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“Association between methylene tetrahydrofolate reductase and glutathione S-transferase M1 gene polymorphisms and chronic myeloid leukemia in a Brazilian population”, vol. 11, pp. 1013-1026, 2012.
, Alves-Silva J, da Silva SM, Guimaraes PE, Ferreira AC, et al. (2000). The ancestry of Brazilian mtDNA lineages. Am. J. Hum. Genet. 67: 444-461.
http://dx.doi.org/10.1086/303004
PMid:10873790
Anisimov VN (2007). Biology of aging and cancer. Cancer Control 14: 23-31.
Barbosa CG, Souza CL, Moura Neto JP, Arruda MGB, et al. (2008). Methylenetetrahydrofolate reductase polymorphisms in myeloid leukemia patients from Northeastern Brazil. Genet. Mol. Biol. 31: 29-32.
http://dx.doi.org/10.1590/S1415-47572008000100005
Barreiro LB, Laval G, Quach H, Patin E, et al. (2008). Natural selection has driven population differentiation in modern humans. Nat. Genet. 40: 340-345.
http://dx.doi.org/10.1038/ng.78
PMid:18246066
Bowen DT, Frew ME, Rollinson S, Roddam PL, et al. (2003). CYP1A1*2B (Val) allele is overrepresented in a subgroup of acute myeloid leukemia patients with poor-risk karyotype associated with NRAS mutation, but not associated with FLT3 internal tandem duplication. Blood 101: 2770-2774.
http://dx.doi.org/10.1182/blood-2002-01-0228
PMid:12468438
Campregher PV, Lorand-Metze I, Grotto HZW and Sonati MF (2004). Haptoglobin phenotypes in Brazilian patients with leukemia. Braz. J. Pathol. Lab. Med. 40: 307-309.
http://dx.doi.org/10.1590/S1676-24442004000500005
Carter K and Worwood M (2007). Haptoglobin: a review of the major allele frequencies worldwide and their association with diseases. Int. J. Lab. Hematol. 29: 92-110.
http://dx.doi.org/10.1111/j.1751-553X.2007.00898.x
PMid:17474882
Chen CL, Liu Q and Relling MV (1996). Simultaneous characterization of glutathione S-transferase M1 and T1 polymorphisms by polymerase chain reaction in American whites and blacks. Pharmacogenetics 6: 187-191.
http://dx.doi.org/10.1097/00008571-199604000-00005
PMid:9156696
Chin YM, Bosco JJ and Koh CL (1992). Analysis of ras gene mutations in acute myeloid leukemia by the polymerase chain reaction and oligonucleotide probes. Singapore Med. J. 33: 48-50.
PMid:1598607
Cotton SC, Sharp L, Little J and Brockton N (2000). Glutathione S-transferase polymorphisms and colorectal cancer: a HuGE review. Am. J. Epidemiol. 151: 7-32.
http://dx.doi.org/10.1093/oxfordjournals.aje.a010124
PMid:10625170
Crump C, Chen C, Appelbaum FR, Kopecky KJ, et al. (2000). Glutathione S-transferase theta 1 gene deletion and risk of acute myeloid leukemia. Cancer Epidemiol. Biomarkers Prev. 9: 457-460.
PMid:10815689
Duthie SJ, Narayanan S, Brand GM, Pirie L, et al. (2002). Impact of folate deficiency on DNA stability. J. Nutr. 132: 2444S-2449S.
PMid:12163709
Franco RF, Morelli V, Lourenco D, Maffei FH, et al. (1999). A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease. Br. J. Haematol. 105: 556-559.
http://dx.doi.org/10.1111/j.1365-2141.1999.01254.x
PMid:10233437
Franco RF, Simoes BP, Tone LG, Gabellini SM, et al. (2001). The methylenetetrahydrofolate reductase C677T gene polymorphism decreases the risk of childhood acute lymphocytic leukaemia. Br. J. Haematol. 115: 616-618.
http://dx.doi.org/10.1046/j.1365-2141.2001.03140.x
PMid:11736945
Frezza M, Tritapepe R, Pozzato G and Di Padova C (1988). Prevention of S-adenosylmethionine of estrogen-induced hepatobiliary toxicity in susceptible women. Am. J. Gastroenterol. 83: 1098-1102.
