Výsledky vyhledávání - "Ming-Xiu Chang"

Ursodeoxycholic acid protects dopaminergic neurons from oxidative stress via regulating mitochondrial function, autophagy, and apoptosis in MPTP/MPP+-induced Parkinson’s disease

Autor: Dong-Fang Shen, Hui-Ping Qi, Ming-Xiu Chang, Huan Wang, Chenggong Jiang

Publikováno v: Neuroscience Letters. 741:135493

Neuroprotection targeting mitochondrial dysfunction has been proposed as a potential therapeutic strategy for Parkinson’s disease (PD). Ursodeoxycholic acid (UDCA) has been shown to prevent neuronal damage; however, the role of UDCA in PD is poorly

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0b006a2b33f469bcf9b9bb4a78337bed
https://doi.org/10.1016/j.neulet.2020.135493

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Mutation analysis of the pathogenic gene in a Chinese family with Brachydactyly type B1

Autor: Feng-yu Wang, Cong-Min Li, Hui-gen Feng, Shu-Li Han, Wei-Wei Sun, Ming-Xiu Chang

Publikováno v: Hereditas (Beijing). 33:147-152

We identified and characterized a Chinese family with autosomal dominant Brachydactyly type B1 (BDB1). Linkage analysis revealed that the disease gene of the Chinese BDB1 family was linked to ROR2 locus. Mutational hot spot of ROR2 gene was amplified

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d2bacce5035ec9c7a09d18cf49cf4169
https://doi.org/10.3724/sp.j.1005.2011.00147

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[Mutation analysis of pathogenic genes in a Henan family affected with congenital stationary night blindness]

Autor: Feng-yu, Wang, Yan-li, Wang, Yang, Yang, Cong-min, Li, Tao, Zhang, Ming-xiu, Chang, Yun-liang, Zhu

Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 29(2)

To detect genetic mutations associated with autosomal dominant congenital stationary night blindness (ADCSNB) in a family from Henan province.Genomic DNA was extracted from peripheral blood samples of 14 family members. Based on 3 genes reported prev

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::142c9465a7ee4d9144ff4fb5f6bb2c72
https://pubmed.ncbi.nlm.nih.gov/22487821

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[Mutation analysis of the pathogenic gene in a Chinese family with Brachydactyly type B1]

Autor: Cong-Min, Li, Feng-Yu, Wang, Wei-Wei, Sun, Shu-Li, Han, Ming-Xiu, Chang, Hui-Gen, Feng

Publikováno v: Yi chuan = Hereditas. 33(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3bbcb9adc146646ca54370891ce63fde
https://pubmed.ncbi.nlm.nih.gov/21377971

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