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2019
I. A. Bento, Silva, K. S. Fe, Moura, K. K. V. O., Júnior, C. L. Ribeiro, and da Costa, I. R., CYP2C19*3 polymorphism in patients with endometriosis, Genetics and Molecular Research, vol. 18, no. 2, 2019.
R. C. P. Ce Silva, de Faria, L. C., Silva, K. S. Fe, Moura, K. K. V. O., Júnior, C. L. Ribeiro, and Guillo, L. A., Endothelial nitric oxide synthase G894T polymorphism increases the risk of infertility in women with endometriosis, Genetics and Molecular Research, vol. 18, no. 2, 2019.
F. R. B. Oliveira, Corrêa, J. F., Silva, K. S. F., Costa, I. A., Mascarenhas, R. S., Barbosa, A. M., Lagares, M. H., Campedelli, F. L., and Moura, K. K. V. O., The eNOS T786C polymorphism is not related to atherosclerosis and cofactors in a Brazilian population, Genetics and Molecular Research, vol. 18, no. 3, 2019.
O. S. Dias Neto, Silva, K. S. Fe, Barbosa, A. M., Rodrigues, D. A., Lagares, M. H., da Costa, I. R., and Moura, K. K. V. O., GSTT1 null genotype in sickle cell anemia and blood transfusion recurrence – a case report, Genetics and Molecular Research, vol. 18, no. 2, 2019.
M. P. Moraes, Silva, K. S. Fe, Lagares, M. H., Barbosa, A. M., Martins, J. V. M., Campedelli, F. L., da Costa, I. R., Rodrigues, D. A., and Moura, K. K. V. O., Polymorphisms of the genes eNOS, GSTT1 and GSTM1 are significantly associated with atherosclerotic disease in hypertensive patients, Genetics and Molecular Research, vol. 18, no. 1, 2019.
I. R. Costa, Santos, T. R., Bento, I. A., Siqueira, B. O., Barbosa, A. M., Silva, K. S. F., Lagares, M. H., Martins, J. V. M., Rodrigues, D. A., Morais, M. P., Campedelle, F. L., and Moura, K. K. V. O., RFLP-PCR is more efficient than ARMS-PCR for identifying CYP2C19*2 polymorphism in atherosclerotic patients, Genetics and Molecular Research, vol. 18, no. 3, 2019.
2016
I. R. Costa, Mascarenhas, R. S., Corrêa, J. F., Oliveira, F. R. B., Fernandes, S. G., Souza, F. O., Reis, G. Mdos, A. Júnior, deP. R., Rodrigues, D. A., Martins, J. V. M., Silva, K. S. Fe, Moura, K. K. V. O., Costa, I. R., Mascarenhas, R. S., Corrêa, J. F., Oliveira, F. R. B., Fernandes, S. G., Souza, F. O., Reis, G. Mdos, A. Júnior, deP. R., Rodrigues, D. A., Martins, J. V. M., Silva, K. S. Fe, and Moura, K. K. V. O., Analysis of the prevalence of polymorphisms in the glutathione S transferase gene (GST) in cataract patients from Goiânia, vol. 15, p. -, 2016.
I. R. Costa, Mascarenhas, R. S., Corrêa, J. F., Oliveira, F. R. B., Fernandes, S. G., Souza, F. O., Reis, G. Mdos, A. Júnior, deP. R., Rodrigues, D. A., Martins, J. V. M., Silva, K. S. Fe, Moura, K. K. V. O., Costa, I. R., Mascarenhas, R. S., Corrêa, J. F., Oliveira, F. R. B., Fernandes, S. G., Souza, F. O., Reis, G. Mdos, A. Júnior, deP. R., Rodrigues, D. A., Martins, J. V. M., Silva, K. S. Fe, and Moura, K. K. V. O., Analysis of the prevalence of polymorphisms in the glutathione S transferase gene (GST) in cataract patients from Goiânia, vol. 15, p. -, 2016.
