-
1
-
-
0032952468
-
Freely associating
-
Editorial. Freely associating. Nature Genet. 22, 1-2 (1999).
-
(1999)
Nature Genet.
, vol.22
, pp. 1-2
-
-
-
2
-
-
0027367546
-
Aminoacid polymorphisms of insulin receptor substrate-1 in non-insulin-dependent diabetes mellitus
-
Almind, K. et al. Aminoacid polymorphisms of insulin receptor substrate-1 in non-insulin-dependent diabetes mellitus. Lancet 342, 828-832 (1993).
-
(1993)
Lancet
, vol.342
, pp. 828-832
-
-
Almind, K.1
-
3
-
-
0028978913
-
Association of a polymorphism in the β 3-adrenergic-receptor gene with features of the insulin resistance syndrome in Finns
-
Widen, E. et al. Association of a polymorphism in the β 3-adrenergic-receptor gene with features of the insulin resistance syndrome in Finns. N. Engl. J. Med. 333, 348-351 (1995).
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 348-351
-
-
Widen, E.1
-
4
-
-
0028940934
-
An amino acid substitution in the human intestinal fatty acid binding protein is associated with increased fatty acid binding, increased fat oxidation, and insulin resistance
-
Baier, L.J. et al. An amino acid substitution in the human intestinal fatty acid binding protein is associated with increased fatty acid binding, increased fat oxidation, and insulin resistance. J. Clin. Invest. 95, 1281-1287 (1995).
-
(1995)
J. Clin. Invest.
, vol.95
, pp. 1281-1287
-
-
Baier, L.J.1
-
5
-
-
0028848010
-
A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus
-
Hager, J. et al. A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus. Nature Genet. 9, 299-304 (1995).
-
(1995)
Nature Genet.
, vol.9
, pp. 299-304
-
-
Hager, J.1
-
6
-
-
0028822448
-
Frequency of mutations of insulin receptor gene in Japanese patients with NIDDM
-
Kan, M. et al. Frequency of mutations of insulin receptor gene in Japanese patients with NIDDM. Diabetes 44, 1081-1086 (1995).
-
(1995)
Diabetes
, vol.44
, pp. 1081-1086
-
-
Kan, M.1
-
7
-
-
0029818742
-
Missense mutation of amylin gene (S20G) in Japanese NIDDM patients
-
Sakagashira, S. et al. Missense mutation of amylin gene (S20G) in Japanese NIDDM patients. Diabetes 45, 1279-1281 (1996).
-
(1996)
Diabetes
, vol.45
, pp. 1279-1281
-
-
Sakagashira, S.1
-
8
-
-
0030000562
-
Codon 972 polymorphism in the insulin receptor substrate-1 gene, obesity, and risk of noninsulin-dependent diabetes mellitus
-
Sigal, R.J., Doria, A., Warram, J.H. & Krolewski, A.S. Codon 972 polymorphism in the insulin receptor substrate-1 gene, obesity, and risk of noninsulin-dependent diabetes mellitus. J. Clin. Endocrinol. Metab. 81, 1657-1659 (1996).
-
(1996)
J. Clin. Endocrinol. Metab.
, vol.81
, pp. 1657-1659
-
-
Sigal, R.J.1
Doria, A.2
Warram, J.H.3
Krolewski, A.S.4
-
9
-
-
15844366738
-
Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians
-
Inoue, H. et al. Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians. Diabetes 45, 825-831 (1996).
-
(1996)
Diabetes
, vol.45
, pp. 825-831
-
-
Inoue, H.1
-
10
-
-
0030983832
-
Paraoxonase-2 gene (PON2) G148 variant associated with elevated fasting plasma glucose in noninsulin-dependent diabetes mellitus
-
Hegele, R.A. et al. Paraoxonase-2 gene (PON2) G148 variant associated with elevated fasting plasma glucose in noninsulin-dependent diabetes mellitus. J. Clin. Endocrinol. Metab. 82, 3373-3377 (1997).
