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Pengzhen Jin

Showing results (11-20 of 23) with videos related to

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Hepatology (Baltimore, Md.)|July 10, 2024
SLC10A5 deficiency causes hypercholanemiaYuqing Xu, Yeqing Qian, Ying Yu, et al.
Frontiers in Genetics|July 19, 2021
Case Report: Identification of Maternal Low-Level Mosaicism in the Dystrophin Gene by Droplet Digital Polymerase Chain ReactionPengzhen Jin, Xiaoyang Gao, Miaomiao Wang, et al.
BMC Pregnancy and Childbirth|May 26, 2026
Prenatal diagnosis of Apert syndrome caused by a de novo FGFR2 mutation in the second trimester: a case reportXiaoying Chen, Pengzhen Jin, Min Chen, et al.
Frontiers in Genetics|November 7, 2022
Case report: Prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in the <i>JAM3</i> geneMin Xu, Pengzhen Jin, Yingzhi Huang, et al.
Frontiers in Cell and Developmental Biology|April 2, 2021
Galectin-14 Promotes Trophoblast Migration and Invasion by Upregulating the Expression of MMP-9 and N-CadherinMiaomiao Wang, Yuqing Xu, Peng Wang, et al.
Frontiers in Genetics|May 27, 2021
Clinical Efficiency of Non-invasive Prenatal Screening for Common Trisomies in Low-Risk and Twin PregnanciesYanfei Xu, Pengzhen Jin, Yu Lei, et al.
Frontiers in Genetics|December 6, 2021
Case Report: A Synonymous Mutation in <i>NF1</i> Located at the Non-canonical Splicing Site Leading to Exon 45 SkippingPengzhen Jin, Kai Yan, Shaofen Ye, et al.
Frontiers in Immunology|December 27, 2021
Pro-Inflammatory Signature in Decidua of Recurrent Pregnancy Loss Regardless of Embryonic Chromosomal AbnormalitiesZaigui Wu, Miaomiao Wang, Guanmian Liang, et al.
The Journal of Gene Medicine|March 26, 2022
Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 genePeng Wang, Pengzhen Jin, Linyan Zhu, et al.
Expert Review of Molecular Diagnostics|March 25, 2024
Performance of noninvasive prenatal screening for fetal sex chromosome aneuploidies in a cohort of 116,862 pregnanciesYanfei Xu, Jianbo Lou, Yeqing Qian, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Hepatology (Baltimore, Md.)|July 10, 2024
SLC10A5 deficiency causes hypercholanemiaYuqing Xu, Yeqing Qian, Ying Yu, et al.
Frontiers in Genetics|July 19, 2021
Case Report: Identification of Maternal Low-Level Mosaicism in the Dystrophin Gene by Droplet Digital Polymerase Chain ReactionPengzhen Jin, Xiaoyang Gao, Miaomiao Wang, et al.
BMC Pregnancy and Childbirth|May 26, 2026
Prenatal diagnosis of Apert syndrome caused by a de novo FGFR2 mutation in the second trimester: a case reportXiaoying Chen, Pengzhen Jin, Min Chen, et al.
Frontiers in Genetics|November 7, 2022
Case report: Prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in the <i>JAM3</i> geneMin Xu, Pengzhen Jin, Yingzhi Huang, et al.
Frontiers in Cell and Developmental Biology|April 2, 2021
Galectin-14 Promotes Trophoblast Migration and Invasion by Upregulating the Expression of MMP-9 and N-CadherinMiaomiao Wang, Yuqing Xu, Peng Wang, et al.
Frontiers in Genetics|May 27, 2021
Clinical Efficiency of Non-invasive Prenatal Screening for Common Trisomies in Low-Risk and Twin PregnanciesYanfei Xu, Pengzhen Jin, Yu Lei, et al.
Frontiers in Genetics|December 6, 2021
Case Report: A Synonymous Mutation in <i>NF1</i> Located at the Non-canonical Splicing Site Leading to Exon 45 SkippingPengzhen Jin, Kai Yan, Shaofen Ye, et al.
Frontiers in Immunology|December 27, 2021
Pro-Inflammatory Signature in Decidua of Recurrent Pregnancy Loss Regardless of Embryonic Chromosomal AbnormalitiesZaigui Wu, Miaomiao Wang, Guanmian Liang, et al.
The Journal of Gene Medicine|March 26, 2022
Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 genePeng Wang, Pengzhen Jin, Linyan Zhu, et al.
Expert Review of Molecular Diagnostics|March 25, 2024
Performance of noninvasive prenatal screening for fetal sex chromosome aneuploidies in a cohort of 116,862 pregnanciesYanfei Xu, Jianbo Lou, Yeqing Qian, et al.
Pageof 3