Výsledky vyhledávání - "S. Sfurti Nath"

Histologic Features and Decreased Lung FOXF1 Gene Expression in Severe Bronchopulmonary Dysplasia without a Genetic Diagnosis of Alveolar Capillary Dysplasia

Autor: C. Galambos, J. Logan, P. Stankiewicz, P. Szafranski, C. Zalles, J. Gonzales, S. Sfurti Nath, S. Patel, S.H. Abman

Severe BPD can be associated with clinical and histologic features that are similar to ACD without evidence of FOXF1 genetic disease. Importantly, lung FOXF1 and TMEM100 gene expression is markedly decreased in severe BPD, suggesting that impaired FO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::699cb84a8cf87e04d313729c9e4f343b
https://doi.org/10.22541/au.167635992.24578122/v1

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