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Zhengchang Li

Showing results (1-10 of 5) with videos related to

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Scientific Reports|April 14, 2026
Human motion recognition based on progressive neural architecture search for efficient and interpretable spatiotemporal learningFeng Wang, Zhengchang Li
The Journal of Steroid Biochemistry and Molecular Biology|November 17, 2025
Urinary metabolomic biomarkers for diagnosing central precocious puberty and revealing sexual dimorphismLingling Wen, Sheng Wu, Jingxia Wu, et al.
Molecular Genetics & Genomic Medicine|May 5, 2021
Confirming the contribution and genetic spectrum of de novo mutation in infantile spasms: Evidence from a Chinese cohortLiying Liu, Fang Liu, Qiuhong Wang, et al.
Brain : a Journal of Neurology|March 4, 2023
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopmentFang Liu, Chen Liang, Zhengchang Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 6, 2021
CNV profiles of Chinese pediatric patients with developmental disordersHaiming Yuan, Shaofang Shangguan, Zhengchang Li, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Scientific Reports|April 14, 2026
Human motion recognition based on progressive neural architecture search for efficient and interpretable spatiotemporal learningFeng Wang, Zhengchang Li
The Journal of Steroid Biochemistry and Molecular Biology|November 17, 2025
Urinary metabolomic biomarkers for diagnosing central precocious puberty and revealing sexual dimorphismLingling Wen, Sheng Wu, Jingxia Wu, et al.
Molecular Genetics & Genomic Medicine|May 5, 2021
Confirming the contribution and genetic spectrum of de novo mutation in infantile spasms: Evidence from a Chinese cohortLiying Liu, Fang Liu, Qiuhong Wang, et al.
Brain : a Journal of Neurology|March 4, 2023
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopmentFang Liu, Chen Liang, Zhengchang Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 6, 2021
CNV profiles of Chinese pediatric patients with developmental disordersHaiming Yuan, Shaofang Shangguan, Zhengchang Li, et al.
Pageof 1