Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Qingxiu Wu"'
Autor:
Jizhu Li, Yuqing Wu, Bingqian Liu, Ying Huang, Qingxiu Wu, Haichun Li, Sainan Xiao, Ying Lin, Tao Li
Publikováno v:
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background A reliable and effective method is required to deliver agent that can aid the in vivo imaging of retinal vessels. The aim of the present study was to evaluate retro-orbital (RO) injection of fluorescein-labeled isothiocyanate dext
Externí odkaz:
https://doaj.org/article/08fd6e6b8e4040db985fca08c56598a6
Autor:
Lihong Tian, Pingping Xiao, Bingrong Zhou, Yishan Chen, Lijuan Kang, Qingqing Wang, Jianfeng Lin, Min Son, Qingxiu Wu
Publikováno v:
Cardiovascular Therapeutics, Vol 2021 (2021)
This meta-analysis was conducted to analyze the effect of NQO1 polymorphism on the warfarin maintenance dosage. Using strict inclusion and exclusion criteria, we searched PubMed, EMBASE, and the Cochrane Library for eligible studies published prior t
Externí odkaz:
https://doaj.org/article/748489c1f0f4414c9e53203c9bafb367
Publikováno v:
Minerva Gastroenterology; Jun2024, Vol. 70 Issue 2, p247-249, 3p
Autor:
Bingqian Liu, Tao Li, Ying Huang, Jizhu Li, Ying Lin, Sainan Xiao, Yuqing Wu, Haichun Li, Qingxiu Wu
Publikováno v:
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Ophthalmology
BMC Ophthalmology
Background A reliable and effective method is required to deliver agent that can aid the in vivo imaging of retinal vessels. The aim of the present study was to evaluate retro-orbital (RO) injection of fluorescein-labeled isothiocyanate dextran (FITC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1491534a2bf00b7e97d5a06e666edb9
https://doaj.org/article/08fd6e6b8e4040db985fca08c56598a6
https://doaj.org/article/08fd6e6b8e4040db985fca08c56598a6
Autor:
Min Son, Bingrong Zhou, Lihong Tian, Qingqing Wang, Jianfeng Lin, Pingping Xiao, Qingxiu Wu, Lijuan Kang, Yishan Chen
Publikováno v:
Cardiovascular Therapeutics
Cardiovascular Therapeutics, Vol 2021 (2021)
Cardiovascular Therapeutics, Vol 2021 (2021)
This meta-analysis was conducted to analyze the effect of NQO1 polymorphism on the warfarin maintenance dosage. Using strict inclusion and exclusion criteria, we searched PubMed, EMBASE, and the Cochrane Library for eligible studies published prior t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9534eff47a3f06e94ce6fa30d36d8f45
http://europepmc.org/articles/PMC8376459
http://europepmc.org/articles/PMC8376459
Autor:
Haichun Li, Lin Lu, Tao Li, Bingqian Liu, Chenjin Jin, Qingxiu Wu, Ying Huang, Yu Lian, Ying Lin, Jizhu Li, Cancan Lyu
Publikováno v:
Experimental and Therapeutic Medicine
Compared to juvenile-onset best vitelliform macular dystrophy (BVMD), adult-onset BVMD is not well characterized and lacks strict diagnostic criteria. The present study aimed to evaluate the clinical and genetic characteristics of four advanced-age C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e53f028781186aae2a1a2ee703fe9e8
https://doi.org/10.3892/etm.2021.10466
https://doi.org/10.3892/etm.2021.10466
Autor:
Lin Lu, Chenjin Jin, Tao Li, Qingxiu Wu, Hongye Jiang, Chenghong Ma, Ying Huang, Yonghao Li, Chuan Chen, Xiaoling Liang, Xinhua Huang, Ying Lin, Yi Zhu, Haichun Li, Hongbin Gao, Bingqian Liu, Jianhua Ye
Publikováno v:
International Journal of Molecular Medicine
Familial exudative vitreoretinopathy (FEVR) is a rare hereditary retinal disorder characterized by the premature arrest of vascularization in the peripheral retina. The aim of the present study was to characterize the clinical presentations of a Chin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df78a1acb808d1a91b81744b6fdcd7e1
http://europepmc.org/articles/PMC5752179
http://europepmc.org/articles/PMC5752179
Autor:
Xiaoling Liang, Yi Zhu, Y. Liu, Yonghao Li, Hongbin Gao, Chuan Chen, Hongye Jiang, Chenjin Jin, Bingqian Liu, Qingxiu Wu, Lin Lu, Jacob V.P. Eswarakumar, Ying Lin, Haichun Li, Siming Ai, Xinhua Huang, Tao Li
Publikováno v:
Molecular Medicine Reports
The aim of the present study was to identify mutations in the fibroblast growth factor receptor 2 (FGFR2) gene in patients with Crouzon syndrome and characterize the associated clinical features. A total of two Chinese patients diagnosed with Crouzon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a761db9d618a54e5cb6d1dfdc6caeade
https://doi.org/10.3892/mmr.2017.7397
https://doi.org/10.3892/mmr.2017.7397
Autor:
Qingxiu Wu
Publikováno v:
2019 International Conference on Robots & Intelligent System (ICRIS).
Due to the approximate characteristics of the ecological footprint model, it has been used by many researchers to solve the evaluation problem of regional industrial ecological coupling degree evaluation. This paper proposes a method of constructing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3855791fc7036c4113802dadf098a195
https://doi.org/10.1109/icris.2019.00109
https://doi.org/10.1109/icris.2019.00109
Autor:
Xiaoling Liang, Chenjin Jin, Ying Huang, Tao Li, Yi Zhu, Cancan Lyu, Chuan Chen, Hongbin Gao, Ying Lin, Xinhua Huang, Qingxiu Wu, Bingqian Liu, Lin Lu, Haichun Li
Publikováno v:
Molecular Medicine Reports
Congenital aniridia is a rare genetic disorder characterized by a variable degree of hypoplasia or absence of iris. It is frequently associated with keratopathy, cataract, juvenile-onset glaucoma and foveal and optic nerve hypoplasia. Mutations in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69db4cd83cd33b04531cdb948631710e
https://doi.org/10.3892/mmr.2018.9469
https://doi.org/10.3892/mmr.2018.9469