-
1
-
-
0034611791
-
Obesity as a medical problem
-
Kopelman P: Obesity as a medical problem. Nature 404:635-643, 2000
-
(2000)
Nature
, vol.404
, pp. 635-643
-
-
Kopelman, P.1
-
2
-
-
0032961820
-
The relative risks of hyperglycaemia, obesity and dyslipidaemia in the relatives of patients with type II diabetes mellitus
-
Shaw J, Purdie D, Neil H, Levy J, Turner R: The relative risks of hyperglycaemia, obesity and dyslipidaemia in the relatives of patients with type II diabetes mellitus. Diabetologia 42:24-27, 1999
-
(1999)
Diabetologia
, vol.42
, pp. 24-27
-
-
Shaw, J.1
Purdie, D.2
Neil, H.3
Levy, J.4
Turner, R.5
-
3
-
-
0032896076
-
Concordance rate for type II diabetes mellitus in monozygotic twins: Actuarial analysis
-
Medici F, Hawa M, Ianari A, Pyke D, Leslie R: Concordance rate for type II diabetes mellitus in monozygotic twins: actuarial analysis. Diabetologia 42:146-150, 1999
-
(1999)
Diabetologia
, vol.42
, pp. 146-150
-
-
Medici, F.1
Hawa, M.2
Ianari, A.3
Pyke, D.4
Leslie, R.5
-
4
-
-
0032953097
-
Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance - A population-based twin study
-
Poulsen P, Kyvik K, Vaag A, Beck-Nielsen H: Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance - a population-based twin study. Diabetologia 42:139-145, 1999
-
(1999)
Diabetologia
, vol.42
, pp. 139-145
-
-
Poulsen, P.1
Kyvik, K.2
Vaag, A.3
Beck-Nielsen, H.4
-
5
-
-
0022896508
-
Relationship of prevalence of non-insulin-dependent diabetes mellitus to Amerindian admixture in the Mexican Americans of San Antonio, Texas
-
Chakraborty R, Ferrell R, Stern M, Haffner S, Hazuda H, Rosenthal M: Relationship of prevalence of non-insulin-dependent diabetes mellitus to Amerindian admixture in the Mexican Americans of San Antonio, Texas. Genet Epidemiol 3:435-454, 1986
-
(1986)
Genet Epidemiol
, vol.3
, pp. 435-454
-
-
Chakraborty, R.1
Ferrell, R.2
Stern, M.3
Haffner, S.4
Hazuda, H.5
Rosenthal, M.6
-
6
-
-
0035106310
-
Putting the genes for type II diabetes on the map
-
Almind K, Doria A, Kahn C: Putting the genes for type II diabetes on the map. Nat Med 7:277-279, 2001
-
(2001)
Nat Med
, vol.7
, pp. 277-279
-
-
Almind, K.1
Doria, A.2
Kahn, C.3
-
7
-
-
0033772073
-
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
-
Horikawa Y, Oda N, Cox NJ, Li X, Orho-Melander M, Hara M, Hinokio Y, Lindner TH, Mashima H, Schwarz PE, Bosque-Plata L, Horikawa Y, Oda Y, Yoshiuchi I, Colilla S, Polonsky KS, Wei S, Concannon P, Iwasaki N, Schulze J, Baier LJ, Bogardus C, Groop L, Boerwinkle E, Hanis CL, Bell GI: Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus. Nat Genet 26:163-175, 2000
-
(2000)
Nat Genet
, vol.26
, pp. 163-175
-
-
Horikawa, Y.1
Oda, N.2
Cox, N.J.3
Li, X.4
Orho-Melander, M.5
Hara, M.6
Hinokio, Y.7
Lindner, T.H.8
Mashima, H.9
Schwarz, P.E.10
Bosque-Plata, L.11
Horikawa, Y.12
Oda, Y.13
Yoshiuchi, I.14
Colilla, S.15
Polonsky, K.S.16
Wei, S.17
Concannon, P.18
Iwasaki, N.19
Schulze, J.20
Baier, L.J.21
Bogardus, C.22
Groop, L.23
Boerwinkle, E.24
Hanis, C.L.25
Bell, G.I.26
more..