A. M. Barbosa, de Souza, S. R., Frare, A. B., Silva, R. C. Costa e, da Costa, I. R., Silva, K. S. Freitas e, Júnior, C. L. Ribeiro, Bordin, B. M., Moura, K. K. V. O., Barbosa, A. M., de Souza, S. R., Frare, A. B., Silva, R. C. Costa e, da Costa, I. R., Silva, K. S. Freitas e, Júnior, C. L. Ribeiro, Bordin, B. M., and Moura, K. K. V. O., Association of CYP1A1 (cytochrome P450) MspI polymorphism in women with endometriosis, vol. 15, p. -, 2016.
A. M. Barbosa, de Souza, S. R., Frare, A. B., Silva, R. C. Costa e, da Costa, I. R., Silva, K. S. Freitas e, Júnior, C. L. Ribeiro, Bordin, B. M., Moura, K. K. V. O., Barbosa, A. M., de Souza, S. R., Frare, A. B., Silva, R. C. Costa e, da Costa, I. R., Silva, K. S. Freitas e, Júnior, C. L. Ribeiro, Bordin, B. M., and Moura, K. K. V. O., Association of CYP1A1 (cytochrome P450) MspI polymorphism in women with endometriosis, vol. 15, p. -, 2016.
K. S. F. Silva, Moura, K. K. V. O., Silva, K. S. F., and Moura, K. K. V. O., Genetic polymorphisms in patients with endometriosis: an analytical study in Goiânia (Central West of Brazil), vol. 15, p. -, 2016.
K. S. F. Silva, Moura, K. K. V. O., Silva, K. S. F., and Moura, K. K. V. O., Genetic polymorphisms in patients with endometriosis: an analytical study in Goiânia (Central West of Brazil), vol. 15, p. -, 2016.
M. P. de Morais, Curado, R. F., Silva, K. S. Fe, Moura, K. K. V. O., and Arruda, J. T., Male idiopathic infertility and the TP53 polymorphism in codon 72, vol. 15, no. 4, p. -, 2016.
Conflicts of interestThe authors declare no conflict of interest.ACKNOWLEDGMENTSResearch supported by funding provided by PUC-GO University. REFERENCESAllan DJ, Harmon BV, Roberts SA, et al (1992). Spermatogonial apoptosis has three morphologically recognizable phases and shows no circadian rhythm during normal spermatogenesis in the rat. Cell Prolif. 25: 241-250. http://dx.doi.org/10.1111/j.1365-2184.1992.tb01399.x Beumer TL, Roepers-Gajadien HL, Gademan IS, van Buul PP, et al (1998). The role of the tumor suppressor p53 in spermatogenesis. Cell Death Differ. 5: 669-677. http://dx.doi.org/10.1038/sj.cdd.4400396 Bojesen SE, Nordestgaard BG, et al (2008). The common germline Arg72Pro polymorphism of p53 and increased longevity in humans. Cell Cycle 7: 158-163. http://dx.doi.org/10.4161/cc.7.2.5249 Brenna SMF, Silva IDCG, Zeferino LC, Pereira J, et al (2004). Prevalence of codon 72 p53 polymorphism in Brazilian women with cervix cancer. Genet. Mol. Biol. 27: 496-499. http://dx.doi.org/10.1590/S1415-47572004000400005 Chowdhury AK, Steinberger E, et al (1964). A quantitative study of the effect of heat on germinal epithelium of rat testes. Am. J. Anat. 115: 509-524. http://dx.doi.org/10.1002/aja.1001150307 Churchman ML, Roig I, Jasin M, Keeney S, et al (2011). Expression of arf tumor suppressor in spermatogonia facilitates meiotic progression in male germ cells. PLoS Genet. 7: e1002157. http://dx.doi.org/10.1371/journal.pgen.1002157 Dumont P, Leu JI, Della Pietra AC3rdGeorgeDL, et al (2003). The codon 72 polymorphic variants of p53 have markedly different apoptotic potential. Nat. Genet. 