-
1
-
-
0016641270
-
A difference between the inheritance of classical juvenile-onset and maturity-onset type diabetes of young people
-
Tattersall RB, Fajans SS. A difference between the inheritance of classical juvenile-onset and maturity-onset type diabetes of young people. Diabetes 1975;24:44-53.
-
(1975)
Diabetes
, vol.24
, pp. 44-53
-
-
Tattersall, R.B.1
Fajans, S.S.2
-
2
-
-
0031914679
-
Maturity-onset diabetes of the young: Clinical heterogeneity explained by genetic heterogeneity
-
Hattersley AT. Maturity-onset diabetes of the young: clinical heterogeneity explained by genetic heterogeneity. Diabet Med 1998;15:15-24.
-
(1998)
Diabet Med
, vol.15
, pp. 15-24
-
-
Hattersley, A.T.1
-
3
-
-
0032857518
-
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.
-
(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
-
5
-
-
0037300839
-
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.
-
(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
-
6
-
-
0036075535
-
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.
-
(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
-
7
-
-
20044396943
-
Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collection
-
Pearson ER, Pruhova S, Tack CJ, Johansen A, Castleden HA, Lumb PJ, et al. Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collection. Diabetologia 2005;48:878-85.
-
(2005)
Diabetologia
, vol.48
, pp. 878-885
-
-
Pearson, E.R.1
Pruhova, S.2
Tack, C.J.3
Johansen, A.4
Castleden, H.A.5
Lumb, P.J.6
-
8
-
-
0035122282
-
beta-cell genes and diabetes: Molecular and clinical characterization of mutations in transcription factors
-
Frayling TM, Evans JC, Bulman MP, Pearson E, Allen L, Owen K, et al. beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors. Diabetes 2001;50 Suppl 1:S94-100.
-
(2001)
Diabetes
, vol.50
, Issue.SUPPL. 1
-
-
Frayling, T.M.1
Evans, J.C.2
Bulman, M.P.3
Pearson, E.4
Allen, L.5
Owen, K.6
-
9
-
-
0036347934
-
Nonsense and missense mutations in the human hepatocyte nuclear factor-1 beta gene (TCF2) and their relation to type 2 diabetes in Japanese
-
Furuta H, Furuta M, Sanke T, Ekawa K, Hanabusa T, Nishi M, et al. Nonsense and missense mutations in the human hepatocyte nuclear factor-1 beta gene (TCF2) and their relation to type 2 diabetes in Japanese. J Clin Endocrinol Metab 2002;87:3859-63.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 3859-3863
-
-
Furuta, H.1
Furuta, M.2
Sanke, T.3
Ekawa, K.4
Hanabusa, T.5
Nishi, M.6
-
10
-
-
22644434767
-
Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus
-
Sagen JV, Baumann ME, Salvesen HB, Molven A, Sovik O, Njolstad PR. Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus. Diabet Med 2005;22:1012-5.
-
(2005)
Diabet Med
, vol.22
, pp. 1012-1015
-
-
Sagen, J.V.1
Baumann, M.E.2
Salvesen, H.B.3
Molven, A.4
Sovik, O.5
Njolstad, P.R.6
-
11
-
-
0030695028
-
Diminished insulin and glucagon secretory responses to arginine in nondiabetic subjects with a mutation in the hepatocyte nuclear factor-4alpha/MODY1 gene
-
Herman WH, Fajans SS, Smith MJ, Polonsky KS, Bell GI, Halter JB. Diminished insulin and glucagon secretory responses to arginine in nondiabetic subjects with a mutation in the hepatocyte nuclear factor-4alpha/MODY1 gene. Diabetes 1997;46:1749-54.
-
(1997)
Diabetes
, vol.46
, pp. 1749-1754
-
-
Herman, W.H.1
Fajans, S.S.2
Smith, M.J.3
Polonsky, K.S.4
Bell, G.I.5
Halter, J.B.6
-
12
-
-
0032589072
-
Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism
-
Lehto M, Bitzen PO, Isomaa B, Wipemo C, Wessman Y, Forsblom C, et al. Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism. Diabetes 1999;48:423-5.