-
(1997)
J. Clin. Endocrinol. Metab.
, vol.82
, pp. 3373-3377
-
-
Hegele, R.A.1
-
11
-
-
0030798067
-
A missense mutation of the muscle glycogen synthase gene (M416V) is associated with insulin resistance in the Japanese population
-
Shimomura, H. et al. A missense mutation of the muscle glycogen synthase gene (M416V) is associated with insulin resistance in the Japanese population. Diabetologia 40, 947-952 (1997).
-
(1997)
Diabetologia
, vol.40
, pp. 947-952
-
-
Shimomura, H.1
-
12
-
-
0031595923
-
A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity
-
Deeb, S.S. et al. A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nature Genet. 20, 284-287 (1998).
-
(1998)
Nature Genet.
, vol.20
, pp. 284-287
-
-
Deeb, S.S.1
-
13
-
-
0031773333
-
Missense mutations in the pancreatic islet β cell inwardly rectifying K+ channel gene (KIR6.2/BIR): A meta-analysis suggests a role in the polygenic basis of type II diabetes mellitus in caucasians
-
Hani, E.H. et al. Missense mutations in the pancreatic islet β cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of type II diabetes mellitus in Caucasians. Diabetologia 41, 1511-1515 (1998).
-
(1998)
Diabetologia
, vol.41
, pp. 1511-1515
-
-
Hani, E.H.1
-
14
-
-
0032587498
-
Association of polymorphisms in the β2-adrenergic receptor gene with obesity, hypertriglyceridaemia, and diabetes mellitus
-
Ishiyama-Shigemoto, S., Yamada, K., Yuan, X., Ichikawa, F. & Nonaka, K. Association of polymorphisms in the β2-adrenergic receptor gene with obesity, hypertriglyceridaemia, and diabetes mellitus. Diabetologia 42, 98-101 (1999).
-
(1999)
Diabetologia
, vol.42
, pp. 98-101
-
-
Ishiyama-Shigemoto, S.1
Yamada, K.2
Yuan, X.3
Ichikawa, F.4
Nonaka, K.5
-
15
-
-
0032988612
-
Prevalence of variants in candidate genes for type 2 diabetes mellitus in the Netherlands: The Rotterdam study and the Hoorn study
-
Hart, L.M. et al. Prevalence of variants in candidate genes for type 2 diabetes mellitus in The Netherlands: the Rotterdam study and the Hoorn study. J. Clin. Endocrinol. Metab. 84, 1002-1006 (1999).
-
(1999)
J. Clin. Endocrinol. Metab.
, vol.84
, pp. 1002-1006
-
-
Hart, L.M.1
-
16
-
-
0033959416
-
Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles
-
Huxtable, S.J. et al. Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles. Diabetes 49, 126-130 (2000).
-
(2000)
Diabetes
, vol.49
, pp. 126-130
-
-
Huxtable, S.J.1
-
17
-
-
0031943552
-
Tumour necrosis factor-α gene promoter polymorphism and decreased insulin resistance
-
Day, C.P. et al. Tumour necrosis factor-α gene promoter polymorphism and decreased insulin resistance. Diabetologia 41, 430-434 (1998).
-
(1998)
Diabetologia
, vol.41
, pp. 430-434
-
-
Day, C.P.1
-
18
-
-
0004509649
-
The Pro115Gln and Pro12Ala PPAR γ gene mutations in obesity and type 2 diabetes
-
Clement, K. et al. The Pro115Gln and Pro12Ala PPAR γ gene mutations in obesity and type 2 diabetes. Int. J. Obes. Relat. Metab. Disord. 24, 391-393 (2000).
-
(2000)
Int. J. Obes. Relat. Metab. Disord.
, vol.24
, pp. 391-393
-
-
Clement, K.1
-
19
-
-
0034728762
-
The Pro12Ala polymorphism in PPAR γ2 may confer resistance to type 2 diabetes
-
Hara, K. et al. The Pro12Ala polymorphism in PPAR γ2 may confer resistance to type 2 diabetes. Biochem. Biophys. Res. Commun. 271, 212-216 (2000).
