메뉴 건너뛰기




Volumn 9, Issue MAY, 2018, Pages

Genetic testing of maturity-onset diabetes of the young current status and future perspectives

Author keywords

Diabetes; Gene mutation; Hyperglycemia; Insulin; Maturity onset diabetes of the young; Sulfonylureas

Indexed keywords

ADENOSINE DEAMINASE; CARBOXYLESTERASE; GLUCOKINASE; HEPATOCYTE NUCLEAR FACTOR 1ALPHA; HEPATOCYTE NUCLEAR FACTOR 4; HEXOKINASE; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; INSULIN; INSULIN RECEPTOR KINASE; LOW DENSITY LIPOPROTEIN CHOLESTEROL; SULFONYLUREA; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PAX4;

EID: 85047247050     PISSN: None     EISSN: 16642392     Source Type: Journal    
DOI: 10.3389/fendo.2018.00253     Document Type: Review
Times cited : (93)

References (137)
  • 1
    • 0036300650 scopus 로고    scopus 로고
    • Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor-4A gene
    • Gloyn AL, Ellard S, Shepherd M, Howell RT, Parry EM, Jefferson A, et al. Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor-4A gene. Diabetes (2001) 51(7):2329-33. doi:10.2337/diabetes.51.7.2329
    • (2001) Diabetes , vol.51 , Issue.7 , pp. 2329-2333
    • Gloyn, A.L.1    Ellard, S.2    Shepherd, M.3    Howell, R.T.4    Parry, E.M.5    Jefferson, A.6
  • 2
    • 0034809513 scopus 로고    scopus 로고
    • Maturity-onset diabetes of the young: from clinical description to molecular genetic characterization
    • Owen K, Hattersley A. Maturity-onset diabetes of the young: from clinical description to molecular genetic characterization. Best Pract Res Clin Endocrinol Metab (2001) 15:309-23. doi:10.1053/beem.2001.0148
    • (2001) Best Pract Res Clin Endocrinol Metab , vol.15 , pp. 309-323
    • Owen, K.1    Hattersley, A.2
  • 3
    • 0035992825 scopus 로고    scopus 로고
    • Different genes, different diabetes: lessons from maturity onset diabetes of the young
    • Stride A, Hattersley AT. Different genes, different diabetes: lessons from maturity onset diabetes of the young. Ann Med (2002) 34:207-16
    • (2002) Ann Med , vol.34 , pp. 207-216
    • Stride, A.1    Hattersley, A.T.2
  • 5
    • 84855161991 scopus 로고    scopus 로고
    • Diagnosis and classification of diabetes mellitus
    • American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care (2012) 35(Suppl 1):S64-71. doi:10.2337/dc12-s064
    • (2012) Diabetes Care , vol.35 , pp. S64-S71
  • 6
    • 84951988949 scopus 로고    scopus 로고
    • Maturity-onset diabetes of the young: what do clinicians need to know?
    • Kim EH. Maturity-onset diabetes of the young: what do clinicians need to know? Diabetes Metab J (2015) 39:468-77. doi:10.4093/dmj.2015.39.6.468
    • (2015) Diabetes Metab J , vol.39 , pp. 468-477
    • Kim, E.H.1
  • 8
    • 10544236911 scopus 로고    scopus 로고
    • Mutations in the hepatocyte nuclear factor-4a gene in maturity-onset diabetes of the young (MODY1)
    • Yamagata K, Furuta H, Oda N, Kaisaki PJ, Menzel S, Cox NJ, et al. Mutations in the hepatocyte nuclear factor-4a gene in maturity-onset diabetes of the young (MODY1). Nature (1996) 384:458-60. doi:10.1038/384458a0
    • (1996) Nature , vol.384 , pp. 458-460
    • Yamagata, K.1    Furuta, H.2    Oda, N.3    Kaisaki, P.J.4    Menzel, S.5    Cox, N.J.6
  • 9
    • 10544249874 scopus 로고    scopus 로고
    • Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
    • Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, et al. Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3). Nature (1996) 384:455-8. doi:10.1038/384455a0
    • (1996) Nature , vol.384 , pp. 455-458
    • Yamagata, K.1    Oda, N.2    Kaisaki, P.J.3    Menzel, S.4    Furuta, H.5    Vaxillaire, M.6
  • 10
    • 0027472126 scopus 로고
    • Familial hyperglycemia due to mutations in glucokinase-definition of a subtype of diabetes mellitus
    • Froguel P, Zouali H, Vionnet N, Velho G, Vaxillaire M, Sun F, et al. Familial hyperglycemia due to mutations in glucokinase-definition of a subtype of diabetes mellitus. N Engl J Med (1993) 328:697-702. doi:10.1056/NEJM199303113281005
    • (1993) N Engl J Med , vol.328 , pp. 697-702
    • Froguel, P.1    Zouali, H.2    Vionnet, N.3    Velho, G.4    Vaxillaire, M.5    Sun, F.6
  • 11
    • 0031453186 scopus 로고    scopus 로고
    • Mutation in hepatocyte nuclear factor-1beta gene (TCF2) associated with MODY
    • Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, et al. Mutation in hepatocyte nuclear factor-1beta gene (TCF2) associated with MODY. Nat Genet (1997) 17:384-5. doi:10.1038/ng1297-384
    • (1997) Nat Genet , vol.17 , pp. 384-385
    • Horikawa, Y.1    Iwasaki, N.2    Hara, M.3    Furuta, H.4    Hinokio, Y.5    Cockburn, B.N.6
  • 12
    • 0024425880 scopus 로고
    • Maturity onset diabetes of the young (MODY)
    • Fajans SS. Maturity onset diabetes of the young (MODY). Diabet Metab Rev (1989) 5:579-606. doi:10.1002/dmr.5610050705
    • (1989) Diabet Metab Rev , vol.5 , pp. 579-606
    • Fajans, S.S.1
  • 13
    • 0031031571 scopus 로고    scopus 로고
    • Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence
    • Stoffers DA, Zinkin NT, Stanojevic V, Clarke WL, Habener JF. Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence. Nat Genet (1997) 15:106-10. doi:10.1038/ng0197-106
    • (1997) Nat Genet , vol.15 , pp. 106-110
    • Stoffers, D.A.1    Zinkin, N.T.2    Stanojevic, V.3    Clarke, W.L.4    Habener, J.F.5
  • 14
    • 58149335251 scopus 로고    scopus 로고
    • Learning from molecular genetics: novel insights arising from the definition of genes for monogenic and type 2 diabetes
    • McCarthy MI, Hattersley AT. Learning from molecular genetics: novel insights arising from the definition of genes for monogenic and type 2 diabetes. Diabetes (2008) 57(11):2889-989. doi:10.2337/db08-0343
    • (2008) Diabetes , vol.57 , Issue.11 , pp. 2889-2989
    • McCarthy, M.I.1    Hattersley, A.T.2
  • 15
    • 33751206505 scopus 로고    scopus 로고
    • Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF1B in human pancreatic development
    • Edghill EL, Bingham C, Slingerland AS, Minton JA, Noordam C, Ellard S, et al. Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF1B in human pancreatic development. Diabet Med (2006) 23:1301-6. doi:10.1111/j.1464-5491.2006.01999.x
    • (2006) Diabet Med , vol.23 , pp. 1301-1306
    • Edghill, E.L.1    Bingham, C.2    Slingerland, A.S.3    Minton, J.A.4    Noordam, C.5    Ellard, S.6
  • 16
    • 0032700272 scopus 로고    scopus 로고
    • Mutations in NEUROD1 are associated with the development of type two diabetes
    • Malecki MT, Jhala U, Antonellis A, Fields L, Doria A, Orban T, et al. Mutations in NEUROD1 are associated with the development of type two diabetes. Nat Genet (1999) 23:323-8. doi:10.1038/15500
    • (1999) Nat Genet , vol.23 , pp. 323-328
    • Malecki, M.T.1    Jhala, U.2    Antonellis, A.3    Fields, L.4    Doria, A.5    Orban, T.6
  • 17
    • 20144389645 scopus 로고    scopus 로고
    • Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function
    • Neve B, Fernandez-Zapico ME, Ashkenazi-Katalan V, Dina C, Hamid YH, Joly E, et al. Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function. Proc Natl Acad Sci U S A (2005) 102:4807-12. doi:10.1073/pnas.0409177102