PMid:3421220
Fryer AA, Zhao L, Alldersea J, Pearson WR, et al. (1993). Use of site-directed mutagenesis of allele-specific PCR primers to identify the GSTM1 A, GSTM1 B, GSTM1 A,B and GSTM1 null polymorphisms at the glutathione S-transferase, GSTM1 locus. Biochem. J. 295: 313-315.
PMid:8216235 PMCid:1134855
Hengstler JG, Arand M, Herrero ME and Oesch F (1998). Polymorphisms of N-acetyltransferases, glutathione S-transferases, microsomal epoxide hydrolase and sulfotransferases: influence on cancer susceptibility. Recent Results Cancer Res. 154: 47-85.
http://dx.doi.org/10.1007/978-3-642-46870-4_4
Hiragi CO, Miranda-Vilela AL, Rocha DMS, Oliveira SF, et al. (2011). Superoxide dismutase, catalase, glutathione Gene polymorphisms associated with CML in Brazil peroxidase and gluthatione S-transferases M1 and T1 gene polymorphisms in three Brazilian population groups. Genet. Mol. Biol. 34: 11-18.
PMid:21637536 PMCid:3085354
Hishida A, Terakura S, Emi N, Yamamoto K, et al. (2005). GSTT1 and GSTM1 deletions, NQO1 C609T polymorphism and risk of chronic myelogenous leukemia in Japanese. Asian Pac. J. Cancer Prev. 6: 251-255.
PMid:16235982
Hur M, Park JY, Cho HC, Lee KM, et al. (2006). Methylenetetrahydrofolate reductase A1298C genotypes are associated with the risks of acute lymphoblastic leukaemia and chronic myelogenous leukaemia in the Korean population. Clin. Lab. Haematol. 28: 154-159.
http://dx.doi.org/10.1111/j.1365-2257.2006.00769.x
PMid:16706930
Ismail SI, Ababneh NA and Awidi A (2009). Methylenetetrahydrofolate reductase (MTHFR) genotype association with the risk of chronic myelogenous leukemia. Jordan Med. J. 43: 8-14.
Kim DH, Xu W, Ma C, Liu X, et al. (2009). Genetic variants in the candidate genes of the apoptosis pathway and susceptibility to chronic myeloid leukemia. Blood 113: 2517-2525.
http://dx.doi.org/10.1182/blood-2008-07-169110
PMid:19141860
Kim I, Lee KH, Kim JH, Ra EK, et al. (2007). Polymorphisms of the methylenetetrahydrofolate reductase gene and clinical outcomes in HLA-matched sibling allogeneic hematopoietic stem cell transplantation. Ann. Hematol. 86: 41-48.
http://dx.doi.org/10.1007/s00277-006-0184-3
PMid:17028897
Landi S (2000). Mammalian class theta GST and differential susceptibility to carcinogens: a review. Mutat. Res. 463: 247-283.
http://dx.doi.org/10.1016/S1383-5742(00)00050-8
Lourenço GJ, Ortega MM, Nascimento H, Teori MT, et al. (2005). Polymorphisms of glutathione S-transferase mu1 (GSTM1) and theta 1 (GSTT1) genes in chronic myeloid leukaemia. Eur. J. Haematol. 75: 530-531.
http://dx.doi.org/10.1111/j.1600-0609.2005.00567.x
PMid:16313269
Ma J, Stampfer MJ, Giovannucci E, Artigas C, et al. (1997). Methylenetetrahydrofolate reductase polymorphism, dietary interactions, and risk of colorectal cancer. Cancer Res. 57: 1098-1102.
PMid:9067278
Maciel ME, Oliveira FK, Propst GB, Bicalho MG, et al. (2009). Population analysis of xenobiotic metabolizing genes in South Brazilian Euro and Afro-descendants. Genet. Mol. Biol. 32: 723-728.
http://dx.doi.org/10.1590/S1415-47572009005000087
PMid:21637445 PMCid:3036891
Miranda-Vilela AL, Alves PC, Akimoto AK, Lordelo GS, et al. (2010). Gene polymorphisms against DNA damage induced by hydrogen peroxide in leukocytes of healthy humans through comet assay: a quasi-experimental study. Environ. Health 9: 21.
