-
1
-
-
0031748728
-
Mutations in the hepatocyte nuclear factor 1b are not a common cause of maturity-onset diabetes of the young in the UK
-
(1998)
Diabetes
, vol.47
, pp. 1152-1154
-
-
Beards, F.1
Frayling, T.2
Bulman, M.3
Horikawa, Y.4
Allen, L.5
Appleton, M.6
Bell, G.I.7
Ellard, S.8
Hattersley, A.T.9
-
2
-
-
15144347575
-
Mutation screening in 18 Caucasian families suggest the existence of other MODY genes
-
(1998)
Diabetologia
, vol.41
, pp. 1017-1023
-
-
Chèvre, J.-C.1
Hani, E.H.2
Boutin, P.3
Vaxillaire, M.4
Blanché, H.5
Vionnet, N.6
Pardini, V.C.7
Timsit, J.8
Larger, E.9
Charpentier, G.10
Beckers, D.11
Maes, M.12
Bellané-Chantelot, C.13
Velho, G.14
Froguel, P.15
-
4
-
-
0032222726
-
Three novel missense mutations in the glucokinase gene (G80S; E221K; G227C) in Italian subjects with maturity-onset diabetes of the young (MODY)
-
(1998)
Hum Mutat
, vol.12
, pp. 1364
-
-
Guazzini, B.1
Gaffi, D.2
Mainieri, D.3
Multari, G.4
Cordera, R.5
Bertolini, S.6
Pozza, G.7
Meschi, F.8
Barbetti, F.9
-
6
-
-
0007333821
-
Screening for mutations in the glucokinase (MODY 2/GCK) and hepatocyte nuclear factor 1-a (MODY 3/HNF 1-a) genes in south-Italian families
-
(1998)
Diabetologia
, vol.41
, Issue.SUPPL. 1
-
-
Bellané-Chantelot, C.1
Iafusco, D.2
Blanché, H.3
Puca, M.R.4
Clauin, S.5
Morel, V.6
Le Gall, I.7
Thomas, G.8
Prisco, F.9
-
8
-
-
0034454416
-
Missense mutations in the human insulin promoter factor-1 (IPF-1) gene and their relation to maturity onset diabetes of the young and late-onset type 2 diabetes mellitus in Caucasians
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 1323-1326
-
-
Hansen, L.1
Uriostel, S.2
Petersen, H.V.3
Jensen, J.N.4
Eiberg, H.5
Barbetti, F.6
Serup, P.7
Hansen, T.8
Pedersen, O.9
-
10
-
-
0041677535
-
Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta
-
(2000)
Kidney Int
, vol.57
, pp. 898-907
-
-
Bingham, C.1
Ellard, S.2
Allen, L.3
Bulman, M.4
Shepherd, M.5
Frayling, T.6
Berry, P.J.7
Clark, P.M.8
Lindner, T.9
Bell, G.I.10
Ryffel, G.U.11
Nicholls, A.J.12
Hattersley, A.T.13
-
11
-
-
0031914679
-
Maturity-onset diabetes of the young: Clinical heterogeneity explained by genetic heterogeneity
-
(1998)
Diabet Med
, vol.15
, pp. 15-24
-
-
Hattersley, A.T.1
-
12
-
-
0030067124
-
Banting Lecture. A lesson in metabolic regulation inspired by the glucokinase glucose sensor paradigm
-
(1996)
Diabetes
, vol.45
, pp. 223-241
-
-
Matschinsky, F.M.1
-
14
-
-
0026608764
-
Close linkage of glucokinase locus on chromosome 7 p to early onset non-insulin dependent diabetes mellitus
-
(1992)
Nature
, vol.356
, pp. 162-164
-
-
Froguel, P.1
Vaxillaire, M.2
Sun, F.3
Velho, G.4
Zouali, H.5
Butel, M.O.6
Lesage, S.7
Vionnet, N.8
Clément, K.9
Fougerousse, F.10
Tanizawa, Y.11
Weissenbach, J.12
Beckman, J.S.13
Lathrop, G.M.14