    • (2005) Proc Natl Acad Sci U S A , vol.102 , pp. 4807-4812
    • Neve, B.1    Fernandez-Zapico, M.E.2    Ashkenazi-Katalan, V.3    Dina, C.4    Hamid, Y.H.5    Joly, E.6
  • 18
    • 77449134528 scopus 로고    scopus 로고
    • Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenetic diabetes
    • Torsvick J, Johannson S, Johansen A, EK J, Minton J, Raeder H, et al. Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenetic diabetes. Hum Genet (2010) 127:55-64. doi:10.1007/s00439-009-0740-8
    • (2010) Hum Genet , vol.127 , pp. 55-64
    • Torsvick, J.1    Johannson, S.2    Johansen, A.3    Ek, J.4    Minton, J.5    Raeder, H.6
  • 20
    • 42449127920 scopus 로고    scopus 로고
    • Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes
    • Molven A, Ringdal M, Nordbø AM, Raeder H, Støy J, Lipkind GM, et al. Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Diabetes (2008) 57(4):1131-5. doi:10.2337/db07-1467
    • (2008) Diabetes , vol.57 , Issue.4 , pp. 1131-1135
    • Molven, A.1    Ringdal, M.2    Nordbø, A.M.3    Raeder, H.4    Støy, J.5    Lipkind, G.M.6
  • 21
    • 42449134450 scopus 로고    scopus 로고
    • Insulin mutation screening in 1.044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood
    • Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, et al. Insulin mutation screening in 1.044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood. Diabetes (2008) 57:11034-42. doi:10.2337/db07-1405
    • (2008) Diabetes , vol.57 , pp. 11034-11042
    • Edghill, E.L.1    Flanagan, S.E.2    Patch, A.M.3    Boustred, C.4    Parrish, A.5    Shields, B.6
  • 22
    • 70149104834 scopus 로고    scopus 로고
    • Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction
    • Borowiec M, Liew CW, Thompson R, Boonyasrisawat W, Hu J, Mlynarski WM, et al. Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction. Proc Natl Acad Sci U S A (2009) 106:14460-5. doi:10.1073/pnas.0906474106
    • (2009) Proc Natl Acad Sci U S A , vol.106 , pp. 14460-14465
    • Borowiec, M.1    Liew, C.W.2    Thompson, R.3    Boonyasrisawat, W.4    Hu, J.5    Mlynarski, W.M.6
  • 24
    • 84862207587 scopus 로고    scopus 로고
    • Whole exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene
    • Bonnefond A, Philippe J, Durand E, Dechaume A, Huyvaert M, Montagne L, et al. Whole exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene. PLoS One (2012) 7:37423. doi:10.1371/journal.pone.0037423
    • (2012) PLoS One , vol.7 , pp. 37423
    • Bonnefond, A.1    Philippe, J.2    Durand, E.3    Dechaume, A.4    Huyvaert, M.5    Montagne, L.6
  • 25
    • 15644378360 scopus 로고
    • The use of tolbutamide in the treatment of young people with mild diabetes mellitus-a progress report
    • Fajans SS, Conn JW. The use of tolbutamide in the treatment of young people with mild diabetes mellitus-a progress report. Diabetes (1962) 11:123-6
    • (1962) Diabetes , vol.11 , pp. 123-126
    • Fajans, S.S.1    Conn, J.W.2
  • 26
    • 0005515077 scopus 로고
    • The early recognition of diabetes mellitus
    • Fajans SS, Conn JW. The early recognition of diabetes mellitus. Ann N Y Acad Sci (1959) 82:208-18. doi:10.1111/j.1749-6632.1959.tb44901.x
    • (1959) Ann N Y Acad Sci , vol.82 , pp. 208-218
    • Fajans, S.S.1    Conn, J.W.2
  • 27
    • 0016244025 scopus 로고
    • Mild familial diabetes with dominant inheritance
    • Tattersall R. Mild familial diabetes with dominant inheritance. Q J Med (1974) 43:339-57
    • (1974) Q J Med , vol.43 , pp. 339-357
    • Tattersall, R.1
  • 28
    • 0016641270 scopus 로고
    • A difference between the inheritance of classical juvenile onset and maturity-onset type diabetes of young people
    • Tattersall R, Fajans S. A difference between the inheritance of classical juvenile onset and maturity-onset type diabetes of young people. Diabetes (1975) 24:44-53. doi:10.2337/diabetes.24.1.44
    • (1975) Diabetes , vol.24 , pp. 44-53
    • Tattersall, R.1    Fajans, S.2
  • 29
    • 0022001972 scopus 로고
    • Insulin gene analysis in a family with maturity-onset diabetes of the young
    • Andreone T, Fajans SS, Rotwein P, Skolnick M, Permutt MA. Insulin gene analysis in a family with maturity-onset diabetes of the young. Diabetes (1985) 34:108-14. doi:10.2337/diab.34.2.108
    • (1985) Diabetes , vol.34 , pp. 108-114
    • Andreone, T.1    Fajans, S.S.2    Rotwein, P.3    Skolnick, M.4    Permutt, M.A.5
  • 30
    • 0026032055 scopus 로고
    • Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q
    • Bell GI, Xiang KS, Newman MV, Wu SH, Wright LG, Fajans SS, et al. Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q. Proc Natl Acad Sci U S A (1991) 1991(88):1484-8. doi:10.1073/pnas.88.4.1484
    • (1991) Proc Natl Acad Sci U S A , vol.1991 , Issue.88 , pp. 1484-1488
    • Bell, G.I.1    Xiang, K.S.2    Newman, M.V.3    Wu, S.H.4    Wright, L.G.5    Fajans, S.S.6
  • 31
    • 0026558807 scopus 로고
    • Identification of genetic markers flanking the locus for maturity-onset diabetes of the young on human chromosome 20
    • Bowden DW, Gravius TC, Akots G, Fajans SS. Identification of genetic markers flanking the locus for maturity-onset diabetes of the young on human chromosome 20. Diabetes (1992) 41:88-92. doi:10.2337/diab.41.1.88
    • (1992) Diabetes , vol.41 , pp. 88-92
    • Bowden, D.W.1    Gravius, T.C.2    Akots, G.3    Fajans, S.S.4
  • 32
    • 0026608764 scopus 로고
    • Close linkage of glucokinase locus on chromosome 7p to early onset non-insulin dependent diabetes mellitus
    • Froguel P, Vaxillaire M, Sun F, Velho G, Zouali H, Butal MO, et al. Close linkage of glucokinase locus on chromosome 7p to early onset non-insulin dependent diabetes mellitus. Nature (1992) 356:162-4. doi:10.1038/356162a0
    • (1992) Nature , vol.356 , pp. 162-164
    • Froguel, P.1    Vaxillaire, M.2    Sun, F.3    Velho, G.4    Zouali, H.5    Butal, M.O.6
  • 33
    • 33747670566 scopus 로고
    • Obesity, insulin resistance and diabetes mellitus in the Pima Indians
    • Kobberling J, Tattersall RB, editors. London: Academic Press
    • Panzram G, Savage PJ, Nagulesparan M, Howar BV, Pettitt DN, Lisse JR, et al. Obesity, insulin resistance and diabetes mellitus in the Pima Indians. In: Kobberling J, Tattersall RB, editors. The Genetics of Diabetes Mellitus. London: Academic Press (1982). p. 243-50
    • (1982) The Genetics of Diabetes Mellitus , pp. 243-250
    • Panzram, G.1    Savage, P.J.2    Nagulesparan, M.3    Howar, B.V.4    Pettitt, D.N.5    Lisse, J.R.6
  • 34
    • 84868292211 scopus 로고    scopus 로고
    • Clinical features and treatment of maturity onset diabetes of the young (MODY)
    • Gardner DS, Tai ES. Clinical features and treatment of maturity onset diabetes of the young (MODY). Diabetes Metab Syndr Obes (2012) 5:101-8. doi:10.2147/DMSO.S23353
    • (2012) Diabetes Metab Syndr Obes , vol.5 , pp. 101-108
    • Gardner, D.S.1    Tai, E.S.2
  • 36
    • 84919402710 scopus 로고    scopus 로고
    • Landscape of monogenetic diabetes in the third millennium
    • Guja C, Guja L. Landscape of monogenetic diabetes in the third millennium. Proc Rom Acad Ser B (2013) 15(3):217-32
    • (2013) Proc Rom Acad Ser B , vol.15 , Issue.3 , pp. 217-232
    • Guja, C.1    Guja, L.2
  • 37
    • 77949450581 scopus 로고    scopus 로고
