-
1
-
-
77956266047
-
The emerging genetics of type 2 diabetes
-
20728409 10.1016/j.molmed.2010.06.004 1:CAS:528:DC%2BC3cXhtFajs7zK
-
Bonnefond A, Froguel P, Vaxillaire M (2010) The emerging genetics of type 2 diabetes. Trends Mol Med 16:407-416
-
(2010)
Trends Mol Med
, vol.16
, pp. 407-416
-
-
Bonnefond, A.1
Froguel, P.2
Vaxillaire, M.3
-
2
-
-
84871941957
-
Diagnosis and classification of diabetes mellitus
-
American Diabetes Association 10.2337/dc13-S067
-
American Diabetes Association (2013) Diagnosis and classification of diabetes mellitus. Diabetes Care 36(Suppl 1):S67-S74
-
(2013)
Diabetes Care
, vol.36
, Issue.SUPPL. 1
-
-
-
3
-
-
80955170054
-
MODY: History, genetics, pathophysiology, and clinical decision making
-
21788644 10.2337/dc11-0035
-
Fajans SS, Bell GI (2011) MODY: history, genetics, pathophysiology, and clinical decision making. Diabetes Care 34:1878-1884
-
(2011)
Diabetes Care
, vol.34
, pp. 1878-1884
-
-
Fajans, S.S.1
Bell, G.I.2
-
4
-
-
0032956493
-
Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes
-
10333942 10.2337/diacare.22.2.253 1:STN:280:DyaK1M3ms1Crtg%3D%3D
-
Doria A, Yang Y, Malecki M et al (1999) Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes. Diabetes Care 22:253-261
-
(1999)
Diabetes Care
, vol.22
, pp. 253-261
-
-
Doria, A.1
Yang, Y.2
Malecki, M.3
-
5
-
-
2342633204
-
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes
-
15115830 10.1056/NEJMoa032922 1:CAS:528:DC%2BD2cXjsVOhtbk%3D
-
Gloyn AL, Pearson ER, Antcliff JF et al (2004) Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes. N Engl J Med 350:1838-1849
-
(2004)
N Engl J Med
, vol.350
, pp. 1838-1849
-
-
Gloyn, A.L.1
Pearson, E.R.2
Antcliff, J.F.3
-
6
-
-
21244487124
-
The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus
-
15784703 10.1210/jc.2005-0096 1:CAS:528:DC%2BD2MXkvFCls7k%3D
-
Yorifuji T, Nagashima K, Kurokawa K et al (2005) The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus. J Clin Endocrinol Metab 90:3174-3178
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 3174-3178
-
-
Yorifuji, T.1
Nagashima, K.2
Kurokawa, K.3
-
7
-
-
84862207587
-
Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene
-
22701567 10.1371/journal.pone.0037423 1:CAS:528:DC%2BC38XovFWisbc%3D
-
Bonnefond A, Philippe J, Durand E et al (2012) Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene. PLoS One 7:e37423
-
(2012)
PLoS One
, vol.7
, pp. 37423
-
-
Bonnefond, A.1
Philippe, J.2
Durand, E.3
-
8
-
-
0028972501
-
Reconstitution of IKATP: An inward rectifier subunit plus the sulfonylurea receptor
-
7502040 10.1126/science.270.5239.1166 1:CAS:528:DyaK2MXpsVykt7Y%3D
-
Inagaki N, Gonoi T, Clement JP 4th et al (1995) Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor. Science 270:1166-1170
-
(1995)
Science
, vol.270
, pp. 1166-1170
-
-
Inagaki, N.1
Gonoi, T.2
Clement IV, J.P.3
-
9
-
-
0032525574
-
Molecular determinants of KATP channel inhibition by ATP
-
9628866 10.1093/emboj/17.12.3290 1:CAS:528:DyaK1cXksFClt7s%3D
-
Tucker SJ, Gribble FM, Proks P et al (1998) Molecular determinants of KATP channel inhibition by ATP. EMBO J 17:3290-3296
-
(1998)
EMBO J
, vol.17
, pp. 3290-3296
-
-
Tucker, S.J.1
Gribble, F.M.2
Proks, P.3
-
10
-
-
61749086774
-
Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic beta cells recapitulates neonatal diabetes
-
19065048 1:CAS:528:DC%2BD1MXmtFChsQ%3D%3D
-
Girard CA, Wunderlich FT, Shimomura K et al (2009) Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic beta cells recapitulates neonatal diabetes. J Clin Invest 119:80-90
-
(2009)
J Clin Invest
, vol.119
, pp. 80-90
