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Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics
Cystic fibrosis is realizing the promise of personalized medicine. Recent advances in drug development that target the causal CFTR directly result in lung function improvement, but variability in response is demanding better prediction of outcomes to improve management decisions. The genetic modifie...
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| 出版年: | Hum Mol Genet |
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| 主要な著者: | , , , , , , , , , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2016
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5886039/ https://ncbi.nlm.nih.gov/pubmed/28171547 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw290 |
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