Non-canonical Wnt signaling pathways in hematopoiesis
Immunologic Research, ISSN: 0257-277X, Vol: 46, Issue: 1-3, Page: 155-164
2010
- 21Citations
- 58Captures
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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.
Metrics Details
- Citations21
- Citation Indexes21
- 21
- CrossRef13
- Captures58
- Readers58
- 58
Review Description
Hematopoietic stem cells (HSCs) are a rare population of cells that are responsible for life-long generation of blood cells of all lineages. In order to maintain their numbers, HSCs must establish a balance between the opposing cell fates of self-renewal and initiation of hematopoietic differentiation. Multiple signaling pathways have been implicated in the regulation of HSC cell fate. One such set of pathways are those activated by the Wnt family of ligands. The function of the canonical Wnt signaling pathway, which utilizes β-catenin to regulate gene expression, has been extensively studied in hematopoiesis. However, there is a growing body of evidence that the other Wnt signaling pathways, termed non-canonical, also play an important role. In this review, we will discuss the regulation of hematopoiesis by the Wnt signaling pathways, focusing on the potential functions of non-canonical Wnt signaling pathways. © 2010 Springer Science+Business Media, LLC.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77949424030&origin=inward; http://dx.doi.org/10.1007/s12026-009-8116-7; http://www.ncbi.nlm.nih.gov/pubmed/19763894; http://link.springer.com/10.1007/s12026-009-8116-7; https://dx.doi.org/10.1007/s12026-009-8116-7; https://link.springer.com/article/10.1007/s12026-009-8116-7; http://www.springerlink.com/index/10.1007/s12026-009-8116-7; http://www.springerlink.com/index/pdf/10.1007/s12026-009-8116-7
Springer Science and Business Media LLC
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