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Volumn 64, Issue 12, 2015, Pages 4322-4332

ABCC8 R1420H loss-of-function variant in a southwest American Indian community: Association with increased birth weight and doubled risk of type 2 diabetes

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM); ABCC8 PROTEIN, HUMAN; RECOMBINANT PROTEIN; SULFONYLUREA RECEPTOR;

EID: 84962168896     PISSN: 00121797     EISSN: 1939327X     Source Type: Journal    
DOI: 10.2337/db15-0459     Document Type: Article
Times cited : (50)

References (66)
  • 1
    • 0025000188 scopus 로고
    • Diabetes mellitus in the Pima Indians: Incidence, risk factors and pathogenesis
    • Knowler WC, Pettitt DJ, Saad MF, Bennett PH. Diabetes mellitus in the Pima Indians: incidence, risk factors and pathogenesis. Diabetes Metab Rev 1990;6:1-27
    • (1990) Diabetes Metab Rev , vol.6 , pp. 1-27
    • Knowler, W.C.1    Pettitt, D.J.2    Saad, M.F.3    Bennett, P.H.4
  • 2
    • 84891821161 scopus 로고    scopus 로고
    • A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes
    • Hanson RL, Muller YL, Kobes S, et al. A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes. Diabetes 2014;63:369-376
    • (2014) Diabetes , vol.63 , pp. 369-376
    • Hanson, R.L.1    Muller, Y.L.2    Kobes, S.3
  • 3
    • 84903525752 scopus 로고    scopus 로고
    • Common genetic variation in the glucokinase gene (GCK) is associated with type 2 diabetes and rates of carbohydrate oxidation and energy expenditure
    • Muller YL, Piaggi P, Hoffman D, et al. Common genetic variation in the glucokinase gene (GCK) is associated with type 2 diabetes and rates of carbohydrate oxidation and energy expenditure. Diabetologia 2014;57:1382-1390
    • (2014) Diabetologia , vol.57 , pp. 1382-1390
    • Muller, Y.L.1    Piaggi, P.2    Hoffman, D.3
  • 4
    • 84891676958 scopus 로고    scopus 로고
    • Strong parent-of-origin effects in the association of KCNQ1 variants with type 2 diabetes in American Indians
    • Hanson RL, Guo T, Muller YL, et al. Strong parent-of-origin effects in the association of KCNQ1 variants with type 2 diabetes in American Indians. Diabetes 2013;62:2984-2991
    • (2013) Diabetes , vol.62 , pp. 2984-2991
    • Hanson, R.L.1    Guo, T.2    Muller, Y.L.3
  • 5
    • 84885805038 scopus 로고    scopus 로고
    • MAP2K3 is reproducibly associated with body mass index in American Indians and Caucasians and may mediate hypothalamic inflammation
    • Bian L, Traurig M, Hanson RL, et al. MAP2K3 is reproducibly associated with body mass index in American Indians and Caucasians and may mediate hypothalamic inflammation. Hum Mol Genet 2013;22:4438-4449
    • (2013) Hum Mol Genet , vol.22 , pp. 4438-4449
    • Bian, L.1    Traurig, M.2    Hanson, R.L.3
  • 6
    • 84555186717 scopus 로고    scopus 로고
    • Greater impact of melanocortin-4 receptor deficiency on rates of growth and risk of type 2 diabetes during childhood compared with adulthood in Pima Indians
    • Thearle MS, Muller YL, Hanson RL, et al. Greater impact of melanocortin-4 receptor deficiency on rates of growth and risk of type 2 diabetes during childhood compared with adulthood in Pima Indians. Diabetes 2012;61:250-257
    • (2012) Diabetes , vol.61 , pp. 250-257
    • Thearle, M.S.1    Muller, Y.L.2    Hanson, R.L.3
  • 7
    • 67650224470 scopus 로고    scopus 로고
    • Common variation in SIM1 is re-producibly associated with BMI in Pima Indians
    • Traurig M, Mack J, Hanson RL, et al. Common variation in SIM1 is re-producibly associated with BMI in Pima Indians. Diabetes 2009;58:1682-1689
