(en) Shanru Li, Joel Weidenfeld et Edward E. Morrisey, « Transcriptional and DNA Binding Activity of the Foxp1/2/4 Family Is Modulated by Heterotypic and Homotypic Protein Interactions », Molecular and Cellular Biology, vol. 24, , p. 809–822 (ISSN0270-7306 et 1098-5549, PMID14701752, PMCID343786, DOI10.1128/MCB.24.2.809-822.2004, lire en ligne, consulté le )
doi.org
dx.doi.org
Bin Wang, Joel Weidenfeld, Min Min Lu et Shanna Maika, « Foxp1 regulates cardiac outflow tract, endocardial cushion morphogenesis and myocyte proliferation and maturation », Development (Cambridge, England), vol. 131, , p. 4477–4487 (ISSN0950-1991, PMID15342473, DOI10.1242/dev.01287, lire en ligne, consulté le )
Jeremy S. Dasen, Alessandro De Camilli, Bin Wang et Philip W. Tucker, « Hox repertoires for motor neuron diversity and connectivity gated by a single accessory factor, FoxP1 », Cell, vol. 134, , p. 304–316 (ISSN1097-4172, PMID18662545, DOI10.1016/j.cell.2008.06.019, lire en ligne, consulté le )
Hui Hu, Bin Wang, Madhuri Borde et Julie Nardone, « Foxp1 is an essential transcriptional regulator of B cell development », Nature Immunology, vol. 7, , p. 819–826 (ISSN1529-2908, PMID16819554, DOI10.1038/ni1358, lire en ligne, consulté le )
(en) Shanru Li, Joel Weidenfeld et Edward E. Morrisey, « Transcriptional and DNA Binding Activity of the Foxp1/2/4 Family Is Modulated by Heterotypic and Homotypic Protein Interactions », Molecular and Cellular Biology, vol. 24, , p. 809–822 (ISSN0270-7306 et 1098-5549, PMID14701752, PMCID343786, DOI10.1128/MCB.24.2.809-822.2004, lire en ligne, consulté le )
Bin Wang, Danjuan Lin, Chuan Li et Philip Tucker, « Multiple domains define the expression and regulatory properties of Foxp1 forkhead transcriptional repressors », The Journal of Biological Chemistry, vol. 278, , p. 24259–24268 (ISSN0021-9258, PMID12692134, DOI10.1074/jbc.M207174200, lire en ligne, consulté le )
Denise Horn, Johannes Kapeller, Núria Rivera-Brugués et Ute Moog, « Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits », Human Mutation, vol. 31, , E1851–1860 (ISSN1098-1004, PMID20848658, PMCID3049153, DOI10.1002/humu.21362, lire en ligne, consulté le )
(en) Anna K. Le Fevre, Sharelle Taylor, Neva H. Malek et Denise Horn, « FOXP1 mutations cause intellectual disability and a recognizable phenotype », American Journal of Medical Genetics Part A, vol. 161, , p. 3166–3175 (ISSN1552-4833, DOI10.1002/ajmg.a.36174, lire en ligne, consulté le )
Marek Mraz, Liguang Chen, Laura Z. Rassenti et Emanuela M. Ghia, « miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1 », Blood, vol. 124, no 1, , p. 84–95 (ISSN1528-0020, PMID24787006, PMCID4125356, DOI10.1182/blood-2013-09-527234, lire en ligne, consulté le )
Bin Wang, Joel Weidenfeld, Min Min Lu et Shanna Maika, « Foxp1 regulates cardiac outflow tract, endocardial cushion morphogenesis and myocyte proliferation and maturation », Development (Cambridge, England), vol. 131, , p. 4477–4487 (ISSN0950-1991, PMID15342473, DOI10.1242/dev.01287, lire en ligne, consulté le )
Jeremy S. Dasen, Alessandro De Camilli, Bin Wang et Philip W. Tucker, « Hox repertoires for motor neuron diversity and connectivity gated by a single accessory factor, FoxP1 », Cell, vol. 134, , p. 304–316 (ISSN1097-4172, PMID18662545, DOI10.1016/j.cell.2008.06.019, lire en ligne, consulté le )
Hui Hu, Bin Wang, Madhuri Borde et Julie Nardone, « Foxp1 is an essential transcriptional regulator of B cell development », Nature Immunology, vol. 7, , p. 819–826 (ISSN1529-2908, PMID16819554, DOI10.1038/ni1358, lire en ligne, consulté le )
