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Xiaocan Hou

Showing results (1-10 of 14) with videos related to

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Gene|May 24, 2024
Mapping cell diversity in human sporadic cerebral cavernous malformationsXiaocan Hou, Feng Liang, Jiaoxing Li, et al.
Communications Medicine|June 1, 2026
Neuromodulation strategies in postburn care for pain rehabilitation and scar remodellingTianjiao Li, Qian Zhang, Xiaocan Hou, et al.
BMC Medical Genetics|January 24, 2018
Birt-Hogg-Dubé syndrome in two Chinese families with mutations in the FLCN geneXiaocan Hou, Yuan Zhou, Yun Peng, et al.
Neurochemical Research|November 5, 2016
Let-7f Regulates the Hypoxic Response in Cerebral Ischemia by Targeting NDRG3Yaobing Yao, Weiwei Wang, Lijun Jing, et al.
Epigenomics|May 31, 2019
Identification of a potential exosomal biomarker in spinocerebellar ataxia Type 3/Machado-Joseph diseaseXiaocan Hou, Xuan Gong, Longbo Zhang, et al.
American Journal of Translational Research|October 12, 2016
Let-7a inhibits migration of melanoma cells via down-regulation of HMGA2 expressionXiaocan Hou, Wencui Wan, Jing Wang, et al.
Frontiers in Genetics|June 29, 2019
RNA Expression Profile and Potential Biomarkers in Patients With Spinocerebellar Ataxia Type 3 From Mainland ChinaTianjiao Li, Xiaocan Hou, Zhao Chen, et al.
Frontiers in Neurology|January 9, 2019
Identifying <i>SYNE1</i> Ataxia With Novel Mutations in a Chinese PopulationYun Peng, Wei Ye, Zhao Chen, et al.
Neurobiology of Aging|July 24, 2018
Investigation on modulation of DNA repair pathways in Chinese MJD patientsChunrong Wang, Zhao Chen, Huirong Peng, et al.
Frontiers in Genetics|March 8, 2019
Is the High Frequency of Machado-Joseph Disease in China Due to New Mutational Origins?Tianjiao Li, Sandra Martins, Yun Peng, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Gene|May 24, 2024
Mapping cell diversity in human sporadic cerebral cavernous malformationsXiaocan Hou, Feng Liang, Jiaoxing Li, et al.
Communications Medicine|June 1, 2026
Neuromodulation strategies in postburn care for pain rehabilitation and scar remodellingTianjiao Li, Qian Zhang, Xiaocan Hou, et al.
BMC Medical Genetics|January 24, 2018
Birt-Hogg-Dubé syndrome in two Chinese families with mutations in the FLCN geneXiaocan Hou, Yuan Zhou, Yun Peng, et al.
Neurochemical Research|November 5, 2016
Let-7f Regulates the Hypoxic Response in Cerebral Ischemia by Targeting NDRG3Yaobing Yao, Weiwei Wang, Lijun Jing, et al.
Epigenomics|May 31, 2019
Identification of a potential exosomal biomarker in spinocerebellar ataxia Type 3/Machado-Joseph diseaseXiaocan Hou, Xuan Gong, Longbo Zhang, et al.
American Journal of Translational Research|October 12, 2016
Let-7a inhibits migration of melanoma cells via down-regulation of HMGA2 expressionXiaocan Hou, Wencui Wan, Jing Wang, et al.
Frontiers in Genetics|June 29, 2019
RNA Expression Profile and Potential Biomarkers in Patients With Spinocerebellar Ataxia Type 3 From Mainland ChinaTianjiao Li, Xiaocan Hou, Zhao Chen, et al.
Frontiers in Neurology|January 9, 2019
Identifying <i>SYNE1</i> Ataxia With Novel Mutations in a Chinese PopulationYun Peng, Wei Ye, Zhao Chen, et al.
Neurobiology of Aging|July 24, 2018
Investigation on modulation of DNA repair pathways in Chinese MJD patientsChunrong Wang, Zhao Chen, Huirong Peng, et al.
Frontiers in Genetics|March 8, 2019
Is the High Frequency of Machado-Joseph Disease in China Due to New Mutational Origins?Tianjiao Li, Sandra Martins, Yun Peng, et al.
Pageof 2