http://dx.doi.org/10.1186/1476-069X-9-21
PMid:20444272 PMCid:2881052
Mitchell RJ, Carzino R and Janardhana V (1988). Associations between the two serum proteins haptoglobin and transferrin and leukaemia. Hum. Hered. 38: 144-150.
http://dx.doi.org/10.1159/000153775
PMid:3397067
Mondal BC, Paria N, Majumdar S, Chandra S, et al. (2005). Glutathione S-transferase M1 and T1 null genotype frequency in chronic myeloid leukaemia. Eur. J. Cancer Prev. 14: 281-284.
http://dx.doi.org/10.1097/00008469-200506000-00014
PMid:15901999
Moon HW, Kim TY, Oh BR, Min HC, et al. (2007). MTHFR 677CC/1298CC genotypes are highly associated with chronic myelogenous leukemia: a case-control study in Korea. Leuk. Res. 31: 1213-1217.
http://dx.doi.org/10.1016/j.leukres.2006.10.016
PMid:17156840
Nei M (1977). F-statistics and analysis of gene diversity in subdivided populations. Ann. Hum. Genet. 41: 225-233.
http://dx.doi.org/10.1111/j.1469-1809.1977.tb01918.x
PMid:596830
Nevo S and Tatarsky I (1986). Serum haptoglobin types and leukemia. Hum. Genet. 73: 240-244.
http://dx.doi.org/10.1007/BF00401236
PMid:3460960
Nowicki MO, Falinski R, Koptyra M, Slupianek A, et al. (2004). BCR/ABL oncogenic kinase promotes unfaithful repair of the reactive oxygen species-dependent DNA double-strand breaks. Blood 104: 3746-3753.
http://dx.doi.org/10.1182/blood-2004-05-1941
PMid:15304390
Oliveira JB, Bidere N, Niemela JE, Zheng L, et al. (2007). NRAS mutation causes a human autoimmune lymphoproliferative syndrome. Proc. Natl. Acad. Sci. U. S. A. 104: 8953-8958.
http://dx.doi.org/10.1073/pnas.0702975104
PMid:17517660 PMCid:1885609
Ozkan Y, Yardim-Akaydin S, Firat H, Caliskan-Can E, et al. (2007). Usefulness of homocysteine as a cancer marker: total thiol compounds and folate levels in untreated lung cancer patients. Anticancer Res. 27: 1185-1189.
PMid:17465261
Queiroz EP (2006). A Migração Intrametropolitana no Distrito Federal e Entorno: O Conseqüente Fluxo Pendular e o Uso dos Equipamentos Urbanos de Saúde e Educação. Available at [http://www.abep.nepo.unicamp.br/encontro2006/docspdf/ABEP2006_724.pdf]. Accessed May 6, 2011.
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
Robien K and Ulrich CM (2003). 5,10-Methylenetetrahydrofolate reductase polymorphisms and leukemia risk: a HuGE minireview. Am. J. Epidemiol. 157: 571-582.
http://dx.doi.org/10.1093/aje/kwg024
PMid:12672676
Robien K, Ulrich CM, Bigler J, Yasui Y, et al. (2004). Methylenetetrahydrofolate reductase genotype affects risk of relapse after hematopoietic cell transplantation for chronic myelogenous leukemia. Clin. Cancer Res. 10: 7592-7598.
http://dx.doi.org/10.1158/1078-0432.CCR-04-1057
PMid:15569990
Rover Júnior L, Höehr NF, Vellasco AP and Kubota LT (2001). Sistema antioxidante envolvendo o ciclo metabólico da glutationa associado a métodos eletroanalíticos na avaliação do estresse oxidativo. Quim. Nova 24: 112-119.
Sattler M, Verma S, Shrikhande G, Byrne CH, et al. (2000). The BCR/ABL tyrosine kinase induces production of reactive oxygen species in hematopoietic cells. J. Biol. Chem. 275: 24273-24278.
http://dx.doi.org/10.1074/jbc.M002094200
PMid:10833515
Serre D and Hudson TJ (2006). Resources for genetic variation studies. Annu. Rev. Genomics Hum. Genet. 7: 443-457.
http://dx.doi.org/10.1146/annurev.genom.7.080505.115806
PMid:16759172
Skibola CF, Smith MT, Kane E, Roman E, et al. (1999). Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults. Proc. Natl. Acad. Sci. U. S. A. 96: 12810-12815.
