[1] | China joint committee on cardiovascular risk assessment and management guidelines. China cardiovascular risk assessment and management guidelines. Chin Circul J, 2019,34(1):4-28. | [1] | 中国心血管病风险评估和管理指南编写联合委员会. 中国心血管病风险评估和管理指南. 中国循环杂志, 2019,34(1):4-28. | [2] | Chen WW, Gao RL, Liu LS, Zhu ML, Wang W, Wang YJ, Wu ZS, Li HJ, Gu DF, Yang YJ, Zheng Z, Jiang LX, Hu SS . Summary of china cardiovascular disease report 2017. Chin Circul J, 2018,33(1):1-8. | [2] | 陈伟伟, 高润霖, 刘力生, 朱曼璐, 王文, 王拥军, 吴兆苏, 李惠君, 顾东风, 杨跃进, 郑哲, 蒋立新, 胡盛寿 . 《中国心血管病报告2017》概要. 中国循环杂志, 2018,33(1):1-8. | [3] | Afouda BA, Lynch AT, de Paiva Alves E, Hoppler S . Genome-wide transcriptomics analysis of genes regulated by GATA4, 5 and 6 during cardiomyogenesis in Xenopus laevis . Data Brief, 2018,17:559-563. | [4] | Lowry JA, Atchley WR . Molecular evolution of the GATA family of transcription factors: conservation within the DNA-binding domain . J Mol Evol, 2000,50(2):103-115. | [5] | Fujiwara T . GATA transcription factors: basic principles and related human disorders. Tohoku J Exp Med, 2017,242(2):83-91. | [6] | Tremblay M, Sanchez-Ferras O, Bouchard M . GATA transcription factors in development and disease. Development, 2018, 145(20) pii:dev164384. | [7] | Suzuki E, Evans T, Lowry J, Truong L, Bell DW, Testa JR, Walsh K . The human GATA-6Gene: structure, chromosomal location, and regulation of expression by tissue-specific and mitogen-responsive signals . Genomics, 1996,38(3):283-290. | [8] | Chou HH, Chiou MJ, Liang FW, Chen LH, Lu TH, Li CY . Association of maternal chronic disease with risk of congenital heart disease in offspring . CMAJ, 2016,188(17-18):E438-E446. | [9] | Maitra M, Koenig SN, Srivastava D, Garg V . Identification of GATA6 sequence variants in patients with congenital heart defects. Pediatr Res, 2010,68(4):281-285. | [10] | Yu L, Bennett JT, Wynn J, Carvill GL, Cheung YH, Shen Y, Mychaliska GB, Azarow KS, Crombleholme TM, Chung DH, Potoka D, Warner BW, Bucher B, Lim FY, Pietsch J, Stolar C, Aspelund G, Arkovitz MS, University of Washington Center for Mendelian Genomics, Mefford H, Chung WK . Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia . J Med Genet, 2014,51(3):197-202. | [11] | Lin X, Huo Z, Liu X, Zhang Y, Li L, Zhao H, Yan B, Liu Y, Yang Y, Chen YH . A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect . J Hum Genet, 2010,55(10):662-667. | [12] | Li C, Li X, Pang S, Chen W, Qin X, Huang W, Zeng C, Yan B . Novel and functional DNA sequence variants within the GATA6 gene promoter in ventricular septal defects . Int J Mol Sci, 2014,15(7):12677-12687.
|
[1] |
Juan Huang, Wenhua Miao, Xiaofeng Guo, Wei Ji.
Diagnosis and genetic testing analysis of limb-girdle muscular dystrophy type 2U caused by a compound heterozygous mutation in the ISPD gene
[J]. Hereditas(Beijing), 2023, 45(6): 536-542.
|
[2] |
Shaozheng Song, Zhengyi He, Yong Cheng, Baoli Yu, Ting Zhang, Dan Li.
MSTN modification in goat mediated by TALENs and performance analysis
[J]. Hereditas(Beijing), 2022, 44(6): 531-542.
|
[3] |
Yuan Zhang, Yuting Zhao, Lenan Zhuang, Jin He.
Transcriptional regulation of transcriptional Mediator complexes in cardiovascular development and disease
[J]. Hereditas(Beijing), 2022, 44(5): 383-397.
|
[4] |
Ruizhi Jiajue, Cheng Xiao, Yiwen Liu, Ran Li, Huabing Zhang, Miao Yu.
Diagnosis, treatment and genetic analysis of two cases of congenital hyperinsulinemic hypoglycemia caused by GCK gene mutation
[J]. Hereditas(Beijing), 2022, 44(11): 1056-1062.
|
[5] |
Cheng Xiao, Jieying Liu, Chunru Yang, Miao Yu.
Advances in lipodystrophy syndrome caused by LMNA gene mutation
[J]. Hereditas(Beijing), 2022, 44(10): 913-925.
|
[6] |
Nan Li, Yajuan Li, Haibin Guo, Xiangqian Zhang.
Design and exploration of genetic comprehensive experiments based on Ds insertion mutants
[J]. Hereditas(Beijing), 2019, 41(12): 1148-1155.
|
[7] |
Furu Xu, Wenjun Jiang, Tao Zhang, Qian Jiang, Ruixue Zhang, Hongsheng Bi.
Fibrillin-2 gene mutations associated with hereditary connective tissue diseases
[J]. Hereditas(Beijing), 2019, 41(10): 919-927.
|
[8] |
Yongyu Wang,Wei Yu,Bin Zhou.
Hippo signaling pathway in cardiovascular development and diseases
[J]. Hereditas(Beijing), 2017, 39(7): 576-587.
|
[9] |
Liu Yuqing, Zhu Xiong, Li Shujin, Yang Yeming, Yang Mu, Zhao Peiquan, Zhu Xianjun.
Identification of LRP5 mutations in families with familial exudative vitreoretinopathy
[J]. Hereditas(Beijing), 2017, 39(3): 241-249.
|
[10] |
Yongxin Zou,Yaoqin Gong.
Aberrant RNA splicing as the molecular basis of some pathogenic variants
[J]. Hereditas(Beijing), 2017, 39(3): 200-207.
|
[11] |
Lijuan Cao,Xinhe Liu,Qing Zha,Qian Song,Ke Yang,Yan Liu.
The relationship of SIRT3 with cellular metabolism and cardiovascular diseases
[J]. HEREDITAS(Beijing), 2015, 37(2): 111-120.
|
[12] |
Shuai Sun, Yuliang Deng.
Single-cell detection of EGFR gene mutation in circulating tumor cells in lung cancer
[J]. HEREDITAS(Beijing), 2015, 37(12): 1251-1257.
|
[13] |
.
The selection of 30 ancestry informative markers and its application in ancestry inference
[J]. HEREDITAS(Beijing), 2014, 36(8): 779-785.
|
[14] |
Yalan Liu, Hua Zhang, Yong Feng.
Progress in the study of syndromic hearing loss resulted from neural crest abnormalities
[J]. HEREDITAS(Beijing), 2014, 36(11): 1131-1144.
|
[15] |
HE Yi-Qun, XU Mei-Fen, YU Han, GENG Jun-Wei, SHI Su-Xue, XUE Ling, LU Zhong-Qiu, GUAN Min-Xin.
Research progress in heritable dyslipidemia
[J]. HEREDITAS, 2013, 35(11): 1237-1243.
|
|
Viewed |
|
|
|
Full text
|
|
|
|
|
Abstract
|
|
|
|
|
|
|
|