Journal Publications

• [21]Zhao S P, Xia K, Chen Y Q, Liu Y X, Jin J Y, Shi X Y, Li J J, Lin M J, Fan L L, Xiang R.The genetic spectrum of familial hypercholesterolemia in the central south region of China[J].Atherosclerosis, 2017, 258: 84-88.
• [22]Xiang R, Li J J, Fan L L, Liu J S.Whole-Exome Sequencing Identifies a Novel Mutation of Desmocollin 2 in a Chinese Family With Arrhythmogenic Right Ventricular Cardiomyopathy[J].Am J Cardiol, 2017, 119 (9) : 1485-1489.
• [23]Xiang R, Xia K, Tao L J, Huang H, Liu X, Zhang H, Fan L L, Liu J S.Whole-Exome Sequencing Identifies Two Novel TTN Mutations in Chinese Families with Dilated Cardiomyopathy[J].Cardiology, 2017, 136 (1) : 10-14.
• [24]Xiang R, Tang J Y, Xia K, Huang H, Jin M, Fan L L, He J Q, Li J J, Jin J Y, Wu P F.A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome[J].Mol Med Rep, 2017, 15 (6) : 3735-3738.
• [25]Chen Y Q, Zhao S P, Huang H, Fan L L, Xiang R.Whole-exome sequencing identifies a novel mutation of DSG2 (Y198C) in a Chinese arrhythmogenic right ventricular cardiomyopathy patient[J].Int J Cardiol, 2016, 214: 1-3.
• [26]Xiang R, Tang J Y, Jin J Y, Fan L L, Fan X F, Guo S, Wu P F.A Novel ZRS Mutation in a Chinese Patient with Preaxial Polydactyly and Triphalangeal Thumb[J].Cytogenet Genome Res, 2016, 149 (3) : 171-175.
• [27]Xiang R, Xia K, Li X P, Fan L L, Huang H, Du RF.A Novel Mutation of FOXC1 (R127L) in an Axenfeld-Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases[J].Ophthalmic Genet, 2016, 37 (1) : 111-115.
• [28]Xiang R, Zhao S P, Xia K, Li J J, Chen Y Q, Huang H, He Z J, Lin M J, Fan L L, Du R.Mutation detection in Chinese patients with familial hypercholesterolemia[J].Springerplus, 2016, 5 (1) : 2095.
• [29]Xiang R, Zhao S P, Xia K, Peng D Q, Huang H, Chen Y Q, Lin M J, Fan L L.Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia[J].Appl Biochem Biotechnol, 2015, 176 (1) : 101-109.
• [30]Xia K, Peng D Q, Li X P, Cao B B, Huang H, Fan L L, Xiang R.A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis[J].Gene, 2014, 534 (2) : 320-323.
• [31]Xiang R, Zhao S, Wu Z, Chen Y.Chemical chaperones reduce ER stress and adipose tissue inflammation in high fat diet-induced mouse model of obesity[J].Sci Rep, 2016, 6: 27486.
• [32]Peng D Q, Hu D, Xiang R, Yu B L.A novel MYH7 mutation in a family with cardiomyopathy presenting with restrictive physiology and varying degrees of left ventricle hypertrophy[J].Eur Heart J, 2015, 36 (3) : 178.
• [33]Yan R, Hu X, Zhang Z, Xiang R, He W, Sharoar M G, Ge Y, Shi Q.Impact of RTN3 deficiency on expression of BACE1 and amyloid deposition[J].J Neurosci, 2014, 34 (42) : 13954-13962.
• [34]项荣, 丁栋博, 范亮亮, 梁龙, 黄皓, 曹贝贝, 蒋昶宇, 黄小忠, 夏昆.稀土氧化锌晶须抗菌效能及安全性研究[J].功能材料, 2013 (S2) : 186-191+197.
• [35]项荣, 黄皓, 范亮亮, 杜然.原发性厚皮性骨膜病的遗传学研究进展[J]. 中国.中华医学遗传学杂志, 2016, 33 (1) : 105-107.
• [36]项荣, 黄威, 高立冬, 张红, 蔡亮, 张帆, 孙倩莱, 周帅锋, 陈雨.2012-2014年湖南省感染性腹泻哨点医院儿童诺如病毒感染及基因型别分析[J].实用预防医学, 2016 (07) : 773-776.
• [37]项荣, 彭元亮, 马立宁, 范亮亮.PI3K/AKT信号通路与心力衰竭[J].生命科学研究, 2015 (1) : 85-90.
• [38]项荣, 范亮亮, 黄皓.HIV-1辅助蛋白负性调节因子下调细胞膜表面分子的研究进展[J].细胞与分子免疫学杂志, 2015 (06) : 848-852.
• [39]夏昆, 黄小忠, 范亮亮, 丁栋博, 项荣.氧化锌的抗菌机制及其安全性研究进展[J].中国组织工程研究, 2014 (03) : 470-475.
• [40]夏昆, 黄皓, 范亮亮, 严经纬, 项荣.动脉粥样硬化中炎性反应与内质网应激的相互作用[J].基础医学与临床, 2014 (02) : 253-256.