-
3
-
-
0035219881
-
Genetic dissection of complex traits: An overview
-
(2001)
Advan. Genet
, vol.42
, pp. 13-32
-
-
Rao, D.C.1
-
9
-
-
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
-
(2000)
Diabetes
, vol.49
, pp. 126-130
-
-
Huxtable, S.J.1
Saker, P.J.2
Haddad, L.3
Walker, M.4
Frayling, T.M.5
Levy, J.C.6
Hitman, G.A.7
O'Rahilly, S.8
Hattersley, A.T.9
McCarthy, M.I.10
-
10
-
-
0026656320
-
Molecular mechanisms of insulin resistance: Lessons from patients with mutations in the insulin-receptor gene
-
(1992)
Diabetes
, vol.41
, pp. 1473-1490
-
-
Tailor, S.I.1
-
13
-
-
0028822448
-
Frequency of mutations of insulin receptor gene in Japanese patients with NIDDM
-
(1995)
Diabetes
, vol.44
, pp. 1081-1086
-
-
Kan, M.1
Danai, F.2
Iida, M.3
Jinnouchi, H.4
Todaka, M.5
Imanaka, T.6
Ito, K.7
Nishioka, Y.8
Ohnishi, T.9
Kamohara, S.10
Hayashi, H.11
Murakami, T.12
Kagawa, S.13
Sano, H.14
Hashimoto, N.15
Yoshida, S.16
Makino, H.17
Ebina, Y.18
-
15
-
-
0034252531
-
Insulin receptor substrate polymorphisms and type 2 diabetes mellitus
-
(2000)
Pharmacogenomics
, vol.1
, pp. 343-357
-
-
Sesti, G.1
-
19
-
-
0029021696
-
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
-
(1995)
Science
, vol.268
, pp. 426-429
-
-
Thomas, P.M.1
Cote, G.J.2
Wohllk, N.3
Haddad, B.4
Mathew, P.M.5
Rabl, W.6
Aguilar-Bryan, L.7
Gagel, R.F.8
Bryan, J.9
-
20
-
-
0029658241
-
Mutations in the Sulfonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews
-
(1996)
Hum. Mol. Genet
, vol.5
, pp. 1813-1822
-
-
Nestorowicz, A.1
Wilson, B.A.2
Schoor, K.P.3
Inoue, H.4
Glaser, B.5
Landau, H.6
Stanley, C.A.7
Thornton, S.8
Clement J.P. IV9
Bryan, J.10
Aguilar-Bryan, L.11
Permutt, M.A.12
-
23
-
-
0033625771
-
Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin
-
(2000)
Diabetes Care
, vol.23
, pp. 70-73
-
-
Rissanen, J.1
Markkanen, A.2
Karkkainen, P.3
Pihlajamaki, J.4
Kekalainen, P.5
Mykkanen, L.6
Kuusisto, J.7
Karhapaa, P.8
Niskanen, L.9
Laakso, M.10
-
24
-
-
0033007968
-
Variants in the sulphonylurea receptor gene: Association of the exon 16-3t variant with type II diabetes mellitus in Dutch Caucasians
-
(1999)
Diabetologia
, vol.42
, pp. 617-620
-
-
Hart, L.M.1
DeKnijff, P.2
Dekker, J.M.3
Stolk, R.P.4
Nijpels, G.5
Van Der Does, F.E.E.6
Ruige, J.B.7
Grobbee, D.E.8
Heine, R.J.9
Maasen, J.A.10
-
25
-
-
15844366738
-
Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians
-
(1996)
Diabetes
, vol.45
, pp. 825-831
-
-
Inoue, H.1
Ferrer, J.2
Welling, C.M.3
Elbein, S.C.4
Hoffman, M.5
Mayorga, R.6
Warren-Perry, M.7
Zhang, Y.8
Millns, H.9
Turner, R.10
Province, M.11
Brya, J.12
Permutt, M.A.13
Aguilar-Bryan, L.14
-
26
-
-
14444273653
-
Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians
-
(1997)
Diabetes
, vol.46
