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Mu-Gen Liu

Showing results (11-20 of 19) with videos related to

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BMC Genomics|March 22, 2005
Comprehensive in silico functional specification of mouse retina transcriptsSamuel Shao-Min Zhang, Xuming Xu, Jinming Li, 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.
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 familyTie Ke, Shang-wu Nie, Qin-bo Yang, et al.
Human Genetics|October 3, 2008
A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33Xiao-Hua Dai, Wen-Wu Chen, Xu Wang, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|August 31, 2006
Mutation p.Arg954Trp of KIF21A causes congenital fibrosis of the extraocular muscles in a Chinese familyXian-Qin Zhang, Jian-Hong Peng, Zhao-Hui Tang, et al.
Yi Chuan = Hereditas|March 21, 2007
[Genetic analysis of GJB2 in a Chinese family with nonsyndromic hearing impairment]Qi-Hui Zhu, Hu Li, Ping Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2003
Cardiomyocyte-restricted knockout of STAT3 results in higher sensitivity to inflammation, cardiac fibrosis, and heart failure with advanced ageJörg J Jacoby, April Kalinowski, Mu-Gen Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 10, 2010
[c.359T>C mutation of the MYH14 gene in two autosomal dominant non-syndromic hearing impairment families with common ancestor]Rong Yang, Hu Li, Cheng-xiong Zhan, et al.
Nature Genetics|March 8, 2011
Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han populationFan Wang, Cheng-Qi Xu, Qing He, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
BMC Genomics|March 22, 2005
Comprehensive in silico functional specification of mouse retina transcriptsSamuel Shao-Min Zhang, Xuming Xu, Jinming Li, 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.
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 familyTie Ke, Shang-wu Nie, Qin-bo Yang, et al.
Human Genetics|October 3, 2008
A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33Xiao-Hua Dai, Wen-Wu Chen, Xu Wang, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|August 31, 2006
Mutation p.Arg954Trp of KIF21A causes congenital fibrosis of the extraocular muscles in a Chinese familyXian-Qin Zhang, Jian-Hong Peng, Zhao-Hui Tang, et al.
Yi Chuan = Hereditas|March 21, 2007
[Genetic analysis of GJB2 in a Chinese family with nonsyndromic hearing impairment]Qi-Hui Zhu, Hu Li, Ping Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2003
Cardiomyocyte-restricted knockout of STAT3 results in higher sensitivity to inflammation, cardiac fibrosis, and heart failure with advanced ageJörg J Jacoby, April Kalinowski, Mu-Gen Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 10, 2010
[c.359T>C mutation of the MYH14 gene in two autosomal dominant non-syndromic hearing impairment families with common ancestor]Rong Yang, Hu Li, Cheng-xiong Zhan, et al.
Nature Genetics|March 8, 2011
Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han populationFan Wang, Cheng-Qi Xu, Qing He, et al.
Pageof 2