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Yanjie Fan

Showing results (11-20 of 59) with videos related to

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Frontiers in Molecular Neuroscience|October 17, 2022
Actin capping protein regulates postsynaptic spine development through CPI-motif interactionsKenneth R Myers, Yanjie Fan, Patrick McConnell, et al.
Molecular Genetics & Genomic Medicine|August 28, 2019
Uniparental isodisomy caused autosomal recessive diseases: NGS-based analysis allows the concurrent detection of homogenous variants and copy-neutral loss of heterozygosityBing Xiao, Lili Wang, Huili Liu, et al.
Gene|January 7, 2022
Extended genetic analysis of exome sequencing for primary hyperoxaluria in pediatric urolithiasis patients with hyperoxaluriaYining Zhao, Yongwei Li, Xiaoliang Fang, et al.
Genome Medicine|September 19, 2024
Combining optical genome mapping and RNA-seq for structural variants detection and interpretation in unsolved neurodevelopmental disordersBing Xiao, Xiaomei Luo, Yi Liu, et al.
Animals : an Open Access Journal From MDPI|December 11, 2025
Low-Altitude UAV-Based Recognition of Porcine Facial Expressions for Early Health MonitoringZhijiang Wang, Ruxue Mi, Haoyuan Liu, et al.
BMC Medical Genetics|April 10, 2020
Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reportsXiaomei Luo, Jiacheng Hu, Xueren Gao, et al.
Annals of Human Genetics|August 11, 2020
RT-PCR analysis of mRNA revealed the splice-altering effect of rare intronic variants in monogenic disordersXia Zhang, Wenjuan Qiu, Huili Liu, et al.
BMC Genomics|September 18, 2015
De novo mutations in ARID1B associated with both syndromic and non-syndromic short statureYongguo Yu, RuEn Yao, Lili Wang, et al.
Frontiers in Genetics|August 1, 2020
Whole Genome Low-Coverage Sequencing Concurrently Detecting Copy Number Variations and Their Underlying Complex Chromosomal Rearrangements by Systematic Breakpoint Mapping in Intellectual Deficiency/Developmental Delay PatientsBing Xiao, Xiantao Ye, Lili Wang, et al.
World Journal of Urology|February 12, 2022
A comparison of the clinical characteristics of pediatric urolithiasis patients with positive and negative molecular diagnosesYining Zhao, Xiaoliang Fang, Lei He, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Frontiers in Molecular Neuroscience|October 17, 2022
Actin capping protein regulates postsynaptic spine development through CPI-motif interactionsKenneth R Myers, Yanjie Fan, Patrick McConnell, et al.
Molecular Genetics & Genomic Medicine|August 28, 2019
Uniparental isodisomy caused autosomal recessive diseases: NGS-based analysis allows the concurrent detection of homogenous variants and copy-neutral loss of heterozygosityBing Xiao, Lili Wang, Huili Liu, et al.
Gene|January 7, 2022
Extended genetic analysis of exome sequencing for primary hyperoxaluria in pediatric urolithiasis patients with hyperoxaluriaYining Zhao, Yongwei Li, Xiaoliang Fang, et al.
Genome Medicine|September 19, 2024
Combining optical genome mapping and RNA-seq for structural variants detection and interpretation in unsolved neurodevelopmental disordersBing Xiao, Xiaomei Luo, Yi Liu, et al.
Animals : an Open Access Journal From MDPI|December 11, 2025
Low-Altitude UAV-Based Recognition of Porcine Facial Expressions for Early Health MonitoringZhijiang Wang, Ruxue Mi, Haoyuan Liu, et al.
BMC Medical Genetics|April 10, 2020
Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reportsXiaomei Luo, Jiacheng Hu, Xueren Gao, et al.
Annals of Human Genetics|August 11, 2020
RT-PCR analysis of mRNA revealed the splice-altering effect of rare intronic variants in monogenic disordersXia Zhang, Wenjuan Qiu, Huili Liu, et al.
BMC Genomics|September 18, 2015
De novo mutations in ARID1B associated with both syndromic and non-syndromic short statureYongguo Yu, RuEn Yao, Lili Wang, et al.
Frontiers in Genetics|August 1, 2020
Whole Genome Low-Coverage Sequencing Concurrently Detecting Copy Number Variations and Their Underlying Complex Chromosomal Rearrangements by Systematic Breakpoint Mapping in Intellectual Deficiency/Developmental Delay PatientsBing Xiao, Xiantao Ye, Lili Wang, et al.
World Journal of Urology|February 12, 2022
A comparison of the clinical characteristics of pediatric urolithiasis patients with positive and negative molecular diagnosesYining Zhao, Xiaoliang Fang, Lei He, et al.
Pageof 6