, pp. 688-694
-
-
Hani, E.H.1
Clement, K.2
Velho, G.3
Vionnet, N.4
Hager, J.5
Philippi, A.6
Dina, C.7
Inoue, H.8
Permutt, M.A.9
Basdevant, A.10
North, M.11
Demenais, F.12
Guy-Grand, B.13
-
27
-
-
0031925068
-
Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor gene
-
(1998)
Diabetes
, vol.47
, pp. 598-605
-
-
Hansen, T.1
Echwald, S.M.2
Hansen, L.3
Moller, A.M.4
Almind, K.5
Clausen, J.O.6
Urhammer, S.A.7
Inoue, H.8
Ferrer, J.9
Bryan, J.10
Aguilar-Bryan, L.11
Permutt, M.A.12
Pedersen, O.13
-
30
-
-
0028209092
-
Variability of the pancreatic islet beta cell/liver (GLUT 2) glucose transporter gene in NIDDM patients
-
(1994)
Diabetologia
, vol.37
, pp. 420-427
-
-
Tanizawa, Y.1
Riggs, A.C.2
Chiu, K.C.3
Janssen, R.C.4
Bell, D.S.H.5
Go, R.P.C.6
Roseman, J.M.7
Acton, R.T.8
-
32
-
-
15144357923
-
A missense mutation in the CD38 gene, a novel factor for insulin secretion: Association with type 2 diabetes mellitus in Japanese subjects and evidence of abnormal function when expressed in vitro
-
(1998)
Diabetologia
, vol.41
, pp. 1024-1028
-
-
Yagui, K.1
Shimada, F.2
Mimura, M.3
Hashimoto, N.4
Suzuki, Y.5
Tokuyama, Y.6
Nata, K.7
Tohgo, A.8
Ikehata, F.9
Takasawa, S.10
Okamoto, H.11
Makino, H.12
Saito, Y.13
Kanatsuka, A.14
-
33
-
-
0026562918
-
Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus
-
(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
Froguel, P.11
Cohen, D.12
-
34
-
-
0027472126
-
Familial hyperglycemia due to mutations in glucokinase
-
(1993)
N. Engl. J. Med
, vol.328
, pp. 697-702
-
-
Froguel, P.1
Zouali, H.2
Vionnet, N.3
Velho, G.4
Vaxillaire, M.5
Sun, F.6
Lesage, S.7
Stoffel, M.8
Takeda, J.9
Passa, P.10
Permutt, A.11
Beckmann, J.S.12
Bell, G.I.13
Cohen, D.14
-
38
-
-
10544236911
-
Mutations in the hepatocyte nuclear factor-4α gene I maturity-onset diabetes of the young (MODY1)
-
(1996)
Nature
, vol.384
, pp. 458-460
-
-
Yamagata, K.1
Furuta, H.2
Oda, N.3
Kaisake, P.J.4
Menzel, S.5
Cox, N.J.6
Fajans, S.S.7
Signorini, S.8
Stoffell, M.9
Bell, G.I.10
-
39
-
-
0032006573
-
A missense mutation in hepatocyte nuclear factor-4α, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus
-
(1998)
J. Clin. Invest
, vol.101
, pp. 521-526
-
-
Hani, E.H.1
Suaud, L.2
Boutin, P.3
Chevre, J.C.4
Durand, E.5
Philippi, A.6
Demenais, F.7
Vionnet, N.8
Furuta, H.9
Velho, G.10
Bell, G.I.11
Laine, B.12
Froguel, P.13
-
40
-
-
10544249874
-
Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3)
-
(1996)
Nature
, vol.384
, pp. 455-457
-
-
Yamagata, K.1
Oda, N.2
Kaisaki, P.J.3
Menzel, S.4
Furuta, H.5
Vaxillaire, M.6
Southams, 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, N.19
Hansen, T.20
Pedersen, O.21
Polonsky, K.S.22
Turner, R.C.23
Velho, G.24
Chevre, J.C.25
Froguel, P.26
Bell, G.I.27
more..