    • Type 2 diabetes, medication-induced diabetes, and monogenic diabetes in Canadian children: a prospective national surveillance study
    • Amed S, Dean HJ, Panagiotopoulos C, Sellers EAC, Hadjiyannakis S, Laubscher TA, et al. Type 2 diabetes, medication-induced diabetes, and monogenic diabetes in Canadian children: a prospective national surveillance study. Diabetes Care (2010) 33:786-91. doi:10.2337/dc09-1013
    • (2010) Diabetes Care , vol.33 , pp. 786-791
    • Amed, S.1    Dean, H.J.2    Panagiotopoulos, C.3    Sellers, E.A.C.4    Hadjiyannakis, S.5    Laubscher, T.A.6
  • 40
    • 0347142258 scopus 로고
    • Heterogeneity between various families with non-insulin dependent diabetes of the MODY type
    • Kobberling J, Tattersall RB, editors. New York: Academic Press
    • Fajans SS. Heterogeneity between various families with non-insulin dependent diabetes of the MODY type. In: Kobberling J, Tattersall RB, editors. The Genetics of Diabetes Mellitus. New York: Academic Press (1982). p. 251-60
    • (1982) The Genetics of Diabetes Mellitus , pp. 251-260
    • Fajans, S.S.1
  • 42
    • 84885224469 scopus 로고    scopus 로고
    • Prevalence, characteristics and clinical diagnosis of maturity onset diabetes of the young due to mutations in HNF1A, HNF4A, and glucokinase: results from the SEARCH for diabetes in youth
    • Pihoker C, Gilliam LK, Ellard S, Dabelea D, Davis C, Dolan LM, et al. Prevalence, characteristics and clinical diagnosis of maturity onset diabetes of the young due to mutations in HNF1A, HNF4A, and glucokinase: results from the SEARCH for diabetes in youth. J Clin Endocrinol Metab (2013) 98:4055-62. doi:10.1210/jc.2013-1279
    • (2013) J Clin Endocrinol Metab , vol.98 , pp. 4055-4062
    • Pihoker, C.1    Gilliam, L.K.2    Ellard, S.3    Dabelea, D.4    Davis, C.5    Dolan, L.M.6
  • 43
    • 20244364399 scopus 로고    scopus 로고
    • Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients
    • Xu JY, Dan QH, Chan V, Wat NM, Tam S, Tiu SC, et al. Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients. Eur J Hum Genet (2004) 13:422-7. doi:10.1038/sj.ejhg.5201347
    • (2004) Eur J Hum Genet , vol.13 , pp. 422-427
    • Xu, J.Y.1    Dan, Q.H.2    Chan, V.3    Wat, N.M.4    Tam, S.5    Tiu, S.C.6
  • 44
    • 0037300839 scopus 로고    scopus 로고
    • Genetic epidemiology of MODY in the Czech Republic: new mutations in the MODY genes HNF-4alpha, GCK and HNF-1alpha
    • Pruhova S, Ek J, Lebl J, Sumnik Z, Saudek F, Andel M, et al. Genetic epidemiology of MODY in the Czech Republic: new mutations in the MODY genes HNF-4alpha, GCK and HNF-1alpha. Diabetologia (2003) 46:291-5. doi:10.1007/s00125-002-1010-7
    • (2003) Diabetologia , vol.46 , pp. 291-295
    • Pruhova, S.1    Ek, J.2    Lebl, J.3    Sumnik, Z.4    Saudek, F.5    Andel, M.6
  • 45
    • 23844518966 scopus 로고    scopus 로고
    • Half of clinically defined maturity onset diabetes of the young patients in Denmark do not have mutations in HNF4A, GCK and TCF1
    • Johansen A, Ek J, Mortensen HB, Pedersen O, Hansen T. Half of clinically defined maturity onset diabetes of the young patients in Denmark do not have mutations in HNF4A, GCK and TCF1. J Clin Endocrinol Metab (2005) 90:4607-14. doi:10.1210/jc.2005-0196
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 4607-4614
    • Johansen, A.1    Ek, J.2    Mortensen, H.B.3    Pedersen, O.4    Hansen, T.5
  • 46
    • 8044260804 scopus 로고    scopus 로고
    • Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY2 families
    • Velho G, Blanche H, Vaxillaire M, Bellanne-Chantelot C, Pardini VC, Timsit J, et al. Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY2 families. Diabetologia (1997) 40:217-24. doi:10.1007/s001250050666
    • (1997) Diabetologia , vol.40 , pp. 217-224
    • Velho, G.1    Blanche, H.2    Vaxillaire, M.3    Bellanne-Chantelot, C.4    Pardini, V.C.5    Timsit, J.6
  • 47
    • 8244219694 scopus 로고    scopus 로고
    • Identification of nine novel mutations in the hepatocyte nuclear factor1alpha gene associated with maturity-onset diabetes of the young (MODY3)
    • Vaxillaire M, Rouard M, Yamagata K, Oda N, Kaisaki PJ, Boriraj VV, et al. Identification of nine novel mutations in the hepatocyte nuclear factor1alpha gene associated with maturity-onset diabetes of the young (MODY3). Hum Mol Genet (1997) 6:583±58. doi:10.1093/hmg/6.4.583
    • (1997) Hum Mol Genet , vol.6
    • Vaxillaire, M.1    Rouard, M.2    Yamagata, K.3    Oda, N.4    Kaisaki, P.J.5    Boriraj, V.V.6
  • 48
    • 0032941772 scopus 로고    scopus 로고
    • Molecular genetics of MODY in Germany
    • Lindner TH, Cockburn BN, Bell GI. Molecular genetics of MODY in Germany. Diabetologia (1999) 42:121-3. doi:10.1007/s001250051128
    • (1999) Diabetologia , vol.42 , pp. 121-123
    • Lindner, T.H.1    Cockburn, B.N.2    Bell, G.I.3
  • 49
    • 30044441418 scopus 로고    scopus 로고
    • Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY)
    • Toaima D, Nake A, Wendenburg J, Praedicow K, Rohayem J, Engel K, et al. Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY). Hum Mutat (2005) 25:503-4. doi:10.1002/humu.9334
    • (2005) Hum Mutat , vol.25 , pp. 503-504
    • Toaima, D.1    Nake, A.2    Wendenburg, J.3    Praedicow, K.4    Rohayem, J.5    Engel, K.6
  • 50
    • 80054961266 scopus 로고    scopus 로고
    • Association of novel variants in the hepatocyte nuclear factor-4A gene with maturity onset diabetes of the young and early onset type 2 diabetes
    • Anuradha S, Radha V, Mohan V. Association of novel variants in the hepatocyte nuclear factor-4A gene with maturity onset diabetes of the young and early onset type 2 diabetes. Clin Genet (2011) 80:541-9. doi:10.1111/j.1399-0004.2010.01577.x
    • (2011) Clin Genet , vol.80 , pp. 541-549
    • Anuradha, S.1    Radha, V.2    Mohan, V.3
  • 51
    • 0034947265 scopus 로고    scopus 로고
    • High prevalence of glucokinase mutations in Italian children with MODY Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI
    • Massa O, Meschi F, Cuesta-Munoz A, Caumo A, Cerutti F, Toni S, et al. High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI. Diabetologia (2001) 44(7):898-905. doi:10.1007/s001250100530
    • (2001) Diabetologia , vol.44 , Issue.7 , pp. 898-905
    • Massa, O.1    Meschi, F.2    Cuesta-Munoz, A.3    Caumo, A.4    Cerutti, F.5    Toni, S.6
  • 52
    • 0242333673 scopus 로고    scopus 로고
    • Identification of eight novel glucokinase mutations in Italian children with maturity-onset diabetes of the young
    • Mantovani V, SalardI S, Cerreta V, Bastia D, Cenci M, Ragni L, et al. Identification of eight novel glucokinase mutations in Italian children with maturity-onset diabetes of the young. Hum Mutat (2003) 22:338. doi:10.1002/humu.9179
    • (2003) Hum Mutat , vol.22 , pp. 338
    • Mantovani, V.1    Salard, I.S.2    Cerreta, V.3    Bastia, D.4    Cenci, M.5    Ragni, L.6
  • 53
    • 0034771385 scopus 로고    scopus 로고
    • Early onset type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor-1alpha and glucokinase
    • Gragnoli C, Cockburn BN, Chiaramonte F, Gorini A, Marietti G, Marozzi G, et al. Early onset type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor-1alpha and glucokinase. Diabetologia (2001) 44:1326-9. doi:10.1007/s001250100644
