Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Binjiao Zheng"'
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Akademický článek
NECTIN-4-redirected T cell Antigen Coupler T cells bearing CD28 show superior antitumor responses against solid tumors
Autor: Cheng Wei, Xin Huang, Tianlong Xu, Yinan Fang, Fabao Wang, Qiaolin He, Peiyuan Zhang, Qianjin Yu, Ying Zhang, Binjiao Zheng, Yue Gao, Yongping Chen, Qichuan Zhuge, Ai Zhao, Jimin Gao, Jinhong Jiang
Publikováno v: Frontiers in Immunology, Vol 15 (2024)
IntroductionT cell Antigen Coupler (TAC) T cells harness all signaling subunits of endogenous T cell receptor (TCR) to trigger T-cell activation and tumor cell lysis, with minimal release of cytokines. Some of the major obstacles to cellular immunoth
Externí odkaz: https://doaj.org/article/a60b92ced82045508b4898d4ffe2b58d
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2
A deafness-associated tRNAAspmutation alters the m1G37 modification, aminoacylation and stability of tRNAAspand mitochondrial function
Autor: Hao Liu, Yong Wang, Binjiao Zheng, Taosheng Huang, Xiaowen Tang, Jing Zheng, Min-Xin Guan, Meng Wang, Yanyan Peng, Xiaofen Jin, Pingping Jiang
Publikováno v: Nucleic Acids Research
In this report, we investigated the pathogenic mechanism underlying the deafness-associated mitochondrial(mt) tRNAAsp 7551A > G mutation. The m.7551A > G mutation is localized at a highly conserved nucleotide(A37), adjacent (3′) to the anticodon, w
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::185054f37c95f57390681d3b0e0823e0
https://doi.org/10.1093/nar/gkw726
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[Analysis of audiological characteristics and genetic background in patients with nonsyndromic deafness and mitochondrial DNA 1555AG mutation]
Autor: Yue, Zhuo, Hao, Wu, Hao, Jin, Haiwei, Liu, Dan, Zhang, Jia, Huang, Binjiao, Zheng
Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 35(5)
To analyze the audiological features and genetic background of patients carrying mitochondrial DNA(mtDNA) 1555AG mutation and factors which may influence the extent of nonsyndromic hearing loss associated with the mutation.A literature search was car
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bb4d94555b5daf2c8028d41952127273
https://pubmed.ncbi.nlm.nih.gov/30298482
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5
[Mutations of mitochondrial tRNA
Autor: Wenlu, Fan, Xiaowen, Tang, Binjiao, Zheng, Minxin, Guan, Ling, Xue
Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 34(1)
Mitochondrial tRNA
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a6a56250c2f1a74f13a7c8b0bbd3ee6d
https://pubmed.ncbi.nlm.nih.gov/28186612
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6
Mitochondrial tRNAIle A4317G mutation may influence the pheno-typic manifestation of deafness-associated 12S rRNA A1555G mutation
Autor: Yue Wu, Min-Xin Guan, Jianxin Lu, Hong-li Xiao, Ya-ling Yang, Binjiao Zheng, Ling-Zhi Liang, Yi Zhu, Qin Cai, Jing Zheng, Xiaowen Tang
Publikováno v: Hereditas (Beijing). 35:752-760
Mitochondrial 12S rRNA A1555G mutation has been associated with both aminoglycoside-induced and nonsyndromic hearing loss. In this report, we performed a clinical and genetic evaluation, and mitochondrial genome analysis of one hearing-impaired Chine
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b4d630fb559c25ead589155c4a26ee81
https://doi.org/10.3724/sp.j.1005.2013.00752
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Mitochondrial 12S rRNA A1555G mutation associated with nonsyn-dromic hearing loss in twenty-five Han Chinese pedigrees
Autor: Ling-Zhi Liang, Min-Xin Guan, Xiao Yu, Jing Zheng, Jianxin Lu, Yi Zhu, Fang Fang, Xiaowen Tang, Yue Wu, Binjiao Zheng, Guang-hua Peng, Benyu Nan, Bobei Chen
Publikováno v: Hereditas (Beijing). 35:62-72
Mitochondrial 12S rRNA A1555AG mutation is one of the important causes of aminoglycoside-induced and nonsyndromic deafness. We report here the clinical, genetic and molecular characterization of 25 Chinese families carrying the A1555G mutation.Clinic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::096d46abd6499a31ab9d8619e7d6a16c
https://doi.org/10.3724/sp.j.1005.2013.00062
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Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Prov-ince
Autor: Fang Fang, Ling-Zhi Liang, Xiaowen Tang, Guang-hua Peng, Benyu Nan, Min-Xin Guan, Yi Zhu, Yue Wu, Binjiao Zheng, Jianxin Lu, Jing Zheng, Bobei Chen
Publikováno v: Hereditas (Beijing). 34:695-704
Mitochondrial DNA (mtDNA) mutations are one of the important causes of deafness. In particular, the 12S rRNA gene is the hot spots for mutations associated with both aminoglycoside ototoxicity and nonsyndromic deafness. In this report, a total of 318
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0733cf6cc242f41a7513d21dfb545396
https://doi.org/10.3724/sp.j.1005.2012.00695
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[Mitochondrial tRNA(Thr)T15943C mutation may be a new position that affects the phenotypic expression of deafness associated 12s rRNA A1555G mutation]
Autor: Hongli, Xiao, Zheyun, He, Yinglong, Gao, Yaling, Yang, Jing, Zheng, Zhaoyang, Cai, Binjiao, Zheng, Xiaowen, Tang, Minxin, Guan
Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 32(2)
To identify secondary mutations associated with deafness in a Chinese family affected with deafness.The family has been subjected to clinical and molecular analyses, in addition with measurement of reactive oxygen species and doubling time after esta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4eee5edb35eb160bf2c4bea37f2a0038
https://pubmed.ncbi.nlm.nih.gov/25863077
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