关注
Tahir Zaib
Tahir Zaib
Postdoctoral Research Assocaite, Shantou University Medical College
在 stu.edu.cn 的电子邮件经过验证
标题
引用次数
引用次数
年份
Assessment of candidate genes and genetic heterogeneity in human non syndromic orofacial clefts specifically non syndromic cleft lip with or without palate
K Saleem, T Zaib, W Sun, S Fu
Heliyon 5 (12), 2019
812019
Emodin succinyl ester inhibits malignant proliferation and migration of hepatocellular carcinoma by suppressing the interaction of AR and EZH2
H Khan, W Jia, Z Yu, T Zaib, J Feng, Y Jiang, H Song, Y Bai, B Yang, ...
Biomedicine & Pharmacotherapy 128, 110244, 2020
222020
Evaluation of a Novel Missense Mutation in ABCB4 Gene Causing Progressive Familial Intrahepatic Cholestasis Type 3
K Saleem, Q Cui, T Zaib, S Zhu, Q Qin, Y Wang, J Dam, W Ji, P Liu, X Jia, ...
Disease Markers 2020 (1), 6292818, 2020
152020
A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family
T Zaib, W Ji, K Saleem, G Nie, C Li, L Cao, B Xu, K Dong, H Yu, X Hao, ...
BMC medical genetics 20, 1-9, 2019
142019
Recent advances in syndactyly: Basis, current status and future perspectives
T Zaib, H Rashid, H Khan, X Zhou, P Sun
Genes 13 (5), 771, 2022
122022
Expression of CD22 in triple-negative breast cancer: a novel prognostic biomarker and potential target for CAR therapy
T Zaib, K Cheng, T Liu, R Mei, Q Liu, X Zhou, L He, H Rashid, Q Xie, ...
International Journal of Molecular Sciences 24 (3), 2152, 2023
82023
SNPs in folate pathway are associated with the risk of nonsyndromic cleft lip with or without cleft palate, a meta-analysis
Q Li, L Xu, X Jia, K Saleem, T Zaib, W Sun, S Fu
Bioscience reports 40 (3), BSR20194261, 2020
82020
[Retracted] Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree
T Zaib, C Zhang, K Saleem, L Xu, Q Qin, Y Wang, W Ji, H Khan, H Yu, ...
Disease Markers 2020 (1), 8360841, 2020
72020
CD22 is a potential target of CAR-NK cell therapy for esophageal squamous cell carcinoma
T Liu, X Dai, Y Xu, T Guan, L Hong, T Zaib, Q Zhou, K Cheng, X Zhou, ...
Journal of Translational Medicine 21 (1), 710, 2023
32023
Combinatorial approach of in silico and in vitro evaluation of MLH1 variant associated with Lynch syndrome like metastatic colorectal cancer
K Saleem, T Zaib, W Ji, C Zhang, Q Qin, Y Wang, L Xu, H Yu, S Zhu, ...
Bioscience Reports 40 (6), BSR20200225, 2020
12020
Two SNPs rs1801133 and rs1801394 in folate pathway are associated with the risk of nonsyndromic cleft lip with or without cleft palate
Q Li, L Xu, X Jia, K Saleem, T Zaib, W Sun, S Fu
2019
WITHDRAWN: A 24-base pair duplication in exon one of HOXD13 gene linked to synpolydactyly type 1 in a Chinese family
T Zaib, W Ji, K Saleem, G Nie, C Li, L Cao, B Xu, K Dong, H Yu, X Hao, ...
Meta Gene, 2018
2018
系统目前无法执行此操作,请稍后再试。
文章 1–12