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Jiyun Yang

Showing results (21-30 of 104) with videos related to

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Genetic Testing and Molecular Biomarkers|February 14, 2018
Identification of Five Novel Variants in Chinese Oculocutaneous Albinism by Targeted Next-Generation SequencingBiyuan Qiu, Tao Ma, Chunyan Peng, et al.
Frontiers in Pediatrics|April 3, 2026
Case Report: A case of Joubert syndrome in twin pregnancy: MRI manifestations and literature reviewSilu Ren, Aitong Li, Jiyun Yang, et al.
Oncology Letters|April 16, 2025
Pancreatic liposarcoma: A case reportYan Zhao, Shikang Hu, Huajun Sun, et al.
Human Mutation|October 22, 2025
Novel Algorithm for Monogenic Noninvasive Prenatal Testing With Highly Similar Parental Pathogenic Haplotypes: A Representative Case of Congenital Adrenal Hyperplasia PedigreeWenjing Zhou, Fulin Liu, Shaojun Li, et al.
Hereditas|November 24, 2020
Two novel likely pathogenic variants of HARS2 identified in a Chinese family with sensorineural hearing lossJing Yu, Wei Jiang, Li Cao, et al.
Epilepsy & Behavior : E&B|September 13, 2020
Alterations of functional connectivity density in a Chinese family with a mild phenotype associated with a novel inherited variant of SCN8AQiong Zhu, Sisi Jiang, Cheng Luo, et al.
Molecular Genetics & Genomic Medicine|April 29, 2026
Identification of a Novel De Novo Heterozygous SEC61A1 Variant in a Patient With Severe Congenital NeutropeniaZixuan Wang, Hui Jing, Yuhan Chen, et al.
Frontiers in Physiology|January 23, 2023
A novel homozygous mutation in <i>LSS</i> gene possibly causes hypotrichosis simplex in two siblings of a Tibetan family from the western Sichuan province of ChinaBei Zhao, Yisi Tang, Wenjing Chen, et al.
Cancer Letters|May 27, 2008
Breast cancer metastasis suppressor 1 inhibits SDF-1alpha-induced migration of non-small cell lung cancer by decreasing CXCR4 expressionJiyun Yang, Ben Zhang, Yin Lin, et al.
Molecular Genetics & Genomic Medicine|November 27, 2018
Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie diseaseJingjing Liu, Jing Zhu, Jiyun Yang, et al.
Pageof 11

Showing results (21-30 of 104) with videos related to

Sort By:
Pageof 11
Genetic Testing and Molecular Biomarkers|February 14, 2018
Identification of Five Novel Variants in Chinese Oculocutaneous Albinism by Targeted Next-Generation SequencingBiyuan Qiu, Tao Ma, Chunyan Peng, et al.
Frontiers in Pediatrics|April 3, 2026
Case Report: A case of Joubert syndrome in twin pregnancy: MRI manifestations and literature reviewSilu Ren, Aitong Li, Jiyun Yang, et al.
Oncology Letters|April 16, 2025
Pancreatic liposarcoma: A case reportYan Zhao, Shikang Hu, Huajun Sun, et al.
Human Mutation|October 22, 2025
Novel Algorithm for Monogenic Noninvasive Prenatal Testing With Highly Similar Parental Pathogenic Haplotypes: A Representative Case of Congenital Adrenal Hyperplasia PedigreeWenjing Zhou, Fulin Liu, Shaojun Li, et al.
Hereditas|November 24, 2020
Two novel likely pathogenic variants of HARS2 identified in a Chinese family with sensorineural hearing lossJing Yu, Wei Jiang, Li Cao, et al.
Epilepsy & Behavior : E&B|September 13, 2020
Alterations of functional connectivity density in a Chinese family with a mild phenotype associated with a novel inherited variant of SCN8AQiong Zhu, Sisi Jiang, Cheng Luo, et al.
Molecular Genetics & Genomic Medicine|April 29, 2026
Identification of a Novel De Novo Heterozygous SEC61A1 Variant in a Patient With Severe Congenital NeutropeniaZixuan Wang, Hui Jing, Yuhan Chen, et al.
Frontiers in Physiology|January 23, 2023
A novel homozygous mutation in <i>LSS</i> gene possibly causes hypotrichosis simplex in two siblings of a Tibetan family from the western Sichuan province of ChinaBei Zhao, Yisi Tang, Wenjing Chen, et al.
Cancer Letters|May 27, 2008
Breast cancer metastasis suppressor 1 inhibits SDF-1alpha-induced migration of non-small cell lung cancer by decreasing CXCR4 expressionJiyun Yang, Ben Zhang, Yin Lin, et al.
Molecular Genetics & Genomic Medicine|November 27, 2018
Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie diseaseJingjing Liu, Jing Zhu, Jiyun Yang, et al.
Pageof 11