-
(1999)
Diabetes
, vol.48
, pp. 423-425
-
-
Lehto, M.1
Bitzen, P.O.2
Isomaa, B.3
Wipemo, C.4
Wessman, Y.5
Forsblom, C.6
-
13
-
-
0034035239
-
Genotype/phenotype relationships in HNF-4alpha/MODY1: Haploinsufficiency is associated with reduced apolipoprotein (AII), apolipoprotein (CIII), lipoprotein(a), and triglyceride levels
-
Shih DQ, Dansky HM, Fleisher M, Assmann G, Fajans SS, Stoffel M. Genotype/phenotype relationships in HNF-4alpha/MODY1: haploinsufficiency is associated with reduced apolipoprotein (AII), apolipoprotein (CIII), lipoprotein(a), and triglyceride levels. Diabetes 2000;49:832-7.
-
(2000)
Diabetes
, vol.49
, pp. 832-837
-
-
Shih, D.Q.1
Dansky, H.M.2
Fleisher, M.3
Assmann, G.4
Fajans, S.S.5
Stoffel, M.6
-
14
-
-
0033791170
-
MODY 2 presenting as neonatal hyperglycaemia: A need to reshape the definition of "neonatal diabetes"?
-
Prisco F, Iafusco D, Franzese A, Sulli N, Barbetti F. MODY 2 presenting as neonatal hyperglycaemia: a need to reshape the definition of "neonatal diabetes"? Diabetologia 2000;43:1331-2.
-
(2000)
Diabetologia
, vol.43
, pp. 1331-1332
-
-
Prisco, F.1
Iafusco, D.2
Franzese, A.3
Sulli, N.4
Barbetti, F.5
-
15
-
-
0027231353
-
Glucokinase gene mutation and impaired glucose uptake by liver
-
Sakura H, Kawamori R, Kubota M, Morishima T, Kamada T, Akanuma Y, et al. Glucokinase gene mutation and impaired glucose uptake by liver. Lancet 1993;341:1532-3.
-
(1993)
Lancet
, vol.341
, pp. 1532-1533
-
-
Sakura, H.1
Kawamori, R.2
Kubota, M.3
Morishima, T.4
Kamada, T.5
Akanuma, Y.6
-
16
-
-
0029864561
-
Impaired hepatic glycogen synthesis in glucokinase-deficient (MODY-2) subjects
-
Velho G, Petersen KF, Perseghin G, Hwang JH, Rothman DL, Pueyo ME, et al. Impaired hepatic glycogen synthesis in glucokinase-deficient (MODY-2) subjects. J Clin Invest 1996;98:1755-61.
-
(1996)
J Clin Invest
, vol.98
, pp. 1755-1761
-
-
Velho, G.1
Petersen, K.F.2
Perseghin, G.3
Hwang, J.H.4
Rothman, D.L.5
Pueyo, M.E.6
-
17
-
-
0031859976
-
Mutations in the glucokinase gene of the fetus result in reduced birth weight
-
Hattersley AT, Beards F, Ballantyne E, Appleton M, Harvey R, Ellard S. Mutations in the glucokinase gene of the fetus result in reduced birth weight. Nat Genet 1998;19:268-70.
-
(1998)
Nat Genet
, vol.19
, pp. 268-270
-
-
Hattersley, A.T.1
Beards, F.2
Ballantyne, E.3
Appleton, M.4
Harvey, R.5
Ellard, S.6
-
18
-
-
0031027502
-
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect
-
Lehto M, Tuomi T, Mahtani MM, Widen E, Forsblom C, Sarelin L, et al. Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect. J Clin Invest 1997;99:582-91.
