Zobrazeno 1 - 10
of 220
pro vyhledávání: '"Zhimei Liu"'
Autor:
Mingming Chen, Yan Li, Xueling Xu, Shuqi Wang, Zhimei Liu, Shiyu Qi, Dandan Si, Zhuo Man, Shoulong Deng, Guoshi Liu, Yue Zhao, Kun Yu, Zhengxing Lian
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-14 (2024)
Abstract Dynamic metabolic reprogramming occurs at different stages of myogenesis and contributes to the fate determination of skeletal muscle satellite cells (MuSCs). Accumulating evidence suggests that mutations in myostatin (MSTN) have a vital rol
Externí odkaz:
https://doaj.org/article/b5bdccdaa8fb4707a04059c9ffcf5bdb
Publikováno v:
Plants, Vol 13, Iss 19, p 2731 (2024)
In this paper, Panax ginseng cyclophilin (PgCyP) was successfully obtained through a genetic engineering technique. A bioinformatics method was used to analyze the physicochemical properties and structure of PgCyP. The results showed that PgCyP belon
Externí odkaz:
https://doaj.org/article/c1ec0db937ed4b63a9c1b92e0605f9bb
Autor:
Yuying Sun, Zhimei Liu, Jianguo Yang, Qingqing Jia, Jinglong Sun, Lei Wang, Fengjiao Liang, Shiyuan Song, Kaixi Wang, Xia Zhou
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
ObjectThe purpose of this study was to evaluate the risk of secondary immune thrombocytopenia in multiple sclerosis patients treated with alemtuzumab through a meta-analysis.MethodsWe searched databases including PubMed, Web of Science, OVID and EMBA
Externí odkaz:
https://doaj.org/article/4e5a8b7af0e5469e92df4f3d61c3cf31
Publikováno v:
Stem Cell Research, Vol 76, Iss , Pp 103346- (2024)
NAD(P)HX dehydratase (NAXD) gene is one of the key enzymes encoding the nicotinamide nucleotide repair system, reportedly associated with Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2 (PEBEL2). Here, we gene
Externí odkaz:
https://doaj.org/article/a18cd896704742279f46964cb21dc8c3
Autor:
Shiwei Zhuang, Zhimei Liu, Jinyao Wu, Yudan Yao, Zongyang Li, Yanxiang Shen, Bin Yu, Donglu Wu
Publikováno v:
Pharmaceuticals, Vol 17, Iss 6, p 664 (2024)
The circulatory system is a closed conduit system throughout the body and consists of two parts as follows: the cardiovascular system and the lymphatic system. Hematological malignancies usually grow and multiply in the circulatory system, directly o
Externí odkaz:
https://doaj.org/article/b357fb8ddfcf4db29e3eec331b271e02
Autor:
Dan Zhao, Ming Liu, Huafang Jiang, Tianyu Song, Chaolong Xu, Xin Duan, Ruoyu Duan, Han Xu, Zhimei Liu, Fang Fang
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Thiamine pyrophosphokinase (TPK) deficiency, is a rare autosomal recessive disorder of congenital metabolic dysfunction caused by variants in the TPK1 gene. TPK1 variants can lead to thiamine metabolic pathway obstacles, and its clinical manifestatio
Externí odkaz:
https://doaj.org/article/0690de52ca3d44f1b7afad743aa18e28
Autor:
Mingming Chen, Yue Zhao, Yao Li, Tiantian Chen, Wendi Zhou, Xiaosheng Zhang, Shoulong Deng, Xueling Xu, Sujun Wu, Zhimei Liu, Shiyu Qi, Luyu Wang, Yan Li, Kun Yu, Zhengxing Lian
Publikováno v:
Frontiers in Veterinary Science, Vol 10 (2023)
IntroductionMyostatin (MSTN) negatively regulates skeletal muscle development. However, its function in reproductive performance and visceral organs has not been thoroughly investigated. Previously, we prepared a MSTN and fibroblast growth factor 5 (
Externí odkaz:
https://doaj.org/article/66c19bcb76614e9bb976ed0488fb7e4c
Publikováno v:
Stem Cell Research, Vol 59, Iss , Pp 102633- (2022)
Mutations in CARS2 gene, encoding for the mitochondrial cysteinyl-tRNA synthetase, has been reported to be associated with early-onset epileptic encephalopathy (EOEE). Here, we generated an induced pluripotent stem cell (iPSC) line from the human der
Externí odkaz:
https://doaj.org/article/643a74abc340444487d3f3323f98be85
Autor:
Dan Sun, Zhimei Liu, Yongchu Liu, Miaojuan Wu, Fang Fang, Xianbo Deng, Zhisheng Liu, Liang Song, Kei Murayama, Chunhua Zhang, Yuanyuan Zhu
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background Short-chain enoyl-CoA hydratase deficiency (ECHS1D), also known as ECHS1 deficiency, is a rare inborn metabolic disorder with clinical presentations characterized by Leigh syndrome (LS). Thirty-four different pathogenic mutations
Externí odkaz:
https://doaj.org/article/069ce8503aa948d08bfd7b599fb27f56
Publikováno v:
ACS Omega, Vol 5, Iss 17, Pp 10106-10114 (2020)
Externí odkaz:
https://doaj.org/article/d422e5069b084abfba51ed4eb1e30533