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A TNFSF13B functional variant is not involved in systemic sclerosis and giant cell arteritis susceptibility
BACKGROUND: The TNFSF13B (TNF superfamily member 13b) gene encodes BAFF, a cytokine with a crucial role in the differentiation and activation of B cells. An insertion-deletion variant (GCTGT→A) of this gene, leading to increased levels of BAFF, has been recently implicated in the genetic predisposit...
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| Vydáno v: | PLoS One |
|---|---|
| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6306228/ https://ncbi.nlm.nih.gov/pubmed/30586461 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0209343 |
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