33: 357-365. http://dx.doi.org/10.1038/ng1093 Fouchécourt S, Livera G, Messiaen S, Fumel B, et al (2016). Apoptosis of Sertoli cells after conditional ablation of murine double minute 2 (Mdm2) gene is p53-dependent and results in male sterility. Cell Death Differ. 23: 521-530. http://dx.doi.org/10.1038/cdd.2015.120 Huckins C, et al (1978). The morphology and kinetics of spermatogonial degeneration in normal adult rats: an analysis using a simplified classification of the germinal epithelium. Anat. Rec. 190: 905-926. http://dx.doi.org/10.1002/ar.1091900410 Jobling MA, Tyler-Smith C, et al (2003). The human Y chromosome: an evolutionary marker comes of age. Nat. Rev. Genet. 4: 598-612. http://dx.doi.org/10.1038/nrg1124 Kerr JB, et al (1992). Spontaneous degeneration of germ cells in normal rat testis: assessment of cell types and frequency during the spermatogenic cycle. J. Reprod. Fertil. 95: 825-830. http://dx.doi.org/10.1530/jrf.0.0950825 Lane DP, et al (1992). Cancer. p53, guardian of the genome. Nature 358: 15-16. http://dx.doi.org/10.1038/358015a0 Lattuada D, Viganò P, Somigliana E, Abbiati A, et al (2004). Analysis of the codon 72 polymorphism of the TP53 gene in patients with endometriosis. Mol. Hum. Reprod. 10: 651-654. http://dx.doi.org/10.1093/molehr/gah093 Li C, Chen K, Liu Z, Wang LE, et al (2008). Polymorphisms of TP53 Arg72Pro, but not p73 G4C14>A4TA4 and p21 Ser31Arg, contribute to risk of cutaneous melanoma. J. Invest. Dermatol. 128: 1585-1588. http://dx.doi.org/10.1038/sj.jid.5701186 Lin HY, Huang CH, Wu WJ, Chang LC, et al (2008). TP53 codon 72 Gene Polymorphism Paradox in Associated with Various Carcinoma Incidences, Invasiveness and Chemotherapy Responses. Int. J. Biomed. Sci. 4: 248-254. Lin YC, Yao PL, Richburg JH, et al (2010). FasL gene-deficient mice display a limited disruption in spermatogenesis and inhibition of mono-(2-ethylhexyl) phthalate-induced germ cell apoptosis. Toxicol. Sci. 114: 335-345. http://dx.doi.org/10.1093/toxsci/kfq015 Lu NX, Xia YK, Gu AH, Liang J, et al (2007). Lack of association between polymorphisms in p53 gene and spermatogenetic failure in a Chinese population. Andrologia 39: 223-228. http://dx.doi.org/10.1111/j.1439-0272.2007.00790.x Matzuk MM, Lamb DJ, et al (2008). The biology of infertility: research advances and clinical challenges. Nat. Med. 14: 1197-1213. http://dx.doi.org/10.1038/nm.f.1895 Murphy ME, et al (2006). Polymorphic variants in the p53 pathway. Cell Death Differ. 13: 916-920. http://dx.doi.org/10.1038/sj.cdd.4401907 Ohta H, Aizawa S, Nishimune Y, et al (2003). Functional analysis of the p53 gene in apoptosis induced by heat stress or loss of stem cell factor signaling in mouse male germ cells. Biol. Reprod. 68: 2249-2254. http://dx.doi.org/10.1095/biolreprod.102.014779 Olesen C, Hansen C, Bendsen E, Byskov AG, et al (2001). Identification of human candidate genes for male infertility by digital differential display. Mol. Hum. Reprod. 