-
8
-
-
0036895104
-
Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians
-
Rasmussen S, Urhammer S, Berglund L, Jensen J, Hansen L, Echwald S, Borch-Johnsen K, Horikawa Y, Mashima H, Lithell H, Cox NJ, Torben Hansen T, Bell GI, Pedersen O: Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians. Diabetes 51:3561-3567, 2002
-
(2002)
Diabetes
, vol.51
, pp. 3561-3567
-
-
Rasmussen, S.1
Urhammer, S.2
Berglund, L.3
Jensen, J.4
Hansen, L.5
Echwald, S.6
Borch-Johnsen, K.7
Horikawa, Y.8
Mashima, H.9
Lithell, H.10
Cox, N.J.11
Torben Hansen, T.12
Bell, G.I.13
Pedersen, O.14
-
9
-
-
0036316935
-
Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort
-
Fingerlin TE, Erdos MR, Watanabe RM, Wiles KR, Stringham HM, Mohlke KL, Silander K, Valle TT, Buchanan TA, Tuomilehto J, Bergman RN, Boehnke M, Collins FS: Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort. Diabetes 51:1644-1648, 2002
-
(2002)
Diabetes
, vol.51
, pp. 1644-1648
-
-
Fingerlin, T.E.1
Erdos, M.R.2
Watanabe, R.M.3
Wiles, K.R.4
Stringham, H.M.5
Mohlke, K.L.6
Silander, K.7
Valle, T.T.8
Buchanan, T.A.9
Tuomilehto, J.10
Bergman, R.N.11
Boehnke, M.12
Collins, F.S.13
-
10
-
-
0036321080
-
Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels
-
Orho-Melander M, Klannemark M, Svensson MK, Ridderstrale M, Lindgren CM, Groop L: Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels. Diabetes 51:2658-2664, 2002
-
(2002)
Diabetes
, vol.51
, pp. 2658-2664
-
-
Orho-Melander, M.1
Klannemark, M.2
Svensson, M.K.3
Ridderstrale, M.4
Lindgren, C.M.5
Groop, L.6
-
11
-
-
0036097653
-
Variation in the calpain-10 gene affects blood glucose levels in the British population
-
Lynn S, Evans JC, White C, Frayling TM, Hattersley AT, Turnbull DM, Horikawa Y, Cox NJ, Bell GI, Walker M: Variation in the calpain-10 gene affects blood glucose levels in the British population. Diabetes 51:247-250, 2002
-
(2002)
Diabetes
, vol.51
, pp. 247-250
-
-
Lynn, S.1
Evans, J.C.2
White, C.3
Frayling, T.M.4
Hattersley, A.T.5
Turnbull, D.M.6
Horikawa, Y.7
Cox, N.J.8
Bell, G.I.9
Walker, M.10
-
12
-
-
0034894047
-
Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom
-
Evans JC, Frayling TM, Cassell PG, Saker PJ, Hitman GA, Walker M, Levy JC, O'Rahilly S, Rao PVS, Bennett AJ, Jones EC, Menzel S, Prestwich P, Simecek N, Wishart M, Dhillon R, Fletcher C, Millward A, Demaine A, Wilkin T, Horikawa Y, Cox NJ, Bell GI, Ellard S, McCarthy MI, Hattersley AT: Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom. Am J Hum Genet 69:544-552, 2001
-
(2001)
Am J Hum Genet
, vol.69
, pp. 544-552
-
-
Evans, J.C.1
Frayling, T.M.2
Cassell, P.G.3
Saker, P.J.4
Hitman, G.A.5
Walker, M.6
Levy, J.C.7
O'Rahilly, S.8
Rao, P.V.S.9
Bennett, A.J.10
Jones, E.C.11
Menzel, S.12
Prestwich, P.13
Simecek, N.14
Wishart, M.15
Dhillon, R.16
Fletcher, C.17
Millward, A.18
Demaine, A.19
Wilkin, T.20
Horikawa, Y.21
Cox, N.J.22
Bell, G.I.23
Ellard, S.24
McCarthy, M.I.25
Hattersley, A.T.26
more..
