Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Xiao-qian Ye"'
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Purpose: Calcitonin gene-related peptide monoclonal antibodies (CGRPmAbs) are new agents approved by the US Food and Drug Administration for preventive treatment of chronic migraine. Comparison between CGRPmAbs and previously approved Botulinum neuro
Externí odkaz:
https://doaj.org/article/74bd8838ee524782a49ae2e7935044a5
Publikováno v:
Frontiers in Pharmacology
Frontiers in Pharmacology, Vol 12 (2021)
Frontiers in Pharmacology, Vol 12 (2021)
Purpose: Calcitonin gene-related peptide monoclonal antibodies (CGRPmAbs) are new agents approved by the US Food and Drug Administration for preventive treatment of chronic migraine. Comparison between CGRPmAbs and previously approved Botulinum neuro
Autor:
Xue-ping Lin, Chong Zong, Yan Lu, Chunwei Xu, Xiao-qian Ye, You-cai Zhu, Wenxian Wang, Kai-qi Du
Publikováno v:
Open Medicine, Vol 12, Iss 1, Pp 257-260 (2017)
Open Medicine
Open Medicine
Hemangiomas of the rib are extremely rare benign neoplasm. Here we present a case in a 47-year-old female, detected by chest X-ray and underwent a surgical resection. Histologically, the tumor was composed of a homogeneous conglomerate, irregular, th
Autor:
Zhihao Zhang, Jin-xian Zhang, Jian Hu, Man-xiang Yin, You-cai Zhu, Chun-wei Xu, Kai-qi Du, Xiao-qian Ye
Publikováno v:
OncoTargets and Therapy. 9:4301-4305
ROS1 rearrangement has recently emerged as a new molecular subtype in non-small cell lung cancer, and is predominantly found in lung adenocarcinomas compared with other oncogenes such as EGFR, KRAS, or ALK. Patients who have both mutations are extrem
Autor:
Dongling Zhong, Yuxi Li, Qiwei Xiao, Lihong Shi, Liuxue Guo, Xiao-Qian Ye, Rongjiang Jin, Juan Li, Huiling Zhang
Publikováno v:
Medicine. 98:e17124
Introduction Spasticity is the most common complication after stroke, which is the main obstacle in the recovery of motor function. Spasticity seriously affects the quality of life and brings a heavy burden to families and society. Acupuncture is an
Autor:
Zhu-qing, Wang, Ping, Wang, Yah-huei, Wu-Chou, Xiao-qian, Ye, Shang-zhi, Huang, Bing, Shi, Ke, Wang, Yuan, Yuan, Dong-jing, Liu, Tao, Wu, Hong, Wang, Terri H, Beaty
Publikováno v:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 47(3)
To explore the association between 10 candidate genes on transforming growth factor-β (TGFB) signaling pathway and non-syndromic cleft lip with or without cleft palate (NSCL/P) among Chinese populations, and to study the gene-environment interaction
Autor:
Li-hong Shi, Liu-xue Guo, Hui-ling Zhang, Yu-xi Li, Dong-ling Zhong, Qi-wei Xiao, Juan Li, Xiao-qian Ye, Rong-jiang Jin, Shi, Li-Hong, Guo, Liu-Xue, Zhang, Hui-Ling, Li, Yu-Xi, Zhong, Dong-Ling, Xiao, Qi-Wei, Li, Juan, Ye, Xiao-Qian, Jin, Rong-Jiang
Publikováno v:
Medicine; Sep2019, Vol. 98 Issue 39, p1-5, 5p
Autor:
Ping, Wang, Hong, Wang, Yah-huei, Wu-chou, Xiao-qian, Ye, Shang-zhi, Huang, Bing, Shi, Kung-yee, Liang, Wei-hua, Cao, Tao, Wu, Terei H, Beaty
Publikováno v:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 45(3)
To explore the association between 18 candidate genes encoding enzymes on the folate/homocysteine metabolism pathway and non-syndromic cleft lip with or without cleft palate (NSCL/P) in Chinese populations.A total of 806 NSCL/P trios were drawn by an
Publikováno v:
Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology. 42(5)
To detect mutations in the ED1 gene in two Chinese pedigrees and a sporadic case with X-linked hypohidrotic ectodermal dysplasia (XLHED) and provide evidences with the mutation analysis for genetic counseling, prenatal diagnosis and confirmation of c
Autor:
Xiao-Qian, Ye, Hui-Xi, Jin, Li-Song, Shi, Ming-Wen, Fan, Guang-Tai, Song, Hua-Li, Fan, Zhuan, Bian
Publikováno v:
International journal of molecular medicine. 16(5)
Van der Woude syndrome (VWS) is an autosomal dominant disorder of syndromic clefts clinically characterized by lower lip pits, cleft lip and/or palate, hypodontia. Mutations in the IRF6 gene have recently been found to cause VWS and more than 70 muta