Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Yu-Wu Jiang"'
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Externí odkaz:
https://doaj.org/article/b278a8e315ca485aa001d24c21526b00
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 12, Pp 1498-1499 (2021)
Externí odkaz:
https://doaj.org/article/ee2f8381e18f4abfb66f1de7961cd59b
Autor:
Zhi-Sheng Liu, Yong-Hua Cui, Dan Sun, Qing Lu, Yu-Wu Jiang, Li Jiang, Jia-Qin Wang, Rong Luo, Fang Fang, Shui-Zhen Zhou, Yi Wang, Fang-Cheng Cai, Qing Lin, Lan Xiong, Yi Zheng, Jiong Qin
Publikováno v:
Frontiers in Psychiatry, Vol 11 (2020)
Tic disorders (TD) are a group neuropsychiatric disorders with childhood onset characterized by tics, i.e. repetitive, sudden, and involuntary movements or vocalizations; and Tourette syndrome (TS) is the most severe form of TD. Their clinical manife
Externí odkaz:
https://doaj.org/article/eccf55b120934b94b5c42e66839b7365
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 6, Pp 672-678 (2016)
Background: Wolf-Hirschhorn syndrome (WHS) is a contiguous gene syndrome that is typically caused by a deletion of the distal portion of the short arm of chromosome 4. However, there are few reports about the features of Chinese WHS patients. This st
Externí odkaz:
https://doaj.org/article/ce8259bcf56e4fe5a2bd01d20de55831
Autor:
Na Chen, Yu-Wu Jiang, Hong-Jun Hao, Ting-Ting Ban, Kai Gao, Zhong-Bin Zhang, Jing-Min Wang, Ye Wu
Publikováno v:
Chinese Medical Journal, Vol 128, Iss 13, Pp 1772-1777 (2015)
Background: Vanishing white matter disease (VWM), a human autosomal recessive inherited leukoencephalopathy, is due to mutations in eukaryotic initiation factor 2B (eIF2B). eIF2B is responsible for the initiation of protein synthesis by its guanine n
Externí odkaz:
https://doaj.org/article/ff0e0c2a3f6e46d0bfcd730dddf67f8d
Autor:
Xiaohong Gong, Yu-Wu Jiang, Xin Zhang, Yu An, Jun Zhang, Ye Wu, Jingmin Wang, Yangfei Sun, Yanyan Liu, Xuewu Gao, Yiping Shen, Xiru Wu, Zilong Qiu, Li Jin, Bai-Lin Wu, Hongyan Wang
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e34739 (2012)
Intellectual disability (ID) is a heterogeneous disorder caused by chromosomal abnormalities, monogenic factors and environmental factors. 22q13 deletion syndrome is a genetic disorder characterized by severe ID. Although the frequency of 22q13 delet
Externí odkaz:
https://doaj.org/article/070aaf91bfd74cc3addfa9d6ddbc4ed6
Autor:
Ma, Jian-wei, Li, Teng-long, Jia, Zhen-yuan, Ye, Tao, Yu, Wu-jiang, Tian, Xue-bao, Wang, Shuang, Liu, Wei
Publikováno v:
In Cryogenics July 2023 133
Akademický článek
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Publikováno v:
World Journal of Pediatrics.
Akademický článek
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