Can Cystic Fibrosis Patients Finally Catch a Breath With Lumacaftor/Ivacaftor?
about
Personalized or Precision Medicine? The Example of Cystic FibrosisDrug-induced dyspnea versus cystic fibrosis exacerbation: a diagnostic dilemma.Managing Innovation to Maximize Value Along the Discovery-Translation-Application Continuum.Drugs for rare disorders.Lumacaftor/ivacaftor, a novel agent for the treatment of cystic fibrosis patients who are homozygous for the F580del CFTR mutation.The CFTR-Associated Ligand Arrests the Trafficking of the Mutant ΔF508 CFTR Channel in the ER Contributing to Cystic Fibrosis.Prolonged co-treatment with HGF sustains epithelial integrity and improves pharmacological rescue of Phe508del-CFTR
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P2860
Can Cystic Fibrosis Patients Finally Catch a Breath With Lumacaftor/Ivacaftor?
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
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name
Can Cystic Fibrosis Patients Finally Catch a Breath With Lumacaftor/Ivacaftor?
@en
type
label
Can Cystic Fibrosis Patients Finally Catch a Breath With Lumacaftor/Ivacaftor?
@en
prefLabel
Can Cystic Fibrosis Patients Finally Catch a Breath With Lumacaftor/Ivacaftor?
@en
P2860
P50
P356
P1476
Can Cystic Fibrosis Patients Finally Catch a Breath With Lumacaftor/Ivacaftor?
@en
P2860
P304
P356
10.1002/CPT.548
P407
P577
2016-11-23T00:00:00Z