Zobrazeno 1 - 10
of 167
pro vyhledávání: '"Lingchao MENG"'
Autor:
Bentuo Zhang, Qiang Gang, Lingchao Meng, Zhenyu Li, Xujun Chu, Haohao Wu, Junsu Yang, Baogang Huang, Kang Du
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-7 (2024)
Abstract Distal hereditary motor neuropathies (dHMN) are a group of heterogeneous diseases and previous studies have reported that the compound heterozygous recessive MME variants cause dHMN. Our study found a novel homozygous MME variant and a repor
Externí odkaz:
https://doaj.org/article/a59a221d562c413cbf2e529d47a4d533
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-20 (2024)
Abstract Assessing and cultivating students’ HOTS are crucial for interior design education in a blended learning environment. However, current research has focused primarily on the impact of blended learning instructional strategies, learning task
Externí odkaz:
https://doaj.org/article/6cabdc69c1a04b4a8587dfef2b4dfd42
Publikováno v:
Journal of Isotopes, Vol 37, Iss 4, Pp 353-362 (2024)
In order to reveal the response relationship between the neutrons and void height of steel-shell concrete composite structures，and establish a new quantitative detection method for the void height，based on the principle of fast neutron moderation
Externí odkaz:
https://doaj.org/article/6e69779c48c845919ef5de051d55ecbf
Publikováno v:
BMC Women's Health, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background The prognostic potential of immune-related genes, particularly immune checkpoint inhibitors (ICIs) and long non-coding RNAs (lncRNAs), is gaining attention for evaluating the prognosis of breast cancer patients. Methods We analyze
Externí odkaz:
https://doaj.org/article/15ad27b205354291a25471738560412f
Autor:
Zhiying Xie, Chang Liu, Haiyan Yu, Zhihao Xie, Chengyue Sun, Ying Zhu, Xiaoyu Hu, Li Bai, Luhua Wei, Peng Sun, Yanyu Lu, Yunlong Lu, Yawen Zhao, Wei Zhang, Zhaoxia Wang, Lingchao Meng, Yun Yuan
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background Pathogenic missense variants in the dystrophin (DMD) gene are rarely reported in dystrophinopathies. Most DMD missense variants are of uncertain significance and their pathogenicity interpretation remains complicated. We aimed to
Externí odkaz:
https://doaj.org/article/86acb045fc3d4749a3f4198b0d35e13c
Autor:
Yunhe Xiong, Qianlin Song, Shurui Zhao, Chuan Wang, Hu Ke, Wenbiao Liao, Lingchao Meng, Lingyan Liu, Chao Song
Publikováno v:
Heliyon, Vol 10, Iss 11, Pp e32482- (2024)
Renal calculi (RC) represent a prevalent disease of the urinary system characterized by a high incidence rate. The traditional clinical diagnosis of RC emphasizes imaging and stone composition analysis. However, the significance of metabolic status i
Externí odkaz:
https://doaj.org/article/3b012276c4d3466c918f15fb00960d09
Autor:
Zhihao Xie, Chang Liu, Chengyue Sun, Yanyu Lu, Shiyi Wu, Yilin Liu, Qi Wang, Yalan Wan, Yikang Wang, Meng Yu, Lingchao Meng, Jianwen Deng, Wei Zhang, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 15, Iss 1, Pp 98-111 (2024)
Abstract Background We aimed to analyse genome‐wide transcriptome differences between Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) patients and identify biomarkers that correlate well with muscle magnetic resonance imaging
Externí odkaz:
https://doaj.org/article/fa65f1eaa6a34093b993df6f469c9b0f
Autor:
Chang Liu, Yanyu Lu, Haiyan Yu, Zhihao Xie, Chengyue Sun, Xinchao Cheng, Fangfang Niu, Yawen Zhao, Jianwen Deng, Lingchao Meng, Zhaoxia Wang, Yun Yuan, Zhiying Xie
Publikováno v:
Heliyon, Vol 10, Iss 6, Pp e28020- (2024)
Most pathogenic DMD variants are detectable and interpretable by standard genetic testing for dystrophinopthies. However, approximately 1∼3% of dystrophinopthies patients still do not have a detectable DMD variant after standard genetic testing, mo
Externí odkaz:
https://doaj.org/article/30c3de73fd56453ba19bca83f52730ad
Autor:
Hui Wang, Yilei Zheng, Jiaxi Yu, Lingchao Meng, Wei Zhang, Daojun Hong, Zhaoxia Wang, Yun Yuan, Jianwen Deng
Publikováno v:
Neurobiology of Disease, Vol 190, Iss , Pp 106391- (2024)
CGG repeat expansion in NOTCH2NLC is the genetic cause of neuronal intranuclear inclusion disease (NIID). Previous studies indicated that the CGG repeats can be translated into polyglycine protein (N2CpolyG) which was toxic to neurons by forming intr
Externí odkaz:
https://doaj.org/article/f3416ec7f874433e9f18c16017094b5e
Publikováno v:
Renal Failure, Vol 45, Iss 1 (2023)
Externí odkaz:
https://doaj.org/article/6bca54c76fc14fc2aa2d96ebf71d50bc