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浏览/检索结果: 共24条，第1-10条 帮助 限定条件 发表日期：2016    专题：山东大学    第一署名单位    第一作者单位    通讯作者单位     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Dietary Fiber Intake Regulates Intestinal Microflora and Inhibits Ovalbumin-Induced Allergic Airway Inflammation in a Mouse Model 期刊论文 PLOS ONE, 2016, 卷号: 11, 期号: 2 作者:  Zhang, Zhiyu;  Shi, Lei;  Pang, Wenhui;  Liu, Wenwen;  Li, Jianfeng 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/16 Preventive Effect of Dihydromyricetin against Cisplatin-Induced Nephrotoxicity In Vitro and In Vivo 期刊论文 EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2016 作者:  Wu, Fei;  Li, Yi;  Song, Haibo;  Zhang, Yuan;  Zhang, Yuzhu 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/16 Effect of lattice misfit on the evolution of the dislocation structure in Ni-based single crystal superalloys during thermal exposure 期刊论文 ACTA MATERIALIA, 2016, 卷号: 120, 页码: 95-107 作者:  Long, Haibo;  Wei, Hua;  Liu, Yinong;  Mao, Shengcheng;  Zhang, Jianxin 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/16 Ni-based superalloys  Dislocations  Aging  Lattice mismatch  Transmission electron microscopy   Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay 期刊论文 BIOMED RESEARCH INTERNATIONAL, 2016 作者:  Zhang, Fengguo;  Xiao, Yun;  Xu, Lei;  Zhang, Xue;  Zhang, Guodong 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/16 Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family 期刊论文 INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 83, 期号: 4, 页码: 179-185 作者:  Ma, Yalin;  Xiao, Yun;  Zhang, Fengguo;  Han, Yuechen;  Li, Jianfeng 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/16 Deafness  Autosomal recessive inheritance  MYO7A gene  Mutation   Selective evolution of secondary gamma' precipitation in a Ni-based single crystal superalloy both in the gamma matrix and at the dislocation nodes 期刊论文 ACTA MATERIALIA, 2016, 卷号: 116, 页码: 343-353 作者:  Xiang, Sisi;  Mao, Shengcheng;  Wei, Hua;  Liu, Yinong;  Zhang, Jianxin 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/16 Ni-based superalloys  Creep  Precipitates  Dislocation node  Order-disorder transition   Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome 期刊论文 INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 85, 页码: 75-79 作者:  Zhang, Fengguo;  Bai, Xiaohui;  Xiao, Yun;  Zhang, Xue;  Zhang, Guodong 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/16 Novel mutation  SLC26A4 gene  EVAS  Nonsense  Chinese family  Pathogenicity   A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss 期刊论文 NEURAL PLASTICITY, 2016 作者:  Zhang, Chi;  Wang, Mingming;  Xiao, Yun 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/16 Protective Effect of Edaravone on Glutamate-Induced Neurotoxicity in Spiral Ganglion Neurons 期刊论文 NEURAL PLASTICITY, 2016 作者:  Bai, Xiaohui;  Zhang, Chi;  Chen, Aiping;  Liu, Wenwen;  Li, Jianfeng 收藏  |  浏览/下载：1/0  |  提交时间：2019/12/16 Irisin reverses platelet derived growth factor-BB-induced vascular smooth muscle cells phenotype modulation through STAT3 signaling pathway 期刊论文 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2016, 卷号: 479, 期号: 2, 页码: 139-145 作者:  Song, Haibo;  Xu, Jia;  Lv, Nan;  Zhang, Yuzhu;  Wu, Fei 收藏  |  浏览/下载：1/0  |  提交时间：2019/12/16 Vascular smooth muscle cells  Phenotype modulation  Irisin  STAT3