Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Qiu‐Xiang Li"'
Publikováno v:
Journal of Management Science and Engineering, Vol 9, Iss 3, Pp 328-347 (2024)
Complex equipment refers to special equipment that differs from general equipment. The collaborative development work of complex equipment in the military-civilian integration context involves numerous suppliers. We consider a two-tier supply network
Externí odkaz:
https://doaj.org/article/6d3f9901887d4334a5402da2cd011f17
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:
Kai‐Yue Zhang, Geng‐Jian Zhang, Hui‐Qian Duan, Qiu‐Xiang Li, Kun Huang, Li‐Qun Xu, Huan Yang, Yue‐Bei Luo
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Calsequestrin 1 (CASQ1) is the most crucial Ca2+ binding protein localized in the sarcoplasmic reticulum (SR) of skeletal muscle. With high capacity and low affinity for Ca2+, CASQ1 plays a significant role in maintaining a large amount of C
Externí odkaz:
https://doaj.org/article/4c66764f85fd49e3987badbc899c1f1b
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundGlycogen storage disease (GSDs) is characterized by abnormally inherited glycogen metabolism. GSD IXd, which is caused by mutations in the PHKA1 gene, is an X-linked rare disease with mild myopathic symptoms. To date, only 13 patients with
Externí odkaz:
https://doaj.org/article/ad0820cdf35141c3ae8fa669a9cc76e3
Publikováno v:
Complexity, Vol 2020 (2020)
This paper considers a Cournot–Bertrand game model based on the relative profit maximization with bounded rational players. The existence and stability of the Nash equilibrium of the dynamic model are investigated. The influence of product differen
Externí odkaz:
https://doaj.org/article/6e2472c36f3c461695a526722d7fd375
Autor:
Kai‐Yue Zhang, Geng‐Jian Zhang, Hui‐Qian Duan, Qiu‐Xiang Li, Kun Huang, Li‐Qun Xu, Huan Yang, Yue‐Bei Luo
Publikováno v:
Clinical Case Reports. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab0a27a1aff3ed356c3ee44409727dfb
https://doi.org/10.1002/ccr3.6689
https://doi.org/10.1002/ccr3.6689
Expanding the clinicopathological‐genetic spectrum of GNE myopathy by a Chinese neuromuscular centre
Publikováno v:
Journal of Cellular and Molecular Medicine
GNE myopathy is a heterogeneous group of ultrarare neuromuscular disorders caused by mutations in the GNE gene. An estimated prevalence of 1~21/1,000,000 leads to a deficiency of data and a lack of availability of samples to conduct clinical research
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b3815ed2ff549dc0116a41642164685
https://doi.org/10.1111/jcmm.16978
https://doi.org/10.1111/jcmm.16978
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 17, Pp 2133-2134 (2018)
Externí odkaz:
https://doaj.org/article/f5a140f1df164195855084c3537f3522
Publikováno v:
Journal of cellular and molecular medicine. 26(14)
Congenital myasthenic syndrome (CMS) encompasses a heterogeneous group of inherited disorders affecting nerve transmission across the neuromuscular junction. The aim of this study was to characterize the clinical, physiological, pathohistological and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f502a336f2af8f17a16a5f30f8466322
https://pubmed.ncbi.nlm.nih.gov/35670010
https://pubmed.ncbi.nlm.nih.gov/35670010
Publikováno v:
Neurogenetics. 23(1)
Limb-girdle muscular dystrophy (LGMD) is a group of clinically and genetically heterogeneous neuromuscular disorders. LGMD-R7, which is caused by telethonin gene (TCAP) mutations, is one of the rarest forms of LGMD, and only a small number of LGMD-R7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::931ecfcd9472cb21487e86ffbff6eb6d
https://pubmed.ncbi.nlm.nih.gov/34982307
https://pubmed.ncbi.nlm.nih.gov/34982307