责任编辑:林颖、梁琦

已发表论文
来源: | 作者:梁琦 | 发布时间: 2019-08-26 | 1533 次浏览 | 分享到:

110.Qu XX, Hao P, Song XJ, Jiang SM, Liu YX, Wang PG, Rao X, Song HD, Wang SY, Zuo Y, Zheng AH, Luo M, Wang HL, Deng F, Wang HZ, Hu ZH, Ding MX, Zhao GP, Deng HK. Identification of Two Critical Amino Acid Residues of the Severe Acute Respiratory Syndrome Coronavirus Spike Protein for Its Variation in Zoonotic Tropism Transition via a Double Substitution Strategy. J Biol Chem 2005; 280(33):29588-95.

111.Miao XX, Xu SJ, Li MH, Li MW, Huang JH, Dai FY, Marino SW, Mills DR, Zeng P, Mita K, Jia SH, Zhang Y, Liu WB, Xiang H, Guo QH, Xu AY, Kong XY, Lin HX, Shi YZ, Lu G, Zhang X, Huang W, Yasukochi Y, Sugasaki T, Shimada T, Nagaraju J, Xiang ZH, Wang SY, Goldsmith MR, Lu C, Zhao GP, Huang YP. Simple sequence repeat-based consensus linkage map of Bombyx mori. Proc Natl Acad SCI U S A. 2005; 102(45):16303-8.

112.Z.H. Zhang, Z.M. Niu, W.T. Yuan, J.J. Zhao, F.X. Jiang, J. Zhang, B. Chai, F. Cui, W. Chen, C.H. Lian, L.H. Xiang, S.J. Xu, W.D. Liu, Z.Z. Zheng and W. Huang. A mutation in SART3 gene in a Chinese pedigree with disseminated superficial actinic porokeratosis. British Journal of Dermatology 2005, 152:658663.

113.Jian-Jun Chen, Wei Huang, Jin-Ping Gui, Sen Yang, Fu-Sheng Zhou, Quan-Geng Xiong, Hong-Bo Wu, Yong Cui, Min Gao, Wei Li, Jin-xian Li, Kai-Lin Yan, Wen-Tao Yuan, Shi-Jie Xu, Jian-Jun Liu, and Xue-Jun Zhang. A Novel Linkage to Generalized Vitiligo on 4q13-q21 Identified in a Genomewide Linkage Analysis of Chinese Families. Am. J. Hum. Genet. 2005; 76:1057-1065.

114.Yu Yang, Sun Lingling, Jin Ying, Li Yushu, Shan Zhongyan, Huang Wei and Teng Weiping.  Association study between the IL4, IL13, IRF1 and UGRP1 genes in chromosomal 5q31 region and Chinese Graves' disease. J Hum Genet. 2005, 50(11):574-582

115.Sen YangMin Gao, Yong Cu, Kai-Lin Yan, Yun-Qing Ren, Guo-Long Zhang, Pei-Guang Wang, Feng-Li Xiao, Wen-Hui Du, Yan-Hua Liang, Liang-Dan Sun, Shi-Jie Xu, Wei Huang and Xue-Jun Zhang. Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3. Journal of Investigative Dermatology 2005; 125(4):711-714

116.Zheng-Hua ZhangWei Huang, Zhen-Min Niu, Wei-Da Liu, Lei-Hong Xiang, Wen-Tao Yuan, Jing-Jun Zhao, Chao-Ying Gu, Bao Chai, Fa-Xing Jiang, Jing Zhang, Shi-Jie Xu and Zhi-Zhong Zheng. Two closely linked variations in actin cytoskeleton pathway in a Chinese pedigree with disseminated superficial actinic porokeratosis. Journal of the American Academy of Dermatology 2005; 52(6):972-976.

117.M. Gao, S. Yang, M. Li, K.L. Yan, Y.X. Jiang, Y. Cui, F.L. Xiao, Y.J. Shen, J.J. Chen, J.B. Liu, S.J. Xu, W. Huang and X.J. Zhang. Refined localization of a punctate palmoplantar keratoderma gene to a 5.06-cM region at 15q22.2-15q22.31. British Journal of Dermatology 2005; 152(5):874-878.

118.Yong Cui, Jun Wang, Sen Yang, Min Gao, Jian-Jun Chen, Kai-Lin Yan, Feng-Li Xiao, Wei Huang and Xue-Jun Zhang. Identification of a novel mutation in the DSRAD gene in a Chinese pedigree with dyschromatosis symmetrica hereditaria. Archives of Dermatological Research 2005; 296(11):543-545.

119.Min Gao, Pei-Guang Wang, Sen Yang, Xiao-Li Hu, Kai-Yue Zhang, Ya-Gang Zhu,Yun-Qing Ren, Wen-Hui Du, Guo-Long Zhang, Yong Cui, Jian-Jun Chen, Kai-Lin Yan, Feng-Li Xiao, Shi-Jie Xu, Wei Huang, Xue-Jun Zhang. Two frameshift mutations in the RNA-specific adenosine deaminase gene associated with dyschromatosis symmetrica hereditaria. Arch Dermatol. 2005; 141(2):193-196.

120.Zeng LC, Han ZG, Ma WJ. Elucidation of subfamily segregation and intramolecular coevolution of the olfactomedin-like proteins by comprehensive phylogenetic analysis and gene expression pattern assessment. FEBS Lett. 2005; 579(25):5443-5453.

121.Ma YY, Qi XF, Song SJ, Zhao ZY, Zhu ZD, Qi J, Zhang X, Xiao HS, Teng Y, Han ZG. cDNA microarray reveals signaling pathways involved in hormones expression of human pituitary. Gen Comp Endocrinol. 2005;143(2):184-192.

122.Lin Y, Xie WF, Chen YX, Zhang X, Zeng X, Qiang H, Chen WZ, Yang XJ, Han ZG, Zhang ZB. Treatment of experimental hepatic fibrosis by combinational delivery of urokinase-type plasminogen activator and hepatocyte growth factor genes. Liver Int. 2005; 25(4):796-807.

123.Zhang X, Wang KS, Wang ZQ, Xu LS, Wang QW, Chen F, Wei DZ, Han ZG. Nuclear localization signal of ING4 plays a key role in its binding to p53. Biochem Biophys Res Commun. 2005; 331(4): 1032-1038.

124.Yi-xuan ZHANG, Yan GENG, Bo BI, Jian-yong HE, Chun-fu WU, Xiao-kui GUO, Guo-ping ZHAO.Identification and classification of all potential hemolysin encoding genes and their products from Leptospira interrogans serogroup Icterohaemorrhagiae serovar Lai. Acta Pharmacologica Sinica 2005 Apr; 26 (4): 453461

125.项佑贵,陆顺元,顾鸣敏,王升跃,任双喜,傅刚,王铸钢。小鼠Nucleophosmin基因的克隆及基因组结构分析. 《遗传学报》. 2005; 32(6):641-9

126.孙玲玲,王艺,黄薇。UGRP1基因及其与疾病相关性的研究。《医学分子生物学杂志》,200523: 185-189

127.张奎星,刘同宝,徐秋霞,朱鼎良,黄薇。血管紧张素Ⅱ 1型受体基因单核苷酸多态性与原发性高血压和冠心病的相关研究。《中华心血管病杂志》,2005; 33(8):720-3

128.宋传贵,黄昌明,刘星,卢辉山,张祥福,黄 薇。CDH1基因-160(CA) 多态与福建地区中国人群胃癌遗传易感性的关联研究。《中华医学遗传学杂志》 2005; 22(5):557-559

129.刘同宝,商惠萍,张奎星,陈良华,朱兴雷,张怡,朱鼎良,黄 薇。血管紧张素转换酶2基因多态性与原发性高血压的关系。《中华医学遗传学杂志》 2005; 22(5):569-571

130.张怡,张奎星,何鑫,袁文涛,王谷亮,茅守玉,高平进,黄薇,朱鼎良。高血压定位区域犬尿氨酸酶基因多态性与高血压病相关。《中华心血管病杂志》2005; 33(7):588-91.

131.张正华,牛振民,袁文涛,赵敬军,蒋法兴,张静,柴宝,熊晓燕,项蕾红,王艺,徐世杰,刘维达,郑志忠,黄薇。播散性浅表性光线性汗孔角化症DSAP1位点的精细定位和候选基因的突变检测, 《遗传学报》 2005; 32(7):667-74.

