教師簡介

  • 專任副教授、榮總兼任副研究員
  • 鍾明怡
  • Ming-Yi Chung
  • 02-2871-2121 ext.3265
  • 榮總致德樓8樓R842
  • 專業領域
  • 分子遺傳
  • 研究興趣
  • 利用分子遺傳學方法找尋並了解基因在致病機轉中所扮演的角色。
  • 研究方向
  • 1-1 家族性滲漏性玻璃體視網膜病變之新基因找尋。

    1-2 家族性滲漏性玻璃體視網膜病變基因在NDP/wnt/β-catenin singaling pathway與 angiogenesis中的角色。

    2. 10q26基因多型性在老年性黃斑部病變的角色。

    3. 偏頭痛與相關表現型之全基因體相關性研究。

    4. 噵致洗腎患者動靜脈廔管阻塞之候選基因因子分析。

  • 執行計畫
  • 科技部 < MOST105-2320-B-010-029 >
    家族性滲漏性玻璃體視網膜病變之分子遺傳學研究 2(2016/08/01-2017/07/31

    科技部 < MOST104-2314-B-010-049 >
    家族性滲漏性玻璃體視網膜病變之分子遺傳學研究(20150801-20160731)

    科技部 < MOST103-2314-B-010-042 >
    血管新生型老年性黃斑部病變之分子遺傳學研究(20140801-20150731)

  • 教授科目
  • 遺傳學概論
    基因體學
    分子遺傳特論
  • 獲獎
  • 1993
    Bacaner Research Award in Basic Medical Science, Minnesota Medical Foundation
  • 經歷
  • Nov, 2013-present
    臺北榮民總醫院醫學研究部
    兼任副研究員
  • Aug, 2006-present
    國立陽明大學
    生命科學系暨基因體科學研究所
    副教授
  • Aug, 2005-Oct, 2013
    臺北榮民總醫院教學研究部
    兼任副研究員
  • Aug, 2005-Jul, 2006
    國立陽明大學遺傳學研究所
    副教授
  • Aug, 2002-Jul, 2005
    國立陽明大學遺傳學研究所
    兼任副教授
  • May, 1997-Aug, 2005
    臺北榮民總醫院教學研究部
    副研究員
  • Oct, 1994-May, 1997
    臺北榮民總醫院
    病理檢驗部臨床細胞遺傳實驗室
    約聘技術師
  • 1994
    美國明尼蘇達大學
    分子遺傳臨床細胞遺傳
    博士後研究
  • 學歷
  • 1993
    美國明尼蘇達大學
    病理生物 博士
  • 1990
    美國明尼蘇達大學
    臨床實驗科學 碩士
  • 1987
    國立臺灣大學
    醫事技術學系 學士

