-
1
-
-
33845881411
-
Mechanisms linking obesity to insulin resistance and type 2 diabetes
-
Kahn SE, Hull RL, Utzschneider KM. Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature 2006;444: 840-846
-
(2006)
Nature
, vol.444
, pp. 840-846
-
-
Kahn, S.E.1
Hull, R.L.2
Utzschneider, K.M.3
-
2
-
-
0028204065
-
Understanding oral glucose tolerance: Comparison of glucose or insulin measurements during the oral glucose tolerance test with specific measurements of insulin resistance and insulin secretion
-
Phillips DI, Clark PM, Hales CN, Osmond C. Understanding oral glucose tolerance: Comparison of glucose or insulin measurements during the oral glucose tolerance test with specific measurements of insulin resistance and insulin secretion. Diabet Med 1994;11: 286-292
-
(1994)
Diabet Med
, vol.11
, pp. 286-292
-
-
Phillips, D.I.1
Clark, P.M.2
Hales, C.N.3
Osmond, C.4
-
3
-
-
84861614905
-
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
-
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium; Multiple Tissue Human Expression Resource (MUTHER) Consortium
-
Manning AK, Hivert MF, Scott RA, et al.; DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium; Multiple Tissue Human Expression Resource (MUTHER) Consortium. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat Genet 2012;44: 659-669
-
(2012)
Nat Genet
, vol.44
, pp. 659-669
-
-
Manning, A.K.1
Hivert, M.F.2
Scott, R.A.3
-
4
-
-
84920882093
-
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population [published correction appears in JAMA 2014;312: 1932]
-
SIGMA Type 2 Diabetes Consortium
-
Estrada K, Aukrust I, Bjørkhaug L, et al.; SIGMA Type 2 Diabetes Consortium. Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population [published correction appears in JAMA 2014;312: 1932]. JAMA 2014;311: 2305-2314
-
(2014)
JAMA
, vol.311
, pp. 2305-2314
-
-
Estrada, K.1
Aukrust, I.2
Bjørkhaug, L.3
-
5
-
-
84893716900
-
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
-
SIGMA Type 2 Diabetes Consortium
-
Williams AL, Jacobs SB, Moreno-Macías H, et al.; SIGMA Type 2 Diabetes Consortium. Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico. Nature 2014;506: 97-101
-
(2014)
Nature
, vol.506
, pp. 97-101
-
-
Williams, A.L.1
Jacobs, S.B.2
Moreno-Macías, H.3
-
6
-
-
84906226932
-
A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes
-
Moltke I, Grarup N, Jørgensen ME, et al. A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes. Nature 2014;512: 190-193
-
(2014)
Nature
, vol.512
, pp. 190-193
-
-
Moltke, I.1
Grarup, N.2
Jørgensen, M.E.3
-
7
-
-
84978128486
-
The genetic architecture of type 2 diabetes
-
Fuchsberger C, Flannick J, Teslovich TM, et al. The genetic architecture of type 2 diabetes. Nature 2016;536: 41-47
-
(2016)
Nature
, vol.536
, pp. 41-47
-
-
Fuchsberger, C.1
Flannick, J.2
Teslovich, T.M.3
-
8
-
-
48349091501
-
Cohort profile: The cardiovascular risk in Young Finns Study
-
Raitakari OT, Juonala M, Rönnemaa T, et al. Cohort profile: The cardiovascular risk in Young Finns Study. Int J Epidemiol 2008;37: 1220-1226
-
(2008)
Int J Epidemiol
, vol.37
, pp. 1220-1226
-
-
Raitakari, O.T.1
Juonala, M.2
Rönnemaa, T.3
-
9
-
-
34247149800
-
Epidemiology, genes and the environment: Lessons learned from the Helsinki Birth Cohort Study
-
Eriksson JG. Epidemiology, genes and the environment: Lessons learned from the Helsinki Birth Cohort Study. J Intern Med 2007;261: 418-425
-
(2007)
J Intern Med
, vol.261
, pp. 418-425
-
-