-
41
-
-
15444341853
-
Mutations in the hepatocyte nuclear factor-1α/MODY3 gene in Japanese subjects with early- and late-onset NIDDM
-
(1997)
Diabetes
, vol.46
, pp. 1504-1508
-
-
Iwasaki, N.1
Oda, N.2
Ogata, M.3
Hara, M.4
Hinokio, Y.5
Oda, Y.6
Yamagata, K.7
Kanematsu, S.8
Ohgawara, H.9
Omori, Y.10
Bell, G.I.11
-
44
-
-
0032742985
-
Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes
-
(1999)
J. Clin. Invest
, vol.104
-
-
Macfarlane, W.M.1
Frayling, T.M.2
Ellard, S.3
Evans, J.C.4
Allen, L.I.S.5
Bulman, M.P.6
Ayres, S.7
Shepherd, A.8
Clark, P.9
Millward, A.10
Demaine, A.11
Wilkin, T.12
Docherty, K.13
Hattersley, A.T.14
-
45
-
-
0034104298
-
The gene MAPK8IP1, encoding islet-brain-1, is a candidate for type 2 diabetes
-
(2000)
Nat. Genet
, vol.24
, pp. 291-295
-
-
Waeber, G.1
Delplanque, J.2
Bonny, C.3
Mooser, V.4
Steinmann, M.5
Widmann, C.6
Maillard, A.7
Miklossy, J.8
Dina, C.9
Hani, E.L.10
Vionnet, N.11
Nicod, P.12
Boutin, P.13
Froguel, P.14
-
46
-
-
0032700272
-
Mutations in NEROD1 are associated with the development of type 2 diabetes mellitus
-
(1999)
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
-
48
-
-
0028365102
-
Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu)(UUR) gene
-
(1994)
Diabetes
, vol.43
, pp. 746-751
-
-
Ouweland, J.M.1
Lemkes, H.H.2
Trembath, R.C.3
Ross, R.4
Velho, G.5
Cohen, D.6
Froguel, P.7
Maassen, J.A.8
-
51
-
-
0027145131
-
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu)(UUR) gene an etiologic hot spot?
-
(1993)
J. Clin. Invest
, vol.92
, pp. 2906-2915
-
-
Moraes, C.T.1
Ciacci, F.2
Bonilla, E.3
Jansen, C.4
Hirano, M.5
Rao, N.6
Lovelace, R.E.7
Rowland, L.P.8
Schon, E.A.9
DiMauro, S.10
-
52
-
-
0025666322
-
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
54
-
-
0032923074
-
Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution
-
(1999)
J. Hum. Genet
, vol.44
, pp. 210-214
-
-
Hirata, K.1
Nakagawa, M.2
Higuchi, I.3
Hashimoto, K.4
Hanada, K.5
Takahashi, K.6
Niiyama, T.7
Izumi, K.8
Sakoda, S.9
Yamada, H.10
Osame, M.11
-
55
-
-
0032540091
-
Novel mitochondrial DNA mutation in tRNA(Lys) (8296A→G) associated with diabetes
-
(1998)
Biochem. Biophys. Res. Commun
, vol.245
, pp. 523-527
-
-
Kameoka, K.1
Isotani, H.2
Tanaka, K.3
Azukari, K.4
Fujimura, Y.5
Shiota, Y.6
Sasaki, E.7
Majima, M.8
Furukawa, K.9
Haginomori, S.10
Kitaoka, H.11
Ohsawa, N.12
-
60
-
-
0031919090
-
An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/Frataxin (Friedreich's ataxia) gene
-
(1998)
Diabetes
, vol.47
, pp. 851-854
-
-
Ristow, M.1
Giannakidou, E.2
Hebinck, J.3
Busch, K.4
Vorgerd, M.5
Kotzka, J.6
Knebel, B.7
Mueller-Berghaus, J.8
Epplen, C.9
Pfeiffer, A.10
Kahn, C.R.11
-
62
-
-
0030846021
-
Regulation of mitochondrial iron accumulation by Yfh1p, a putative homologue of Frataxin
-
(1997)
Science
, vol.276
, pp. 1709-1712
-
-
Babcock, M.1
deSilva, D.2
Oaks, R.3
Davis-Kaplan, S.4
Jiralerspong, S.5
Montermini, L.6
Pandolfo, M.7
Kaplan, J.8
-
63
-
-
0027741390
-
Rad: A member of the Ras family overexpressed in muscle of type ii diabetic humans
-
(1993)
Science
, vol.262
, pp. 1441-1444
-
-
Reynet, C.1
Kahn, C.R.2
-
71
-
-
0033599038
-
Dominant negative mutations in human PPARG associated with severe insulin resistance, diabetes mellitus and hypertension
-
(1999)
Nature
, vol.402
, pp. 880-883
-
-
Barroso, I.1
Gurnell, M.2
Crowley, V.E.3
Agostini, M.4
Schwabe, J.W.5
Soos, M.A.6
Maslen, G.L.7
Williams, T.D.8
Lewis, H.9
Schafer, A.J.10
-
72
-
-
0345164399
-
