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Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy
Transforming growth factor (TGF)-α1 (encoded by TGFB1) is the prototypic member of the TGF-β family of 33 proteins that orchestrate embryogenesis, development and tissue homeostasis(1,2). Following its discovery(3), enormous interest and numerous controversies have emerged about the role of TGF-β in...
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| Gepubliceerd in: | Nat Genet |
|---|---|
| Hoofdauteurs: | , , , , , , , , , , , , , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6309869/ https://ncbi.nlm.nih.gov/pubmed/29483653 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41588-018-0063-6 |
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