Publications

Found 24 results
Filters: Author is Q. Liu  [Clear All Filters]
2016
Z. Cheng, Dai, L. L., Liu, Q., Liu, M., Wang, Q., Li, P. F., Wang, H., Jia, L. Q., An, L., Cheng, Z., Dai, L. L., Liu, Q., Liu, M., Wang, Q., Li, P. F., Wang, H., Jia, L. Q., and An, L., Correlation between polymorphisms in the glucocorticoid receptor gene NR3C1 and susceptibility to asthma in a Chinese population from the Henan Province, vol. 15, p. -, 2016.
Z. Cheng, Dai, L. L., Liu, Q., Liu, M., Wang, Q., Li, P. F., Wang, H., Jia, L. Q., An, L., Cheng, Z., Dai, L. L., Liu, Q., Liu, M., Wang, Q., Li, P. F., Wang, H., Jia, L. Q., and An, L., Correlation between polymorphisms in the glucocorticoid receptor gene NR3C1 and susceptibility to asthma in a Chinese population from the Henan Province, vol. 15, p. -, 2016.
X. X. Wu, Li, J., Wu, X. D., Liu, Q., Wang, Z. K., Liu, S. S., Li, S. N., Ma, Y. L., Sun, J., Zhao, L., Li, H. Y., Li, D. M., Li, W. B., Su, A. Y., Wu, X. X., Li, J., Wu, X. D., Liu, Q., Wang, Z. K., Liu, S. S., Li, S. N., Ma, Y. L., Sun, J., Zhao, L., Li, H. Y., Li, D. M., Li, W. B., and Su, A. Y., Ectopic expression of Arabidopsis thaliana Na+(K+)/H+ antiporter gene, AtNHX5, enhances soybean salt tolerance, vol. 15, p. -, 2016.
X. X. Wu, Li, J., Wu, X. D., Liu, Q., Wang, Z. K., Liu, S. S., Li, S. N., Ma, Y. L., Sun, J., Zhao, L., Li, H. Y., Li, D. M., Li, W. B., Su, A. Y., Wu, X. X., Li, J., Wu, X. D., Liu, Q., Wang, Z. K., Liu, S. S., Li, S. N., Ma, Y. L., Sun, J., Zhao, L., Li, H. Y., Li, D. M., Li, W. B., and Su, A. Y., Ectopic expression of Arabidopsis thaliana Na+(K+)/H+ antiporter gene, AtNHX5, enhances soybean salt tolerance, vol. 15, p. -, 2016.
X. G. Zhang, Zhang, H., Liang, X. L., Liu, Q., Wang, H. Y., Cao, B., Cao, J., Liu, S., Long, Y. J., Xie, W. Y., Peng, D. Z., Zhang, X. G., Zhang, H., Liang, X. L., Liu, Q., Wang, H. Y., Cao, B., Cao, J., Liu, S., Long, Y. J., Xie, W. Y., and Peng, D. Z., Epigenetic mechanism of maternal post-traumatic stress disorder in delayed rat offspring development: dysregulation of methylation and gene expression, vol. 15, p. -, 2016.
X. G. Zhang, Zhang, H., Liang, X. L., Liu, Q., Wang, H. Y., Cao, B., Cao, J., Liu, S., Long, Y. J., Xie, W. Y., Peng, D. Z., Zhang, X. G., Zhang, H., Liang, X. L., Liu, Q., Wang, H. Y., Cao, B., Cao, J., Liu, S., Long, Y. J., Xie, W. Y., and Peng, D. Z., Epigenetic mechanism of maternal post-traumatic stress disorder in delayed rat offspring development: dysregulation of methylation and gene expression, vol. 15, p. -, 2016.
J. Shi, Li, L. H., Duan, X. Y., Liu, Q., Sun, L. L., Tian, Y. T., Shi, J., Li, L. H., Duan, X. Y., Liu, Q., Sun, L. L., and Tian, Y. T., Gly71Arg UGT1A1 polymorphism is associated with breast cancer susceptibility in Han Chinese women, vol. 15, p. -, 2016.
J. Shi, Li, L. H., Duan, X. Y., Liu, Q., Sun, L. L., Tian, Y. T., Shi, J., Li, L. H., Duan, X. Y., Liu, Q., Sun, L. L., and Tian, Y. T., Gly71Arg UGT1A1 polymorphism is associated with breast cancer susceptibility in Han Chinese women, vol. 15, p. -, 2016.
M. F. Zhang, Liu, Q., Jia, G. X., Zhang, M. F., Liu, Q., and Jia, G. X., Reference gene selection for gene expression studies in lily using quantitative real-time PCR, vol. 15, p. -, 2016.
M. F. Zhang, Liu, Q., Jia, G. X., Zhang, M. F., Liu, Q., and Jia, G. X., Reference gene selection for gene expression studies in lily using quantitative real-time PCR, vol. 15, p. -, 2016.
Q. Liu, Chen, H. B., Luo, M., Zheng, H., Liu, Q., Chen, H. B., Luo, M., and Zheng, H., Serum soluble RAGE level inversely correlates with left ventricular hypertrophy in essential hypertension patients, vol. 15, p. -, 2016.
Q. Liu, Chen, H. B., Luo, M., Zheng, H., Liu, Q., Chen, H. B., Luo, M., and Zheng, H., Serum soluble RAGE level inversely correlates with left ventricular hypertrophy in essential hypertension patients, vol. 15, p. -, 2016.
