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Hongxu Pan

Showing results (51-60 of 61) with videos related to

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Computational and Structural Biotechnology Journal|March 29, 2021
<i>De novo</i> mutations in folate-related genes associated with common developmental disordersTengfei Luo, Kuokuo Li, Zhengbao Ling, et al.
Cell|April 25, 2025
SLC7A11 is an unconventional H<sup>+</sup> transporter in lysosomesNan Zhou, Jingzhi Chen, Meiqin Hu, et al.
European Journal of Neurology|November 17, 2023
GGC expansions in NOTCH2NLC contribute to Parkinson disease and dopaminergic neuron degenerationQiong Liu, Juan Chen, Jin Xue, et al.
Frontiers in Genetics|May 23, 2022
Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read SequencingZhenhua Liu, Guihu Zhao, Yuhui Xiao, et al.
Acta Neuropathologica|February 18, 2021
ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland populationYuwen Zhao, Hongxu Pan, Yige Wang, et al.
Computational and Structural Biotechnology Journal|April 19, 2021
GPCards: An integrated database of genotype-phenotype correlations in human genetic diseasesBin Li, Zheng Wang, Qian Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 3, 2025
Genetic Variation Analysis of Essential Tremor: Insights from the China Essential Tremor Alliance CohortMingqiang Li, Yuwen Zhao, Yuzheng Wang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 3, 2022
The Chinese Parkinson's Disease Registry (CPDR): Study Design and Baseline Patient CharacteristicsXiaoxia Zhou, Zhenhua Liu, Xiaoting Zhou, et al.
NPJ Parkinson'S Disease|March 28, 2026
The genetic spectrum of LRRK2 variants in Parkinson's disease: findings from a large Chinese cohortJuan Wan, Hongxu Pan, Dong Chang, et al.
Brain : a Journal of Neurology|July 3, 2020
The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland populationYuwen Zhao, Lixia Qin, Hongxu Pan, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Computational and Structural Biotechnology Journal|March 29, 2021
<i>De novo</i> mutations in folate-related genes associated with common developmental disordersTengfei Luo, Kuokuo Li, Zhengbao Ling, et al.
Cell|April 25, 2025
SLC7A11 is an unconventional H<sup>+</sup> transporter in lysosomesNan Zhou, Jingzhi Chen, Meiqin Hu, et al.
European Journal of Neurology|November 17, 2023
GGC expansions in NOTCH2NLC contribute to Parkinson disease and dopaminergic neuron degenerationQiong Liu, Juan Chen, Jin Xue, et al.
Frontiers in Genetics|May 23, 2022
Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read SequencingZhenhua Liu, Guihu Zhao, Yuhui Xiao, et al.
Acta Neuropathologica|February 18, 2021
ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland populationYuwen Zhao, Hongxu Pan, Yige Wang, et al.
Computational and Structural Biotechnology Journal|April 19, 2021
GPCards: An integrated database of genotype-phenotype correlations in human genetic diseasesBin Li, Zheng Wang, Qian Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 3, 2025
Genetic Variation Analysis of Essential Tremor: Insights from the China Essential Tremor Alliance CohortMingqiang Li, Yuwen Zhao, Yuzheng Wang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 3, 2022
The Chinese Parkinson's Disease Registry (CPDR): Study Design and Baseline Patient CharacteristicsXiaoxia Zhou, Zhenhua Liu, Xiaoting Zhou, et al.
NPJ Parkinson'S Disease|March 28, 2026
The genetic spectrum of LRRK2 variants in Parkinson's disease: findings from a large Chinese cohortJuan Wan, Hongxu Pan, Dong Chang, et al.
Brain : a Journal of Neurology|July 3, 2020
The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland populationYuwen Zhao, Lixia Qin, Hongxu Pan, et al.
Pageof 7