    • (2001) Diabetologia , vol.44 , pp. 1326-1329
    • Gragnoli, C.1    Cockburn, B.N.2    Chiaramonte, F.3    Gorini, A.4    Marietti, G.5    Marozzi, G.6
  • 54
    • 0030798412 scopus 로고    scopus 로고
    • Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene
    • Gragnoli C, Lindner T, Cockburn BN, Kaisaki PJ, Gragnoli F, Marozzi G, et al. Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene. Diabetes (1997) 46:1648-51. doi:10.2337/diacare.46.10.1648
    • (1997) Diabetes , vol.46 , pp. 1648-1651
    • Gragnoli, C.1    Lindner, T.2    Cockburn, B.N.3    Kaisaki, P.J.4    Gragnoli, F.5    Marozzi, G.6
  • 57
    • 17544403804 scopus 로고    scopus 로고
    • Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families
    • Costa A, Bescos M, Velho G, Chevre J, Vidal J, Sesmilo G, et al. Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families. Eur J Endocrinol (2000) 142:380-6. doi:10.1530/eje.0.1420380
    • (2000) Eur J Endocrinol , vol.142 , pp. 380-386
    • Costa, A.1    Bescos, M.2    Velho, G.3    Chevre, J.4    Vidal, J.5    Sesmilo, G.6
  • 58
    • 0036075535 scopus 로고    scopus 로고
    • Nine novel mutations in maturity-onset diabetes of the young (MODY) candidate genes in 22 Spanish families
    • Barrio R, Bellanne-Chantelot C, Moreno JC, Morel V, Calle H, Alonso M, et al. Nine novel mutations in maturity-onset diabetes of the young (MODY) candidate genes in 22 Spanish families. J Clin Endocrinol Metab (2002) 87:2532-9. doi:10.1210/jcem.87.6.8530
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 2532-2539
    • Barrio, R.1    Bellanne-Chantelot, C.2    Moreno, J.C.3    Morel, V.4    Calle, H.5    Alonso, M.6
  • 59
    • 0032857518 scopus 로고    scopus 로고
    • High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes
    • Lehto M, Wipemo C, Ivarsson SA, Lindgren C, Lipsanen-Nyman M, Weng J, et al. High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes. Diabetologia (1999) 42:1131-7. doi:10.1007/s001250051281
    • (1999) Diabetologia , vol.42 , pp. 1131-1137
    • Lehto, M.1    Wipemo, C.2    Ivarsson, S.A.3    Lindgren, C.4    Lipsanen-Nyman, M.5    Weng, J.6
  • 61
    • 14444278300 scopus 로고    scopus 로고
    • Mutations in the hepatocyte nuclear factor 1 alpha gene are a common cause of maturity-onset diabetes of the young in the United Kingdom
    • Frayling T, Bulman MP, Ellard S, Appleton M, Dronsfield M, Mackie A, et al. Mutations in the hepatocyte nuclear factor 1 alpha gene are a common cause of maturity-onset diabetes of the young in the United Kingdom. Diabetes (1997) 46:720-5. doi:10.2337/diab.46.4.720
    • (1997) Diabetes , vol.46 , pp. 720-725
    • Frayling, T.1    Bulman, M.P.2    Ellard, S.3    Appleton, M.4    Dronsfield, M.5    Mackie, A.6
  • 62
    • 43549084587 scopus 로고    scopus 로고
    • Monogenetic diabetes of young, pharmacogenetics and relevance to multifactorial forms of type 2 diabetes
    • Vaxillaire M, Froguel P. Monogenetic diabetes of young, pharmacogenetics and relevance to multifactorial forms of type 2 diabetes. Endocr Rev (2008) 29:254-64
    • (2008) Endocr Rev , vol.29 , pp. 254-264
    • Vaxillaire, M.1    Froguel, P.2
  • 63
    • 0025690311 scopus 로고
    • Liver enriched transcription factor HNF-4 Is a novel member of the steroid hormone receptor superfamily
    • Sladek FM, Zhong WM, Lai E, Darnell JE Jr. Liver enriched transcription factor HNF-4 Is a novel member of the steroid hormone receptor superfamily. Genes Dev (1990) 4:2353-65. doi:10.1101/gad.4.12b.2353
    • (1990) Genes Dev , vol.4 , pp. 2353-2365
    • Sladek, F.M.1    Zhong, W.M.2    Lai, E.3    Darnell, J.E.4
  • 64
    • 0026555197 scopus 로고
    • A transcriptional hierarchy involved in mammalian cell-type specification
    • Kuo CJ, Conley PB, Chen L, Sladek FM, Darnell JE Jr., Crabtree GR. A transcriptional hierarchy involved in mammalian cell-type specification. Nature (1992) 355:457-61. doi:10.1038/355457a0
    • (1992) Nature , vol.355 , pp. 457-461
    • Kuo, C.J.1    Conley, P.B.2    Chen, L.3    Sladek, F.M.4    Darnell, J.E.5    Crabtree, G.R.6
  • 65
    • 0026636624 scopus 로고
    • Transcriptional regulation of human apolipoprotein genes ApoB, ApoCIII, and ApoAII by members of the steroid hormone receptor superfamily HNF-4, ARP-1, EAR-2, and EAR-3
    • Ladias JA, Hadzopoulou-Cladaras M, Kardassis D, Cardot P, Cheng J, Zannis V, et al. Transcriptional regulation of human apolipoprotein genes ApoB, ApoCIII, and ApoAII by members of the steroid hormone receptor superfamily HNF-4, ARP-1, EAR-2, and EAR-3. J Biol Chem (1992) 267:15849-60
    • (1992) J Biol Chem , vol.267 , pp. 15849-15860
    • Ladias, J.A.1    Hadzopoulou-Cladaras, M.2    Kardassis, D.3    Cardot, P.4    Cheng, J.5    Zannis, V.6
  • 66
    • 0030695445 scopus 로고    scopus 로고
    • The maturity-onset diabetes of the young (MODY1) transcription factor HNF4a regulates expression of genes required for glucose transport and metabolism
    • Stoffel M, Duncan SA. The maturity-onset diabetes of the young (MODY1) transcription factor HNF4a regulates expression of genes required for glucose transport and metabolism. Proc Natl Acad U S A (1997) 94:13209-14. doi:10.1073/pnas.94.24.13209
    • (1997) Proc Natl Acad U S A , vol.94 , pp. 13209-13214
    • Stoffel, M.1    Duncan, S.A.2
  • 67
    • 0034680936 scopus 로고    scopus 로고
    • Hepatocyte nuclear factor 4a regulates the expression of pancreatic b-cell genes implicated in glucose metabolism and nutrient-induced insulin secretion
    • Wang H, Maechler P, Antinozzi PA, Hagenfeldt KA, Wollheim CB. Hepatocyte nuclear factor 4a regulates the expression of pancreatic b-cell genes implicated in glucose metabolism and nutrient-induced insulin secretion. J Biol Chem (2000) 275:35953-9. doi:10.1074/jbc. M006612200
    • (2000) J Biol Chem , vol.275 , pp. 35953-35959
    • Wang, H.1    Maechler, P.2    Antinozzi, P.A.3    Hagenfeldt, K.A.4    Wollheim, C.B.5
  • 68
    • 79954416864 scopus 로고    scopus 로고
    • Hepatocyte nuclear factor-4a gene mutation associated with familial neonatal hyperinsulinism and maturity onset diabetes of the young
    • Pingul MM, Hughes N, Wu A, Stanley CA, Gruppuso PA. Hepatocyte nuclear factor-4a gene mutation associated with familial neonatal hyperinsulinism and maturity onset diabetes of the young. J Pediatr (2011) 158:852-4. doi:10.1016/j.jpeds.2011.01.003
    • (2011) J Pediatr , vol.158 , pp. 852-854
    • Pingul, M.M.1    Hughes, N.2    Wu, A.3    Stanley, C.A.4    Gruppuso, P.A.5
  • 69
    • 77951662347 scopus 로고    scopus 로고
    • Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF1A gene mutation
    • Flanagan SE, Kapoor RR, Mali G. Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF1A gene mutation. Eur J Endocrinol (2010) 162:987-92. doi:10.1530/EJE-09-0861
    • (2010) Eur J Endocrinol , vol.162 , pp. 987-992
    • Flanagan, S.E.1    Kapoor, R.R.2    Mali, G.3
  • 70
    • 84890145303 scopus 로고    scopus 로고
    • Maturity onset diabetes if the young; identification and diagnosis
    • McDonald TJ, Ellard S. Maturity onset diabetes if the young; identification and diagnosis. Ann Clin Biochem (2013) 50(Pt):403-15. doi:10.1177/0004563213483458
