12967_2020_2445_MOESM1_ESM.docx (522.81 kB)
Additional file 1 of Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defects
journal contribution
posted on 2020-08-08, 03:28 authored by Shuang Zhou, Qingjie Wang, Zhuo Meng, Jiayu Peng, Yue Zhou, Wenting Song, Jian Wang, Sun Chen, Kun SunAdditional file 1: Table S1. Primer pairs used to amplify the coding regions contain candidate variants. Table S2. Primer pairs used to screen of downstream target genes of FGF8 and FGF10. Figure S1. Cardiac ultrasound results in patients. A and B Echocardiography of a patient with TOF labeled F150, C Echocardiography of a patient with single atrium and single ventricle labeled S033. Figure S2. Screening of downstream target genes of FGF8 and FGF10. A and C Screening of downstream target genes of FGF8 in human cardiomyocytes and HEK293T cells, B and D Screening of downstream target genes of FGF10 in human cardiomyocytes and HEK293T cells (n = 3). GAPDH was used as an internal control.