Zobrazeno 1 - 10
of 18
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, 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:
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
Publikováno v:
Genes. 13(5)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b726ff6128e6b8891680324faedc4c0
https://pubmed.ncbi.nlm.nih.gov/35627156
https://pubmed.ncbi.nlm.nih.gov/35627156
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
Volume 24
Issue 3
Pages: 2152
Volume 24
Issue 3
Pages: 2152
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3ac67040761de3c99f7f86a345a9e28
https://doi.org/10.3390/ijms24032152
https://doi.org/10.3390/ijms24032152
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b06952d9fe54d392a9cebc5a0f651ac6
http://www.sciencedirect.com/science/article/pii/S0753332220304364
http://www.sciencedirect.com/science/article/pii/S0753332220304364
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31b359a75c1c4e2a30d72b6a2ca62b75
https://doi.org/10.1042/bsr20200225
https://doi.org/10.1042/bsr20200225
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cccd596b7847fb593f6162af243ddfad
https://doi.org/10.1042/bsr20194261
https://doi.org/10.1042/bsr20194261
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7da432416645bfc86b814031fcb8925
https://pubmed.ncbi.nlm.nih.gov/32626542
https://pubmed.ncbi.nlm.nih.gov/32626542
Autor:
Songbin Fu, Wei Ji, Lidan Xu, Chunhui Zhang, Hanfei Yu, Jie Wu, Wei Gao, Hanif Khan, Siqi Zhu, Yanqiao Zhang, Hongtao Song, Wenjing Sun, Yun Huang, Xueyuan Jia, Komal Saleem, Yusi Wang, Tahir Zaib, Qian Qin
Publikováno v:
Disease Markers
Disease Markers, Vol 2020 (2020)
Disease Markers, Vol 2020 (2020)
Lynch syndrome (LS) is the most common hereditary colorectal cancer (CRCs) inherited in an autosomal-dominant manner. Here, we reported a multigeneration Chinese family clinically diagnosed with LS according to the Amsterdam II criteria. To identify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a31b13f837c4ab85f795226b0490d488