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There are 12493 results for: content related to: Functional polymorphisms of circadian positive feedback regulation genes and clinical outcome of Chinese patients with resected colorectal cancer

  1. Variant of the clock circadian regulator (CLOCK) gene and related haplotypes are associated with the prevalence of type 2 diabetes in the Japanese population

    Journal of Diabetes

    Volume 8, Issue 5, September 2016, Pages: 667–676, Hirokazu Uemura, Sakurako Katsuura-Kamano, Miwa Yamaguchi, Kokichi Arisawa, Nobuyuki Hamajima, Asahi Hishida, Sayo Kawai, Isao Oze, Koichi Shinchi, Naoyuki Takashima, Sadao Suzuki, Noriko Nakahata, Haruo Mikami, Keizo Ohnaka, Nagato Kuriyama, Michiaki Kubo, Hideo Tanaka and for the Japan Multi-Institutional Collaborative Cohort (J-MICC) Study Group

    Version of Record online : 1 DEC 2015, DOI: 10.1111/1753-0407.12344

  2. Association of IRS1, CAPN10, and PPARG gene polymorphisms with type 2 diabetes mellitus in the high-risk population of Hyderabad, India 在印度海得拉巴高风险人群中IRS1CAPN10以及PPARG基因多态性与2型糖尿病的关系

    Journal of Diabetes

    Volume 6, Issue 6, November 2014, Pages: 564–573, Uma Jyothi Kommoju, Jayaraj Maruda, Subburaj Kadarkarai Samy, Kumuda Irgam, Jaya Prasad Kotla and Battini Mohan Reddy

    Version of Record online : 3 APR 2014, DOI: 10.1111/1753-0407.12142

  3. Interactions of several genetic polymorphisms and alcohol consumption on blood pressure levels

    BioFactors

    Volume 41, Issue 5, September/October 2015, Pages: 339–351, Rui-Xing Yin, Lynn Htet Htet Aung, Xing-Jiang Long, Ting-Ting Yan, Xiao-Li Cao, Feng Huang, Jin-Zhen Wu, De-Zhai Yang, Wei-Xiong Lin and Shang-Ling Pan

    Version of Record online : 10 SEP 2015, DOI: 10.1002/biof.1234

  4. Differential modification of genetic susceptibility to childhood eczema by two probiotics

    Clinical & Experimental Allergy

    Volume 44, Issue 10, October 2014, Pages: 1255–1265, A. R. Morgan, D. Y. Han, K. Wickens, C. Barthow, E. A. Mitchell, T. V. Stanley, J. Dekker, J. Crane and L. R. Ferguson

    Version of Record online : 22 SEP 2014, DOI: 10.1111/cea.12394

  5. You have full text access to this Open Access content
    Intron-1 rs3761548 is related to the defective transcription of Foxp3 in psoriasis through abrogating E47/c-Myb binding

    Journal of Cellular and Molecular Medicine

    Volume 14, Issue 1-2, January-February 2010, Pages: 226–241, Z. Shen, L. Chen, F. Hao, G. Wang, P. Fan and Y. Liu

    Version of Record online : 24 MAY 2008, DOI: 10.1111/j.1582-4934.2008.00370.x

  6. Interactions of several single nucleotide polymorphisms and high body mass index on serum lipid traits

    BioFactors

    Volume 39, Issue 3, May/June 2013, Pages: 315–325, Rui-Xing Yin, Dong-Feng Wu, Lin Miao, Lynn Htet Htet Aung, Xiao-Li Cao, Ting-Ting Yan, Xing-Jiang Long, Wan-Ying Liu, Lin Zhang and Meng Li

    Version of Record online : 28 JAN 2013, DOI: 10.1002/biof.1073

  7. PER2 variantion is associated with depression vulnerability

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 2, March 2010, Pages: 570–581, Catharina Lavebratt, Louise K. Sjöholm, Timo Partonen, Martin Schalling and Yvonne Forsell

