Resultados da pesquisa - JABS, ETHYLIN WANG

A TWIST in the fate of human osteoblasts identifies signaling molecules involved in skull development Por Jabs, Ethylin Wang

Obter o texto integral Obter o texto integral

Oral Clefting in China Over the Last Decade: 205,679 Patients Por Kling, Rochelle R., Taub, Peter J., Ye, Xiaoqian, Jabs, Ethylin Wang

Obter o texto integral Obter o texto integral Obter o texto integral

Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses Por Heuzé, Yann, Holmes, Gregory, Peter, Inga, Richtsmeier, Joan T., Jabs, Ethylin Wang

Obter o texto integral Obter o texto integral Obter o texto integral

Embryonic Craniofacial Bone Volume and Bone Mineral Density in Fgfr2(+/P253R) and Nonmutant Mice Por Percival, Christopher J., Huang, Yuan, Jabs, Ethylin Wang, Li, Runze, Richtsmeier, Joan T.

Obter o texto integral Obter o texto integral Obter o texto integral

BCL11B expression in intramembranous osteogenesis during murine craniofacial suture development Por Holmes, Greg, van Bakel, Harm, Zhou, Xueyan, Losic, Bojan, Jabs, Ethylin Wang

Obter o texto integral Obter o texto integral Obter o texto integral

Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues Por Heuzé, Yann, Singh, Nandini, Basilico, Claudio, Jabs, Ethylin Wang, Holmes, Greg, Richtsmeier, Joan T

Obter o texto integral Obter o texto integral Obter o texto integral

Choanal Atresia and Craniosynostosis: Development and Disease Por Lesciotto, Kate M., Heuzé, Yann, Jabs, Ethylin Wang, Bernstein, Joseph M., Richtsmeier, Joan T.

Obter o texto integral Obter o texto integral Obter o texto integral

The study of abnormal bone development in the Apert syndrome Fgfr2(+/S252W) mouse using a 3D hydrogel culture model Por Yang, Fan, Wang, Yingli, Zhang, Zijun, Hsu, Bryan, Jabs, Ethylin Wang, Elisseeff, Jennifer H.

Obter o texto integral Obter o texto integral Obter o texto integral

FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Por Martínez-Abadías, Neus, Heuzé, Yann, Wang, Yingli, Jabs, Ethylin Wang, Aldridge, Kristina, Richtsmeier, Joan T.

Obter o texto integral Obter o texto integral Obter o texto integral

Tyrosine-Dependent Basolateral Targeting of Human Connexin43-eYFP in Madin-Darby Canine Kidney Cells Can Be Disrupted by the Oculodentodigital Dysplasia Mutation L90V Por Chtchetinin, Jana, Gifford, Wes D., Li, Sichen, Paznekas, William A., Jabs, Ethylin Wang, Lai, Albert

Obter o texto integral Obter o texto integral Obter o texto integral

Ten-year experience of more than 35,000 orofacial clefts in Africa Por Conway, Julia C, Taub, Peter J, Kling, Rochelle, Oberoi, Kurun, Doucette, John, Jabs, Ethylin Wang

Obter o texto integral Obter o texto integral Obter o texto integral

From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome Por Martínez-Abadías, Neus, Holmes, Greg, Pankratz, Talia, Wang, Yingli, Zhou, Xueyan, Jabs, Ethylin Wang, Richtsmeier, Joan T.

Obter o texto integral Obter o texto integral Obter o texto integral

Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes Por Rucker, Janet C., Webb, Bryn D., Frempong, Tamiesha, Gaspar, Harald, Naidich, Thomas P., Jabs, Ethylin Wang

Obter o texto integral Obter o texto integral Obter o texto integral

Mirror Movements Identified in Patients with Moebius Syndrome Por Webb, Bryn D., Frempong, Tamiesha, Naidich, Thomas P., Gaspar, Harald, Jabs, Ethylin Wang, Rucker, Janet C.

Obter o texto integral Obter o texto integral Obter o texto integral

Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex Por Motch Perrine, Susan M., Wu, Meng, Holmes, Greg, Bjork, Bryan C., Jabs, Ethylin Wang, Richtsmeier, Joan T.

Obter o texto integral Obter o texto integral Obter o texto integral

The Paternal-Age Effect in Apert Syndrome Is Due, in Part, to the Increased Frequency of Mutations in Sperm Por Glaser, Rivka L., Broman, Karl W., Schulman, Rebecca L., Eskenazi, Brenda, Wyrobek, Andrew J., Jabs, Ethylin Wang

Obter o texto integral Obter o texto integral

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice Por Motch Perrine, Susan M, Cole, Theodore M, Martínez-Abadías, Neus, Aldridge, Kristina, Jabs, Ethylin Wang, Richtsmeier, Joan T

Obter o texto integral Obter o texto integral Obter o texto integral

Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public Por Sanderson, Saskia C., Suckiel, Sabrina A., Zweig, Micol, Bottinger, Erwin P., Jabs, Ethylin Wang, Richardson, Lynne D.

Obter o texto integral Obter o texto integral Obter o texto integral

C-type natriuretic peptide analog treatment of craniosynostosis in a Crouzon syndrome mouse model Por Holmes, Greg, Zhang, Lening, Rivera, Joshua, Murphy, Ryan, Assouline, Claudia, Sullivan, Lorraine, Oppeneer, Todd, Jabs, Ethylin Wang

Obter o texto integral Obter o texto integral Obter o texto integral

TISSUE SPECIFIC RESPONSES TO ABERRANT FGF SIGNALING IN COMPLEX HEAD PHENOTYPES Por Martínez-Abadías, Neus, Motch, Susan M., Pankratz, Talia L., Wang, Yingli, Aldridge, Kristina, Jabs, Ethylin Wang, Richtsmeier, Joan T.

Obter o texto integral Obter o texto integral Obter o texto integral