http://dx.doi.org/10.1073/pnas.96.22.12810
Souza CL, Barbosa CG, Neto JPM, Barreto JH, et al. (2008). Polymorphisms in the glutathione S-transferase theta and mu genes and susceptibility to myeloid leukemia in Brazilian patients. Genet. Mol. Biol. 31: 39-41.
http://dx.doi.org/10.1590/S1415-47572008000100008
Suarez-Kurtz G (2004). Pharmacogenomics in admixed populations: the Brazilian pharmacogenetics/pharmacogenomics network - REFARGEN. Pharmacogenomics J. 4: 347-348.
http://dx.doi.org/10.1038/sj.tpj.6500287
PMid:15549130
Ulrich CM, Kampman E, Bigler J, Schwartz SM, et al. (1999). Colorectal adenomas and the C677T MTHFR polymorphism: evidence for gene-environment interaction? Cancer Epidemiol. Biomarkers Prev. 8: 659-668.
PMid:10744125
van der Put NM, Gabreels F, Stevens EM, Smeitink JA, et al. (1998). A second common mutation in the methylenetet-rahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am. J. Hum. Genet. 62: 1044-1051.
http://dx.doi.org/10.1086/301825
PMid:9545395
Yano A, Yamamoto Y, Miyaishi S and Ishizu H (1998). Haptoglobin genotyping by allele-specific polymerase chain reaction amplification. Acta Med. Okayama 52: 173-181.
PMid:9781267
Yi P, Pogribny I and Jill JS (2002). Multiplex PCR for simultaneous detection of 677 C→T and 1298 A→C polymorphisms in methylenetetrahydrofolate reductase gene for population studies of cancer risk. Cancer Lett. 181: 209.
http://dx.doi.org/10.1016/S0304-3835(02)00060-5
“Evidence for an association between haptoglobin and MnSOD (Val9Ala) gene polymorphisms in essential hypertension based on a Brazilian case-control study”, vol. 9, pp. 2166-2175, 2010.
, Akyol O, Yanik M, Elyas H, Namli M, et al. (2005). Association between Ala-9Val polymorphism of Mn-SOD gene and schizophrenia. Prog. Neuropsychopharmacol. Biol. Psychiatry 29: 123-131.
http://dx.doi.org/10.1016/j.pnpbp.2004.10.014
PMid:15610954
Alexander RW (1995). Hypertension and the Pathogenesis of Atherosclerosis. Hypertension 25: 155-161.
http://dx.doi.org/10.1161/01.HYP.25.2.155
PMid:7843763
Alves-Silva J, da Silva SM, Guimaraes PE, Ferreira AC, et al. (2000). The ancestry of Brazilian mtDNA lineages. Am. J. Hum. Genet. 67: 444-461.
http://dx.doi.org/10.1086/303004
PMid:10873790 PMCid:1287189
Barreiro LB, Laval G, Quach H, Patin E, et al. (2008). Natural selection has driven population differentiation in modern humans. Nat. Genet. 40: 340-345.
http://dx.doi.org/10.1038/ng.78
PMid:18246066
Bastaki M, Huen K, Manzanillo P, Chande N, et al. (2006). Genotype-activity relationship for Mn-superoxide dismutase, glutathione peroxidase 1 and catalase in humans. Pharmacogenet. Genomics 16: 279-286.
http://dx.doi.org/10.1097/01.fpc.0000199498.08725.9c
PMid:16538174
Boing AC and Boing AF (2007). Hipertensão arterial sistêmica: o que nos dizem os sistemas brasileiros de cadastramentos e informações em saúde. Rev. Bras. Hipertens. 14: 84-88.
Carretero OA and Oparil S (2000). Essential hypertension. Part I: definition and etiology. Circulation 101: 329-335.
http://dx.doi.org/10.1161/01.CIR.101.3.329
PMid:10645931
Carter K and Worwood M (2007). Haptoglobin: a review of the major allele frequencies worldwide and their association with diseases. Int. J. Lab. Hematol. 29: 92-110.
http://dx.doi.org/10.1111/j.1751-553X.2007.00898.x
PMid:17474882
Caulfield M, Lavender P, Farrall M, Munroe P, et al. (1994). Linkage of the angiotensinogen gene to essential hypertension. N. Engl. J. Med. 330: 1629-1633.
