Pulmonary Fibrosis in Response to Environmental Cues and Molecular Targets Involved in Its Pathogenesis
Author:
Affiliation:
1. Laboratory of Pathology, Toxicology Division, The Institute of Environmental Toxicology
2. The Institute of Environmental Toxicology
Publisher
Japanese Society of Toxicologic Pathology
Subject
Toxicology,Pathology and Forensic Medicine
Link
http://www.jstage.jst.go.jp/article/tox/24/1/24_1_9/_pdf
Reference158 articles.
1. 1.Greaves P. Respiratory tract. In: Histopathology of Preclinical Toxicity Studies: Interpretation and Relevance in Drug Safety Evaluation, Third Edition. Elsevier Inc., Oxford, UK. 215-269. 2007.
2. 2.King Jr TE. Clinical advances in the diagnosis and therapy of the interstitial lung diseases. Am J Respir Crit Care Med.172: 268-279. 2005.
3. 3.American Thoracic Society European Respiratory Society American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias(This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001). Am J Respir Crit Care Med.165: 277-304. 2002.
4. 4.Maher TM, Wells AU, and Laurent GJ. Idiopathic pulmonary fibrosis: multiple causes and multiple mechanisms?Eur Respir J.30: 835-839. 2007.
5. 5.Visscher DW, and Myers JL. Histologic spectrum of idiopathic interstitial pneumonias. Proc Am Thorac Soc.3: 322-329. 2006.
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