Hasil Pencarian - Longlong Lin
Anda harus masuk terlebih dahulu
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1
Effective Temporal Graph Learning via Personalized PageRank oleh Ziyu Liao, Tao Liu, Yue He, Longlong Lin
Diterbitkan 2024-07-01
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2
A Dual-Band, Dual-Polarized Filtering Antenna Based on Cross-Shaped Dielectric Strip Resonator oleh Lixin Jin, Hui Tang, Jin Shi, Longlong Lin, Kai Xu
Diterbitkan 2022-11-01
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3
A Balanced Substrate Integrated Waveguide Phase Shifter with Wideband Common-Mode Suppression oleh Wei Zhang, Jin Shi, Gangxiong Wu, Longlong Lin, Kai Xu
Diterbitkan 2023-01-01
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4
Photovoltaic power prediction based on dilated causal convolutional network and stacked LSTM oleh Chongyi Tian, Longlong Lin, Yi Yan, Ruiqi Wang, Fan Wang, Qingqing Chi
Diterbitkan 2024-01-01
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Design of a Switchable Filter for Reflectionless-Bandpass-to-Reflectionless-Bandstop Responses oleh Gangxiong Wu, Hao Wu, Wei Qin, Jin Shi, Wei Zhang, Longlong Lin, Qian Li
Diterbitkan 2023-02-01
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7
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy oleh Xiaoang Sun, Xiaona Luo, Longlong Lin, Simei Wang, Chunmei Wang, Fang Yuan, Xiaoping Lan, Jingbin Yan, Yucai Chen
Diterbitkan 2023-09-01
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8
Two heterozygous mutations in the calcium/calmodulin‐dependent serine protein kinase gene (CASK) in cases with developmental disorders oleh Kunfang Yang, Longlong Lin, Fang Yuan, Xiaoguang Li, Zhiping Liu, Xiaoping Lan, Yilin Wang, Yun Ren, Jiaoyan Li, Yucai Chen
Diterbitkan 2022-11-01
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Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases oleh Meiyan Liu, Xiaoang Sun, Longlong Lin, Xiaona Luo, Simei Wang, Chunmei Wang, Yuanfeng Zhang, Quanmei Xu, Wuhen Xu, Shengnan Wu, Xiaoping Lan, Yucai Chen, Yucai Chen
Diterbitkan 2022-11-01
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11
Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13 oleh Fang Yuan, Chunmei Wang, Jiaming Xi, Simei Wang, Longlong Lin, Yilin Wang, Anqi Wang, Chao Wang, Xiaona Luo, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Xiaomin Sun, Yucai Chen
Diterbitkan 2020-05-01
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12
MED12-Related Disease in a Chinese Girl: Clinical Characteristics and Underlying Mechanism oleh Chao Wang, Longlong Lin, Yan Xue, Yilin Wang, Zhao Liu, Zicheng Ou, Shengnan Wu, Xiaoping Lan, Yuanfeng Zhang, Fang Yuan, Xiaona Luo, Chunmei Wang, Jiaming Xi, Xiaomin Sun, Yucai Chen
Diterbitkan 2020-02-01
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13
Clinical Study of 8 Cases of CHD2 Gene Mutation–Related Neurological Diseases and Their Mechanisms oleh 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, Yucai Chen
Diterbitkan 2022-03-01
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14
Generation of an induced pluripotent stem cell line from an Ohtahara syndrome patient with the hemizygous mutation p.Q503Afs*28 (c.1507_1508del) in the ARX gene oleh 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
Diterbitkan 2022-03-01
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15
Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndro... oleh Yilin Wang, Fang Yuan, Anqi Wang, Chao Wang, Longlong Lin, Simei Wang, Chunmei Wang, Xiaona Luo, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Xiaomin Sun, Jiaming Xi, Jingbin Yan, Fanyi Zeng, Yucai Chen
Diterbitkan 2020-07-01
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16
Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.... oleh 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
Diterbitkan 2022-07-01
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17
Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan–Herndon–Dudley syndrome oleh Anqi Wang, Jiaming Xi, Fang Yuan, Yilin Wang, Simei Wang, Chunmei Wang, Chao Wang, Longlong Lin, Xiaona Luo, Quanmei Xu, Rongrong Yin, Hongyi Cheng, Yuanfeng Zhang, Xiaomin Sun, Jie Yang, Jingbin Yan, Fanyi Zeng, Yucai Chen
Diterbitkan 2020-07-01
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18
Segawa syndrome caused by TH gene mutation and its mechanism oleh 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
Diterbitkan 2022-12-01
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Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene oleh 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, Yucai Chen
Diterbitkan 2021-11-01
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