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2016
I. A. Gutiérrez-Hurtado, Puebla-Pérez, A. M., Delgado-Saucedo, J. I., Figuera, L. E., Zúñiga-González, G. M., Gomez-Mariscal, K., Ronquillo-Carreón, C. A., Gallegos-Arreola, M. P., Gutiérrez-Hurtado, I. A., Puebla-Pérez, A. M., Delgado-Saucedo, J. I., Figuera, L. E., Zúñiga-González, G. M., Gomez-Mariscal, K., Ronquillo-Carreón, C. A., and Gallegos-Arreola, M. P., Association between TNF-α-308G>A and -238G>A gene polymorphisms and TNF-α serum levels in Mexican colorectal cancer patients, vol. 15, p. -, 2016.
I. A. Gutiérrez-Hurtado, Puebla-Pérez, A. M., Delgado-Saucedo, J. I., Figuera, L. E., Zúñiga-González, G. M., Gomez-Mariscal, K., Ronquillo-Carreón, C. A., Gallegos-Arreola, M. P., Gutiérrez-Hurtado, I. A., Puebla-Pérez, A. M., Delgado-Saucedo, J. I., Figuera, L. E., Zúñiga-González, G. M., Gomez-Mariscal, K., Ronquillo-Carreón, C. A., and Gallegos-Arreola, M. P., Association between TNF-α-308G>A and -238G>A gene polymorphisms and TNF-α serum levels in Mexican colorectal cancer patients, vol. 15, p. -, 2016.
A. Marin-Medina, Brambila-Tapia, A. J. L., Picos-Cárdenas, V. J., Gallegos-Arreola, M. P., and Figuera, L. E., eNOS gene Glu298Asp and 4b/a polymorphisms are associated with renal function parameters in Mexican patients with Fabry disease, vol. 15, no. 4, p. -, 2016.
Conflicts of interestThe authors declare no conflict of interest.ACKNOWLEDGMENTSWe want to acknowledge the doctoral fellowship granted to A. Marin-Medina by CONACyT. REFERENCESAlFadhli S, et al (2013). Influence of endothelial nitric oxide synthase gene intron-4 27bp repeat polymorphism on its expression in autoimmune diseases. Dis. Markers 34: 349-356. http://dx.doi.org/10.1155/2013/613978 Dellamea BS, Pinto LC, Leitão CB, Santos KG, et al (2014). Endothelial nitric oxide synthase gene polymorphisms and risk of diabetic nephropathy: a systematic review and meta-analysis. BMC Med. Genet. 15: 9. http://dx.doi.org/10.1186/1471-2350-15-9 Heltianu C, Costache G, Azibi K, Poenaru L, et al (2002). Endothelial nitric oxide synthase gene polymorphisms in Fabry’s disease. Clin. Genet. 61: 423-429. http://dx.doi.org/10.1034/j.1399-0004.2002.610605.x Heltianu C, Costache G, Gafencu A, Diaconu M, et al (2005). Relationship of eNOS gene variants to diseases that have in common an endothelial cell dysfunction. J. Cell. Mol. Med. 9: 135-142. http://dx.doi.org/10.1111/j.1582-4934.2005.tb00343.x Hingorani AD, et al (2003). Endothelial nitric oxide synthase polymorphisms and hypertension. Curr. Hypertens. Rep. 5: 19-25. http://dx.doi.org/10.1007/s11906-003-0006-0 Hingorani AD, Liang CF, Fatibene J, Lyon A, et al (1999). A common variant of the endothelial nitric oxide synthase (Glu298-->Asp) is a major risk factor for coronary artery disease in the UK. Circulation 100: 1515-1520. http://dx.doi.org/10.1161/01.CIR.100.14.1515 McDonald DM, Alp NJ, Channon KM, et al (2004). Functional comparison of the endothelial nitric oxide synthase Glu298Asp polymorphic variants in human endothelial cells. Pharmacogenetics 14: 831-839. http://dx.doi.org/10.1097/00008571-200412000-00006 Miller SA, Dykes DD, Polesky HF, et al (1988). A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 16: 1215. http://dx.doi.org/10.1093/nar/16.3.1215 Qi HP, Fraser WD, Luo ZC, Julien P, et al (2013). Endothelial nitric oxide synthase gene polymorphisms and risk of preeclampsia. Am. J. Perinatol. 30: 795-804. http://dx.doi.org/10.1055/s-0032-1333406 Ramos-Kuri M, Olvera D, Morales JJ, Rodriguez-Espino BA, et al (2014). Clinical, histological and molecular characteristics of Mexican patients with Fabry disease and significant renal involvement. Arch. Med. Res. 45: 257-262. http://dx.doi.org/10.1016/j.arcmed.2014.03.005 Sandoughi M, Salimi S, Zakeri Z, Darbandi EJ, et al (2014). Association of eNOS gene polymorphisms and systemic lupus erythematosus in southeast Iran. Int. J. Rheum. Dis.http://dx.doi.org/10.1111/1756-185X.12510 Tesauro M, Thompson WC, Rogliani P, Qi L, et al (2000). Intracellular processing of endothelial nitric oxide synthase isoforms associated with differences in severity of cardiopulmonary diseases: cleavage of proteins with aspartate vs. glutamate at position 298. Proc. Natl. Acad. Sci. USA 97: 2832-2835. http://dx.doi.org/10.1073/pnas.97.6.2832 Waldek S, Feriozzi S, et al (2014). Fabry nephropathy: a review - how can we optimize the management of Fabry nephropathy? BMC Nephrol. 