110-119.
-
Construction of Gpm6a/ReelinGFPCreERT2 by BAC recombination using a specific gene in hepatic mesothelial or stellate cells. World J Gastroenterol. 2017 Jan 14; 23(2):224-231.