"Stem Cells" 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.
Relatively undifferentiated cells that retain the ability to divide and proliferate throughout postnatal life to provide progenitor cells that can differentiate into specialized cells.
| Descriptor ID |
D013234
|
| MeSH Number(s) |
A11.872
|
| Concept/Terms |
Stem Cells- Stem Cells
- Cell, Stem
- Cells, Stem
- Stem Cell
- Progenitor Cells
- Cell, Progenitor
- Cells, Progenitor
- Progenitor Cell
- Mother Cells
- Cell, Mother
- Cells, Mother
- Mother Cell
Colony-Forming Unit- Colony-Forming Unit
- Colony Forming Unit
- Colony-Forming Units
- Colony Forming Units
|
Below are MeSH descriptors whose meaning is more general than "Stem Cells".
Below are MeSH descriptors whose meaning is more specific than "Stem Cells".
This graph shows the total number of publications written about "Stem Cells" by people in this website by year, and whether "Stem Cells" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Stem Cells" by people in Profiles.
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Single-Cell Transcriptomic Analysis of Human Lung Provides Insights into the Pathobiology of Pulmonary Fibrosis. Am J Respir Crit Care Med. 2019 06 15; 199(12):1517-1536.
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Cryptosporidium parvum infection attenuates the ex vivo propagation of murine intestinal enteroids. Physiol Rep. 2016 Dec; 4(24).
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Special issue on stem cells. J Comp Neurol. 2014 Aug 15; 522(12):2689-90.
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Extending in silico mechanism-of-action analysis by annotating targets with pathways: application to cellular cytotoxicity readouts. Future Med Chem. 2014; 6(18):2029-56.
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Differential regulation of integrin-mediated proplatelet formation and megakaryocyte spreading. J Cell Physiol. 1995 Jun; 163(3):597-607.
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Megakaryocyte proplatelet-like process formation in vitro is inhibited by serum prothrombin, a process which is blocked by matrix-bound glycosaminoglycans. Exp Hematol. 1993 Feb; 21(2):372-81.