Antigens, Differentiation
"Antigens, Differentiation" 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.
Antigens expressed primarily on the membranes of living cells during sequential stages of maturation and differentiation. As immunologic markers they have high organ and tissue specificity and are useful as probes in studies of normal cell development as well as neoplastic transformation.
| Descriptor ID |
D000943
|
| MeSH Number(s) |
D23.050.301.264 D23.101.100
|
| Concept/Terms |
Antigens, Differentiation- Antigens, Differentiation
- Differentiation Markers
- Markers, Differentiation
- Differentiation Antigens
- Marker Antigens
- Antigens, Marker
|
Below are MeSH descriptors whose meaning is more general than "Antigens, Differentiation".
Below are MeSH descriptors whose meaning is more specific than "Antigens, Differentiation".
This graph shows the total number of publications written about "Antigens, Differentiation" by people in this website by year, and whether "Antigens, Differentiation" 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 | 0 | 1 | 1 |
| 1995 | 0 | 3 | 3 |
| 1996 | 3 | 3 | 6 |
| 1997 | 4 | 2 | 6 |
| 1998 | 7 | 0 | 7 |
| 1999 | 6 | 1 | 7 |
| 2000 | 6 | 2 | 8 |
| 2001 | 5 | 8 | 13 |
| 2002 | 6 | 1 | 7 |
| 2003 | 4 | 2 | 6 |
| 2004 | 4 | 4 | 8 |
| 2005 | 1 | 2 | 3 |
| 2006 | 3 | 3 | 6 |
| 2007 | 1 | 0 | 1 |
| 2008 | 3 | 2 | 5 |
| 2009 | 3 | 0 | 3 |
| 2011 | 2 | 0 | 2 |
| 2012 | 0 | 1 | 1 |
| 2013 | 1 | 1 | 2 |
| 2015 | 0 | 2 | 2 |
| 2016 | 0 | 1 | 1 |
| 2017 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Antigens, Differentiation" by people in Profiles.
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Probing the interaction interface of the GADD45ß/MKK7 and MKK7/DTP3 complexes by chemical cross-linking mass spectrometry. Int J Biol Macromol. 2018 Jul 15; 114:114-123.
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GADD45ß Loss Ablates Innate Immunosuppression in Cancer. Cancer Res. 2018 03 01; 78(5):1275-1292.
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Dendritic Cells but Not Macrophages Sense Tumor Mitochondrial DNA for Cross-priming through Signal Regulatory Protein a Signaling. Immunity. 2017 08 15; 47(2):363-373.e5.
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Nanoparticulate Mineralized Collagen Scaffolds and BMP-9 Induce a Long-Term Bone Cartilage Construct in Human Mesenchymal Stem Cells. Adv Healthc Mater. 2016 07; 5(14):1821-30.
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"Velcro" engineering of high affinity CD47 ectodomain as signal regulatory protein a (SIRPa) antagonists that enhance antibody-dependent cellular phagocytosis. J Biol Chem. 2015 May 15; 290(20):12650-63.
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The innate immune system contributes to tissue-engineered vascular graft performance. FASEB J. 2015 Jun; 29(6):2431-8.
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Induced maturation of hepatic progenitor cells in vitro. Braz J Med Biol Res. 2013 Jul; 46(7):559-66.
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Engineered SIRPa variants as immunotherapeutic adjuvants to anticancer antibodies. Science. 2013 Jul 05; 341(6141):88-91.
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Loss of the urothelial differentiation marker FOXA1 is associated with high grade, late stage bladder cancer and increased tumor proliferation. PLoS One. 2012; 7(5):e36669.
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All-trans retinoic acid inhibits tumor growth of human osteosarcoma by activating Smad signaling-induced osteogenic differentiation. Int J Oncol. 2012 Jul; 41(1):153-60.