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Qian Pan

Showing results (111-120 of 282) with videos related to

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Archives of Neurology|January 21, 2004
Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegiaBeisha Tang, Guohua Zhao, Kun Xia, et al.
Investigative Ophthalmology & Visual Science|February 25, 2011
A novel locus for congenital simple microphthalmia family mapping to 17p12-q12Zhengmao Hu, Changhong Yu, Jingzhi Li, et al.
Epilepsy Research|February 6, 2008
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsionsHaiyan Li, Nan Li, Lu Shen, et al.
Human Molecular Genetics|August 8, 2015
Pathogenic Cx31 is un/misfolded to cause skin abnormality via a Fos/JunB-mediated mechanismChengyuan Tang, Xiang Chen, Jingwei Chi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 22, 2009
Spinocerebellar ataxia type 11 in the Chinese Han populationQian Xu, Xiaohui Li, Junling Wang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 24, 2025
Angiotensin II: A novel biomarker in vascular diseasesQin-Yi Zhou, Jin-Qian Pan, Wang Liu, et al.
Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao Acta Biochimica Et Biophysica Sinica|June 21, 2002
Cloning of Human Myelin Protein Zero-like Genes by Bioinformatics StrategyDong-Sheng Tang, Kuan-Ping Yu, Xi-Xiang Tang, et al.
Journal of the Neurological Sciences|June 28, 2005
Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four familiesHong Jiang, Beisha Tang, Kun Xia, et al.
Human Genetics|November 2, 2004
Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese familyBaorong Zhang, Kun Xia, Meiping Ding, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 9, 2013
[Cloning and localization of A3IP -a novel protein that interacts with ataxin-3]Feng-zhen Huang, Xuan Hou, Guo Wang, et al.
Pageof 29

Showing results (111-120 of 282) with videos related to

Sort By:
Pageof 29
Archives of Neurology|January 21, 2004
Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegiaBeisha Tang, Guohua Zhao, Kun Xia, et al.
Investigative Ophthalmology & Visual Science|February 25, 2011
A novel locus for congenital simple microphthalmia family mapping to 17p12-q12Zhengmao Hu, Changhong Yu, Jingzhi Li, et al.
Epilepsy Research|February 6, 2008
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsionsHaiyan Li, Nan Li, Lu Shen, et al.
Human Molecular Genetics|August 8, 2015
Pathogenic Cx31 is un/misfolded to cause skin abnormality via a Fos/JunB-mediated mechanismChengyuan Tang, Xiang Chen, Jingwei Chi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 22, 2009
Spinocerebellar ataxia type 11 in the Chinese Han populationQian Xu, Xiaohui Li, Junling Wang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 24, 2025
Angiotensin II: A novel biomarker in vascular diseasesQin-Yi Zhou, Jin-Qian Pan, Wang Liu, et al.
Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao Acta Biochimica Et Biophysica Sinica|June 21, 2002
Cloning of Human Myelin Protein Zero-like Genes by Bioinformatics StrategyDong-Sheng Tang, Kuan-Ping Yu, Xi-Xiang Tang, et al.
Journal of the Neurological Sciences|June 28, 2005
Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four familiesHong Jiang, Beisha Tang, Kun Xia, et al.
Human Genetics|November 2, 2004
Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese familyBaorong Zhang, Kun Xia, Meiping Ding, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 9, 2013
[Cloning and localization of A3IP -a novel protein that interacts with ataxin-3]Feng-zhen Huang, Xuan Hou, Guo Wang, et al.
Pageof 29