Zobrazeno 1 - 10
of 157
pro vyhledávání: '"Xiao rong Liu"'
Autor:
Na He, Bao‐Zhu Guan, Jie Wang, Han‐Kui Liu, Yong Mao, Zhi‐Gang Liu, Fei Yin, Jing Peng, Bo Xiao, Bei‐sha Tang, Dong Zhou, Guang Huang, Qi‐Lin Dai, Ying Zeng, Hong Han, Qiong‐Xiang Zhai, Bin Li, Bin Tang, Wen‐Bin Li, Wang Song, Liu Liu, Yi‐Wu Shi, Bing‐Mei Li, Tao Su, Peng Zhou, Xiao‐Rong Liu, Li‐Wu Guo, Yong‐Hong Yi, Wei‐Ping Liao
Publikováno v:
Clinical and Translational Medicine, Vol 13, Iss 6, Pp n/a-n/a (2023)
Abstract Background HCFC1 encodes transcriptional co‐regulator HCF‐1, which undergoes an unusual proteolytic maturation at a centrally located proteolysis domain. HCFC1 variants were associated with X‐linked cobalamin metabolism disorders and m
Externí odkaz:
https://doaj.org/article/b7aa36b3436b4440a085e851cb780fae
Autor:
Wang Song, Wen- Jun Bian, Hua Li, Qing- Hui Guo, Jie Wang, Bin Tang, Jia- Yuan Zhang, Wei Wei, Xiao- Rong Liu, Wei- Ping Liao, Bin Li, Na He
Publikováno v:
Journal of Medical Genetics; Sep2024, Vol. 61 Issue 9, p895-903, 9p
Retraction Note: Mir20a/106a-WTX axis regulates RhoGDIa/CDC42 signaling and colon cancer progression
Autor:
Gui-fang Zhu, Yang-wei Xu, Jian Li, Hui-lin Niu, Wen-xia Ma, Jia Xu, Pei-rong Zhou, Xia Liu, Dan-li Ye, Xiao-rong Liu, Tao Yan, Wei-ke Zhai, Zhi-jun Xu, Chun Liu, Lei Wang, Hao Wang, Jia-mao Luo, Li Liu, Xuan-qi Li, Suiqun Guo, Hui-ping Jiang, Peng Shen, Hui-kuan Lin, Di-hua Yu, Yan-qing Ding, Qing-ling Zhang
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/cd9207c07ef1431d916b21d2494179fe
Autor:
Bao-Xing Huang, Zi-Chang Jia, Xue Yang, Chao-Lin Cheng, Xiao-Rong Liu, Jianhua Zhang, Mo-Xian Chen, Jing-Fang Yang, Yun-Sheng Chen
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
The gene SYF2—an RNA splicing factor—can interact with Cyclin D-type binding protein 1 (GICP) in many biological processes, including splicing regulation, cell cycle regulation, and DNA damage repair. In our previous study we performed genome-wid
Externí odkaz:
https://doaj.org/article/800876d7dcec4289b03f9e450f497bca
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Externí odkaz:
https://doaj.org/article/b278a8e315ca485aa001d24c21526b00
Autor:
Sheng Luo, Zhi-Gang Liu, Juan Wang, Jun-Xia Luo, Xing-Guang Ye, Xin Li, Qiong-Xiang Zhai, Xiao-Rong Liu, Jie Wang, Liang-Di Gao, Fu-Li Liu, Zi-Long Ye, Huan Li, Zai-Fen Gao, Qing-Hui Guo, Bing-Mei Li, Yong-Hong Yi, Wei-Ping Liao
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
ObjectiveThe LAMA5 gene encodes the laminin subunit α5, the most abundant laminin α subunit in the human brain. It forms heterotrimers with the subunit β1/β2 and γ1/γ3 and regulates neurodevelopmental processes. Genes encoding subunits of the l
Externí odkaz:
https://doaj.org/article/4e0afead762e4a949294f4e33dce5d1f
Autor:
Ming-Feng He, Li-Hong Liu, Sheng Luo, Juan Wang, Jia-Jun Guo, Peng-Yu Wang, Qiong-Xiang Zhai, Su-Li He, Dong-Fang Zou, Xiao-Rong Liu, Bing-Mei Li, Hai-Yan Ma, Jing-Da Qiao, Peng Zhou, Na He, Yong-Hong Yi, Wei-Ping Liao
Publikováno v:
Journal of Medical Genetics; Jul2024, Vol. 61 Issue 7, p652-660, 14p
Publikováno v:
Journal of Integrative Nursing, Vol 2, Iss 4, Pp 203-206 (2020)
Objective: The objective of this study is to investigate the effect of mild moxibustion on quality of life of patients with type 2 diabetic peripheral neuropathy (DPN). Materials and Methods: Fifty-five patients with type 2 DPN from October 2018 to J
Externí odkaz:
https://doaj.org/article/da5036e45b9f46a69d08582502733ba3
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2022)
Objective: An overwhelming majority of the genetic variants associated with genetic disorders are missense. The association between the nature of substitution and the functional alteration, which is critical in determining the pathogenicity of varian
Externí odkaz:
https://doaj.org/article/a858231cdca34078a998212e88f8aeec
Autor:
Xiao-Rong Liu, Xing-Xing Xu, Si-Mei Lin, Cui-Ying Fan, Ting-Ting Ye, Bin Tang, Yi-Wu Shi, Tao Su, Bing-Mei Li, Yong-Hong Yi, Jian-Hong Luo, Wei-Ping Liao
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Objective: The objective of this study is to explore the role of GRIN2A gene in idiopathic generalized epilepsies and the potential underlying mechanism for phenotypic variation.Methods: Whole-exome sequencing was performed in a cohort of 88 patients
Externí odkaz:
https://doaj.org/article/b804738b5f7a465d8119396683083633