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New Therapeutic Targets in Idiopathic Pulmonary Fibrosis. Aiming to Rein in Runaway Wound-Healing Responses

Idiopathic pulmonary fibrosis (IPF) is a devastating disease, with a median survival as short as 3 years from the time of diagnosis and no pharmacological therapies yet approved by the U.S. Food and Drug Administration. To address the great unmet need for effective IPF therapy, a number of new drugs...

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Detalhes bibliográficos
Publicado no:Am J Respir Crit Care Med
Main Authors: Ahluwalia, Neil, Shea, Barry S., Tager, Andrew M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4299574/
https://ncbi.nlm.nih.gov/pubmed/25090037
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201403-0509PP
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