Zobrazeno 1 - 10
of 5 411
pro vyhledávání: '"Wei-Qian"'
Autor:
Ke-Mi Xu, Chao Liu, Lei Wang, Feng-Chun Pang, Xin-Jing Zhao, Xian-Bin Li, Qi-Dai Chen, Wei-Qian Zhao
Publikováno v:
Light: Advanced Manufacturing, Vol 5, Pp 1-8 (2024)
The manipulation of micro/nanostructures to customise their inherent material characteristics has garnered considerable attention. In this study, we present the selective activation of gallium arsenide (GaAs) via ultrafast laser-induced decomposition
Externí odkaz:
https://doaj.org/article/aa38f44b5fd54d3382a467c888b369d7
Autor:
Jing Song, Wei-Qian Lin
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Alcohol consumption is known to be associated with an increased risk of type 2 diabetes (T2DM). However, the effect of alcohol intake on the incidence of T2DM remains controversial due to inconsistent results across studies. This
Externí odkaz:
https://doaj.org/article/f97d1426376345efb2f08455da98a81f
Autor:
Kun Huang, Dan-Dan Wang, Wen-Bao Hu, Wei-Qian Zeng, Xia Xu, Qiu-Xiang Li, Fang-Fang Bi, Huan Yang, Jian Qiu
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-10 (2022)
Abstract Background Myotonic dystrophy type 1 (DM1), one of the most common forms of adult-onset muscular dystrophy, is caused by abnormally expanded CTG repeats in the 3′ untranslated region of the DMPK gene. The CUG repeats transcribed from the e
Externí odkaz:
https://doaj.org/article/9908958568a04201bf93ea59e4e0e755
Autor:
Jin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, Sha-Sha Huang, Guo-Jian Wang, Yu Su, Jin-Cao Xu, Ying Fu, Dong-Yang Kang, Kun Yang, Xin Zhang, Xing Liu, Xue Gao, Yong-Yi Yuan, Pu Dai
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-16 (2022)
Abstract Pathogenic variants in MYO15A are known to cause autosomal recessive nonsyndromic hearing loss (ARNSHL), DFNB3. We have previously reported on one ARNSHL family including two affected siblings and identified MYO15A c.5964+3G > A and c.8375 T
Externí odkaz:
https://doaj.org/article/ee9185e4b81c4596b2cae7e39d7fd8bc
Autor:
Kun Yang, Xi Wang, Wei‐Qian Wang, Ming‐Yu Han, Li‐Min Hu, Dong‐Yang Kang, Jin‐Yuan Yang, Min Liu, Xue Gao, Yong‐Yi Yuan, Jin‐Cao Xu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract Background Myhre syndrome is a rare multisystem genetic disorder that is caused by de novo heterozygous gain‐of‐function variants in SMAD4. Patients with Myhre syndrome exhibit several phenotypes at different ages such as small size, aut
Externí odkaz:
https://doaj.org/article/72523bacc75d4f989e2a04bb15ec1358
Autor:
Jin‐jin Ma, Jun Ying, Jin‐yu Wang, Tao‐tao Xu, Han‐ting Xia, Hong‐ting Jin, Lu‐wei Xiao, Wen‐jun Shang, Wei‐qian Wang, Jian‐yin Feng
Publikováno v:
Orthopaedic Surgery, Vol 14, Iss 5, Pp 946-954 (2022)
Objective To observe expression of CD38, a key modulator of nicotinamide dinucleotide (NAD+) metabolism in mice with knee osteoarthritis, and protective effect of CD38 inhibition during the osteoarthritis (OA) development. Method The destabilization
Externí odkaz:
https://doaj.org/article/87c407cb154c497c919dd25905c706c9
Autor:
Yi-Qi Chen, Dan Cheng, Lin Zhu, Wei-Qian Gao, Jia-Feng Yu, Jun Wang, Xin-Yi Deng, Ji-Wei Tao, Jia Qu, Li-Jun Shen
Publikováno v:
International Journal of Ophthalmology, Vol 15, Iss 2, Pp 255-260 (2022)
AIM: To investigate the feasibility of teaching minimally invasive vitreoretinal surgery with a robot-assisted surgical system and a three-dimensional (3D) visualization system. METHODS: Enucleated porcine eyes were established as an animal model for
Externí odkaz:
https://doaj.org/article/c308c5b0a64c4717b0eb6649c505ce80
Publikováno v:
Frontiers in Nutrition, Vol 9 (2022)
ObjectiveTo assess the effect of a novel naturally cultured rice with high resistant starch (RS) on postprandial glycemia in patients with type 2 diabetes compared to ordinary rice.DesignThis study is a randomized, double-blinded controlled trial.Met
Externí odkaz:
https://doaj.org/article/b6abb043eaee4fba9d5a697f93258950
Autor:
Rui Wang, Wei-Qian Wang, Xiao-Qin Li, Juan Zhao, Kun Yang, Yong Feng, Meng-Meng Guo, Min Liu, Xing Liu, Xi Wang, Yong-Yi Yuan, Xue Gao, Jin-Cao Xu
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
Abstract Mutations in the Forkhead Box C1 (FOXC1) are known to cause autosomal dominant hereditary Axenfeld-Rieger syndrome, which is a genetic disorder characterized by ocular and systemic features including glaucoma, variable dental defects, cranio
Externí odkaz:
https://doaj.org/article/01e95e3556b74eb9b9985d9b000e849b
In sensor networks characterized by irregular layouts and poor connectivity, anisotropic properties can significantly reduce the accuracy of distance estimation between nodes, consequently impairing the localization precision of unidentified nodes. S
Externí odkaz:
http://arxiv.org/abs/2411.08902
