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Heterogeneous expression of CFTR in insulin-secreting β-cells of the normal human islet
Cystic fibrosis (CF) is due to mutations in the CF-transmembrane conductance regulator (CFTR) and CF-related diabetes (CFRD) is its most common co-morbidity, affecting ~50% of all CF patients, significantly influencing pulmonary function and longevity. Yet, the complex pathogenesis of CFRD remains u...
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| Vydáno v: | PLoS One |
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| Hlavní autoři: | , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7710116/ https://ncbi.nlm.nih.gov/pubmed/33264332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0242749 |
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