2015
X. Z. Wang, Liu, Q., Sun, J. J., Zuo, W. S., Hu, D. W., Ma, S. G., Mu, D. B., and Yu, Z. Y., Correlation between p53 and epidermal growth factor receptor expression in breast cancer classification, vol. 14, pp. 4282-4290, 2015.
D. G. Li, Li, J. L., Sun, D. Q., Sun, X. B., Sun, X. G., and Liu, Q., Lentinan depresses 3T3-L1 fat cell formation by inhibiting PPARγ/AKT signaling pathway, vol. 14, pp. 8084-8090, 2015.
Y. Y. Wu, Zhao, J. M., Liu, Q., Guo, Q., Liu, Z., Wang, X. X., Wang, C. Y., Li, R. Y., Zhang, Y. Z., and Zhang, S. T., miR-71b regulation of insulin/IGF-1 signaling during starvation in planarians, vol. 14, pp. 11905-11914, 2015.
Y. Yu, Lv, F., Lin, H., Qian, G., Jiang, Y. S., Pang, L. X., Wang, Y. P., Wang, X. F., Kang, Y. M., Li, C. B., Liu, Q., Xu, J. Z., and You, W., Mitochondrial ND3 G10398A mutation: a biomarker for breast cancer, vol. 14, pp. 17426-17431, 2015.
Y. P. Lu, Han, W. T., Liu, Q., Li, J. X., Li, Z. J., Jiang, M., and Xu, W., Variations in WNT3 gene are associated with incidence of non-syndromic cleft lip with or without cleft palate in a northeast Chinese population, vol. 14, pp. 12646-12653, 2015.
W. H. Wu, Zhang, M. P., Yang, S. J., Liu, Q., Bai, X., Qin, J. H., Peng, B., Ou, S. T., Liu, J., Zhao, C. Y., Zhang, Q., Hu, Q. D., and Xue, L., Zhi-Long-Huo-Xue-Tong-Yu modulates mitochondrial fission through the ROCK1 pathway in mitochondrial dysfunction caused by streptozotocin-induced diabetic kidney injury, vol. 14, pp. 4593-4606, 2015.
2013
Q. Liu, Qi, X. F., Ye, F., Yao, J., and Xu, J., Lack of mutations of G4.5 in three families from China with noncompaction of the ventricular myocardium, vol. 12, pp. 53-58, 2013.
Bleyl SB, Mumford BR, Thompson V, Carey JC, et al. (1997). Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome. Am. J. Hum. Genet. 61: 868-872. http://dx.doi.org/10.1086/514879 PMid:9382097 PMCid:1715997   Chen R, Tsuji T, Ichida F, Bowles KR, et al. (2002). Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction. Mol. Genet. Metab. 77: 319-325. http://dx.doi.org/10.1016/S1096-7192(02)00195-6   Chin TK, Perloff JK, Williams RG, Jue K, et al. (1990). Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation 82: 507-513. http://dx.doi.org/10.1161/01.CIR.82.2.507 PMid:2372897   Ichida F, Tsubata S, Bowles KR, Haneda N, et al. (2001). Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome. Circulation 103: 1256-1263. http://dx.doi.org/10.1161/01.CIR.103.9.1256 PMid:11238270   Jenni R, Oechslin E, Schneider J, Attenhofer JC, et al. (2001). Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy. Heart 86: 666-671. http://dx.doi.org/10.1136/heart.86.6.666 PMid:11711464 PMCid:1730012   Kasifoglu T, Cavusoglu Y, Korkmaz C and Birdane A (2007). Noncompaction of the ventricular myocardium in a patient with Behcet's disease showing multiple thrombus formations in the right atrium, inferior vena cava and right iliac vein: A case report. Int. J. Angiol. 16: 69-72. http://dx.doi.org/10.1055/s-0031-1278252 PMid:22477276 PMCid:2733008   Kenton AB, Sanchez X, Coveler KJ, Makar KA, et al. (2004). Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12. Mol. Genet. Metab. 82: 162-166. http://dx.doi.org/10.1016/j.ymgme.2004.02.009 PMid:15172004   Klaassen S, Probst S, Oechslin E, Gerull B, et al. (2008). Mutations in sarcomere protein genes in left ventricular noncompaction. Circulation 117: 2893-2901. http://dx.doi.org/10.1161/CIRCULATIONAHA.107.746164 PMid:18506004   Maron BJ, Towbin JA, Thiene G, Antzelevitch C, et al. (2006). Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation 113: 1807-1816. http://dx.doi.org/10.1161/CIRCULATIONAHA.106.174287 PMid:16567565   Richardson P, McKenna W, Bristow M, Maisch B, et al. (1996). Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. Circulation 93: 841-842. http://dx.doi.org/10.1161/01.CIR.93.5.841 PMid:8598070   Sasse-Klaassen S, Gerull B, Oechslin E, Jenni R, et al. (2003). Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients. Am. J. Med. Genet. A 119A: 162-167. http://dx.doi.org/10.1002/ajmg.a.20075 PMid:12749056   Weiford BC, Subbarao VD and Mulhern KM (2004). Noncompaction of the ventricular myocardium. Circulation 109: 2965-2971. http://dx.doi.org/10.1161/01.CIR.0000132478.60674.D0 PMid:15210614   Zambrano E, Marshalko SJ, Jaffe CC and Hui P (2002). Isolated noncompaction of the ventricular myocardium: clinical and molecular aspects of a rare cardiomyopathy. Lab Invest 82: 117-122. http://dx.doi.org/10.1038/labinvest.3780404 PMid:11850525