(en) Shanru Li, Joel Weidenfeld et Edward E. Morrisey, « Transcriptional and DNA Binding Activity of the Foxp1/2/4 Family Is Modulated by Heterotypic and Homotypic Protein Interactions », Molecular and Cellular Biology, vol. 24, , p. 809–822 (ISSN0270-7306 et 1098-5549, PMID14701752, PMCID343786, DOI10.1128/MCB.24.2.809-822.2004, lire en ligne, consulté le )
Bin Wang, Danjuan Lin, Chuan Li et Philip Tucker, « Multiple domains define the expression and regulatory properties of Foxp1 forkhead transcriptional repressors », The Journal of Biological Chemistry, vol. 278, , p. 24259–24268 (ISSN0021-9258, PMID12692134, DOI10.1074/jbc.M207174200, lire en ligne, consulté le )
Denise Horn, Johannes Kapeller, Núria Rivera-Brugués et Ute Moog, « Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits », Human Mutation, vol. 31, , E1851–1860 (ISSN1098-1004, PMID20848658, PMCID3049153, DOI10.1002/humu.21362, lire en ligne, consulté le )
(en) Anna K. Le Fevre, Sharelle Taylor, Neva H. Malek et Denise Horn, « FOXP1 mutations cause intellectual disability and a recognizable phenotype », American Journal of Medical Genetics Part A, vol. 161, , p. 3166–3175 (ISSN1552-4833, DOI10.1002/ajmg.a.36174, lire en ligne, consulté le )
Marek Mraz, Liguang Chen, Laura Z. Rassenti et Emanuela M. Ghia, « miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1 », Blood, vol. 124, no 1, , p. 84–95 (ISSN1528-0020, PMID24787006, PMCID4125356, DOI10.1182/blood-2013-09-527234, lire en ligne, consulté le )
Bin Wang, Joel Weidenfeld, Min Min Lu et Shanna Maika, « Foxp1 regulates cardiac outflow tract, endocardial cushion morphogenesis and myocyte proliferation and maturation », Development (Cambridge, England), vol. 131, , p. 4477–4487 (ISSN0950-1991, PMID15342473, DOI10.1242/dev.01287, lire en ligne, consulté le )
Jeremy S. Dasen, Alessandro De Camilli, Bin Wang et Philip W. Tucker, « Hox repertoires for motor neuron diversity and connectivity gated by a single accessory factor, FoxP1 », Cell, vol. 134, , p. 304–316 (ISSN1097-4172, PMID18662545, DOI10.1016/j.cell.2008.06.019, lire en ligne, consulté le )
Hui Hu, Bin Wang, Madhuri Borde et Julie Nardone, « Foxp1 is an essential transcriptional regulator of B cell development », Nature Immunology, vol. 7, , p. 819–826 (ISSN1529-2908, PMID16819554, DOI10.1038/ni1358, lire en ligne, consulté le )
(en) Shanru Li, Joel Weidenfeld et Edward E. Morrisey, « Transcriptional and DNA Binding Activity of the Foxp1/2/4 Family Is Modulated by Heterotypic and Homotypic Protein Interactions », Molecular and Cellular Biology, vol. 24, , p. 809–822 (ISSN0270-7306 et 1098-5549, PMID14701752, PMCID343786, DOI10.1128/MCB.24.2.809-822.2004, lire en ligne, consulté le )
Bin Wang, Danjuan Lin, Chuan Li et Philip Tucker, « Multiple domains define the expression and regulatory properties of Foxp1 forkhead transcriptional repressors », The Journal of Biological Chemistry, vol. 278, , p. 24259–24268 (ISSN0021-9258, PMID12692134, DOI10.1074/jbc.M207174200, lire en ligne, consulté le )
Denise Horn, Johannes Kapeller, Núria Rivera-Brugués et Ute Moog, « Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits », Human Mutation, vol. 31, , E1851–1860 (ISSN1098-1004, PMID20848658, PMCID3049153, DOI10.1002/humu.21362, lire en ligne, consulté le )
Marek Mraz, Liguang Chen, Laura Z. Rassenti et Emanuela M. Ghia, « miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1 », Blood, vol. 124, no 1, , p. 84–95 (ISSN1528-0020, PMID24787006, PMCID4125356, DOI10.1182/blood-2013-09-527234, lire en ligne, consulté le )
(en) Anna K. Le Fevre, Sharelle Taylor, Neva H. Malek et Denise Horn, « FOXP1 mutations cause intellectual disability and a recognizable phenotype », American Journal of Medical Genetics Part A, vol. 161, , p. 3166–3175 (ISSN1552-4833, DOI10.1002/ajmg.a.36174, lire en ligne, consulté le )