-
13
-
-
0242524453
-
The inherited basis of diabetes mellitus: Implications for the genetic analysis of complex traits
-
Florez JC, Hirschhorn J, Altshuler D: The inherited basis of diabetes mellitus: implications for the genetic analysis of complex traits. Annu Rev Genomics Hum Genet 4:257-291, 2003
-
(2003)
Annu Rev Genomics Hum Genet
, vol.4
, pp. 257-291
-
-
Florez, J.C.1
Hirschhorn, J.2
Altshuler, D.3
-
14
-
-
0036300603
-
The gene INPPL1, encoding the lipid phosphatase SHIP 2, is a candidate for type 2 diabetes in rat and man
-
Marion E, Kaisaki PJ, Pouillon V, Gueydan C, Levy JC, Bodson A, Krzentowski G, Daubresse JC, Mockel J, Behrends J, Servais G, Szpirer C, Kruys V, Gauguier D, Schurmans S: The gene INPPL1, encoding the lipid phosphatase SHIP2, is a candidate for type 2 diabetes in rat and man. Diabetes 51:2012-2017, 2002
-
(2002)
Diabetes
, vol.51
, pp. 2012-2017
-
-
Marion, E.1
Kaisaki, P.J.2
Pouillon, V.3
Gueydan, C.4
Levy, J.C.5
Bodson, A.6
Krzentowski, G.7
Daubresse, J.C.8
Mockel, J.9
Behrends, J.10
Servais, G.11
Szpirer, C.12
Kruys, V.13
Gauguier, D.14
Schurmans, S.15
-
15
-
-
0032837860
-
Mouse ENU mutagenesis
-
Justice MJ, Noveroske JK, Weber JS, Zheng B, Bradley A: Mouse ENU mutagenesis. Hum Mol Genet 8:1955-1963, 1999
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1955-1963
-
-
Justice, M.J.1
Noveroske, J.K.2
Weber, J.S.3
Zheng, B.4
Bradley, A.5
-
16
-
-
0034425410
-
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse
-
Nolan PM, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray IC, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson J, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel KP, Voegeling S, Guenet JL, Nickols C, Sadri R, Naase M, Isaacs A, Davies KE, Browne M, Fisher EMC, Martin J, Rastan S, Brown SDM, Hunter JA: A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. Nat Genet 25:440-443, 2000
-
(2000)
Nat Genet
, vol.25
, pp. 440-443
-
-
Nolan, P.M.1
Peters, J.2
Strivens, M.3
Rogers, D.4
Hagan, J.5
Spurr, N.6
Gray, I.C.7
Vizor, L.8
Brooker, D.9
Whitehill, E.10
Washbourne, R.11
Hough, T.12
Greenaway, S.13
Hewitt, M.14
Liu, X.15
McCormack, S.16
Pickford, K.17
Selley, R.18
Wells, C.19
Tymowska-Lalanne, Z.20
Roby, P.21
Glenister, P.22
Thornton, C.23
Thaung, C.24
Stevenson, J.25
Arkell, R.26
Mburu, P.27
Hardisty, R.28
Kiernan, A.29
Erven, A.30
Steel, K.P.31
Voegeling, S.32
Guenet, J.L.33
Nickols, C.34
Sadri, R.35
Naase, M.36
Isaacs, A.37
Davies, K.E.38
Browne, M.39
Fisher, E.M.C.40
Martin, J.41
Rastan, S.42
Brown, S.D.M.43
Hunter, J.A.44
more..
