Zobrazeno 1 - 10
of 76
pro vyhledávání: '"XIN-KAI QU"'
Autor:
Yu-Min Sun, Jun Wang, Xing-Biao Qiu, Fang Yuan, Ruo-Gu Li, Ying-Jia Xu, Xin-Kai Qu, Hong-Yu Shi, Xu-Min Hou, Ri-Tai Huang, Song Xue, Yi-Qing Yang
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 4, Pp 987-992 (2016)
Congenital heart disease (CHD) is the most common developmental abnormality, and is the leading noninfectious cause of mortality in neonates. Increasing evidence demonstrates that genetic defects play an important role in the pathogenesis of CHD. How
Externí odkaz:
https://doaj.org/article/32aee88e8521494cadfdefd540e6a566
Publikováno v:
Clinics, Vol 69, Iss 1, Pp 15-22 (2014)
OBJECTIVE: This study aimed to identify novel PITX2c mutations responsible for idiopathic atrial fibrillation. METHODS: A cohort of 210 unrelated patients with idiopathic atrial fibrillation and 200 unrelated, ethnically matched healthy individuals u
Externí odkaz:
https://doaj.org/article/e96b82a49a3244abbf97046fbbc32d24
Autor:
Wen-Hui Xie, Cheng Chang, Ying-Jia Xu, Ruo-Gu Li, Xin-Kai Qu, Wei-Yi Fang, Xu Liu, Yi-Qing Yang
Publikováno v:
Clinics, Vol 68, Iss 6, Pp 777-784 (2013)
OBJECTIVE: The aim of this study was to evaluate the prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation (AF). METHODS: A cohort of 136 unrelated patients with idiopathic atrial fibrillation and 200 unrelated, e
Externí odkaz:
https://doaj.org/article/dba8a729f4cf4366b36eac9a2e6f405a
Publikováno v:
International Journal of Oral and Maxillofacial Surgery. 50:391-397
The objective of this study was to compare the implant longevity following two methods of peri-implant soft tissue optimization following free fibula flap (FFF): thinning of skin paddle (SP) and collagen matrix (CM). All patients who underwent rehabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6c959afcc160277894b3a417809baa
https://doi.org/10.1016/j.ijom.2020.07.028
https://doi.org/10.1016/j.ijom.2020.07.028
Autor:
Yi-Qing Yang, Juan Wang, Ruo-Gu Li, Song Xue, Xing-Biao Qiu, Ri-Tai Huang, Xing-Yuan Liu, Xiao-Hui Qiao, Ying-Jia Xu, Yan-Jie Li, Qian Wang, Min Zhang, Xin-Kai Qu
Publikováno v:
European Journal of Medical Genetics. 61:197-203
Congenital heart defect (CHD) is the most common type of birth defect in humans and a leading cause of infant morbidity and mortality. Previous studies have demonstrated that genetic defects play a pivotal role in the pathogenesis of CHD. However, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9742b88882fca3da01689c4708a3ff87
https://doi.org/10.1016/j.ejmg.2017.12.003
https://doi.org/10.1016/j.ejmg.2017.12.003
Autor:
Min Zhang, Hua Liu, Ri-Tai Huang, Ruo-Gu Li, Hong-Yu Shi, Yan-Jie Li, Fang Yuan, Li Li, Xing-Biao Qiu, Juan Wang, Xing-Yuan Liu, Song Xue, Ying-Jia Xu, Xin-Kai Qu, Yi-Qing Yang
Publikováno v:
The American Journal of Cardiology. 121:469-474
Aggregating evidence suggests that genetic determinants play a pivotal role in the pathogenesis of the congenitally bicuspid aortic valve (BAV). BAV is of pronounced genetic heterogeneity, and the genetic components underlying BAV in an overwhelming
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccc4751f71791f8ac24b4451ca9c18cf
https://doi.org/10.1016/j.amjcard.2017.11.012
https://doi.org/10.1016/j.amjcard.2017.11.012
Autor:
Shaofeng Guan, Wei-Yi Fang, Jianwei Ma, Wenzheng Han, Ping Yang, Ruo-Gu Li, Shuping Wang, Xu-Min Hou, Min Zhang, Zhicheng Pan, Xin-Kai Qu, Hua Liu, Tiantong Ou
Publikováno v:
Molecular and Cellular Biochemistry. 437:45-53
Endothelial inflammation and monocyte plays an essential role in the initiation and progression of atherosclerosis. Ghrelin is beneficial for atherosclerosis progression. However, the detailed and precise molecular mechanisms of how ghrelin regulates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d863e5080672472696c9c00a3b376b5
https://doi.org/10.1007/s11010-017-3094-x
https://doi.org/10.1007/s11010-017-3094-x
Autor:
Kaizheng Gong, Ming Wang, Yan-Jie Li, Wei-Yi Fang, Xin-Kai Qu, Qian Gan, Shaofeng Guan, Wenzheng Han
Publikováno v:
Journal of the American Society of Hypertension. 11:314-320
Recently, the effectiveness of renal sympathetic nerve denervation for treatment of hypertension has been doubted after SYMPLICITY HTN-3 trial. An ideal animal model is still unavailable for preclinical study about catheter-based renal sympathetic ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2f1ec8f4fb0dcab7f89c40f4628646e
https://doi.org/10.1016/j.jash.2017.02.006
https://doi.org/10.1016/j.jash.2017.02.006
Autor:
Hong-Yu Shi, Ruo-Gu Li, Jiahong Xu, Hua Liu, Hong Zhang, Xin-Kai Qu, Ying-Jia Xu, Yu-Han Guo, Xing-Biao Qiu, Jian-Yun Gu, Yi-Qing Yang, Xiaoxiao Yang
Publikováno v:
International Heart Journal. 58:521-529
Dilated cardiomyopathy (DCM), the most common form of primary myocardial disease, is a leading cause of congestive heart failure and the most common indication for heart transplantation. Recently, NKX2-5 mutations have been involved in the pathogenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ffccc5fd0613509429e9daa927b663f
https://doi.org/10.1536/ihj.16-440
https://doi.org/10.1536/ihj.16-440
Autor:
Jia Hong Xu, Song Xue, Jian Yun Gu, Xiaoxiao Yang, Yan‑Jie Li, Ruo‑Gu Li, Yi-Qing Yang, Xin‑Kai Qu, Xiao Dong Zhang, Ning Li, Xing‑Biao Qiu, Hua Liu, Ying‑Jia Xu, Juan Wang, Ri‑Tai Huang
Publikováno v:
Gene. 595:62-68
As the most common form of birth defect in humans, congenital heart disease (CHD) is associated with substantial morbidity and mortality in both children and adults. Increasing evidence demonstrates that genetic defects play a pivotal role in the pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f9e8f3922bd234482daeb5611ed6810
https://doi.org/10.1016/j.gene.2016.09.044
https://doi.org/10.1016/j.gene.2016.09.044