Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aixia Jin"'
Autor:
Aixia Jin, Qingqing Zhao, Shuting Liu, Zi-bing Jin, Shuyan Li, Mengqing Xiang, Mingbing Zeng, Kangxin Jin
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Congenital hereditary cataract is genetically heterogeneous and the leading cause of visual impairment in children. Identification of hereditary causes is critical to genetic counselling and family planning. Here, we examined a four-generation Chines
Externí odkaz:
https://doaj.org/article/bf5490a3b93e484c874adadff226a960
Autor:
Ying Yao, Xiaoyong Miao, Liping Wang, Zhengyu Jiang, Lingxia Li, Ping Jiang, Yifei Wang, Aixia Jin, Na Li, Changli Wang, Kezhe Tan, Yan Meng, Jinjun Bian, Yan Zhang, Xiaoming Deng, Jianping Cao
Publikováno v:
Journal of Immunology Research, Vol 2022 (2022)
Allergic asthma is associated with allergen-induced airway hyperresponsiveness and inflammatory cell infiltration. While moderate-to-severe asthma with refractory symptoms is difficult to treat, methane is protective against organ damage. In this stu
Externí odkaz:
https://doaj.org/article/52fa805f544e40ff83d94ba275c1c305
Autor:
Aixia Jin, Xiaotong Han, Jiaqing Zhang, Xiaozhang Qiu, Yifan Zhang, Bo Qu, Xuhua Tan, Lixia Luo
Publikováno v:
Translational Vision Science & Technology. 12:13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7894b5554222d32347cdcad2296ab924
https://doi.org/10.1167/tvst.12.3.13
https://doi.org/10.1167/tvst.12.3.13
Autor:
Aixia Jin, Qingqing Zhao, Shuting Liu, Zi-bing Jin, Shuyan Li, Mengqing Xiang, Mingbing Zeng, Kangxin Jin
Publikováno v:
Frontiers in cell and developmental biology. 10
Congenital hereditary cataract is genetically heterogeneous and the leading cause of visual impairment in children. Identification of hereditary causes is critical to genetic counselling and family planning. Here, we examined a four-generation Chines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::471d9a2caaf879906088656531f63afb
https://pubmed.ncbi.nlm.nih.gov/35531093
https://pubmed.ncbi.nlm.nih.gov/35531093
Publikováno v:
Current Eye Research. 45:483-489
Purpose: To identify the pathogenetic mutations in a four-generation Chinese family with dominant congenital cataracts and microphthalmia.Methods: A four-generation Chinese family with dominant congenital cataracts were recruited. Genomic DNAs were c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9d9794aee11ef989e146961e1b3b994
https://doi.org/10.1080/02713683.2019.1675176
https://doi.org/10.1080/02713683.2019.1675176
Publikováno v:
EURASIP Journal on Wireless Communications and Networking, Vol 2018, Iss 1, Pp 1-15 (2018)
Abstract Using wireless relay nodes to cooperate is a very important helpful way to improve the physical layer security performance. In this paper, in the presence of an eavesdropping node between the source and destination nodes, a decoded and forwa
Externí odkaz:
https://doaj.org/article/98ae304598514dc6831cbe1eb49e4c2f