代表著作

  • Wu, J.H., Liu, J.H., Ko, Y.C., Wang, C.T., Chung, Y.C., Chu, K.C., Liu, T.T., Chao, H.M., Jiang, Y.J., Chen, S.J. and Chung, M.Y. (2016) Haploinsufficiency of RCBTB1 is Associated with Coats Disease and Familial Exudative Vitreoretinopathy. Hum Mol Genet, in press.
  • Yu, C.J., Du, J.C., Chiou, H.C., Yang, S.H., Liao, K.W., Yang, W., Chung, M.Y., Chien, L.C., Hwang, B. and Chen, M.L. (2016) Attention Deficit/Hyperactivity Disorder and Urinary Nonylphenol Levels: A Case-Control Study in Taiwanese Children. PLoS One, 11, e0149558.
  • Lee, K.H., Tsai, W.J., Chen, Y.W., Yang, W.C., Lee, C.Y., Ou, S.M., Chen, Y.T., Chien, C.C., Lee, P.C., Chung, M.Y. et al. (2016) Genotype polymorphisms of genes regulating nitric oxide synthesis determine long-term arteriovenous fistula patency in male hemodialysis patients. Ren Fail, 38, 228-237.
  • Fuh, J.L., Chung, M.Y., Yao, S.C., Chen, P.K., Liao, Y.C., Hsu, C.L., Wang, P.J., Wang, Y.F., Chen, S.P., Fann, C.S. et al. (2015) Susceptible genes of restless legs syndrome in migraine. Cephalalgia, in press.
  • Tseng, S.H., Cheng, C.Y., Huang, M.Z., Chung, M.Y. and Su, T.S. (2013) Modulation of formation of the 3'-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism. Int J Biochem Mol Biol, 4, 179-190.
  • Lin, C.C., Chung, M.Y., Yang, W.C., Lin, S.J. and Lee, P.C. (2013) Length polymorphisms of heme oxygenase-1 determine the effect of far-infrared therapy on the function of arteriovenous fistula in hemodialysis patients: a novel physicogenomic study. Nephrol Dial Transplant, 28, 1284-1293.
  • Chang, C.F., Lu, T.M., Yang, W.C., Lin, S.J., Lin, C.C. and Chung, M.Y. (2013) Gene polymorphisms of interleukin-10 and tumor necrosis factor-alpha are associated with contrast-induced nephropathy. Am J Nephrol, 37, 110-117.
  • Lin, C.S., Wang, L.S., Chang, S.C., Chou, T.Y., Hsu, W.H., Liu, C.S., Lee, M.H., Chung, M.Y. and Wei, Y.H. (2012) Associated microsatellite alterations in mitochondrial DNA and in TP53 in thoracic esophageal squamous cell carcinoma. Oncol Rep, 28, 69-76.
  • Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung MY, Mundwiller E, Shakkottai V, Liu TT, Tesson C, Lu YC, Brice A, Tsuji S, Burmeister M, Stevanin G, Soong BW. (2012) Mutations in KCND3 cause spinocerebellar ataxia type 22. Annals of Neurology, 72, 859-869.
  • Hsu, C.P., Lin, S.J., Chung, M.Y. and Lu, T.M. (2012) Asymmetric dimethylarginine predicts clinical outcomes in ischemic chronic heart failure. Atherosclerosis, 225, 504-510.
  • Chiang, C.H., Lin, M.W., Chung, M.Y. and Yang, U.C. (2012) The association between the IL-4, ADRbeta2 and ADAM 33 gene polymorphisms and asthma in the Taiwanese population. J Chin Med Assoc, 75, 635-643.
  • Zhang, L., Su, T.P., Choi, K., Maree, W., Li, C.T., Chung, M.Y., Chen, Y.S., Bai, Y.M., Chou, Y.H., Barker, J.L. et al. (2011) P11 (S100A10) as a potential biomarker of psychiatric patients at risk of suicide. J Psychiatr Res, 45, 435-441.
  • Zhang, L., Li, C.T., Su, T.P., Hu, X.Z., Lanius, R.A., Webster, M.J., Chung, M.Y., Chen, Y.S., Bai, Y.M., Barker, J.L. et al. (2011) P11 expression and PET in bipolar disorders. J Psychiatr Res, 45, 1426-1430.
  • Lu, T.M., Lin, S.J., Lin, M.W., Hsu, C.P. and Chung, M.Y. (2011) The association of dimethylarginine dimethylaminohydrolase 1 gene polymorphism with type 2 diabetes: a cohort study. Cardiovasc Diabetol, 10, 16.
  • Lu, T.M., Chung, M.Y., Lin, M.W., Hsu, C.P. and Lin, S.J. (2011) Plasma asymmetric dimethylarginine predicts death and major adverse cardiovascular events in individuals referred for coronary angiography. Int J Cardiol, in press.
  • Lu, T.M., Chung, M.Y., Lin, C.C., Hsu, C.P. and Lin, S.J. (2011) Asymmetric dimethylarginine and clinical outcomes in chronic kidney disease. Clin J Am Soc Nephrol, 6, 1566-1572.