    • (2013) Ann Clin Biochem , vol.50 , Issue.PART , pp. 403-415
    • McDonald, T.J.1    Ellard, S.2
  • 71
  • 72
    • 23844433186 scopus 로고    scopus 로고
    • Glucokinase, glucose homeostasis, and diabetes mellitus
    • Matschinsky FM. Glucokinase, glucose homeostasis, and diabetes mellitus. Curr Diab Rep (2005) 5:171-6. doi:10.1007/s11892-005-0005-4
    • (2005) Curr Diab Rep , vol.5 , pp. 171-176
    • Matschinsky, F.M.1
  • 73
    • 0028353674 scopus 로고
    • Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations
    • Byrne MM, Sturis J, Clément K, Vionnet N, Pueyo ME, Stoffel M, et al. Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations. J Clin Invest (1994) 93(3):1120-30. doi:10.1172/JCI117064
    • (1994) J Clin Invest , vol.93 , Issue.3 , pp. 1120-1130
    • Byrne, M.M.1    Sturis, J.2    Clément, K.3    Vionnet, N.4    Pueyo, M.E.5    Stoffel, M.6
  • 74
    • 0034000635 scopus 로고    scopus 로고
    • A high prevalence of glucokinase mutation in gestational diabetic subjects selected by clinical criteria
    • Ellard S, Beards F, Allen LI, Shepherd M, Ballantyne E, Harvey R, et al. A high prevalence of glucokinase mutation in gestational diabetic subjects selected by clinical criteria. Diabetologia (2000) 43:250-3. doi:10.1007/s001250050038
    • (2000) Diabetologia , vol.43 , pp. 250-253
    • Ellard, S.1    Beards, F.2    Allen, L.I.3    Shepherd, M.4    Ballantyne, E.5    Harvey, R.6
  • 75
    • 0035960122 scopus 로고    scopus 로고
    • Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young
    • Fajan SS, Bell GI, Polonsky KS. Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. N Engl J Med (2001) 345:971-80. doi:10.1056/NEJMra002168
    • (2001) N Engl J Med , vol.345 , pp. 971-980
    • Fajan, S.S.1    Bell, G.I.2    Polonsky, K.S.3
  • 76
    • 0026562918 scopus 로고
    • Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus
    • Vionnet N, Stoffel M, Takeda J, Yasuda K, Bell GI, Zouali H, et al. Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus. Nature (1992) 356:721-2. doi:10.1038/356721a0
    • (1992) Nature , vol.356 , pp. 721-722
    • Vionnet, N.1    Stoffel, M.2    Takeda, J.3    Yasuda, K.4    Bell, G.I.5    Zouali, H.6
  • 78
    • 0242384237 scopus 로고    scopus 로고
    • Glucokinase (GCK) mutations in hyper-and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy
    • Gloyn AL. Glucokinase (GCK) mutations in hyper-and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy. Hum Mutat (2003) 22:353-62. doi:10.1002/humu.10277
    • (2003) Hum Mutat , vol.22 , pp. 353-362
    • Gloyn, A.L.1
  • 79
    • 30044443396 scopus 로고    scopus 로고
    • Effects of novel maturity-onset diabetes of the young (MODY)-associated mutations on glucokinase activity and protein stability
    • Galán M, Vincent O, Roncero I, Azriel S, Boix-Pallares P, Delgado-Alvarez E, et al. Effects of novel maturity-onset diabetes of the young (MODY)-associated mutations on glucokinase activity and protein stability. Biochem J (2006) 393:386-96. doi:10.1042/BJ20051137
    • (2006) Biochem J , vol.393 , pp. 386-396
    • Galán, M.1    Vincent, O.2    Roncero, I.3    Azriel, S.4    Boix-Pallares, P.5    Delgado-Alvarez, E.6
  • 80
    • 20244377376 scopus 로고    scopus 로고
    • Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young
    • Gloyn AL, Odili S, Zelent D, Buettger C, Castleden HAJ, Steele AM, et al. Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young. J Biol Chem (2005) 280:14105-13. doi:10.1074/jbc. M413146200
    • (2005) J Biol Chem , vol.280 , pp. 14105-14113
    • Gloyn, A.L.1    Odili, S.2    Zelent, D.3    Buettger, C.4    Castleden, H.A.J.5    Steele, A.M.6
  • 81
    • 70350741368 scopus 로고    scopus 로고
    • Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia
    • Osbak KK, Colclough K, Saint-Martin C, Beer NL, Bellanné-Chantelot C, Ellard S, et al. Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia. Hum Mutat (2009) 30(11):1512-26. doi:10.1002/humu.21110
    • (2009) Hum Mutat , vol.30 , Issue.11 , pp. 1512-1526
    • Osbak, K.K.1    Colclough, K.2    Saint-Martin, C.3    Beer, N.L.4    Bellanné-Chantelot, C.5    Ellard, S.6
  • 82
    • 33845270456 scopus 로고    scopus 로고
    • Transcription factors regulating beta cell function
    • Cerf ME. Transcription factors regulating beta cell function. Eur J Endocrinol (2006) 155:671-9. doi:10.1530/eje.1.02277
    • (2006) Eur J Endocrinol , vol.155 , pp. 671-679
    • Cerf, M.E.1
  • 83
    • 79952837279 scopus 로고    scopus 로고
    • Differential effects of HNF-1a mutations associated with familial young onset diabetes on target gene regulation
    • Galan M, Garcia-Herrero CM, Azriel S, Gargallo M, Durán M, Gorgojo JJ, et al. Differential effects of HNF-1a mutations associated with familial young onset diabetes on target gene regulation. Mol Med (2011) 17:256-65. doi:10.2119/molmed.2010.00097
    • (2011) Mol Med , vol.17 , pp. 256-265
    • Galan, M.1    Garcia-Herrero, C.M.2    Azriel, S.3    Gargallo, M.4    Durán, M.5    Gorgojo, J.J.6
  • 84
    • 0027323856 scopus 로고
    • Administration of sulfonylureas can increase glucose-induced insulin secretion for decades in patients with maturity-onset diabetes of the young
    • Fajans SS, Brown MB. Administration of sulfonylureas can increase glucose-induced insulin secretion for decades in patients with maturity-onset diabetes of the young. Diabetes Care (1993) 16:1254-61. doi:10.2337/diacare.16.9.1254
    • (1993) Diabetes Care , vol.16 , pp. 1254-1261
    • Fajans, S.S.1    Brown, M.B.2
  • 85
    • 25644460500 scopus 로고    scopus 로고
    • A prevalent amino acid polymorphism at codon 98 (Ala98Val) of the hepatocyte nuclear factor-1alpha is associated with maturity-onset diabetes of the young and younger age at onset of type 2 diabetes in Asian Indians
    • Anuradha S, Radha V, Deepa R, Hansen T, Carstensen B, Pedersen O, et al. A prevalent amino acid polymorphism at codon 98 (Ala98Val) of the hepatocyte nuclear factor-1alpha is associated with maturity-onset diabetes of the young and younger age at onset of type 2 diabetes in Asian Indians. Diabetes Care (2005) 28(10):2430-5. doi:10.2337/diacare.28.10.2430
    • (2005) Diabetes Care , vol.28 , Issue.10 , pp. 2430-2435
    • Anuradha, S.1    Radha, V.2    Deepa, R.3    Hansen, T.4    Carstensen, B.5    Pedersen, O.6
  • 86
    • 21544451980 scopus 로고    scopus 로고
    • Cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in hepatocyte nuclear factor-1alpha mutation carriers
    • Stride A, Ellard S, Clark P, Shakespeare L, Salzmann M, Shepherd M, et al. Cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in hepatocyte nuclear factor-1alpha mutation carriers. Diabetes Care (2005) 28:1751-6. doi:10.2337/diacare.28.7.1751
    • (2005) Diabetes Care , vol.28 , pp. 1751-1756
    • Stride, A.1    Ellard, S.2    Clark, P.3    Shakespeare, L.4    Salzmann, M.5    Shepherd, M.6
  • 87
    • 84865720828 scopus 로고    scopus 로고
    • Serum levels of pancreatic stone protein (PSP)/reg1A as an indicator of beta cell apoptosis suggest an increased apoptosis rate in hepatocyte nuclear factor-1 alpha (HNF1A-MODY) carriers from the third decade of life onward
