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Molecular Human Reproduction|January 19, 2020
The identification of novel mutations in PLCZ1 responsible for human fertilization failure and a therapeutic intervention by artificial oocyte activationJian Mu, Zhihua Zhang, Ling Wu, et al.Human Genetics|September 28, 2023
Homozygous variants in CDC23 cause female infertility characterized by oocyte maturation defectsHuizhen Fan, Zhou Zhou, Wei Zheng, et al.EMBO Molecular Medicine|May 12, 2026
CCDC174 deficiency impaired human fertility by affecting the alternative splicing of maternal mRNAsWeijie Wang, Zhiqi Pan, Huixia Jing, et al.Human Reproduction (Oxford, England)|June 22, 2026
Pathogenic variants in ACTRT3 lead to male infertility characterized by fertilization defectsHongying Zhu, Rong Shi, Guowei Zou, et al.Journal of Medical Genetics|June 9, 2016
Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryosRuizhi Feng, Zheng Yan, Bin Li, et al.Human Reproduction (Oxford, England)|May 30, 2021
FBXO43 variants in patients with female infertility characterized by early embryonic arrestWeijie Wang, Wenjing Wang, Yao Xu, et al.Human Molecular Genetics|May 3, 2023
Bi-allelic variants in ASTL cause abnormal fertilization or oocyte maturation defectsYang Zeng, Biaobang Chen, Yiming Sun, et al.Human Genetics|February 28, 2019
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formationZhou Zhou, Caixia Ni, Ling Wu, et al.Human Genetics|January 22, 2024
Bi-allelic missense variants in MEI4 cause preimplantation embryonic arrest and female infertilityZhiqi Pan, Weijie Wang, Ling Wu, et al.The Journal of Clinical Endocrinology and Metabolism|August 9, 2019
Pregnancy and Live Birth In Women With Pathogenic LHCGR Variants Using Their Own OocytesXuefeng Lu, Zheng Yan, Renfei Cai, et al.Pageof 7