-
17
-
-
0034425715
-
Genome-wide, large-scale production of mutant mice by ENU mutagenesis
-
Hrabe de Angelis MH, Flaswinkel H, Fuchs H, Rathkolb B, Soewarto D, Marschall S, Heffner S, Pargent W, Wuensch K, Jung M, Reis A, Richter T, Alessandrini F, Jakob T, Fuchs E, Kolb H, Kremmer E, Schaeble K, Rollinski B, Roscher A, Peters C, Meitinger T, Strom T, Steckler T, Holsboer F, Klopstock T, Gekeler F, Schindewolf C, Jung T, Avraham K, Behrendt H, Ring J, Zimmer A, Schughart K, Pfeffer K, Wolf E, Balling R: Genome-wide, large-scale production of mutant mice by ENU mutagenesis. Nat Genet 25:444-447, 2000
-
(2000)
Nat Genet
, vol.25
, pp. 444-447
-
-
Hrabe De Angelis, M.H.1
Flaswinkel, H.2
Fuchs, H.3
Rathkolb, B.4
Soewarto, D.5
Marschall, S.6
Heffner, S.7
Pargent, W.8
Wuensch, K.9
Jung, M.10
Reis, A.11
Richter, T.12
Alessandrini, F.13
Jakob, T.14
Fuchs, E.15
Kolb, H.16
Kremmer, E.17
Schaeble, K.18
Rollinski, B.19
Roscher, A.20
Peters, C.21
Meitinger, T.22
Strom, T.23
Steckler, T.24
Holsboer, F.25
Klopstock, T.26
Gekeler, F.27
Schindewolf, C.28
Jung, T.29
Avraham, K.30
Behrendt, H.31
Ring, J.32
Zimmer, A.33
Schughart, K.34
Pfeffer, K.35
Wolf, E.36
Balling, R.37
more..
-
18
-
-
0036509698
-
A gene-driven approach to the identification of ENU mutants in the mouse
-
Coghill EL, Hugill A, Parkinson N, Davison C, Glenister P, Clements S, Hunter J, Cox RD, Brown SD: A gene-driven approach to the identification of ENU mutants in the mouse. Nat Genet 30:255-256, 2002
-
(2002)
Nat Genet
, vol.30
, pp. 255-256
-
-
Coghill, E.L.1
Hugill, A.2
Parkinson, N.3
Davison, C.4
Glenister, P.5
Clements, S.6
Hunter, J.7
Cox, R.D.8
Brown, S.D.9
-
19
-
-
0036800873
-
Novel phenotypes identified by plasma biochemical screening in the mouse
-
Hough TA, Nolan PM, Tsipouri V, Toye AA, Gray IC, Goldsworthy M, Moir L, Cox RD, Clements S, Glenister PH, Wood J, Selley RL, Strivens MA, Vizor L, McCormack SL, Peters J, Fisher EM, Spurr N, Rastan S: Novel phenotypes identified by plasma biochemical screening in the mouse. Mamm Genome 13:595-602, 2002
-
(2002)
Mamm Genome
, vol.13
, pp. 595-602
-
-
Hough, T.A.1
Nolan, P.M.2
Tsipouri, V.3
Toye, A.A.4
Gray, I.C.5
Goldsworthy, M.6
Moir, L.7
Cox, R.D.8
Clements, S.9
Glenister, P.H.10
Wood, J.11
Selley, R.L.12
Strivens, M.A.13
Vizor, L.14
McCormack, S.L.15
Peters, J.16
Fisher, E.M.17
Spurr, N.18
Rastan, S.19
-
20
-
-
0028302127
-
A genetic map of the mouse with 4,006 simple sequence length polymorphisms
-
Dietrich WF, Miller JC, Steen RG, Merchant M, Damron D, Nahf R, Gross A, Joyce DC, Wessel M, Dredge RD, Marquis A, Stein LD, Goodman N, Page DC, Lander ES: A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nat Genet 7:220-245, 1994
-
(1994)
Nat Genet
, vol.7
, pp. 220-245
-
-
Dietrich, W.F.1
Miller, J.C.2
Steen, R.G.3
Merchant, M.4
Damron, D.5
Nahf, R.6
Gross, A.7
Joyce, D.C.8
Wessel, M.9
Dredge, R.D.10
Marquis, A.11
Stein, L.D.12
Goodman, N.13
Page, D.C.14
Lander, E.S.15
-
21
-
-
0035164656
-
Map Manager QTX, cross-platform software for genetic mapping
-
Manly KF, Cudmore RH Jr, Meer JM: Map Manager QTX, cross-platform software for genetic mapping. Mamm Genome 12:930-932, 2001
