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Associations of MTHFR C677T and MTRR A66G gene polymorphisms with metabolic syndrome: a case-control study in Northern China.
Yang, Boyi; Fan, Shujun; Zhi, Xueyuan; Wang, Da; Li, Yongfang; Wang, Yinuo; Wang, Yanxun; Wei, Jian; Zheng, Quanmei; Sun, Guifan.
Afiliación
  • Yang B; Environment and Non-Communicable Disease Research Center, School of Public Health, China Medical University, Shenyang 110013, China. boyiyangcmu@163.com.
  • Fan S; Environment and Non-Communicable Disease Research Center, School of Public Health, China Medical University, Shenyang 110013, China. fanfan0721ykl@163.com.
  • Zhi X; Environment and Non-Communicable Disease Research Center, School of Public Health, China Medical University, Shenyang 110013, China. zhixy90smile@126.com.
  • Wang D; Environment and Non-Communicable Disease Research Center, School of Public Health, China Medical University, Shenyang 110013, China. 472594283@163.com.
  • Li Y; Environment and Non-Communicable Disease Research Center, School of Public Health, China Medical University, Shenyang 110013, China. liyongfang17@163.com.
  • Wang Y; Division of Molecular Preventive Medicine, Shanghai Institute of Targeted Therapy and Molecular Medicine, Shanghai 200433, China. 13817895706@163.com.
  • Wang Y; Division of Molecular Preventive Medicine, Shanghai Institute of Targeted Therapy and Molecular Medicine, Shanghai 200433, China. 13817895706@163.com.
  • Wei J; Brain Disease Center, Tianjin Dagang Oil Field General Hospital, Tianjin 300280, China. weijiantianjin@163.com.
  • Zheng Q; Environment and Non-Communicable Disease Research Center, School of Public Health, China Medical University, Shenyang 110013, China. qmzheng@mail.cmu.edu.cn.
  • Sun G; Environment and Non-Communicable Disease Research Center, School of Public Health, China Medical University, Shenyang 110013, China. sungf@mail.cmu.edu.cn.
Int J Mol Sci ; 15(12): 21687-702, 2014 Nov 25.
Article en En | MEDLINE | ID: mdl-25429430
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Síndrome Metabólico / Metilenotetrahidrofolato Reductasa (NADPH2) / Estudios de Asociación Genética / Ferredoxina-NADP Reductasa Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Int J Mol Sci Año: 2014 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Síndrome Metabólico / Metilenotetrahidrofolato Reductasa (NADPH2) / Estudios de Asociación Genética / Ferredoxina-NADP Reductasa Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Int J Mol Sci Año: 2014 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza