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Revision as of 10:13, 19 September 2012
Welcome to the Basson lab at King's College London
Our research is aimed at uncovering the signalling mechanisms that control morphogenesis of complex structures and organs in the developing embryo and newborn
The Basson laboratory is located on the 27th floor of Guy's Hospital in the Department of Craniofacial and Stem Cell Biology and affiliated with the MRC Centre for Developmental Neurobiology on Guy's Campus 
FGF signalling in development and disease
All organs in the body originate from relatively simple structures in the embryo. For example a simple epithelial tube, the neural tube, develops into the highly complex brain. The many forces and growth factors that act upon embryonic tissues are precisely coordinated to shape the morphogenesis of more complex structures. We are interested in understanding how signalling centres are established in the embryo and how signalling pathways are regulated during development. Current research projects in the lab primarily focus on the fibroblast growth factor (FGF) signalling pathway and our aim is to understand how deregulated FGF signalling results in birth defects and cellular malfunction. We are particularly interested in elucidating the functions of the Sprouty genes, which encode FGF antagonists; Tbx1, a T-box transcription factor implicated in DiGeorge syndrome and Chd7, a chromatin remodeller, mutated in CHARGE syndrome.
In the press
Our work on the cerebellum and autism features in a new article in International Innovation:
Image:Basson International Innovation.pdf
Manuscripts in press
- Chakkalakal, J., Jones, K., Basson, M.A. & Brack, A.S. (2012) The aged niche disrupts muscle stem cell quiescence. Nature (in press).
- Magnani, D., Amaniti, E-M., Benadiba, C., Hasenpusch-Theil, K., Yu, T., Basson, M.A., Price, D.J., Lebrand, C. & Theil, T. (2012) Gli3 controls corpus callosum formation by positioning midline guideposts during telencephalic patterning. Cerebral Cortex (in press).
- Pitera, J.E., Woolf, A.S., Basson, M.A. & Scambler, P.J. (2012) Sprouty1 haploinsufficiency permits kidney maturation in Fraser syndrome renal agenesis mice. J. Am. Soc. Nephrol. (in press).
== Publications in press ==