Zobrazeno 1 - 10
of 569
pro vyhledávání: '"Xue-jun Li"'
Autor:
Yu-qian Li, Lu-yao Li, Xue Yang, Qi-qi Lei, Liu-yan Xiang, Yuan-ru Wang, Si-meng Gu, Ya-jun Cao, Yan Pan, Lu Tie, Xue-jun Li
Publikováno v:
BMC Complementary Medicine and Therapies, Vol 23, Iss 1, Pp 1-15 (2023)
Abstract Background Cardiovascular disease and cancer are the main causes of morbidity and mortality worldwide. Studies have shown that these two diseases may have some common risk factors. Atorvastatin is mainly used for the treatment of atheroscler
Externí odkaz:
https://doaj.org/article/84a1fdf5c77e43e8a3a986ad0e1cba0e
Autor:
Yongchao Mou, Ghata Nandi, Sukhada Mukte, Eric Chai, Zhenyu Chen, Jorgen E. Nielsen, Troels T. Nielsen, Chiara Criscuolo, Craig Blackstone, Matthew J. Fraidakis, Xue-Jun Li
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-16 (2023)
Abstract Background Biallelic mutations in CYP27A1 and CYP7B1, two critical genes regulating cholesterol and bile acid metabolism, cause cerebrotendinous xanthomatosis (CTX) and hereditary spastic paraplegia type 5 (SPG5), respectively. These rare di
Externí odkaz:
https://doaj.org/article/da1bf0a071b64f849bc224f6de04b0b9
Publikováno v:
Neurobiology of Disease, Vol 187, Iss , Pp 106293- (2023)
Spastic paraplegia type 11 (SPG11) is a common autosomal recessive form of hereditary spastic paraplegia (HSP) characterized by the degeneration of cortical motor neuron axons, leading to muscle spasticity and weakness. Impaired lipid trafficking is
Externí odkaz:
https://doaj.org/article/5920107ee5f14e7f82e27187ba3e1e37
Autor:
Zhenyu Chen, Xue-Jun Li
Publikováno v:
Neural Regeneration Research, Vol 20, Iss 5, Pp 1397-1398 (2025)
Externí odkaz:
https://doaj.org/article/8b4fd027b6864743890a4d0452f14598
Autor:
Lei Wang, Song-peng Jia, Lan Zhang, Fang-ran Ma, Meng Zhang, Miao Yu, Hong-xia Jiang, Zhi-gang Qiao, Xue-jun Li
Publikováno v:
Aquaculture Reports, Vol 25, Iss , Pp 101194- (2022)
This study compared the physical characteristics, nutritional components, mineral elements, and volatile matter of the muscle of the Yellow River carp (Cyprinus carpio haematopterus) grown under the traditional pond system (TPS), in-pond raceway syst
Externí odkaz:
https://doaj.org/article/211a7da5ab7448e587c25aac3de56c17
Autor:
Yongchao Mou, Yi Dong, Zhenyu Chen, Kyle R. Denton, Michael O. Duff, Craig Blackstone, Su-Chun Zhang, Xue-Jun Li
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-20 (2020)
Abstract Hereditary spastic paraplegias (HSPs) are caused by a length-dependent axonopathy of long corticospinal neurons, but how axons of these cortical projection neurons (PNs) degenerate remains elusive. We generated isogenic human pluripotent ste
Externí odkaz:
https://doaj.org/article/2f4a0eef358e44248cac7d0af78e78cc
Autor:
Fei‐yi‐fan Wang, Si‐yi Wang‐gou, Hang Cao, Nian Jiang, Qi Yang, Qi Huang, Chun‐hai Huang, Xue‐jun Li
Publikováno v:
Cancer Communications, Vol 40, Iss 10, Pp 518-530 (2020)
Abstract Background Glioma, the most frequent primary tumor of the central nervous system, has poor prognosis. The epidermal growth factor receptor (EGFR) pathway and angiogenesis play important roles in glioma growth, invasion, and recurrence. The p
Externí odkaz:
https://doaj.org/article/36e97a1678dc4c26a55e1462527265d0
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Charcot-Marie-Tooth (CMT) disease is one of the most common genetically inherited neurological disorders and CMT type 2A (CMT 2A) is caused by dominant mutations in the mitofusin-2 (MFN2) gene. MFN2 is located in the outer mitochondrial membrane and
Externí odkaz:
https://doaj.org/article/1addfe128ab1428db019033d0e387914
Autor:
Xue-Jun Li
Publikováno v:
Neural Regeneration Research, Vol 17, Iss 6, Pp 1265-1266 (2022)
Externí odkaz:
https://doaj.org/article/91909e44d5794b5c98f1ba58b6ba4bef
Autor:
Yongchao Mou, Xue-Jun Li
Publikováno v:
Neural Regeneration Research, Vol 14, Iss 4, Pp 574-577 (2019)
Impaired axonal development and degeneration underlie debilitating neurodegenerative diseases including hereditary spastic paraplegia, a large group of inherited diseases. Hereditary spastic paraplegia is caused by retrograde degeneration of the long
Externí odkaz:
https://doaj.org/article/da2cf9eb02e248bdba546ef52e1ab993