http://dx.doi.org/10.1056/NEJM199406093302301
PMid:8177268
Chen CL, Liu Q and Relling MV (1996). Simultaneous characterization of glutathione S-transferase M1 and T1 polymorphisms by polymerase chain reaction in American whites and blacks. Pharmacogenetics 6: 187-191.
http://dx.doi.org/10.1097/00008571-199604000-00005
PMid:9156696
Choi JY, Neuhouser ML, Barnett MJ, Hong CC, et al. (2008). Iron intake, oxidative stress-related genes (MnSOD and MPO) and prostate cancer risk in CARET cohort. Carcinogenesis 29: 964-970.
http://dx.doi.org/10.1093/carcin/bgn056
PMid:18296681 PMCid:2902382
Cotton SC, Sharp L, Little J and Brockton N (2000). Glutathione S-transferase polymorphisms and colorectal cancer: a HuGE review. Am. J. Epidemiol. 151: 7-32.
http://dx.doi.org/10.1093/oxfordjournals.aje.a010124
PMid:10625170
Delanghe JR, Duprez DA, De Buyzere ML, Bergez BM, et al. (1995). Refractory hypertension is associated with the haptoglobin 2-2 phenotype. J. Cardiovasc. Risk 2: 131-136.
http://dx.doi.org/10.1097/00043798-199504000-00008
PMid:7606649
Delanghe J, Cambier B, Langlois M, De Buyzere M, et al. (1997). Haptoglobin polymorphism, a genetic risk factor in coronary artery bypass surgery. Atherosclerosis 132: 215-219.
http://dx.doi.org/10.1016/S0021-9150(97)00089-0
Dominiczak AF, Negrin DC, Clark JS, Brosnan MJ, et al. (2000). Genes and hypertension: from gene mapping in experimental models to vascular gene transfer strategies. Hypertension 35: 164-172.
http://dx.doi.org/10.1161/01.HYP.35.1.164
PMid:10642293
Ferreira ALA and Matsubara LS (1997). Radicais livres: conceitos, doenças relacionadas, sistema de defesa e estresse oxidativo. Rev. Assoc. Med. Bras. 43: 61-68.
http://dx.doi.org/10.1590/S0104-42301997000100014
PMid:9224995
Guéye PM, Glasser N, Ferard G and Lessinger JM (2006). Influence of human haptoglobin polymorphism on oxidative stress induced by free hemoglobin on red blood cells. Clin. Chem. Lab. Med. 44: 542-547.
http://dx.doi.org/10.1515/CCLM.2006.095
PMid:16681422
Harrison D, Griendling KK, Landmesser U, Hornig B, et al. (2003). Role of oxidative stress in atherosclerosis. Am. J. Cardiol. 91: 7A-11A.
http://dx.doi.org/10.1016/S0002-9149(02)03144-2
Hermes-Lima M (2004). Oxygen in Biology and Biochemistry: Role of Free Radicals. In: Functional Metabolism: Regulation and Adaptation. (Storey KB, ed.). Hoboken, New Jersey, 319-368.
Li JJ and Chen JL (2005). Inflammation may be a bridge connecting hypertension and atherosclerosis. Med. Hypotheses 64: 925-929.
http://dx.doi.org/10.1016/j.mehy.2004.10.016
PMid:15780486
Messerli FH, Williams B and Ritz E (2007). Essential hypertension. Lancet 370: 591-603.
http://dx.doi.org/10.1016/S0140-6736(07)61299-9
Mitrunen K, Sillanpaa P, Kataja V, Eskelinen M, et al. (2001). Association between manganese superoxide dismutase (MnSOD) gene polymorphism and breast cancer risk. Carcinogenesis 22: 827-829.
http://dx.doi.org/10.1093/carcin/22.5.827
PMid:11323405
Nakazono K, Watanabe N, Matsuno K, Sasaki J, et al. (1991). Does superoxide underlie the pathogenesis of hypertension? Proc. Natl. Acad. Sci U. S. A. 88: 10045-10048.
http://dx.doi.org/10.1073/pnas.88.22.10045
PMid:1658794 PMCid:52864
Neder MM and Borges AAN (2006). Hipertensão arterial sistêmica no Brasil: o que avançamos no conhecimento de sua epidemiologia? Rev. Bras. Hipertens. 13: 126-133.
