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Hafiz Muhammad Jafar Hussain
Hafiz Muhammad Jafar Hussain
在 bcm.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
A DNAH17 missense variant causes flagella destabilization and asthenozoospermia
B Zhang, H Ma, T Khan, A Ma, T Li, H Zhang, J Gao, J Zhou, Y Li, C Yu, ...
Journal of Experimental Medicine 217 (2), 2020
1072020
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
472018
A highly sensitive DNAzyme-based SERS biosensor for quantitative detection of lead ions in human serum
W Xu, A Zhao, F Zuo, R Khan, HMJ Hussain, J Li
Analytical and Bioanalytical Chemistry 412, 4565-4574, 2020
382020
CDKN2A/P16INK4A variants association with breast cancer and their in-silico analysis
A Aftab, S Shahzad, HMJ Hussain, R Khan, S Irum, S Tabassum
Breast Cancer 26, 11-28, 2019
382019
Discovery of selective inhibitors for cyclic AMP response element-binding protein: A combined ligand and structure-based resources pipeline
I Muneer, MT ul Qamar, K Tusleem, SA Rauf, HMJ Hussain, AR Siddiqi
Anti-Cancer Drugs 30 (4), 363-373, 2019
332019
Au@ Ag core-shell nanoparticles for microRNA-21 determination based on duplex-specific nuclease signal amplification and surface-enhanced Raman scattering
W Xu, A Zhao, F Zuo, R Khan, HMJ Hussain, J Chang
Microchimica Acta 187, 1-9, 2020
272020
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
192020
A “turn-off” SERS aptasensor based DNAzyme-gold nanorod for ultrasensitive lead ion detection
W Xu, A Zhao, F Zuo, HMJ Hussain, R Khan
Analytica Chimica Acta: X 2, 100020, 2019
192019
Hypophosphatemia is an independent risk factor for AKI among hospitalized patients with COVID-19 infection
Z Chen, C Gao, H Yu, L Lu, J Liu, W Chen, X Xiang, HMJ Hussain, BJ Lee, ...
Renal Failure 43 (1), 1329-1337, 2021
182021
The testis-specifically expressed Dpep3 is not essential for male fertility in mice
Y Xie, R Khan, F Wahab, HMJ Hussain, A Ali, H Ma, H Jiang, J Xu, ...
Gene 711, 143925, 2019
152019
Particulate matter of air pollution may increase risk of kidney failure in IgA nephropathy
C Luo, Y Ouyang, S Shi, G Li, Z Zhao, H Luo, F Xu, L Shao, Z Chen, S Yu, ...
Kidney International 102 (6), 1382-1391, 2022
142022
Clinical and genetic analysis of lipoprotein glomerulopathy patients caused by APOE mutations
M Yang, Q Weng, X Pan, HMJ Hussain, S Yu, J Xu, X Yu, Y Liu, Y Jin, ...
Molecular Genetics & Genomic Medicine 8 (8), e1281, 2020
142020
A validation study comparing risk prediction models of IgA nephropathy
Y Ouyang, Z Zhao, G Li, H Luo, F Xu, L Shao, Z Chen, S Yu, Y Jin, J Xu, ...
Frontiers in immunology 12, 753901, 2021
132021
Computational analysis of Cyclin D1 gene SNPs and association with breast cancer
A Aftab, R Khan, W Shah, M Azhar, A Unar, HM Jafar Hussain, A Waqas
Bioscience Reports 41 (1), BSR20202269, 2021
132021
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
Glomerular transcriptome profiles in focal glomerulosclerosis: new genes and pathways for steroid resistance
J Tong, Y Jin, Q Weng, S Yu, HM Jafar Hussain, H Ren, J Xu, W Zhang, ...
American journal of nephrology 51 (6), 442-452, 2020
82020
TP53LNC-DB, the database of lncRNAs in the p53 signalling network
MR Khan, I Bukhari, R Khan, HMJ Hussain, M Wu, RF Thorne, J Li, G Liu
Database 2019, bay136, 2019
82019
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
Possible potential outcomes from COVID-19 complications on testes: Lesson from SARS infection
R Khan, T Naseem, MJ Hussain, MA Hussain, SS Malik
Brain 32, 14-37, 2020
72020
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
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