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FGF10 missense mutations in aplasia of lacrimal and salivary glands (ALSG)An intronic alteration of the fibroblast growth factor 10 gene causing ALSG-(aplasia of lacrimal and salivary glands) syndromeHomozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontiaFgf10 is required for specification of non-sensory regions of the cochlear epithelium.Structural basis for reduced FGFR2 activity in LADD syndrome: Implications for FGFR autoinhibition and activationEvidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse modelPlatelet-derived growth factor receptor regulates salivary gland morphogenesis via fibroblast growth factor expressionTwist1 Is Essential for Tooth Morphogenesis and Odontoblast DifferentiationSalivary Gland Dysplasia in Fgf10 Heterozygous Mice: A New Mouse Model of Xerostomia.Identification of differentially expressed genes in early inner ear developmentHighly efficient targeted mutagenesis in one-cell mouse embryos mediated by the TALEN and CRISPR/Cas systems.Differential interactions of FGFs with heparan sulfate control gradient formation and branching morphogenesis.The Fibroblast Growth Factor signaling pathwayFibroblast growth factors: biology, function, and application for tissue regeneration.Chromodomain proteins in development: lessons from CHARGE syndrome.Submandibular parasympathetic gangliogenesis requires sprouty-dependent Wnt signals from epithelial progenitors.A breath of fresh air on the mesenchyme: impact of impaired mesenchymal development on the pathogenesis of bronchopulmonary dysplasia.Mechanisms involved in injury and repair of the murine lacrimal gland: role of programmed cell death and mesenchymal stem cellsThe FGF family: biology, pathophysiology and therapyMolecular pathology of the fibroblast growth factor family.Case report: Presentation of lacrimo-auriculodento- digital (LADD) syndrome in a young female patient.Role of FGFs/FGFRs in skeletal development and bone regeneration.Salivary gland organogenesis.Fibroblast growth factor signaling in mammalian tooth development.Walking along the Fibroblast Growth Factor 10 Route: A Key Pathway to Understand the Control and Regulation of Epithelial and Mesenchymal Cell-Lineage Formation during Lung Development and Repair after Injury.Salivary gland development and disease.Molecular studies on the roles of Runx2 and Twist1 in regulating FGF signaling.Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast growth factor 10 (FGF10)-FGF receptor 2 signaling pathway.Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glands.A Case of Lacrimo-Auriculo-Dento-Digital Syndrome with Multiple Congenitally Missing Teeth.Retinoic acid signaling regulates Krt5 and Krt14 independently of stem cell markers in submandibular salivary gland epithelium.Dynamic relationship of the epithelium and mesenchyme during salivary gland initiation: the role of Fgf10A branching morphogenesis program governs embryonic growth of the thyroid gland.A new syndrome associated with absence of lower lid lacrimal punctum, ptosis, elevation deficiency of both eyes and mild facial dysmorphism.The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.The Role of Fibroblast Growth Factors in Tooth Development and Incisor Renewal.Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies.Regulation of FGF10 Signaling in Development and Disease
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
LADD syndrome is caused by FGF10 mutations.
@en
LADD syndrome is caused by FGF10 mutations.
@nl
type
label
LADD syndrome is caused by FGF10 mutations.
@en
LADD syndrome is caused by FGF10 mutations.
@nl
prefLabel
LADD syndrome is caused by FGF10 mutations.
@en
LADD syndrome is caused by FGF10 mutations.
@nl
P2093
P2860
P1433
P1476
LADD syndrome is caused by FGF10 mutations.
@en
P2093
P2860
P304
P356
10.1111/J.1399-0004.2006.00597.X
P577
2006-04-01T00:00:00Z