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Life Science Alliance|October 10, 2022
VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndromeSara Cioffi, Gemma Flore, Stefania Martucciello, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 20, 2020
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3Stefania Martucciello, Maria Giuseppina Turturo, Marchesa Bilio, et al.Genetic Testing and Molecular Biomarkers|July 17, 2009
GPR143 mutational analysis in two Italian families with X-linked ocular albinismLucia Micale, Bartolomeo Augello, Carmela Fusco, et al.European Journal of Human Genetics : EJHG|July 2, 2009
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patientGiovanni Battista Ferrero, Cédric Howald, Lucia Micale, et al.European Journal of Human Genetics : EJHG|October 22, 2009
Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosisLucia Micale, Maria Giuseppina Turturo, Carmela Fusco, et al.Cell Cycle (Georgetown, Tex.)|January 21, 2012
TRIM8 modulates p53 activity to dictate cell cycle arrestMariano Francesco Caratozzolo, Lucia Micale, Maria Giuseppina Turturo, et al.Pageof 1