Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Hua Sheng Xiao"'
Autor:
Xingyu Pan, Jingrong Zhao, Zhiying Zhou, Jijun Chen, Zhenxing Yang, Yuxuan Wu, Meizhu Bai, Yang Jiao, Yun Yang, Xuye Hu, Tianling Cheng, Qianyun Lu, Bin Wang, Chang-Lin Li, Ying-Jin Lu, Lei Diao, Yan-Qing Zhong, Jing Pan, Jianmin Zhu, Hua-Sheng Xiao, Zi-Long Qiu, Jinsong Li, Zefeng Wang, Jingyi Hui, Lan Bao, Xu Zhang
Publikováno v:
eLife, Vol 10 (2021)
The congenital intellectual disability (ID)-causing gene mutations remain largely unclear, although many genetic variations might relate to ID. We screened gene mutations in Chinese Han children suffering from severe ID and found a single-nucleotide
Externí odkaz:
https://doaj.org/article/421c9d4b8f844bb7ba651e3f10b6f7d3
Autor:
Xu Zhang, Hua-Sheng Xiao, Tianling Cheng, Yang Jiao, Zilong Qiu, Xu-Ye Hu, Zhiying Zhou, Yuxuan Wu, Zhenxing Yang, Bin Wang, Xingyu Pan, Meizhu Bai, Jing Pan, Qianyun Lu, Jianmin Zhu, Jingyi Hui, Jinsong Li, Zefeng Wang, Lei Diao, Chang-Lin Li, Yan-Qing Zhong, Jijun Chen, Ying-Jin Lu, Jingrong Zhao, Lan Bao, Yun Yang
Publikováno v:
eLife, Vol 10 (2021)
The congenital intellectual disability (ID)-causing gene mutations remain largely unclear, although many genetic variations might relate to ID. We screened gene mutations in Chinese Han children suffering from severe ID and found a single-nucleotide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5aa9a454e28e2c5f73947631ef6d6f3
https://doi.org/10.7554/elife.63021
https://doi.org/10.7554/elife.63021
Autor:
Jingrong Zhao, Zefeng Wang, Lan Bao, Qianyun Lu, Xingyu Pan, Chang-Lin Li, Xu-Ye Hu, Lei Diao, Jinsong Li, Yang Jiao, Yun Yang, Jing Pan, Zhiying Zhou, Meizhu Bai, Ying-Jin Lu, Jijun Chen, Jianmin Zhu, Tianling Cheng, Yuxuan Wu, Xu Zhang, Yan-Qing Zhong, Zilong Qiu, Zhenxing Yang, Bin Wang, Jingyi Hui, Hua-Sheng Xiao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5ee953a7e34701def511a0e60ce22bf
https://doi.org/10.7554/elife.63021.sa2
https://doi.org/10.7554/elife.63021.sa2
Autor:
Xingyu, Pan, Jingrong, Zhao, Zhiying, Zhou, Jijun, Chen, Zhenxing, Yang, Yuxuan, Wu, Meizhu, Bai, Yang, Jiao, Yun, Yang, Xuye, Hu, Tianling, Cheng, Qianyun, Lu, Bin, Wang, Chang-Lin, Li, Ying-Jin, Lu, Lei, Diao, Yan-Qing, Zhong, Jing, Pan, Jianmin, Zhu, Hua-Sheng, Xiao, Zi-Long, Qiu, Jinsong, Li, Zefeng, Wang, Jingyi, Hui, Lan, Bao, Xu, Zhang
Publikováno v:
eLife
The congenital intellectual disability (ID)-causing gene mutations remain largely unclear, although many genetic variations might relate to ID. We screened gene mutations in Chinese Han children suffering from severe ID and found a single-nucleotide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7a85472722292e07c0505fe06edd2fb4
https://pubmed.ncbi.nlm.nih.gov/34184986
https://pubmed.ncbi.nlm.nih.gov/34184986
Analyses of copy number variation of GK rat reveal new putative type 2 diabetes susceptibility loci.
Autor:
Zhi-Qiang Ye, Shen Niu, Yang Yu, Hui Yu, Bao-Hong Liu, Rong-Xia Li, Hua-Sheng Xiao, Rong Zeng, Yi-Xue Li, Jia-Rui Wu, Yuan-Yuan Li
Publikováno v:
PLoS ONE, Vol 5, Iss 11, p e14077 (2010)
Large efforts have been taken to search for genes responsible for type 2 diabetes (T2D), but have resulted in only about 20 in humans due to its complexity and heterogeneity. The GK rat, a spontanous T2D model, offers us a superior opportunity to sea
Externí odkaz:
https://doaj.org/article/de2f08df41944090b4231706c5a1edb2
Publikováno v:
Acta Pharmacologica Sinica. 36:1200-1211
Cancer is an extremely diverse and complex disease that results from various genetic and epigenetic changes such as DNA copy-number variations, mutations, and aberrant mRNA and/or protein expression caused by abnormal transcriptional regulation. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f8bd11dbef3649a72aecc19feb0472d
https://doi.org/10.1038/aps.2015.67
https://doi.org/10.1038/aps.2015.67
Autor:
Kai-Cheng Li, Bei-Bei Zhou, Xu Zhang, Chang-Lin Li, Jingrong Zhao, Sashuang Wang, D. J. Wu, Hao Luo, Lan Bao, Ying-Jin Lu, Rui Hou, Xu-Ye Hu, Hua-Sheng Xiao, Yan-Qing Zhong, Ming-Ming Sun, Yan Chen
Sensory neurons are distinguished by distinct signaling networks and receptive characteristics. Thus, sensory neuron types can be defined by linking transcriptome-based neuron typing with the sensory phenotypes. Here we classify somatosensory neurons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90d0cf8dc314202d0c9b9afe768459e0
https://europepmc.org/articles/PMC4973338/
https://europepmc.org/articles/PMC4973338/
Autor:
Jun-Ru Yao, Rohini Kuner, Lan Bao, Qiong Wang, Hua-Sheng Xiao, Mingyan Yu, Yu-Qiu Zhang, Kai-Cheng Li, Xiang Gao, Kai-Hua Zhang, Mei Han, Yan-Qing Zhong, Xu Zhang, Ying-Jin Lu, Fang-Xiong Zhang, Xiao-Li Ma, Jin-Yuan Wang, Feng Wang, Li-Bo Lin, Chang-Lin Li
Publikováno v:
Neuron. 69(5):974-987
SummaryExcitatory synaptic transmission is modulated by inhibitory neurotransmitters and neuromodulators. We found that the synaptic transmission of somatic sensory afferents can be rapidly regulated by a presynaptically secreted protein, follistatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c90160955058ef2bf93e2982ee4b51e2
Publikováno v:
The Tohoku Journal of Experimental Medicine. 224:119-125
Lymphotoxin-alpha (LTA), a pro-inflammatory cytokine, has been implicated in the pathogenesis of coronary atherosclerosis. Meanwhile, association of some single nucleotide polymorphisms (SNPs) of LTA gene with coronary artery disease (CAD) has been e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b21b3d3f9d36d4799408e6ca2dd1623
https://doi.org/10.1620/tjem.224.119
https://doi.org/10.1620/tjem.224.119
Publikováno v:
Academic Journal of Second Military Medical University. 30:1109-1113
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a621821502547727b12f8421398d7385
https://doi.org/10.3724/sp.j.1008.2010.01109
https://doi.org/10.3724/sp.j.1008.2010.01109