-
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 24:44-53, 1975
-
(1975)
Diabetes
, vol.24
, pp. 44-53
-
-
Tattersall, R.B.1
Fajans, S.S.2
-
2
-
-
0026562918
-
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, Lesage S, Velho G, Iris F, Passa P, et al.: Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus. Nature 356:721-722, 1992
-
(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
Lesage, S.7
Velho, G.8
Iris, F.9
Passa, P.10
-
3
-
-
0026937234
-
Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes
-
Stoffel M, Patel P, Lo YM, Hattersley AT, Lucassen AM, Page R, Bell JI, Bell GI, Turner RC, Wainscoat JS: Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes. Nat Genet 2:153-156, 1992
-
(1992)
Nat Genet
, vol.2
, pp. 153-156
-
-
Stoffel, M.1
Patel, P.2
Lo, Y.M.3
Hattersley, A.T.4
Lucassen, A.M.5
Page, R.6
Bell, J.I.7
Bell, G.I.8
Turner, R.C.9
Wainscoat, J.S.10
-
4
-
-
10544249874
-
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young
-
Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, Southam L, Cox RD, Lathrop GM, Boriraj VV, Chen X, Cox NJ, Oda Y, Yano H, Le Beau MM, Yamada S, Nishigori H, Takeda J, Fajans SS, Hattersley AT, Iwasaki N, Hansen T, Pedersen O, Polonsky KS, Bell GI, et al.: Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young. Nature 384:455-458, 1996
-
(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
Southam, L.7
Cox, R.D.8
Lathrop, G.M.9
Boriraj, V.V.10
Chen, X.11
Cox, N.J.12
Oda, Y.13
Yano, H.14
Le Beau, M.M.15
Yamada, S.16
Nishigori, H.17
Takeda, J.18
Fajans, S.S.19
Hattersley, A.T.20
Iwasaki, N.21
Hansen, T.22
Pedersen, O.23
Polonsky, K.S.24
Bell, G.I.25
more..
-
5
-
-
10544236911
-
Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young
-
Yamagata K, Furuta H, Oda N, Kaisaki PJ, Menzel S, Cox NJ, Fajans SS, Signorini S, Stoffel M, Bell GI: Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young. Nature 384:458-460, 1996
-
(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
Fajans, S.S.7
Signorini, S.8
Stoffel, M.9
Bell, G.I.10
-
6
-
-
0031253820
-
Early-onset type-II diabetes mellitus (MODY4) linked to IPF 1
-
Stoffers DA, Ferrer J, Clarke WL, Habener JF: Early-onset type-II diabetes mellitus (MODY4) linked to IPF1. Nat Genet 17:138-139, 1997
-
(1997)
Nat Genet
, vol.17
, pp. 138-139
-
-
Stoffers, D.A.1
Ferrer, J.2
Clarke, W.L.3
Habener, J.F.4
-
7
-
-
0031453186
-
Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY
-
Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, Lindner T, Yamagata K, Ogata M, Tomonaga O, Kuroki H, Kasahara T, Iwamoto Y, Bell GI: Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY. Nat Genet 17:384-385, 1997
-
(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
Lindner, T.7
Yamagata, K.8
Ogata, M.9
Tomonaga, O.10
Kuroki, H.11
Kasahara, T.12
Iwamoto, Y.13
Bell, G.I.14
-
8
-
-
0032700272
-
Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus
-
Malecki MT, Jhala US, Antonellis A, Fields L, Doria A, Orban T, Saad M, Warram JH, Montminy M, Krolewski AS: Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus. Nat Genet 23:323-328, 1997
-
(1997)
Nat Genet
, vol.23
, pp. 323-328
-
-
Malecki, M.T.1
Jhala, U.S.2
Antonellis, A.3
Fields, L.4
Doria, A.5
Orban, T.6
Saad, M.7
Warram, J.H.8
Montminy, M.9
Krolewski, A.S.10
-
9
-
-
0038691467
-
Determinants of the development of diabetes (MODY3) in carriers of HNF-1α mutations: Evidence for a parent of origin effect