7: 11-20. http://dx.doi.org/10.1093/molehr/7.1.11 Pelúzio MCG, Volp ACP, Queiroz IC, Brito CJ, et al (2006). As proteínas supressoras em neoplasias malignas - Conhecendo seu papel. Rev. Bras. Nutr. Clín. 21: 233-238. Print CG, Loveland KL, et al (2000). Germ cell suicide: new insights into apoptosis during spermatogenesis. BioEssays 22: 423-430. http://dx.doi.org/10.1002/(SICI)1521-1878(200005)22:5<423::AID-BIES4>3.0.CO;2-0 Rotter V, Schwartz D, Almon E, Goldfinger N, et al (1993). Mice with reduced levels of p53 protein exhibit the testicular giant-cell degenerative syndrome. Proc. Natl. Acad. Sci. USA 90: 9075-9079. http://dx.doi.org/10.1073/pnas.90.19.9075 Schwartz D, Goldfinger N, Rotter V, et al (1993). Expression of p53 protein in spermatogenesis is confined to the tetraploid pachytene primary spermatocytes. Oncogene 8: 1487-1494. Shikone T, Billig H, Hsueh AJ, et al (1994). Experimentally induced cryptorchidism increases apoptosis in rat testis. Biol. Reprod. 51: 865-872. http://dx.doi.org/10.1095/biolreprod51.5.865 Show MD, Hill CM, Anway MD, Wright WW, et al (2008). Phosphorylation of mitogen-activated protein kinase 8 (MAPK8) is associated with germ cell apoptosis and redistribution of the Bcl2-modifying factor (BMF). J. Androl. 29: 338-344. http://dx.doi.org/10.2164/jandrol.107.003558 Siddique M, Sabapathy K, et al (2006). Trp53-dependent DNA-repair is affected by the codon 72 polymorphism. Oncogene 25: 3489-3500. http://dx.doi.org/10.1038/sj.onc.1209405 Stankiewicz P, Lupski JR, et al (2002). Genome architecture, rearrangements and genomic disorders. Trends Genet. 18: 74-82. http://dx.doi.org/10.1016/S0168-9525(02)02592-1 Tada M, Furuuchi K, Kaneda M, Matsumoto J, et al (2001). Inactivate the remaining p53 allele or the alternate p73? Preferential selection of the Arg72 polymorphism in cancers with recessive p53 mutants but not transdominant mutants. Carcinogenesis 22: 515-517. http://dx.doi.org/10.1093/carcin/22.3.515 WHO (1999). World Health Organization Laboratory manual for the examination of human semen and sperm-cervical mucus interaction. 4th edn. Cambridge University Press, Cambridge.  
2012
A. M. Barbosa, Frare, A. B., Costa, N. B., Silva, R. E., and Moura, K. K. V. O., GSTM1 polymorphism in patients with primary open-angle glaucoma, vol. 11, pp. 3256-3262, 2012.
Abu-Amero KK, Morales J, Mohamed GH, Osman MN, et al. (2008). Glutathione S-transferase M1 and T1 polymorphisms in Arab glaucoma patients. Mol. Vis. 14: 425-430. PMid:18334963 PMCid:2268859   Board PG, Baker RT, Chelvanayagam G and Jermiin LS (1997). Zeta, a novel class of glutathione transferases in a range of species from plants to humans. Biochem. J. 328: 929-935. PMid:9396740 PMCid:1219006   Dias JFP and Almeida HG (2000). Glaucoma. 2ª ed. Cultura Médica, Rio de Janeiro.   Izzotti A, Bagnis A and Sacca SC (2006). The role of oxidative stress in glaucoma. Mutat. Res. 612: 105-114. http://dx.doi.org/10.1016/j.mrrev.2005.11.001 PMid:16413223   Juronen E, Tasa G, Veromann S, Parts L, et al. (2000). Polymorphic glutathione S-transferase M1 is a risk factor of primary open-angle glaucoma among Estonians. Exp. Eye Res. 71: 447-452. http://dx.doi.org/10.1006/exer.2000.0899 PMid:11040079   Kamal D and Hitchings R (1998). Normal tension glaucoma - a practical approach. Br. J. Ophthalmol. 