"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.
Surface ligands, usually glycoproteins, that mediate cell-to-cell adhesion. Their functions include the assembly and interconnection of various vertebrate systems, as well as maintenance of tissue integration, wound healing, morphogenic movements, cellular migrations, and metastasis.
| Descriptor ID |
D015815
|
| MeSH Number(s) |
D12.776.395.550.200 D12.776.543.550.200 D23.050.301.350
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Cell Adhesion Molecules".
Below are MeSH descriptors whose meaning is more specific than "Cell Adhesion Molecules".
This graph shows the total number of publications written about "Cell Adhesion Molecules" by people in this website by year, and whether "Cell Adhesion Molecules" 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 |
|---|
| 1994 | 1 | 0 | 1 |
| 1997 | 0 | 1 | 1 |
| 1998 | 0 | 3 | 3 |
| 1999 | 1 | 1 | 2 |
| 2000 | 0 | 1 | 1 |
| 2001 | 0 | 3 | 3 |
| 2002 | 0 | 4 | 4 |
| 2003 | 1 | 2 | 3 |
| 2004 | 2 | 1 | 3 |
| 2005 | 1 | 0 | 1 |
| 2006 | 0 | 4 | 4 |
| 2007 | 3 | 1 | 4 |
| 2008 | 2 | 3 | 5 |
| 2009 | 1 | 2 | 3 |
| 2010 | 2 | 2 | 4 |
| 2011 | 1 | 2 | 3 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 1 | 1 | 2 |
| 2016 | 3 | 1 | 4 |
| 2017 | 21 | 27 | 48 |
| 2018 | 8 | 17 | 25 |
| 2019 | 6 | 7 | 13 |
| 2020 | 2 | 1 | 3 |
| 2021 | 2 | 3 | 5 |
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Below are the most recent publications written about "Cell Adhesion Molecules" by people in Profiles.
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ACE2, TMPRSS2, and L-SIGN Expression in Placentae From HIV-Positive Pregnancies Exposed to Antiretroviral Therapy-Implications for SARS-CoV-2 Placental Infection. J Infect Dis. 2021 Dec 08; 224(Supplement_6):S631-S641.
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Cell Adhesion Molecules and Vascular Endothelial Growth Factor at the Systemic and Alveolar Level in Coronavirus Disease 2019 Acute Respiratory Distress Syndrome. J Infect Dis. 2021 09 17; 224(6):1101-1103.
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Comment on: Cell Adhesion Molecules and Vascular Endothelial Growth Factor at the Systemic and Alveolar Level in Coronavirus Disease 2019 Acute Respiratory Distress Syndrome. J Infect Dis. 2021 09 17; 224(6):1103-1104.
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Lectins enhance SARS-CoV-2 infection and influence neutralizing antibodies. Nature. 2021 10; 598(7880):342-347.
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A proteome-wide genetic investigation identifies several SARS-CoV-2-exploited host targets of clinical relevance. Elife. 2021 08 17; 10.
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Immunoglobulin G Immune Complexes May Contribute to Neutrophil Activation in the Course of Severe Coronavirus Disease 2019. J Infect Dis. 2021 08 16; 224(4):575-585.
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Neutrophil Extracellular Traps in Fatal COVID-19-Associated Lung Injury. Dis Markers. 2021; 2021:5566826.
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L-SIGN is a receptor on liver sinusoidal endothelial cells for SARS-CoV-2 virus. JCI Insight. 2021 07 22; 6(14).
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Poly-l-lysine Glycoconjugates Inhibit DC-SIGN-mediated Attachment of Pandemic Viruses. ChemMedChem. 2021 08 05; 16(15):2345-2353.
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sMAdCAM: IL-6 Ratio Influences Disease Progression and Anti-Viral Responses in SARS-CoV-2 Infection. Front Immunol. 2021; 12:619906.