Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Xiuli Zhao"'
Autor:
Shumin, Wang, Shaojie, Guo, Ying, Han, Siyang, Ni, Feng, Wu, Yuyang, Dai, Qiang, Xia, Yan, Yang, Xiuli, Zhao
Publikováno v:
Clinical Pharmacology in Drug Development. 11:1481-1488
Linezolid, an oxazolidinone antibacterial agent with several formulations, has been widely used for over 20 years. This study aimed to compare the bioequivalence, pharmacokinetics, and safety of test and reference linezolid tablets after a single ora
Autor:
Shumin, Wang, Feng, Wu, Ying, Han, Siyang, Ni, Shaojie, Guo, Yuyang, Dai, Qiang, Xia, Di, Chang, Ju, Zhang, Huiwen, Wei, Xiuli, Zhao
Publikováno v:
Clinical Pharmacology in Drug Development. 11:949-956
Misoprostol is a synthetic prostaglandin E1 derivative that has been used to treat duodenal and gastric ulcers, and to prevent ulcers caused by nonsteroidal anti-inflammatory drugs in many countries. Misoprostol can also be used for medical abortion.
Publikováno v:
Journal of visualized experiments : JoVE. (185)
An increasing body of evidence now shows that the majority of children in China experience lower levels of physical activity (PA) than the recommended guideline. Table tennis is a compound and technically difficult game that is popular in China; unde
Autor:
Yixuan Cao, Yi You, Qiong Wang, Xiuzhi Ren, Shan Li, Lulu Li, Weibo Xia, Xin Guan, Tao Yang, Shiro Ikegawa, Zheng Wang, Xiuli Zhao
Publikováno v:
BMC Medical Genomics. 15
Background Hypophosphatemic rickets (HR) is a rare genetic disorder associated with renal phosphate wasting and characterized by bone defects. Inactivating mutations in the phosphate regulating endopeptidase homolog X‑linked gene (PHEX) account for
Autor:
Shaoke Chen, Mei Li, Jennifer E Posey, Yue Ming, Yanning Song, Guixing Qiu, Pengfei Liu, Jianguo Zhang, Chenxi Yu, Di Wu, Chunxiu Gong, Xiuli Zhao, Shuyang Zhang, Weibo Xia, Qiang Zhang, COmorbidities (Disco) study, Xinzhuang Yang, James R. Lupski, Shiyu Luo, Zihui Yan, Yuchen Niu, Nan Wu, Chuan Li, Yi Wang, Zhihong Wu, Hui Pan, Deciphering Disorders Involving Scoliosis, Sen Zhao, Lijun Fan, Baoheng Gui, Xin Fan, Xiaoxin Li
Publikováno v:
Journal of Genetics and Genomics. 48:396-402
Short stature is among the most common endocrinological disease phenotypes of childhood and may occur as an isolated finding or in conjunction with other clinical manifestations. Although the diagnostic utility of clinical genetic testing in short st
Publikováno v:
Journal of clinical pharmacy and therapeuticsREFERENCES. 47(9)
Patients with optic neuritis (ON) have significant individual differences in their response to high-dose intravenous methylprednisolone (HIMP) therapy. This study aims to evaluate the association between gene polymorphisms and the efficacy of HIMP th
Publikováno v:
Molecular Genetics & Genomic Medicine. 10
Spondyloepi(meta)physeal dysplasias (SE[M]D) are a group of inherited skeletal disorders that mainly affect bone and cartilage, and next-generation sequencing has aided the detection of genetic defects of such diseases. In this study, we aimed to ide
Autor:
Yan Gao, Zilin Song, Li Jia, Yi Tang, Chengcheng Wang, Xiuli Zhao, Haiyang Hu, Dawei Chen, Mingxi Qiao
Publikováno v:
Biomaterials. 291:121902
Despite the important role of reactive oxygen species (ROS) in battling cancer, ROS production with current approaches has been severely limited by the deficiency of oxy-substrates in tumor microenvironment. Herein, an atorvastatin (Ato)-catalytic se
Autor:
Jiulong Zhang, Xiaoyan Sun, Mengdan Xu, Xiufeng Zhao, Chunrong Yang, Kexin Li, Fan Zhao, Haiyang Hu, Mingxi Qiao, Dawei Chen, Xiuli Zhao
Publikováno v:
Acta biomaterialia. 149
Circumventing immune resistance and boosting immune response is the ultimate goal of cancer immunotherapy. Herein, we reported a tumor-associated macrophage (TAM) membrane-camouflaged nanodecoy containing a self-amplifying reactive oxygen species (RO
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(2)
To identify the causative variants in 13 Chinese pedigrees affected with oculocutaneous albinism (OCA) so as to provide genetic counseling and prenatal diagnosis to them.Thirteen unrelated pedigrees with clinically diagnosed OCA were collected and cl