Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Zi-wen Yu"'
Autor:
Bin Jiang, Qi Liu, Jian-Peng Li, Si-Ning Lin, Hui-Juan Wan, Zi-Wen Yu, Jing Wang, Wei Zhuang, Jia-Hui Tang, Cai-Hong Chen, Fa-Yin Li, Min Bi, Nai-An Xiao, Kun-Mu Zheng
Publikováno v:
BMC Geriatrics, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background With the aging population, the number of individuals with dementia in China is increasing rapidly. This community-based study aimed to investigate the prevalence and risk factors for dementia and mild cognitive impairment (MCI) am
Externí odkaz:
https://doaj.org/article/001f3ce7cda74677b62d8ba7dec49d3e
A Pathogenic Variant p.Phe177Val in PSEN1 Causes Early-Onset Alzheimer’s Disease in a Chinese Family
Autor:
Bin Jiang, Min Bi, Jun Li, Qi Liu, Nai-An Xiao, Jie Fang, Man-Yi Shi, Zi-Wen Yu, Qi-Lin Ma, Sui-Jun Tong, Kun-Mu Zheng
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Familial Alzheimer’s disease (FAD) present as a positive family history of cognitive decline, with early onset and an autosomal dominant inheritance pattern. FAD is mainly caused by the mutations in the genes encoding for amyloid precursor protein
Externí odkaz:
https://doaj.org/article/808c3657ce574fceb94a3c337aefecd3
Autor:
Kun Fan, Song‐Song Bao, Zi‐Wen Yu, Xin‐Da Huang, Yu‐Jie Liu, Mohamedally Kurmoo, Li‐Min Zheng
Publikováno v:
Chinese Journal of Chemistry. 40:931-938
Autor:
Qi Liu, Bin Jiang, Min Zou, Hui-Juan Wan, Zi-Wen Yu, Jing Wang, Chu-Chuan Xu, Si-Ning Lin, Kun-Mu Zheng, Nai-An Xiao, Min Bi, Jian-Peng Li
Publikováno v:
Neuroscience letters. 790
Genetic factors play an important role in early-onset Parkinson's disease (EOPD). The genetic spectrum of patients with EOPD varies widely among different ethnicities, with extensive investigations having been performed in Caucasian populations; howe
Autor:
Li-Min Zheng, Xin-Da Huang, Ran Huo, Song-Song Bao, Yu-Jie Liu, Zi-Wen Yu, Mohamedally Kurmoo, Kun Fan
Publikováno v:
Inorganic Chemistry Frontiers. 7:4580-4592
A series of iridium(III)–lanthanide(III) bimetallic coordination polymers were successfully obtained by hydrothermal reactions based on the Ir unit [Ir(ppy)2(Hdcbpy)], namely, [Ln{Ir(ppy)2(dcbpy)}2(NO3)(H2O)n]·solvent (Ir2Ln, n = 5, Ln = Gd and Dy
Autor:
Ying Xiao, Ya-qian Jia, Wen-juan Liu, Chun Niu, Zhan-hai Mai, Jia-qi Dong, Xiao-song Zhang, Zi-wen Yuan, Peng Ji, Yan-ming Wei, Yong-li Hua
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
Ethnopharmacological relevance: Pulsatilla decoction (PD) is a classical prescription for the treatment of ulcerative colitis. Previous studies have demonstrated that the therapeutic efficacy of PD is closely associated with the activation of Farneso
Externí odkaz:
https://doaj.org/article/e8eb0cf3c18046c596c32f43dca1e6cc
Autor:
Peng Ji, Nian-Shou Zhao, Fan-Lin Wu, Yan-Ming Wei, Ci-Dan Laba, Cuo-Mu Wujin, Yong-Li Hua, Zi-Wen Yuan, Wan-Ling Yao
Publikováno v:
BMC Complementary Medicine and Therapies, Vol 24, Iss 1, Pp 1-12 (2024)
Abstract Background Leguminous Sophora moorcroftiana (SM) is a genuine medicinal material in Tibet. Many research results have reveal the Sophora moorcroftiana alkaloids (SMA), as the main active substance, have a wide range of effects, such as antib
Externí odkaz:
https://doaj.org/article/7b6efbdaed8f44688dc89df42c260c95
A Pathogenic Variant p.Phe177Val in PSEN1 Causes Early-Onset Alzheimer’s Disease in a Chinese Family
Autor:
Zi-Wen Yu, Qi Liu, Jiang Bin, Jie Fang, Nai-An Xiao, Suijun Tong, Min Bi, Kun-Mu Zheng, Man-Yi Shi, Qi-Lin Ma, Jun Li
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Familial Alzheimer’s disease (FAD) present as a positive family history of cognitive decline, with early onset and an autosomal dominant inheritance pattern. FAD is mainly caused by the mutations in the genes encoding for amyloid precursor protein
Autor:
Bin, Jiang, Min, Bi, Jun, Li, Qi, Liu, Nai-An, Xiao, Jie, Fang, Man-Yi, Shi, Zi-Wen, Yu, Qi-Lin, Ma, Sui-Jun, Tong, Kun-Mu, Zheng
Publikováno v:
Frontiers in Genetics
Familial Alzheimer’s disease (FAD) present as a positive family history of cognitive decline, with early onset and an autosomal dominant inheritance pattern. FAD is mainly caused by the mutations in the genes encoding for amyloid precursor protein
Publikováno v:
Emerging Developments in the Power and Energy Industry ISBN: 9780429295300
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::033118bc343adadbe39d5625616b4eb2
https://doi.org/10.1201/9780429295300-40
https://doi.org/10.1201/9780429295300-40