Damage Effect of Amorphous Carbon Black Nanoparticle Aggregates on Model Phospholipid Membranes: Surface Charge, Exposure Concentration and Time Dependence

por Wang, Xiao-Feng, Xu, Kun, Li, Xin-Rui, Liu, Ya-Xin, Cheng, Jie-Min
Publicado 2023

Possible Role of Docosahexaenoic Acid in Response to Diarrhetic Shellfish Toxins in the Mussel Perna viridis

por Yuan, Kuan-Kuan, Chen, Zi-Min, Liu, Ya-Xin, Li, Hong-Ye, Yang, Wei-Dong
Publicado 2023

Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report

por Fan, Peng, Zhang, Di, Yang, Kun-Qi, Tian, Tao, Luo, Fang, Liu, Ya-Xin, Wang, Lin-Ping, Zhou, Xian-Liang
Publicado 2020

Clinical Characteristics and Prognosis of End-stage Hypertrophic Cardiomyopathy

por Xiao, Yan, Yang, Kun-Qi, Yang, Yan-Kun, Liu, Ya-Xin, Tian, Tao, Song, Lei, Jiang, Xiong-Jing, Zhou, Xian-Liang
Publicado 2015

A Human Health Risk Assessment of Trace Elements Present in Chinese Wine

por Deng, Zhi-Hao, Zhang, Ang, Yang, Zhi-Wei, Zhong, Ya-Li, Mu, Jian, Wang, Fei, Liu, Ya-Xin, Zhang, Jin-Jie, Fang, Yu-Lin
Publicado 2019

Etiology spectrum and clinical characteristics of renal artery stenosis in a Chinese cohort

por MENG, Xu, ZHOU, Yi, JIANG, Xiong-Jing, CAI, Jun, ZHANG, Hui-Min, WU, Hai-Ying, MA, Wen-Jun, LOU, Ying, LIU, Ya-Xin, ZHOU, Xian-Liang
Publicado 2021

A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension

por Lu, Yi-Ting, Liu, Xin-Chang, Zhou, Ze-Ming, Zhang, Di, Sun, Lin, Zhang, Ying, Fan, Peng, Zhang, Lin, Liu, Ya-Xin, Luo, Fang, Zhou, Xian-Liang
Publicado 2022

A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation

por Yang, Kun-Qi, Lu, Chao-Xia, Zhang, Ying, Yang, Yan-Kun, Li, Jia-Cheng, Lan, Tian, Meng, Xu, Fan, Peng, Tian, Tao, Wang, Lin-Ping, Liu, Ya-Xin, Zhang, Xue, Zhou, Xian-Liang
Publicado 2017

Implication of a novel truncating mutation in titin as a cause of autosomal dominant left ventricular noncompaction

por DONG, Xue-Qi, ZHANG, Di, QU, Yi, HU, Yu-Xiao, YANG, Chun-Xue, TIAN, Tao, XU, Nan, JIANG, Hai-Lun, ZENG, Li, XIA, Peng-Yan, LIU, Ya-Xin, LIU, Rui, ZHOU, Xian-Liang
Publicado 2022

Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family

por Zhang, Di, Qu, Yi, Dong, Xue-Qi, Lu, Yi-Ting, Yang, Kun-Qi, Liu, Xin-Chang, Fan, Peng, Hu, Yu-Xiao, Yang, Chun-Xue, Gao, Ling-Gen, Liu, Ya-Xin, Zhou, Xian-Liang
Publicado 2022

Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family

por Zhang, Di, Qu, Yi, Dong, Xue-Qi, Lu, Yi-Ting, Yang, Kun-Qi, Liu, Xin-Chang, Fan, Peng, Hu, Yu-Xiao, Yang, Chun-Xue, Gao, Ling-Gen, Liu, Ya-Xin, Zhou, Xian-Liang
Publicado 2022

A novel missense mutation in obscurin gene in a Chinese consanguineous family with left ventricular noncompaction

por DONG, Xue-Qi, QIN, Pei-Pei, ZHANG, Di, ZHANG, Qiong-Yu, QU, Yi, ZHAO, Lin, LU, Yi-Ting, HU, Yu-Xiao, YANG, Chun-Xue, LIU, Xin-Chang, LIU, Ya-Xin, ZHOU, Xian-Liang
Publicado 2022

A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia

por Fan, Peng, Zhao, Yu-Mo, Zhang, Di, Liao, Ying, Yang, Kun-Qi, Tian, Tao, Lou, Ying, Luo, Fang, Ma, Wen-Jun, Zhang, Hui-Min, Song, Lei, Cai, Jun, Liu, Ya-Xin, Zhou, Xian-Liang
Publicado 2019

Anemia in patients with Takayasu arteritis: prevalence, clinical features, and treatment

por Zhang, Ying, Zhang, Di, Qu, Yi, Fan, Peng, Liu, Ya-Xin, Zhang, Hui-Min, Song, Lei, Ma, Wen-Jun, Wu, Hai-Ying, Cai, Jun, Luo, Fang, Zhou, Xian-Liang, Zheng, De-Yu, Liu, Li-Sheng
Publicado 2019

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension

por Fan, Peng, Pan, Xiao-Cheng, Zhang, Di, Yang, Kun-Qi, Zhang, Ying, Tian, Tao, Luo, Fang, Ma, Wen-Jun, Liu, Ya-Xin, Wang, Lin-Ping, Zhang, Hui-Min, Song, Lei, Cai, Jun, Zhou, Xian-Liang
Publicado 2020

Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B

por Fan, Peng, Lu, Chao-Xia, Zhang, Di, Yang, Kun-Qi, Lu, Pei-Pei, Zhang, Ying, Meng, Xu, Hao, Su-Fang, Luo, Fang, Liu, Ya-Xin, Zhang, Hui-Min, Song, Lei, Cai, Jun, Zhang, Xue, Zhou, Xian-Liang
Publicado 2018

Efficient Photocatalytic Hydrogen Evolution over TiO(2-X) Mesoporous Spheres-ZnO Nanorods Heterojunction

por Zhang, BingKe, Li, Qi, Wang, Dongbo, Wang, Jinzhong, Jiang, Baojiang, Jiao, Shujie, Liu, DongHao, Zeng, Zhi, Zhao, ChenChen, Liu, YaXin, Xun, ZhiKun, Fang, Xuan, Gao, ShiYong, Zhang, Yong, Zhao, LianCheng
Publicado 2020

Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2 and characterized by early-onset hypertension and hypokalemia

por Fan, Peng, Lu, Yi-Ting, Yang, Kun-Qi, Zhang, Di, Liu, Xue-Ying, Tian, Tao, Luo, Fang, Wang, Lin-Ping, Ma, Wen-Jun, Liu, Ya-Xin, Zhang, Hui-Min, Song, Lei, Cai, Jun, Lou, Ying, Zhou, Xian-Liang
Publicado 2020

A novel phenotype with splicing mutation identified in a Chinese family with desminopathy

por Fan, Peng, Lu, Chao-Xia, Dong, Xue-Qi, Zhu, Di, Yang, Kun-Qi, Liu, Ke-Qiang, Zhang, Di, Zhang, Ying, Meng, Xu, Tan, Hui-Qiong, Yu, Li-Tian, Dou, Ke-Fei, Liu, Ya-Xin, Zhang, Xue, Zhou, Xian-Liang
Publicado 2019