Obserwuj
Manan Khan
Manan Khan
Xuanwu Hospital Capital Medical University, Beijing China &Hazar University Mansehra Pakistan
Zweryfikowany adres z hu.edu.pk
Tytuł
Cytowane przez
Cytowane przez
Rok
A homozygous FANCM frameshift pathogenic variant causes male infertility
H Yin, H Ma, S Hussain, H Zhang, X Xie, L Jiang, X Jiang, F Iqbal, ...
Genetics in Medicine 21 (1), 62-70, 2019
982019
Specific Deletion of Cdh2 in Sertoli Cells Leads to Altered Meiotic Progression and Subfertility of Mice
X Jiang, T Ma, Y Zhang, H Zhang, S Yin, W Zheng, L Wang, Z Wang, ...
Biology of reproduction 92 (3), 79, 1-12, 2015
642015
The evolutionarily conserved genes: Tex37, Ccdc73, Prss55 and Nxt2 are dispensable for fertility in mice
M Khan, N Jabeen, T Khan, HMJ Hussain, A Ali, R Khan, L Jiang, T Li, ...
Scientific Reports 8 (1), 4975, 2018
482018
Histone acetyltransferase KAT8 is essential for mouse oocyte development by regulating reactive oxygen species levels
S Yin, X Jiang, H Jiang, Q Gao, F Wang, S Fan, T Khan, N Jabeen, ...
Development 144 (12), 2165-2174, 2017
432017
A TOP6BL mutation abolishes meiotic DNA double-strand break formation and causes human infertility
Y Jiao, S Fan, N Jabeen, H Zhang, R Khan, G Murtaza, H Jiang, A Ali, Y Li, ...
Science Bulletin 65 (24), 2120-2129, 2020
222020
Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice
R Khan, Q Zaman, J Chen, M Khan, A Ma, J Zhou, B Zhang, A Ali, ...
Frontiers in Endocrinology 12, 765639, 2021
142021
The deubiquitinating gene Usp29 is dispensable for fertility in male mice
Z Huang, M Khan, J Xu, T Khan, H Ma, R Khan, HMJ Hussain, X Jiang, ...
Science China Life Sciences 62, 544-552, 2019
92019
Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani family
T Khan, M Khan, A Yousaf, S Khan, M Naeem, A Shah, G Murtaza, A Ali, ...
Journal of Human Genetics 63 (10), 1071-1076, 2018
82018
Whole exome sequencing revealed a novel nonsense variant in the GNRHR gene causing normosmic hypogonadotropic hypogonadism in a Pakistani family
HMJ Hussain, G Murtaza, X Jiang, R Khan, M Khan, MBS Kakakhel, ...
Hormone Research in Paediatrics 91 (1), 9-16, 2019
72019
A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella
A Ali, A Unar, Z Muhammad, S Dil, B Zhang, H Sadaf, M Khan, M Ali, ...
Journal of Assisted Reproduction and Genetics 41 (1), 109-120, 2024
52024
Inactivation of testis-specific gene C4orf46 is dispensable for spermatogenesis and fertility in mouse
B Shah, R Khan, W Shah, A Aftab, M Khan, S Dil, Q Shi
Mammalian Genome 32 (5), 364-370, 2021
52021
Deficiency in a special dynein DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and mice
M Yang, HMJ Hussain, M Khan, Z Muhammad, J Zhou, A Ma, X Huang, ...
bioRxiv, 2024.06. 20.599934, 2024
22024
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