Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred.
By Alan Q. Thomas, K. Lane, J. Phillips, M. Prince, C. Markin, M. Speer, David A. Schwartz, Radhika Gaddipati, A. Marney, Joyce E. Johnson and 4 more. American Journal of Respiratory and Critical Care Medicine, 2002
632 citations recorded by the source corpus.
Subfields: Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/66e1de397d9030857ad09d4c9cc8ae3219270f70
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In Pulmonary and Respiratory Medicine
Citations in the corpus
- Short telomeres are a risk factor for idiopathic pulmonary fibrosis (2008, background): “Histological features of IPF and other IIP subtypes are often present in the same individual and in individuals from a single family, indicating that IIPs could share a common etiology (3, 4).”
- TGF-β1 Signaling and Tissue Fibrosis. (2018, background): “Genetic analysis of patients with familial interstitial pneumonitis point to type II alveolar epithelial dysfunction as a consequence of SP gene mutations and as a causal mechanism for pulmonary fibrosis (Nogee et al. 2001; Thomas et al. 2002; Wang et al. 2009; Garcia 2011).”