    • (2009) Diabetes , vol.58 , pp. 1682-1689
    • Traurig, M.1    Mack, J.2    Hanson, R.L.3
  • 8
    • 0030609143 scopus 로고    scopus 로고
    • Octameric stoichiometry of the KATP channel complex
    • Shyng S, Nichols CG. Octameric stoichiometry of the KATP channel complex. J Gen Physiol 1997;110:655-664
    • (1997) J Gen Physiol , vol.110 , pp. 655-664
    • Shyng, S.1    Nichols, C.G.2
  • 9
    • 23644442552 scopus 로고    scopus 로고
    • ATP-sensitive potassium channelopathies: Focus on insulin secretion
    • Ashcroft FM. ATP-sensitive potassium channelopathies: focus on insulin secretion. J Clin Invest 2005;115:2047-2058
    • (2005) J Clin Invest , vol.115 , pp. 2047-2058
    • Ashcroft, F.M.1
  • 10
    • 0037317981 scopus 로고    scopus 로고
    • ATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes
    • ATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes. Diabetes 2003;52:568-572
    • (2003) Diabetes , vol.52 , pp. 568-572
    • Gloyn, A.L.1    Weedon, M.N.2    Owen, K.R.3
  • 11
    • 34249885875 scopus 로고    scopus 로고
    • A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
    • Scott LJ, Mohlke KL, Bonnycastle LL, et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 2007;316:1341-1345
    • (2007) Science , vol.316 , pp. 1341-1345
    • Scott, L.J.1    Mohlke, K.L.2    Bonnycastle, L.L.3
  • 12
    • 84962097359 scopus 로고    scopus 로고
    • Role of established type 2 diabetes-susceptibility genetic variants in a high prevalence American Indian population
    • Hanson RL, Rong R, Kobes S, et al. Role of established type 2 diabetes-susceptibility genetic variants in a high prevalence American Indian population. Diabetes 2015;64:2646-2657
    • (2015) Diabetes , vol.64 , pp. 2646-2657
    • Hanson, R.L.1    Rong, R.2    Kobes, S.3
  • 15
    • 84873643510 scopus 로고    scopus 로고
    • Genotype and phenotype correlations in 417 children with congenital hyperinsulinism
    • Snider KE, Becker S, Boyajian L, et al. Genotype and phenotype correlations in 417 children with congenital hyperinsulinism. J Clin Endocrinol Metab 2013; 98:E355-E363
    • (2013) J Clin Endocrinol Metab , vol.98 , pp. E355-E363
    • Snider, K.E.1    Becker, S.2    Boyajian, L.3
  • 16
    • 48649093189 scopus 로고    scopus 로고
    • Glucose intolerance and diabetes are observed in the long-term follow-up of nonpancreatectomized patients with persistent hyperinsulinemic hypoglycemia of infancy due to mutations in the ABCC8 gene
    • Gussinyer M, Clemente M, Cebrián R, Yeste D, Albisu M, Carrascosa A. Glucose intolerance and diabetes are observed in the long-term follow-up of nonpancreatectomized patients with persistent hyperinsulinemic hypoglycemia of infancy due to mutations in the ABCC8 gene. Diabetes Care 2008;31:1257-1259
    • (2008) Diabetes Care , vol.31 , pp. 1257-1259
    • Gussinyer, M.1    Clemente, M.2    Cebrián, R.3    Yeste, D.4    Albisu, M.5    Carrascosa, A.6
  • 17
    • 0033594787 scopus 로고    scopus 로고
    • The fetal insulin hypothesis: An alternative explanation of the association of low birthweight with diabetes and vascular disease
    • Hattersley AT, Tooke JE. The fetal insulin hypothesis: an alternative explanation of the association of low birthweight with diabetes and vascular disease. Lancet 1999;353:1789-1792
    • (1999) Lancet , vol.353 , pp. 1789-1792
    • Hattersley, A.T.1    Tooke, J.E.2
  • 18
    • 34247500820 scopus 로고    scopus 로고
    • Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene
