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Oxidative Medicine and Cellular Longevity
|
March 29, 2021
Regulation of Superoxide by BAP31 through Its Effect on p22<sup>phox</sup> and Keap1/Nrf2/HO-1 Signaling Pathway in Microglia
Xia Liu, Qing Yuan, Guo-Xun Li, et al.
Zhen Ci Yan Jiu = Acupuncture Research
|
July 18, 2024
Effect of electroacupuncture pre-conditioning on the expression rhythm of core clock gene Bmal1 in uterine tissue of controlled hyperstimulation rats
Qian Zhu, Jing-Yu Liu, Sai-Nan Hao, et al.
Investigative Ophthalmology & Visual Science
|
May 24, 2020
FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus Syndrome
Lei Jiang, Yulei Li, Kangjuan Yang, et al.
Frontiers in Endocrinology
|
August 2, 2021
Differential Gene Expression and Biological Analyses of Primary Hepatocytes Following D-Chiro-Inositol Supplement
Feier Cheng, Shao-Jun Yun, Jin-Ling Cao, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology
|
February 9, 2010
[Analysis of PAX6 gene in a Chinese family with congenital aniridia]
Peng-cheng Li, Qi Yao, Xiang Ren, et al.
Cornea
|
March 10, 2015
Identification of corneal neovascularization-related long noncoding RNAs through microarray analysis
Jin Huang, Yu-Jie Li, Jing-Yu Liu, et al.
Natural Product Research
|
October 11, 2021
Contact toxicity and repellence of essential oil from <i>Senecio scandens</i> and its major components against three stored product insects
Fang He, Jing-Yu Liu, Li-Jiang Chen, et al.
Journal of Human Genetics
|
May 23, 2007
Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation
Jing Yu Liu, Xiang Ren, Xiufeng Yang, et al.
Journal of Human Genetics
|
October 27, 2006
A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia
Changzheng Huang, Qinbo Yang, Tie Ke, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 10, 2006
The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family
Tie Ke, Shang-wu Nie, Qin-bo Yang, et al.
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Search research articles
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Showing results (71-80 of 130) with videos related to
Sort By:
Page
of 13
Oxidative Medicine and Cellular Longevity
|
March 29, 2021
Regulation of Superoxide by BAP31 through Its Effect on p22<sup>phox</sup> and Keap1/Nrf2/HO-1 Signaling Pathway in Microglia
Xia Liu, Qing Yuan, Guo-Xun Li, et al.
Zhen Ci Yan Jiu = Acupuncture Research
|
July 18, 2024
Effect of electroacupuncture pre-conditioning on the expression rhythm of core clock gene Bmal1 in uterine tissue of controlled hyperstimulation rats
Qian Zhu, Jing-Yu Liu, Sai-Nan Hao, et al.
Investigative Ophthalmology & Visual Science
|
May 24, 2020
FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus Syndrome
Lei Jiang, Yulei Li, Kangjuan Yang, et al.
Frontiers in Endocrinology
|
August 2, 2021
Differential Gene Expression and Biological Analyses of Primary Hepatocytes Following D-Chiro-Inositol Supplement
Feier Cheng, Shao-Jun Yun, Jin-Ling Cao, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology
|
February 9, 2010
[Analysis of PAX6 gene in a Chinese family with congenital aniridia]
Peng-cheng Li, Qi Yao, Xiang Ren, et al.
Cornea
|
March 10, 2015
Identification of corneal neovascularization-related long noncoding RNAs through microarray analysis
Jin Huang, Yu-Jie Li, Jing-Yu Liu, et al.
Natural Product Research
|
October 11, 2021
Contact toxicity and repellence of essential oil from <i>Senecio scandens</i> and its major components against three stored product insects
Fang He, Jing-Yu Liu, Li-Jiang Chen, et al.
Journal of Human Genetics
|
May 23, 2007
Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation
Jing Yu Liu, Xiang Ren, Xiufeng Yang, et al.
Journal of Human Genetics
|
October 27, 2006
A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia
Changzheng Huang, Qinbo Yang, Tie Ke, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 10, 2006
The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family
Tie Ke, Shang-wu Nie, Qin-bo Yang, et al.
Page
of 13