Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
about
Novel insights into the bovine polled phenotype and horn ontogenesis in BovidaeGJC2 missense mutations cause human lymphedemaThe murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesisFOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domainProtein tyrosine phosphatase PTPN14 is a regulator of lymphatic function and choanal development in humansAnalysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasiaBiomedicine and diseases: the Klippel-Trenaunay syndrome, vascular anomalies and vascular morphogenesisFoxc2 transcription factor: a newly described regulator of angiogenesisLinkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairsGDF6, a novel locus for a spectrum of ocular developmental anomaliesGene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regionsDevelopment of the mammalian lymphatic vasculatureThe neural crest in cardiac congenital anomaliesVascular anomalies: from genetics toward models for therapeutic trialsEvidence for SH2 domain-containing 5'-inositol phosphatase-2 (SHIP2) contributing to a lymphatic dysfunctionA case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutationGenetics of lymphatic anomaliesFoxf2: a novel locus for anterior segment dysgenesis adjacent to the Foxc1 geneThe evolution of Fox genes and their role in development and diseaseDiscontinuous LYVE-1 expression in corneal limbal lymphatics: dual function as microvalves and immunological hot spots.Elevated expression of VEGFR-3 in lymphatic endothelial cells from lymphangiomasPhosphorylation regulates FOXC2-mediated transcription in lymphatic endothelial cellsIdentification and analysis of evolutionary selection pressures acting at the molecular level in five forkhead subfamilies.Cleft lip and palate genetics and application in early embryological development.Dermal collagen and lipid deposition correlate with tissue swelling and hydraulic conductivity in murine primary lymphedema.Genomic identification of regulatory elements by evolutionary sequence comparison and functional analysisLong-range control of gene expression: emerging mechanisms and disruption in disease.The lymphatic system in health and disease.Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndromeMolecular mechanisms of pituitary organogenesis: In search of novel regulatory genes.Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review.Current views on the function of the lymphatic vasculature in health and diseaseRecent progress in histochemistry and cell biology.Human Lymphatic Architecture and Dynamic Transport Imaged Using Near-infrared Fluorescence.Pleural function and lymphatics.Gastrointestinal lymphatics in health and diseaseGenetic effects on human cognition: lessons from the study of mental retardation syndromesSystematic analysis of palatal transcriptome to identify cleft palate genes within TGFβ3-knockout mice alleles: RNA-Seq analysis of TGFβ3 Mice.Lymphatic and angiogenic candidate genes predict the development of secondary lymphedema following breast cancer surgery.
P2860
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P2860
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
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2000 nî lūn-bûn
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2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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name
Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
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P2093
P2860
P356
P1476
Mutations in FOXC2 (MFH-1), a ...... mphedema-distichiasis syndrome
@en
P2093
J L Gorski
L H Seaver
R P Erickson
S L Dagenais
T W Glover
P2860
P304
P356
10.1086/316915
P407
P577
2000-11-08T00:00:00Z