Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Pan-feng Tao"'
Publikováno v:
Shipin yu jixie, Vol 38, Iss 2, Pp 81-87 (2022)
Objective: To solve the difficulty of head and tail orientation in crayfish mechanized treatment. Methods: A crayfish head and tail orientation method was proposed by using the difference of crayfish head and tail shape, which was composed of a rolle
Externí odkaz:
https://doaj.org/article/757d94e5437f44c98872eee91e55d550
Autor:
Guo-min Li, Xu Han, Ye Wu, Wei Wang, Hong-xia Tang, Mei-ping Lu, Xue-mei Tang, Yi Lin, Fan Deng, Jun Yang, Xin-ning Wang, Cong-cong Liu, Wen-jie Zheng, Bing-bing Wu, Fang Zhou, Hong Luo, Liang Zhang, Hai-mei Liu, Wan-zhen Guan, Shi-hao Wang, Pan-feng Tao, Tai-jie Jin, Ran Fang, Yuan Wu, Jie Zhang, Yao Zhang, Tian-nan Zhang, Wei Yin, Li Guo, Wen-jing Tang, Hong Chang, Qiu-ye Zhang, Xiao-zhong Li, Jian-guo Li, Zhi-xuan Zhou, Si-rui Yang, Kang-kang Yang, Hong Xu, Hong-mei Song, Natalie T. Deuitch, Pui Y. Lee, Qing Zhou, Li Sun
Publikováno v:
Journal of Clinical Immunology. 43:835-845
Purpose Deficiency of adenosine deaminase 2 (DADA2), an autosomal recessive autoinflammatory disorder caused by biallelic loss-of-function variants in adenosine deaminase 2 (ADA2), has not been systemically investigated in Chinese population yet. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edd1a0a59391a46812cb1ad71b32a583
https://doi.org/10.1007/s10875-023-01432-8
https://doi.org/10.1007/s10875-023-01432-8
Autor:
Guomin Li, Xu Han, Ye Wu, Wei Wang, Hong-xia Tang, Mei-ping Lu, Xue-mei Tang, Yi Lin, Fan Deng, Jun Yang, Xin-ning Wang, Cong-cong Liu, Wen-jie Zheng, Bing-bing Wu, Fang Zhou, Hong Luo, Liang Zhang, Hai-mei Liu, Wan-zhen Guan, Shi-hao Wang, Pan-feng Tao, Tai-jie Jin, Ran Fang, Yuan Wu, Jie Zhang, yao Zhang, Tian-nan Zhang, Wei Yin, Li Guo, Wen-jing Tang, Hong Chang, Qiu-ye Zhang, Xiao-zhong Li, Jian-guo Li, Zhi-xuan Zhou, Si-rui Yang, Kang-kang Yang, Hong Xu, Hong-mei Song, Qing Zhou, Li Sun
Purpose: Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive autoinflammatory disorder caused by biallelic loss-of-function mutations in ADA2, characterized by systemic inflammation, vasculitis, immunodeficiency, and/or hematologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21acf02859118646a227307eadd660f8
https://doi.org/10.21203/rs.3.rs-1796745/v1
https://doi.org/10.21203/rs.3.rs-1796745/v1