    Version of Record online : 19 AUG 2009, DOI: 10.1002/ajmg.b.31021

  8. Genetic association of FOXP3 gene polymorphisms with allograft rejection in renal transplant patients

    Nephrology

    Volume 17, Issue 4, May 2012, Pages: 423–430, XIAO-YAN QIU, ZHENG JIAO, MING ZHANG, JIAN-PING CHEN, XIAO-JIN SHI and MING-KANG ZHONG

    Version of Record online : 17 APR 2012, DOI: 10.1111/j.1440-1797.2012.01561.x

  9. The possible involvement of genetic variants of NET1 in the etiology of attention-deficit/hyperactivity disorder comorbid with oppositional defiant disorder

    Journal of Child Psychology and Psychiatry

    Volume 56, Issue 1, January 2015, Pages: 58–66, Lu Liu, Jia Cheng, Haimei Li, Li Yang, Qiujin Qian and Yufeng Wang

    Version of Record online : 19 JUN 2014, DOI: 10.1111/jcpp.12278

  10. You have free access to this content
    Genetic susceptibility to heroin addiction: a candidate gene association study

    Genes, Brain and Behavior

    Volume 7, Issue 7, October 2008, Pages: 720–729, O. Levran, , D. Londono, K. O’Hara, D. A. Nielsen, E. Peles, J. Rotrosen, P. Casadonte, S. Linzy, M. Randesi, J. Ott, , M. Adelson and ,, M. J. Kreek

    Version of Record online : 2 JUN 2008, DOI: 10.1111/j.1601-183X.2008.00410.x

  11. You have full text access to this OnlineOpen article
    Significant association between FOXP3 gene polymorphism and steroid-resistant acute rejection in living donor liver transplantation

    Hepatology Communications

    Volume 1, Issue 5, July 2017, Pages: 406–420, Sapana Verma, Yuka Tanaka, Seiichi Shimizu, Naoki Tanimine and Hideki Ohdan

    Version of Record online : 8 JUN 2017, DOI: 10.1002/hep4.1052

  12. Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 3, 5 April 2006, Pages: 234–241, Caroline M. Nievergelt, Daniel F. Kripke, Thomas B. Barrett, Elyssa Burg, Ronald A. Remick, A. Dessa Sadovnick, Susan L. McElroy, Paul E. Keck Jr, Nicholas J. Schork and John R. Kelsoe

    Version of Record online : 9 MAR 2006, DOI: 10.1002/ajmg.b.30252

  13. You have free access to this content
    Replication and Extension of Association Between Common Genetic Variants in SIM1 and Human Adiposity

    Obesity

    Volume 19, Issue 12, December 2011, Pages: 2394–2403, Michael M. Swarbrick, Daniel S. Evans, Maria. I. Valle, Hélène Favre, Shi-Hsuan Wu, Omer T. Njajou, Rongling Li, Joseph M. Zmuda, Iva Miljkovic, Tamara B. Harris, Pui-Yan Kwok, Christian Vaisse and Wen-Chi Hsueh

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2011.79

  14. Association of tryptophan 2,3 dioxygenase gene polymorphism with autism

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 125B, Issue 1, 15 February 2004, Pages: 63–68, Rafiqun Nabi, Fatema J. Serajee, Diane C. Chugani, Hailang Zhong and A.H.M. Mahbubul Huq

    Version of Record online : 24 SEP 2003, DOI: 10.1002/ajmg.b.20147

  15. Chronic consumption of a low-fat diet improves cardiometabolic risk factors according to the CLOCK gene in patients with coronary heart disease

    Molecular Nutrition & Food Research

    Volume 59, Issue 12, December 2015, Pages: 2556–2564, Francisco Gomez-Delgado, Antonio Garcia-Rios, Juan Francisco Alcala-Diaz, Oriol Rangel-Zuñiga, Javier Delgado-Lista, Elena M. Yubero-Serrano, Javier Lopez-Moreno, Francisco Jose Tinahones, Jose M. Ordovas, Marta Garaulet, Jose Lopez-Miranda and Pablo Perez-Martinez

