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“Cytotoxic T lymphocyte antigen-4 (CTLA-4) rs231775 and rs5792909 polymorphisms are not associated with adult- and childhood-onset type 1 diabetes in a Southern Brazilian population”, Genetics and Molecular Research, vol. 20, no. 2, 2021.
, “The IL18 rs1946518 and PTPN22 rs2476601 polymorphisms are not associated with adult- and childhood-onset type 1 diabetes mellitus”, Genetics and Molecular Research, vol. 19, no. 4, 2020.
, “Polymorphism V362F (rs2304256) of tyrosine kinase 2 is not associated with childhood- or adulthood-onset type 1 diabetes in southern Brazil”, Genetics and Molecular Research, vol. 18, 3 vol., no. 3. 2019.
, “Polymorphisms rs1800795 of interleukin-6 and rs2228145 of interleukin-6 receptor genes in Euro-Brazilians with adult-onset type 1 diabetes mellitus”, Genetics and Molecular Research, vol. 18, no. 3, 2019.
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“Low prevalence of glucokinase gene mutations in gestational diabetic patients with good glycemic control”, vol. 11, pp. 1433-1441, 2012.
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American Diabetes Association (2010). Diagnosis and classification of diabetes mellitus. Diabetes Care 33 (Suppl 1): S62-S69.
http://dx.doi.org/10.2337/dc10-S062
PMid:20042775 PMCid:2797383
American Diabetes Association (2011). Diagnosis and classification of diabetes mellitus. Diabetes Care 34 (Suppl 1): S62-S69.
http://dx.doi.org/10.2337/dc11-S062
PMid:21193628 PMCid:3006051
Arden C, Harbottle A, Baltrusch S, Tiedge M, et al. (2004). Glucokinase is an integral component of the insulin granules in glucose-responsive insulin secretory cells and does not translocate during glucose stimulation. Diabetes 53: 2346-2352.
http://dx.doi.org/10.2337/diabetes.53.9.2346
PMid:15331544
Ben-Haroush A, Yogev Y and Hod M (2004). Epidemiology of gestational diabetes mellitus and its association with Type 2 diabetes. Diabet. Med. 21: 103-113.
http://dx.doi.org/10.1046/j.1464-5491.2003.00985.x
PMid:14984444
de la Iglesia N, Veiga-da-Cunha M, Van Schaftingen E, Guinovart JJ, et al. (1999). Glucokinase regulatory protein is essential for the proper subcellular localisation of liver glucokinase. FEBS Lett. 456: 332-338.
http://dx.doi.org/10.1016/S0014-5793(99)00971-0
Ellard S, Beards F, Allen LI, Shepherd M, et al. (2000). A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria. Diabetologia 43: 250-253.
http://dx.doi.org/10.1007/s001250050038
PMid:10753050
Gloyn AL (2003). Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy. Hum. Mutat. 22: 353-362.
http://dx.doi.org/10.1002/humu.10277
PMid:14517946
Greeley SA, Tucker SE, Worrell HI, Skowron KB, et al. (2010). Update in neonatal diabetes. Curr. Opin. Endocrinol. Diabetes Obes. 17: 13-19.
PMid:19952737
Grundy SM, Cleeman JI, Daniels SR, Donato KA, et al. (2006). Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute scientific statement. Curr. Opin. Cardiol. 21: 1-6.
http://dx.doi.org/10.1097/01.hco.0000200416.65370.a0
PMid:16355022
Hayashi K (1991). PCR-SSCP: a simple and sensitive method for detection of mutations in the genomic DNA. PCR Methods Appl. 1: 34-38.
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Iynedjian PB (2009). Molecular physiology of mammalian glucokinase. Cell Mol. Life Sci. 66: 27-42.
http://dx.doi.org/10.1007/s00018-008-8322-9
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Jetton TL, Liang Y, Pettepher CC, Zimmerman EC, et al. (1994). Analysis of upstream glucokinase promoter activity in transgenic mice and identification of glucokinase in rare neuroendocrine cells in the brain and gut. J. Biol. Chem. 269: 3641-3654.
