Resultats de la cerca - Xi, Qiongchao

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

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

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

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

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

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

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

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