-
-
Girard, C.A.1
Wunderlich, F.T.2
Shimomura, K.3
-
11
-
-
0036894342
-
Sulfonylurea stimulation of insulin secretion
-
12475777 10.2337/diabetes.51.2007.S368 1:CAS:528:DC%2BD38XpsVagtLo%3D
-
Proks P, Reimann F, Green N, Gribble F, Ashcroft F (2002) Sulfonylurea stimulation of insulin secretion. Diabetes 51(Suppl 3):S368-S376
-
(2002)
Diabetes
, vol.51
, Issue.SUPPL. 3
-
-
Proks, P.1
Reimann, F.2
Green, N.3
Gribble, F.4
Ashcroft, F.5
-
12
-
-
0037317981
-
Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes
-
12540637 10.2337/diabetes.52.2.568 1:CAS:528:DC%2BD3sXhtFansbY%3D
-
Gloyn AL, Weedon MN, Owen KR et al (2003) Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes. Diabetes 52:568-572
-
(2003)
Diabetes
, vol.52
, pp. 568-572
-
-
Gloyn, A.L.1
Weedon, M.N.2
Owen, K.R.3
-
13
-
-
0034048298
-
Diverse roles of KATP channels learned from Kir6. 2 genetically engineered mice
-
10868950 10.2337/diabetes.49.3.311 1:CAS:528:DC%2BD3cXlsFCruro%3D
-
Seino S, Iwanaga T, Nagashima K, Miki T (2000) Diverse roles of KATP channels learned from Kir6. 2 genetically engineered mice. Diabetes 49:311-318
-
(2000)
Diabetes
, vol.49
, pp. 311-318
-
-
Seino, S.1
Iwanaga, T.2
Nagashima, K.3
Miki, T.4
-
14
-
-
0030671407
-
Abnormalities of pancreatic islets by targeted expression of a dominant-negative KATP channel
-
9342346 10.1073/pnas.94.22.11969 1:CAS:528:DyaK2sXntFSmsLo%3D
-
Miki T, Tashiro F, Iwanaga T et al (1997) Abnormalities of pancreatic islets by targeted expression of a dominant-negative KATP channel. Proc Natl Acad Sci U S A 94:11969-11973
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 11969-11973
-
-
Miki, T.1
Tashiro, F.2
Iwanaga, T.3
-
15
-
-
12644260472
-
High prevalence of mitochondrial diabetes mellitus in Japanese patients with major risk factors
-
9225833 10.1016/S0026-0495(97)90124-4 1:CAS:528:DyaK2sXksFGjsrs%3D
-
Fukui M, Nakano K, Obayashi H et al (1997) High prevalence of mitochondrial diabetes mellitus in Japanese patients with major risk factors. Metabolism 46:793-795
-
(1997)
Metabolism
, vol.46
, pp. 793-795
-
-
Fukui, M.1
Nakano, K.2
Obayashi, H.3
-
16
-
-
75149130955
-
Diagnosis and classification of diabetes mellitus
-
American Diabetes Association 10.2337/dc10-S062
-
American Diabetes Association (2010) Diagnosis and classification of diabetes mellitus. Diabetes Care 33(Suppl 1):S62-S69
-
(2010)
Diabetes Care
, vol.33
, Issue.SUPPL. 1
-
-
-
17
-
-
10544249874
-
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
-
8945470 10.1038/384455a0 1:CAS:528:DyaK28XnsFWqtbk%3D
-
Yamagata K, Oda N, Kaisaki PJ et al (1996) Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3). Nature 384:455-458
-
(1996)
Nature
, vol.384
, pp. 455-458
-
-
Yamagata, K.1
Oda, N.2
Kaisaki, P.J.3
-
18
-
-
10544236911
-
Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)
-
8945471 10.1038/384458a0 1:CAS:528:DyaK28XnsFWqur0%3D
-
Yamagata K, Furuta H, Oda N et al (1996) Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1). Nature 384:458-460
-
(1996)
Nature
, vol.384
, pp. 458-460
-
-
Yamagata, K.1
Furuta, H.2
Oda, N.3
-
19
-
-
0027472126
-
Familial hyperglycemia due to mutations in glucokinase: Definition of a subtype of diabetes mellitus
-
8433729 10.1056/NEJM199303113281005 1:STN:280:DyaK3s7msFSqsA%3D%3D
-
Froguel P, Zouali H, Vionnet N et al (1993) Familial hyperglycemia due to mutations in glucokinase: definition of a subtype of diabetes mellitus. N Engl J Med 328:697-702
-
(1993)
N Engl J Med
, vol.328
, pp. 697-702
-
-
Froguel, P.1
Zouali, H.2
Vionnet, N.3
-
20
-
-
2642709182
-
Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French Caucasians
-
9588460 10.2337/diabetes.47.5.843
-
Chèvre JC, Hani EH, Stoffers DA, Habener JF, Froguel P (1998) Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French Caucasians. Diabetes 47:843-844
-
(1998)
Diabetes
, vol.47
, pp. 843-844
-
-
Chèvre, J.C.1
Hani, E.H.2
Stoffers, D.A.3
Habener, J.F.4
Froguel, P.5
-
21
-
-
0031748728
-
Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K
-
9648841 10.2337/diabetes.47.7.1152 1:CAS:528:DyaK1cXkt1amu74%3D
-
Beards F, Frayling T, Bulman M et al (1998) Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K. Diabetes 47:1152-1154
-
(1998)
Diabetes
, vol.47
, pp. 1152-1154
-
-
Beards, F.1
Frayling, T.2
Bulman, M.3
-
22
-
-
0032700272
-
Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus
-
10545951 10.1038/15500 1:CAS:528:DyaK1MXnt1Gns7o%3D
-
Malecki MT, Jhala US, Antonellis A et al (1999) Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus. Nat Genet 23:323-328
-
(1999)
Nat Genet
, vol.23
, pp. 323-328
-
-
Malecki, M.T.1
Jhala, U.S.2
Antonellis, A.3
-
23
-
-
0012431804
-
Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus (position statement)
-
The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus
-
The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus (2003) Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus (position statement). Diabetes Care 26(Suppl 1):S5-S20
-
(2003)
Diabetes Care
, vol.26
, Issue.SUPPL. 1
-
-
-
24
-
-
14544298750
-
Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification
-
15723059 10.1038/nn1411 1:CAS:528:DC%2BD2MXhslyqsbo%3D
-
Pegan S, Arrabit C, Zhou W et al (2005) Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification. Nat Neurosci 8:279-287
-
(2005)
Nat Neurosci
, vol.8
, pp. 279-287
-
-
Pegan, S.1
Arrabit, C.2
Zhou, W.3
-
25
-
-
13444274375
-
Functional analysis of a structural model of the ATP-binding site of the KATP channel Kir6.2 subunit
-
15650751 10.1038/sj.emboj.7600487 1:CAS:528:DC%2BD2MXmslOnsw%3D%3D
-
Antcliff JF, Haider S, Proks P, Sansom MS, Ashcroft FM (2005) Functional analysis of a structural model of the ATP-binding site of the KATP channel Kir6.2 subunit. EMBO J 24:229-239
-
(2005)
EMBO J
, vol.24
, pp. 229-239
-
-
Antcliff, J.F.1
Haider, S.2
Proks, P.3
Sansom, M.S.4
Ashcroft, F.M.5
-
26
-
-
84859906039
-
Diabetes caused by Kir6.2 mutation: Successful treatment with oral glibenclamide switched from continuous subcutaneous insulin infusion in the early phase of the disease
-
22507152 10.1111/j.1442-200X.2011.03413.x 1:CAS:528:DC%2BC38Xpt1yru70%3D
-
Nagano N, Urakami T, Mine Y et al (2012) Diabetes caused by Kir6.2 mutation: successful treatment with oral glibenclamide switched from continuous subcutaneous insulin infusion in the early phase of the disease. Pediatr Int 54:277-279
-
(2012)
Pediatr Int
, vol.54
, pp. 277-279
-
-
Nagano, N.1
Urakami, T.2
Mine, Y.3
-
27
-
-
33746686369
-
Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations
-
16885550 10.1056/NEJMoa061759 1:CAS:528:DC%2BD28XnslyktrY%3D
-
Pearson ER, Flechtner I, Njølstad PR et al (2006) Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med 355:467-477
-
(2006)
N Engl J Med
, vol.355
, pp. 467-477
-
-
Pearson, E.R.1
Flechtner, I.2
Njølstad, P.R.3
-
28
-
-
41049091884
-
Centile charts for birthweight for gestational age for Scottish singleton births
-
18298810 10.1186/1471-2393-8-5
-
Bonellie S, Chalmers J, Gray R, Greer I, Jarvis S, Williams C (2008) Centile charts for birthweight for gestational age for Scottish singleton births. BMC Pregnancy Childbirth 8:5
-
(2008)
BMC Pregnancy Childbirth
