Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Chu-qin Zhang"'
Publikováno v:
International Journal of Neuroscience. 131:994-1003
Objective: To expound the roles of mTOR and NF-kB signaling pathway in intermittent hypoxia (IH)-induced damage of hippocampal neurons.Methods: For rat experiments, mTOR inhibitor (Rapamycin, Rapa) and NF-κB signaling inhibitor (ammonium pyrrolidine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66eeefe58c8f0d2fd502992e00a2c790
https://doi.org/10.1080/00207454.2020.1766460
https://doi.org/10.1080/00207454.2020.1766460
Autor:
Zaizai Cao, Haijie Xiang, Xiang Zhan, Ruru Chen, Bobei Chen, Chu-qin Zhang, Saiyu Huang, Jinjian Gao, Bo Zheng
Publikováno v:
Audiologyneuro-otology. 24(1)
Background: Recently, genetic factors have been considered as an important risk factor for sudden sensorineural hearing loss (SSNHL). Many studies analyzed the association between SSNHL and polymorphisms. However, most of them gave inconclusive resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d375475154abe4164186940b6e027c1f
https://pubmed.ncbi.nlm.nih.gov/30870848
https://pubmed.ncbi.nlm.nih.gov/30870848
Autor:
Min-Xin Guan, Saiyu Huang, Yu-Yao Zhang, Benyu Nan, Xuejun Liu, Xiao Yu, Chu-qin Zhang, Jing Zheng, Jinjian Gao, Ying-Ying Chen, Bobei Chen
Publikováno v:
Hereditas (Beijing). 35:352-358
To evaluate the correlation between genetic mutations and the age in nonsyndromic hearing impairment (NSHI) and the clinical characteristics of NSHI, 215 patients with NSHI were enrolled between April 2006 and April 2012. All patients were divided in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad7d4fbb2e027c4b8779f1e857a1d7c2
https://doi.org/10.3724/sp.j.1005.2013.00352
https://doi.org/10.3724/sp.j.1005.2013.00352
Autor:
Ying-Ying Chen, Chu-qin Zhang, Min-Xin Guan, Jia-Yun Huang, Bobei Chen, Dongmei Sun, Song-Jie Xiang
Publikováno v:
Hereditas (Beijing). 30:1406-1410
GJB2, SLC26A4 (PDS) and mitochondrial DNA (mtDNA) have been associated with sensorineural hearing loss. In the present study, the clinical, genetic and molecular analysis of 14 cochlear implant recipients and their parents was studied from April 2006
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a531e2a28c54301124fbcd66f3b09a4
https://doi.org/10.3724/sp.j.1005.2008.01406
https://doi.org/10.3724/sp.j.1005.2008.01406
Autor:
Xiao, Yu, Bo-bei, Chen, Hai-jie, Xiang, Ben-yu, Nan, Jing, Zheng, Chu-qin, Zhang, Jin-jian, Gao, Bin-jiao, Zheng, Ying-ying, Chen, Min-xin, Guan
Publikováno v:
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery. 48(12)
To assess the possible genotype-phenotype correlation for GJB2.Retrospectively analyzed GJB2 gene mutations with non-syndromic hearing impairment (NSHI) patients and their families audiological data. Individuals were grouped, according to non-truncat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b6512c220a6a3b1db49b6272cf03c84
https://pubmed.ncbi.nlm.nih.gov/24506997
https://pubmed.ncbi.nlm.nih.gov/24506997
Autor:
Chu-Qin, Zhang, Bo-Bei, Chen, Ying-Ying, Chen, Xue-Jun, Liu, Jing, Zheng, Jin-Jian, Gao, Sai-Yu, Huang, Ben-Yu, Nan, Yu-Yao, Zhang, Xiao, Yu, Min-Xin, Guan
Publikováno v:
Yi chuan = Hereditas. 35(3)
To evaluate the correlation between genetic mutations and the age in nonsyndromic hearing impairment (NSHI) and the clinical characteristics of NSHI, 215 patients with NSHI were enrolled between April 2006 and April 2012. All patients were divided in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce66aaae64424f3777f2afb33a661708
https://pubmed.ncbi.nlm.nih.gov/23575541
https://pubmed.ncbi.nlm.nih.gov/23575541
Publikováno v:
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery. 47(6)
To investigate the safety of peri-operative management on children with juvenile recurrent respiratory papilloma (JORRP).A retrospective analysis was conducted on preoperative assessment, anesthesia methods and options, operative procedure, and posto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::42bae5be76d4c134770cf5d0d14b76cf
https://pubmed.ncbi.nlm.nih.gov/22932135
https://pubmed.ncbi.nlm.nih.gov/22932135
Autor:
Sha-sha, Gong, Bo-bei, Chen, Guang-hua, Peng, Jing, Zheng, Ting, Zhang, Bin-jiao, Zheng, Fang, Fang, Chu-qin, Zhang, Jian-xin, Lv, Min-xin, Guan
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 29(4)
To evaluate the effect of mitochondrial DNA(mtDNA) secondary mutations, haplotypes, GJB2 gene mutations on phenotype of 1494CT mutation, and to study the molecular pathogenic mechanism of maternally transmitted aminoglycoside-induced and nonsyndromic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::215436b697d6983a100deb3c3e40236f
https://pubmed.ncbi.nlm.nih.gov/22875491
https://pubmed.ncbi.nlm.nih.gov/22875491
Autor:
Ting, Zhang, Bo-bei, Chen, Jing, Zheng, Sha-sha, Gong, Chu-qin, Zhang, Jian-xin, Lv, Min-xin, Guan
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 28(4)
To study the effect of the mitochondrial 12S rRNA mutations on aminoglycoside-induced and nonsyndromic hearing loss, to carry out the clinical and molecular characterization of five Han Chinese pedigrees with maternally transmitted aminoglycoside-ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9b3833929469c79303014584e2dbb49f
https://pubmed.ncbi.nlm.nih.gov/21811972
https://pubmed.ncbi.nlm.nih.gov/21811972
Autor:
Chu-Qin, Zhang, Bo-Bei, Chen, Jia-Yun, Huang, Dong-Mei, Sun, Ying-Ying, Chen, Song-Jie, Xiang, Min-Xin, Guan
Publikováno v:
Yi chuan = Hereditas. 30(11)
GJB2, SLC26A4 (PDS) and mitochondrial DNA (mtDNA) have been associated with sensorineural hearing loss. In the present study, the clinical, genetic and molecular analysis of 14 cochlear implant recipients and their parents was studied from April 2006
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::339113ac5615eba515232409f0b7870c
https://pubmed.ncbi.nlm.nih.gov/19073547
https://pubmed.ncbi.nlm.nih.gov/19073547