-
Klupa T, Warram JH, Antonellis A, Pezzolesi M, Nam M, Malecki MT, Doria A, Rich SS, Krolewski AS: Determinants of the development of diabetes (MODY3) in carriers of HNF-1α mutations: evidence for a parent of origin effect. Diabetes Care 25:2292-2301, 2002
-
(2002)
Diabetes Care
, vol.25
, pp. 2292-2301
-
-
Klupa, T.1
Warram, J.H.2
Antonellis, A.3
Pezzolesi, M.4
Nam, M.5
Malecki, M.T.6
Doria, A.7
Rich, S.S.8
Krolewski, A.S.9
-
10
-
-
0031027502
-
Characterization of the MODY3 phenotype: Early-onset diabetes caused by an insulin secretion defect
-
Lehto M, Tuomi T, Mahtani MM, Widen E, et al.: Characterization of the MODY3 phenotype: early-onset diabetes caused by an insulin secretion defect. J Clin Invest 99:582-591, 1997
-
(1997)
J Clin Invest
, vol.99
, pp. 582-591
-
-
Lehto, M.1
Tuomi, T.2
Mahtani, M.M.3
Widen, E.4
-
11
-
-
0032956493
-
Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes
-
Doria A, Yang Y, Malecki M, Scotti S, Dreyfus J, O'Keeffe C, Wantman M, Orban T, Warram JH, Krolewski AS: 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
-
(1999)
Diabetes Care
, vol.22
, pp. 253-261
-
-
Doria, A.1
Yang, Y.2
Malecki, M.3
Scotti, S.4
Dreyfus, J.5
O'Keeffe, C.6
Wantman, M.7
Orban, T.8
Warram, J.H.9
Krolewski, A.S.10
-
12
-
-
0033911995
-
Phenotypes of patients with simple Mendelian disorders are complex traits: Thresholds, modifiers, and system dynamics
-
Dipple KM, McCabe ER: Phenotypes of patients with simple Mendelian disorders are complex traits: thresholds, modifiers, and system dynamics. Am J Hum Genet 66:1729-1735, 2000
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1729-1735
-
-
Dipple, K.M.1
McCabe, E.R.2
-
13
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
Almasy L, Blangero J: Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet 62:1198-211, 1998
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
14
-
-
0029920402
-
Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q 31
-
Field LL, Tobias R, Thomson G, Plon S: Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31. Genomics 33:1-8, 1996
-
(1996)
Genomics
, vol.33
, pp. 1-8
-
-
Field, L.L.1
Tobias, R.2
Thomson, G.3
Plon, S.4
-
15
-
-
0037312885
-
Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: Evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q 24
-
Hsueh WC, St Jean PL, Mitchell BD, Pollin TI, Knowler WC, Ehm MG, Bell CJ, Sakul H, Wagner MJ, Burns DK, Shuldiner AR: Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24. Diabetes 52:550-557, 2003
-
(2003)
Diabetes
, vol.52
, pp. 550-557
-
-
Hsueh, W.C.1
St. Jean, P.L.2
Mitchell, B.D.3
Pollin, T.I.4
Knowler, W.C.5
Ehm, M.G.6
Bell, C.J.7
Sakul, H.8
Wagner, M.J.9
Burns, D.K.10
Shuldiner, A.R.11
-
16
-
-
0031678880
-
Cloning and characterization of Sel-11, a murine homolog of the C. elegans sel-1 gene
-
Donoviel DB, Donoviel MS, Fan E, Hadjantonakis AK, Bernstein A: Cloning and characterization of Sel-11, a murine homolog of the C. elegans sel-1 gene. Mech Dev 78:203-207, 1998
-
(1998)
Mech Dev
, vol.78
, pp. 203-207
-
-
Donoviel, D.B.1
Donoviel, M.S.2
Fan, E.3
Hadjantonakis, A.K.4
Bernstein, A.5
-
17
-
-
0031042083
-
Structure, function, and expression of SEL-1, a negative regulator of LIN-12 and GLP-1 in C. elegans
-