    • Pearson ER, Boj SF, Steele AM, et al. Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene. PLoS Med 2007;4:e118
    • (2007) PLoS Med , vol.4 , pp. e118
    • Pearson, E.R.1    Boj, S.F.2    Steele, A.M.3
  • 19
    • 84894061194 scopus 로고    scopus 로고
    • HNF4A mutation: Switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin response
    • Arya VB, Rahman S, Senniappan S, Flanagan SE, Ellard S, Hussain K. HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin response. Diabet Med 2014;31:e11-e15
    • (2014) Diabet Med , vol.31 , pp. e11-e15
    • Arya, V.B.1    Rahman, S.2    Senniappan, S.3    Flanagan, S.E.4    Ellard, S.5    Hussain, K.6
  • 21
    • 0012431804 scopus 로고    scopus 로고
    • Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus
    • Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care 2003;26(Suppl. 1):S5-S20
    • (2003) Diabetes Care , vol.26 , pp. S5-S20
  • 22
    • 0021813187 scopus 로고
    • Homeostasis model assessment: Insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man
    • Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985;28: 412-419
    • (1985) Diabetologia , vol.28 , pp. 412-419
    • Matthews, D.R.1    Hosker, J.P.2    Rudenski, A.S.3    Naylor, B.A.4    Treacher, D.F.5    Turner, R.C.6
  • 23
    • 0034650163 scopus 로고    scopus 로고
    • Evaluation of simple indices of insulin sensitivity and insulin secretion for use in epidemiologic studies
    • Hanson RL, Pratley RE, Bogardus C, et al. Evaluation of simple indices of insulin sensitivity and insulin secretion for use in epidemiologic studies. Am J Epidemiol 2000;151:190-198
    • (2000) Am J Epidemiol , vol.151 , pp. 190-198
    • Hanson, R.L.1    Pratley, R.E.2    Bogardus, C.3
  • 24
    • 0019308550 scopus 로고
    • Gestational diabetes: Infant and maternal complications of pregnancy in relation to third-trimester glucose tolerance in the Pima Indians
    • Pettitt DJ, Knowler WC, Baird HR, Bennett PH. Gestational diabetes: infant and maternal complications of pregnancy in relation to third-trimester glucose tolerance in the Pima Indians. Diabetes Care 1980;3:458-464
    • (1980) Diabetes Care , vol.3 , pp. 458-464
    • Pettitt, D.J.1    Knowler, W.C.2    Baird, H.R.3    Bennett, P.H.4
  • 25
    • 0033851979 scopus 로고    scopus 로고
    • Secular trends in birth weight, BMI, and diabetes in the offspring of diabetic mothers
    • Lindsay RS, Hanson RL, Bennett PH, Knowler WC. Secular trends in birth weight, BMI, and diabetes in the offspring of diabetic mothers. Diabetes Care 2000;23:1249-1254
    • (2000) Diabetes Care , vol.23 , pp. 1249-1254
    • Lindsay, R.S.1    Hanson, R.L.2    Bennett, P.H.3    Knowler, W.C.4
  • 26
    • 0027762766 scopus 로고
    • Insulin resistance and insulin secretory dysfunction as precursors of non-insulin-dependent diabetes mellitus. Prospective studies of Pima Indians
    • Lillioja S, Mott DM, Spraul M, et al. Insulin resistance and insulin secretory dysfunction as precursors of non-insulin-dependent diabetes mellitus. Prospective studies of Pima Indians. N Engl J Med 1993;329:1988-1992
    • (1993) N Engl J Med , vol.329 , pp. 1988-1992
    • Lillioja, S.1    Mott, D.M.2    Spraul, M.3
  • 27
    • 0022468357 scopus 로고
    • Individual admixture estimates: Disease associations and individual risk of diabetes and gallbladder disease among Mexican-Americans in Starr County, Texas
