Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Tahir Zaib"'
Autor:
Tingdang Liu, Ximing Dai, Yien Xu, Tian Guan, Liangli Hong, Tahir Zaib, Qi Zhou, Ke Cheng, Xiaoling Zhou, Changchun Ma, Pingnan Sun
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-12 (2023)
Abstract Background Chimeric antigen receptor NK (CAR-NK) cell therapy is one of the most promising immunotherapies. Although it has shown a significant therapeutic effect in hematologic malignancies, few successes have been obtained in solid tumors
Externí odkaz:
https://doaj.org/article/fd0ef2247af04e3c8ce3dbe5021c98f9
Autor:
Tahir Zaib, Ke Cheng, Tingdang Liu, Ruyi Mei, Qin Liu, Xiaoling Zhou, Lifang He, Hibba Rashid, Qingdong Xie, Hanif Khan, Yien Xu, Pingnan Sun, Jundong Wu
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2152 (2023)
Triple-negative breast cancer (TNBC) accounts for 15–20% of all breast cancer cases. Due to the lack of expression of well-known molecular targets [estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HE
Externí odkaz:
https://doaj.org/article/b99a4361ee324acd92b57a904b5c7dc0
Autor:
Tahir Zaib, Wei Ji, Komal Saleem, Guangchen Nie, Chao Li, Lin Cao, Baijun Xu, Kexian Dong, Hanfei Yu, Xuguang Hao, Yan Xue, Shuhan Si, Xueyuan Jia, Jie Wu, Xuelong Zhang, Rongwei Guan, Guohua Ji, Jing Bai, Feng Chen, Yong Liu, Wenjing Sun, Songbin Fu
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background Synpolydactyly type 1 (SPD1), also known as syndactyly type II, is an autosomal dominant limb deformity generally results in webbing of 3rd and 4th fingers, duplication of 4th or 5th toes. It is most commonly caused by mutation in
Externí odkaz:
https://doaj.org/article/08ae1d772caf4e608fea4fa8a07f1b5c
Publikováno v:
Genes, Vol 13, Iss 5, p 771 (2022)
A comprehensive summary of recent knowledge in syndactyly (SD) is important for understanding the genetic etiology of SD and disease management. Thus, this review article provides background information on SD, as well as insights into phenotypic and
Externí odkaz:
https://doaj.org/article/2845c5af794b4a66a82a9a20d745bb19
Autor:
Hanif Khan, Wenting Jia, Zhuo Yu, Tahir Zaib, Jun Feng, Yanan Jiang, Haibin Song, Yunlong Bai, Baofeng Yang, Hai Feng
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 128, Iss , Pp 110244- (2020)
Emodin is a promising anti-cancer reagent. To improve the physicochemical and anti-cancer property, we modified its structure and get a derivative called emodin succinyl ester (ESE). Here, we investigated the effect of ESE on the suppression of hepat
Externí odkaz:
https://doaj.org/article/08b65a0832904e5ebe3f2d7638c55da7
Publikováno v:
Heliyon, Vol 5, Iss 12, Pp e03019- (2019)
Non syndromic orofacial clefts specifically non-syndromic cleft lip/palate are one of the most common craniofacial malformation among birth defects in human having multifactorial etiology with an incidence of 1:700/1000. On the basis of association w
Externí odkaz:
https://doaj.org/article/4d22877d127141e1a67e32cbd2df7127
Autor:
Jun Feng, Hai Feng, Hanif Khan, Haibin Song, Tahir Zaib, Zhuo Yu, Baofeng Yang, Wenting Jia, Yanan Jiang, Yunlong Bai
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 128, Iss, Pp 110244-(2020)
Emodin is a promising anti-cancer reagent. To improve the physicochemical and anti-cancer property, we modified its structure and get a derivative called emodin succinyl ester (ESE). Here, we investigated the effect of ESE on the suppression of hepat
Autor:
Shuhan Si, Jie Wu, Siqi Zhu, Songbin Fu, Kexian Dong, Qian Qin, Wenjing Sun, Wei Ji, Xueyuan Jia, Chunhui Zhang, Tahir Zaib, Yusi Wang, Lidan Xu, Hanfei Yu, Komal Saleem
Publikováno v:
Bioscience Reports. 40
Colorectal cancer (CRC) is the third most developing cancer worldwide and Lynch syndrome (LS) accounts for 3–4% of CRC. Genetic alteration in any of DNA mismatch repair (MMR) gene is the major cause of LS that disrupt the normal upstream and downst
Publikováno v:
Bioscience Reports
Background: Prenatal intake of folic acid is important for prevention of NSCL/P (nonsyndromic cleft lip with or without cleft palate). Associated genes in folate pathway are major enzymes of folic acid metabolism that is crucial for preventing birth
Autor:
Komal, Saleem, Qingbo, Cui, Tahir, Zaib, Siqi, Zhu, Qian, Qin, Yusi, Wang, Jinxi, Dam, Wei, Ji, Peng, Liu, Xueyuan, Jia, Jie, Wu, Jing, Bai, Songbin, Fu, Wenjing, Sun
Publikováno v:
Disease Markers
Progressive familial intrahepatic cholestasis type 3 (PFIC3) is a hepatic disorder occurring predominantly in childhood and is difficult to diagnose. PFIC3, being a rare autosomal recessive disease, is caused by genetic mutations in both alleles of A