Chemical structure, properties and potential applications of surfactin, as well as advanced strategies for improving its microbial production

por Zhen, Cheng, Ge, Xian-Feng, Lu, Yi-Ting, Liu, Wen-Zheng
Publicado 2023

Making a Decision between Acute Appendicitis and Acute Gastroenteritis

por Lu, Yi-Ting, Chen, Po-Cheng, Huang, Ying-Hsien, Huang, Fu-Chen
Publicado 2020

Trapped interfacial redox introduces reversibility in the oxygen reduction reaction in a non-aqueous Ca(2+) electrolyte

por Lu, Yi-Ting, Neale, Alex R., Hu, Chi-Chang, Hardwick, Laurence J.
Publicado 2021

Tandem Mach Zehnder Directional Coupler Design and Simulation on Silicon Platform for Optical Coherence Tomography Applications

por Lu, Yi-Ting, Widhianto, Benedictus Yohanes Bagus, Hsu, Shih-Hsiang, Chang, Che-Chang
Publicado 2020

Apparent mineralocorticoid excess: comprehensive overview of molecular genetics

por Lu, Yi-ting, Zhang, Di, Zhang, Qiong-yu, Zhou, Ze-ming, Yang, Kun-qi, Zhou, Xian-liang, Peng, Fan
Publicado 2022

Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing NF1 Mutation

por Lu, Yi-Ting, Rejiepu, Buweimairemu, Zhang, Di, Cai, Dong-Cheng, Yang, Kun-Qi, Tian, Tao, Zhou, Xian-Liang, Fan, Peng
Publicado 2023

RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas

por Zhao, Lin, Yang, Kun-Qi, Fan, Peng, Gong, Ding-Xu, Zhang, Lin, Lu, Yi-Ting, Meng, Xu, Zhou, Xian-Liang
Publicado 2022

Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension

por Lu, Yi-Ting, Zhang, Di, Liu, Xin-Chang, Zhang, Qiong-Yu, Dong, Xue-Qi, Fan, Peng, Xiao, Yan, Zhou, Xian-Liang
Publicado 2021

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia

por Lu, Yi-Ting, Fan, Peng, Zhang, Di, Zhang, Ying, Meng, Xu, Zhang, Qiong-Yu, Zhao, Lin, Yang, Kun-Qi, Zhou, Xian-Liang
Publicado 2021

The Effect of Degrees of Inversion on the Electronic Structure of Spinel NiCo(2)O(4): A Density Functional Theory Study

por Chang, Tzu-Chien, Lu, Yi-Ting, Lee, Chih-Heng, Gupta, Jyoti K., Hardwick, Laurence J., Hu, Chi-Chang, Chen, Hsin-Yi Tiffany
Publicado 2021

Percutaneous Transluminal Renal Angioplasty for Fibromuscular Dysplasia and Prognostic Risk Factors: A Retrospective Chinese Cohort Study

por Lu, Yi-Ting, Zhou, Ze-Ming, Zhang, Di, Sun, Lin, Liu, Xin-Chang, Yang, Yan-Kun, Jiang, Xiong-Jing, Zhou, Xian-Liang
Publicado 2022

Prognostic value of plasma big endothelin-1 in left ventricular non-compaction cardiomyopathy

por Fan, Peng, Zhang, Ying, Lu, Yi-Ting, Yang, Kun-Qi, Lu, Pei-Pei, Zhang, Qiong-Yu, Luo, Fang, Lin, Ya-Hui, Zhou, Xian-Liang, Tian, Tao
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

Hsa_Circ_0098181 Suppresses Hepatocellular Carcinoma by Sponging miR-18a-3p and Targeting PPARA

por Luo, Yuan-Yuan, Tao, Ke-Gong, Lu, Yi-Ting, Li, Bin-Bin, Wu, Kai-Ming, Ding, Chen-Hong, Yan, Fang-Zhi, Liu, Yue, Lin, Yong, Zhang, Xin, Zeng, Xin
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

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