Eriksson, J.G.1
-
10
-
-
70349263990
-
OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism
-
Perttilä J, Merikanto K, Naukkarinen J, et al. OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism. J Mol Med (Berl) 2009;87: 825-835
-
(2009)
J Mol Med (Berl)
, vol.87
, pp. 825-835
-
-
Perttilä, J.1
Merikanto, K.2
Naukkarinen, J.3
-
11
-
-
77952721703
-
Thirty-five-year trends in cardiovascular risk factors in Finland
-
Vartiainen E, Laatikainen T, Peltonen M, et al. Thirty-five-year trends in cardiovascular risk factors in Finland. Int J Epidemiol 2010;39: 504-518
-
(2010)
Int J Epidemiol
, vol.39
, pp. 504-518
-
-
Vartiainen, E.1
Laatikainen, T.2
Peltonen, M.3
-
12
-
-
84880062762
-
Best practices and joint calling of the HumanExome BeadChip: The CHARGE Consortium
-
Grove ML, Yu B, Cochran BJ, et al. Best practices and joint calling of the HumanExome BeadChip: The CHARGE Consortium. PLoS One 2013;8: E68095
-
(2013)
PLoS One
, vol.8
, pp. e68095
-
-
Grove, M.L.1
Yu, B.2
Cochran, B.J.3
-
13
-
-
0032821965
-
Insulin sensitivity indices obtained from oral glucose tolerance testing: Comparison with the euglycemic insulin clamp
-
Matsuda M, DeFronzo RA. Insulin sensitivity indices obtained from oral glucose tolerance testing: Comparison with the euglycemic insulin clamp. Diabetes Care 1999;22: 1462-1470
-
(1999)
Diabetes Care
, vol.22
, pp. 1462-1470
-
-
Matsuda, M.1
DeFronzo, R.A.2
-
14
-
-
84893756641
-
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56000 whites and blacks
-
NHLBI GO Exome Sequencing Project
-
Peloso GM, Auer PL, Bis JC, et al.; NHLBI GO Exome Sequencing Project. Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. Am J Hum Genet 2014;94: 223-232
-
(2014)
Am J Hum Genet
, vol.94
, pp. 223-232
-
-
Peloso, G.M.1
Auer, P.L.2
Bis, J.C.3
-
15
-
-
26444496137
-
Adjusting for treatment effects in studies of quantitative traits: Antihypertensive therapy and systolic blood pressure
-
Tobin MD, Sheehan NA, Scurrah KJ, Burton PR. Adjusting for treatment effects in studies of quantitative traits: Antihypertensive therapy and systolic blood pressure. Stat Med 2005;24: 2911-2935
-
(2005)
Stat Med
, vol.24
, pp. 2911-2935
-
-
Tobin, M.D.1
Sheehan, N.A.2
Scurrah, K.J.3
Burton, P.R.4
-
16
-
-
77950301214
-
Variance component model to account for sample structure in genome-wide association studies
-
Kang HM, Sul JH, Service SK, et al. Variance component model to account for sample structure in genome-wide association studies. Nat Genet 2010;42: 348-354
-
(2010)
Nat Genet
, vol.42
, pp. 348-354
-
-
Kang, H.M.1
Sul, J.H.2
Service, S.K.3
-
17
-
-
77955894071
-
METAL: Fast and efficient meta-analysis of genomewide association scans
-
Willer CJ, Li Y, Abecasis GR. METAL: Fast and efficient meta-analysis of genomewide association scans. Bioinformatics 2010;26: 2190-2191
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
18
-
-
84929200986
-
Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus
-
T2D-GENES Consortium GoT2D Consortium
-
Mahajan A, Sim X, Ng HJ, et al.; T2D-GENES Consortium, GoT2D Consortium. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. PLoS Genet 2015;11: E1004876
-
(2015)
PLoS Genet
, vol.11
, pp. e1004876
-
-
Mahajan, A.1
Sim, X.2
Ng, H.J.3
-
19
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu MC, Lee S, Cai T, Li Y, Boehnke M, Lin X. Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet 2011;89: 82-93
-
(2011)
Am J Hum Genet
