Zobrazeno 1 - 10
of 429
pro vyhledávání: '"Bingbing wu"'
Publikováno v:
Chinese Journal of Mechanical Engineering, Vol 37, Iss 1, Pp 1-11 (2024)
Abstract Considering that the clutch cover assembly and driven disc assembly show common effect on the engagement/disengagement characteristics of the pull-type diaphragm spring clutches for heavy-duty commercial vehicles, the diaphragm spring, cushi
Externí odkaz:
https://doaj.org/article/2d449e63e50b43809c13bab98111ed65
Autor:
Fucheng Dong, Xiuge Wang, Tao Huang, Yingying Yin, Sai Xiao, Yanjie Ma, Huafang Wei, Bingbing Wu, Ruidan Zhang, Liying Wang, Xuejiang Guo, Fei Gao, Chao Liu, Hongbin Liu, Jianguo Zhao, Wei Li
Publikováno v:
Genes and Diseases, Vol 11, Iss 6, Pp 101132- (2024)
Externí odkaz:
https://doaj.org/article/4ef0cecee5d7460a9a03db7ba602d22c
Autor:
Bingbing Wu, Yongxiao Wang, Xiaoming Liu, Di Zhang, Shuhao Zhou, Lingrui Deng, Liqiang Wang, Hui Li
Publikováno v:
Journal of Materials Research and Technology, Vol 30, Iss , Pp 5963-5976 (2024)
The aluminum alloy components on automobile often experience high strain rate deformation during accidents. The dynamic deformation behavior and constitutive model are crucial for analysis of vehicle body collisions and failures. In this work, the 7A
Externí odkaz:
https://doaj.org/article/40128c428fd148338a1f9ba2698248d9
Autor:
Mingyu Gan, Yanyan Zhang, Gangfeng Yan, Yixue Wang, Guoping Lu, Bingbing Wu, Weiming Chen, Wenhao Zhou
Publikováno v:
Annals of Clinical Microbiology and Antimicrobials, Vol 23, Iss 1, Pp 1-9 (2024)
Abstract Background Antimicrobial resistance (AMR) is a major threat to children’s health, particularly in respiratory infections. Accurate identification of pathogens and AMR is crucial for targeted antibiotic treatment. Metagenomic next-generatio
Externí odkaz:
https://doaj.org/article/57d36b3c39d94970af92684b71b9b008
Autor:
Jiangfeng Shen, Kaijin Lu, Fuxing Liu, Xia Chen, Quan Chen, Bingbing Wu, Hailan Wang, Pengfei Ge, Guang Han, Fei Wang, Peng Zhang, Pei Yin, Weiguang Jia, Yiming Zheng, Pengcheng Wang, Fei Sun
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
BackgroundCarcinosarcoma is a rare esophageal tumor, accounting for approximately 0.27-2.8% of malignant esophageal tumors. This study aims to investigate the clinical pathological characteristics, surgical treatment outcomes, and analysis of prognos
Externí odkaz:
https://doaj.org/article/f0a48361120645288e54561259ca70b7
Publikováno v:
Stem Cell Research, Vol 78, Iss , Pp 103451- (2024)
Hereditary fructose intolerance (HFI) is an autosomal recessive metabolic disease associated with a mutation in the aldolase B gene on chromosome 9q31. In this study, we generated a human-induced pluripotent stem cell (hiPSC) line, FDCHi015-A, from p
Externí odkaz:
https://doaj.org/article/fa8adbb01d1b43eea5c6651157e13d22
Autor:
Qi Ni, Meiling Tang, Xiang Chen, Yulan Lu, Bingbing Wu, Huijun Wang, Wenhao Zhou, Xinran Dong
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
ObjectiveFructose-1,6-bisphosphatase deficiency (FBP1D) is a rare inborn error due to mutations in the FBP1 gene. The genetic spectrum of FBP1D in China is unknown, also nonspecific manifestations confuse disease diagnosis. We systematically estimate
Externí odkaz:
https://doaj.org/article/c285b8ae1aa64b5ea23274f29c49c07b
Autor:
Hui Xiao, Huiyao Chen, Xiang Chen, Yulan Lu, Bingbing Wu, Huijun Wang, Yun Cao, Liyuan Hu, Xinran Dong, Wenhao Zhou, Lin Yang
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-15 (2023)
Abstract Background In China, ~1,072,100 small for gestational age (SGA) births occur annually. These SGA newborns are a high-risk population of developmental delay. Our study aimed to evaluate the genetic profile of SGA newborns in the newborn inten
Externí odkaz:
https://doaj.org/article/a13219e6102b4b708d625471812653ae
Publikováno v:
Stem Cell Research, Vol 76, Iss , Pp 103369- (2024)
Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities (NEDASB) is a rare autosomal dominant disorder caused by a heterozygous mutation in the NOVA2 gene on chromosome 19q13. Here, we describe the generati
Externí odkaz:
https://doaj.org/article/e7492c268c724264b4d0313198dbb424
Autor:
Yinmo Jiang, Bingbing Wu, Xi Zhang, Lin Yang, Sujuan Wang, Huiping Li, Shuizhen Zhou, Yanyan Qian, Huijun Wang
Publikováno v:
Children, Vol 11, Iss 8, p 897 (2024)
Background: Neurodevelopmental disorders (NDDs) are a group of diseases that severely affect the physical and mental health of children. The PPP2R5D gene encodes B56δ, the regulatory subunit of protein phosphatase 2A (PP2A). NDDs related to the PPP2
Externí odkaz:
https://doaj.org/article/030f7586661749f59d1895380dc50193