| Q28365965 | 5' flanking sequence of the human immediate early responsive gene ccn1 (cyr61) and mapping of polymorphic CA repeat sequence motifs in the human ccn1 (cyr61) locus |
| Q35888906 | A Shh-Foxf-Fgf18-Shh Molecular Circuit Regulating Palate Development |
| Q36686738 | A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human |
| Q22011171 | A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle |
| Q51323089 | A novel missense mutation in the transcription factor FOXF1 cosegregating with infantile hypertrophic pyloric stenosis in the extended pedigree linked to IHPS5 on chromosome 16q24. |
| Q28478096 | Abnormal notochord branching is associated with foregut malformations in the adriamycin treated mouse model |
| Q43103690 | Alternative functional in vitro models of human intestinal epithelia. |
| Q58713813 | Alveolar capillary dysplasia with misalignment of the pulmonary veins: clinical, histological, and genetic aspects |
| Q75341117 | Differences in the embryonic expression patterns of mouse Foxf1 and -2 match their distinct mutant phenotypes |
| Q34489962 | Differential epithelial expression of SHH and FOXF1 in usual and nonspecific interstitial pneumonia |
| Q32128097 | Differential expression of forkhead box transcription factors following butylated hydroxytoluene lung injury |
| Q47706203 | Effect of abnormal notochord delamination on hindgut development in the Adriamycin mouse model |
| Q47684571 | Expression of FoxC, FoxF, FoxL1, and FoxQ1 genes in the dogfish Scyliorhinus canicula defines ancient and derived roles for Fox genes in vertebrate development |
| Q91179708 | FOXF1 transcription factor promotes lung morphogenesis by inducing cellular proliferation in fetal lung mesenchyme |
| Q35933347 | Forkhead Box F1 promotes breast cancer cell migration by upregulating lysyl oxidase and suppressing Smad2/3 signaling |
| Q47741187 | Forkhead Box F1 represses cell growth and inhibits COL1 and ARPC2 expression in lung fibroblasts in vitro. |
| Q28587296 | Forkhead box F1 is essential for migration of mesenchymal cells and directly induces integrin-beta3 expression |
| Q52168199 | Forkhead transcription factor FoxF2 is expressed in mesodermal tissues involved in epithelio-mesenchymal interactions. |
| Q52103985 | Forkhead transcription factor Foxf2 (LUN)-deficient mice exhibit abnormal development of secondary palate. |
| Q40618445 | Foxf1haploinsufficiency reduces Notch-2 signaling during mouse lung development |
| Q50512840 | Foxf2 is required for secondary palate development and Tgfβ signaling in palatal shelf mesenchyme. |
| Q48786316 | Functional characterization of evolutionarily conserved DNA regions in forkhead box f1 gene locus |
| Q39455902 | Functional conservation of regulatory elements in the pdx-1 gene: PDX-1 and hepatocyte nuclear factor 3beta transcription factors mediate beta-cell-specific expression |
| Q51721142 | Fusion of lung lobes and vessels in mouse embryos heterozygous for the forkhead box f1 targeted allele. |
| Q35442856 | Gene expression signatures identify novel regulatory pathways during murine lung development: implications for lung tumorigenesis |
| Q41826361 | Genomic and Epigenetic Complexity of the FOXF1 Locus in 16q24.1: Implications for Development and Disease. |
| Q47919129 | Genomic structure and embryonic expression of the Xenopus winged helix factors XFD-13/13'. |
| Q28513845 | HOXA13 Is essential for placental vascular patterning and labyrinth endothelial specification |
| Q33481774 | Identification of regulatory elements in the Isl1 gene locus |
| Q36515335 | In control of biology: of mice, men and Foxes |
| Q104073668 | Loss of FOXF1 expression promotes human lung-resident mesenchymal stromal cell migration via ATX/LPA/LPA1 signaling axis |
| Q53115903 | Maternal somatic mosaicism of FOXF1 mutation causes recurrent alveolar capillary dysplasia with misalignment of pulmonary veins in siblings. |
| Q36874650 | Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain. |
| Q24291515 | Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation |
| Q28508589 | Sonic hedgehog signaling regulates Gli3 processing, mesenchymal proliferation, and differentiation during mouse lung organogenesis |
| Q40811358 | Structural characterization of the mouse Foxf1a gene |
| Q43861815 | TRAIL and inhibitors of apoptosis are opposing determinants for NF-kappaB-dependent, genotoxin-induced apoptosis of cancer cells |
| Q48327016 | The forkhead box F1 transcription factor is expressed in brain and head mesenchyme during mouse embryonic development |
| Q34210079 | Transcription factors in mouse lung development and function |
| Q33337226 | Transcription profiling of lung adenocarcinomas of c-myc-transgenic mice: identification of the c-myc regulatory gene network |
| Q43988488 | Wild-type levels of the mouse Forkhead Box f1 gene are essential for lung repair |
| Q40424508 | biniou (FoxF), a central component in a regulatory network controlling visceral mesoderm development and midgut morphogenesis in Drosophila |