    • Bacon S, Kyithar MP, Schmid J, Rizvi SR, Bonner C, Graf R, et al. Serum levels of pancreatic stone protein (PSP)/reg1A as an indicator of beta cell apoptosis suggest an increased apoptosis rate in hepatocyte nuclear factor-1 alpha (HNF1A-MODY) carriers from the third decade of life onward. BMC Endocr Disord (2012) 12:13. doi:10.1186/1472-6823-12-13
    • (2012) BMC Endocr Disord , vol.12 , pp. 13
    • Bacon, S.1    Kyithar, M.P.2    Schmid, J.3    Rizvi, S.R.4    Bonner, C.5    Graf, R.6
  • 88
    • 0036544854 scopus 로고    scopus 로고
    • L. Pbx1 inactivation disrupts pancreas development and in Ipf1-deficient mice promotes diabetes mellitus
    • Kim SK, Selleri L, Lee JS, Zhang AY, Gu X, Jacobs Y, et al. L. Pbx1 inactivation disrupts pancreas development and in Ipf1-deficient mice promotes diabetes mellitus. Nature Genet (2002) 30:430-5. doi:10.1038/ng860
    • (2002) Nature Genet , vol.30 , pp. 430-435
    • Kim, S.K.1    Selleri, L.2    Lee, J.S.3    Zhang, A.Y.4    Gu, X.5    Jacobs, Y.6
  • 89
    • 0141787919 scopus 로고    scopus 로고
    • Agenesis of human pancreas due to decreased half-life of insulin promoter factor 1
    • Schwitzgebel VM, Mamin A, Brun T, Ritz-Laser B, Zaiko M, Maret A, et al. Agenesis of human pancreas due to decreased half-life of insulin promoter factor 1. J Clin Endocr Metab (2003) 88:4398-406. doi:10.1210/jc.2003-030046
    • (2003) J Clin Endocr Metab , vol.88 , pp. 4398-4406
    • Schwitzgebel, V.M.1    Mamin, A.2    Brun, T.3    Ritz-Laser, B.4    Zaiko, M.5    Maret, A.6
  • 90
    • 0034454416 scopus 로고    scopus 로고
    • Mis-sense mutation in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in Caucasians
    • Hansen L, Urioste S, Petersen HV, Jensen JN, Eiberg H, Barbetti F, et al. Mis-sense mutation in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in Caucasians. J Clin Endocrinol Metab (2000) 85:1323-6. doi:10.1210/jc.85.3.1323
    • (2000) J Clin Endocrinol Metab , vol.85 , pp. 1323-1326
    • Hansen, L.1    Urioste, S.2    Petersen, H.V.3    Jensen, J.N.4    Eiberg, H.5    Barbetti, F.6
  • 91
    • 0028149890 scopus 로고
    • Insulin-promoter-factor 1 is required for pancreas development in mice
    • Jonsson J, Carlsson L, Edlund T, Edlund H. Insulin-promoter-factor 1 is required for pancreas development in mice. Nature (1994) 371:606-9. doi:10.1038/371606a0
    • (1994) Nature , vol.371 , pp. 606-609
    • Jonsson, J.1    Carlsson, L.2    Edlund, T.3    Edlund, H.4
  • 92
    • 0032525981 scopus 로고    scopus 로고
    • Beta-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the beta-cell phenotype and maturity onset diabetes
    • Ahlgren U, Jonsson J, Jonsson L, Simu K, Edlund H. Beta-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the beta-cell phenotype and maturity onset diabetes. Genes Dev (1998) 12:1763-8. doi:10.1101/gad.12.12.1763
    • (1998) Genes Dev , vol.12 , pp. 1763-1768
    • Ahlgren, U.1    Jonsson, J.2    Jonsson, L.3    Simu, K.4    Edlund, H.5
  • 94
    • 0037408284 scopus 로고    scopus 로고
    • Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1-beta gene mutation
    • Bingham C, Ellard S, Van't HoffWG, Simmonds HA, Marinaki AM, Badman MK, et al. Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1-beta gene mutation. Kidnet Int (2003) 63:1645-51. doi:10.1046/j.1523-1755.2003.00903.x
    • (2003) Kidnet Int , vol.63 , pp. 1645-1651
    • Bingham, C.1    Ellard, S.2    Van't Hoff, W.G.3    Simmonds, H.A.4    Marinaki, A.M.5    Badman, M.K.6
  • 95
    • 84963796403 scopus 로고    scopus 로고
    • Idetification and functional characterization of P159L mutation in HNF1B in a family with maturity-onset diabetes of the young5 (MODY5)
    • Kim EK, Lee JS, Cheong HI, Chung SS, Kwak SH, Park KS. Idetification and functional characterization of P159L mutation in HNF1B in a family with maturity-onset diabetes of the young5 (MODY5). Genomics Inform (2014) 12:240-6. doi:10.5808/GI.2014.12.4.240
    • (2014) Genomics Inform , vol.12 , pp. 240-246
    • Kim, E.K.1    Lee, J.S.2    Cheong, H.I.3    Chung, S.S.4    Kwak, S.H.5    Park, K.S.6
  • 96
    • 0030886674 scopus 로고    scopus 로고
    • Diabetes, defective pancreatic morphogenesis, and abnormal enteroendocrine differentiation in BETA2/neuroD-deficient mice
    • Naya FJ, Huang H-P, Qiu Y, Mutoh H, DeMayo FJ, Leiter AB, et al. Diabetes, defective pancreatic morphogenesis, and abnormal enteroendocrine differentiation in BETA2/neuroD-deficient mice. Genes Dev (1997) 11:2323-34. doi:10.1101/gad.11.18.2323
    • (1997) Genes Dev , vol.11 , pp. 2323-2334
    • Naya, F.J.1    Huang, H.-P.2    Qiu, Y.3    Mutoh, H.4    DeMayo, F.J.5    Leiter, A.B.6
  • 98
    • 0032475869 scopus 로고    scopus 로고
    • Molecular cloning and characterization of TIEG2 reveals a new subfamily of transforming growth factor-beta-inducible Sp1-like zinc finger-encoding genes involved in the regulation of cell growth
    • Cook T, Gebelein B, Mesa K, Mladek A, Urrutia R. Molecular cloning and characterization of TIEG2 reveals a new subfamily of transforming growth factor-beta-inducible Sp1-like zinc finger-encoding genes involved in the regulation of cell growth. J Biol Chem (1998) 273(40):25929-36. doi:10.1074/jbc.273.40.25929
    • (1998) J Biol Chem , vol.273 , Issue.40 , pp. 25929-25936
    • Cook, T.1    Gebelein, B.2    Mesa, K.3    Mladek, A.4    Urrutia, R.5
  • 99
    • 0034672494 scopus 로고    scopus 로고
    • Identification of KLF13 and KLF14 (SP6), novel members of the SP/XKLF transcription factor family
    • Scohy S, Gabant P, Van Reeth T, Hertveldt V, Dreze PL, Van Vooren P, et al. Identification of KLF13 and KLF14 (SP6), novel members of the SP/XKLF transcription factor family. Genomics (2001) 70(1):93-101. doi:10.1006/geno.2000.6362
    • (2001) Genomics , vol.70 , Issue.1 , pp. 93-101
    • Scohy, S.1    Gabant, P.2    Van Reeth, T.3    Hertveldt, V.4    Dreze, P.L.5    Van Vooren, P.6
  • 100
    • 0842284799 scopus 로고    scopus 로고
    • Beta-cell glucose toxicity, lipotoxicity, and chronic oxidative stress in type 2 diabetes
    • Robertson RP, Harmon J, Tran PO, Poitout V. Beta-cell glucose toxicity, lipotoxicity, and chronic oxidative stress in type 2 diabetes. Diabetes (2004) 53:S119-24. doi:10.2337/diabetes.53.2007.S119
    • (2004) Diabetes , vol.53 , pp. S119-S124
    • Robertson, R.P.1    Harmon, J.2    Tran, P.O.3    Poitout, V.4
  • 101
    • 0035968445 scopus 로고    scopus 로고
    • Carboxyl ester lipase: its pathophysiological implications
    • Lombardo DY, Howles PN. Carboxyl ester lipase: its pathophysiological implications. Biochem Biophy Acta (2001) 1533:1-28
    • (2001) Biochem Biophy Acta , vol.1533 , pp. 1-28
    • Lombardo, D.Y.1    Howles, P.N.2
  • 102
    • 0036915534 scopus 로고    scopus 로고
    • Carboxyl ester lipase: structure-function relationship and physiological role in lipoprotein metabolism and arterosclerosis
    • Hui DY, Howles PN. Carboxyl ester lipase: structure-function relationship and physiological role in lipoprotein metabolism and arterosclerosis. J Lipid Res (2002) 43:2017-30. doi:10.1194/jlr. R200013-JLR200
    • (2002) J Lipid Res , vol.43 , pp. 2017-2030
    • Hui, D.Y.1    Howles, P.N.2
  • 103