-
(2001)
Mamm Genome
, vol.12
, pp. 930-932
-
-
Manly, K.F.1
Cudmore Jr., R.H.2
Meer, J.M.3
-
22
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L: Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet, 11:241-247, 1995
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
23
-
-
0026559651
-
Heterogeneous expression of glucokinase among pancreatic beta cells
-
Jetton TL, Magnuson MA: Heterogeneous expression of glucokinase among pancreatic beta cells. Proc Natl Acad Sci U S A 89:2619-2623, 1992
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 2619-2623
-
-
Jetton, T.L.1
Magnuson, M.A.2
-
24
-
-
0030963661
-
Cell-specific expression and regulation of a glucokinase gene locus transgene
-
Niswender KD, Postic C, Jetton TL, Bennett BD, Piston DW, Efrat S, Magnuson MA: Cell-specific expression and regulation of a glucokinase gene locus transgene. J Biol Chem 272:22564-22569, 1997
-
(1997)
J Biol Chem
, vol.272
, pp. 22564-22569
-
-
Niswender, K.D.1
Postic, C.2
Jetton, T.L.3
Bennett, B.D.4
Piston, D.W.5
Efrat, S.6
Magnuson, M.A.7
-
25
-
-
0031043316
-
Effects of altered glucokinase gene copy number on blood glucose homoeostasis
-
Niswender KD, Postic C, Shiota M, Jetton TL, Magnuson MA: Effects of altered glucokinase gene copy number on blood glucose homoeostasis. Biochem Soc Trans 25:113-117, 1997
-
(1997)
Biochem Soc Trans
, vol.25
, pp. 113-117
-
-
Niswender, K.D.1
Postic, C.2
Shiota, M.3
Jetton, T.L.4
Magnuson, M.A.5
-
26
-
-
0028826361
-
Transgenic knockouts reveal a critical requirement for pancreatic beta cell glucokinase in maintaining glucose homeostasis
-
Grupe A, Hultgren B, Ryan A, Ma YH, Bauer M, Stewart TA: Transgenic knockouts reveal a critical requirement for pancreatic beta cell glucokinase in maintaining glucose homeostasis. Cell 83:69-78, 1995
-
(1995)
Cell
, vol.83
, pp. 69-78
-
-
Grupe, A.1
Hultgren, B.2
Ryan, A.3
Ma, Y.H.4
Bauer, M.5
Stewart, T.A.6
-
27
-
-
0026639928
-
Human glucokinase gene: Isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus
-
Stoffel M, Froguel P, Taked J, Zouali H, Vionnet N, Nishi S, Weber IT, Harrison RW, Pilkis SJ, Lesage S, Vaxillaire M, Velho G, Sun F, Iris F, Passa P, Cohen D, Bell GI: Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus. Proc Natl Acad Sci U S A 89:7698-7702, 1992
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 7698-7702
-
-
Stoffel, M.1
Froguel, P.2
Taked, J.3
Zouali, H.4
Vionnet, N.5
Nishi, S.6
Weber, I.T.7
Harrison, R.W.8
Pilkis, S.J.9
Lesage, S.10
Vaxillaire, M.11
Velho, G.12
Sun, F.13
Iris, F.14
Passa, P.15
Cohen, D.16
Bell, G.I.17
-
28
-
-
8044260804
-
Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families
-
Velho G, Blanche H, Vaxillaire M, Bellanne-Chantelot C, Pardini VC, Timsit J, Passa P, Deschamps I, Robert JJ, Weber IT, Marotta D, Pilkis SJ, Lipkind GM, Bell GI, Froguel P: Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families. Diabetologia 40:217-224, 1997
-
(1997)
Diabetologia
, vol.40
, pp. 217-224
-
-
Velho, G.1
Blanche, H.2
Vaxillaire, M.3
Bellanne-Chantelot, C.4