Passa, P.15
Permutt, M.A.16
Cohen, D.17
-
15
-
-
0026032055
-
Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20
-
(1991)
Proc Natl Acad Sci USA
, vol.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
Spielman, R.S.7
Cox, N.J.8
-
20
-
-
0030707689
-
Early diabetes and abnormal pancreatic islet development in mice lacking Glut2
-
(1997)
Nat Genet
, vol.17
, pp. 327-330
-
-
Guillam, M.1
Hummler, E.2
Schaerer, E.3
Yeh, J.4
Birnbaum, M.5
Beermann, F.6
Schmidt, A.7
Deriaz, N.8
Thorens, B.9
-
21
-
-
0030667885
-
Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome
-
(1997)
Nat Genet
, vol.17
, pp. 324-326
-
-
Santer, R.1
Schneppenheim, R.2
Dombrowski, A.3
Gotze, H.4
Steinmann, B.5
Schaub, J.6
-
24
-
-
0026969347
-
Genetic and environmental determinants of non-insulin-dependent diabetes mellitus(NIDDM)
-
(1992)
Diabetes Metab Rev
, vol.8
, pp. 287-338
-
-
Hamman, R.F.1
-
25
-
-
0030897315
-
Genetic analyses of glucose transporter genes in French non-insulin-dependent diabetic families
-
(1997)
Diabetes Metab
, vol.23
, pp. 137-142
-
-
Lesage, S.1
Zouali, H.2
Vionnet, N.3
Philippi, A.4
Velho, G.5
Serradas, P.6
Passa, P.7
Demenais, F.8
Froguel, P.9
-
26
-
-
0028174912
-
Affected sib-pair analysis of the GLUT1 glucose transporter gene locus in non-insulin-dependent diabetes mellitus (NIDDM): Evidence for no linkage
-
(1994)
Hum Genet
, vol.93
, pp. 675-680
-
-
Baroni, M.G.1
Alcolado, J.C.2
Gragnoli, C.3
Franciosi, A.M.4
Cavallo, M.G.5
Fiore, V.6
Pozzilli, P.7
Galton, D.J.8
-
28
-
-
0031948951
-
High frequency of polymorphism but no mutations found in the GLUT1 glucose transporter gene in NIDDM and familial obesity by single strand conformation polymorphism analysis
-
(1998)
Hum Genet
, vol.102
, pp. 479-482
-
-
Baroni, M.G.1
D'Andrea, M.P.2
Capici, F.3
Buzzetti, R.4
Cavallo, M.G.5
Fallucca, F.6
Giovannini, C.7
Pozzilli, P.8
-
30
-
-
0030038406
-
Normal values of first-phase insulin response to intravenous glucose in healthy Italian children and adolescents
-
(1996)
Diabetologia
, vol.39
, pp. 370-371
-
-
Lorini, R.1
Vanelli, M.2
-
32
-
-
17344367164
-
GLUT1 deficiency syndrome caused by haploinsufficiency of the blood brain barrier hexose carrier
-
(1998)
Nat Genet
, vol.18
, pp. 188-191
-
-
Seidner, G.1
Alvarez, M.G.2
Yeh, J.I.3
O'Driscoll, K.R.4
Klepper, J.5
Stump, T.S.6
Wang, D.7
Spinner, N.B.8
Birnbaum, M.J.9
De Vivo, D.C.10
-
33
-
-
0344614690
-
GLUT1 glucose transporter gene transcription is repressed by Sp3. Evidence for a regulatory role of Sp3 during myogenesis
-
(1999)
J Mol Biol
, vol.294
, pp. 103-119
-
-
Fandos, C.1
Sanchez-Feutrie, M.2
Santalucia Vinals, T.F.3
Cadefau, J.4
Guma, A.5
Cusso, R.6
Kaliman, P.7
Canicio, J.8
Palacin, M.9
Zorzano, A.10
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