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Linghan Gao

Showing results (11-20 of 25) with videos related to

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Molecular Vision|November 6, 2007
The E233del mutation in BFSP2 causes a progressive autosomal dominant congenital cataract in a Chinese familyXiaobo Cui, Linghan Gao, Yan Jin, et al.
Molecular Vision|December 24, 2011
An Arg124His mutation in TGFBI associated to Avellino corneal dystrophy in a Chinese pedigreeZhensheng Gu, Peiquan Zhao, Guang He, et al.
Plos One|April 9, 2014
Identification of duplication downstream of BMP2 in a Chinese family with brachydactyly type A2 (BDA2)Xudong Liu, Linghan Gao, Aman Zhao, et al.
Human Mutation|September 24, 2015
Variants in TRIM44 Cause Aniridia by Impairing PAX6 ExpressionXibo Zhang, Gang Qin, Guilan Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 10, 2018
[Analysis of TGFBI gene mutation in a pedigree affected with corneal dystrophy]Anli Shu, Gen Li, Hai Luo, et al.
BMC Medical Genetics|October 10, 2013
Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataractXueyuan Jia, Feng Zhang, Jing Bai, et al.
Genomics|February 8, 2012
Mutation identification of the DSPP in a Chinese family with DGI-II and an up-to-date bioinformatic analysisDaxu Li, Xiaoyun Du, Rui Zhang, et al.
Clinical Science (London, England : 1979)|February 7, 2009
Association between the PDE4D gene and ischaemic stroke in the Chinese Han populationYun Sun, Yanyan Huang, Xu Chen, et al.
The Journal of Nutritional Biochemistry|December 31, 2010
Proteome alterations of cortex and hippocampus tissues in mice subjected to vitamin A depletionMing Zhang, Ke Huang, Zhao Zhang, et al.
Neuroscience Letters|October 12, 2010
No association between the KCNH1, KCNJ10 and KCNN3 genes and schizophrenia in the Han Chinese populationQi Shen, Jing Zhang, Yang Wang, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Molecular Vision|November 6, 2007
The E233del mutation in BFSP2 causes a progressive autosomal dominant congenital cataract in a Chinese familyXiaobo Cui, Linghan Gao, Yan Jin, et al.
Molecular Vision|December 24, 2011
An Arg124His mutation in TGFBI associated to Avellino corneal dystrophy in a Chinese pedigreeZhensheng Gu, Peiquan Zhao, Guang He, et al.
Plos One|April 9, 2014
Identification of duplication downstream of BMP2 in a Chinese family with brachydactyly type A2 (BDA2)Xudong Liu, Linghan Gao, Aman Zhao, et al.
Human Mutation|September 24, 2015
Variants in TRIM44 Cause Aniridia by Impairing PAX6 ExpressionXibo Zhang, Gang Qin, Guilan Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 10, 2018
[Analysis of TGFBI gene mutation in a pedigree affected with corneal dystrophy]Anli Shu, Gen Li, Hai Luo, et al.
BMC Medical Genetics|October 10, 2013
Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataractXueyuan Jia, Feng Zhang, Jing Bai, et al.
Genomics|February 8, 2012
Mutation identification of the DSPP in a Chinese family with DGI-II and an up-to-date bioinformatic analysisDaxu Li, Xiaoyun Du, Rui Zhang, et al.
Clinical Science (London, England : 1979)|February 7, 2009
Association between the PDE4D gene and ischaemic stroke in the Chinese Han populationYun Sun, Yanyan Huang, Xu Chen, et al.
The Journal of Nutritional Biochemistry|December 31, 2010
Proteome alterations of cortex and hippocampus tissues in mice subjected to vitamin A depletionMing Zhang, Ke Huang, Zhao Zhang, et al.
Neuroscience Letters|October 12, 2010
No association between the KCNH1, KCNJ10 and KCNN3 genes and schizophrenia in the Han Chinese populationQi Shen, Jing Zhang, Yang Wang, et al.
Pageof 3