Molecular scanning of the human peroxisome proliferator activated receptor gamma (hPPAR gamma) gene in diabetic Caucasians: Identification of a Pro12A1a PPAR gamma 2 missense mutation
-
(1997)
Biochem. Biophys. Res. Commun
, vol.241
, pp. 270-274
-
-
Yen, C.J.1
Beamer, B.A.2
Negri, C.3
Silver, K.4
Brown, K.A.5
Yarnall, D.P.6
Burns, D.K.7
Roth, J.8
Shuldiner, A.R.9
-
73
-
-
0032500747
-
Effect of the Pro12Ala variant of the human peroxisome proliferator-activated receptor gamma 2 gene on adiposity, fat distribution, and insulin sensitivity in Japanese men
-
(1998)
Biochem. Biophys. Res. Commun
, vol.251
, pp. 195-198
-
-
Mori, Y.1
Kim-Motoyama, H.2
Katakura, T.3
Yasuda, K.4
Kadowaki, H.5
Beamer, B.A.6
Shuldiner, A.R.7
Akanuma, Y.8
Yazaki, Y.9
Kadowaki, T.10
-
74
-
-
0031595923
-
A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity
-
(1998)
Nat. Genet
, vol.20
, pp. 284-287
-
-
Deeb, S.S.1
Fajas, L.2
Nemoto, M.3
Pihlajamaki, J.4
Mykkanen, L.5
Kuusisto, J.6
Laakso, M.7
Fujimoto, W.8
Auwerx, J.9
-
75
-
-
0033624575
-
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
-
(2000)
Nat. Genet
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
Hirschhorn, J.N.2
Klannemark, M.3
Lindgren, C.M.4
Vohl, M.C.5
Nemesh, J.6
Lane, C.R.7
Schaffner, S.F.8
Bolk, S.9
Brewer, C.10
-
77
-
-
0027160178
-
Identification of a simple tandem repeat DNA polymorphism in the human glycogen synthase gene and linkage to five markers on chromosome 19q
-
(1993)
Diabetes
, vol.42
, pp. 930-932
-
-
Vionnet, N.1
Bell, G.I.2
-
79
-
-
0030048997
-
Association of the glycogen synthase locus on 19q13 with NIDDM in Pima Indians
-
(1996)
Diabetologia
, vol.39
, pp. 314-321
-
-
Majer, M.1
Mott, D.M.2
Mochizuki, H.3
Rowles, J.C.4
Pedersen, O.5
Knowler, W.C.6
Bogardus, C.7
Prochazka, M.8
-
80
-
-
0027511164
-
Association between polymorphism of the glycogen synthase gene and non-insulin dependent diabetes mellitus
-
(1993)
N. Engl. J. Med
, vol.328
, pp. 10-14
-
-
Groop, L.C.1
Kankuri, M.2
Schalin-Jantti, C.3
Edstrand, A.4
Nikula-Ijas, P.5
Widen, E.6
Kuismanen, E.7
Eriksson, J.8
Franssila-Kallunki, A.9
Saloranta, C.10
Koskimies, S.11
-
84
-
-
0031688058
-
A common variant in PPP1R3 associated with insulin resistance and type 2 diabetes
-
(1998)
Diabetes
, vol.47
, pp. 1519-1524
-
-
Xia, J.1
Scherer, S.W.2
Cohen, P.T.W.3
Majer, M.4
Xi, T.5
Norman, R.A.6
Knowler, W.C.7
Bogardus, C.8
Prochazka, M.9
-
85
-
-
0032987981
-
The 3′-untranslated region polymorphism of the gene for skeletal muscle-specific glycogen-targeting subunit of protein phosphatase 1 in the type 2 diabetic Japanese population
-
(1999)
Diabetes
, vol.48
, pp. 1469-1472
-
-
Maegawa, H.1
Shi, K.2
Hidaka, H.3
Iwai, N.4
Nishio, Y.5
Egawa, K.6
Kojima, H.7
Haneda, M.8
Yasuda, H.9
Nakamura, Y.10
Kinoshita, M.11
Kikkawa, R.12
Kashiwagi, A.13
-
86
-
-
0031763878
-
Variation in the AU(AT)-rich element within the 3′-untranslated region of PPP1R3 is associated with variation in plasma glucose in Aboriginal Canadians
-
(1998)
J. Clin. Endocrinol. Metab
, vol.83
, pp. 3980-3983
-
-
Hegele, R.A.1
Harris, S.B.2
Bernard, Z.3
Wang, J.4
Cao, H.5
Hanley, A.J.G.6
Tsui, L.C.7
Scherer, S.W.8
-
89
-
-
0028848010
-
A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus
-
(1995)
Nat. Genet
, vol.9
, pp. 299-305
-
-
Hager, J.1
Hansen, L.2
Vaisse, C.3
Vionnet, N.4
Philippi, A.5
Poller, W.6
Welho, G.7
Carcassi, C.8
Contu, L.9
Julier, C.10
-
90
-
-
0029119111
-
Mutation of the glucagon receptor gene and diabetes mellitus in the UK: Association or founder effect?