, vol.8
, pp. 5
-
-
Bonellie, S.1
Chalmers, J.2
Gray, R.3
Greer, I.4
Jarvis, S.5
Williams, C.6
-
29
-
-
0034820065
-
Familial early-onset type 2 diabetes in Chinese patients: Obesity and genetics have more significant roles than autoimmunity
-
11315828 10.2337/diacare.24.4.663 1:CAS:528:DC%2BD3MXivVOmur4%3D
-
Ng MC, Lee SC, Ko GT et al (2001) Familial early-onset type 2 diabetes in Chinese patients: obesity and genetics have more significant roles than autoimmunity. Diabetes Care 24:663-671
-
(2001)
Diabetes Care
, vol.24
, pp. 663-671
-
-
Ng, M.C.1
Lee, S.C.2
Ko, G.T.3
-
30
-
-
20244364399
-
Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients
-
15657605 10.1038/sj.ejhg.5201347 1:CAS:528:DC%2BD2MXisFKitbo%3D
-
Xu JY, Dan QH, Chan V et al (2005) Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients. Eur J Hum Genet 13:422-427
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 422-427
-
-
Xu, J.Y.1
Dan, Q.H.2
Chan, V.3
-
31
-
-
34547896613
-
A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family
-
17440689 10.1007/s11010-007-9463-0 1:CAS:528:DC%2BD2sXoslGhs78%3D
-
Liu L, Furuta H, Minami A et al (2007) A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family. Mol Cell Biochem 303:115-120
-
(2007)
Mol Cell Biochem
, vol.303
, pp. 115-120
-
-
Liu, L.1
Furuta, H.2
Minami, A.3
-
32
-
-
68049137605
-
Kir6.2 variant E23K increases ATP-sensitive K+ channel activity and is associated with impaired insulin release and enhanced insulin sensitivity in adults with normal glucose tolerance
-
19491206 10.2337/db09-0025 1:CAS:528:DC%2BD1MXpsV2mtbY%3D
-
Villareal DT, Koster JC, Robertson H et al (2009) Kir6.2 variant E23K increases ATP-sensitive K+ channel activity and is associated with impaired insulin release and enhanced insulin sensitivity in adults with normal glucose tolerance. Diabetes 58:1869-1878
-
(2009)
Diabetes
, vol.58
, pp. 1869-1878
-
-
Villareal, D.T.1
Koster, J.C.2
Robertson, H.3
-
33
-
-
0036314298
-
Kir6.2 polymorphism predisposes to type 2 diabetes by inducing overactivity of pancreatic beta-cell ATP-sensitive K+ channels
-
11872696 10.2337/diabetes.51.3.875 1:CAS:528:DC%2BD38XitFSgt78%3D
-
Schwanstecher C, Meyer U, Schwanstecher M (2002) Kir6.2 polymorphism predisposes to type 2 diabetes by inducing overactivity of pancreatic beta-cell ATP-sensitive K+ channels. Diabetes 51:875-879
-
(2002)
Diabetes
, vol.51
, pp. 875-879
-
-
Schwanstecher, C.1
Meyer, U.2
Schwanstecher, M.3
-
34
-
-
20044387060
-
The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: Evidence for heterogeneity of beta cell function among carriers of the R201H mutation
-
10.1007/s00125-005-1731-5
-
Klupa T, Edghill EL, Nazim J et al (2005) The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R201H mutation. Diabetologia 8:1029-1031
-
(2005)
Diabetologia
, vol.8
, pp. 1029-1031
-
-
Klupa, T.1
Edghill, E.L.2
Nazim, J.3
-
35
-
-
33751089560
-
Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes
-
17021801 10.1007/s00424-006-0112-3 1:CAS:528:DC%2BD28Xht1WhsbjN
-
Girard CA, Shimomura K, Proks P et al (2006) Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes. Pflugers Arch 453:323-332
-
(2006)
Pflugers Arch
, vol.453
, pp. 323-332
-
-
Girard, C.A.1
Shimomura, K.2
Proks, P.3
-
36
-
-
34347387276
-
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood
-
17446535 10.2337/db07-0043 1:CAS:528:DC%2BD2sXnvVWisrk%3D
-
Flanagan SE, Patch AM, Mackay DJ et al (2007) Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood. Diabetes 56:1930-1937
-
(2007)
Diabetes
, vol.56
, pp. 1930-1937
-
-
Flanagan, S.E.1
Patch, A.M.2
