Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Rongrong Yin"'
Autor:
Rongrong Yin, Ahmadjan Muhammadhaji
Publikováno v:
AIMS Mathematics, Vol 9, Iss 2, Pp 4962-4989 (2024)
This paper studies a delayed rumor propagation model with logistic growth and saturation incidence. The next generation matrix method, some inequality techniques, the Lyapunov-LaSalle invariance principle, and the Lyapunov method are used in this pap
Externí odkaz:
https://doaj.org/article/bab71b35796a415498d275aa1493b076
Publikováno v:
Buildings, Vol 13, Iss 9, p 2193 (2023)
Using coral debris as coarse and fine aggregates and seawater as mixing water has been proposed to address transportation and material shortage issues in island and reef construction projects. However, the utilization of coral may result in impuritie
Externí odkaz:
https://doaj.org/article/771edbf2bc5245f8be09fc5230f64364
Autor:
Yilin Wang, Chunmei Wang, Meiyan Liu, Wuhen Xu, Simei Wang, Fang Yuan, Xiaona Luo, Quanmei Xu, Rongrong Yin, Anqi Wang, Miao Guo, Longlong Lin, Chao Wang, Hongyi Cheng, Zhiping Liu, Yuanfeng Zhang, Fanyi Zeng, Jingbin Yan, Yucai Chen
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Dopa-responsive dystonia (DRD), also known as Segawa syndrome, is a rare neurotransmitter disease. The decrease in dopamine caused by tyrosine hydroxylase (TH) gene mutation may lead to dystonia, tremor and severe encephalopathy in children. Although
Externí odkaz:
https://doaj.org/article/b4c72c20fa7b4310acb4c5086f031a5c
Autor:
Xiaona Luo, Yilin Wang, Fang Yuan, Longlong Lin, Anqi Wang, Chao Wang, Miao Guo, Simei Wang, Chunmei Wang, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Zhiping Liu, Wuhen Xu, Jingbin Yan, Fanyi Zeng, Yucai Chen
Publikováno v:
Stem Cell Research, Vol 62, Iss , Pp 102798- (2022)
Epilepsy of infancy with migrating focal seizures (EIMFS) is a kind of epileptic encephalopathy with high genetic heterogeneity. The most common pathogenic gene for EIMFS is potassium sodium-activated channel subfamily T member 1 (KCNT1). Using Senda
Externí odkaz:
https://doaj.org/article/1dc604a960284801bdf68e662f6e9500
Publikováno v:
IEEE Access, Vol 9, Pp 49025-49035 (2021)
Many real-world networks have scale-free characteristics and can be abstracted into scale-free networks. Aiming at the problem that scale-free networks have low fault tolerance in the face of malicious attacks, we focus on the selective forwarding at
Externí odkaz:
https://doaj.org/article/e7c8298d6a3440d5afe4d2fddda9550b
Publikováno v:
JACS Au, Vol 1, Iss 2, Pp 164-173 (2020)
Externí odkaz:
https://doaj.org/article/db14f5cc19fb420697110c082d98b228
Autor:
Chunmei Wang, Yilin Wang, Wuhen Xu, Xuefeng Lin, Jiaming Xi, Simei Wang, Longlong Lin, Fang Yuan, Anqi Wang, Chao Wang, Xiaona Luo, Quanmei Xu, Rongrong Yin, Yuanfeng Zhang, Xiaoyi Huang, Yucai Chen
Publikováno v:
Stem Cell Research, Vol 59, Iss , Pp 102621- (2022)
Aristaless-related homeobox (ARX)-related disorders are recessive X-linked intellectual disability disorders. We encountered a patient with a hemizygous mutation (c.1507_1508del) showing intellectual disability, early-onset epileptic encephalopathy a
Externí odkaz:
https://doaj.org/article/c84f59a0d89241e687288fd4ac511985
Autor:
Xiaona Luo, Chunmei Wang, Longlong Lin, Fang Yuan, Simei Wang, Yilin Wang, Anqi Wang, Chao Wang, Shengnan Wu, Xiaoping Lan, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Jiaming Xi, Jie Zhang, Xiaomin Sun, Jingbin Yan, Fanyi Zeng, Yucai Chen
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
The gene encoding collagen like tail subunit of asymmetric acetylcholinesterase (COLQ) is responsible for the transcription of three strands of collagen of acetylcholinesterase, which is attached to the endplate of neuromuscular junctions. Mutations
Externí odkaz:
https://doaj.org/article/6939934fb6e9403f8f54ed0089c01920
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 24, p 15858 (2022)
Iron overload is an independent risk factor for disuse osteoporosis. Hibernating animals are natural models of anti-disuse osteoporosis; however, whether iron metabolism is involved in bone adaptation and maintenance during hibernation is unclear. To
Externí odkaz:
https://doaj.org/article/433a3d25fb2c4a4e95a4b10a3768510d
Autor:
Fang Yuan, Simei Wang, Yilin Wang, Anqi Wang, Chao Wang, Xiaona Luo, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Chunmei Wang, Miao Guo, Yuanfeng Zhang, Jiaming Xi, Jie Yang, Xiaomin Sun, Jingbin Yan, Fanyi Zeng, Yucai Chen
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102292- (2021)
Mental retardation, X-linked 21/34 (MRX21/34), is a rare intellectual disability disease caused by mutations in the IL1RAPL1 (Interleukin-1 Receptor Accessory Protein-Like 1) gene. Using Sendai virus-mediated reprogramming, we established an induced
Externí odkaz:
https://doaj.org/article/e6bd3271acae4c959b3c8b6e82b8f793