Mechanical Properties of Calvarial Bones in a Mouse Model for Craniosynostosis

por Moazen, Mehran, Peskett, Emma, Babbs, Christian, Pauws, Erwin, Fagan, Michael J.
Publicado 2015

Mechanical loading of cranial joints minimizes the craniofacial phenotype in Crouzon syndrome

por Moazen, Mehran, Hejazi, Mahbubeh, Savery, Dawn, Jones, Dominic, Marghoub, Arsalan, Alazmani, Ali, Pauws, Erwin
Publicado 2022

Analysis of the Fgfr2(C342Y) mouse model shows condensation defects due to misregulation of Sox9 expression in prechondrocytic mesenchyme

por Peskett, Emma, Kumar, Samin, Baird, William, Jaiswal, Janhvi, Li, Ming, Patel, Priyanca, Britto, Jonathan A., Pauws, Erwin
Publicado 2017

Overexpression of Fgfr2c causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouse

por Lee, Kevin K. L., Peskett, Emma, Quinn, Charlotte M., Aiello, Rosanna, Adeeva, Liliya, Moulding, Dale A., Stanier, Philip, Pauws, Erwin
Publicado 2018

Tbx22(null) mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes

por Pauws, Erwin, Hoshino, Aya, Bentley, Lucy, Prajapati, Suresh, Keller, Charles, Hammond, Peter, Martinez-Barbera, Juan-Pedro, Moore, Gudrun E., Stanier, Philip
Publicado 2009

Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening

por Adams, David, Baldock, Richard, Bhattacharya, Shoumo, Copp, Andrew J., Dickinson, Mary, Greene, Nicholas D. E., Henkelman, Mark, Justice, Monica, Mohun, Timothy, Murray, Stephen A., Pauws, Erwin, Raess, Michael, Rossant, Janet, Weaver, Tom, West, David
Publicado 2013

Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening

por Adams, David, Baldock, Richard, Bhattacharya, Shoumo, Copp, Andrew J., Dickinson, Mary, Greene, Nicholas D. E., Henkelman, Mark, Justice, Monica, Mohun, Timothy, Murray, Stephen A., Pauws, Erwin, Raess, Michael, Rossant, Janet, Weaver, Tom, West, David
Publicado 2013

Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability

por Twigg, Stephen R.F., Forecki, Jennifer, Goos, Jacqueline A.C., Richardson, Ivy C.A., Hoogeboom, A. Jeannette M., van den Ouweland, Ans M.W., Swagemakers, Sigrid M.A., Lequin, Maarten H., Van Antwerp, Daniel, McGowan, Simon J., Westbury, Isabelle, Miller, Kerry A., Wall, Steven A., van der Spek, Peter J., Mathijssen, Irene M.J., Pauws, Erwin, Merzdorf, Christa S., Wilkie, Andrew O.M.
Publicado 2015

Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

por Fratta, Pietro, Sivakumar, Prasanth, Humphrey, Jack, Lo, Kitty, Ricketts, Thomas, Oliveira, Hugo, Brito‐Armas, Jose M, Kalmar, Bernadett, Ule, Agnieszka, Yu, Yichao, Birsa, Nicol, Bodo, Cristian, Collins, Toby, Conicella, Alexander E, Mejia Maza, Alan, Marrero‐Gagliardi, Alessandro, Stewart, Michelle, Mianne, Joffrey, Corrochano, Silvia, Emmett, Warren, Codner, Gemma, Groves, Michael, Fukumura, Ryutaro, Gondo, Yoichi, Lythgoe, Mark, Pauws, Erwin, Peskett, Emma, Stanier, Philip, Teboul, Lydia, Hallegger, Martina, Calvo, Andrea, Chiò, Adriano, Isaacs, Adrian M, Fawzi, Nicolas L, Wang, Eric, Housman, David E, Baralle, Francisco, Greensmith, Linda, Buratti, Emanuele, Plagnol, Vincent, Fisher, Elizabeth MC, Acevedo‐Arozena, Abraham
Publicado 2018