15: 72. http://dx.doi.org/10.1186/1471-2369-15-72 Yang Y, Du K, Liu Z, Lu X, et al (2014). Endothelial nitric oxide synthase (eNOS) 4b/a gene polymorphisms and coronary artery disease: evidence from a meta-analysis. Int. J. Mol. Sci. 15: 7987-8003. http://dx.doi.org/10.3390/ijms15057987 Zhang L, Chen LM, Wang MN, Chen XJ, et al (2014). The G894t, T-786c and 4b/a polymorphisms in Enos gene and cancer risk: a meta-analysis. J. Evid. Based Med. 7: 263-269. http://dx.doi.org/10.1111/jebm.12126 Zhang MX, Ou H, Shen YH, Wang J, et al (2005). Regulation of endothelial nitric oxide synthase by small RNA. Proc. Natl. Acad. Sci. USA 102: 16967-16972. http://dx.doi.org/10.1073/pnas.0503853102 Zhang MX, Zhang C, Shen YH, Wang J, et al (2008). Effect of 27nt small RNA on endothelial nitric-oxide synthase expression. Mol. Biol. Cell 19: 3997-4005. http://dx.doi.org/10.1091/mbc.E07-11-1186  
2012
M. P. Gallegos-Arreola, Figuera-Villanueva, L. E., Puebla-Pérez, A. M., Montoya-Fuentes, H., Suarez-Rincon, A. E., and Zúñiga-González, G. M., Association of TP53 gene codon 72 polymorphism with endometriosis in Mexican women, vol. 11, pp. 1401-1408, 2012.
Akahane T, Sekizawa A, Purwosunu Y, Nagatsuka M, et al. (2007). The role of p53 mutation in the carcinomas arising from endometriosis. Int. J. Gynecol. Pathol. 26: 345-351. http://dx.doi.org/10.1097/pgp.0b013e31802b41a8 PMid:17581423   Ammendola M, Gloria-Bottini F, Sesti F, Piccione E, et al. (2008). Association of p53 codon 72 polymorphism with endometriosis. Fertil. Steril. 90: 406-408. http://dx.doi.org/10.1016/j.fertnstert.2007.06.051 PMid:17931634   Ayala YR and Mota GM (2007). Endometriosis: physiopathology and investigation trends (first part). Ginecol. Obstet. Mex. 75: 477-483.   Chang CC, Hsieh YY, Tsai FJ, Tsai CH, et al. (2002). The proline form of p53 codon 72 polymorphism is associated with endometriosis. Fertil. Steril. 77: 43-45. http://dx.doi.org/10.1016/S0015-0282(01)02938-7   Chiurillo MA, Moran Y, Cañas M and Valero G (2010). Distribución del polimorfismo codon 72 de TP53 en Venezuela: implicaciones étnicas y Geográficas. Interciencia 35: 202-206.   Doosti A, Zamani M, Ghasemi P, Taherin S, et al. (2011). Association of the p53 codon 72 polymorphism with colorectal cancer in South West of Iran. Sci. Res. Essays 6: 3148-3152.   Dunselman G (2002). Endometriosis. Patogenia de los Implantes Endometriósicos. In: Reproducción Humana (Pellicer A and Simón C, eds.). Mc GrawHill, España, 191-197.   Felix A, Nogales FF and Arias-Stella J (2010). Polypoid endometriosis of the uterine cervix with Arias-Stella reaction in a patient taking phytoestrogens. Int. J. Gynecol. Pathol. 29: 185-188. http://dx.doi.org/10.1097/PGP.0b013e3181b7015e PMid:20173505   Ghasemi N, Karimi-Zarchi M, Mortazavi-Zadeh MR and Atash-Afza A (2010). Evaluation of the frequency of TP53 gene codon 72 polymorphisms in Iranian patients with endometrial cancer. Cancer Genet. Cytogenet. 196: 167-170. http://dx.doi.org/10.1016/j.cancergencyto.2009.09.013 PMid:20082853   Giudice LC and Kao LC (2004). Endometriosis. Lancet 364: 1789-1799. http://dx.doi.org/10.1016/S0140-6736(04)17403-5   Goodman C, Jeyendran RS and Coulam CB (2009). P53 tumor suppressor factor, plasminogen activator inhibitor, and vascular endothelial growth factor gene polymorphisms and recurrent implantation failure. Fertil. Steril. 92: 494-498. http://dx.doi.org/10.1016/j.fertnstert.2008.07.022 PMid:18829023   Gruppo Italiano per lo Studio dell'Endometriosi (2001). Relationship between stage, site and morphological characteristics of pelvic endometriosis and pain. Hum. Reprod. 