A citation-based method for searching scientific literature

E A Lindsay, A Botta, V Jurecic, S Carattini-Rivera, Y C Cheah, H M Rosenblatt, A Bradley, A Baldini. Nature 1999
Times Cited: 299



Zhen Zhang, Tuong Huynh, Antonio Baldini. Development 2006
Times Cited: 126




List of shared articles



Times cited

Importance of endothelial Hey1 expression for thoracic great vessel development and its distal enhancer for Notch-dependent endothelial transcription.
Yusuke Watanabe, Daiki Seya, Dai Ihara, Shuhei Ishii, Taiki Uemoto, Atsushi Kubo, Yuji Arai, Yoshie Isomoto, Atsushi Nakano, Takaya Abe,[...]. J Biol Chem 2020
1

Importance of endothelial Hey1 expression for thoracic great vessel development and its distal enhancer for Notch-dependent endothelial transcription.
Yusuke Watanabe, Daiki Seya, Dai Ihara, Shuhei Ishii, Taiki Uemoto, Atsushi Kubo, Yuji Arai, Yoshie Isomoto, Atsushi Nakano, Takaya Abe,[...]. J Biol Chem 2020
0


Failed Progenitor Specification Underlies the Cardiopharyngeal Phenotypes in a Zebrafish Model of 22q11.2 Deletion Syndrome.
Burcu Guner-Ataman, Juan Manuel González-Rosa, Harsh N Shah, Vincent L Butty, Spencer Jeffrey, Maryline Abrial, Laurie A Boyer, C Geoffrey Burns, Caroline E Burns. Cell Rep 2018
9

Temporally Distinct Six2-Positive Second Heart Field Progenitors Regulate Mammalian Heart Development and Disease.
Zhengfang Zhou, Jingying Wang, Chaoshe Guo, Weiting Chang, Jian Zhuang, Ping Zhu, Xue Li. Cell Rep 2017
28

SDF1-CXCR4 signaling: A new player involved in DiGeorge/22q11-deletion syndrome.
Jean-Loup Duband, Sophie Escot, Claire Fournier-Thibault. Rare Dis 2016
4

p53 Suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome.
Cinzia Caprio, Antonio Baldini. Proc Natl Acad Sci U S A 2014
21

Jun is required in Isl1-expressing progenitor cells for cardiovascular development.
Tao Zhang, Junchen Liu, Jue Zhang, Eldhose B Thekkethottiyil, Timothy L Macatee, Fraz A Ismat, Fen Wang, Jason Z Stoller. PLoS One 2013
8

The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.
Irinna Papangeli, Peter Scambler. Wiley Interdiscip Rev Dev Biol 2013
41

Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome.
Shan Gao, Xiao Li, Brad A Amendt. Curr Allergy Asthma Rep 2013
20

Tbx1, subpulmonary myocardium and conotruncal congenital heart defects.
Pauline Parisot, Karim Mesbah, Magali ThĂ©veniau-Ruissy, Robert G Kelly. Birth Defects Res A Clin Mol Teratol 2011
29


Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21.
Huojun Cao, Sergio Florez, Melanie Amen, Tuong Huynh, Ziedonis Skobe, Antonio Baldini, Brad A Amendt. Dev Biol 2010
29