-
(1995)
Hum. Mol. Genet
, vol.4
, pp. 1609-1612
-
-
Gough, S.C.L.1
Saker, P.J.2
Pritchard, L.E.3
Merriman, T.R.4
Merriman, M.E.5
Rowe, B.R.6
Kumar, S.7
Aitman, T.8
Barnett, A.H.9
Turner, R.C.10
-
95
-
-
0027392074
-
3-adrenergic receptor mRNA in man
-
(1993)
J. Clin. Invest
, vol.91
, pp. 344-349
-
-
Krief, S.1
Lonnqvist, F.2
Raimbault, S.3
Baude, B.4
Van Spronsen, A.5
Arner, P.6
Strosberg, A.D.7
Ricquier, D.8
Emorine, L.J.9
-
98
-
-
0029084088
-
3-adrenergic-receptor gene
-
(1995)
N. Engl. J. Med
, vol.333
, pp. 343-347
-
-
Walston, J.1
Silver, K.2
Bogardus, C.3
Knowler, W.C.4
Celi, F.S.5
Austin, S.6
Manning, B.7
Strosberg, A.D.8
Stern, M.P.9
Raben, N.10
-
99
-
-
0028978910
-
3-adrenergic-receptor and an increased capacity to gain weight in patients with morbid obesity
-
(1995)
N. Engl. J. Med
, vol.333
, pp. 352-354
-
-
Clement, K.1
Vaisse, C.2
Manning, B.S.3
Basdevant, A.4
Guy-Grand, B.5
Ruiz, J.6
Silver, K.D.7
Shuldiner, A.R.8
Froguel, P.9
Strosberg, A.D.10
-
100
-
-
9044228020
-
3-adrenergic-receptor with NIDDM and body weight gain
-
(1996)
Diabetologia
, vol.39
, pp. 349-352
-
-
Fujisawa, T.1
Ikegami, H.2
Yamato, E.3
Takekawa, K.4
Nakagawa, Y.5
Hamada, Y.6
Oga, T.7
Ueda, H.8
Shintani, A.9
Fukuda, M.10
Ogihara, T.11
-
102
-
-
0027468540
-
Linkage of chromosomal markers on 4q with a putative gene determining maximal insulin action in Pima Indians
-
(1993)
Diabetes
, vol.42
, pp. 514-519
-
-
Prochazka, M.1
Lillioja, S.2
Tait, J.F.3
Knowler, W.C.4
Mott, D.M.5
Spraul, M.6
Bennett, P.H.7
Bogardus, C.8
-
103
-
-
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
-
(1995)
J. Clin. Invest
, vol.95
, pp. 1281-1287
-
-
Baier, L.J.1
Sacchettini, J.C.2
Knowler, W.C.3
Eads, J.4
Paolisso, G.5
Tataranni, P.A.6
Mochizuki, H.7
Bennett, P.H.8
Bogardus, C.9
Prochazka, M.10
-
107
-
-
0031912535
-
Human hormone-sensitive lipase: Genetic mapping, identification of a new dinucleotide repeat, and association with obesity and NIDDM
-
(1998)
Diabetes
, vol.47
, pp. 284-286
-
-
Magre, J.1
Laurell, H.2
Fizames, C.3
Antoine, P.J.4
Dib, C.5
Vigouroux, C.6
Bourut, C.7
Capeau, J.8
Weissenbach, J.9
Langin, D.10
-
108
-
-
0031796690
-
The putative role of the hormone-sensitive lipase gene in the pathogenesis of type 2 diabetes mellitus and abdominal obesity
-
(1998)
Diabetologia
, vol.41
, pp. 1516-1522
-
-
Klannemark, M.1
Orho, M.2
Langin, D.3
Laurell, H.4
Holm, C.5
Reynisdottir, S.6
Arner, P.7
Groop, L.8
-
109
-
-
0344450708
-
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