16: 2668-2671.   Gylfason JT, Kristjansson KA, Sverrisdottir G, Jonsdottir K, et al. (2010). Pelvic endometriosis diagnosed in an entire nation over 20 years. Am. J. Epidemiol. 172: 237-243. http://dx.doi.org/10.1093/aje/kwq143 PMid:20616202   Hsieh YY and Lin CS (2006). P53 codon 11, 72, and 248 gene polymorphisms in endometriosis. Int. J. Biol. Sci. 2: 188- 193. http://dx.doi.org/10.7150/ijbs.2.188 PMid:16896365 PMCid:1525214   Kang HJ, Feng Z, Sun Y, Atwal G, et al. (2009). Single-nucleotide polymorphisms in the p53 pathway regulate fertility in humans. Proc. Natl. Acad. Sci. U. S. A. 106: 9761-9766. http://dx.doi.org/10.1073/pnas.0904280106 PMid:19470478 PMCid:2700980   Kern SE, Kinzler KW, Bruskin A, Jarosz D, et al. (1991). Identification of p53 as a sequence-specific DNA-binding protein. Science 252: 1708-1711. http://dx.doi.org/10.1126/science.2047879 PMid:2047879   Kobayashi H, Kajiwara H, Kanayama S, Yamada Y, et al. (2009). Molecular pathogenesis of endometriosis-associated clear cell carcinoma of the ovary (review). Oncol. Rep. 22: 233-240. PMid:19578761   Liu G, Miller DP, Zhou W, Thurston SW, et al. (2001). Differential association of the codon 72 p53 and GSTM1 polymorphisms on histological subtype of non-small cell lung carcinoma. Cancer Res. 61: 8718-8722. PMid:11751390   Mandai M, Yamaguchi K, Matsumura N, Baba T, et al. (2009). Ovarian cancer in endometriosis: molecular biology, pathology, and clinical management. Int. J. Clin. Oncol. 14: 383-391. http://dx.doi.org/10.1007/s10147-009-0935-y PMid:19856044   Miller SA, Dykes DD and Polesky HF (1988). A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 16: 1215. http://dx.doi.org/10.1093/nar/16.3.1215 PMid:3344216 PMCid:334765   Nouri K, Ott J, Krupitz B, Huber JC, et al. (2010). Family incidence of endometriosis in first-, second-, and third-degree relatives: case-control study. Reprod. Biol. Endocrinol. 8: 85. http://dx.doi.org/10.1186/1477-7827-8-85 PMid:20618992 PMCid:2911462   Peppone LJ, Piazza KM, Mahoney MC, Morrow GR, et al. (2009). Associations between adult and childhood smoke exposures and fecundity and fetal loss among women who visited a cancer hospital. Tob. Control 18: 115-120. http://dx.doi.org/10.1136/tc.2008.027961 PMid:19039010 PMCid:2886518   Ribeiro Junior CL, Arruda JT, Silva CT and Moura KK (2009). Analysis of p53 codon 72 gene polymorphism in Brazilian patients with endometriosis. Genet. Mol. Res. 8: 494-499. http://dx.doi.org/10.4238/vol8-2gmr593 PMid:19551637   Sanguinetti CJ, Dias NE and Simpson AJ (1994). Rapid silver staining and recovery of PCR products separated on polyacrylamide gels. Biotechniques 17: 914-921. PMid:7840973   Shiverick KT and Salafia C (1999). Cigarette smoking and pregnancy I: ovarian, uterine and placental effects. Placenta 20: 265-272. http://dx.doi.org/10.1053/plac.1998.0377 PMid:10329346   Själander A, Birgander R, Saha N, Beckman L, et al. (1996). p53 polymorphisms and haplotypes show distinct differences between major ethnic groups. Hum. Hered. 46: 41-48. http://dx.doi.org/10.1159/000154324 PMid:8825462   Suárez-Rincon AE, Moran-Moguel MC, Montoya-Fuentes H, Gallegos-Arreola MP, et al. (2002). Polymorphism in codon 72 of the p53 gene and cervico-uterine cancer risk in Mexico. Ginecol. Obstet. Mex. 70: 344-348. PMid:12221910   Sunderam S, Chang J, Flowers L, Kulkarni A, et al. (2009). Assisted reproductive technology surveillance-United States, 2006. MMWR Surveill Summ. 58: 1-25. PMid:19521336   Thomas M, Kalita A, Labrecque S, Pim D, et al. (1999). Two polymorphic variants of wild-type p53 differ biochemically and biologically. Mol. Cell Biol. 19: 1092-1100. PMid:9891044 PMCid:116039   Troyer MR (2007). Differential diagnosis of endometriosis in a young adult woman with nonspecific low back pain. Phys. Ther. 87: 801-810. http://dx.doi.org/10.2522/ptj.20060141 PMid:17442838