Grant B, Greenwald I: Structure, function, and expression of SEL-1, a negative regulator of LIN-12 and GLP-1 in C. elegans. Development 124:637-644, 1997
-
(1997)
Development
, vol.124
, pp. 637-644
-
-
Grant, B.1
Greenwald, I.2
-
18
-
-
0032242705
-
Notch signaling and the control of cell fate choices in vertebrates
-
Lewis J: Notch signaling and the control of cell fate choices in vertebrates. Semin Cell Dev Biol 9:583-589, 1998
-
(1998)
Semin Cell Dev Biol
, vol.9
, pp. 583-589
-
-
Lewis, J.1
-
19
-
-
0033606972
-
Notch signaling controls pancreatic cell differentiation
-
Apelqvist A, LI H, Sommer L, Beatus P, Anderson DJ, Honjo T, Hrabe de Angelis M, Lendhal U, Edlund H: Notch signaling controls pancreatic cell differentiation. Nature 400:877-881, 1999
-
(1999)
Nature
, vol.400
, pp. 877-881
-
-
Apelqvist, A.1
Li, H.2
Sommer, L.3
Beatus, P.4
Anderson, D.J.5
Honjo, T.6
Hrabe de Angelis, M.7
Lendhal, U.8
Edlund, H.9
-
20
-
-
0032522927
-
An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians
-
Pratley RE, Thompson DB, Prochazka M, Baier L, Mott D, Ravussin E, Sakul H, Ehm MG, Burns DK, Foroud T, Garvey WT, Hanson RL, Knowler WC, Bennett PH, Bogardus C: An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians. J Clin Invest 101:1757-1764, 1998
-
(1998)
J Clin Invest
, vol.101
, pp. 1757-1764
-
-
Pratley, R.E.1
Thompson, D.B.2
Prochazka, M.3
Baier, L.4
Mott, D.5
Ravussin, E.6
Sakul, H.7
Ehm, M.G.8
Burns, D.K.9
Foroud, T.10
Garvey, W.T.11
Hanson, R.L.12
Knowler, W.C.13
Bennett, P.H.14
Bogardus, C.15
-
21
-
-
0031945356
-
Hereditary fructose intolerance
-
Ali M, Rellos P, Cox TM: Hereditary fructose intolerance. J Med Genet 35:353-365, 1998
-
(1998)
J Med Genet
, vol.35
, pp. 353-365
-
-
Ali, M.1
Rellos, P.2
Cox, T.M.3
-
22
-
-
17944362243
-
The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome
-
Comuzzie AG, Funahashi T, Sonnenberg G, Martin LJ, Jacob HJ, Black AE, Maas D, Takahashi M, Kihara S, Tanaka S, Matsuzawa Y, Blangero J, Cohen D, Kissebah A: The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome. J Clin Endocrinol Metab 86:4321-4325, 2001
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 4321-4325
-
-
Comuzzie, A.G.1
Funahashi, T.2
Sonnenberg, G.3
Martin, L.J.4
Jacob, H.J.5
Black, A.E.6
Maas, D.7
Takahashi, M.8
Kihara, S.9
Tanaka, S.10
Matsuzawa, Y.11
Blangero, J.12
Cohen, D.13
Kissebah, A.14
-
23
-
-
0029837937
-
A clinical approach for the diagnosis of diabetes mellitus: An analysis using glycosylated hemoglobin levels: Meta-analysis Research Group on the Diagnosis of Diabetes Using Glycated Hemoglobin Levels
-
Peters AL, Davidson MB, Schriger DL, Hasselblad V: A clinical approach for the diagnosis of diabetes mellitus: an analysis using glycosylated hemoglobin levels: Meta-analysis Research Group on the Diagnosis of Diabetes Using Glycated Hemoglobin Levels. JAMA 276:1246-1252, 1996
-
(1996)
JAMA
, vol.276
, pp. 1246-1252
-
-
Peters, A.L.1
Davidson, M.B.2
Schriger, D.L.3
Hasselblad, V.4
-
24
-
-
0035228946
-
Genotyping for human whole-genome scans: Past, present, and future
-
Weber JL, Broman KW: Genotyping for human whole-genome scans: past, present, and future. Adv Genet 42:77-96, 2001
-
(2001)
Adv Genet
, vol.42
, pp. 77-96
-
-
Weber, J.L.1
Broman, K.W.2
-
25
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE: PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 63:259-266, 1998
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
|