Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Guoli Tian"'
Autor:
Maosheng Cheng, Shuang Chen, Kang Li, Ganping Wang, Gan Xiong, Rongsong Ling, Caihua Zhang, Zhihui Zhang, Hui Han, Zhi Chen, Xiaochen Wang, Yu Liang, Guoli Tian, Ruoxing Zhou, Yan Zhu, Jieyi Ma, Jiahong Liu, Shuibin Lin, Hao Xu, Demeng Chen, Yang Li, Liang Peng
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-17 (2024)
Abstract Interplay between innate and adaptive immune cells is important for the antitumor immune response. However, the tumor microenvironment may turn immune suppressive, and tumor associated macrophages are playing a role in this transition. Here,
Externí odkaz:
https://doaj.org/article/73b9a51ecf3d46e89fc737e515933959
Autor:
Zhixing Zhu, Georgi Z. Genchev, Yanmin Wang, Wei Ji, Xiaofen Zhang, Hui Lu, Sira Sriswasdi, Guoli Tian
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-14 (2023)
Abstract Background The peroxisome is a ubiquitous single membrane-enclosed organelle with an important metabolic role. Peroxisomal disorders represent a class of medical conditions caused by deficiencies in peroxisome function and are segmented into
Externí odkaz:
https://doaj.org/article/07e1aa6dcf004addaffa4290fcf2b61f
Autor:
Zhixing Zhu, Georgi Z. Genchev, Yanmin Wang, Wei Ji, Xiaofen Zhang, Hui Lu, Sira Sriswasdi, Guoli Tian
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/1eacf27162fd438f9ea7f245ccc476b7
Autor:
Zhixing Zhu, Jianlei Gu, Georgi Z. Genchev, Xiaoshu Cai, Yangmin Wang, Jing Guo, Guoli Tian, Hui Lu
Publikováno v:
Frontiers in Molecular Biosciences, Vol 7 (2020)
Phenylketonuria (PKU) is a common genetic metabolic disorder that affects the infant's nerve development and manifests as abnormal behavior and developmental delay as the child grows. Currently, a triple–quadrupole mass spectrometer (TQ-MS) is a co
Externí odkaz:
https://doaj.org/article/7f211335713d4f13892b636dea9d86d1
Autor:
Fan Song, Chen Hou, Jianfeng Liang, Hongshi Cai, Guoli Tian, Yaoqi Jiang, Ziyi Wang, Danqi Qiu, Jinsong Hou
Background Intracellular lactate is shown to drive a novel type of post-translational modification (PTM), lysine lactylation (Kla), which has been confirmed to affect the malignant progression of tumors such as hepatocellular carcinoma (HCC) and gast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed1686c7e21d8839423fe69cd754edd6
https://doi.org/10.21203/rs.3.rs-2901339/v1
https://doi.org/10.21203/rs.3.rs-2901339/v1
Publikováno v:
Journal of Zhejiang University (Medical Sciences). 50:481-486
To investigate the value of very long chain acylcarnitine (VLCAC) and lysophosphatidylcholine (LPC) in screening of peroxisomal disease in children. Eighteen children with peroxisomal disease, including 14 cases of X-linked adrenoleukodystrophy (X-AL
Autor:
Qianming Chen, Zihao Wei, Yuye Liang, Xin Zeng, Lu Jiang, Peiyang Yuan, Xuemei Qiu, Xin-hua Liang, Guoli Tian
Publikováno v:
The Journal of Dermatology. 47
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 39(10)
L-2-hydroxyglutaric aciduria is a genetic metabolic disorder. Its clinical features include elevated levels of hydroxyglutaric acid in body fluids and abnormal magnetic resonance imaging (MRI) in the subcortical white matter, which are affected by th
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