Odawara M, Matsunuma A and Yamashita K (1997). Mistyping frequency of the angiotensin-converting enzyme gene polymorphism and an improved method for its avoidance. Hum. Genet. 100: 163-166.
http://dx.doi.org/10.1007/s004390050484
PMid:9254843
Olson SH, Carlson MDA, Ostrer H, Harlap S, et al. (2004). Genetic variants in SOD2, MPO, and NQO1, and risk of ovarian cancer. Gynecol. Oncol. 93: 615-620.
http://dx.doi.org/10.1016/j.ygyno.2004.03.027
PMid:15196853
Oparil S, Zaman MA and Calhoun DA (2003). Pathogenesis of hypertension. Ann. Intern. Med. 139: 761-776.
http://dx.doi.org/10.7326/0003-4819-139-9-200311040-00011
PMid:14597461
Pasha MA, Khan AP, Kumar R, Ram RB, et al. (2002). Variations in angiotensin-converting enzyme gene insertion/ deletion polymorphism in Indian populations of different ethnic origins. J. Biosci. 27: 67-70.
http://dx.doi.org/10.1007/BF02703684
PMid:11927778
Passos VMA, Assis TD and Barreto SM (2006). Hipertensão arterial no Brasil: estimativa de prevalência a partir de estudos de base populacional. Epidemiol. Serv. Saúde 15: 35-45.
Prabha S, Padma T and Ramaswamy M (1987). Haptoglobin patterns in essential hypertension and associated conditions - increased risk for Hp 2-2. Hum. Hered. 37: 345-348.
http://dx.doi.org/10.1159/000153732
Queiroz EP (2006). A Migração Intrametropolitana no Distrito Federal e Entorno: o Conseqüente Fluxo Pendular e o Uso dos Equipamentos Urbanos de Saúde e Educação. http://www.abep.nepo.unicamp.br/encontro2006/docspdf/ABEP2006_724.pdf. Accessed June 20, 2010.
Rola MG and Ferreira LB (2008). Polimorfismos genéticos associados à hipertensão arterial sistêmica. Univ. Cienc. Saúde 6: 57-68.
Rigat B, Hubert C, Corvol P and Soubrier F (1992). PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1). Nucleic Acids Res. 20: 1433.
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PMid:1313972 PMCid:312213
Sagnella GA, Rothwell MJ, Onipinla AK, Wicks PD, et al. (1999). A population study of ethnic variations in the angiotensin-converting enzyme I/D polymorphism: relationships with gender, hypertension and impaired glucose metabolism. J. Hypertens. 17: 657-664.
http://dx.doi.org/10.1097/00004872-199917050-00009
PMid:10403609
Thomas GN, Young RP, Tomlinson B, Woo KS, et al. (2000). Renin-angiotensin-aldosterone system gene polymorphisms and hypertension in Hong Kong Chinese. Clin. Exp. Hypertens. 22: 87-97.
http://dx.doi.org/10.1081/CEH-100100064
PMid:10685727
Ukkola O, Erkkila PH, Savolainen MJ and Kesaniemi YA (2001). Lack of association between polymorphisms of catalase, copper-zinc superoxide dismutase (SOD), extracellular SOD and endothelial nitric oxide synthase genes and macroangiopathy in patients with type 2 diabetes mellitus. J. Intern. Med. 249: 451-459.
http://dx.doi.org/10.1046/j.1365-2796.2001.00828.x
PMid:11350569
Wang Z and Hoy WE (2004). Waist circumference, body mass index, hip circumference and waist-to-hip ratio as predictors of cardiovascular disease in Aboriginal people. Eur. J. Clin. Nutr. 58: 888-893.
http://dx.doi.org/10.1038/sj.ejcn.1601891
PMid:15164109
Yano A, Yamamoto Y, Miyaishi S and Ishizu H (1998). Haptoglobin genotyping by allele-specific polymerase chain reaction amplification. Acta Med. Okayama 52: 173-181.
PMid:9781267
Zhao H, Liang D, Grossman HB and Wu X (2005). Glutathione peroxidase 1 gene polymorphism and risk of recurrence in patients with superficial bladder cancer. Urology 66: 769-774.
http://dx.doi.org/10.1016/j.urology.2005.04.033
PMid:16230136