The CAA Repeat Polymorphism in the ZFHX3 Gene Is Associated with Risk of Coronary Heart Disease in a Chinese Population
Author:
Affiliation:
1. Central Laboratory, Shenzhen Baoan Hospital, Southern Medical University
2. Department of Emergency Medicine, Shenzhen Baoan Hospital, Southern Medical University
Publisher
Tohoku University Medical Press
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
https://www.jstage.jst.go.jp/article/tjem/235/4/235_261/_pdf
Reference25 articles.
1. Axford, M.M., Wang, Y.H., Nakamori, M., Zannis-Hadjopoulos, M., Thornton, C.A. & Pearson, C.E. (2013) Detection of slipped-DNAs at the trinucleotide repeats of the myotonic dystrophy type I disease locus in patient tissues. PLoS Genet., 9, e1003866.
2. Benjamin, E.J., Rice, K.M., Arking, D.E., Pfeufer, A., van Noord, C., Smith, A.V., Schnabel, R.B., Bis, J.C., Boerwinkle, E., Sinner, M.F., Dehghan, A., Lubitz, S.A., D’Agostino, R.B. Sr., Lumley, T., Ehret, G.B., et al. (2009) Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat. Genet., 41, 879-881.
3. Chen, S., Xie, X., Wang, Y., Gao, Y., Xie, X., Yang, J. & Ye, J. (2014) Association between leukocyte mitochondrial DNA content and risk of coronary heart disease: a case-control study. Atherosclerosis, 237, 220-226.
4. Dong, X.Y., Fu, X., Fan, S., Guo, P., Su, D. & Dong, J.T. (2012) Oestrogen causes ATBF1 protein degradation through the oestrogen-responsive E3 ubiquitin ligase EFP. Biochem. J., 444, 581-590.
5. Dong, X.Y., Guo, P., Sun, X., Li, Q. & Dong, J.T. (2011) Estrogen up-regulates ATBF1 transcription but causes its protein degradation in estrogen receptor-alpha-positive breast cancer cells. J. Biol. Chem., 286, 13879-13890.
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