132.马会利,葛均波,王颖,黄薇,孙爱军,牛玉宏,方业明,马永莉,冯军,赵洁,王克强。纤维蛋白原及其相关基因[3148[3854多态性与冠心病发病的相关性。《中国动脉硬化杂志》2005l33):351-354

133.梁燕华,何平平,杨森,王红艳,陈建军,刘宏胜,徐世杰,崔勇,黄薇,张学军。多发性家族性毛发上皮瘤基因的确定。《中华皮肤科杂志》2005382):71-73

134.金丽威,牛振民,袁文涛,张静,鲁智勇,郑捷。SPRR2E基因编码区单核苷酸多态性与银屑病。《中华皮肤科杂志》2005383):143-145

135.朱弘,周宇波,曾令春,杨鸿蒙,韩泽广。一个富含谷氨酸的人类分泌蛋白基因hMGRAP的克隆与表达分析, 《遗传》2005; 27(1): 7-13

136.潘勤, 谢渭芬, 张忠兵, 张新, 韩泽广。细胞外信号调节激酶对肝纤维化逆转的影响及其机制. 《第二军医大学学报 》2005;26(9)

137.彭永德,曲建,张新,韩泽广,陈家伦。hTRIP 15对甲状腺激素受体功能的影响. 《上海第二医科大学学报》 2005;25(4)

138.彭永德,宋怀东, 曲建,张新, 韩泽广, 陈家伦。酵母双杂交文库筛选及hTRIP15Y盒结合蛋白-1相互作用的探讨.《生命科学研究》 2005;9(1)

139.杨妙芳, 张新, 强晖, 孙田美, 谢渭芬。核糖体S6激酶与大鼠肝纤维化相关性研究 《中华消化杂志》 2005;25(2)

140.沈坤堂,秦新裕,宋陆军,张新,韩泽广。人胰岛素基因在大鼠肝细胞中的可调节性表达 《中华实验外科杂志》2005;22(1)

141.张敏, 张新,韩泽广。DLK1研究进展. 《医学分子生物学杂志》2005;2(5): 243-246.

142.方彩云,翟建军,刘锋,杨芃原。基质中加入少量盐类可改善MALDI-TOF MS的谱图信噪比 《高等学校化学学报》 2005;26(4):660662

143.潘勤, 谢渭芬, 张忠兵, 张新, 韩泽广。大鼠CCI4所致肝纤维化自发逆转的基因表达谱研究 《世界华人消化杂志》2005;13(13):1544-1549

144.卜云萍、王光凤、陈竺。转基因高-亚麻酸大豆抗肿瘤作用的研究。《中国生物工程杂志》2005257):92-97

145.Chen S, Zhou Y, et al. Genetic and structural analyses suggest that a novel SPG3A mutation causes severe phenotypes of hereditary spastic paraplegia. Chinese Science Bullitin English version. 2006, 51(16): 2038-40.

146.Huang Weijun ,Li Caixia ,Labu ,Zhou Yan ,Li Peixing,Hu Bin,Pubuzhuoma,Gesangzhuogab, Fang Jiqian and Wang Yiming. High resolution linkage disequilibrium and haplotype maps for the genes in the centromeric region of chromosome 15 in Tibetans and comparisons with Han population. Chinese Science Bullitin English version. 2006;51(5):542-551

147.Qin XY, Shen KT, Song LJ, Zhang X, Han ZG. Regulated production of mature insulin in rat hepatoma cells: insulin production is up-regulated by dexamethasone and down-regulated by insulin. Acta Biochim Biophys Sin (Shanghai). 2006 ; 38(2):89-94.

148.Wang XR, Zhou YB, Liu F, Wang KS, Shen Y, Liu JH, Han ZG. A novel recently evolved gene C19orf24 encodes a non-classical secreted protein. Cell Mol Biol Lett. 2006;11(2):161-70. 

149.Wang PG, Gao M, Lin GS, Yang S, Lin D, Liang YH, Zhang GL, Zhu YG, Cui Y, Zhang KY, Huang W, and Zhang XJ.  Genetic heterogeneity in acrokeratosis verruciformis of Hopf. Clinical and Experimental Dermatology 2006 Jun;31(4):558-63

150.Sen Yang, Kai-Lin Yan, Xue-Jun Zhang, Feng-Li Xiao, Xing Fan, Min Gao, Yong Cui, Peng-Guang Wang, Guo-Long Zhang, Liang-Dan Sun, Zhi-Min Wang, Da-Zhi Wang, Kai-Yue Zhang, Wei Huang, Jian-Jun Liu.  Systematic evaluation of association between the microsomal glutathione S-transferase 2 common variation and psoriasis vulgaris in Chinese population. Arch Dermatol Res 2006, 298:107112

151.Qi J, Zhang X, Zhang HK, Yang HM, Zhou YB, Han ZG. ZBTB34, a novel human BTB/POZ zinc finger protein, is a potential transcriptional repressor. Mol Cell Biochem. 2006;290:159-167