82: 835-840. http://dx.doi.org/10.1136/bjo.82.7.835 PMid:9924383 PMCid:1722650   Kanski JJ (2003). Oftalmologia Clínica: Uma Abordagem Sistemática. 5ª ed. Elsevier, Rio de Janeiro.   Katoh T, Yamano Y, Tsuji M and Watanabe M (2008). Genetic polymorphisms of human cytosol glutathione S-transferases and prostate cancer. Pharmacogenomics 9: 93-104. http://dx.doi.org/10.2217/14622416.9.1.93 PMid:18154451   Leske MC (1983). The epidemiology of open-angle glaucoma: a review. Am. J. Epidemiol. 118: 166-191. PMid:6349332   Marigo FA, Cronemberger S and Calixto N (2001). Neuroproteção: situação atual no glaucoma. Arq. Bras. Oftalmol. 64: 167-171. http://dx.doi.org/10.1590/S0004-27492001000200016   Quigley HA (1996). Number of people with glaucoma worldwide. Br. J. Ophthalmol. 80: 389-393. http://dx.doi.org/10.1136/bjo.80.5.389 PMid:8695555 PMCid:505485   Quigley HA and Broman AT (2006). The number of people with glaucoma worldwide in 2010 and 2020. Br. J. Ophthalmol. 90: 262-267. http://dx.doi.org/10.1136/bjo.2005.081224 PMid:16488940 PMCid:1856963   Quigley HA, Nickells RW, Kerrigan LA, Pease ME, et al. (1995). Retinal ganglion cell death in experimental glaucoma and after axotomy occurs by apoptosis. Invest. Ophthalmol. Vis. Sci. 36: 774-786. PMid:7706025   Racette L, Wilson MR, Zangwill LM, Weinreb RN, et al. (2003). Primary open-angle glaucoma in blacks: a review. Surv. Ophthalmol. 48: 295-313. http://dx.doi.org/10.1016/S0039-6257(03)00028-6   Rebbeck TR (1997). Molecular epidemiology of the human glutathione S-transferase genotypes GSTM1 and GSTT1 in cancer susceptibility. Cancer Epidemiol. Biomarkers Prev. 6: 733-743. PMid:9298582   Ritch R, Shields MB and Krupin T (1996). The Glaucomas. Basic Sciences Vol. 1. 2nd edn. Mosby - Year Book, St. Louis.   Sarfarazi M, Akarsu AN, Hossain A, Turacli ME, et al. (1995). Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics 30: 171-177. http://dx.doi.org/10.1006/geno.1995.9888 PMid:8586416   Uhm KB and Shin DH (1992). Positive family history of glaucoma is a risk factor for increased IOP rather than glaucomatous optic nerve damage (POAG vs OH vs normal control). Korean J. Ophthalmol. 6: 100-104. PMid:1301446   Unal M, Guven M, Devranoglu K, Ozaydin A, et al. (2007). Glutathione S transferase M1 and T1 genetic polymorphisms are related to the risk of primary open-angle glaucoma: a study in a Turkish population. Br. J. Ophthalmol. 91: 527-530. http://dx.doi.org/10.1136/bjo.2006.102418 PMid:16973661 PMCid:1994754   Wiggs JL (2007). Genetic etiologies of glaucoma. Arch. Ophthalmol. 125: 30-37. http://dx.doi.org/10.1001/archopht.125.1.30 PMid:17210849
2011
I. R. Costa, Silva, R. C. P. C., Frare, A. B., Silva, C. T. X., Bordin, B. M., Souza, S. R., Júnior, C. L. Ribeiro, and Moura, K. K. V. O., Polymorphism of the progesterone receptor gene associated with endometriosis in patients from Goiás, Brazil, vol. 10, pp. 1364-1370, 2011.
