Wnt3a(−/−)-like phenotype and limb deficiency in Lef1(−/−)Tcf1(−/−) mice

por Galceran, Juan, Fariñas, Isabel, Depew, Michael J., Clevers, Hans, Grosschedl, Rudolf
Publicado em 1999

Reassessing the Dlx code: the genetic regulation of branchial arch skeletal pattern and development

por Depew, Michael J, Simpson, Carol A, Morasso, Maria, Rubenstein, John LR
Publicado em 2005

DLX5 Regulates Development of Peripheral and Central Components of the Olfactory System

por Long, Jason E., Garel, Sonia, Depew, Michael J., Tobet, Stuart, Rubenstein, John L. R.
Publicado no J Neurosci (2003)

Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch

por Trumpp, Andreas, Depew, Michael J., Rubenstein, John L.R., Bishop, J. Michael, Martin, Gail R.
Publicado em 1999

Gas1 is a modifier for holoprosencephaly and genetically interacts with sonic hedgehog

por Seppala, Maisa, Depew, Michael J., Martinelli, David C., Fan, Chen-Ming, Sharpe, Paul T., Cobourne, Martyn T.
Publicado em 2007

Sonic hedgehog signalling inhibits palatogenesis and arrests tooth development in a mouse model of the nevoid basal cell carcinoma syndrome

por Cobourne, Martyn T., Xavier, Guilherme M., Depew, Michael, Hagan, Louise, Sealby, Jane, Webster, Zoe, Sharpe, Paul T.
Publicado em 2009

Satb2 Haploinsufficiency Phenocopies 2q32-q33 Deletions, whereas Loss Suggests a Fundamental Role in the Coordination of Jaw Development

por Britanova, Olga, Depew, Michael J., Schwark, Manuela, Thomas, Bethan L., Miletich, Isabelle, Sharpe, Paul, Tarabykin, Victor
Publicado em 2006

Fgf8 Dosage Determines Midfacial Integration and Polarity within the Nasal and Optic Capsules

por Griffin, John N., Compagnucci, Claudia, Hu, Diane, Fish, Jennifer, Klein, Ophir, Marcucio, Ralph, Depew, Michael J.
Publicado em 2012

Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene

por McGonnell, Imelda M, Graham, Anthony, Richardson, Joanna, Fish, Jennifer L, Depew, Michael J, Dee, Chris T, Holland, Peter WH, Takahashi, Tokiharu
Publicado em 2011

Heterogeneous Conservation of Dlx Paralog Co-Expression in Jawed Vertebrates

por Debiais-Thibaud, Mélanie, Metcalfe, Cushla J., Pollack, Jacob, Germon, Isabelle, Ekker, Marc, Depew, Michael, Laurenti, Patrick, Borday-Birraux, Véronique, Casane, Didier
Publicado em 2013

A Conserved Pbx-Wnt-p63-Irf6 Regulatory Module Controls Face Morphogenesis by Promoting Epithelial Apoptosis

por Ferretti, Elisabetta, Li, Bingsi, Zewdu, Rediet, Wells, Victoria, Hebert, Jean M., Karner, Courtney, Anderson, Matthew J., Williams, Trevor, Dixon, Jill, Dixon, Michael J., Depew, Michael J., Selleri, Licia
Publicado em 2011

ESCRT-II/Vps25 constrains digit number by endosome-mediated selective modulation of FGF-SHH signaling

por Handschuh, Karen, Feenstra, Jennifer, Koss, Matthew, Ferretti, Elisabetta, Risolino, Maurizio, Zewdu, Rediet, Sahai, Michelle A., Bénazet, Jean-Denis, Peng, Xiao P., Depew, Michael J., Quintana, Laura, Sharpe, James, Wang, Baolin, Alcorn, Heather, Rivi, Roberta, Butcher, Stephen, Manak, J Robert, Vaccari, Thomas, Weinstein, Harel, Anderson, Kathryn V., Lacy, Elizabeth, Selleri, Licia
Publicado no Cell Rep (2014)

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

por Bogani, Debora, Willoughby, Catherine, Davies, Jennifer, Kaur, Kulvinder, Mirza, Ghazala, Paudyal, Anju, Haines, Heather, McKeone, Richard, Cadman, Matthew, Pieles, Guido, Schneider, Jürgen E., Bhattacharya, Shoumo, Hardy, Andrea, Nolan, Patrick M., Tripodis, Nikos, Depew, Michael J., Chandrasekara, Ramya, Duncan, Gimara, Sharpe, Paul T., Greenfield, Andy, Denny, Paul, Brown, Steve D. M., Ragoussis, Jiannis, Arkell, Ruth M.
Publicado em 2005