About this Research Topic
In addition to these embryonic activities Fgf10 is also critical in the adult mouse for repair after injury. Fgf10 has also been associated with breast cancer in humans and mutations in this gene and/or its receptor are associated with multiple human diseases such as Aplasia of the Lacrimal and Salivary gland syndrome (ALSG) as well as Lacrimal-Auriculo-dental digital syndrome (LADD). Fgf10 mutations are also associated with the development of Chronic obstructive pulmonary disease in humans. In the future recombinant Fgf10 could be instrumental to treat diseases associated with organ failure or/and involving defective wound healing.
With this Research Topic, we hope to create a collection of articles addressing the importance of FGF10, in particular its role in development, homeostasis, disease and repair. The following article types will be considered: Original Research and Reviews.
Keywords: FGF10
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