Abrão MS, Podgaec S and Dias JA Jr (2007). Endometriose, a mulher moderna e o Brasil. Prat. Hosp. 50: 73-77. Berbel BT, Podgaec S and Abrão MS (2008). Análise da associação entre o quadro clínico referido pelas pacientes portadoras de endometriose e o local de acometimento da doença. Rev. Med. 87: 195-200. Carvalho CV, D’Amota P, Sato H, Girão MJBC, et al. (2004). Polimorfismo do gene do receptor de progesterona (PROGINS) em mulheres com endometriose pélvica. RBGO 26: 613-617. doi:10.1590/S0100-72032004000800004 Dentillo DB (2007). Expressão Gênica Diferencial em Tecido Endometrial Tópico e Lesões Endometrióticas. Doctoral thesis, Faculdade de Medicina de Ribeirão Preto, USP, Ribeirão Preto. Donaldson CJ, Crapanzano JP, Watson JC, Levine EA, et al. (2002). PROGINS Alu insertion and human genomic diversity. Mutat. Res. 501: 137-141. doi:10.1016/S0027-5107(02)00015-5 Giordano MG (1998). Ginecologia Endócrina e da Reprodução. Fundo Editorial BYK, São Paulo, 225. Gomes MTV, Castro RA, Villanova FE, Silva IDCG, et al. (2006). Relação entre polimorfismo do gene do receptor de progesterona, raça, paridade e ocorrência de leiomioma uterino. Rev. Bras. Ginecol. Obstet. 28: 278-284. doi:10.1590/S0100-72032006000500003 Hurtado R (2008). Análise Inter e Intra-Observador no Diagnóstico Anátomo-Patológico de Endometriose. Master’s thesis, Faculdade de Medicina, UFMG, Belo Horizente. Johnson MCP, Pinto CO, Alves ALC, Palomino AA, et al. (2004). P450 arom y microambiente estrogénico en endometrios eutópicos de mujeres con endometriosis. Rev. Med. Chile 132: 1475-1482. PMid:15743158 Kamergorodsky G (2007). Avaliação da Classificação Histológica da Endometriose Observada em Implantes de Mulheres Portadoras de Endometriose Pélvica Superficial e Profunda. Master’s thesis, Faculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo. Lattuada D, Viganò P, Somigliana E, Abbiati A, et al. (2004). Analysis of the codon 72 polymorphism of the TP53 gene in patients with endometriosis. Mol. Hum. Reprod. 10: 651-654. doi:10.1093/molehr/gah093 PMid:15273281 Moura MD, Pereira TN, Nogueira AA, Ferriani RA, et al. (1999). Avaliação do tratamento clínico da endometriose. Rev. Bras. Ginecol. Obstet. 21: 85-90. Nakata LC, Goloni-Bertollo EM, Dos Santos I, Oliani AH, et al. (2004). Biomarcadores de susceptibilidade à endometriosis. RBGO 26: 299-304. doi:10.1590/S0100-72032004000400006 Pearce CL, Hirschhorn JN, Wu AH, Burtt NP, et al. (2005). Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis. J. Natl. Cancer Inst. 97: 51-59. doi:10.1093/jnci/dji007 PMid:15632380 Ranney B (1980). Endometriosis: Pathogenesis, symptoms, and findings. Clin. Obstet. Gynecol. 23: 865-874. doi:10.1097/00003081-198023030-00016 PMid:7418286 Renner SP, Strick R, Oppelt P, Fasching PA, et al. (2006). Evaluation of clinical parameters and estrogen receptor alpha gene polymorphisms for patients with endometriosis. Reproduction 131: 153-161. doi:10.1530/rep.1.00787 PMid:16388018 Riachi SHMS (2008). Imunoexpressão da Enzima Aromatase p450 em Espécimes Cirúrgicos de Mulheres Portadoras de Endometriose Pélvica Profunda. Master’s thesis, Faculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo. Sampson JA (1927). Peritoneal endometriosis due to the menstrual dissemination of endometrial tissue into the peritonial cavity. Am. J. Obstet. Gynecol. 14: 469. Tempfer CB, Simoni M, Destenaves B and Fauser BC (2009). Functional genetic polymorphisms and female reproductive disorders: part II - endometriosis. Hum. Reprod. Update 15: 97-118. doi:10.1093/humupd/dmn040 PMid:18805939    PMCid:2639061 Treloar SA, Zhao ZZ, Armitage T, Duffy DL, et al. (2005). Association between polymorphisms in the progesterone receptor gene and endometriosis. Mol. Hum. Reprod. 11: 641-647. doi:10.1093/molehr/gah221 PMid:16126772 van Kaam KJ, Romano A, Schouten JP, Dunselman GA, et al. (2007). Progesterone receptor polymorphism +331G/A is associated with a decreased risk of deep infiltrating endometriosis. Hum. Reprod. 22: 129-135. doi:10.1093/humrep/del325 PMid:16920727 Wieser F, Scheneeberger C, Tong D, Tempfer C, et al. (2002). PROGINS receptor gene polymorphism is associated with endometrioses. Fertil Steril. 77: 309-312. doi:10.1016/S0015-0282(01)02984-3
R. C. P. C. Silva, Costa, I. R., Bordin, B. M., Silva, C. T. X., Souza, S. R., Júnior, C. L. R., Frare, A. B., and Moura, K. K. V. O., RsaI polymorphism of the ERβgene in women with endometriosis, vol. 10, pp. 465-470, 2011.