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http://dx.doi.org/10.2337/diacare.3.3.416
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Kousta E, Ellard S, Allen LI, Saker PJ, et al. (2001). Glucokinase mutations in a phenotypically selected multiethnic group of women with a history of gestational diabetes. Diabet. Med. 18: 683-684.
http://dx.doi.org/10.1046/j.1464-5491.2001.00530.x
PMid:11553210
Lahiri DK and Nurnberger JI Jr (1991). A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies. Nucleic Acids Res. 19: 5444.
http://dx.doi.org/10.1093/nar/19.19.5444
PMid:1681511 PMCid:328920
Liang Z, Dong M, Cheng Q and Chen D (2010). Gestational diabetes mellitus screening based on the gene chip technique. Diabetes Res. Clin. Pract. 89: 167-173.
http://dx.doi.org/10.1016/j.diabres.2010.04.001
PMid:20554072
Magnuson MA and Shelton KD (1989). An alternate promoter in the glucokinase gene is active in the pancreatic beta cell. J. Biol. Chem. 264: 15936-15942.
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Marcinkevage JA and Narayan KM (2011). Gestational diabetes mellitus: taking it to heart. Prim. Care Diabetes 5: 81-88.
http://dx.doi.org/10.1016/j.pcd.2010.10.002
PMid:21106447
Matschinsky FM (2009). Assessing the potential of glucokinase activators in diabetes therapy. Nat. Rev. Drug. Discov. 8: 399-416.
http://dx.doi.org/10.1038/nrd2850
PMid:19373249
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Matschinsky FM, Magnuson MA, Zelent D, Jetton TL, et al. (2006). The network of glucokinase-expressing cells in glucose homeostasis and the potential of glucokinase activators for diabetes therapy. Diabetes 55: 1-12.
http://dx.doi.org/10.2337/diabetes.55.01.06.db05-0926
PMid:16380470
Metzger BE, Phelps RL, Freinkel N and Navickas IA (1980). Effects of gestational diabetes on diurnal profiles of plasma glucose, lipids, and individual amino acids. Diabetes Care 3: 402-409.
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Meyers-Seifer CH and Vohr BR (1996). Lipid levels in former gestational diabetic mothers. Diabetes Care 19: 1351-1356.
http://dx.doi.org/10.2337/diacare.19.12.1351
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PMid:2565038 PMCid:286999
Osbak KK, Colclough K, Saint-Martin C, Beer NL, et al. (2009). Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia. Hum. Mutat. 30: 1512-1526.
http://dx.doi.org/10.1002/humu.21110
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http://dx.doi.org/10.1146/annurev.nu.13.070193.002335
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Riskin-Mashiah S, Younes G, Damti A and Auslender R (2009). First-trimester fasting hyperglycemia and adverse pregnancy outcomes. Diabetes Care 32: 1639-1643.
http://dx.doi.org/10.2337/dc09-0688
PMid:19549728 PMCid:2732138
Rivero K, Portal VL, Vieira M and Behle I (2008). Prevalence of the impaired glucose metabolism and its association with risk factors for coronary artery disease in women with gestational diabetes. Diabetes Res. Clin. Pract. 79: 433-437.
http://dx.doi.org/10.1016/j.diabres.2007.10.015
PMid:18045723
Rose CS, Ek J, Urhammer SA, Glumer C, et al. (2005). A -30G>A polymorphism of the beta-cell-specific glucokinase promoter associates with hyperglycemia in the general population of whites. Diabetes 54: 3026-3031.
http://dx.doi.org/10.2337/diabetes.54.10.3026
PMid:16186409
Rosenberg TJ, Garbers S, Lipkind H and Chiasson MA (2005). Maternal obesity and diabetes as risk factors for adverse pregnancy outcomes: differences among 4 racial/ethnic groups. Am. J. Public. Health 95: 1545-1551.
http://dx.doi.org/10.2105/AJPH.2005.065680
PMid:16118366 PMCid:1449396
Rubio-Cabezas O, Klupa T and Malecki MT (2011). Permanent neonatal diabetes mellitus - the importance of diabetes differential diagnosis in neonates and infants. Eur. J. Clin. Invest. 41: 323-333.
http://dx.doi.org/10.1111/j.1365-2362.2010.02409.x
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Ruzzo A, Andreoni F and Magnani M (1998). Structure of the human hexokinase type I gene and nucleotide sequence of the 5' flanking region. Biochem. J. 331 (Pt 2): 607-613.
