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Qing Sang

Showing results (151-160 of 159) with videos related to

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European Journal of Human Genetics : EJHG|October 10, 2018
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertilityBiaobang Chen, Wenjing Wang, Xiandong Peng, et al.
Human Reproduction (Oxford, England)|May 26, 2021
Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failureJie Dong, Hong Zhang, Xiaoyan Mao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 27, 2022
Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrestLin Zhao, Qun Li, Yanping Kuang, et al.
Protein & Cell|July 16, 2020
Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic developmentLin Zhao, Songguo Xue, Zhongyuan Yao, et al.
The Journal of Clinical Investigation|January 17, 2023
Karyopherin α deficiency contributes to human preimplantation embryo arrestWenjing Wang, Yoichi Miyamoto, Biaobang Chen, et al.
Genome Biology|April 6, 2023
Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defectsQun Li, Lin Zhao, Yang Zeng, et al.
The New England Journal of Medicine|January 21, 2016
Mutations in TUBB8 and Human Oocyte Meiotic ArrestRuizhi Feng, Qing Sang, Yanping Kuang, et al.
Cell Genomics|September 26, 2025
Genetic landscape of human oocyte/embryo defectsBiaobang Chen, Weijie Wang, Juanzi Shi, et al.
Molecular Ecology Resources|May 14, 2011
Permanent Genetic Resources added to Molecular Ecology Resources Database 1 August 2009-30 September 2009, Doukary Abdoullaye, I Acevedo, et al.
Pageof 16

Showing results (151-160 of 159) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 159 results.
European Journal of Human Genetics : EJHG|October 10, 2018
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertilityBiaobang Chen, Wenjing Wang, Xiandong Peng, et al.
Human Reproduction (Oxford, England)|May 26, 2021
Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failureJie Dong, Hong Zhang, Xiaoyan Mao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 27, 2022
Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrestLin Zhao, Qun Li, Yanping Kuang, et al.
Protein & Cell|July 16, 2020
Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic developmentLin Zhao, Songguo Xue, Zhongyuan Yao, et al.
The Journal of Clinical Investigation|January 17, 2023
Karyopherin α deficiency contributes to human preimplantation embryo arrestWenjing Wang, Yoichi Miyamoto, Biaobang Chen, et al.
Genome Biology|April 6, 2023
Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defectsQun Li, Lin Zhao, Yang Zeng, et al.
The New England Journal of Medicine|January 21, 2016
Mutations in TUBB8 and Human Oocyte Meiotic ArrestRuizhi Feng, Qing Sang, Yanping Kuang, et al.
Cell Genomics|September 26, 2025
Genetic landscape of human oocyte/embryo defectsBiaobang Chen, Weijie Wang, Juanzi Shi, et al.
Molecular Ecology Resources|May 14, 2011
Permanent Genetic Resources added to Molecular Ecology Resources Database 1 August 2009-30 September 2009, Doukary Abdoullaye, I Acevedo, et al.
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