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Miaofei Xu

Showing results (1-10 of 18) with videos related to

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Andrologia|February 2, 2021
Deficiency of TBL1XR1 causes asthenozoospermiaQiao Zhou, Miaofei Xu, Xin Wang, et al.
Oncotarget|September 9, 2017
Mitochondrial DNA sequencing and large-scale genotyping identifies <i>MT-ND4</i> gene mutation m.11696G>A associated with idiopathic oligoasthenospermiaJuan Ji, Miaofei Xu, Zhenyao Huang, 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.
Ecotoxicology and Environmental Safety|July 2, 2017
Interaction between Y chromosome haplogroup O3<sup>*</sup> and 4-n-octylphenol exposure reduces the susceptibility to spermatogenic impairment in Han ChineseWeiyue Hu, Minjian Chen, Juan Ji, et al.
Molecular Human Reproduction|October 29, 2013
Pathogenic variants screening in five non-obstructive azoospermia-associated genesChuncheng Lu, Miaofei Xu, Rong Wang, et al.
Plos One|January 16, 2013
Genetic variants in meiotic program initiation pathway genes are associated with spermatogenic impairment in a Han Chinese populationChuncheng Lu, Miaofei Xu, Ying Wang, et al.
Plos One|December 5, 2013
Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese populationMiaofei Xu, Yufeng Qin, Jianhua Qu, et al.
Mitochondrion|August 2, 2015
A genome-wide association study of mitochondrial DNA in Chinese men identifies two risk single nucleotide substitutions for idiopathic oligoasthenospermiaChuncheng Lu, Miaofei Xu, Rong Wang, et al.
Reproductive Biomedicine Online|September 22, 2018
Human mitochondrial DNA haplogroup M8a influences the penetrance of m.8684C>T in Han Chinese men with non-obstructive azoospermiaJuan Ji, Miaofei Xu, Rong Wang, et al.
Human Molecular Genetics|August 20, 2011
Additional genomic duplications in AZFc underlie the b2/b3 deletion-associated risk of spermatogenic impairment in Han Chinese populationChuncheng Lu, Feng Zhang, Hua Yang, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Andrologia|February 2, 2021
Deficiency of TBL1XR1 causes asthenozoospermiaQiao Zhou, Miaofei Xu, Xin Wang, et al.
Oncotarget|September 9, 2017
Mitochondrial DNA sequencing and large-scale genotyping identifies <i>MT-ND4</i> gene mutation m.11696G>A associated with idiopathic oligoasthenospermiaJuan Ji, Miaofei Xu, Zhenyao Huang, 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.
Ecotoxicology and Environmental Safety|July 2, 2017
Interaction between Y chromosome haplogroup O3<sup>*</sup> and 4-n-octylphenol exposure reduces the susceptibility to spermatogenic impairment in Han ChineseWeiyue Hu, Minjian Chen, Juan Ji, et al.
Molecular Human Reproduction|October 29, 2013
Pathogenic variants screening in five non-obstructive azoospermia-associated genesChuncheng Lu, Miaofei Xu, Rong Wang, et al.
Plos One|January 16, 2013
Genetic variants in meiotic program initiation pathway genes are associated with spermatogenic impairment in a Han Chinese populationChuncheng Lu, Miaofei Xu, Ying Wang, et al.
Plos One|December 5, 2013
Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese populationMiaofei Xu, Yufeng Qin, Jianhua Qu, et al.
Mitochondrion|August 2, 2015
A genome-wide association study of mitochondrial DNA in Chinese men identifies two risk single nucleotide substitutions for idiopathic oligoasthenospermiaChuncheng Lu, Miaofei Xu, Rong Wang, et al.
Reproductive Biomedicine Online|September 22, 2018
Human mitochondrial DNA haplogroup M8a influences the penetrance of m.8684C>T in Han Chinese men with non-obstructive azoospermiaJuan Ji, Miaofei Xu, Rong Wang, et al.
Human Molecular Genetics|August 20, 2011
Additional genomic duplications in AZFc underlie the b2/b3 deletion-associated risk of spermatogenic impairment in Han Chinese populationChuncheng Lu, Feng Zhang, Hua Yang, et al.
Pageof 2