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Chengqing Yang

Showing results (21-30 of 58) with videos related to

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International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 26, 2022
A novel de novo frameshift variation in the SON gene causing severe global developmental delay and seizures in a Chinese femaleZhi Yi, Zhenfeng Song, Fei Li, et al.
Italian Journal of Pediatrics|June 3, 2024
A case of variant of GBS with positive serum ganglioside GD3 IgG antibodyJiao Xue, Zhenfeng Song, Hongshan Zhao, et al.
Italian Journal of Pediatrics|July 11, 2020
Report of a de novo c.2605C > T (p.Pro869Ser) change in the MED13L gene and review of the literature for MED13L-related intellectual disabilityZhi Yi, Ying Zhang, Zhenfeng Song, et al.
Journal of Molecular Neuroscience : MN|September 25, 2021
A Novel De Novo TUBB3 Variant Causing Developmental Delay, Epilepsy and Mild Ophthalmological Symptoms in a Chinese ChildJiao Xue, Zhenfeng Song, Shuyin Ma, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|April 29, 2021
De novo frameshift variants of HNRNPU in patients with early infantile epileptic encephalopathy: Two case reports and literature reviewZhenfeng Song, Ying Zhang, Chengqing Yang, et al.
Tuberculosis (Edinburgh, Scotland)|December 31, 2020
Activation of hypoxia-inducible factor 1 (Hif-1) enhanced bactericidal effects of macrophages to Mycobacterium tuberculosisQuan Li, Yuyu Xie, Zhangbo Cui, et al.
Frontiers in Immunology|May 28, 2024
The regulation and potential role of interleukin-32 in tuberculous pleural effusionXuan Wang, Chengqing Yang, Chao Quan, et al.
Frontiers in Genetics|August 5, 2025
Case Report: Pediatric CNS-isolated hemophagocytic lymphohistiocytosis secondary to uniparental disomy of <i>PRF1</i> mutationJiao Xue, Zhenfeng Song, Hongshan Zhao, et al.
Medicine|October 1, 2025
Mapping cerebrospinal fluid biomarkers to dementia risk through Mendelian randomizationXiaomin Zhu, Wei Chen, Guifeng Zhuo, et al.
Frontiers in Neuroscience|March 19, 2026
A pediatric patient with Warsaw breakage syndrome presenting with epilepsy: a case report and literature reviewYixuan Zhang, Zhi Yi, Ying Zhang, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 26, 2022
A novel de novo frameshift variation in the SON gene causing severe global developmental delay and seizures in a Chinese femaleZhi Yi, Zhenfeng Song, Fei Li, et al.
Italian Journal of Pediatrics|June 3, 2024
A case of variant of GBS with positive serum ganglioside GD3 IgG antibodyJiao Xue, Zhenfeng Song, Hongshan Zhao, et al.
Italian Journal of Pediatrics|July 11, 2020
Report of a de novo c.2605C > T (p.Pro869Ser) change in the MED13L gene and review of the literature for MED13L-related intellectual disabilityZhi Yi, Ying Zhang, Zhenfeng Song, et al.
Journal of Molecular Neuroscience : MN|September 25, 2021
A Novel De Novo TUBB3 Variant Causing Developmental Delay, Epilepsy and Mild Ophthalmological Symptoms in a Chinese ChildJiao Xue, Zhenfeng Song, Shuyin Ma, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|April 29, 2021
De novo frameshift variants of HNRNPU in patients with early infantile epileptic encephalopathy: Two case reports and literature reviewZhenfeng Song, Ying Zhang, Chengqing Yang, et al.
Tuberculosis (Edinburgh, Scotland)|December 31, 2020
Activation of hypoxia-inducible factor 1 (Hif-1) enhanced bactericidal effects of macrophages to Mycobacterium tuberculosisQuan Li, Yuyu Xie, Zhangbo Cui, et al.
Frontiers in Immunology|May 28, 2024
The regulation and potential role of interleukin-32 in tuberculous pleural effusionXuan Wang, Chengqing Yang, Chao Quan, et al.
Frontiers in Genetics|August 5, 2025
Case Report: Pediatric CNS-isolated hemophagocytic lymphohistiocytosis secondary to uniparental disomy of <i>PRF1</i> mutationJiao Xue, Zhenfeng Song, Hongshan Zhao, et al.
Medicine|October 1, 2025
Mapping cerebrospinal fluid biomarkers to dementia risk through Mendelian randomizationXiaomin Zhu, Wei Chen, Guifeng Zhuo, et al.
Frontiers in Neuroscience|March 19, 2026
A pediatric patient with Warsaw breakage syndrome presenting with epilepsy: a case report and literature reviewYixuan Zhang, Zhi Yi, Ying Zhang, et al.
Pageof 6