Publications by authors named "Kai-Xiang Liu"
[Investigation on the Influencing Factors of Adult Dyslipidemia in Shunqing District of Nanchong City].
Sichuan Da Xue Xue Bao Yi Xue Ban
January 2020
Article Synopsis
- - The study aimed to identify the risk factors contributing to dyslipidemia among adult residents in the Shunqing District of Nanchong City using a comprehensive sampling and analysis method from 2013 to 2018.
- - The findings revealed a 34.2% prevalence rate of dyslipidemia, with higher rates in males (38.11%) compared to females (31.91%), and linked dyslipidemia to conditions like hypertension, diabetes, and coronary heart disease.
- - Key risk factors identified include gender, body mass index, education level, smoking history, and existing health conditions, indicating that targeting these factors could help address dyslipidemia in this urban population.
Evidence of the pressure-induced conductivity switching of yttrium-doped SrTiO3.
J Phys Condens Matter
November 2016
The electrical transport properties of undoped and yttrium-doped strontium titanate (Sr(Ti1 - x Y x )O3 - δ , x = 0, 0.02) under high pressure were investigated with in situ impedance spectroscopy measurements. A pressure-induced conductivity switching for undoped and 2 mole% Y-doped strontium titanate is observed at around ~10.
View Article and Find Full Text PDF[A new mutation in the GJB1 gene of a Chinese family with Charcot-Marie-Tooth disease associated with vocal cord paresis].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
October 2010
Objective: To report an X-linked dominant Charcot-Marie-Tooth disease (CMTX) Chinese family with vocal cord paresis and to identify the mutation of gap junction protein beta 1 gene (GJB1).
Methods: Part of the family members with dysphagia, dysphonia and lethal respiratory failure were studied through flexible laryngoscope, clinical, brain MRI and electrophysiological examinations. After excluding large fragment tandem duplication containing peripheral myelin protein 22 gene (PMP22), direct sequencing was performed to analyze the mutation of the GJB1 gene in 5 patients including the proband, 5 unaffected family members and 50 unrelated healthy individuals.