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Xiaoqiao Li

Showing results (1-10 of 18) with videos related to

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Molecular Vision|April 25, 2009
A novel GPR143 duplication mutation in a Chinese family with X-linked congenital nystagmusYuanyuan Peng, Yan Meng, Zheng Wang, et al.
Reproductive Toxicology (Elmsford, N.Y.)|November 5, 2013
Knockdown of p66Shc by siRNA injection rescues arsenite-induced developmental retardation in mouse preimplantation embryosKai Ren, Xiaoqiao Li, Jinting Yan, et al.
Journal of Personalized Medicine|March 25, 2022
Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the LiteratureFenqi Gao, Xiu Zhao, Bingyan Cao, et al.
Current Eye Research|July 6, 2010
A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese familyXiaobo Gao, Jie Cheng, Cailing Lu, et al.
Pediatric Investigation|August 28, 2020
Efficacy and safety of octreotide treatment for diazoxide-unresponsive congenital hyperinsulinism in ChinaBingyan Cao, Wu Di, Chang Su, et al.
Endocrine Connections|October 15, 2025
Long-term intranasal oxytocin therapy in patients with hypothalamic syndrome: case series and literature reviewYusi Wang, Yi Wang, Bingyan Cao, et al.
Toxicology Letters|May 23, 2012
Arsenic impairs embryo development via down-regulating Dvr1 expression in zebrafishXiaoqiao Li, Yan Ma, Dan Li, et al.
Epilepsy Research|April 19, 2011
The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsyHui Liu, Cailing Lu, Zhenzhong Li, et al.
Pediatric Investigation|September 19, 2025
Clinical and genetic characteristics of Cornelia de Lange syndrome in pediatric patientsXiaoqiao Li, Ming Cheng, Min Liu, et al.
BMC Medical Genomics|December 5, 2020
The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapyXuyun Hu, Di Wu, Yuchuan Li, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Molecular Vision|April 25, 2009
A novel GPR143 duplication mutation in a Chinese family with X-linked congenital nystagmusYuanyuan Peng, Yan Meng, Zheng Wang, et al.
Reproductive Toxicology (Elmsford, N.Y.)|November 5, 2013
Knockdown of p66Shc by siRNA injection rescues arsenite-induced developmental retardation in mouse preimplantation embryosKai Ren, Xiaoqiao Li, Jinting Yan, et al.
Journal of Personalized Medicine|March 25, 2022
Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the LiteratureFenqi Gao, Xiu Zhao, Bingyan Cao, et al.
Current Eye Research|July 6, 2010
A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese familyXiaobo Gao, Jie Cheng, Cailing Lu, et al.
Pediatric Investigation|August 28, 2020
Efficacy and safety of octreotide treatment for diazoxide-unresponsive congenital hyperinsulinism in ChinaBingyan Cao, Wu Di, Chang Su, et al.
Endocrine Connections|October 15, 2025
Long-term intranasal oxytocin therapy in patients with hypothalamic syndrome: case series and literature reviewYusi Wang, Yi Wang, Bingyan Cao, et al.
Toxicology Letters|May 23, 2012
Arsenic impairs embryo development via down-regulating Dvr1 expression in zebrafishXiaoqiao Li, Yan Ma, Dan Li, et al.
Epilepsy Research|April 19, 2011
The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsyHui Liu, Cailing Lu, Zhenzhong Li, et al.
Pediatric Investigation|September 19, 2025
Clinical and genetic characteristics of Cornelia de Lange syndrome in pediatric patientsXiaoqiao Li, Ming Cheng, Min Liu, et al.
BMC Medical Genomics|December 5, 2020
The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapyXuyun Hu, Di Wu, Yuchuan Li, et al.
Pageof 2