Zobrazeno 1 - 10
of 491
pro vyhledávání: '"Chu Liao"'
Autor:
Cheng‐Tsung Hsiao, Tzu‐Yun Tsai, Ting‐Yi Shen, Yu‐Shuen Tsai, Yi‐Chu Liao, Yi‐Chung Lee, Pei‐Chien Tsai
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 7, Pp 1909-1920 (2024)
Abstract Objective TFG mutations have previously been implicated in autosomal recessive hereditary spastic paraplegia (HSP), also known as SPG57. This study aimed to investigate the clinical and molecular features of TFG mutations in a Taiwanese HSP
Externí odkaz:
https://doaj.org/article/283eded396fc435b9379fe01b6dea680
Autor:
Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 5, Pp 1091-1114 (2024)
Abstract PAR3/INSC/LGN form an evolutionarily conserved complex required for asymmetric cell division in the developing brain, but its post-developmental function and disease relevance in the peripheral nervous system (PNS) remains unknown. We mapped
Externí odkaz:
https://doaj.org/article/5359f09eb23c4e93a0c5ca897d7a0804
Autor:
Pei-Chen Chen, Tzu-Pei Tsai, Yi-Chu Liao, Yu-Chieh Liao, Hung-Wei Cheng, Yi-Hsiu Weng, Chiao-Mei Lin, Cheng-Yuan Kao, Chih-Cheng Tai, Jhen-Wei Ruan
Publikováno v:
npj Biofilms and Microbiomes, Vol 10, Iss 1, Pp 1-15 (2024)
Abstract Gut microbiota rearrangement induced by cold temperature is crucial for browning in murine white adipose tissue. This study provides evidence that DUSP6, a host factor, plays a critical role in regulating cold-induced gut microbiota rearrang
Externí odkaz:
https://doaj.org/article/51ecacbb03f84f84a591fed8779acc1b
Publikováno v:
Journal of Stroke, Vol 26, Iss 1, Pp 112-115 (2024)
Externí odkaz:
https://doaj.org/article/4210a7b8e62642059e5c3ff9bc5cc374
Autor:
Chien-Hsun Huang, Chih-Ting Huang, Hsu-Yun Tsai, Yi-Chu Liao, Chiao-Mei Lin, Pei-Chen Chen, Jong-Shian Liou, Chin-Lin Hsu, Shih-Hau Chiu, Chien-Chi Chen, Sung-Yuan Hsieh, Hsin-Bai Zou, Cheng-Chih Hsu, Pai-Sheng Chen, Cheng-Yuan Kao, Jhen-Wei Ruan
Publikováno v:
Journal of Functional Foods, Vol 115, Iss , Pp 106110- (2024)
The emergence of next-generation probiotics (NGPs) has illuminated new possibilities for improving various diseases through food-grade supplements. In this study, a new gut bacterial species, designated as Akkermansia sp. BCRC 18949, was isolated fro
Externí odkaz:
https://doaj.org/article/3cdfef7df1024ee5bc06a784d08bf519
Autor:
Jhen-Wei Ruan, Yi-Chu Liao, Pei-Chen Chen, Yen-Ju Chen, Yi-Hsiu Tsai, Pei-Jane Tsai, Yao-Jong Yang, Chi-Chang Shieh, Yung-Chieh Lin, Chia-Yu Chi
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 56, Iss 5, Pp 1084-1097 (2023)
Background/purpose(s): Human breastmilk (BM) is important for microbiome maturation in infants across different body sites. Streptococcus and Staphylococcus are considered universally predominant genera in the BM microbiota. However, whether the diff
Externí odkaz:
https://doaj.org/article/7ad8867b9e4146e685c547453a5d8037
Autor:
Ying‐Tsen Chou, Shao‐Lun Hsu, Yu‐Shuen Tsai, Yi‐Jiun Lu, Kai‐Wei Yu, Hsiu‐Mei Wu, Yi‐Chu Liao, Yi‐Chung Lee
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 9, Pp 1603-1612 (2023)
Abstract Objective Hereditary spastic paraplegias (HSPs) are a group of inherited neurodegenerative disorders characterized by slowly progressive lower limb spasticity and weakness. HSP type 54 (SPG54) is autosomal recessively inherited and caused by
Externí odkaz:
https://doaj.org/article/54fb5979efc84d9ba071e5980d4e8893
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Clopidogrel is the most-widely used platelet P2Y12-inhibitor for secondary-prevention of ischemic stroke. Platelet P2Y12 reactivity before and after inhibitors can be measured with blood sampling by commercialized system. We aimed to evaluat
Externí odkaz:
https://doaj.org/article/41fc3eb655284bf797517608c995d9ac
Autor:
Yu‐Wen Cheng, Yi‐Chu Liao, Chih‐Hao Chen, Chih‐Ping Chung, Cathy S. J. Fann, Chien‐Ching Chang, Yi‐Chung Lee, Sung‐Chun Tang
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 22 (2023)
Background Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most prevalent monogenic cerebral small‐vessel disease. Phenotype variability in CADASIL suggests the possible role of genetic mo
Externí odkaz:
https://doaj.org/article/a9bd1c2a016446cc97097b2007db40fd
Autor:
Shih‐Yu Fang, Ying‐Tsen Chou, Kuo‐Chou Hsu, Shao‐Lun Hsu, Kai‐Wei Yu, Yu‐Shuen Tsai, Yi‐Chu Liao, Pei‐Chien Tsai, Yi‐Chung Lee
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 3, Pp 353-362 (2023)
Abstract Objective NIPA1 mutations have been implicated in hereditary spastic paraplegia (HSP) as the cause of spastic paraplegia type 6 (SPG6). The aim of this study was to investigate the clinical and genetic features of SPG6 in a Taiwanese HSP coh
Externí odkaz:
https://doaj.org/article/512e80aa1e98488187e6baa056a3fd06