Peroxisome-proliferator-activated receptor-binding protein (PBP) is essential for the growth of active Notch4-immortalized mammary epithelial cells by activating SOX10 expression

Por Zhu, Yiwei Tony, Jia, Yuzhi, Hu, Liping, Qi, Chao, Prasad, Megana K., McCallion, Andrew S., Zhu, Yi-Jun
Publicado em 2009

Close association of olfactory placode precursors and cranial neural crest cells does not predestine cell mixing

Por Harden, Maegan V., Pereiro, Luisa, Ramialison, Mirana, Wittbrodt, Jochen, Prasad, Megana K., McCallion, Andrew S., Whitlock, Kathleen E.
Publicado no Dev Dyn (2012)

A Polymorphic 3’UTR Element in ATP1B1 Regulates Alternative Polyadenylation and Is Associated with Blood Pressure

Por Prasad, Megana K., Bhalla, Kavita, Pan, Zhen Hua, O’Connell, Jeffrey R., Weder, Alan B., Chakravarti, Aravinda, Tian, Bin, Chang, Yen-Pei C.
Publicado em 2013

SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer

Por Prasad, Megana K, Reed, Xylena, Gorkin, David U, Cronin, Julia C, McAdow, Anthony R, Chain, Kristopher, Hodonsky, Chani J, Jones, Erin A, Svaren, John, Antonellis, Anthony, Johnson, Stephen L, Loftus, Stacie K, Pavan, William J, McCallion, Andrew S
Publicado em 2011

Gpnmb is a Melanoblast-Expressed, MITF-Dependent Gene

Por Loftus, Stacie K., Antonellis, Anthony, Matera, Ivana, Renaud, Gabriel, Baxter, Laura L., Reid, Duncan, Wolfsberg, Tyra G., Chen, Yidong, Wang, ChenWei, Prasad, Megana K., Bessling, Seneca L., McCallion, Andrew S., Green, Eric D., Bennett, Dorothy C., Pavan, William J.
Publicado em 2008

Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta

Por Huckert, Mathilde, Stoetzel, Corinne, Morkmued, Supawich, Laugel-Haushalter, Virginie, Geoffroy, Véronique, Muller, Jean, Clauss, François, Prasad, Megana K., Obry, Frédéric, Raymond, Jean Louis, Switala, Marzena, Alembik, Yves, Soskin, Sylvie, Mathieu, Eric, Hemmerlé, Joseph, Weickert, Jean-Luc, Dabovic, Branka Brukner, Rifkin, Daniel B., Dheedene, Annelies, Boudin, Eveline, Caluseriu, Oana, Cholette, Marie-Claude, Mcleod, Ross, Antequera, Reynaldo, Gellé, Marie-Paule, Coeuriot, Jean-Louis, Jacquelin, Louis-Frédéric, Bailleul-Forestier, Isabelle, Manière, Marie-Cécile, Van Hul, Wim, Bertola, Debora, Dollé, Pascal, Verloes, Alain, Mortier, Geert, Dollfus, Hélène, Bloch-Zupan, Agnès
Publicado no Hum Mol Genet (2015)

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

Por Prasad, Megana K, Geoffroy, Véronique, Vicaire, Serge, Jost, Bernard, Dumas, Michael, Le Gras, Stéphanie, Switala, Marzena, Gasse, Barbara, Laugel-Haushalter, Virginie, Paschaki, Marie, Leheup, Bruno, Droz, Dominique, Dalstein, Amelie, Loing, Adeline, Grollemund, Bruno, Muller-Bolla, Michèle, Lopez-Cazaux, Séréna, Minoux, Maryline, Jung, Sophie, Obry, Frédéric, Vogt, Vincent, Davideau, Jean-Luc, Davit-Beal, Tiphaine, Kaiser, Anne-Sophie, Moog, Ute, Richard, Béatrice, Morrier, Jean-Jacques, Duprez, Jean-Pierre, Odent, Sylvie, Bailleul-Forestier, Isabelle, Rousset, Monique Marie, Merametdijan, Laure, Toutain, Annick, Joseph, Clara, Giuliano, Fabienne, Dahlet, Jean-Christophe, Courval, Aymeric, El Alloussi, Mustapha, Laouina, Samir, Soskin, Sylvie, Guffon, Nathalie, Dieux, Anne, Doray, Bérénice, Feierabend, Stephanie, Ginglinger, Emmanuelle, Fournier, Benjamin, de la Dure Molla, Muriel, Alembik, Yves, Tardieu, Corinne, Clauss, François, Berdal, Ariane, Stoetzel, Corinne, Manière, Marie Cécile, Dollfus, Hélène, Bloch-Zupan, Agnès
Publicado no J Med Genet (2016)