Regulation of dendritic cell development by STATs
Jak-Stat Signaling: From Basics to Disease, Page: 169-186
2012
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Book Chapter Description
Dendritic cells (DCs) serve as a critical link between the innate and adaptive immune responses due to their ability to sense pathogens and respond by activating adaptive immune cell types. Delineating the molecular control of DC development will provide important information about the generation of natural immunity as well as approaches to regulate DCs in clinical settings. DCs are generated from hematopoietic stem cells through specialized progenitor subsets in response to cytokine and transcriptional cues, with FMS-like tyrosine kinase 3 ligand (Flt3L) and Flt3L receptor (Flt3) signaling providing a major pathway supporting homeostatic DC generation. Recent work has indicated that granulocyte-macrophage colony-stimulating factor (GM-CSF) and type I interferons (IFNs) also play important roles in regulating DC subset production. Here we review new insight into the mechanisms by which cytokine-activated STAT proteins control the DC developmental process.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84930590339&origin=inward; http://dx.doi.org/10.1007/978-3-7091-0891-8_11; https://link.springer.com/10.1007/978-3-7091-0891-8_11; http://www.springerlink.com/index/10.1007/978-3-7091-0891-8_11; http://www.springerlink.com/index/pdf/10.1007/978-3-7091-0891-8_11; https://dx.doi.org/10.1007/978-3-7091-0891-8_11; https://link.springer.com/chapter/10.1007/978-3-7091-0891-8_11
Springer Science and Business Media LLC
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