-
(1998)
Nature
, vol.392
, pp. 398-401
-
-
Clement, K.1
Vaisse, C.2
Lahlou, N.3
Cabrol, S.4
Pelloux, V.5
Cassuto, D.6
Gourmelen, M.7
Dina, C.8
Chambaz, J.9
Lacorte, J.M.10
Basdevant, A.11
Bougnères, P.12
Lebouc, Y.13
Froguel, P.14
Guy-Grand, B.15
-
110
-
-
0032788234
-
Combination of polymorphisms in OB-R and the OB gene associated with insulin resistance in Nauruan males
-
(1999)
Int. J. Obesity
, vol.23
, pp. 816-822
-
-
De Silva, A.M.1
Walder, K.R.2
Aitman, T.J.3
Gotoda, T.4
Goldstone, A.P.5
Hodge, A.M.6
De Courten, M.P.7
Zimmet, P.Z.8
Collier, G.R.9
-
113
-
-
0028121082
-
Relationships between angiotensin I converting enzyme gene polymorphism, plasma levels, and diabetic retinal and renal complications
-
(1994)
Diabetes
, vol.43
, pp. 384-388
-
-
Marre, M.1
Bernadet, P.2
Gellois, Y.3
Savagner, F.4
Guyene, T.T.5
Hallab, M.6
Cambien, F.7
Passa, P.8
Alhenc-Gelas, F.9
-
117
-
-
17344366286
-
Association of a human G-protein B3 subunit variant with hypertension
-
(1998)
Nat. Genet
, vol.18
, pp. 45-48
-
-
Siffert, W.1
Rosskopf, D.2
Siffert, G.3
Busch, S.4
Moritz, A.5
Erbel, R.6
Sharma, A.M.7
Ritz, E.8
Wichmann, H.E.9
Jakobs, K.H.10
Horsthemke, B.11
-
119
-
-
0034736343
-
Interaction of the G Protein β3 subunit T825 allele and the IRS-1 Arg972 variant in type 2 diabetes
-
(2000)
Eur. J. Med. Res
, vol.5
, pp. 484-490
-
-
Rosskopf, D.1
Frey, U.2
Eckhardt, S.3
Schmidt, S.4
Ritz, E.5
Hofmann, S.6
Jaksch, M.7
Muller, N.8
Husing, J.9
Siffert, W.10
Jockel, K.H.11
-
120
-
-
9044243415
-
A genome-wide search for human non-insulin dependent (type 2) diabetes genes reveal a major susceptibility locus on chromosome 2
-
(1996)
Nat. Genet
, vol.13
, pp. 161-166
-
-
Hanis, C.L.1
-
121
-
-
0033772073
-
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
-
(2000)
Nat. Genet
, vol.26
, pp. 163-175
-
-
Horikawa, Y.1
Oda, N.2
Cox, N.J.3
Li, X.-Q.4
Orho-Melander, M.5
Hara, M.6
Hinokio, Y.7
Lindner, T.H.8
Mashima, H.9
Schwarz, P.E.H.10
Bosque-Plata, L.D.11
Horikawa, Y.12
Oda, Y.13
Yoshiuchi, I.14
Colilla, S.15
Polonsky, K.16
Wei, S.17
Concannon, P.18
Iwasaki, L.J.19
Bogardus, C.20
Groop, L.21
Boerwinkle, E.22
Hanis, C.L.23
Bell, G.I.24
more..
-
127
-
-
0030949271
-
Obesity and impaired prohormone processing associated with mutation in the human prohormone convertase 1 gene
-
(1997)
Nat. Genet
, vol.16
, pp. 303-306
-
-
Jackson, R.S.1
Creemers, J.W.M.2
Ohagi, S.3
Raffin-Sanson, M.L.4
Sanders, L.5
Montague, C.T.6
Hutton, J.C.7
O'Rahilly, S.8
|