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Renqian Du

Showing results (1-10 of 23) with videos related to

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Human Molecular Genetics|October 18, 2014
Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genomeZhen Peng, Weichen Zhou, Wenqing Fu, et al.
Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology|November 27, 2009
[Recombinant human gapM1 expressed in Pichia pastoris and its anti-diabetic effect]Xiang Mei, Renqian Du, Xi Li, et al.
BMC Bioinformatics|February 22, 2014
Evaluation of copy number variation detection for a SNP array platformXin Zhang, Renqian Du, Shilin Li, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|July 26, 2017
CNVbase: Batch identification of novel and rare copy number variations based on multi-ethnic population dataCheng Zhang, Jianqi Lu, Haiyi Lou, et al.
Brain & Development|August 26, 2015
Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophyJuan Ding, Dandan Zhao, Renqian Du, et al.
Genes & Genomics|September 17, 2022
The infertile individual analysis based on whole-exome sequencing in chinese multi-ethnic groupsQiongzhen Zhao, Yanqi Li, Qi Liang, et al.
Journal of Human Genetics|June 8, 2012
Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplificationRenqian Du, Chuncheng Lu, Zhengwen Jiang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 6, 2024
[Analysis and clinical application of preimplantation genetic testing for monogenic disorders in a case with Spinal muscular atrophy "2+0" genotype]Shaoying Li, Jianchun He, Wenzhi He, et al.
Journal of Human Genetics|July 8, 2016
SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humansJing Guan, Dayong Wang, Wenjian Cao, et al.
Genome Research|June 17, 2018
Predicting human genes susceptible to genomic instability associated with <i>Alu</i>/<i>Alu</i>-mediated rearrangementsXiaofei Song, Christine R Beck, Renqian Du, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|October 18, 2014
Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genomeZhen Peng, Weichen Zhou, Wenqing Fu, et al.
Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology|November 27, 2009
[Recombinant human gapM1 expressed in Pichia pastoris and its anti-diabetic effect]Xiang Mei, Renqian Du, Xi Li, et al.
BMC Bioinformatics|February 22, 2014
Evaluation of copy number variation detection for a SNP array platformXin Zhang, Renqian Du, Shilin Li, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|July 26, 2017
CNVbase: Batch identification of novel and rare copy number variations based on multi-ethnic population dataCheng Zhang, Jianqi Lu, Haiyi Lou, et al.
Brain & Development|August 26, 2015
Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophyJuan Ding, Dandan Zhao, Renqian Du, et al.
Genes & Genomics|September 17, 2022
The infertile individual analysis based on whole-exome sequencing in chinese multi-ethnic groupsQiongzhen Zhao, Yanqi Li, Qi Liang, et al.
Journal of Human Genetics|June 8, 2012
Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplificationRenqian Du, Chuncheng Lu, Zhengwen Jiang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 6, 2024
[Analysis and clinical application of preimplantation genetic testing for monogenic disorders in a case with Spinal muscular atrophy "2+0" genotype]Shaoying Li, Jianchun He, Wenzhi He, et al.
Journal of Human Genetics|July 8, 2016
SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humansJing Guan, Dayong Wang, Wenjian Cao, et al.
Genome Research|June 17, 2018
Predicting human genes susceptible to genomic instability associated with <i>Alu</i>/<i>Alu</i>-mediated rearrangementsXiaofei Song, Christine R Beck, Renqian Du, et al.
Pageof 3