Loss of Cystic Fibrosis Transmembrane Conductance Regulator Function Produces Abnormalities in Tracheal Development in Neonatal Pigs and Young Children - Concepedia

Concepedia

Publication | Open Access

Loss of Cystic Fibrosis Transmembrane Conductance Regulator Function Produces Abnormalities in Tracheal Development in Neonatal Pigs and Young Children

DOI Full Paper Access

199

Citations

53

References

2010

Year

David K. Meyerholz, David A. Stoltz, Eman Namati, Shyam Ramachandran, Alejandro A. Pezzulo, Amanda R. Smith, Michael V. Rector, Melissa J. Suter, Simon C. Kao, Geoffrey McLennan,

American Journal of Respiratory and Critical Care Medicine

Abstract

Our findings in newborn CF pigs and young patients with CF suggest that airway changes begin during fetal life and may contribute to CF pathogenesis and clinical disease during postnatal life.

References

	Year	Citations

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