    • 29444440400 scopus 로고    scopus 로고
    • Mutations in the CEL-VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction
    • Raeder H, Johansson S, Holm PI, Haldorsen IS, Mas E, Sbarra V, et al. Mutations in the CEL-VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction. Nat Genet (2006) 38:54-62. doi:10.1038/ng1708
    • (2006) Nat Genet , vol.38 , pp. 54-62
    • Raeder, H.1    Johansson, S.2    Holm, P.I.3    Haldorsen, I.S.4    Mas, E.5    Sbarra, V.6
  • 104
    • 0030897629 scopus 로고    scopus 로고
    • The Pax4 gene is essential for differentiation of insulin-producing cells in the mammalian pancreas
    • Sosa-Pineda B, Chowdhury K, Torres M, Oliver G, Gruss P. The Pax4 gene is essential for differentiation of insulin-producing cells in the mammalian pancreas. Nature (1997) 386:399-402. doi:10.1038/386399a0
    • (1997) Nature , vol.386 , pp. 399-402
    • Sosa-Pineda, B.1    Chowdhury, K.2    Torres, M.3    Oliver, G.4    Gruss, P.5
  • 105
    • 0033499662 scopus 로고    scopus 로고
    • Paired-homeodomain transcription factor PAX4 acts as a transcriptional repressor in early pancreatic development
    • Smith SB, Ee HC, Conners JR, German MS. Paired-homeodomain transcription factor PAX4 acts as a transcriptional repressor in early pancreatic development. Mol Cell Biol (1999) 19:8272-80. doi:10.1128/MCB.19.12.8272
    • (1999) Mol Cell Biol , vol.19 , pp. 8272-8280
    • Smith, S.B.1    Ee, H.C.2    Conners, J.R.3    German, M.S.4
  • 106
    • 17444409580 scopus 로고    scopus 로고
    • Association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to cell regenerative capacity
    • Biason-Lauber A, Boehm B, Lang-Muritano M, Gauthier BR, Brun T, Wollheim CB, et al. Association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to cell regenerative capacity. Diabetologia (2005) 48:900-5. doi:10.1007/s00125-005-1723-5
    • (2005) Diabetologia , vol.48 , pp. 900-905
    • Biason-Lauber, A.1    Boehm, B.2    Lang-Muritano, M.3    Gauthier, B.R.4    Brun, T.5    Wollheim, C.B.6
  • 108
    • 0034915177 scopus 로고    scopus 로고
    • Insulin inhibits intranuclear nuclear factor kappa-B and stimulates I-kappa-B in mononuclear cells in obese subjects: evidence for an anti-inflammatory effect?
    • Dandona P, Aljada A, Mohanty P, Ghanim H, Hamouda W, Assian E, et al. Insulin inhibits intranuclear nuclear factor kappa-B and stimulates I-kappa-B in mononuclear cells in obese subjects: evidence for an anti-inflammatory effect? J Clin Endocr Metab (2001) 86:3257-65. doi:10.1210/jcem.86.7.7623
    • (2001) J Clin Endocr Metab , vol.86 , pp. 3257-3265
    • Dandona, P.1    Aljada, A.2    Mohanty, P.3    Ghanim, H.4    Hamouda, W.5    Assian, E.6
  • 109
    • 0028797601 scopus 로고
    • Molecular cloning, characterization, and chromosomal localization of a human lymphoid tyrosine kinase relayed to murine BLK
    • Islam KB, Rabbani H, Larsson C, Sanders R, Smith CI. Molecular cloning, characterization, and chromosomal localization of a human lymphoid tyrosine kinase relayed to murine BLK. J Immunol (1995) 154:1265-72
    • (1995) J Immunol , vol.154 , pp. 1265-1272
    • Islam, K.B.1    Rabbani, H.2    Larsson, C.3    Sanders, R.4    Smith, C.I.5
  • 110
    • 0028893443 scopus 로고
    • Molecular cloning and chromosomal localization of the human homologue of a B-lymphocyte specific protein tyrosine kinase (Blk)
    • Drebin JA, Hartzell SW, Griffin C, Campbell MJ, Niederhuber JE. Molecular cloning and chromosomal localization of the human homologue of a B-lymphocyte specific protein tyrosine kinase (Blk). Oncogene (1995) 10(3):477-86
    • (1995) Oncogene , vol.10 , Issue.3 , pp. 477-486
    • Drebin, J.A.1    Hartzell, S.W.2    Griffin, C.3    Campbell, M.J.4    Niederhuber, J.E.5
  • 111
    • 2342539735 scopus 로고    scopus 로고
    • Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23
    • Kim SH, Ma X, Weremowicz S, Ercolino T, Powers C, Mlynarski W, et al. Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23. Diabetes (2004) 53:1375-84. doi:10.2337/diabetes.53.5.1375
    • (2004) Diabetes , vol.53 , pp. 1375-1384
    • Kim, S.H.1    Ma, X.2    Weremowicz, S.3    Ercolino, T.4    Powers, C.5    Mlynarski, W.6
  • 112
    • 48249151437 scopus 로고    scopus 로고
    • A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults
    • Tarasov AI, Nicolson TJ, Riveline JP, Taneja TK, Baldwin SA, Baldwin JM, et al. A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults. Diabetes (2008) 57:1595-604. doi:10.2337/db07-1547
    • (2008) Diabetes , vol.57 , pp. 1595-1604
    • Tarasov, A.I.1    Nicolson, T.J.2    Riveline, J.P.3    Taneja, T.K.4    Baldwin, S.A.5    Baldwin, J.M.6
  • 114
    • 0028972501 scopus 로고
    • Reconstruction of I (KATP): an inward rectifier subunit plus the sulfonylurea receptor
    • Inagaki N, Gonoi T, Clement JP, Namba N, Inazawa J, Gonzalez G, et al. Reconstruction of I (KATP): an inward rectifier subunit plus the sulfonylurea receptor. Science (1995) 270:1166-70. doi:10.1126/science.270.5239.1166
    • (1995) Science , vol.270 , pp. 1166-1170
    • Inagaki, N.1    Gonoi, T.2    Clement, J.P.3    Namba, N.4    Inazawa, J.5    Gonzalez, G.6
  • 115
    • 4043088022 scopus 로고    scopus 로고
    • Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 gene encoding the kir6.2 subunit of the beta-cell potassium adenosine triphosphate channel
    • Gloyn AL, Cummings EA, Edghill EL, Harries LW, Scott R, Costa T, et al. Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 gene encoding the kir6.2 subunit of the beta-cell potassium adenosine triphosphate channel. J Clin Endocrinol Metab (2004) 89:3932-5. doi:10.1210/jc.2004-0568
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 3932-3935
    • Gloyn, A.L.1    Cummings, E.A.2    Edghill, E.L.3    Harries, L.W.4    Scott, R.5    Costa, T.6
  • 116
    • 21244487124 scopus 로고    scopus 로고
    • The C42R mutation in the Kir6.2(KCNJ11) gene as a cause of transient neonatal diabetes, or later-onset, apparently type 2 diabetes mellitus
    • Yorifuji T, Nagashima K, Kurokawa K, Kawai M, Oishi M, Akazawa Y, et al. The C42R mutation in the Kir6.2(KCNJ11) gene as a cause of transient neonatal diabetes, or later-onset, apparently type 2 diabetes mellitus. J Clin Endocrinol Metab (2005) 90:3174-8. doi:10.1210/jc.2005-0096
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 3174-3178
    • Yorifuji, T.1    Nagashima, K.2    Kurokawa, K.3    Kawai, M.4    Oishi, M.5    Akazawa, Y.6
  • 117
    • 19944427182 scopus 로고    scopus 로고
    • KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes
    • Massa O, Iafusco D, D'Amato E, Gloyn AL, Hattersly AT, Pasquino B, et al. KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes. Hum Mutat (2005) 25:22-7. doi:10.1002/humu.20124
    • (2005) Hum Mutat , vol.25 , pp. 22-27
    • Massa, O.1    Iafusco, D.2    D'Amato, E.3    Gloyn, A.L.4    Hattersly, A.T.5    Pasquino, B.6
  • 118
    • 44049086392 scopus 로고    scopus 로고
    • Destabilization of ATP-sensitive potassium channel activity by novel KCNJ11 mutations identified in congenital hyperinsulinism
