Hasil Pencarian - YaXin Liu
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1
Deformation Behavior of Coarse-Grained Soil as an Embankment Filler under Cyclic Loading oleh Zhong-Ming He, Da Xiang, Ya-Xin Liu, Qian-Feng Gao, Han-Bing Bian
Diterbitkan 2020-01-01
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Clinical Characteristics and Prognosis of End-stage Hypertrophic Cardiomyopathy oleh Yan Xiao, Kun-Qi Yang, Yan-Kun Yang, Ya-Xin Liu, Tao Tian, Lei Song, Xiong-Jing Jiang, Xian-Liang Zhou
Diterbitkan 2015-01-01
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4
Enhancement of ionospheric heating effect by chemical release oleh Hai-Sheng Zhao, Jie Feng, Zheng-Wen Xu, Ya-Xin Liu, Kun Xue, Jian Wu, Cheng Wang, Shou-Zhi Xie, Huai-Yun Peng
Diterbitkan 2024-06-01
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5
A Human Health Risk Assessment of Trace Elements Present in Chinese Wine oleh Zhi-Hao Deng, Ang Zhang, Zhi-Wei Yang, Ya-Li Zhong, Jian Mu, Fei Wang, Ya-Xin Liu, Jin-Jie Zhang, Yu-Lin Fang
Diterbitkan 2019-01-01
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6
A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension oleh Yi-Ting Lu, Xin-Chang Liu, Ze-Ming Zhou, Di Zhang, Lin Sun, Ying Zhang, Peng Fan, Lin Zhang, Ya-Xin Liu, Fang Luo, Xian-Liang Zhou
Diterbitkan 2022-06-01
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7
A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation oleh Kun-Qi Yang, Chao-Xia Lu, Ying Zhang, Yan-Kun Yang, Jia-Cheng Li, Tian Lan, Xu Meng, Peng Fan, Tao Tian, Lin-Ping Wang, Ya-Xin Liu, Xue Zhang, Xian-Liang Zhou
Diterbitkan 2017-05-01
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8
Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family oleh Di Zhang, Yi Qu, Xue-Qi Dong, Yi-Ting Lu, Kun-Qi Yang, Xin-Chang Liu, Peng Fan, Yu-Xiao Hu, Chun-Xue Yang, Ling-Gen Gao, Ya-Xin Liu, Xian-Liang Zhou
Diterbitkan 2022-05-01
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9
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome oleh Kun-Qi Yang, Chao-Xia Lu, Peng Fan, Ying Zhang, Xu Meng, Xue-Qi Dong, Fang Luo, Ya-Xin Liu, Hui-Min Zhang, Hai-Ying Wu, Jun Cai, Xue Zhang, Xian-Liang Zhou
Diterbitkan 2018-02-01
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10
Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family oleh Di Zhang, Yi Qu, Xue-Qi Dong, Yi-Ting Lu, Kun-Qi Yang, Xin-Chang Liu, Peng Fan, Yu-Xiao Hu, Chun-Xue Yang, Ling-Gen Gao, Ya-Xin Liu, Xian-Liang Zhou
Diterbitkan 2022-06-01
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11
Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation oleh Peng Fan, Di Zhang, Xiao-Cheng Pan, Kun-Qi Yang, Qiong-Yu Zhang, Yi-Ting Lu, Ying Zhang, Xue-Ying Liu, Wen-Jun Ma, Hui-Min Zhang, Lei Song, Jun Cai, Ya-Xin Liu, Xian-Liang Zhou
Diterbitkan 2020-07-01
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12
Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B oleh Peng Fan, Chao-Xia Lu, Di Zhang, Kun-Qi Yang, Pei-Pei Lu, Ying Zhang, Xu Meng, Su-Fang Hao, Fang Luo, Ya-Xin Liu, Hui-Min Zhang, Lei Song, Jun Cai, Xue Zhang, Xian-Liang Zhou
Diterbitkan 2018-12-01
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13
Efficient Photocatalytic Hydrogen Evolution over TiO<sub>2-X</sub> Mesoporous Spheres-ZnO Nanorods Heterojunction oleh BingKe Zhang, Qi Li, Dongbo Wang, Jinzhong Wang, Baojiang Jiang, Shujie Jiao, DongHao Liu, Zhi Zeng, ChenChen Zhao, YaXin Liu, ZhiKun Xun, Xuan Fang, ShiYong Gao, Yong Zhang, LianCheng Zhao
Diterbitkan 2020-10-01
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14
A novel phenotype with splicing mutation identified in a Chinese family with desminopathy oleh Peng Fan, Chao-Xia Lu, Xue-Qi Dong, Di Zhu, Kun-Qi Yang, Ke-Qiang Liu, Di Zhang, Ying Zhang, Xu Meng, Hui-Qiong Tan, Li-Tian Yu, Ke-Fei Dou, Ya-Xin Liu, Xue Zhang, Xian-Liang Zhou, Yi Cui
Diterbitkan 2019-01-01
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