Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice

Overview of attention for article published in BMC Developmental Biology, February 2010

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Victoria, a co-author of this paper, is a Ramapo College Bioinformatics Alumna. She worked on a gene involved in skull…

I helped discover that p38 was involved in the skull abnormalities of Apert Syndrome mice: http://www.ncbi.nlm.nih.gov/pmc/arti…

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