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Santos IC, Daga DR, Frigeri HR, Rea RR, et al. (2010a). The functional polymorphisms -429T>C and -374T>A of the RAGE gene promoter are not associated with gestational diabetes in Euro-Brazilians. Genet. Mol. Res. 9: 1130-1135.
http://dx.doi.org/10.4238/vol9-2gmr817
PMid:20568058
Santos IC, Frigeri HR, Rea RR, Almeida AC, et al. (2010b). The glucokinase gene promoter polymorphism -30G>A (rs1799884) is associated with fasting glucose in healthy pregnant women but not with gestational diabetes. Clin. Chim. Acta 411: 892-893.
http://dx.doi.org/10.1016/j.cca.2010.03.011
PMid:20227404
Schmidt MI, Matos MC, Reichelt AJ, Forti AC, et al. (2000). Prevalence of gestational diabetes mellitus - do the new WHO criteria make a difference? Brazilian Gestational Diabetes Study Group. Diabet. Med. 17: 376-380.
http://dx.doi.org/10.1046/j.1464-5491.2000.00257.x
PMid:10872537
Souza RL, Mikami LR, Maegawa RO and Chautard-Freire-Maia EA (2005). Four new mutations in the BCHE gene of human butyrylcholinesterase in a Brazilian blood donor sample. Mol. Genet. Metab. 84: 349-353.
http://dx.doi.org/10.1016/j.ymgme.2004.12.005
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Tinto N, Zagari A, Capuano M, De Simone A, et al. (2008). Glucokinase gene mutations: structural and genotype-phenotype analyses in MODY children from South Italy. PLoS One 3: e1870.
Weedon MN, Frayling TM, Shields B, Knight B, et al. (2005). Genetic regulation of birth weight and fasting glucose by a common polymorphism in the islet cell promoter of the glucokinase gene. Diabetes 54: 576-581.
http://dx.doi.org/10.2337/diabetes.54.2.576
PMid:15677518
“Virulence characteristics and antimicrobial susceptibility of uropathogenic Escherichia coli strains”, vol. 10, pp. 4114-4125, 2011.
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Abe CM, Salvador FA, Falsetti IN, Vieira MA, et al. (2008). Uropathogenic Escherichia coli (UPEC) strains may carry virulence properties of diarrhoeagenic E. coli. FEMS Immunol. Med. Microbiol. 52: 397-406.
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Arslan H, Azap OK, Ergönül Ö and Timurkaynak F (2005). Risk factors for ciprofloxacin resistance among Escherichia coli strains isolated from community-adquired urinary tract infections in Turkey. J. Antimicrob. Chemother. 56: 914-918.
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“The functional polymorphisms -429T>C and -374T>A of the RAGE gene promoter are not associated with gestational diabetes in Euro-Brazilians”, vol. 9. pp. 1130-1135, 2010.
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Dos Santos KG, Canani LH, Gross JL, Tschiedel B, et al. (2005). The -374A allele of the receptor for advanced glycation end products gene is associated with a decreased risk of ischemic heart disease in African-Brazilians with type 2 diabetes. Mol. Genet. Metab. 85: 149-156.
http://dx.doi.org/10.1016/j.ymgme.2005.02.010
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Falcone C, Campo I, Emanuele E, Buzzi MP, et al. (2004). Relationship between the -374T/A RAGE gene polymorphism and angiographic coronary artery disease. Int. J. Mol. Med. 14: 1061-1064.
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Hudson BI, Stickland MH, Futers TS and Grant PJ (2001a). Effects of novel polymorphisms in the RAGE gene on transcriptional regulation and their association with diabetic retinopathy. Diabetes 50: 1505-1511.
http://dx.doi.org/10.2337/diabetes.50.6.1505
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Hudson BI, Stickland MH, Grant PJ and Futers TS (2001b). Characterization of allelic and nucleotide variation between the RAGE gene on chromosome 6 and a homologous pseudogene sequence to its 5' regulatory region on chromosome 3: implications for polymorphic studies in diabetes. Diabetes 50: 2646-2651.
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PMid:11723045
JiXiong X, BiLin X, MingGong Y and ShuQin L (2003). -429T/C and -374T/A polymorphisms of RAGE gene promoter are not associated with diabetic retinopathy in Chinese patients with type 2 diabetes. Diabetes Care 26: 2696-2697.
Kankova K, Stejskalova A, Hertlova M and Znojil V (2005). Haplotype analysis of the RAGE gene: identification of a haplotype marker for diabetic nephropathy in type 2 diabetes mellitus. Nephrol. Dial. Transplant. 20: 1093-1102.
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Lahiri DK and Nurnberger JI Jr (1991). A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies. Nucleic Acids Res. 19: 5444.
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