Aschim EL, Giwercman A, Stahl O, Eberhard J, et al. (2005). The RsaI polymorphism in the estrogen receptor-beta gene is associated with male infertility. J. Clin. Endocrinol. Metab. 90: 5343-5348. http://dx.doi.org/10.1210/jc.2005-0263 PMid:15998774   Chang PL, Zeitoun KM, Chan LK, Thornton MH, et al. (2002). GnRH antagonist in older IVF patients. Retrieval rates and clinical outcome. J. Reprod. Med. 47: 253-258. PMid:12012875   Enmark E, Pelto-Huikko M, Grandien K, Lagercrantz S, et al. (1997). Human estrogen receptor beta-gene structure, chromosomal localization, and expression pattern. J. Clin. Endocrinol. Metab. 82: 4258-4265. http://dx.doi.org/10.1210/jc.82.12.4258 PMid:9398750   Galliano D (2009). Polimorfismos Genéticos da Rota Estrogênica que Influenciam a Duração da Janela Fértil na Mulher. Masther's thesis, Departamento de Ginecologia e Obstetrícia da Faculdade de Medicina, Universidade de Granada, Granada.   Hapangama DK, Turner MA, Drury JA, Quenby S, et al. (2008). Endometriosis is associated with aberrant endometrial expression of telomerase and increased telomere length. Hum. Reprod. 23: 1511-1519. http://dx.doi.org/10.1093/humrep/den172 PMid:18456668   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   Miller AS, 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   Nakata LC, Goloni-Bertollo EM, Dos Santos I, Antonio H, et al. (2004). Biomarcadores de susceptibilidade à endometriosis. Rev. Bras. Ginecol. Obstet. 26: 299-304. http://dx.doi.org/10.1590/S0100-72032004000400006   Renner SP, Strick R, Oppelt P, Fasching PA, et al. (2006). Evaluation of clinical parameters and estrogen receptor alpha gene polymorphisms for patients with endometriosis. Reproduction 131: 153-161. http://dx.doi.org/10.1530/rep.1.00787 PMid:16388018   Sneige N, Liu B, Yin G, Gong Y, et al. (2006). Correlation of cytologic findings and chromosomal instability detected by fluorescence in situ hybridization in breast fine-needle aspiration specimens from women at high risk for breast cancer. Mod. Pathol. 19: 622-629. http://dx.doi.org/10.1038/modpathol.3800571 PMid:16528376   Sundarrajan C, Liao WX, Roy AC and Ng SC (2001). Association between estrogen receptor-beta gene polymorphisms and ovulatory dysfunctions in patients with menstrual disorders. J. Clin. Endocrinol. Metab. 86: 135-139. http://dx.doi.org/10.1210/jc.86.1.135 PMid:11231990   Tempfer CB, Simoni M, Destenaves B and Fauser BC (2009). Functional genetic polymorphisms and female reproductive disorders: Part II - endometriosis. Hum. Reprod. Update 15: 97-118. http://dx.doi.org/10.1093/humupd/dmn040 PMid:18805939 PMCid:2639061   Tsukamoto K, Inoue S, Hosoi T, Orimo H, et al. (1998). Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human estrogen receptor beta locus. J. Hum. Genet. 43: 73-74. http://dx.doi.org/10.1007/s100380050043 PMid:9610005   Zhao Y, Kreger DO and Brannian JD (2000). Serum leptin concentrations in women during gonadotropin stimulation cycles. J. Reprod. Med. 45: 121-125. PMid:10710742
2010
C. O. A. Melo, Danin, A. R., Silva, D. M., Tacon, J. A., Moura, K. K. V. O., Costa, E. O. A., and da Cruz, A. D., Association between male infertility and androgen receptor mutations in Brazilian patients, vol. 9, pp. 128-133, 2010.
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