    • Hanis CL, Chakraborty R, Ferrell RE, Schull WJ. Individual admixture estimates: disease associations and individual risk of diabetes and gallbladder disease among Mexican-Americans in Starr County, Texas. Am J Phys Anthropol 1986;70:433-441
    • (1986) Am J Phys Anthropol , vol.70 , pp. 433-441
    • Hanis, C.L.1    Chakraborty, R.2    Ferrell, R.E.3    Schull, W.J.4
  • 28
    • 34250861441 scopus 로고    scopus 로고
    • A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping
    • Tian C, Hinds DA, Shigeta R, et al. A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping. Am J Hum Genet 2007;80:1014-1023
    • (2007) Am J Hum Genet , vol.80 , pp. 1014-1023
    • Tian, C.1    Hinds, D.A.2    Shigeta, R.3
  • 29
    • 68149165614 scopus 로고    scopus 로고
    • Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
    • Kumar P, Henikoff S, Ng PC. Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat Protoc 2009;4: 1073-1081
    • (2009) Nat Protoc , vol.4 , pp. 1073-1081
    • Kumar, P.1    Henikoff, S.2    Ng, P.C.3
  • 30
    • 77951640946 scopus 로고    scopus 로고
    • A method and server for predicting damaging missense mutations
    • Adzhubei IA, Schmidt S, Peshkin L, et al. A method and server for predicting damaging missense mutations. Nat Methods 2010;7:248-249
    • (2010) Nat Methods , vol.7 , pp. 248-249
    • Adzhubei, I.A.1    Schmidt, S.2    Peshkin, L.3
  • 31
    • 0035516193 scopus 로고    scopus 로고
    • Changes in BMI and weight before and after the development of type 2 diabetes
    • Looker HC, Knowler WC, Hanson RL. Changes in BMI and weight before and after the development of type 2 diabetes. Diabetes Care 2001;24:1917-1922
    • (2001) Diabetes Care , vol.24 , pp. 1917-1922
    • Looker, H.C.1    Knowler, W.C.2    Hanson, R.L.3
  • 32
    • 0034731305 scopus 로고    scopus 로고
    • Functional analysis of a mutant sulfonylurea receptor, SUR1-R1420C, that is responsible for persistent hyper-insulinemic hypoglycemia of infancy
    • Matsuo M, Trapp S, Tanizawa Y, et al. Functional analysis of a mutant sulfonylurea receptor, SUR1-R1420C, that is responsible for persistent hyper-insulinemic hypoglycemia of infancy. J Biol Chem 2000;275:41184-41191
    • (2000) J Biol Chem , vol.275 , pp. 41184-41191
    • Matsuo, M.1    Trapp, S.2    Tanizawa, Y.3
  • 33
    • 17144452397 scopus 로고    scopus 로고
    • Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: Nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1
    • Tanizawa Y, Matsuda K, Matsuo M, et al. Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1. Diabetes 2000;49:114-120
    • (2000) Diabetes , vol.49 , pp. 114-120
    • Tanizawa, Y.1    Matsuda, K.2    Matsuo, M.3
  • 34
    • 0031799545 scopus 로고    scopus 로고
    • Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy
    • Shyng SL, Ferrigni T, Shepard JB, et al. Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy. Diabetes 1998;47:1145-1151
    • (1998) Diabetes , vol.47 , pp. 1145-1151
    • Shyng, S.L.1    Ferrigni, T.2    Shepard, J.B.3
  • 35
    • 57649183334 scopus 로고    scopus 로고
    • Functional clustering of mutations in the dimer interface of the nucleotide binding folds of the sulfonylurea receptor
    • Masia R, Nichols CG. Functional clustering of mutations in the dimer interface of the nucleotide binding folds of the sulfonylurea receptor. J Biol Chem 2008;283:30322-30329
    • (2008) J Biol Chem , vol.283 , pp. 30322-30329
    • Masia, R.1    Nichols, C.G.2
  • 36
    • 84856729217 scopus 로고    scopus 로고
    • Heterozygous ABCC8 mutations are a cause of MODY
