Frontal Bone Insufficiency in Gsk3β Mutant Mice

por Szabo-Rogers, Heather, Yakob, Wardati, Liu, Karen J.
Publicado 2016

Novel Reporter Alleles of GSK-3α and GSK-3β

por Barrell, William B., Szabo-Rogers, Heather L., Liu, Karen J.
Publicado 2012

Prickle1 regulates differentiation of frontal bone osteoblasts

por Wan, Yong, Lantz, Brandi, Cusack, Brian J., Szabo-Rogers, Heather L.
Publicado 2018

Trps1 Regulates Development of Craniofacial Skeleton and Is Required for the Initiation of Palatal Shelves Fusion

por Cho, Kah Yan, Kelley, Brian P., Monier, Daisy, Lee, Brendan, Szabo-Rogers, Heather, Napierala, Dobrawa
Publicado 2019

Finding the Unicorn, a New Mouse Model of Midfacial Clefting

por Lantz, Brandi, White, Casey, Liu, Xinyun, Wan, Yong, Gabriel, George, Lo, Cecilia W. Y., Szabo-Rogers, Heather L.
Publicado 2020

The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis, and mouse embryonic development

por Gray, Ryan S., Abitua, Philip B., Wlodarczyk, Bogdan J., Szabo-Rogers, Heather L., Blanchard, Otis, Lee, Insuk, Weiss, Greg S., Liu, Karen J., Marcotte, Edward M., Wallingford, John B., Finnell, Richard H.
Publicado 2009

Fuz Mutant Mice Reveal Shared Mechanisms between Ciliopathies and FGF-Related Syndromes

por Tabler, Jacqueline M., Barrell, William B., Szabo-Rogers, Heather L., Healy, Christopher, Yeung, Yvonne, Perdiguero, Elisa Gomez, Schulz, Christian, Yannakoudakis, Basil Z., Mesbahi, Aida, Wlodarczyk, Bogdan, Geissmann, Frederic, Finnell, Richard H., Wallingford, John B., Liu, Karen J.
Publicado 2013

Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects

por Gibbs, Brian C., Damerla, Rama Rao, Vladar, Eszter K., Chatterjee, Bishwanath, Wan, Yong, Liu, Xiaoqin, Cui, Cheng, Gabriel, George C., Zahid, Maliha, Yagi, Hisato, Szabo-Rogers, Heather L., Suyama, Kaye L., Axelrod, Jeffrey D., Lo, Cecilia W.
Publicado 2016

PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits

por Liu, Dongjing, Ban, Hyo-Jeong, El Sergani, Ahmed M., Lee, Myoung Keun, Hecht, Jacqueline T., Wehby, George L., Moreno, Lina M., Feingold, Eleanor, Marazita, Mary L., Cha, Seongwon, Szabo-Rogers, Heather L., Weinberg, Seth M., Shaffer, John R.
Publicado 2021

Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape

por Goovaerts, Seppe, Hoskens, Hanne, Eller, Ryan J., Herrick, Noah, Musolf, Anthony M., Justice, Cristina M., Yuan, Meng, Naqvi, Sahin, Lee, Myoung Keun, Vandermeulen, Dirk, Szabo-Rogers, Heather L., Romitti, Paul A., Boyadjiev, Simeon A., Marazita, Mary L., Shaffer, John R., Shriver, Mark D., Wysocka, Joanna, Walsh, Susan, Weinberg, Seth M., Claes, Peter
Publicado 2023