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Kalinichenko, V.V., Gusarova, G.A., Kim, I.M., Shin, B., Yoder, H.M., Clark, J., Sapozhnikov, A.M., Whitsett, J.A. and Costa, R.H. (2004) Foxf1 Haploinsufficiency Reduces Notch-2 Signaling during Mouse Lung Development. American Journal of Physiology—Lung Cellular and Molecular, 286, L521-L530.
http://dx.doi.org/10.1152/ajplung.00212.2003

has been cited by the following article:

• TITLE: A Novel Mutation in FOXF1 Gene Associated with a Delayed Presentation of Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins

  AUTHORS: Maxine S. Eikani, Vladimir V. Kalinichenko, Arun Pradhan, Julie Noe

  KEYWORDS: Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins, Persistent Pulmonary Hypertension, FOXF1

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.4 No.3, March 18, 2015

  ABSTRACT: Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is a rare, fatal developmental lung disorder of neonates and infants, associated with severe persistent pulmonary hypertension unresponsive to treatment. We reported the case of a term newborn with delayed presentation of ACD/MPV and a novel mutation of FOXF1 gene that received supportive cardiopulmonary treatments, inhaled nitric oxide, oral sildenafil and nebulized iloprost with no clinical improvement. DNA sequence analysis of FOXF1 gene identified a novel heterozygous variant c.257G > C; p.R86P, in exon 1. At autopsy, lung histology showed the characteristic features of ACD/MPV. FOXF1 has been identified as one of the genes responsible for ACD/MPV associated with multiple congenital malformations. This is a report of a novel heterozygous variant c.257G > C; p.R86P, in the first exon of FOXF1, in a patient with delayed presentation of ACD/MPV.