    • Bowman P, Flanagan SE, Edghill EL, et al. Heterozygous ABCC8 mutations are a cause of MODY. Diabetologia 2012;55:123-127
    • (2012) Diabetologia , vol.55 , pp. 123-127
    • Bowman, P.1    Flanagan, S.E.2    Edghill, E.L.3
  • 37
    • 84861476229 scopus 로고    scopus 로고
    • Exome sequencing and genetic testing for MODY
    • Johansson S, Irgens H, Chudasama KK, et al. Exome sequencing and genetic testing for MODY. PLoS One 2012;7:e38050
    • (2012) PLoS One , vol.7 , pp. e38050
    • Johansson, S.1    Irgens, H.2    Chudasama, K.K.3
  • 38
    • 48249102392 scopus 로고    scopus 로고
    • Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence [published correction in Diabetes 2008;57:2552]
    • Abdulhadi-Atwan M, Bushman J, Tornovsky-Babaey S, et al. Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence [published correction in Diabetes 2008;57:2552]. Diabetes 2008;57:1935-1940
    • (2008) Diabetes , vol.57 , pp. 1935-1940
    • Abdulhadi-Atwan, M.1    Bushman, J.2    Tornovsky-Babaey, S.3
  • 39
    • 77958523353 scopus 로고    scopus 로고
    • Hyperinsulinemic hypo-glycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation
    • Vieira TC, Bergamin CS, Gurgel LC, Moisés RS. Hyperinsulinemic hypo-glycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation. Pediatr Diabetes 2010;11:505-508
    • (2010) Pediatr Diabetes , vol.11 , pp. 505-508
    • Vieira, T.C.1    Bergamin, C.S.2    Gurgel, L.C.3    Moisés, R.S.4
  • 40
    • 80053894221 scopus 로고    scopus 로고
    • ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglyce-mia
    • Glaser B, Blech I, Krakinovsky Y, et al. ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglyce-mia. Genet Med 2011;13:891-894
    • (2011) Genet Med , vol.13 , pp. 891-894
    • Glaser, B.1    Blech, I.2    Krakinovsky, Y.3
  • 41
    • 84975795680 scopus 로고    scopus 로고
    • An integrated map of genetic variation form 1,092 human genomes
    • Abecasis GR, Auton A, Brooks LD, et al.; 1000 Genomes Project Consortium. An integrated map of genetic variation form 1,092 human genomes. Nature 2012;491:56-65
    • (2012) Nature , vol.491 , pp. 56-65
    • Abecasis, G.R.1    Auton, A.2    Brooks, L.D.3
  • 43
    • 84867886439 scopus 로고    scopus 로고
    • Nateglinide is effective for diabetes mellitus with reactive hypoglycemia in a child with a compound heterozygous ABCC8 mutation
    • Saito-Hakoda A, Yorifuji T, Kanno J, Kure S, Fujiwara I. Nateglinide is effective for diabetes mellitus with reactive hypoglycemia in a child with a compound heterozygous ABCC8 mutation. Clin Pediatr Endocrinol 2012;21:45-52
    • (2012) Clin Pediatr Endocrinol , vol.21 , pp. 45-52
    • Saito-Hakoda, A.1    Yorifuji, T.2    Kanno, J.3    Kure, S.4    Fujiwara, I.5
  • 44
    • 80054092390 scopus 로고    scopus 로고
    • Hyperinsulinaemic hypo-glycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations
    • Kapoor RR, Flanagan SE, James CT, et al. Hyperinsulinaemic hypo-glycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations. Diabetologia 2011;54:2575-2583
    • (2011) Diabetologia , vol.54 , pp. 2575-2583
    • Kapoor, R.R.1    Flanagan, S.E.2    James, C.T.3
  • 45
    • 84877810871 scopus 로고    scopus 로고
    • Prematurity, mac-rosomia, hyperinsulinaemic hypoglycaemia and a dominant ABCC8 gene mutation
    • Khoriati D, Arya VB, Flanagan SE, Ellard S, Hussain K. Prematurity, mac-rosomia, hyperinsulinaemic hypoglycaemia and a dominant ABCC8 gene mutation. BMJ Case Rep 2013;2013:bcr2013008767
    • (2013) BMJ Case Rep , vol.2013
    • Khoriati, D.1    Arya, V.B.2    Flanagan, S.E.3    Ellard, S.4    Hussain, K.5
