Adult

Study on the association of UGT1A9 gene c.98T>C polymorphism and mycophenolic acid plasma levels in renal transplant patients.

L. R. Ruschel, Schmitt, V. M., Silva, A. B., Oliveira, C. S. A., Flach, K., d'Avila, D. O., and Thiesen, F. V., “Study on the association of UGT1A9 gene c.98T>C polymorphism and mycophenolic acid plasma levels in renal transplant patients.”, Genet Mol Res, vol. 16, no. 2, 2017.

Lack of association between human leukocyte antigen polymorphisms rs9277535 and rs7453920 and chronic hepatitis B in a Brazilian population.

V. R. Z. B. Pereira, Wolf, J. M., Stumm, G. Z., Boeira, T. R., Galvan, J., Simon, D., and Lunge, V. R., “Lack of association between human leukocyte antigen polymorphisms rs9277535 and rs7453920 and chronic hepatitis B in a Brazilian population.”, Genet Mol Res, vol. 16, no. 2, 2017.

SETD5 gene variant associated with mild intellectual disability - a case report.

E. Stur, Soares, L. A., and Louro, I. D., “SETD5 gene variant associated with mild intellectual disability - a case report.”, Genet Mol Res, vol. 16, no. 2, 2017.

Detection of damage on single- or double-stranded DNA in a population exposed to arsenic in drinking water.

J. Jiménez-Villarreal, Rivas-Armendáriz, D. I., Pineda-Belmontes, C. P., Betancourt-Martínez, N. D., Macías-Corral, M. A., Guerra-Alanis, A. J., Niño-Castañeda, M. S., and Morán-Martínez, J., “Detection of damage on single- or double-stranded DNA in a population exposed to arsenic in drinking water.”, Genet Mol Res, vol. 16, no. 2, 2017.

Prevalence of human papillomavirus, Chlamydia trachomatis, and Trichomonas vaginalis infections in Amazonian women with normal and abnormal cytology.

E. Costa-Lira, Jacinto, A. H. V. L., Silva, L. M., Napoleão, P. F. R., Barbosa-Filho, R. A. A., Cruz, G. J. S., Astolfi-Filho, S., and Borborema-Santos, C. M., “Prevalence of human papillomavirus, Chlamydia trachomatis, and Trichomonas vaginalis infections in Amazonian women with normal and abnormal cytology.”, Genet Mol Res, vol. 16, no. 2, 2017.

Association of interleukin-6 gene polymorphisms and circulating levels with keloid scars in a Chinese Han population.

X. J. Zhu, Li, W. Z., Li, H., Fu, C. Q., and Liu, J., “Association of interleukin-6 gene polymorphisms and circulating levels with keloid scars in a Chinese Han population.”, Genet Mol Res, vol. 16, no. 2, 2017.

Polymorphism E23K (rs5219) in the KCNJ11 gene in Euro-Brazilian subjects with type 1 and 2 diabetes.

S. W. Souza, Alcazar, L. P., Arakaki, P. A., Santos-Weiss, I. C. R., Alberton, D., Picheth, G., and Rego, F. G. M., “Polymorphism E23K (rs5219) in the KCNJ11 gene in Euro-Brazilian subjects with type 1 and 2 diabetes.”, Genet Mol Res, vol. 16, no. 2, 2017.

Association between interleukin-4 polymorphisms and risk of pre-eclampsia in a population of Chinese pregnant women.

J. Chen, Zhong, M., and Yu, Y. H., “Association between interleukin-4 polymorphisms and risk of pre-eclampsia in a population of Chinese pregnant women.”, Genet Mol Res, vol. 16, no. 2, 2017.

TNFR1 -383 A˃C polymorphism and ankylosing spondylitis in a Russian Caucasian population: a preliminary study.

V. Mordovskii, Semenchukov, A., Nikulina, S. Y., Salmina, A. B., Chernova, A., Kapustina, E., Kents, A., Ohapkina, A., Moskaleva, E., Maltese, P. E., Convertini, P., and Bertelli, M., “TNFR1 -383 A˃C polymorphism and ankylosing spondylitis in a Russian Caucasian population: a preliminary study.”, Genet Mol Res, vol. 16, no. 1, 2017.

Leptin (rs7799039) and solute carrier family 30 zinc transporter (rs13266634) polymorphisms in Euro-Brazilian pregnant women with gestational diabetes.

A. Teleginski, Welter, M., Frigeri, H. R., Réa, R. R., Souza, E. M., Alberton, D., Rego, F. G. M., and Picheth, G., “Leptin (rs7799039) and solute carrier family 30 zinc transporter (rs13266634) polymorphisms in Euro-Brazilian pregnant women with gestational diabetes.”, Genet Mol Res, vol. 16, no. 1, 2017.

Pages