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Primary cilia disruption differentially affects the infiltrating and resident macrophage compartment in the liver
Hepatorenal fibrocystic disease (HRFCD) is characterized by cysts in the kidney and liver with associated fibrosis and is the result of defects in proteins required for cilia function or assembly. Previous reports indicate that macrophages, mainly M2-like macrophages, contribute to HRFCD, although t...
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| Publicado en: | Am J Physiol Gastrointest Liver Physiol |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Physiological Society
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6048441/ https://ncbi.nlm.nih.gov/pubmed/29543508 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpgi.00381.2017 |
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