Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Haimei OuYang"'
Autor:
Shu Liu, Zhiqing Wang, Xianhua Zheng, Ye Zhang, Sisi Wei, Haimei OuYang, Jinqun Liang, Nuan Chen, Weihong Zeng, Jianhui Jiang
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundSevere hyperlipidemia is characterized by markedly elevated blood triglyceride levels and severe early-onset cardiovascular diseases, pancreatitis, pancreatic necrosis or persistent multiple organ failure if left untreated. It is a rare aut
Externí odkaz:
https://doaj.org/article/43a5fa846ce94740bdb310118e87de4a
Autor:
Chenhong Zhang, Aihua Yin, Hongde Li, Ruirui Wang, Guojun Wu, Jian Shen, Menghui Zhang, Linghua Wang, Yaping Hou, Haimei Ouyang, Yan Zhang, Yinan Zheng, Jicheng Wang, Xiaofei Lv, Yulan Wang, Feng Zhang, Benhua Zeng, Wenxia Li, Feiyan Yan, Yufeng Zhao, Xiaoyan Pang, Xiaojun Zhang, Huaqing Fu, Feng Chen, Naisi Zhao, Bruce R. Hamaker, Laura C. Bridgewater, David Weinkove, Karine Clement, Joel Dore, Elaine Holmes, Huasheng Xiao, Guoping Zhao, Shengli Yang, Peer Bork, Jeremy K. Nicholson, Hong Wei, Huiru Tang, Xiaozhuang Zhang, Liping Zhao
Publikováno v:
EBioMedicine, Vol 2, Iss 8, Pp 968-984 (2015)
Gut microbiota has been implicated as a pivotal contributing factor in diet-related obesity; however, its role in development of disease phenotypes in human genetic obesity such as Prader–Willi syndrome (PWS) remains elusive. In this hospitalized i
Externí odkaz:
https://doaj.org/article/5ec5bb4f691e4712aeebac59885ecc16
Autor:
Yaping Hou, Fuli Deng, Jia Guo, Lijuan Lv, Haimei Ouyang, Xingwang Wang, Yasha Luo, Xiuwen Chen, Fanghua Wang
Publikováno v:
Endocrinology.
Lipid metabolism is tightly linked to adiposity. Prader-Willi syndrome (PWS) is a typical genetic disorder caused obesity, however, the distinct lipidomic profiles in PWS children have not been thoroughly investigated. Herein, serum lipidomics analys
Autor:
Shu Liu, Nuan Chen, Weihong Zeng, Haimei OuYang, Xunjie Xie, Sisi Wei, Zhiqing Wang, Jinqun Liang, Liying Chen, Jianhui Jiang
Publikováno v:
Cytogenetic and Genome Research. 154:201-208
Ring chromosome 6, r(6), is an extremely rare cytogenetic abnormality with clinical heterogeneity which arises typically de novo. The phenotypes of r(6) can be highly variable, ranging from almost normal to severe malformations and neurological defec
Autor:
Shu Liu, Zhiqing Wang, Weihong Zeng, Sisi Wei, Jianhui Jiang, Qingshan Hong, Xianqiong Luo, Jinqun Liang, Ye Zhang, Haimei OuYang, Nuan Chen
Publikováno v:
Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]. 20(3)
Johanson–Blizzard Syndrome (JBS) is a rare autosomal recessive genetic disorder characterized by exocrine pancreatic insufficiency, distinct abnormal facial appearance and varying degrees of growth retardation. Variants in UBR1 gene are considered
Autor:
Liying Chen, Xunjie Xie, Shu Liu, Jianhui Jiang, Weihong Zeng, Sisi Wei, Haimei OuYang, Nuan Chen, Jinqun Liang, Zhiqing Wang
Publikováno v:
Steroids. 144
