Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Longlong Lin"'
Publikováno v:
Mathematical Biosciences and Engineering, Vol 21, Iss 1, Pp 1167-1185 (2024)
Due to the crucial role of photovoltaic power prediction in the integration, scheduling and operation of intelligent grid systems, the accuracy of prediction has garnered increasing attention from both the research and industry sectors. Addressing th
Externí odkaz:
https://doaj.org/article/1de3ce97afce40b1808d41c515d526b7
Publikováno v:
Entropy, Vol 26, Iss 7, p 588 (2024)
Graph representation learning aims to map nodes or edges within a graph using low-dimensional vectors, while preserving as much topological information as possible. During past decades, numerous algorithms for graph representation learning have emerg
Externí odkaz:
https://doaj.org/article/784d0e88a3364c0f84c0997dc77b5fd2
Autor:
Xiaoang Sun, Xiaona Luo, Longlong Lin, Simei Wang, Chunmei Wang, Fang Yuan, Xiaoping Lan, Jingbin Yan, Yucai Chen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 9, Pp n/a-n/a (2023)
Abstract Background Lysine acetyltransferase 6B (KAT6B) encodes a highly conserved histone acetyltransferase that regulates the expression of multiple genes and is essential for human growth and development. Methods We identified a novel frameshift v
Externí odkaz:
https://doaj.org/article/248af0dbeef44c17913336d1b8e29dca
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:
Meiyan Liu, Xiaoang Sun, Longlong Lin, Xiaona Luo, Simei Wang, Chunmei Wang, Yuanfeng Zhang, Quanmei Xu, Wuhen Xu, Shengnan Wu, Xiaoping Lan, Yucai Chen
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundProline-rich transmembrane protein 2 (PRRT2) plays an important role in the central nervous system and mutations in the gene are implicated in a variety of neurological disorders. This study aimed to summarize the clinical characteristics a
Externí odkaz:
https://doaj.org/article/670301d0ffc2493382032d19678ff992
Autor:
Kunfang Yang, Longlong Lin, Fang Yuan, Xiaoguang Li, Zhiping Liu, Xiaoping Lan, Yilin Wang, Yun Ren, Jiaoyan Li, Yucai Chen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Background The calcium/calmodulin‐dependent serine protein kinase gene (CASK) is an essential gene in mammals, critical for neurodevelopment. The purpose of this study is to expand the understanding of the diagnosis of CASK‐linked disord
Externí odkaz:
https://doaj.org/article/c7c8fa2a30fd4178bdd9f26872ba5c94
Publikováno v:
IET Microwaves, Antennas & Propagation, Vol 15, Iss 9, Pp 1076-1085 (2021)
Abstract A design approach is presented based on insights into power division among modes for a dual‐band filtering power divider using a single multimode resonator. The relationship between the energy of the input port under different modes and th
Externí odkaz:
https://doaj.org/article/79defed5b21e4b1c99f9e6985fba60b4
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
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, Xiaoang Sun, Yilin Wang, Longlong Lin, Fang Yuan, Simei Wang, Wenjing Zhang, Xiaobing Ji, Meiyan Liu, Shengnan Wu, Xiaoping Lan, Jie Zhang, Jingbin Yan, Fanyi Zeng, Yucai Chen
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Background: The chromodomain helicase DNA-binding protein 2 (CHD2) gene, is an ATPase and part of the CHD family of chromatin remodelers. Mutations in the CHD2 gene are inherited in an autosomal-dominant manner and can lead to intellectual disability
Externí odkaz:
https://doaj.org/article/97f6639bab4744f8bed5ed741c3ba30f