-
(1997)
J Clin Invest
, vol.99
, pp. 582-591
-
-
Lehto, M.1
Tuomi, T.2
Mahtani, M.M.3
Widen, E.4
Forsblom, C.5
Sarelin, L.6
-
19
-
-
0028848246
-
Localization of MODY3 to a 5-cM region of human chromosome 12
-
Menzel S, Yamagata K, Trabb JB, Nerup J, Permutt MA, Fajans SS, et al. Localization of MODY3 to a 5-cM region of human chromosome 12. Diabetes 1995;44:1408-13.
-
(1995)
Diabetes
, vol.44
, pp. 1408-1413
-
-
Menzel, S.1
Yamagata, K.2
Trabb, J.B.3
Nerup, J.4
Permutt, M.A.5
Fajans, S.S.6
-
20
-
-
0035807972
-
Dissecting the transcriptional network of pancreatic islets during development and differentiation
-
Shih DQ, Stoffel M. Dissecting the transcriptional network of pancreatic islets during development and differentiation. Proc Natl Acad Sci U S A 2001;98:14189-91.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 14189-14191
-
-
Shih, D.Q.1
Stoffel, M.2
-
21
-
-
0031894649
-
Chronic diabetic complications in patients with MODY3 diabetes
-
Isomaa B, Henricsson M, Lehto M, Forsblom C, Karanko S, Sarelin L, et al. Chronic diabetic complications in patients with MODY3 diabetes. Diabetologia 1998;41:467-73.
-
(1998)
Diabetologia
, vol.41
, pp. 467-473
-
-
Isomaa, B.1
Henricsson, M.2
Lehto, M.3
Forsblom, C.4
Karanko, S.5
Sarelin, L.6
-
22
-
-
0142186278
-
Genetic cause of hyperglycaemia and response to treatment in diabetes
-
Pearson ER, Starkey BJ, Powell RJ, Gribble FM, Clark PM, Hattersley AT. Genetic cause of hyperglycaemia and response to treatment in diabetes. Lancet 2003;362:1275-81.
-
(2003)
Lancet
, vol.362
, pp. 1275-1281
-
-
Pearson, E.R.1
Starkey, B.J.2
Powell, R.J.3
Gribble, F.M.4
Clark, P.M.5
Hattersley, A.T.6
-
23
-
-
0031031571
-
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.
-
(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
-
24
-
-
12144286598
-
Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations
-
Bellanne-Chantelot C, Chauveau D, Gautier JF, Dubois-Laforgue D, Clauin S, Beaufils S, et al. Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations. Ann Intern Med 2004;140:510-7.
-
(2004)
Ann Intern Med
, vol.140
, pp. 510-517
-
-
Bellanne-Chantelot, C.1
Chauveau, D.2
Gautier, J.F.3
Dubois-Laforgue, D.4
Clauin, S.5
Beaufils, S.6
-
25
-
-
17544379409
-
Genetic testing for maturity onset diabetes of the young: Uptake, attitudes and comparison with hereditary non-polyposis colorectal cancer
-
Liljestrom B, Aktan-Collan K, Isomaa B, Sarelin L, Uutela A, Groop L, et al. Genetic testing for maturity onset diabetes of the young: uptake, attitudes and comparison with hereditary non-polyposis colorectal cancer. Diabetologia 2005;48:242-50.
-
(2005)
Diabetologia
, vol.48
, pp. 242-250
-
-
Liljestrom, B.1
Aktan-Collan, K.2
Isomaa, B.3
Sarelin, L.4
Uutela, A.5
Groop, L.6
-
26
-
-
0242363725
-
No deterioration in glycemic control in HNF-1alpha maturity-onset diabetes of the young following transfer from long-term insulin to sulphonylureas
-
Shepherd M, Pearson ER, Houghton J, Salt G, Ellard S, Hattersley AT. No deterioration in glycemic control in HNF-1alpha maturity-onset diabetes of the young following transfer from long-term insulin to sulphonylureas. Diabetes Care 2003;26:3191-2.
-
(2003)
Diabetes Care
, vol.26
, pp. 3191-3192
-
-
Shepherd, M.1
Pearson, E.R.2
Houghton, J.3
Salt, G.4
Ellard, S.5
Hattersley, A.T.6
|