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Hui Ma
Basic Medical Sciences
University of Science and Technology of China
Anhui
Language: English, Chinese
Spermatogenesis
Maturation
Molecular Mechanisms
Disorders
Meiosis
Regulation
Human
Recombination
Genetics
Fertility
Areas of Focus
- Molecular mechanisms of human spermatogenesis and maturation disorders
- Regulatory mechanisms of meiosis
Work Experience
- 2014-2015 - National University of Singapore, School of Medicine - Research Assistant
- 2015-2017 - University of Science and Technology of China, School of Life Sciences - Postdoctoral Researcher
- 2017-2022 - University of Science and Technology of China, School of Life Sciences and Medicine - Special Associate Researcher
- 2022-present - University of Science and Technology of China, School of Life Sciences and Medicine - Associate Researcher
Academic Background & Achievements
- 2006-2010 Bachelor: Zhejiang University, School of Life Sciences
- 2010-2014 PhD: National University of Singapore, School of Medicine
- Received funding from National Natural Science Foundation of China
Publications
- M1AP interacts with the mammalian ZZS complex and promotes male meiotic recombination., Li Y, Wu Y, Khan I, Zhou J, Lu Y, Ye J, Liu J, Xie X, Hu C, Jiang H, Fan S, Zhang H, Zhang Y, Jiang X, Xu B, Ma H, Shi Q, 2023
- RAD51AP2 is required for efficient meiotic recombination between X and Y chromosomes., Ma H, Li T, Xie X, Jiang L, Ye J, Gong C, Jiang H, Fan S, Zhang H, Shi B, Zhang B, Jiang X, Li Y, Zhou J, Xu J, Zhang X, Hou X, Yin H, Zhang Y, Shi Q, 2022
- ZFP541 maintains the repression of pre-pachytene transcriptional programs and promotes male meiosis progression., Xu J, Gao J, Liu J, Huang X, Zhang H, Ma A, Ye J, Zhang X, Li Y, Yang G, Yin H, Khan R, Li T, Fan S, Jiang X, Ma H, Shi Q, 2022
- Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees., Xie X, Murtaza G, Li Y, Zhou J, Ye J, Khan R, Jiang L, Khan I, Zubair M, Yin H, Jiang H, Liu W, Shi B, Hou X, Gong C, Fan S, Wang Y, Jiang X, Zhang Y, Zhang H, Ma H, Shi Q, 2022
- Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormality of the flagella., Ma H, Zhang B, Khan A, Zhao D, Ma A, Jianteng Z, Khan I, Khan K, Zhang H, Zhang Y, Xiaohua J, Dil S, Zeb A, Rahim F, Shi Q, 2021
- A DNAH17 missense variant causes destabilization of doublets 4-7 in flagella and asthenozoospermia., Zhang B, Ma H, Khan T, Li T, Zhang H, Gao J, Zhou J, Ma A, Li Y, Yu C, Bao J, Ali A, Murtaza G, Yin H, Gao Q, Jiang X, Zhang F, Liu C, Khan I, Zubair M, Hussain H. M. J., Khan R, Yousaf A, Yuan L, Lu Y, Tao Q, Hao Q, Fang H, Cheng H, Zhang Y, Shi Q, 2020
- A TOP6BL mutation abolishes meiotic DNA double-strand break formation and causes human infertility., Jiao Y, Fan S, Jabeen N, Zhang H, Khan R, Murtaza G, Jiang H, Ali A, Li Y, Bao J, Zhang B, Xu J, Xu B, Hussain HMJ, Zaman Q, Khan I, Bukhari I, Iqbal F, Yousaf A, Dil S, Khan M, Ahmad N, Ma H, Jiang X, Zhang Y, Shi Q, 2020
- The testis specific LINC component SUN3 is essential for sperm head shaping during mouse spermiogenesis., Gao Q, Khan R, Yu C, Alsheimer M, Jiang X, Ma H, Shi Q, 2020
- A homozygous FANCM frameshift pathogenic variant causes male infertility., Yin H, Ma H, Hussain S, Zhang H, Xie X, Jiang L, Jiang X, Iqbal F, Bukhari I, Jiang H, Ali A, Zhong L, Li T, Fan S, Zhang B, Gao J, Li Y, Nazish J, Khan T, Khan M, Zubair M, Hao Q, Fang H, Huang J, Huleihel M, Sha J, Pandita TK, Zhang Y, Shi Q, 2019
- Zfp322a regulates mouse ES cell pluripotency and enhances reprogramming efficiency., Ma H, Ng HM, Teh X, Li H, Lee YH, Chong YM, Loh YH, Collins JJ, Feng B, Yang H, Wu Q, 2014
Awards
- National Natural Science Foundation of China General Program
- Youth Science Fund
- Postdoctoral Science Fund (First Class)
