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Dongdong Tang

Showing results (81-90 of 105) with videos related to

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Journal of Assisted Reproduction and Genetics|March 2, 2023
Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryosFei Tang, Yang Gao, KuoKuo Li, et al.
Systems Biology in Reproductive Medicine|June 19, 2024
Association of lifestyle and occupational exposure factors with human semen quality: a cross-sectional study of 1060 participantsWen Yang, Zongliu Duan, Guanjian Li, et al.
Journal of Medical Genetics|January 2, 2023
Biallelic mutations in <i>CFAP54</i> cause male infertility with severe MMAF and NOAShixiong Tian, Chaofeng Tu, Xiaojin He, et al.
Journal of Medical Internet Research|February 25, 2021
Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control StudyGuanjian Li, Weiran Li, Bing Song, et al.
Environmental Science and Pollution Research International|March 11, 2024
Atlas and source of the microplastics of male reproductive system in human and miceWen Yang, Longmei Wu, Guanjian Li, et al.
Iscience|July 29, 2024
Further evidence from <i>DNAH12</i> supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variantsHao Geng, Kai Wang, Dan Liang, et al.
Cells|May 28, 2022
Activation of MT1/MT2 to Protect Testes and Leydig Cells against Cisplatin-Induced Oxidative Stress through the SIRT1/Nrf2 Signaling PathwayJunqiang Zhang, Yuan Fang, Dongdong Tang, et al.
Clinical Genetics|May 11, 2022
Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in humanYang Gao, Liting Liu, Qunshan Shen, et al.
American Journal of Human Genetics|December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and miceChen Tan, Lanlan Meng, Mingrong Lv, et al.
Human Mutation|September 22, 2022
Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humansGuanxiong Wang, Xiaoyu Zhu, Yang Gao, et al.
Pageof 11

Showing results (81-90 of 105) with videos related to

Sort By:
Pageof 11
Journal of Assisted Reproduction and Genetics|March 2, 2023
Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryosFei Tang, Yang Gao, KuoKuo Li, et al.
Systems Biology in Reproductive Medicine|June 19, 2024
Association of lifestyle and occupational exposure factors with human semen quality: a cross-sectional study of 1060 participantsWen Yang, Zongliu Duan, Guanjian Li, et al.
Journal of Medical Genetics|January 2, 2023
Biallelic mutations in <i>CFAP54</i> cause male infertility with severe MMAF and NOAShixiong Tian, Chaofeng Tu, Xiaojin He, et al.
Journal of Medical Internet Research|February 25, 2021
Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control StudyGuanjian Li, Weiran Li, Bing Song, et al.
Environmental Science and Pollution Research International|March 11, 2024
Atlas and source of the microplastics of male reproductive system in human and miceWen Yang, Longmei Wu, Guanjian Li, et al.
Iscience|July 29, 2024
Further evidence from <i>DNAH12</i> supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variantsHao Geng, Kai Wang, Dan Liang, et al.
Cells|May 28, 2022
Activation of MT1/MT2 to Protect Testes and Leydig Cells against Cisplatin-Induced Oxidative Stress through the SIRT1/Nrf2 Signaling PathwayJunqiang Zhang, Yuan Fang, Dongdong Tang, et al.
Clinical Genetics|May 11, 2022
Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in humanYang Gao, Liting Liu, Qunshan Shen, et al.
American Journal of Human Genetics|December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and miceChen Tan, Lanlan Meng, Mingrong Lv, et al.
Human Mutation|September 22, 2022
Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humansGuanxiong Wang, Xiaoyu Zhu, Yang Gao, et al.
Pageof 11