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EMBO Molecular Medicine
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April 13, 2023
Bi-allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility
Weijie Wang, Jing Guo, Juanzi Shi, et al.
Reproductive Biomedicine Online
|
April 3, 2018
Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest
Xueqian Wang, Di Song, Dmytro Mykytenko, et al.
Journal of Assisted Reproduction and Genetics
|
June 12, 2020
Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations
Lin Zhao, Yichun Guan, Wenjing Wang, et al.
Cancer Immunology, Immunotherapy : CII
|
April 29, 2025
Targeting interleukin-2-inducible T cell kinase ameliorates immune-mediated aplastic anemia
Weiwang Li, Yu Lian, Lele Zhang, et al.
Science Translational Medicine
|
March 29, 2019
A pannexin 1 channelopathy causes human oocyte death
Qing Sang, Zhihua Zhang, Juanzi Shi, et al.
Frontiers in Cell and Developmental Biology
|
April 26, 2021
Identification of Novel Mutations in <i>CDC20</i>: Expanding the Mutational Spectrum for Female Infertility
Lin Zhao, Yichun Guan, Qingxia Meng, et al.
European Journal of Human Genetics : EJHG
|
October 10, 2018
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility
Biaobang Chen, Wenjing Wang, Xiandong Peng, et al.
Nature Biomedical Engineering
|
October 29, 2025
Improved specificity and efficiency of in vivo adenine base editing therapies with hybrid guide RNAs
Madelynn N Whittaker, Lauren C Testa, Aidan Quigley, 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 failure
Jie 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 arrest
Lin Zhao, Qun Li, Yanping Kuang, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 208) with videos related to
Sort By:
Page
of 21
EMBO Molecular Medicine
|
April 13, 2023
Bi-allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility
Weijie Wang, Jing Guo, Juanzi Shi, et al.
Reproductive Biomedicine Online
|
April 3, 2018
Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest
Xueqian Wang, Di Song, Dmytro Mykytenko, et al.
Journal of Assisted Reproduction and Genetics
|
June 12, 2020
Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations
Lin Zhao, Yichun Guan, Wenjing Wang, et al.
Cancer Immunology, Immunotherapy : CII
|
April 29, 2025
Targeting interleukin-2-inducible T cell kinase ameliorates immune-mediated aplastic anemia
Weiwang Li, Yu Lian, Lele Zhang, et al.
Science Translational Medicine
|
March 29, 2019
A pannexin 1 channelopathy causes human oocyte death
Qing Sang, Zhihua Zhang, Juanzi Shi, et al.
Frontiers in Cell and Developmental Biology
|
April 26, 2021
Identification of Novel Mutations in <i>CDC20</i>: Expanding the Mutational Spectrum for Female Infertility
Lin Zhao, Yichun Guan, Qingxia Meng, et al.
European Journal of Human Genetics : EJHG
|
October 10, 2018
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility
Biaobang Chen, Wenjing Wang, Xiandong Peng, et al.
Nature Biomedical Engineering
|
October 29, 2025
Improved specificity and efficiency of in vivo adenine base editing therapies with hybrid guide RNAs
Madelynn N Whittaker, Lauren C Testa, Aidan Quigley, 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 failure
Jie 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 arrest
Lin Zhao, Qun Li, Yanping Kuang, et al.
Page
of 21