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MUC5B and Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF), a fatal disease that is a result of complex interactions between genetics and the environment, has limited treatment options. We have identified the MUC5B promoter polymorphism and other common genetic variants that in aggregate explain roughly one-third of disea...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Ann Am Thorac Soc
Päätekijät: Yang, Ivana V., Fingerlin, Tasha E., Evans, Christopher M., Schwarz, Marvin I., Schwartz, David A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Thoracic Society 2015
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4722833/
https://ncbi.nlm.nih.gov/pubmed/26595739
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/AnnalsATS.201503-110AW
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