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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 26, 2010
Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermisAlessio Lancioni, Mariateresa Pizzo, Bianca Fontanella, et al.Frontiers in Cell and Developmental Biology|October 5, 2020
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse CellsAndrea Cirino, Ilaria Aurigemma, Monica Franzese, et al.Communications Biology|March 22, 2024
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiationIlaria Aurigemma, Olga Lanzetta, Andrea Cirino, et al.International Journal of Molecular Sciences|January 23, 2020
TBX1 and Basal Cell Carcinoma: Expression and Interactions with Gli2 and Dvl2 SignalingCinzia Caprio, Silvia Varricchio, Marchesa Bilio, et al.Development (Cambridge, England)|May 30, 2025
Tbx1 stabilizes differentiation of the cardiopharyngeal mesoderm and drives morphogenesis in the pharyngeal apparatusOlga Lanzetta, Marchesa Bilio, Johannes Liebig, et al.American Journal of Medical Genetics. Part A|July 2, 2003
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrumFrancesca De Falco, Silvia Cainarca, Grazia Andolfi, et al.Pageof 2