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.3
Li, Y.4
Boehnke, M.5
Lin, X.6
-
20
-
-
84895808047
-
Meta-analysis of gene-level tests for rare variant association
-
Liu DJ, Peloso GM, Zhan X, et al. Meta-analysis of gene-level tests for rare variant association. Nat Genet 2014;46: 200-204
-
(2014)
Nat Genet
, vol.46
, pp. 200-204
-
-
Liu, D.J.1
Peloso, G.M.2
Zhan, X.3
-
21
-
-
84880294630
-
General framework for metaanalysis of rare variants in sequencing association studies
-
Lee S, Teslovich TM, Boehnke M, Lin X. General framework for metaanalysis of rare variants in sequencing association studies. Am J Hum Genet 2013; 93: 42-53
-
(2013)
Am J Hum Genet
, vol.93
, pp. 42-53
-
-
Lee, S.1
Teslovich, T.M.2
Boehnke, M.3
Lin, X.4
-
22
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J, Howie B, Myers S, McVean G, Donnelly P. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 2007; 39: 906-913
-
(2007)
Nat Genet
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
23
-
-
84942755762
-
-
Exome Aggregation Consortium Available from Accessed 29 January
-
Exome Aggregation Consortium. ExAC Browser. Available from http://exac .broadinstitute.org/. Accessed 29 January 2016
-
(2016)
ExAC Browser
-
-
-
25
-
-
0036681416
-
Scoring residue conservation
-
Valdar WS. Scoring residue conservation. Proteins 2002;48: 227-241
-
(2002)
Proteins
, vol.48
, pp. 227-241
-
-
Valdar, W.S.1
-
27
-
-
79959564695
-
The IntFOLD server: An integrated web resource for protein fold recognition, 3D model quality assessment, intrinsic disorder prediction, domain prediction and ligand binding site prediction
-
Roche DB, Buenavista MT, Tetchner SJ, McGuffin LJ. The IntFOLD server: An integrated web resource for protein fold recognition, 3D model quality assessment, intrinsic disorder prediction, domain prediction and ligand binding site prediction. Nucleic Acids Res 2011;39: W171-6
-
(2011)
Nucleic Acids Res
, vol.39
, pp. W171-176
-
-
Roche, D.B.1
Buenavista, M.T.2
Tetchner, S.J.3
McGuffin, L.J.4
-
29
-
-
84929001104
-
Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
-
GTEx Consortium
-
GTEx Consortium. Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans. Science 2015;348: 648-660
-
(2015)
Science
, vol.348
, pp. 648-660
-
-
-
30
-
-
85028171423
-
Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins
-
Buil A, Brown AA, Lappalainen T, et al. Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins. Nat Genet 2015; 47: 88-91
-
(2015)
Nat Genet
, vol.47
, pp. 88-91
-
-
Buil, A.1
Brown, A.A.2
Lappalainen, T.3
-
31
-
-
84899627083
-
Genetic interactions affecting human gene expression identified by variance association mapping
-
Brown AA, Buil A, Viñuela A, et al. Genetic interactions affecting human gene expression identified by variance association mapping. eLife 2014;3: E01381
-
(2014)
ELife
, vol.3
, pp. e01381
-
-
Brown, A.A.1
Buil, A.2
Viñuela, A.3
-
32
-
-
85014326417
-
Genetic regulation of adipose gene expression and cardio-metabolic traits
-
Civelek M, Wu Y, Pan C, et al. Genetic regulation of adipose gene expression and cardio-metabolic traits. Am J Hum Genet 2017;100: 428-443
-
(2017)
Am J Hum Genet
, vol.100
, pp. 428-443
-
-
Civelek, M.1
Wu, Y.2
Pan, C.3
-
33
-
-
42449084951
-
Quantitative linkage analysis for pancreatic B-cell function and insulin resistance in a large twin cohort
-
Falchi M, Wilson SG, Paximadas D, Swaminathan R, Spector TD. Quantitative linkage analysis for pancreatic B-cell function and insulin resistance in a large twin cohort. Diabetes 2008;57: 1120-1124
