Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic disease

Por Rasouly, Hila Milo, Kumar, Sudhir, Chan, Stefanie, Pisarek-Horowitz, Anna, Sharma, Richa, Xi, Qiongchao J., Nishizaki, Yuriko, Higashi, Yujiro, Salant, David J., Maas, Richard L., Lu, Weining
Publicado no Kidney Int (2016)

Pax6- and Six3-Mediated Induction of Lens Cell Fate in Mouse and Human ES Cells

Por Anchan, Raymond M., Lachke, Salil A., Gerami-Naini, Behzad, Lindsey, Jennifer, Ng, Nicholas, Naber, Catherine, Nickerson, Michael, Cavallesco, Resy, Rowan, Sheldon, Eaton, Jennifer L., Xi, Qiongchao, Maas, Richard L.
Publicado no PLoS One (2014)

Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis(†)

Por Mukherjee, Kusumika, Ishii, Kana, Pillalamarri, Vamsee, Kammin, Tammy, Atkin, Joan F., Hickey, Scott E., Xi, Qiongchao J., Zepeda, Cinthya J., Gusella, James F., Talkowski, Michael E., Morton, Cynthia C., Maas, Richard L., Liao, Eric C.
Publicado no Hum Mol Genet (2016)

Crim1 regulates integrin signaling in murine lens development

Por Zhang, Ying, Fan, Jieqing, Ho, Joshua W. K., Hu, Tommy, Kneeland, Stephen C., Fan, Xueping, Xi, Qiongchao, Sellarole, Michael A., de Vries, Wilhelmine N., Lu, Weining, Lachke, Salil A., Lang, Richard A., John, Simon W. M., Maas, Richard L.
Publicado no Development (2016)

The Cell-Adhesion Gene PVRL3 is Associated with Congenital Ocular Defects

Por Lachke, Salil A., Higgins, Anne W., Inagaki, Maiko, Saadi, Irfan, Xi, Qiongchao, Long, Michelle, Quade, Bradley J., Talkowski, Michael E., Gusella, James F., Fujimoto, Atsuko, Robinson, Michael L., Yang, Ying, Duong, Quynh T., Shapira, Irit, Motro, Benny, Miyoshi, Jun, Takai, Yoshimi, Morton, Cynthia C., Maas, Richard L.
Publicado em 2011

MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus

Por Quintero-Rivera, Fabiola, Xi, Qiongchao J., Keppler-Noreuil, Kim M., Lee, Ji Hyun, Higgins, Anne W., Anchan, Raymond M., Roberts, Amy E., Seong, Ihn Sik, Fan, Xueping, Lage, Kasper, Lu, Lily Y., Tao, Joanna, Hu, Xuchen, Berezney, Ronald, Gelb, Bruce D., Kamp, Anna, Moskowitz, Ivan P., Lacro, Ronald V., Lu, Weining, Morton, Cynthia C., Gusella, James F., Maas, Richard L.
Publicado no Hum Mol Genet (2015)

Disruption of ROBO2 Is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux

Por Lu, Weining, van Eerde, Albertien M., Fan, Xueping, Quintero-Rivera, Fabiola, Kulkarni, Shashikant, Ferguson, Heather, Kim, Hyung-Goo, Fan, Yanli, Xi, Qiongchao, Li, Qing-gang, Sanlaville, Damien, Andrews, William, Sundaresan, Vasi, Bi, Weimin, Yan, Jiong, Giltay, Jacques C., Wijmenga, Cisca, de Jong, Tom P. V. M., Feather, Sally A., Woolf, Adrian S., Rao, Yi, Lupski, James R., Eccles, Michael R., Quade, Bradley J., Gusella, James F., Morton, Cynthia C., Maas, Richard L.
Publicado em 2007

NFIA Haploinsufficiency Is Associated with a CNS Malformation Syndrome and Urinary Tract Defects

Por Lu, Weining, Quintero-Rivera, Fabiola, Fan, Yanli, Alkuraya, Fowzan S, Donovan, Diana J, Xi, Qiongchao, Turbe-Doan, Annick, Li, Qing-Gang, Campbell, Craig G, Shanske, Alan L, Sherr, Elliott H, Ahmad, Ayesha, Peters, Roxana, Rilliet, Benedict, Parvex, Paloma, Bassuk, Alexander G, Harris, David J, Ferguson, Heather, Kelly, Chantal, Walsh, Christopher A, Gronostajski, Richard M, Devriendt, Koenraad, Higgins, Anne, Ligon, Azra H, Quade, Bradley J, Morton, Cynthia C, Gusella, James F, Maas, Richard L
Publicado em 2007