• 已选条件：
  • × Wang, Jing
  • × 期刊论文
  • × 2015
 全选  【符合条件的数据共：26条】

1 Self-assembly of size-controlled liposomes on DNA nanotemplates, [期刊论文]

Collaborative Research: Molecular Programming Architectures, Abstractions, Algorithms, and Applications,,A7942015年

Yang, Yang, Wang, Jing, Shigematsu, Hideki, Xu, Weiming, Shih, William M, Rothman, James E, Lin, Chenxiang. 

LicenseType:Others | 英文

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2 Self-assembly of size-controlled liposomes on DNA nanotemplates, [期刊论文]

Collaborative Research: Molecular Programming Architectures, Abstractions, Algorithms, and Applications,,A7892015年

Yang, Yang, Wang, Jing, Shigematsu, Hideki, Xu, Weiming, Shih, William M, Rothman, James E, Lin, Chenxiang. 

LicenseType:Others | 英文

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3 Correlates of self-reported dietary cruciferous vegetable intake and urinary isothiocyanate from two cohorts in China [期刊论文]

PUBLIC HEALTH NUTRITION,,182015年

Vogtmann, Emily, Yang, Gong, Li, Hong-Lan, Wang, Jing, Han, Li-Hua, Wu, Qi-Jun, Xie, Li, Cai, Quiyin, Li, Guo-Liang, Waterbor, John W., Levitan, Emily B., Zhang, Bin, Gao, Yu-Tang, Zheng, Wei, Xiang, Yong-Bing, Shu, Xiao-Ou

英文

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4 Impact of Perceived Barriers to Healthy Eating on Diet and Weight in a 24-Month Behavioral Weight Loss Trial [期刊论文]

JOURNAL OF NUTRITION EDUCATION AND BEHAVIOR,,472015年

Wang, Jing, Ye, Lei, Zheng, Yaguang, Burke, Lora E.

英文

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5 Effect of beta-aminobutyric acid on cell wall modification and senescence in sweet cherry during storage at 20 degrees C [期刊论文]

FOOD CHEMISTRY,,1752015年

Wang, Lei, Jin, Peng, Wang, Jing, Jiang, Lulu, Shan, Timin, Zheng, Yonghua

英文

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6 Association of Alzheimer's disease GWAS loci with MRI markers of brain aging [期刊论文]

NEUROBIOLOGY OF AGING,,362015年

Chauhan, Ganesh, Adams, Hieab H. H., Bis, Joshua C., Weinstein, Galit, Yu, Lei, Toglhofer, Anna Maria, Smith, Albert Vernon, van der Lee, Sven J., Gottesmanm, Rebecca F., Thomson, Russell, Wang, Jing, Yang, Qiong, Niessen, Wiro J., Lopez, Oscar L., Becker, James T., Phan, Thanh G., Beare, Richard J., Arfanakis, Konstantinos, Fleischman, Debra, Vernooij, Meike W., Mazoyer, Bernard, Schmidt, Helena, Srikanth, Velandai, Knopman, David S., Jack, Clifford R., Jr., Amouyel, Philippe, Hofman, Albert, DeCarli, Charles, Tzourio, Christophe, van Duijnc, Cornelia M., Bennett, David A., Schmidt, Reinhold, Longstreth, William T., Jr., Mosley, Thomas H., Fornage, Myriam, Launer, Lenore J., Seshadri, Sudha, Ikramc, M. Arfan, Debette, Stephanie

LicenseType:Free |

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Whether novel risk variants of Alzheimer's disease (AD) identified through genome-wide association studies also influence magnetic resonance imaging-based intermediate phenotypes of AD in the general population is unclear. We studied association of 24 AD risk loci with intracranial volume, total brain volume, hippocampal volume (HV), white matter hyperintensity burden, and brain infarcts in a meta-analysis of genetic association studies from large population-based samples (N = 8175-11,550). In single-SNP based tests, AD risk allele of APOE (rs2075650) was associated with smaller HV (p = 0.0054) and CD33 (rs3865444) with smaller intracranial volume (p = 0.0058). In gene-based tests, there was associations of HLA-DRB1 with total brain volume (p = 0.0006) and BIN1 with HV (p = 0.00089). A weighted AD genetic risk score was associated with smaller HV (beta +/- SE = -0.047 +/- 0.013, p = 0.00041), even after excluding the APOE locus (p = 0.029). However, only association of AD genetic risk score with HV, including APOE, was significant after multiple testing correction (including number of independent phenotypes tested). These results suggest that novel AD genetic risk variants may contribute to structural brain aging in nondemented older community persons. (C) 2015 Elsevier Inc. All rights reserved.