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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 embryos
Fei 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 participants
Wen 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 NOA
Shixiong 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 Study
Guanjian 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 mice
Wen 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 variants
Hao 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 Pathway
Junqiang 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 human
Yang 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 mice
Chen 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 humans
Guanxiong Wang, Xiaoyu Zhu, Yang Gao, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 105) with videos related to
Sort By:
Page
of 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 embryos
Fei 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 participants
Wen 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 NOA
Shixiong 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 Study
Guanjian 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 mice
Wen 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 variants
Hao 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 Pathway
Junqiang 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 human
Yang 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 mice
Chen 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 humans
Guanxiong Wang, Xiaoyu Zhu, Yang Gao, et al.
Page
of 11