The role of p53 in developmental syndromes

por Bowen, Margot E, Attardi, Laura D
Publicado 2019

SHP2 Regulates Chondrocyte Terminal Differentiation, Growth Plate Architecture and Skeletal Cell Fates

por Bowen, Margot E., Ayturk, Ugur M., Kurek, Kyle C., Yang, Wentian, Warman, Matthew L.
Publicado 2014

Presphenoidal synchondrosis fusion in DBA/2J mice

por Adams, Allysa, McBratney-Owen, Brandeis, Newby, Brittany, Bowen, Margot E., Olsen, Bjorn R., Warman, Matthew L.
Publicado 2012

Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Chd7 Mutant Mouse Ear

por Durruthy-Durruthy, Robert, Sperry, Ethan D., Bowen, Margot E., Attardi, Laura D., Heller, Stefan, Martin, Donna M.
Publicado 2018

SHP2 regulates skeletal cell fate by modifying SOX9 expression and transcriptional activity

por Zuo, Chunlin, Wang, Lijun, Kamalesh, Raghavendra M., Bowen, Margot E., Moore, Douglas C., Dooner, Mark S., Reginato, Anthony M., Wu, Qian, Schorl, Christoph, Song, Yueming, Warman, Matthew L., Neel, Benjamin G., Ehrlich, Michael G., Yang, Wentian
Publicado 2018

Loss-of-Function Mutations in PTPN11 Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome

por Bowen, Margot E., Boyden, Eric D., Holm, Ingrid A., Campos-Xavier, Belinda, Bonafé, Luisa, Superti-Furga, Andrea, Ikegawa, Shiro, Cormier-Daire, Valerie, Bovée, Judith V., Pansuriya, Twinkal C., de Sousa, Sérgio B., Savarirayan, Ravi, Andreucci, Elena, Vikkula, Miikka, Garavelli, Livia, Pottinger, Caroline, Ogino, Toshihiko, Sakai, Akinori, Regazzoni, Bianca M., Wuyts, Wim, Sangiorgi, Luca, Pedrini, Elena, Zhu, Mei, Kozakewich, Harry P., Kasser, James R., Seidman, Jon G., Kurek, Kyle C., Warman, Matthew L.
Publicado 2011