  • 46
    • 84961353466 scopus 로고    scopus 로고
    • Congenital hyperinsulinism in a newborn with a novel homozygous mutation (p.Q392H) in the ABCC8 gene
    • Ince DA, Sahin NM, Ecevit A, et al. Congenital hyperinsulinism in a newborn with a novel homozygous mutation (p.Q392H) in the ABCC8 gene. J Pediatr Endocrinol Metab 2014;27:1253-1255
    • (2014) J Pediatr Endocrinol Metab , vol.27 , pp. 1253-1255
    • Ince, D.A.1    Sahin, N.M.2    Ecevit, A.3
  • 48
    • 77955558577 scopus 로고    scopus 로고
    • Type 2 diabetes risk alleles near ADCY5, CDKAL1 and HHEX-IDE are associated with reduced birthweight
    • Andersson EA, Pilgaard K, Pisinger C, et al. Type 2 diabetes risk alleles near ADCY5, CDKAL1 and HHEX-IDE are associated with reduced birthweight. Dia-betologia 2010;53:1908-1916
    • (2010) Dia-betologia , vol.53 , pp. 1908-1916
    • Andersson, E.A.1    Pilgaard, K.2    Pisinger, C.3
  • 49
    • 34250827858 scopus 로고    scopus 로고
    • Type 2 diabetes TCF7L2 risk genotypes alter birth weight: A study of 24,053 individuals
    • Freathy RM, Weedon MN, Bennett A, et al. Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals. Am J Hum Genet 2007;80:1150-1161
    • (2007) Am J Hum Genet , vol.80 , pp. 1150-1161
    • Freathy, R.M.1    Weedon, M.N.2    Bennett, A.3
  • 50
    • 0034737811 scopus 로고    scopus 로고
    • Sur1 knockout mice. A model for K(ATP) channel-independent regulation of insulin secretion
    • Seghers V, Nakazaki M, DeMayo F, Aguilar-Bryan L, Bryan J. Sur1 knockout mice. A model for K(ATP) channel-independent regulation of insulin secretion. J Biol Chem 2000;275:9270-9277
    • (2000) J Biol Chem , vol.275 , pp. 9270-9277
    • Seghers, V.1    Nakazaki, M.2    DeMayo, F.3    Aguilar-Bryan, L.4    Bryan, J.5
  • 51
    • 84891686905 scopus 로고    scopus 로고
    • A mouse model of human hyperin-sulinism produced by the E1506K mutation in the sulphonylurea receptor SUR1
    • Shimomura K, Tusa M, Iberl M, et al. A mouse model of human hyperin-sulinism produced by the E1506K mutation in the sulphonylurea receptor SUR1. Diabetes 2013;62:3797-3806
    • (2013) Diabetes , vol.62 , pp. 3797-3806
    • Shimomura, K.1    Tusa, M.2    Iberl, M.3
  • 52
    • 9444254642 scopus 로고    scopus 로고
    • Diet-induced glucose intolerance in mice with decreased beta-cell ATP-sensitive K+ channels
    • Remedi MS, Koster JC, Markova K, et al. Diet-induced glucose intolerance in mice with decreased beta-cell ATP-sensitive K+ channels. Diabetes 2004;53: 3159-3167
    • (2004) Diabetes , vol.53 , pp. 3159-3167
    • Remedi, M.S.1    Koster, J.C.2    Markova, K.3
  • 53
    • 84907197887 scopus 로고    scopus 로고
    • Congenital hyperinsulinism: Current status and future perspectives
    • Yorifuji T. Congenital hyperinsulinism: current status and future perspectives. Ann Pediatr Endocrinol Metab 2014;19:57-68
    • (2014) Ann Pediatr Endocrinol Metab , vol.19 , pp. 57-68
    • Yorifuji, T.1
  • 54
    • 0033853921 scopus 로고    scopus 로고
    • Glaser B. β-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy
    • Kassem SA, Ariel I, Thornton PS, Scheimberg I, Glaser B. β-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy. Diabetes 2000;49:1325-1333
    • (2000) Diabetes , vol.49 , pp. 1325-1333
    • Kassem, S.A.1    Ariel, I.2    Thornton, P.S.3    Scheimberg, I.4
  • 56
    • 53949097376 scopus 로고    scopus 로고
    • Endoplasmic reticulum stress in beta cells: Latent mechanism of secondary sulfonylurea failure in type 2 diabetes?
