| Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development Z Zhang, T Huynh, A Baldini Development 133 (18), 3587-3595, 2006 | 218 | 2006 |
| Subepicardial endothelial cells invade the embryonic ventricle wall to form coronary arteries X Tian, T Hu, H Zhang, L He, X Huang, Q Liu, W Yu, L He, Z Yang, ... Cell research 23 (9), 1075, 2013 | 198 | 2013 |
| Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development Z Zhang, F Cerrato, H Xu, F Vitelli, M Morishima, J Vincentz, Y Furuta, ... Development 132 (23), 5307-5315, 2005 | 144 | 2005 |
| In vivo response to high-resolution variation of Tbx1 mRNA dosage Z Zhang, A Baldini Human molecular genetics 17 (1), 150-157, 2007 | 125 | 2007 |
| Wdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeleton C Cui, B Chatterjee, TP Lozito, Z Zhang, RJ Francis, H Yagi, LM Swanhart, ... PLoS biology 11 (11), e1001720, 2013 | 108 | 2013 |
| Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm A Dastjerdi, L Robson, R Walker, J Hadley, Z Zhang, ... Developmental dynamics: an official publication of the American Association …, 2007 | 82 | 2007 |
| Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy Z Zhang, D Alpert, R Francis, B Chatterjee, Q Yu, T Tansey, SL Sabol, ... Proceedings of the National Academy of Sciences 106 (9), 3219-3224, 2009 | 80 | 2009 |
| Rebalancing gene haploinsufficiency in vivo by targeting chromatin FG Fulcoli, M Franzese, X Liu, Z Zhang, C Angelini, A Baldini Nature communications 7, 11688, 2016 | 73 | 2016 |
| Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells H Xu, A Viola, Z Zhang, CP Gerken, EA Lindsay-Illingworth, A Baldini Developmental biology 302 (2), 670-682, 2007 | 64 | 2007 |
| Early thyroid development requires a Tbx1–Fgf8 pathway G Lania, Z Zhang, T Huynh, C Caprio, AM Moon, F Vitelli, A Baldini Developmental biology 328 (1), 109-117, 2009 | 54 | 2009 |
| Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants F Vitelli, Z Zhang, T Huynh, A Sobotka, A Mupo, A Baldini Developmental biology 295 (2), 559-570, 2006 | 51 | 2006 |
| Tbx1 is a negative modulator of Mef2c LS Pane, Z Zhang, R Ferrentino, T Huynh, L Cutillo, A Baldini Human molecular genetics 21 (11), 2485-2496, 2012 | 50 | 2012 |
| Bach2 deficiency leads to spontaneous expansion of IL-4-producing T follicular helper cells and autoimmunity H Zhang, Q Hu, M Zhang, F Yang, C Peng, Z Zhang, C Huang Frontiers in immunology 10, 2050, 2019 | 42 | 2019 |
| Familial Nonsyndromic Patent Ductus Arteriosus Caused by Mutations in TFAP2B YW Chen, W Zhao, ZF Zhang, Q Fu, J Shen, Z Zhang, W Ji, J Wang, F Li Pediatric cardiology 32 (7), 958-965, 2011 | 38 | 2011 |
| Inhibition of autophagy potentiates the efficacy of Gli inhibitor GANT-61 in MYCN-amplified neuroblastoma cells J Wang, S Gu, J Huang, S Chen, Z Zhang, M Xu BMC cancer 14 (1), 768, 2014 | 33 | 2014 |
| An Avascular Niche Created by Axitinib‐Loaded PCL/Collagen Nanofibrous Membrane Stabilized Subcutaneous Chondrogenesis of Mesenchymal Stromal Cells TJ Ji, B Feng, J Shen, M Zhang, YQ Hu, AX Jiang, DQ Zhu, YW Chen, W Ji, ... Advanced Science 8 (20), 2100351, 2021 | 28 | 2021 |
| Lmod2 piggyBac mutant mice exhibit dilated cardiomyopathy S Li, K Mo, H Tian, C Chu, S Sun, L Tian, S Ding, T Li, X Wu, F Liu, ... Cell & bioscience 6 (1), 38, 2016 | 26 | 2016 |
| A neonatal rat model of increased right ventricular afterload by pulmonary artery banding S Wang, L Ye, H Hong, C Tang, M Li, Z Zhang, J Liu The Journal of thoracic and cardiovascular surgery 154 (5), 1734-1739, 2017 | 20 | 2017 |
| The protective autophagy activated by GANT-61 in MYCN amplified neuroblastoma cells is mediated by PERK J Wang, S Huang, R Tian, J Chen, H Gao, C Xie, Y Shan, Z Zhang, S Gu, ... Oncotarget 9 (18), 14413, 2018 | 18 | 2018 |
| A gain-of-function ACTC1 3′ UTR mutation that introduces a miR-139-5p target site may be associated with a dominant familial atrial septal defect Y Wang, X Du, Z Zhou, J Jiang, Z Zhang, L Ye, H Hong Scientific reports 6, 25404, 2016 | 16 | 2016 |
