 Vascular Cell Adhesion Molecule-1
"Vascular Cell Adhesion Molecule-1" 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.
Cytokine-induced cell adhesion molecule present on activated endothelial cells, tissue macrophages, dendritic cells, bone marrow fibroblasts, myoblasts, and myotubes. It is important for the recruitment of leukocytes to sites of inflammation. (From Pigott & Power, The Adhesion Molecule FactsBook, 1993, p154)
| Descriptor ID |
D019010
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| MeSH Number(s) |
D12.776.395.550.200.920 D12.776.543.550.200.920 D23.050.301.350.920
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| Concept/Terms |
Vascular Cell Adhesion Molecule-1- Vascular Cell Adhesion Molecule-1
- Vascular Cell Adhesion Molecule 1
- Inducible Cell Adhesion Molecule 110
- CD106 Antigens
- VCAM-1
- CD106 Antigen
- Antigen, CD106
- Antigens, CD106
- Vascular Cell Adhesion Molecule
- INCAM-110
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Below are MeSH descriptors whose meaning is more general than "Vascular Cell Adhesion Molecule-1".
Below are MeSH descriptors whose meaning is more specific than "Vascular Cell Adhesion Molecule-1".
This graph shows the total number of publications written about "Vascular Cell Adhesion Molecule-1" by people in this website by year, and whether "Vascular Cell Adhesion Molecule-1" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 | | 1996 | 1 | 0 | 1 | | 1997 | 1 | 1 | 2 | | 1998 | 1 | 0 | 1 | | 1999 | 1 | 1 | 2 | | 2000 | 1 | 0 | 1 | | 2001 | 1 | 0 | 1 | | 2002 | 1 | 3 | 4 | | 2003 | 2 | 1 | 3 | | 2005 | 0 | 3 | 3 | | 2007 | 0 | 1 | 1 | | 2008 | 0 | 3 | 3 | | 2010 | 0 | 1 | 1 | | 2011 | 0 | 1 | 1 | | 2013 | 0 | 2 | 2 | | 2014 | 1 | 2 | 3 | | 2016 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2021 | 0 | 1 | 1 | | 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Vascular Cell Adhesion Molecule-1" by people in Profiles.
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Zhai Y, Ao L, Yao Q, The E, Fullerton DA, Meng X. Elevated Expression of TLR2 in Aging Hearts Exacerbates Cardiac Inflammatory Response and Adverse Remodeling Following Ischemia and Reperfusion Injury. Front Immunol. 2022; 13:891570.
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Gergen AK, Jarrett MJ, Li A, Cheng L, Tilva KR, Madsen HJ, Meng X, Fullerton DA, Weyant MJ. Expression of Adhesion Molecules in a Gastroduodenal Reflux Murine Model. Ann Thorac Surg. 2022 03; 113(3):926-933.
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Tenório TRS, Balagopal PB, Andersen LB, Ritti-Dias RM, Hill JO, Lofrano-Prado MC, Prado WL. Effect of Low- Versus High-Intensity Exercise Training on Biomarkers of Inflammation and Endothelial Dysfunction in Adolescents With Obesity: A 6-Month Randomized Exercise Intervention Study. Pediatr Exerc Sci. 2018 02 01; 30(1):96-105.
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Gu P, Theiss A, Han J, Feagins LA. Increased Cell Adhesion Molecules, PECAM-1, ICAM-3, or VCAM-1, Predict Increased Risk for Flare in Patients With Quiescent Inflammatory Bowel Disease. J Clin Gastroenterol. 2017 Jul; 51(6):522-527.
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Attia EF, Jolley SE, Crothers K, Schnapp LM, Liles WC. Soluble Vascular Cell Adhesion Molecule-1 (sVCAM-1) Is Elevated in Bronchoalveolar Lavage Fluid of Patients with Acute Respiratory Distress Syndrome. PLoS One. 2016; 11(2):e0149687.
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Radecke CE, Warrick AE, Singh GD, Rogers JH, Simon SI, Armstrong EJ. Coronary artery endothelial cells and microparticles increase expression of VCAM-1 in myocardial infarction. Thromb Haemost. 2015 Mar; 113(3):605-16.
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Brown JD, Lin CY, Duan Q, Griffin G, Federation A, Paranal RM, Bair S, Newton G, Lichtman A, Kung A, Yang T, Wang H, Luscinskas FW, Croce K, Bradner JE, Plutzky J. NF-?B directs dynamic super enhancer formation in inflammation and atherogenesis. Mol Cell. 2014 Oct 23; 56(2):219-231.
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Sato J, Kinugasa M, Satomi-Kobayashi S, Hatakeyama K, Knox AJ, Asada Y, Wierman ME, Hirata K, Rikitake Y. Family with sequence similarity 5, member C (FAM5C) increases leukocyte adhesion molecules in vascular endothelial cells: implication in vascular inflammation. PLoS One. 2014; 9(9):e107236.
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Fenner EK, Boguniewicz J, Tucker RM, Sokol RJ, Mack CL. High-dose IgG therapy mitigates bile duct-targeted inflammation and obstruction in a mouse model of biliary atresia. Pediatr Res. 2014 Jul; 76(1):72-80.
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Hadi NR, Yousif NG, Abdulzahra MS, Mohammad BI, Al-Amran FG, Majeed ML, Yousif MG. Role of NF-?ß and oxidative pathways in atherosclerosis: cross-talk between dyslipidemia and candesartan. Cardiovasc Ther. 2013 Dec; 31(6):381-7.
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