Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Xinli Zhan"'
Publikováno v:
Medicine. 101:e31725
Growing evidence indicates that lncRNAs are involved in the progression of several diseases, including osteoarthritis (OA). However, the role of the lncRNA PVT1 in OA is still unclear. The present study was aimed at exploring the impact of PVT1 on OA
Autor:
Jiemei Cen, Tuo Liang, Zhaojun Lu, Jie Jiang, Xihua Sun, Xinli Zhan, Zide Zhang, Tianyou Chen, Jiarui Chen, Liyi Chen, Shengsheng Huang, Chong Liu, Hao Li, Guoyong Xu
Publikováno v:
Medicine. 100:e26582
Background Tuberculosis (TB) is a global health problem that brings us numerous difficulties. Diverse genetic factors play a significant role in the progress of TB disease. However, still no key genes for TB susceptibility have been reported. This st
Autor:
Tuo Liang, Jie Jiang, Shian Liao, Zequn Wang, Hongyu Liao, Zide Zhang, Guoyong Xu, Juliang He, Jian Guan, Zuowei Liao, Xinli Zhan, Hao Mo, Zhaojun Lu, Chong Liu, Jiarui Chen, Zhenchao Yuan, Chaojie Yu
Publikováno v:
Medicine
Background: Autophagy is closely related to skin cutaneous melanoma (SKCM), but the mechanism involved is unclear. Therefore, exploration of the role of autophagy-related genes (ARGs) in SKCM is necessary. Materials and methods: Differential expressi
Autor:
Zequn Wang, Tuo Liang, Zhaojun Lu, Jiarui Chen, Chong Liu, Shian Liao, Guoyong Xu, Hao Li, Xinli Zhan, Tianyou Chen, Chaojie Yu, Zide Zhang, Jie Jiang
Publikováno v:
Medicine
Background: Ewing sarcoma (ES), the second most prevalent bone malignant tumor has no widely known prognostic biomarker. Earlier studies have suggested that chaperonin containing TCP1 complex 6A (CCT6A), which encodes a molecular protein chaperone, i
Autor:
Xinli Zhan, Guoyong Xu, Tuo Liang, Chong Liu, Zequn Wang, Jiang Xue, Xin Zhou, Zhaojie Qin, Haopeng Zeng, Jie Jiang, Zhaojun Lu, Chaojie Yu, Zide Zhang, Jiarui Chen
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
Background: In pediatric tumors, immunotherapy exhibits less toxicity than chemotherapy and radiation. The current study aims to identify potential immune targets in immune-related genes of C
Background: In pediatric tumors, immunotherapy exhibits less toxicity than chemotherapy and radiation. The current study aims to identify potential immune targets in immune-related genes of C
Autor:
Zhaojie Qin, Xinli Zhan, Chao Jie Yu, Guoyong Xu, Chong Liu, Jie Jiang, Tuo Liang, Jiarui Chen, Zide Zhang
Publikováno v:
Medicine
Background: Ossification of the posterior longitudinal ligament (OPLL) refers to an ectopic ossification disease originating from the posterior longitudinal ligament of the spine. Pressing on the spinal cord or nerve roots can cause limb sensory and
Autor:
Guoyong Xu, Zide Zhang, Jiang Xue, Chong Liu, Chaojie Yu, Haopeng Zeng, Jiemei Cen, Jie Jiang, Jiarui Chen, Xinli Zhan, Zequn Wang, Tuo Liang, Zhaojun Lu, Jian Zeng
Publikováno v:
Medicine
Background: The incidence of triple negative breast cancer (TNBC) is at a relatively high level, and our study aimed to identify differentially expressed genes (DEGs) in TNBC and explore the key pathways and genes of TNBC. Methods: The gene expressio
Publikováno v:
Medicine
Background: This meta-analysis was conducted to compare the effects and safety of teriparatide with risedronate in the treatment of osteoporosis. Material and methods: PubMed, Embase, Web of Science and Cochrane library database were systematically r
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
The Ladybird Homeobox 1 (LBX1) gene has been implicated in the etiology of adolescent idiopathic scoliosis (AIS). The association between LBX1 gene polymorphisms and AIS has been investigated
The Ladybird Homeobox 1 (LBX1) gene has been implicated in the etiology of adolescent idiopathic scoliosis (AIS). The association between LBX1 gene polymorphisms and AIS has been investigated
Publikováno v:
Medicine. 98:e15796
miRNAs and genes play significant roles in the etiology and pathogenesis of intervertebral disc degeneration (IDD). This study aimed to identify aberrantly expressed miRNAs, genes, and pathways in IDD through a comprehensive bioinformatics analysis.D