Pardini, V.C.5
Timsit, J.6
Passa, P.7
Deschamps, I.8
Robert, J.J.9
Weber, I.T.10
Marotta, D.11
Pilkis, S.J.12
Lipkind, G.M.13
Bell, G.I.14
Froguel, P.15
-
29
-
-
0028353674
-
Insulin secretory abnormalities in subjects with hyperglycaemia due to glucokinase mutations
-
Byrne M, Sturis J, Clement K, Vionnet N, Pueyo M, Stoffel I, Takeda J, Passa P, Cohen D, Bell GI, Velho G, Froguel P, Polonsky KS: Insulin secretory abnormalities in subjects with hyperglycaemia due to glucokinase mutations. J Clin Invest 93:1120-1130, 1994
-
(1994)
J Clin Invest
, vol.93
, pp. 1120-1130
-
-
Byrne, M.1
Sturis, J.2
Clement, K.3
Vionnet, N.4
Pueyo, M.5
Stoffel, I.6
Takeda, J.7
Passa, P.8
Cohen, D.9
Bell, G.I.10
Velho, G.11
Froguel, P.12
Polonsky, K.S.13
-
30
-
-
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 19:268-270, 1998
-
(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
-
31
-
-
0342902204
-
Neonatal diabetes mellitus due to complete glucokinase deficiency
-
Njolstad PR, Sovik O, Cuesta-Munoz A, Bjorkhaug L, Massa O, Barbetti F, Undlien DE, Shiota C, Magnuson MA, Molven A, Matschinsky FM, Bell GI: Neonatal diabetes mellitus due to complete glucokinase deficiency. N Engl J Med 344:1588-1592, 2001
-
(2001)
N Engl J Med
, vol.344
, pp. 1588-1592
-
-
Njolstad, P.R.1
Sovik, O.2
Cuesta-Munoz, A.3
Bjorkhaug, L.4
Massa, O.5
Barbetti, F.6
Undlien, D.E.7
Shiota, C.8
Magnuson, M.A.9
Molven, A.10
Matschinsky, F.M.11
Bell, G.I.12
-
32
-
-
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, Froguel P, Cohen D: 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
Froguel, P.11
Cohen, D.12
-
33
-
-
0026583193
-
Linkage of type 2 diabetes to the glucokinase gene
-
Hattersley AT, Turner RC, Permutt MA, Patel P, Tanizawa Y, Chiu KC, O'Rahilly S, Watkins PJ, Wainscoat JS: Linkage of type 2 diabetes to the glucokinase gene. Lancet 339:1307-1310, 1992
-
(1992)
Lancet
, vol.339
, pp. 1307-1310
-
-
Hattersley, A.T.1
Turner, R.C.2
Permutt, M.A.3
Patel, P.4
Tanizawa, Y.5
Chiu, K.C.6
O'Rahilly, S.7
Watkins, P.J.8
Wainscoat, J.S.9
-
34
-
-
0032556969
-
Familial hyperinsulinism caused by an activating glucokinase mutation
-
Glaser B, Kesavan P, Heyman M, Davis E, Cuesta A, Buchs A, Stanley CA, Thornton PS, Permutt M, Matschinsky FM, Herold KC: Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med 338:226-230, 1998
-
(1998)
N Engl J Med
, vol.338
, pp. 226-230
-
-
Glaser, B.1
Kesavan, P.2
Heyman, M.3
Davis, E.4
Cuesta, A.5
Buchs, A.6
Stanley, C.A.7
Thornton, P.S.8
Permutt, M.9
Matschinsky, F.M.10
Herold, K.C.11
-
35
-
-
0032942836
-
Congenital hyperinsulinism: Molecular basis of a heterogeneous disease
-
Meissner T, Beinbrech B, Mayatepek E: Congenital hyperinsulinism: molecular basis of a heterogeneous disease. Hum Mutat 13:351-361, 1999
-
(1999)
Hum Mutat
, vol.13
, pp. 351-361
-
-
Meissner, T.1
Beinbrech, B.2
Mayatepek, E.3
-
36
-
-
0029155957
-
Animal models for maturity-onset diabetes of the young generated by disruption of the mouse glucokinase gene
-