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.271
, pp. 212-216
-
-
Hara, K.1
-
20
-
-
0033060302
-
Pro12Ala substitution in the peroxisome proliferator-activated receptor-γ2 is not associated with type 2 diabetes
-
Mancini, P.P. et al. Pro12Ala substitution in the peroxisome proliferator-activated receptor-γ2 is not associated with type 2 diabetes. Diabetes 48, 1466-1468 (1999).
-
(1999)
Diabetes
, vol.48
, pp. 1466-1468
-
-
Mancini, P.P.1
-
21
-
-
0001491179
-
Impact of the peroxisome proliferator activated receptor γ2 Pro12Ala polymorphism on adiposity, lipids and non-insulin-dependent diabetes mellitus
-
Meirhaeghe, A. et al. Impact of the peroxisome proliferator activated receptor γ2 Pro12Ala polymorphism on adiposity, lipids and non-insulin-dependent diabetes mellitus. Int. J. Obes. Relat. Metab. Disord. 24, 195-199 (2000).
-
(2000)
Int. J. Obes. Relat. Metab. Disord.
, vol.24
, pp. 195-199
-
-
Meirhaeghe, A.1
-
22
-
-
0033582258
-
Pro12Ala missense mutation of the peroxisome proliferator activated receptor γ and diabetes mellitus
-
Ringel, J., Engeli, S., Distler, A. & Sharma, A.M. Pro12Ala missense mutation of the peroxisome proliferator activated receptor γ and diabetes mellitus. Biochem. Biophys. Res. Commun. 254, 450-453 (1999).
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.254
, pp. 450-453
-
-
Ringel, J.1
Engeli, S.2
Distler, A.3
Sharma, A.M.4
-
23
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman, R.S., McGinnis, R.E. & Ewens, W.J. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am. J. Hum. Genet. 52, 506-516 (1993).
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
24
-
-
0031912715
-
A sibship test for linkage in the presence of association: The sib transmission/disequilibrium test
-
Spielman, R.S. & Ewens, W.J. A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test. Am. J. Hum. Genet. 62, 450-458 (1998).
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 450-458
-
-
Spielman, R.S.1
Ewens, W.J.2
-
25
-
-
0031028361
-
Transmission-disequilibrium tests for quantitative traits
-
Allison, D.B. Transmission-disequilibrium tests for quantitative traits. Am. J. Hum. Genet. 60, 676-690 (1997).
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 676-690
-
-
Allison, D.B.1
-
26
-
-
0028641559
-
Stimulation of adipogenesis in fibroblasts by PPAR γ 2, a lipid-activated transcription factor
-
Tontonoz, P., Hu, E. & Spiegelman, B.M. Stimulation of adipogenesis in fibroblasts by PPAR γ 2, a lipid-activated transcription factor. Cell 79, 1147-1156 (1994).
-
(1994)
Cell
, vol.79
, pp. 1147-1156
-
-
Tontonoz, P.1
Hu, E.2
Spiegelman, B.M.3
-
27
-
-
0029016829
-
An antidiabetic thiazolidinedione is a high affinity ligand for peroxisome proliferator-activated receptor γ (PPAR γ)
-
Lehmann, J.M. et al. An antidiabetic thiazolidinedione is a high affinity ligand for peroxisome proliferator-activated receptor γ (PPAR γ), J. Biol. Chem. 270, 12953-12956 (1995).
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 12953-12956
-
-
Lehmann, J.M.1
-
28
-
-
0029024314
-
Cloning of the β cell high-affinity sulfonylurea receptor: A regulator of insulin secretion
-
Aguilar-Bryan, L. et al. Cloning of the β cell high-affinity sulfonylurea receptor: a regulator of insulin secretion. Science 268, 423-426 (1995).
-
(1995)
Science
, vol.268
, pp. 423-426
-
-
Aguilar-Bryan, L.1
-
29
-
-
0034607051
-
Inhibitory effect of a proline-to-alanine substitution at codon 12 of peroxisome proliferator-activated receptor-γ 2 on thiazolidinedione-induced adipogenesis
-
Masugi, J., Tamori, Y., Mori, H., Koike, T. & Kasuga, M. Inhibitory effect of a proline-to-alanine substitution at codon 12 of peroxisome proliferator-activated receptor-γ 2 on thiazolidinedione-induced adipogenesis. Biochem. Biophys. Res. Commun. 268, 178-182 (2000).
