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

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

Prickle1 regulates differentiation of frontal bone osteoblasts

por Wan, Yong, Lantz, Brandi, Cusack, Brian J., Szabo-Rogers, Heather L.
Publicado no Sci Rep (2018)

Localization of Tfap2β, Casq2, Penk, Zic1, and Zic3 Expression in the Developing Retina, Muscle, and Sclera of the Embryonic Mouse Eye

por Wan, Yong, White, Casey, Robert, Nadine, Rogers, Matthew B., Szabo-Rogers, Heather L.
Publicado no J Histochem Cytochem (2019)

Growth factor signaling alters the morphology of the zebrafish ethmoid plate

por Cusack, Brian J., Parsons, Trish E., Weinberg, Seth M., Vieira, Alexandre R., Szabo‐Rogers, Heather L.
Publicado no J Anat (2017)

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 no Genes (Basel) (2020)

Neural crest origin of olfactory ensheathing glia

por Barraud, Perrine, Seferiadis, Anastasia A., Tyson, Luke D., Zwart, Maarten F., Szabo-Rogers, Heather L., Ruhrberg, Christiana, Liu, Karen J., Baker, Clare V. H.
Publicado em 2010

Accelerated enamel mineralization in Dspp mutant mice

por Verdelis, Kostas, Szabo-Rogers, Heather L., Xu, Yang, Chong, Rong, Kang, Ryan, Cusack, Brian J., Jani, Priyam, Boskey, Adele L., Qin, Chunlin, Beniash, Elia
Publicado no Matrix Biol (2016)

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 em 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 em 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 no Biol Open (2016)