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Journal of Human Genetics|April 17, 2019
Translocation breakpoint disrupting the host SNHG14 gene but not coding genes or snoRNAs in typical Prader-Willi syndromeMing Lei, Satomi Mitsuhashi, Noriko Miyake, et al.Analytica Chimica Acta|May 21, 2024
Sensitive and visual detection of SARS-CoV-2 using RPA-Cas12a one-step assay with ssDNA-modified crRNAQinlong Zeng, Miaojin Zhou, Weiheng Deng, et al.Life (Basel, Switzerland)|November 27, 2021
An Episomal CRISPR/Cas12a System for Mediating Efficient Gene EditingNannan Duan, Shuqing Tang, Baitao Zeng, et al.Journal of Ovarian Research|March 31, 2022
Mutation analysis of the TUBB8 gene in primary infertile women with oocyte maturation arrestZhongyuan Yao, Jun Zeng, Huimin Zhu, et al.Biosensors|May 28, 2022
Cas14a1-Mediated Nucleic Acid Diagnostics for Spinal Muscular AtrophyZhiqing Hu, Miaomiao Chen, Chunhua Zhang, et al.Annals of Laboratory Medicine|August 25, 2020
Detection of Spinal Muscular Atrophy Using a Duplexed Real-Time PCR Approach With Locked Nucleic Acid-Modified PrimersJianyan Pan, Chunhua Zhang, Yanling Teng, et al.BMC Bioinformatics|January 2, 2019
Constructing a database for the relations between CNV and human genetic diseases via systematic text miningXi Yang, Zhuo Song, Chengkun Wu, et al.Biosensors|August 26, 2021
CRISPR/Cas12a-Based Ultrasensitive and Rapid Detection of <i>JAK2</i> V617F Somatic Mutation in Myeloproliferative NeoplasmsMiaomiao Chen, Chunhua Zhang, Zhiqing Hu, et al.BMC Pregnancy and Childbirth|November 25, 2025
Whole exome sequencing in fetal cardiac rhabdomyoma detected by ultrasonography: an analysis of 12 casesJing Liu, Jun He, Wanglan Tang, et al.International Journal of Molecular Sciences|April 13, 2024
Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia ARou Xiao, Yan Chen, Zhiqing Hu, et al.Pageof 20