    • Lin Y-W, Bushman JD, Yan F-F, Haidar S, MacMullen C, Ganguly A, et al. Destabilization of ATP-sensitive potassium channel activity by novel KCNJ11 mutations identified in congenital hyperinsulinism. J Biol Chem (2008) 283:9146-56. doi:10.1074/jbc. M708798200
    • (2008) J Biol Chem , vol.283 , pp. 9146-9156
    • Lin, Y.-W.1    Bushman, J.D.2    Yan, F.-F.3    Haidar, S.4    MacMullen, C.5    Ganguly, A.6
  • 119
    • 42949092018 scopus 로고    scopus 로고
    • The endosomal protein Appl1 mediates Akt substrate specificity and cell survival in vertebrate development
    • Schenck A, Goto-Silva L, Collinet C, Rhinn M, Giner A, Habermann B, et al. The endosomal protein Appl1 mediates Akt substrate specificity and cell survival in vertebrate development. Cell (2008) 133:486-97. doi:10.1016/j.cell.2008.02.044
    • (2008) Cell , vol.133 , pp. 486-497
    • Schenck, A.1    Goto-Silva, L.2    Collinet, C.3    Rhinn, M.4    Giner, A.5    Habermann, B.6
  • 120
    • 84862526033 scopus 로고    scopus 로고
    • The development and validation of a clinical prediction model to determine the probability of MODY in patients with young-onset diabetes
    • Shields BM, McDonald TJ, Ellard S, Campbell MJ, Hyde C, Hattersley AT. The development and validation of a clinical prediction model to determine the probability of MODY in patients with young-onset diabetes. Diabetologia (2012) 55(5):1265-72. doi:10.1007/s00125-011-2418-8
    • (2012) Diabetologia , vol.55 , Issue.5 , pp. 1265-1272
    • Shields, B.M.1    McDonald, T.J.2    Ellard, S.3    Campbell, M.J.4    Hyde, C.5    Hattersley, A.T.6
  • 121
    • 0036049411 scopus 로고    scopus 로고
    • Heterogeneity in young adult onset aetiology alters clinical characteristics
    • Owen KR, Shepherd M, Stride A, Ellard S, Hattersley AT. Heterogeneity in young adult onset aetiology alters clinical characteristics. Diabet Med (2002) 19(9):758-61. doi:10.1046/j.1464-5491.2002.00766.x
    • (2002) Diabet Med , vol.19 , Issue.9 , pp. 758-761
    • Owen, K.R.1    Shepherd, M.2    Stride, A.3    Ellard, S.4    Hattersley, A.T.5
  • 122
    • 84896141306 scopus 로고    scopus 로고
    • Positivity for islet cell autoantibodies in patients with monogenic diabetes is associated with later diabetes onset and higher HbA1c level
    • Urbanová J, Rypácková B, Procházková Z, Kucera P, Cerná M, Andel M, et al. Positivity for islet cell autoantibodies in patients with monogenic diabetes is associated with later diabetes onset and higher HbA1c level. Diabet Med (2014) 31:466-71. doi:10.1111/dme.12314
    • (2014) Diabet Med , vol.31 , pp. 466-471
    • Urbanová, J.1    Rypácková, B.2    Procházková, Z.3    Kucera, P.4    Cerná, M.5    Andel, M.6
  • 123
    • 80054692207 scopus 로고    scopus 로고
    • A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes
    • Thanabalasingham G, Shah N, Vaxillaire M, Hansen T, Tuomi T, Gašperíková D, et al. A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes. Diabetologia (2011) 54(11):2801-10. doi:10.1007/s00125-011-2261-y
    • (2011) Diabetologia , vol.54 , Issue.11 , pp. 2801-2810
    • Thanabalasingham, G.1    Shah, N.2    Vaxillaire, M.3    Hansen, T.4    Tuomi, T.5    Gašperíková, D.6
  • 124
    • 0034304925 scopus 로고    scopus 로고
    • HNF1 alpha controls renal glucose reabsorption in mouse and man
    • Pontoglio M, Prié D, Cheret C, Doyen A, Leroy C, Froguel P, et al. HNF1 alpha controls renal glucose reabsorption in mouse and man. EMBO Rep (2000) 1(4):359-65. doi:10.1093/embo-reports/kvd071
    • (2000) EMBO Rep , vol.1 , Issue.4 , pp. 359-365
    • Pontoglio, M.1    Prié, D.2    Cheret, C.3    Doyen, A.4    Leroy, C.5    Froguel, P.6
  • 125
    • 41149139275 scopus 로고    scopus 로고
    • Best practice guidelines for the molecular genetics diagnosis of maturity onset diabetes of the young
    • Ellard S, Bellanné-Chantelot C, Hattersley AT. Best practice guidelines for the molecular genetics diagnosis of maturity onset diabetes of the young. Diabetologia (2008) 51:546-53. doi:10.1007/s00125-008-0942-y
    • (2008) Diabetologia , vol.51 , pp. 546-553
    • Ellard, S.1    Bellanné-Chantelot, C.2    Hattersley, A.T.3
  • 126
    • 84881614898 scopus 로고    scopus 로고
    • Improved genetic testing for monogenic diabetes using targeted next-generation sequencing
    • Ellard S, Allen HL, Franco ED, Flanagan SE, Hysenaj G, Colclough K, et al. Improved genetic testing for monogenic diabetes using targeted next-generation sequencing. Diabetologia (2013) 56:1958-63. doi:10.1007/s00125-013-2962-5
    • (2013) Diabetologia , vol.56 , pp. 1958-1963
    • Ellard, S.1    Allen, H.L.2    Franco, E.D.3    Flanagan, S.E.4    Hysenaj, G.5    Colclough, K.6
  • 128
    • 84877157032 scopus 로고    scopus 로고
    • Maturity onset diabetes of the young: clinical characteristics, diagnosis and management
    • Kavvoura FK, Owen KR. Maturity onset diabetes of the young: clinical characteristics, diagnosis and management. Pediatr Endocrinol Rev (2012) 10:234-42
    • (2012) Pediatr Endocrinol Rev , vol.10 , pp. 234-242
    • Kavvoura, F.K.1    Owen, K.R.2
  • 131
  • 132
    • 84884527899 scopus 로고    scopus 로고
    • Monogenetic diabetes: old and new approaches of diagnosis
    • Owen KR. Monogenetic diabetes: old and new approaches of diagnosis. Clin Med (2013) 13(13):278-81. doi:10.7861/clinmedicine.13-3-278
    • (2013) Clin Med , vol.13 , Issue.13 , pp. 278-281
    • Owen, K.R.1
  • 133
    • 64249170094 scopus 로고    scopus 로고
    • A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients
    • Shepherd M, Shields B, Ellard S, Rubio-Cabezas O, Hattersley AT. A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients. Diabet Med (2009) 26:437-41. doi:10.1111/j.1464-5491.2009.02690.x
    • (2009) Diabet Med , vol.26 , pp. 437-441
    • Shepherd, M.1    Shields, B.2    Ellard, S.3    Rubio-Cabezas, O.4    Hattersley, A.T.5
  • 136
    • 84903548465 scopus 로고    scopus 로고
    • Glucose-lowering effects and low risk of hypoglycemia in patients with maturity-onset diabetes of the young when treated with a GLP-1 receptor agonist: a double-blind, randomized, crossover trial
    • Østoft SH, Bagger JI, Hansen T, Pedersen O, Faber J, Holst JJ, et al. Glucose-lowering effects and low risk of hypoglycemia in patients with maturity-onset diabetes of the young when treated with a GLP-1 receptor agonist: a double-blind, randomized, crossover trial. Diabetes Care (2014) 37(7):1797-805. doi:10.2337/dc13-3007
    • (2014) Diabetes Care , vol.37 , Issue.7 , pp. 1797-1805
    • Østoft, S.H.1    Bagger, J.I.2    Hansen, T.3    Pedersen, O.4    Faber, J.5    Holst, J.J.6
  • 137
    • 33646337684 scopus 로고    scopus 로고
    • Improved prandial glucose control with lower risk of hypoglycemia with nateglinide than with glibenclamide in patients with maturity-onset diabetes of the young type 3
    • Tuomi T, Honkanen EH, Isomaa B, Sarelin L, Groop LC. Improved prandial glucose control with lower risk of hypoglycemia with nateglinide than with glibenclamide in patients with maturity-onset diabetes of the young type 3. Diabetes Care (2006) 23(2):189-94. doi:10.2337/diacare.29.02.06.dc05-1314
    • (2006) Diabetes Care , vol.23 , Issue.2 , pp. 189-194
    • Tuomi, T.1    Honkanen, E.H.2    Isomaa, B.3    Sarelin, L.4    Groop, L.C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.