Bali D, Svetlanov A, Lee H, Fusco-DeMane D, Leiser M, Li B, Barzilai N, Surana M, Hou H, Fleischer N, Depinho R, Rossetti L, Efrat S: Animal models for maturity-onset diabetes of the young generated by disruption of the mouse glucokinase gene. J Biol Chem 37:21464-21467, 1995
-
(1995)
J Biol Chem
, vol.37
, pp. 21464-21467
-
-
Bali, D.1
Svetlanov, A.2
Lee, H.3
Fusco-DeMane, D.4
Leiser, M.5
Li, B.6
Barzilai, N.7
Surana, M.8
Hou, H.9
Fleischer, N.10
Depinho, R.11
Rossetti, L.12
Efrat, S.13
-
37
-
-
0029417331
-
Pancreatic β-cell-specific targeted disruption of glucokinase gene
-
Terauchi Y, Sakura H, Yasuda K, Iwamoto K, Takahashi N, Ito K, Kasai H, Suzuld H, Ueda O, Kamada N, Jishage K, Komeda K, Noda M, Kanazawa Y, Taniguchi S, Miwa I, Akanuma Y, Kodama T, Yazaki Y, Kadowaki T: Pancreatic β-cell-specific targeted disruption of glucokinase gene. J Biol Chem 270:30253-30256, 1995
-
(1995)
J Biol Chem
, vol.270
, pp. 30253-30256
-
-
Terauchi, Y.1
Sakura, H.2
Yasuda, K.3
Iwamoto, K.4
Takahashi, N.5
Ito, K.6
Kasai, H.7
Suzuld, H.8
Ueda, O.9
Kamada, N.10
Jishage, K.11
Komeda, K.12
Noda, M.13
Kanazawa, Y.14
Taniguchi, S.15
Miwa, I.16
Akanuma, Y.17
Kodama, T.18
Yazaki, Y.19
Kadowaki, T.20
more..
-
38
-
-
0032898369
-
Dual roles for glucokinase in glucose homeostasis as determined by liver and pancreatic cell-specific gene knock-outs using Cre recombinase
-
Postic C, Shiota M, Niswender K, Jetto T, Chen Y, Moates J, Shelton K, Lindner J, Cherrington A, Magnuson ML: Dual roles for glucokinase in glucose homeostasis as determined by liver and pancreatic cell-specific gene knock-outs using Cre recombinase J Biol Chem 274:305-315, 1999
-
(1999)
J Biol Chem
, vol.274
, pp. 305-315
-
-
Postic, C.1
Shiota, M.2
Niswender, K.3
Jetto, T.4
Chen, Y.5
Moates, J.6
Shelton, K.7
Lindner, J.8
Cherrington, A.9
Magnuson, M.L.10
-
39
-
-
0035787576
-
Cell-specific roles of glucokinase in glucose homeostasis
-
Postic C, Shiota M, Magnuson MA: Cell-specific roles of glucokinase in glucose homeostasis. Recent Prog Horm Res 56:195-217, 2001
-
(2001)
Recent Prog Horm Res
, vol.56
, pp. 195-217
-
-
Postic, C.1
Shiota, M.2
Magnuson, M.A.3
-
40
-
-
0033199955
-
Cell-biological assessment of human glucokinase mutants causing maturity-onset diabetes of the young type 2 (MODY) or glucokinase-linked hyperisulinaemia (GK-HI)
-
Burke C, Buettger C, Davis E, McClane S, Matschinksy F, Raper S: Cell-biological assessment of human glucokinase mutants causing maturity-onset diabetes of the young type 2 (MODY) or glucokinase-linked hyperisulinaemia (GK-HI). Biochem J 342:345-352, 1999
-
(1999)
Biochem J
, vol.342
, pp. 345-352
-
-
Burke, C.1
Buettger, C.2
Davis, E.3
McClane, S.4
Matschinksy, F.5
Raper, S.6
-
41
-
-
0031259747
-
Variable expression of hepatic glucokinase in mice is due to a regulational locus that cosegregates with the glucokinase gene
-
Moates JM, Postic C, Decaux JF, Girard J, Magnuson MA: Variable expression of hepatic glucokinase in mice is due to a regulational locus that cosegregates with the glucokinase gene. Genomics 45:185-193, 1997
-
(1997)
Genomics
, vol.45
, pp. 185-193
-
-
Moates, J.M.1
Postic, C.2
Decaux, J.F.3
Girard, J.4
Magnuson, M.A.5
|