-
(2008)
Diabetes
, vol.57
, pp. 1120-1124
-
-
Falchi, M.1
Wilson, S.G.2
Paximadas, D.3
Swaminathan, R.4
Spector, T.D.5
-
34
-
-
65549163338
-
Changes in insulin sensitivity and insulin release in relation to glycemia and glucose tolerance in 6,414 Finnish men
-
Stancáková A, Javorský M, Kuulasmaa T, Haffner SM, Kuusisto J, Laakso M. Changes in insulin sensitivity and insulin release in relation to glycemia and glucose tolerance in 6,414 Finnish men. Diabetes 2009;58: 1212-1221
-
(2009)
Diabetes
, vol.58
, pp. 1212-1221
-
-
Stancáková, A.1
Javorský, M.2
Kuulasmaa, T.3
Haffner, S.M.4
Kuusisto, J.5
Laakso, M.6
-
35
-
-
0035368548
-
Insulin resistance and a diabetes mellitus-like syndrome in mice lacking the protein kinase Akt2 (PKB beta)
-
Cho H, Mu J, Kim JK, et al. Insulin resistance and a diabetes mellitus-like syndrome in mice lacking the protein kinase Akt2 (PKB beta). Science 2001;292: 1728-1731
-
(2001)
Science
, vol.292
, pp. 1728-1731
-
-
Cho, H.1
Mu, J.2
Kim, J.K.3
-
36
-
-
85047693348
-
Severe diabetes, age-dependent loss of adipose tissue, and mild growth deficiency in mice lacking Akt2/PKB beta
-
Garofalo RS, Orena SJ, Rafidi K, et al. Severe diabetes, age-dependent loss of adipose tissue, and mild growth deficiency in mice lacking Akt2/PKB beta. J Clin Invest 2003;112: 197-208
-
(2003)
J Clin Invest
, vol.112
, pp. 197-208
-
-
Garofalo, R.S.1
Orena, S.J.2
Rafidi, K.3
-
37
-
-
80055087787
-
An activating mutation of AKT2 and human hypoglycemia
-
Hussain K, Challis B, Rocha N, et al. An activating mutation of AKT2 and human hypoglycemia. Science 2011;334: 474
-
(2011)
Science
, vol.334
, pp. 474
-
-
Hussain, K.1
Challis, B.2
Rocha, N.3
-
38
-
-
84893815531
-
Activating AKT2 mutation: Hypoinsulinemic hypoketotic hypoglycemia
-
Arya VB, Flanagan SE, Schober E, Rami-Merhar B, Ellard S, Hussain K. Activating AKT2 mutation: Hypoinsulinemic hypoketotic hypoglycemia. J Clin Endocrinol Metab 2014;99: 391-394
-
(2014)
J Clin Endocrinol Metab
, vol.99
, pp. 391-394
-
-
Arya, V.B.1
Flanagan, S.E.2
Schober, E.3
Rami-Merhar, B.4
Ellard, S.5
Hussain, K.6
-
39
-
-
2542528670
-
A family with severe insulin resistance and diabetes due to a mutation in AKT2
-
George S, Rochford JJ, Wolfrum C, et al. A family with severe insulin resistance and diabetes due to a mutation in AKT2. Science 2004;304: 1325-1328
-
(2004)
Science
, vol.304
, pp. 1325-1328
-
-
George, S.1
Rochford, J.J.2
Wolfrum, C.3
-
40
-
-
33847410199
-
Analysis of genetic variation in Akt2/PKB-beta in severe insulin resistance, lipodystrophy, type 2 diabetes, and related metabolic phenotypes
-
Tan K, Kimber WA, Luan J, et al. Analysis of genetic variation in Akt2/PKB-beta in severe insulin resistance, lipodystrophy, type 2 diabetes, and related metabolic phenotypes. Diabetes 2007;56: 714-719
-
(2007)
Diabetes
, vol.56
, pp. 714-719
-
-
Tan, K.1
Kimber, W.A.2
Luan, J.3
-
41
-
-
84869774399
-
Disruption of PH-kinase domain interactions leads to oncogenic activation of AKT in human cancers
-
Parikh C, Janakiraman V, Wu WI, et al. Disruption of PH-kinase domain interactions leads to oncogenic activation of AKT in human cancers. Proc Natl Acad Sci U S A 2012;109: 19368-19373
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 19368-19373
-
-
Parikh, C.1
Janakiraman, V.2
Wu, W.I.3
-
42
-
-
0034845958
-
PKB/Akt: A key mediator of cell proliferation, survival and insulin responses?
