Publications
Found 7 results
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, “Association of CYP1A1 (cytochrome P450) MspI polymorphism in women with endometriosis”, vol. 15, p. -, 2016.
, “Association of CYP1A1 (cytochrome P450) MspI polymorphism in women with endometriosis”, vol. 15, p. -, 2016.
, “Association between CYP1A1m1 gene polymorphism and primary open-angle glaucoma”, vol. 13, pp. 10382-10389, 2014.
, “GSTM1 and GSTT1 polymorphisms in endometriosis in women from Goiás, Brazil”, vol. 12, pp. 2764-2770, 2013.
, “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
, “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
, “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