검색결과 : 12건
| No. | Article |
|---|---|
| 1 |
Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients Dianatpour S, Khatami M, Heidari MM, Hadadzadeh M Applied Biochemistry and Biotechnology, 190(3), 896, 2020 |
| 2 |
Notch1 signaling mediated dysfunction of bone marrow mesenchymal stem cells derived from cyanotic congenital heart disease Wang TT, Xing JY, Ying YQ, Tang H, Li J, Wei YJ, Zhang H Biochemical and Biophysical Research Communications, 527(4), 847, 2020 |
| 3 |
Maternal exosomes in diabetes contribute to the cardiac development deficiency Shi RJ, Zhao LB, Cai WB, Wei MY, Zhou XY, Yang GD, Yuan LJ Biochemical and Biophysical Research Communications, 483(1), 602, 2017 |
| 4 |
Novel and Functional DNA Sequence Variants within the GATA6 Gene Promoter in Ventricular Septal Defects Li CY, Li XK, Pang SC, Chen W, Qin XY, Huang WH, Zeng CQ, Yan B International Journal of Molecular Sciences, 15(7), 12677, 2014 |
| 5 |
Analysis of MTHFR and MTRR Gene Polymorphisms in Iranian Ventricular Septal Defect Subjects Pishva SR, Vasudevan R, Etemad A, Heidari F, Komara M, Ismail P, Othman F, Karimi A, Sabri MR International Journal of Molecular Sciences, 14(2), 2739, 2013 |
| 6 |
CITED2 mutation links congenital heart defects to dysregulation of the cardiac gene VEGF and PITX2C expression Li Q, Pan H, Guan L, Su DM, Ma X Biochemical and Biophysical Research Communications, 423(4), 895, 2012 |
| 7 |
Genetic analysis of the SIRT1 gene promoter in ventricular septal defects Shan JP, Pang SC, Wanyan HX, Xie W, Qin XY, Yan B Biochemical and Biophysical Research Communications, 425(4), 741, 2012 |
| 8 |
Corticosteroid enhances heme oxygenase-1 production by circulating monocytes by up-regulating hemoglobin scavenger receptor and amplifying the receptor-mediated uptake of hemoglobin-haptoglobin complex Yamazaki H, Ohta K, Tsukiji H, Toma T, Hashida Y, Ishizaki A, Saito T, Arai S, Koizumi S, Yachie A Biochemical and Biophysical Research Communications, 358(2), 506, 2007 |
| 9 |
Human chromosome 21q22.2-qter carries a gene(s) responsible for downregulation of mlc2a and PEBP in Down syndrome model mice Kazuki Y, Kimura M, Nishigaki R, Kai Y, Abe S, Okita C, Shirayoshi Y, Schulz TC, Tomizuka K, Hanaoka K, Inoue T, Oshimura M Biochemical and Biophysical Research Communications, 317(2), 491, 2004 |
| 10 |
An extra human chromosome 21 reduces mlc-2a expression in chimeric mice and Down syndrome Nishigaki R, Shinohara T, Toda T, Omori A, Ichinose S, Itoh M, Shirayoshi Y, Kurimasa A, Oshimura M Biochemical and Biophysical Research Communications, 295(1), 112, 2002 |