FGF10 gene

INTRODUCTION Several candidate loci have been suggested as influencing mandibular prognathism (1p22.1, 1p22.2, 1p36, 3q26.2, 5p13… Expand

During early lung development, airway tubes change shape. Tube length increases more than circumference as a large proportion of… Expand

Tbx1, the major gene underlying del22q11.2 or DiGeorge syndrome in humans, is required for normal development and septation of… Expand

Hypospadias is a common malformation, which results from failure of urethral tube closure, and whose molecular mechanisms are… Expand

Lacrimo-auriculo-dento-digital syndrome [LADD (MIM 149730)] is an autosomal-dominant multiple congenital anomaly disorder… Expand

Lacrimo-auriculo-dento-digital (LADD) syndrome is characterized by lacrimal duct aplasia, malformed ears and deafness, small… Expand

The highly ordered process of wound healing involves the coordinated regulation of cell proliferation and migration and tissue… Expand

Development of the arterial pole of the heart is a critical step in cardiogenesis, yet its embryological origin remains obscure… Expand

Here, we characterized the skin and hair phenotype of mice lacking the fibroblast growth factor 10 gene (Fgf10), a newly… Expand

We cloned the mouse homolog of FGF10, which was recently reported as a new member of the FGF family. The predicted molecular mass… Expand