Adult

MiR-214 regulates oral cancer KB cell apoptosis through targeting RASSF5.

T. K. Li, Yin, K., Chen, Z., Bao, Y., and Zhang, S. X., “MiR-214 regulates oral cancer KB cell apoptosis through targeting RASSF5.”, Genet Mol Res, vol. 16, no. 1, 2017.

Interactions among methylenetetrahydrofolate reductase (MTHFR) and cystathionine β-synthase (CBS) polymorphisms - a cross-sectional study: multiple heterozygosis as a risk factor for higher homocysteine levels and vaso-occlusive episodes.

F. M. Amaral, Miranda-Vilela, A. L., Lordelo, G. S., Ribeiro, I. F., Daldegan, M. B., and Grisolia, C. K., “Interactions among methylenetetrahydrofolate reductase (MTHFR) and cystathionine β-synthase (CBS) polymorphisms - a cross-sectional study: multiple heterozygosis as a risk factor for higher homocysteine levels and vaso-occlusive episodes.”, Genet Mol Res, vol. 16, no. 1, 2017.

Inhibition of invasion and migration of prostate cancer cells by miRNA-509-5p via targeting MDM2.

X. M. Tian, Luo, Y. Z., He, P., Li, J., Ma, Z. W., and An, Y., “Inhibition of invasion and migration of prostate cancer cells by miRNA-509-5p via targeting MDM2.”, Genet Mol Res, vol. 16, no. 1, 2017.

A large-scale analysis study on the clinical and viral characteristics of hepatitis B infection with concurrence of hepatitis B surface or E antigens and their corresponding antibodies.

Y. Xiang, Chen, P., Xia, J. R., and Zhang, L. P., “A large-scale analysis study on the clinical and viral characteristics of hepatitis B infection with concurrence of hepatitis B surface or E antigens and their corresponding antibodies.”, Genet Mol Res, vol. 16, no. 1, 2017.

Polymorphisms in interleukin-6 and interleukin-10 may be associated with risk of preeclampsia.

D. M. Fan, Wang, Y., Liu, X. L., Zhang, A., and Xu, Q., “Polymorphisms in interleukin-6 and interleukin-10 may be associated with risk of preeclampsia.”, Genet Mol Res, vol. 16, no. 1, 2017.

Mutations in codons 12 and 13 of K-ras exon 2 in colorectal tumors of Saudi Arabian patients: frequency, clincopathological associations, and clinical outcomes.

J. Zekri, Al-Shehri, A., Mahrous, M., Al-Rehaily, S., Darwish, T., Bassi, S., H Taani, E., A Zahrani, A., Elsamany, S., Al-Maghrabi, J., and Sadiq, B. B., “Mutations in codons 12 and 13 of K-ras exon 2 in colorectal tumors of Saudi Arabian patients: frequency, clincopathological associations, and clinical outcomes.”, Genet Mol Res, vol. 16, no. 1, 2017.

Polymorphism in the third intron of the interferonγ gene is associated with susceptibility to multiple sclerosis.

X. L. Wang, Meng, F. R., Wang, X., Wang, S. H., and Guo, L., “Polymorphism in the third intron of the interferonγ gene is associated with susceptibility to multiple sclerosis.”, Genet Mol Res, vol. 16, no. 1, 2017.

Matrix metalloproteinase gene polymorphisms and susceptibility to systemic sclerosis.

T. F. Rech, Moraes, S. B. C., Bredemeier, M., de Paoli, J., Brenol, J. C. T., Xavier, R. M., Chies, J. A. B., and Simon, D., “Matrix metalloproteinase gene polymorphisms and susceptibility to systemic sclerosis.”, Genet Mol Res, vol. 15, no. 4, 2016.

Association between -174G/C and -572G/C interleukin 6 gene polymorphisms and severe radiographic damage to the hands of Mexican patients with rheumatoid arthritis: a preliminary report.

S. A. Zavaleta-Muñiz, Gonzalez-Lopez, L., Murillo-Vazquez, J. D., Saldaña-Cruz, A. M., Vazquez-Villegas, M. L., Martín-Márquez, B. T., Vasquez-Jimenez, J. C., Sandoval-Garcia, F., Ruiz-Padilla, A. J., Fajardo-Robledo, N. S., Ponce-Guarneros, J. M., Rocha-Muñoz, A. D., Alcaraz-Lopez, M. F., Cardona-Müller, D., Totsuka-Sutto, S. E., Rubio-Arellano, E. D., and Gamez-Nava, J. I., “Association between -174G/C and -572G/C interleukin 6 gene polymorphisms and severe radiographic damage to the hands of Mexican patients with rheumatoid arthritis: a preliminary report.”, Genet Mol Res, vol. 15, no. 4, 2016.

Association between COL9A2 Gln326Arg mutations and the development of intervertebral disc disease in a Chinese population.

T. Meng, Ren, Q., Wang, J. M., Shi, H., Zhang, S. T., and Liu, M. T., “Association between COL9A2 Gln326Arg mutations and the development of intervertebral disc disease in a Chinese population.”, Genet Mol Res, vol. 15, no. 4, 2016.

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