    Version of Record online : 8 OCT 2015, DOI: 10.1002/mnfr.201500375

  16. Association between angiotensin II type 1 receptor polymorphisms and the occurrence of nonalcoholic fatty liver disease

    Liver International

    Volume 29, Issue 7, August 2009, Pages: 1078–1085, Masato Yoneda, Kikuko Hotta, Yuichi Nozaki, Hiroki Endo, Takashi Uchiyama, Hironori Mawatari, Hiroshi Iida, Shingo Kato, Koji Fujita, Hirokazu Takahashi, Hiroyuki Kirikoshi, Noritoshi Kobayashi, Masahiko Inamori, Yasunobu Abe, Kensuke Kubota, Satoru Saito, Shiro Maeyama, Koichiro Wada and Atsushi Nakajima

    Version of Record online : 3 MAR 2009, DOI: 10.1111/j.1478-3231.2009.01988.x

  17. You have free access to this content
    Identification of IDUA and WNT16 Phosphorylation-Related Non-Synonymous Polymorphisms for Bone Mineral Density in Meta-Analyses of Genome-Wide Association Studies

    Journal of Bone and Mineral Research

    Volume 31, Issue 2, February 2016, Pages: 358–368, Tianhua Niu, Ning Liu, Xun Yu, Ming Zhao, Hyung Jin Choi, Paul J Leo, Matthew A Brown, Lei Zhang, Yu-Fang Pei, Hui Shen, Hao He, Xiaoying Fu, Shan Lu, Xiang-Ding Chen, Li-Jun Tan, Tie-Lin Yang, Yan Guo, Nam H Cho, Jie Shen, Yan-Fang Guo, Geoffrey C Nicholson, Richard L Prince, John A Eisman, Graeme Jones, Philip N Sambrook, Qing Tian, Xue-Zhen Zhu, Christopher J Papasian, Emma L Duncan, André G Uitterlinden, Chan Soo Shin, Shuanglin Xiang and Hong-Wen Deng

    Version of Record online : 11 SEP 2015, DOI: 10.1002/jbmr.2687

  18. Common quantitative trait locus downstream of RETN gene identified by genome-wide association study is associated with risk of type 2 diabetes mellitus in Han Chinese: a Mendelian randomization effect

    Diabetes/Metabolism Research and Reviews

    Volume 30, Issue 3, March 2014, Pages: 232–240, Chia-Min Chung, Tsung-Hsien Lin, Jaw-Wen Chen, Hsin-Bang Leu, Wei-Hsian Yin, Hung-Yun Ho, Sheng-Hsiung Sheu, Wei-Chuan Tsai, Jyh-Hong Chen, Shing-Jong Lin and Wen-Harn Pan

    Version of Record online : 3 MAR 2014, DOI: 10.1002/dmrr.2481

  19. Common single nucleotide variants underlying drug addiction: more than a decade of research

    Addiction Biology

    Volume 20, Issue 5, September 2015, Pages: 845–871, Kora-Mareen Bühler, Elena Giné, Victor Echeverry-Alzate, Javier Calleja-Conde, Fernando Rodriguez de Fonseca and Jose Antonio López-Moreno

    Version of Record online : 21 JAN 2015, DOI: 10.1111/adb.12204

  20. A toll-like receptor 3 single nucleotide polymorphism in Japanese patients with sarcoidosis

    Tissue Antigens

    Volume 85, Issue 3, March 2015, Pages: 204–208, K. Ikezoe, T. Handa, K. Tanizawa, T. Kubo, I. Ito, A. Sokai, Y. Nakatsuka, S. Nagai, T. Izumi and M. Mishima

    Version of Record online : 26 FEB 2015, DOI: 10.1111/tan.12535