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.268
, pp. 178-182
-
-
Masugi, J.1
Tamori, Y.2
Mori, H.3
Koike, T.4
Kasuga, M.5
-
30
-
-
0033599038
-
Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension
-
Barroso, I. et al. Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension. Nature 402, 880-883 (1999).
-
(1999)
Nature
, vol.402
, pp. 880-883
-
-
Barroso, I.1
-
31
-
-
0032189782
-
Obesity associated with a mutation in a genetic regulator of adipocyte differentiation
-
Ristow, M., Muller-Wieland, D., Pfeiffer, A., Krone, W. & Kahn, C.R. Obesity associated with a mutation in a genetic regulator of adipocyte differentiation. N. Engl. J. Med. 339, 953-959 (1998).
-
(1998)
N. Engl. J. Med.
, vol.339
, pp. 953-959
-
-
Ristow, M.1
Muller-Wieland, D.2
Pfeiffer, A.3
Krone, W.4
Kahn, C.R.5
-
32
-
-
0003014882
-
Metabolic consequences of a family history of NIDDM (the Botnia study): Evidence for sex-specific parental effects
-
Groop, L. et al. Metabolic consequences of a family history of NIDDM (the Botnia study): evidence for sex-specific parental effects. Diabetes 45, 1585-1593 (1996).
-
(1996)
Diabetes
, vol.45
, pp. 1585-1593
-
-
Groop, L.1
-
33
-
-
0031851293
-
Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: Diagnosis and classification of diabetes mellitus provisional report of a WHO consultation
-
Alberti, K.G. & Zimmet, P.Z. Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet. Med. 15, 539-553 (1998).
-
(1998)
Diabet. Med.
, vol.15
, pp. 539-553
-
-
Alberti, K.G.1
Zimmet, P.Z.2
-
34
-
-
15444359998
-
Predictors of progression from impaired glucose tolerance to NIDDM: An analysis of six prospective studies
-
Edelstein, S.L. et al. Predictors of progression from impaired glucose tolerance to NIDDM: an analysis of six prospective studies. Diabetes 46, 701-710 (1997).
-
(1997)
Diabetes
, vol.46
, pp. 701-710
-
-
Edelstein, S.L.1
-
35
-
-
0033042346
-
Impaired fasting glucose or impaired glucose tolerance. What best predicts future diabetes in Mauritius?
-
Shaw, J.E. et al. Impaired fasting glucose or impaired glucose tolerance. What best predicts future diabetes in Mauritius? Diabetes Care 22, 399-402(1999).
-
(1999)
Diabetes Care
, vol.22
, pp. 399-402
-
-
Shaw, J.E.1
-
36
-
-
0030885877
-
Fluorescence energy transfer detection as a homogeneous DNA diagnostic method. Proc
-
Chen, X., Zehnbauer, B., Gnirke, A. & Kwok, P.Y. Fluorescence energy transfer detection as a homogeneous DNA diagnostic method. Proc. Natl Acad. Sci. USA 94, 10756-10761 (1997).
-
(1997)
Natl Acad. Sci. USA
, vol.94
, pp. 10756-10761
-
-
Chen, X.1
Zehnbauer, B.2
Gnirke, A.3
Kwok, P.Y.4
-
37
-
-
0033058730
-
Fluorescence polarization in homogeneous nucleic acid analysis
-
Chen, X., Levine, L. & Kwok, P.Y. Fluorescence polarization in homogeneous nucleic acid analysis. Genome Res. 9, 492-498 (1999).
-
(1999)
Genome Res.
, vol.9
, pp. 492-498
-
-
Chen, X.1
Levine, L.2
Kwok, P.Y.3
-
38
-
-
0031949273
-
Genetic association mapping based on discordant sib pairs: The discordant-alleles test
-
Boehnke, M. & Langefeld, C.D. Genetic association mapping based on discordant sib pairs: the discordant-alleles test. Am. J. Hum. Genet. 62, 950-961 (1998).
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 950-961
-
-
Boehnke, M.1
Langefeld, C.D.2
|