Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Meiling Lai"'
Autor:
Yijuan Han, Huiquan Chen, Meiling Lai, Zhongyuan Lin, Yongji Huang, Weiqi Tang, Yanbing Zhu, Yange Zhang, Zonghua Wang, Hui Ni, Xiaofeng Chen, Songbiao Chen
Publikováno v:
Foods, Vol 13, Iss 19, p 3150 (2024)
Smooth cordgrass (Spartina alterniflora) is a native salt marsh plant along the Atlantic coast but has become an invasive species in coastal regions in China, as well as other areas. Utilizing it for resources has become a control measure in reducing
Externí odkaz:
https://doaj.org/article/842b0af0cd0b4ba09706054978551371
Publikováno v:
Journal of Electrical and Computer Engineering, Vol 2015 (2015)
Spectrum sensing is one of the key tasks in cognitive radio. This paper proposes a fast two-step energy detection (FED) algorithm for spectrum sensing via improving the sampling process of conventional energy detection (CED). The algorithm adaptively
Externí odkaz:
https://doaj.org/article/486dccc28cec4796b455097804550b38
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 25:743-746
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e9cb358d0406b2a475f3228eb744762
https://doi.org/10.1111/j.1468-3083.2010.03773.x
https://doi.org/10.1111/j.1468-3083.2010.03773.x
Autor:
Yan Hu, Meiling Lai, Chengrang Li, Lijia Yang, Ming Li, Cheng Jin, Zhirong Yao, Guolong Zhang, Jin ji
Publikováno v:
Archives of Dermatological Research. 302:469-476
Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant cutaneous disorder characterized by a mixture of hyperpigmented and hypopigmented macules of various sizes on the extremities and caused by the mutations of adenosine deaminase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46dfa6f13a85da15f4c580d1c6a95222
https://doi.org/10.1007/s00403-010-1039-2
https://doi.org/10.1007/s00403-010-1039-2
Publikováno v:
Genetics and molecular research : GMR. 11(2)
Dyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant cutaneous disorder, characterized by a mixture of hyperpigmented and hypopigmented macules mostly on the dorsal portions of the extremities. Pathogenic mutations have been identifie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34d0c5976b90234104071771a65edbfe
https://pubmed.ncbi.nlm.nih.gov/22843049
https://pubmed.ncbi.nlm.nih.gov/22843049
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 27(1)
To identify the mutation in the keratin 6A(K6A) gene in a pedigree with pachyonychia congenita type I (PC-I).Blood samples were obtained from 2 affected, 3 unaffected members in this family, and 100 unrelated healthy individuals. Mutation detection w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf5ce875eb0fb6110867aa4399d8b79f
https://pubmed.ncbi.nlm.nih.gov/20140871
https://pubmed.ncbi.nlm.nih.gov/20140871
Autor:
Ming Li, Lijia Yang, Chengrang Li, Cheng Jin, Meiling Lai, Guolong Zhang, Yan Hu, Jin ji, Zhirong Yao
Publikováno v:
Archives of Dermatological Research; Jul2010, Vol. 302 Issue 6, p469-476, 8p, 1 Color Photograph, 3 Charts, 1 Graph