Androgen insensitivity syndrome (AIS), a rare X-linked recessive genetic disorder with a normal 46, XY karyotype, is caused by defect of androgen receptor gene (AR) leading to resistance of the target tissues to androgenic hormones. There is a wide s
Autor:
Yaping Hou, Xiaofei Lv, Ai-hua Yin, Haimei Ouyang, Haishan Peng, Qing-Qing He, Hailiang Liu, Jie Li, Yi-Nan Zheng, Qun Wang, Shao-Chuan Li
Publikováno v:
BioMed Research International
Objective. To investigate the gut microbiota differences of obese children compared with the control healthy cohort to result in further understanding of the mechanism of obesity development. Methods. We evaluated the 16S rRNA gene, the enterotypes,
Autor:
Haimei Ouyang, Ning Ye, Fang Fang Zeng, Dan Feng, Ai-hua Yin, Wenhua Ling, Xiaozhuang Zhang, Yuan Zhang, Xiaofei Lv, Dan Li
Publikováno v:
Clinical Rheumatology. 33:1801-1805
Gout is a common metabolic disorder with high heritability. We tried to explore the association between rs2231142 and gout. We searched “rs2231142 or Q141K and gout” in four databases and scholar searching website until 1 June, 2013 and included
Autor:
Jinqun Liang, Haimei OuYang, Weihong Zeng, Nuan Chen, Liying Chen, Xunjie Xie, Zhiqing Wang, Jianhui Jiang, Shu Liu
Publikováno v:
Archivos argentinos de pediatria. 115(4)
Nonketotic hyperglycinemia is an extremely rare autosomal recessively inherited glycine encephalopathy caused by a deficiency in the mitochondrial glycine cleavage system, which leads to severe clinical symptoms. Nonketotic hyperglycinemia is charact
Autor:
Menghui Zhang, Karine Clément, Benhua Zeng, Hongde Li, Huasheng Xiao, Yulan Wang, Shengli Yang, Feiyan Yan, Huaqing Fu, Guojun Wu, R.Z. Wang, David Weinkove, Joël Doré, Hong Wei, Huiru Tang, Jicheng Wang, Aihua Yin, Xiaozhuang Zhang, Yufeng Zhao, Liping Zhao, Wenxia Li, Jeremy K. Nicholson, Laura C. Bridgewater, Chenhong Zhang, Yaping Hou, Feng Zhang, Haimei Ouyang, Linghua Wang, Guoping Zhao, Yi-Nan Zheng, Xiaofei Lv, Elaine Holmes, Peer Bork, Naisi Zhao, Jian Shen, Feng Chen, Yan Zhang, Xiaoyan Pang, Bruce R. Hamaker, Xiaojun Zhang
Publikováno v:
EBioMedicine
EBioMedicine, Elsevier, 2015, 2 (8), pp.968-984. ⟨10.1016/j.ebiom.2015.07.007⟩
EBioMedicine, 2015, Vol.2(8), pp.968-984 [Peer Reviewed Journal]
EBioMedicine 8 (2), 968-984. (2015)
EBioMedicine, Vol 2, Iss 8, Pp 968-984 (2015)
EBioMedicine, Elsevier, 2015, 2 (8), pp.968-984. ⟨10.1016/j.ebiom.2015.07.007⟩
EBioMedicine, 2015, Vol.2(8), pp.968-984 [Peer Reviewed Journal]
EBioMedicine 8 (2), 968-984. (2015)
EBioMedicine, Vol 2, Iss 8, Pp 968-984 (2015)
International audience; Gut microbiota has been implicated as a pivotal contributing factor in diet-related obesity; however, its role in development of disease phenotypes in human genetic obesity such as Prader-Willi syndrome (PWS) remains elusive.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f356c3c309563ce125e97563d2e406f
https://hal.inrae.fr/hal-02641529/file/2015_Zhang_EBioMedicine_1.pdf
https://hal.inrae.fr/hal-02641529/file/2015_Zhang_EBioMedicine_1.pdf