    • Qian L, Zhang S, Xu L, Peng Y. Endoplasmic reticulum stress in beta cells: latent mechanism of secondary sulfonylurea failure in type 2 diabetes? Med Hypotheses 2008;71:889-891
    • (2008) Med Hypotheses , vol.71 , pp. 889-891
    • Qian, L.1    Zhang, S.2    Xu, L.3    Peng, Y.4
  • 57
    • 84865592405 scopus 로고    scopus 로고
    • The diabetic β-cell: Hyperstimulated vs. Hyper-excited
    • Nichols CG, Remedi MS. The diabetic β-cell: hyperstimulated vs. hyper-excited. Diabetes Obes Metab 2012;14(Suppl. 3):129-135
    • (2012) Diabetes Obes Metab , vol.14 , pp. 129-135
    • Nichols, C.G.1    Remedi, M.S.2
  • 58
    • 55949116427 scopus 로고    scopus 로고
    • Chronic antidiabetic sulfonylureas in vivo: Reversible effects on mouse pancreatic beta-cells
    • Remedi MS, Nichols CG. Chronic antidiabetic sulfonylureas in vivo: reversible effects on mouse pancreatic beta-cells. PLoS Med 2008;5:e206
    • (2008) PLoS Med , vol.5 , pp. e206
    • Remedi, M.S.1    Nichols, C.G.2
  • 59
    • 35148847369 scopus 로고    scopus 로고
    • Beta-Cell hyperexcitability: From hy-perinsulinism to diabetes
    • Nichols CG, Koster JC, Remedi MS. beta-Cell hyperexcitability: from hy-perinsulinism to diabetes. Diabetes Obes Metab 2007;9(Suppl. 2):81-88
    • (2007) Diabetes Obes Metab , vol.9 , pp. 81-88
    • Nichols, C.G.1    Koster, J.C.2    Remedi, M.S.3
  • 60
    • 34447554544 scopus 로고    scopus 로고
    • Regulation of KATP channel subunit gene expression by hyperglycemia in the mediobasal hypothalamus of female rats
    • Acosta-Martínez M, Levine JE. Regulation of KATP channel subunit gene expression by hyperglycemia in the mediobasal hypothalamus of female rats. Am J Physiol Endocrinol Metab 2007;292:E1801-E1807
    • (2007) Am J Physiol Endocrinol Metab , vol.292 , pp. E1801-E1807
    • Acosta-Martínez, M.1    Levine, J.E.2
  • 61
    • 17844379717 scopus 로고    scopus 로고
    • Hypothalamic K(ATP) channels control hepatic glucose production
    • Pocai A, Lam TK, Gutierrez-Juarez R, et al. Hypothalamic K(ATP) channels control hepatic glucose production. Nature 2005;434:1026-1031
    • (2005) Nature , vol.434 , pp. 1026-1031
    • Pocai, A.1    Lam, T.K.2    Gutierrez-Juarez, R.3
  • 62
    • 84895823423 scopus 로고    scopus 로고
    • Hypothalamic glucagon signals through the KATP channels to regulate glucose production
    • Abraham MA, Yue JT, LaPierre MP, et al. Hypothalamic glucagon signals through the KATP channels to regulate glucose production. Mol Metab 2014;3: 202-208
    • (2014) Mol Metab , vol.3 , pp. 202-208
    • Abraham, M.A.1    Yue, J.T.2    LaPierre, M.P.3
  • 63
    • 0032190017 scopus 로고    scopus 로고
    • Paternal mutation of the sulfo-nylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia
    • Verkarre V, Fournet JC, de Lonlay P, et al. Paternal mutation of the sulfo-nylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. J Clin Invest 1998;102:1286-1291
    • (1998) J Clin Invest , vol.102 , pp. 1286-1291
    • Verkarre, V.1    Fournet, J.C.2    De Lonlay, P.3
  • 64
    • 0037312864 scopus 로고    scopus 로고
    • The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes
    • Nielsen EM, Hansen L, Carstensen B, et al. The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes. Diabetes 2003;52:573-577
    • (2003) Diabetes , vol.52 , pp. 573-577
    • Nielsen, E.M.1    Hansen, L.2    Carstensen, B.3
  • 65
    • 84864797156 scopus 로고    scopus 로고
    • ATP-sensitive potassium channel-deficient mice show hyperphagia but are resistant to obesity
    • Park YB, Choi YJ, Park SY, et al. ATP-sensitive potassium channel-deficient mice show hyperphagia but are resistant to obesity. Diabetes Metab J 2011;35:219-225
    • (2011) Diabetes Metab J , vol.35 , pp. 219-225
    • Park, Y.B.1    Choi, Y.J.2    Park, S.Y.3
  • 66
    • 73049095036 scopus 로고    scopus 로고
    • Sarcolemmal ATP-sensitive K(+) channels control energy expenditure determining body weight
    • Alekseev AE, Reyes S, Yamada S, et al. Sarcolemmal ATP-sensitive K(+) channels control energy expenditure determining body weight. Cell Metab 2010; 11:58-69
    • (2010) Cell Metab , vol.11 , pp. 58-69
    • Alekseev, A.E.1    Reyes, S.2    Yamada, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.