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pro vyhledávání: '"Siying Fang"'
Autor:
Peipei Ma, Shu Zhang, Hao Zhang, Siying Fang, Yuru Dong, Yan Zhang, Weiwei Hao, Shiwen Wu, Yuying Zhao
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-10 (2018)
Abstract Background Dystrophinopathies are a set of severe and incurable X-linked neuromuscular disorders caused by mutations in the dystrophin gene (DMD). These mutations form a complex spectrum. A national registration network is essential not only
Externí odkaz:
https://doaj.org/article/dda22994a8a0408a83022283fe88f252
Autor:
Peipei Ma, Shu Zhang, Hao Zhang, Siying Fang, Yuru Dong, Yan Zhang, Weiwei Hao, Shiwen Wu, Yuying Zhao
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-1 (2021)
An amendment to this paper has been published and can be accessed via the original article.
Externí odkaz:
https://doaj.org/article/63cde046d01d4d17b9565b3f46953c0f
Autor:
Siying Fang, Yuying Zhao, Weiwei Hao, Yan Zhang, Shu Zhang, Yuru Dong, Hao Zhang, Peipei Ma, Shiwen Wu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-1 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Dystrophinopathies are a set of severe and incurable X-linked neuromuscular disorders caused by mutations in the dystrophin gene (DMD). These mutations form a complex spectrum. A national registration network is essential not only to provide more inf
Autor:
Peipei Ma, Zhang, Shu, Zhang, Hao, Siying Fang, Yuru Dong, Zhang, Yan, Weiwei Hao, Shiwen Wu, Yuying Zhao
Clinical and genetic information of patients with small mutations. (PDF 93Â kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bec04e0ef6d3bbb6d89df6bde40a19d6
Publikováno v:
Talanta. 167
A sensitive and selective fluorescent method for detection of cholesterol based on β-cyclodextrin functionalized carbon quantum dots (β-CD-CQD) nanoprobe through competitive host-guest recognition has been developed. The bright fluorescence of β-C