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Zhe Long

Showing results (41-50 of 113) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|June 4, 2026
Genomic Landscape and Phenotypic Spectrum of Autosomal Recessive Cerebellar Ataxia in ChinaXiaokai Shen, Zhao Chen, Huirong Peng, et al.
Plos One|June 11, 2015
Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in ChinaFengzhen Huang, Zhe Long, Zhao Chen, et al.
Gene|April 12, 2025
Pathogenicity analysis of three SCA14-associated missense mutations in PRKCG gene of Chinese patients with ataxiaHongyu Yuan, Zhao Chen, Linlin Wan, et al.
Genomics Data|December 24, 2015
miRNA profiling in autism spectrum disorder in ChinaFengzhen Huang, Tieqiao Zhou, Xiaoxi Yao, et al.
Frontiers in Neurology|March 3, 2020
Corrigendum: Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic StudyHuirong Peng, Xiaochun Liang, Zhe Long, et al.
Scientific Reports|February 6, 2016
Identification of a de novo DYNC1H1 mutation via WES according to published guidelinesDongxue Ding, Zhao Chen, Kai Li, et al.
Plos One|October 7, 2015
Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine PerspectiveZhao Chen, Wei Ye, Zhe Long, et al.
American Journal of Otolaryngology|April 27, 2012
Pattern of expression of cyclooxygenase-2 in malignant transformation of sinonasal inverted papillomaGun-Ho Lee, Yeo-Hoon Yoon, Yong Min Kim, et al.
Frontiers in Genetics|June 22, 2023
Case report: Autosomal recessive type 3 Stickler syndrome caused by compound heterozygous mutations in <i>COL11A2</i>Ying Su, Chun-Qiong Ran, Zhe-Long Liu, et al.
Human Pathology|December 31, 2010
Differential expression of Yes-associated protein is correlated with expression of cell cycle markers and pathologic TNM staging in non-small-cell lung carcinomaJin Man Kim, Dong Wook Kang, Liang Zhe Long, et al.
Pageof 12

Showing results (41-50 of 113) with videos related to

Sort By:
Pageof 12
Movement Disorders : Official Journal of the Movement Disorder Society|June 4, 2026
Genomic Landscape and Phenotypic Spectrum of Autosomal Recessive Cerebellar Ataxia in ChinaXiaokai Shen, Zhao Chen, Huirong Peng, et al.
Plos One|June 11, 2015
Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in ChinaFengzhen Huang, Zhe Long, Zhao Chen, et al.
Gene|April 12, 2025
Pathogenicity analysis of three SCA14-associated missense mutations in PRKCG gene of Chinese patients with ataxiaHongyu Yuan, Zhao Chen, Linlin Wan, et al.
Genomics Data|December 24, 2015
miRNA profiling in autism spectrum disorder in ChinaFengzhen Huang, Tieqiao Zhou, Xiaoxi Yao, et al.
Frontiers in Neurology|March 3, 2020
Corrigendum: Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic StudyHuirong Peng, Xiaochun Liang, Zhe Long, et al.
Scientific Reports|February 6, 2016
Identification of a de novo DYNC1H1 mutation via WES according to published guidelinesDongxue Ding, Zhao Chen, Kai Li, et al.
Plos One|October 7, 2015
Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine PerspectiveZhao Chen, Wei Ye, Zhe Long, et al.
American Journal of Otolaryngology|April 27, 2012
Pattern of expression of cyclooxygenase-2 in malignant transformation of sinonasal inverted papillomaGun-Ho Lee, Yeo-Hoon Yoon, Yong Min Kim, et al.
Frontiers in Genetics|June 22, 2023
Case report: Autosomal recessive type 3 Stickler syndrome caused by compound heterozygous mutations in <i>COL11A2</i>Ying Su, Chun-Qiong Ran, Zhe-Long Liu, et al.
Human Pathology|December 31, 2010
Differential expression of Yes-associated protein is correlated with expression of cell cycle markers and pathologic TNM staging in non-small-cell lung carcinomaJin Man Kim, Dong Wook Kang, Liang Zhe Long, et al.
Pageof 12