Zobrazeno 1 - 7
of 7
pro vyhledávání: '"ZHAO LI"'
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Abstract Background Thoracic aortic aneurysm and dissection (TAAD) is a common condition associated with high mortality. It is predominantly inherited in an autosomal dominant manner with reduced penetrance and variable expression. The genetic basis
Externí odkaz:
https://doaj.org/article/b16d84731be2409fa6a41def0a520acb
Publikováno v:
Stem Cells International, Vol 2021 (2021)
Myocardial infarction (MI) is a devastating disease with high morbidity and mortality caused by the irreversible loss of functional cardiomyocytes and heart failure (HF) due to the restricted blood supply. Mesenchymal stem cells (MSCs) have been emer
Externí odkaz:
https://doaj.org/article/8a31c77d5a5a432bb8339ccc4846a3fa
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disorder characterized by progressive cyst formation and expansion in the kidneys, which culminates in end-stage renal disease. Aortic dissec
Externí odkaz:
https://doaj.org/article/16d5aa6855974b949824f17c3bca2f2c
Publikováno v:
Cardiovascular Diabetology; 2013, Vol. 12 Issue 1, p1-7, 7p, 2 Charts, 4 Graphs
Autor:
Jiang Fuman, Ren Jinghui, Chen Fang, Zhou Yuqiu, Xie Jiansheng, Dan Shan, Su Yue, Xie Jianhong, Yin Baomin, Su Wen, Zhang Huakun, Wang Wei, Chai Xianghua, Lin Linhua, Guo Hui, Li Qiyun, Li Peipei, Yuan Yuying, Pan Xiaoyu, Li Yihan, Liu Lifu, Chen Huifei, Xuan Zhaoling, Chen Shengpei, Zhang Chunlei, Zhang Hongyun, Tian Zhongming, Zhang Zhengyu, Jiang Hui, Zhao Lijian, Zheng Weimou, Li Songgang, Li Yingrui, Wang Jun, Wang Jian, Zhang Xiuqing
Publikováno v:
BMC Medical Genomics, Vol 5, Iss 1, p 57 (2012)
Abstract Background Conventional prenatal screening tests, such as maternal serum tests and ultrasound scan, have limited resolution and accuracy. Methods We developed an advanced noninvasive prenatal diagnosis method based on massively parallel sequ
Externí odkaz:
https://doaj.org/article/3c0f0ca4528b46b4aea5e1aefe12a75f
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 77 (2012)
Abstract Background 5,10-methylenetetrahydrofolate reductase (MTHFR) variants, C677T and A1298C, have been reported to be associated with decreased risk of acute lymphoblastic leukemia (ALL). However, results derived from individually underpowered st
Externí odkaz:
https://doaj.org/article/34190c3dce9a4738b6c0c5ef5820cdac
Autor:
Bracken Michael B, Zhao Linlu
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 93 (2011)
Abstract Background Asthma is a phenotypically diverse disease with genetic susceptibility. A single nucleotide polymorphism (SNP) in the CD14 gene at position -260 (also known as -159) C>T has been inconsistently associated with asthma. The aim of t
Externí odkaz:
https://doaj.org/article/a1fd8424421c4cfcaa0059f74b6a8581