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Shengwen Huang

Showing results (11-20 of 53) with videos related to

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Frontiers in Neurology|January 9, 2023
Case report: Two unique nonsense mutations in <i>HTRA1</i>-related cerebral small vessel disease in a Chinese population and literature reviewWeijie Chen, Yuanyuan Wang, Shengwen Huang, et al.
Stem Cell Research|June 29, 2023
Human induced pluripotent stem cells derived from a patient with a mutation of SERPINC1 c.236G>A (p.R79H)Weijie Chen, Yuanyuan Wang, Liwei Shen, et al.
Hemoglobin|February 29, 2024
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid DifferentiationDan Xie, Yuanyuan Han, Wenyi Zhang, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|October 26, 2022
A Three-Year Prospective Study Assessing the Application of Chromosomal Microarray Analysis in 576 High-Risk Pregnant WomenMinmin Jiang, Shengwen Huang, Xingwei Ma, et al.
Biochemical Genetics|July 2, 2025
Functional Analysis of a Novel Missense Mutation c.1039A > G of TUBB8 in Infertile WomenMin Guo, Fangfang Li, Lingyan Ren, et al.
Medicine|February 17, 2023
A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case reportDan Xie, Jiangfen Wu, Wenyi Zhang, et al.
Journal of Assisted Reproduction and Genetics|May 26, 2021
Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic developmentJuan Liu, Zongjian Tan, Jun He, et al.
Heliyon|May 31, 2024
Functional analysis of a novel intronic variant of <i>MCPH1</i> with autosomal recessive primary microcephalyShulin Luo, Lingyan Ren, Rongping Wang, et al.
Acta Biochimica Et Biophysica Sinica|August 14, 2016
Adenosine monophosphate-activated protein kinase attenuates cardiomyocyte hypertrophy through regulation of FOXO3a/MAFbx signaling pathwayBaolin Chen, Qiang Wu, Zhaojun Xiong, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2015
[Mutation analysis of the TRAPPC2 gene in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda]Xian Wu, Kaixian Deng, Chunjiao Wang, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
Frontiers in Neurology|January 9, 2023
Case report: Two unique nonsense mutations in <i>HTRA1</i>-related cerebral small vessel disease in a Chinese population and literature reviewWeijie Chen, Yuanyuan Wang, Shengwen Huang, et al.
Stem Cell Research|June 29, 2023
Human induced pluripotent stem cells derived from a patient with a mutation of SERPINC1 c.236G>A (p.R79H)Weijie Chen, Yuanyuan Wang, Liwei Shen, et al.
Hemoglobin|February 29, 2024
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid DifferentiationDan Xie, Yuanyuan Han, Wenyi Zhang, et al.
Evidence-Based Complementary and Alternative Medicine : Ecam|October 26, 2022
A Three-Year Prospective Study Assessing the Application of Chromosomal Microarray Analysis in 576 High-Risk Pregnant WomenMinmin Jiang, Shengwen Huang, Xingwei Ma, et al.
Biochemical Genetics|July 2, 2025
Functional Analysis of a Novel Missense Mutation c.1039A > G of TUBB8 in Infertile WomenMin Guo, Fangfang Li, Lingyan Ren, et al.
Medicine|February 17, 2023
A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case reportDan Xie, Jiangfen Wu, Wenyi Zhang, et al.
Journal of Assisted Reproduction and Genetics|May 26, 2021
Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic developmentJuan Liu, Zongjian Tan, Jun He, et al.
Heliyon|May 31, 2024
Functional analysis of a novel intronic variant of <i>MCPH1</i> with autosomal recessive primary microcephalyShulin Luo, Lingyan Ren, Rongping Wang, et al.
Acta Biochimica Et Biophysica Sinica|August 14, 2016
Adenosine monophosphate-activated protein kinase attenuates cardiomyocyte hypertrophy through regulation of FOXO3a/MAFbx signaling pathwayBaolin Chen, Qiang Wu, Zhaojun Xiong, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2015
[Mutation analysis of the TRAPPC2 gene in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda]Xian Wu, Kaixian Deng, Chunjiao Wang, et al.
Pageof 6