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Ao Ma

Showing results (91-100 of 100) with videos related to

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Frontiers in Endocrinology|December 6, 2021
Novel Loss-of-Function Mutations in <i>DNAH1</i> Displayed Different Phenotypic Spectrum in Humans and MiceRanjha Khan, Qumar Zaman, Jing Chen, et al.
Zoological Research|January 27, 2022
Computationally predicted pathogenic <i>USP9X</i> mutation identified in infertile men does not affect spermatogenesis in miceWei Liu, Yue-Wen Wang, Huan Zhang, et al.
Cell Reports|March 23, 2022
ZFP541 maintains the repression of pre-pachytene transcriptional programs and promotes male meiosis progressionJianze Xu, Jianing Gao, Junyan Liu, et al.
Asian Journal of Andrology|March 9, 2022
A recurrent homozygous missense mutation in <i>CCDC103</i> causes asthenoteratozoospermia due to disorganized dynein armsMuhammad Zubair, Ranjha Khan, Ao Ma, et al.
Nature Cell Biology|March 8, 2011
Drosophila katanin is a microtubule depolymerase that regulates cortical-microtubule plus-end interactions and cell migrationDong Zhang, Kyle D Grode, Shannon F Stewman, et al.
Nature Communications|January 3, 2024
Tubeimosides are pan-coronavirus and filovirus inhibitors that can block their fusion protein binding to Niemann-Pick C1Ilyas Khan, Sunan Li, Lihong Tao, et al.
Elife|March 27, 2025
Deficiency in DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and miceMenglei Yang, Hafiz Muhammad Jafar Hussain, Manan Khan, et al.
Clinical Genetics|October 18, 2020
Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and miceBeibei Zhang, Ihsan Khan, Chunyu Liu, et al.
JCI Insight|February 8, 2023
Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and miceAo Ma, Jianteng Zhou, Haider Ali, et al.
The Journal of Experimental Medicine|October 30, 2019
A DNAH17 missense variant causes flagella destabilization and asthenozoospermiaBeibei Zhang, Hui Ma, Teka Khan, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Frontiers in Endocrinology|December 6, 2021
Novel Loss-of-Function Mutations in <i>DNAH1</i> Displayed Different Phenotypic Spectrum in Humans and MiceRanjha Khan, Qumar Zaman, Jing Chen, et al.
Zoological Research|January 27, 2022
Computationally predicted pathogenic <i>USP9X</i> mutation identified in infertile men does not affect spermatogenesis in miceWei Liu, Yue-Wen Wang, Huan Zhang, et al.
Cell Reports|March 23, 2022
ZFP541 maintains the repression of pre-pachytene transcriptional programs and promotes male meiosis progressionJianze Xu, Jianing Gao, Junyan Liu, et al.
Asian Journal of Andrology|March 9, 2022
A recurrent homozygous missense mutation in <i>CCDC103</i> causes asthenoteratozoospermia due to disorganized dynein armsMuhammad Zubair, Ranjha Khan, Ao Ma, et al.
Nature Cell Biology|March 8, 2011
Drosophila katanin is a microtubule depolymerase that regulates cortical-microtubule plus-end interactions and cell migrationDong Zhang, Kyle D Grode, Shannon F Stewman, et al.
Nature Communications|January 3, 2024
Tubeimosides are pan-coronavirus and filovirus inhibitors that can block their fusion protein binding to Niemann-Pick C1Ilyas Khan, Sunan Li, Lihong Tao, et al.
Elife|March 27, 2025
Deficiency in DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and miceMenglei Yang, Hafiz Muhammad Jafar Hussain, Manan Khan, et al.
Clinical Genetics|October 18, 2020
Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and miceBeibei Zhang, Ihsan Khan, Chunyu Liu, et al.
JCI Insight|February 8, 2023
Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and miceAo Ma, Jianteng Zhou, Haider Ali, et al.
The Journal of Experimental Medicine|October 30, 2019
A DNAH17 missense variant causes flagella destabilization and asthenozoospermiaBeibei Zhang, Hui Ma, Teka Khan, et al.
Pageof 10