FOXF1

A gene on chromosome 16q24 that encodes a member of the forkhead family of transcription factors, which may play a role in embryonic development and in regulating lung-specific genes.

References in periodicals archive ?

Differential epithelial expression of SHH and FOXF1 in usual and nonspecific interstitial pneumonia.

Honeycomb Lung: Time for a Change

FOXF1 FOXF1 has high expression in normal prostate and its expression decreases in prostate cancer (39).

Comparative analysis of prostate cancer gene regulatory networks via hub type Variation

The p53-p21WAF1 checkpoint pathway plays a protective role in preventing DNA replication induced by abrogation of FOXF1 function.

[beta]-Asarone induces senescence in colorectal cancer cells by inducing lamin B1 expression

1, que consta de cuatro genes, FOXF1, MTHFSD FOXC2, y FOXL1, como causantes de un fenotipo parecido a la asociacion VACTERL, con anomalias vertebrales, atresias gastrointestinal (esofago, duodeno o ano), cardiopatias congenitas y malformaciones del tracto urinario, asi como una rara anomalia letal de desarrollo del pulmon, la displasia capilar alveolar.

Presentacion de un caso con multiples malformaciones congenitas: asociacion VACTERL / a case with multiple congenital malformations: VACTERL association

The disease that usually kills the infants born with it within the first month of life results from deletions or mutations in the FOXF1 transcription factor gene, said a consortium of researchers led by Baylor College of Medicine (www.