Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Zheyun, He"'
Publikováno v:
Frontiers in Microbiology, Vol 15 (2024)
Non-alcoholic fatty liver disease (NAFLD) is a prevalent chronic liver condition observed globally, with the potential to progress to non-alcoholic steatohepatitis (NASH), cirrhosis, and even hepatocellular carcinoma. Currently, the US Food and Drug
Externí odkaz:
https://doaj.org/article/34a1cd6967814e0caba81bfd1bc554b5
Autor:
Jing Zheng, Zhengbiao Ying, Zhaoyang Cai, Dongmei Sun, Zheyun He, Yinglong Gao, Ting Zhang, Yi Zhu, Ye Chen, Min-Xin Guan
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128691 (2015)
Mutations in Gap Junction Beta 2 (GJB2) have been reported to be a major cause of non-syndromic hearing loss in many populations worldwide. The spectrums and frequencies of GJB2 variants vary substantially among different ethnic groups, and the genot
Externí odkaz:
https://doaj.org/article/f89b69ba003d4be895dcb78c4bdd9506
Publikováno v:
Journal of Hepatology. 77:S304
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b9df383d8d600bf6c80fee31a7b4b5a
https://doi.org/10.1016/s0168-8278(22)00974-6
https://doi.org/10.1016/s0168-8278(22)00974-6
Autor:
Jun Qin Mo, Mi Zhou, Zheyun He, Feilong Meng, Xiaofen Jin, Xiaoyan Ren, Xiaowen Tang, Qiang Shu, Meng Wang, Shasha Gong, Min-Xin Guan, Jing Zheng, Yi Zhu
Publikováno v:
Journal of Biological Chemistry. 293:3321-3334
The 1555A→G mutation in mitochondrial 12S rRNA has been associated with aminoglycoside-induced and non-syndromic deafness in many individuals worldwide. Mitochondrial genetic modifiers are proposed to influence the phenotypic expression of m.1555A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51ae52a1a2f4b8c3d842fdaaafcfbf9d
https://doi.org/10.1074/jbc.ra117.000530
https://doi.org/10.1074/jbc.ra117.000530
Publikováno v:
American Journal of Rhinology & Allergy. 30:e176-e180
Purpose To assess the efficacy and safety of bupivacaine compared with lidocaine in local anesthesia of nasopharynx through meta-analysis. Methods A number of medical literature data bases were searched electronically. Relevant journals and reference
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd95a5acd05c01a236086c5389f3cdee
https://doi.org/10.2500/ajra.2016.30.4357
https://doi.org/10.2500/ajra.2016.30.4357
Autor:
Min-Xin Guan, Zhengbiao Ying, Hui Wang, Xiaowen Tang, Jing Zheng, Juan Yao, Han Yu, Ya-ling Yang, Ye Chen, Zhaoyang Cai, Yinglong Gao, Zheyun He
Publikováno v:
Mitochondrion. 23:17-24
Mutations in the mitochondrial DNA have been associated with hearing loss. However, the prevalence and spectrum of mitochondrial tRNA mutations in hearing-impaired subjects are poorly understood. In this report, we have investigated the prevalence an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5530ae8c31cca64e7c619b35198f05f9
https://doi.org/10.1016/j.mito.2015.05.001
https://doi.org/10.1016/j.mito.2015.05.001
Autor:
Feilong, Meng, Zheyun, He, Xiaowen, Tang, Jing, Zheng, Xiaofen, Jin, Yi, Zhu, Xiaoyan, Ren, Mi, Zhou, Meng, Wang, Shasha, Gong, Jun Qin, Mo, Qiang, Shu, Min-Xin, Guan
Publikováno v:
The Journal of biological chemistry. 293(9)
The 1555A→G mutation in mitochondrial 12S rRNA has been associated with aminoglycoside-induced and non-syndromic deafness in many individuals worldwide. Mitochondrial genetic modifiers are proposed to influence the phenotypic expression of m.1555A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::098929d87b59db8c0a022520eadb7fe7
https://pubmed.ncbi.nlm.nih.gov/29348176
https://pubmed.ncbi.nlm.nih.gov/29348176
Autor:
Yan-Hong Sun, Min Liang, Yanchun Ji, Yi Tong, Yinglong Gao, Zheyun He, Fuxin Zhao, Min-Xin Guan, Han Yu, Jia Qu, Xiangtian Zhou, Juanjuan Zhang, Qun Fu, Xiaoling Liu, Taosheng Huang, Pingping Jiang, Minglian Zhang
Publikováno v:
Investigative ophthalmologyvisual science. 56(8)
Purpose To investigate the prevalence and spectrum of mitochondrial ND4 mutations in subjects with Leber's hereditary optic neuropathy (LHON). Methods A cohort of 1281 Chinese Han probands and 478 control subjects underwent clinical and genetic evalu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78decde2cc8512a6ffbe03c74d97949e
https://pubmed.ncbi.nlm.nih.gov/26218905
https://pubmed.ncbi.nlm.nih.gov/26218905
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
https://pubmed.ncbi.nlm.nih.gov/25863077
Autor:
Xiao, Yu, Zheyun, He, Haijie, Xiang, Jing, Zheng, Benyu, Nan, Binjiao, Zheng, Jinjian, Gao, Saiyu, Huang, Minxin, Guan, Bobei, Chen
Publikováno v:
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery. 49(11)
To investigate the correlation between nonsyndromic deafness and mitochondrial 12s rRNA A839G mutation.According to the clinical manifestations of mitochondrial DNA sequencing and analysis to find and determine family containing mitochondrial 12s rRN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a5f7fb9fa9b2be1822169213b2263d70
https://pubmed.ncbi.nlm.nih.gov/25598369
https://pubmed.ncbi.nlm.nih.gov/25598369