Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome
Hasten, Erica, McDonald-McGinn, Donna M, Crowley, Terrence B, Zackai, Elaine, Emanuel, Beverly S, Morrow, Bernice E, Racedo, Silvia E
Published in Human molecular genetics (01.06.2018)
Published in Human molecular genetics (01.06.2018)
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Journal Article
Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome
Racedo, Silvia E, Hasten, Erica, Lin, Mingyan, Devakanmalai, Gnanapackiam Sheela, Guo, Tingwei, Ozbudak, Ertugrul M, Cai, Chen-Leng, Zheng, Deyou, Morrow, Bernice E
Published in PLoS genetics (01.03.2017)
Published in PLoS genetics (01.03.2017)
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Journal Article
Development of an Image-Based HCS-Compatible Method for Endothelial Barrier Function Assessment
Dubrovskyi, Oleksii, Hasten, Erica, Dudek, Steven M., Flavin, Michael T., Chan, Leo Li-Ying
Published in SLAS discovery (01.10.2021)
Published in SLAS discovery (01.10.2021)
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Journal Article
Reduced dosage of [beta]-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome
Racedo, Silvia E, Hasten, Erica, Lin, Mingyan, Devakanmalai, Gnanapackiam Sheela, Guo, Tingwei, Ozbudak, Ertugrul M, Cai, Chen-Leng, Zheng, Deyou, Morrow, Bernice E
Published in PLoS genetics (27.03.2017)
Published in PLoS genetics (27.03.2017)
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Journal Article