Mackay, D.J.3
-
37
-
-
0347359228
-
Hyperinsulinism in infancy: From basic science to clinical disease
-
14715916 10.1152/physrev.00022.2003 1:CAS:528:DC%2BD2cXotl2qsA%3D%3D
-
Dunne MJ, Cosgrove KE, Shepherd RM, Aynsley-Green A, Lindley KJ (2004) Hyperinsulinism in infancy: from basic science to clinical disease. Physiol Rev 84:239-275
-
(2004)
Physiol Rev
, vol.84
, pp. 239-275
-
-
Dunne, M.J.1
Cosgrove, K.E.2
Shepherd, R.M.3
Aynsley-Green, A.4
Lindley, K.J.5
-
38
-
-
78751472528
-
Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management
-
20980454 10.2337/db10-0731 1:CAS:528:DC%2BC3MXosVWgtA%3D%3D
-
Loechner KJ, Akrouh A, Kurata HT et al (2011) Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management. Diabetes 60:209-217
-
(2011)
Diabetes
, vol.60
, pp. 209-217
-
-
Loechner, K.J.1
Akrouh, A.2
Kurata, H.T.3
-
39
-
-
0037464795
-
A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1
-
12559865 10.1016/S0140-6736(03)12325-2 1:CAS:528:DC%2BD3sXmt1antw%3D%3D
-
Huopio H, Otonkoski T, Vauhkonen I, Reimann F, Ashcroft FM, Laakso M (2003) A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1. Lancet 361:301-307
-
(2003)
Lancet
, vol.361
, pp. 301-307
-
-
Huopio, H.1
Otonkoski, T.2
Vauhkonen, I.3
Reimann, F.4
Ashcroft, F.M.5
Laakso, M.6
-
40
-
-
35148847369
-
β-cell hyperexcitability: From hyperinsulinism to diabetes
-
17919182 10.1111/j.1463-1326.2007.00778.x 1:CAS:528:DC%2BD2sXhtlOhsLfO
-
Nichols CG, Koster JC, Remedi MS (2007) β-cell hyperexcitability: from hyperinsulinism to diabetes. Diabetes Obes Metab 9(Suppl 2):81-88
-
(2007)
Diabetes Obes Metab
, vol.9
, Issue.SUPPL. 2
, pp. 81-88
-
-
Nichols, C.G.1
Koster, J.C.2
Remedi, M.S.3
-
41
-
-
32844459139
-
Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism
-
16357843 10.1038/modpathol.3800497 1:CAS:528:DC%2BD2MXhtlSqu7zP
-
Suchi M, MacMullen CM, Thornton PS et al (2006) Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism. Mod Pathol 19:122-129
-
(2006)
Mod Pathol
, vol.19
, pp. 122-129
-
-
Suchi, M.1
Macmullen, C.M.2
Thornton, P.S.3
-
42
-
-
33747033470
-
Spontaneous recovery from hyperglycemia by regeneration of pancreatic beta-cells in Kir6.2G132S transgenic mice
-
16804060 10.2337/db05-1459 1:CAS:528:DC%2BD28XmvVChtrY%3D
-
Oyama K, Minami K, Ishizaki K, Fuse M, Miki T, Seino S (2006) Spontaneous recovery from hyperglycemia by regeneration of pancreatic beta-cells in Kir6.2G132S transgenic mice. Diabetes 55:1930-1938
-
(2006)
Diabetes
, vol.55
, pp. 1930-1938
-
-
Oyama, K.1
Minami, K.2
Ishizaki, K.3
Fuse, M.4
Miki, T.5
Seino, S.6
-
43
-
-
33751322380
-
Genetic and clinical characteristics of Korean maturity-onset diabetes of the young (MODY) patients
-
16632067 10.1016/j.diabres.2006.03.002 1:CAS:528:DC%2BD28XptlyksLo%3D
-
Hwang JS, Shin CH, Yang SW, Jung SY, Huh N (2006) Genetic and clinical characteristics of Korean maturity-onset diabetes of the young (MODY) patients. Diabetes Res Clin Pract 74:75-81
-
(2006)
Diabetes Res Clin Pract
, vol.74
, pp. 75-81
-
-
Hwang, J.S.1
Shin, C.H.2
Yang, S.W.3
Jung, S.Y.4
Huh, N.5
-
44
-
-
66149107461
-
Mutations of maturity-onset diabetes of the young (MODY) genes in Thais with early-onset type 2 diabetes mellitus
-
10.1111/j.1365-2265.2008.03397.x 1:CAS:528:DC%2BD1MXmvVCjsbs%3D
-
Plengvidhya N, Boonyasrisawat W, Chongjaroen N et al (2009) Mutations of maturity-onset diabetes of the young (MODY) genes in Thais with early-onset type 2 diabetes mellitus. Clin Endocrinol (Oxf) 70:847-853
-
(2009)
Clin Endocrinol (Oxf)
, vol.70
, pp. 847-853
-
-
Plengvidhya, N.1
Boonyasrisawat, W.2
Chongjaroen, N.3
|