Correction: PIAS1 Is a GATA4 SUMO Ligase That Regulates GATA4-Dependent Intestinal Promoters Independent of SUMO Ligase Activity and GATA4 Sumoylation

Por Belaguli, Narasimhaswamy S., Zhang, Mao, Hernández-Garcia, Andrés, Berger, David H.
Publicado em 2012

P2Y2 purinergic receptor activation is essential for efficient hepatocyte proliferation in response to partial hepatectomy

Por Tackett, Bryan C., Sun, Hongdan, Mei, Yu, Maynard, Janielle P., Cheruvu, Sayuri, Mani, Arunmani, Hernandez-Garcia, Andres, Vigneswaran, Nadarajah, Karpen, Saul J., Thevananther, Sundararajah
Publicado no Am J Physiol Gastrointest Liver Physiol (2014)

Novel Frem1-Related Mouse Phenotypes and Evidence of Genetic Interactions with Gata4 and Slit3

Por Beck, Tyler F., Shchelochkov, Oleg A., Yu, Zhiyin, Kim, Bum Jun, Hernández-García, Andrés, Zaveri, Hitisha P., Bishop, Colin, Overbeek, Paul A., Stockton, David W., Justice, Monica J., Scott, Daryl A.
Publicado em 2013

An Allelic Series of Mice Reveals a Role for RERE in the Development of Multiple Organs Affected in Chromosome 1p36 Deletions

Por Kim, Bum Jun, Zaveri, Hitisha P., Shchelochkov, Oleg A., Yu, Zhiyin, Hernández-García, Andrés, Seymour, Michelle L., Oghalai, John S., Pereira, Fred A., Stockton, David W., Justice, Monica J., Lee, Brendan, Scott, Daryl A.
Publicado em 2013

ATP release after partial hepatectomy regulates liver regeneration in the rat

Por Gonzales, Emmanuel, Julien, Boris, Serrière-Lanneau, Valérie, Nicou, Alexandra, Doignon, Isabelle, Lagoudakis, Laura, Garcin, Isabelle, Azoulay, Daniel, Duclos-Vallée, Jean-Charles, Castaing, Denis, Samuel, Didier, Hernandez-Garcia, Andres, Awad, Samir S., Combettes, Laurent, Thevananther, Sundararajah, Tordjmann, Thierry
Publicado em 2009

Identification of Critical Regions and Candidate Genes for Cardiovascular Malformations and Cardiomyopathy Associated with Deletions of Chromosome 1p36

Por Zaveri, Hitisha P., Beck, Tyler F., Hernández-García, Andrés, Shelly, Katharine E., Montgomery, Tara, van Haeringen, Arie, Anderlid, Britt-Marie, Patel, Chirag, Goel, Himanshu, Houge, Gunnar, Morrow, Bernice E., Cheung, Sau Wai, Lalani, Seema R., Scott, Daryl A.
Publicado em 2014

Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1

Por Wat, Margaret J., Beck, Tyler F., Hernández-García, Andrés, Yu, Zhiyin, Veenma, Danielle, Garcia, Monica, Holder, Ashley M., Wat, Jeanette J., Chen, Yuqing, Mohila, Carrie A., Lally, Kevin P., Dickinson, Mary, Tibboel, Dick, de Klein, Annelies, Lee, Brendan, Scott, Daryl A.
Publicado em 2012

FBN1 Contributing to Familial Congenital Diaphragmatic Hernia

Por Beck, Tyler F., Campeau, Philippe M., Jhangiani, Shalini N., Gambin, Tomasz, Li, Alexander H., Abo-Zahrah, Reem, Jordan, Valerie K., Hernandez-Garcia, Andres, Wiszniewski, Wojciech K., Muzny, Donna, Gibbs, Richard A., Boerwinkle, Eric, Lupski, James R., Lee, Brendan, Reardon, Willie, Scott, Daryl A.
Publicado no Am J Med Genet A (2015)

De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions

Por Fregeau, Brieana, Kim, Bum Jun, Hernández-García, Andrés, Jordan, Valerie K., Cho, Megan T., Schnur, Rhonda E., Monaghan, Kristin G., Juusola, Jane, Rosenfeld, Jill A., Bhoj, Elizabeth, Zackai, Elaine H., Sacharow, Stephanie, Barañano, Kristin, Bosch, Daniëlle G.M., de Vries, Bert B.A., Lindstrom, Kristin, Schroeder, Audrey, James, Philip, Kulch, Peggy, Lalani, Seema R., van Haelst, Mieke M., van Gassen, Koen L.I., van Binsbergen, Ellen, Barkovich, A. James, Scott, Daryl A., Sherr, Elliott H.
Publicado no Am J Hum Genet (2016)