Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Huajing You"'
Autor:
Huajing You, Tengteng Wu, Gang Du, Yue Huang, Yixuan Zeng, Lishan Lin, Dingbang Chen, Chao Wu, Xunhua Li, Jean-marc Burgunder, Zhong Pei
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Objective: Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder. Neurofilament light protein (NfL) is correlated with clinical severity of HD but relative data are the lack in the Chinese population. Reactive astrocytes are r
Externí odkaz:
https://doaj.org/article/7597e9b8b9594d0e9cd79cb62e077540
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Background The presence of more than one polyQ‐related gene within a single individual is a rare incidence, which may provide the potential opportunity to study the combined effects of these spinocerebellar ataxia (SCA) genes. Methods We r
Externí odkaz:
https://doaj.org/article/d149d41c72c141048938b0485d5091aa
Autor:
Jie Yang, Dingbang Chen, Li Feng, Zhicong Yan, Chao Wu, Huajing You, Bing Liao, Jinlang Wu, Xunhua Li
Publikováno v:
Neurological Sciences. 43:2137-2139
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77fa3d0eef71738ba84c957c6148d793
https://doi.org/10.1007/s10072-021-05788-w
https://doi.org/10.1007/s10072-021-05788-w
Autor:
Jie Yang, Zihuan Huang, Huiming Yang, Yue Luo, Huajing You, Dingbang Chen, Zhong Pei, Xunhua Li
Publikováno v:
Parkinsonismrelated disorders. 95
Neurofilament light chain (NfL) was recently proposed as a promising blood biomarker for nervous system diseases, including Wilson's disease (WD). In this study, we investigated plasma NfL concentrations in patients with different types of WD and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::856380c41a020850dfdd375c7466041f
https://pubmed.ncbi.nlm.nih.gov/34942565
https://pubmed.ncbi.nlm.nih.gov/34942565
Autor:
Chao Wu, Huajing You, Zhong Pei, Xue‐jiao Li, Hui-Hua Yang, Hong-Yu Zhang, Qing-Ling Fu, Yukun Feng, Tengteng Wu, Xunhua Li, Shu-Bin Fang, Ge Li
Publikováno v:
Stem Cell Research & Therapy, Vol 11, Iss 1, Pp 1-11 (2020)
Stem Cell Research & Therapy
Stem Cell Research & Therapy
Background Machado-Joseph disease is the most common autosomal dominant hereditary ataxia worldwide without effective treatment. Mesenchymal stem cells (MSCs) could slow the disease progression, but side effects limited their clinical application. Be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e11e899325b354b2cb971b6169e837d8
https://doi.org/10.1186/s13287-020-01727-2
https://doi.org/10.1186/s13287-020-01727-2
Autor:
Dingbang Chen, Li Feng, Chao Wu, Jiwei Zhang, Xiang-xue Zhou, Xiu-Ling Liang, Huajing You, Zhong Pei, Xun-hua Li
Publikováno v:
CNS neurosciencetherapeutics. 23(4)
AIMS: To detect specific oculomotor deficits in preclinical stage of spinocerebellar ataxia type 3 (SCA3) and evaluate whether these abnormalities prove useful as potential biomarkers of disease progression. METHODS: A Chinese cohort of 56 patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6b0826404b385b488cc4ce1de65cbbe
https://pubmed.ncbi.nlm.nih.gov/28195427
https://pubmed.ncbi.nlm.nih.gov/28195427
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background The presence of more than one polyQ‐related gene within a single individual is a rare incidence, which may provide the potential opportunity to study the combined effects of these spinocerebellar ataxia (SCA) genes. Methods We retrospect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eef49bc3b027556676bcb68b9f04a31f
https://doi.org/10.1002/mgg3.663
https://doi.org/10.1002/mgg3.663