-
Lawlor MA, Alessi DR. PKB/Akt: A key mediator of cell proliferation, survival and insulin responses? J Cell Sci 2001;114: 2903-2910
-
(2001)
J Cell Sci
, vol.114
, pp. 2903-2910
-
-
Lawlor, M.A.1
Alessi, D.R.2
-
43
-
-
0034881622
-
AKT-1, -2, and -3 are expressed in both normal and tumor tissues of the lung, breast, prostate, and colon
-
Zinda MJ, Johnson MA, Paul JD, et al. AKT-1, -2, and -3 are expressed in both normal and tumor tissues of the lung, breast, prostate, and colon. Clin Cancer Res 2001;7: 2475-2479
-
(2001)
Clin Cancer Res
, vol.7
, pp. 2475-2479
-
-
Zinda, M.J.1
Johnson, M.A.2
Paul, J.D.3
-
44
-
-
0038624395
-
Dwarfism, impaired skin development, skeletal muscle atrophy, delayed bone development, and impeded adipogenesis in mice lacking Akt1 and Akt2
-
Peng XD, Xu PZ, Chen ML, et al. Dwarfism, impaired skin development, skeletal muscle atrophy, delayed bone development, and impeded adipogenesis in mice lacking Akt1 and Akt2. Genes Dev 2003;17: 1352-1365
-
(2003)
Genes Dev
, vol.17
, pp. 1352-1365
-
-
Peng, X.D.1
Xu, P.Z.2
Chen, M.L.3
-
45
-
-
70450193472
-
Human genetics illuminates the paths to metabolic disease
-
O'Rahilly S. Human genetics illuminates the paths to metabolic disease. Nature 2009;462: 307-314
-
(2009)
Nature
, vol.462
, pp. 307-314
-
-
O'Rahilly, S.1
-
46
-
-
84905460411
-
Distribution and medical impact of loss-of-function variants in the Finnish founder population
-
Sequencing Initiative Suomi (SISu) Project
-
Lim ET, Würtz P, Havulinna AS, et al.; Sequencing Initiative Suomi (SISu) Project. Distribution and medical impact of loss-of-function variants in the Finnish founder population. PLoS Genet 2014;10: E1004494
-
(2014)
PLoS Genet
, vol.10
, pp. e1004494
-
-
Lim, E.T.1
Würtz, P.2
Havulinna, A.S.3
-
47
-
-
67249108808
-
A truncation mutation in TBC1D4 in a family with acanthosis nigricans and postprandial hyperinsulinemia
-
Dash S, Sano H, Rochford JJ, et al. A truncation mutation in TBC1D4 in a family with acanthosis nigricans and postprandial hyperinsulinemia. Proc Natl Acad Sci U S A 2009;106: 9350-9355
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 9350-9355
-
-
Dash, S.1
Sano, H.2
Rochford, J.J.3
-
48
-
-
33745668478
-
SiRNA-based gene silencing reveals specialized roles of IRS-1/Akt2 and IRS-2/Akt1 in glucose and lipid metabolism in human skeletal muscle
-
Bouzakri K, Zachrisson A, Al-Khalili L, et al. siRNA-based gene silencing reveals specialized roles of IRS-1/Akt2 and IRS-2/Akt1 in glucose and lipid metabolism in human skeletal muscle. Cell Metab 2006;4: 89-96
-
(2006)
Cell Metab
, vol.4
, pp. 89-96
-
-
Bouzakri, K.1
Zachrisson, A.2
Al-Khalili, L.3
-
49
-
-
55049094499
-
Identification of a novel AS160 splice variant that regulates GLUT4 translocation and glucose-uptake in rat muscle cells
-
Baus D, Heermeier K, De Hoop M, et al. Identification of a novel AS160 splice variant that regulates GLUT4 translocation and glucose-uptake in rat muscle cells. Cell Signal 2008;20: 2237-2246
-
(2008)
Cell Signal
, vol.20
, pp. 2237-2246
-
-
Baus, D.1
Heermeier, K.2
De Hoop, M.3
-
50
-
-
0035914388
-
Akt1/PKBalpha is required for normal growth but dispensable for maintenance of glucose homeostasis in mice
-
Cho H, Thorvaldsen JL, Chu Q, Feng F, Birnbaum MJ. Akt1/PKBalpha is required for normal growth but dispensable for maintenance of glucose homeostasis in mice. J Biol Chem 2001;276: 38349-38352
-
(2001)
J Biol Chem
, vol.276
, pp. 38349-38352
-
-
Cho, H.1
Thorvaldsen, J.L.2
Chu, Q.3
Feng, F.4
Birnbaum, M.J.5
-
51
-
-
84901437003
-
Signaling specificity in the Akt pathway in biology and disease
-
Toker A, Marmiroli S. Signaling specificity in the Akt pathway in biology and disease. Adv Biol Regul 2014;55: 28-38
-
(2014)
Adv Biol Regul
, vol.55
, pp. 28-38
-
-
Toker, A.1
Marmiroli, S.2
-
52
-
-
23144449547
-
Essential role of protein kinase B gamma (PKB gamma/Akt3) in postnatal brain development but not in glucose homeostasis
-
Tschopp O, Yang ZZ, Brodbeck D, et al. Essential role of protein kinase B gamma (PKB gamma/Akt3) in postnatal brain development but not in glucose homeostasis. Development 2005;132: 2943-2954
-
(2005)
Development
, vol.132
, pp. 2943-2954
-
-
Tschopp, O.1
Yang, Z.Z.2
Brodbeck, D.3
-
53
-
-
0344375097
-
Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferatoractivated receptor-gamma
-
Savage DB, Tan GD, Acerini CL, et al. Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferatoractivated receptor-gamma. Diabetes 2003;52: 910-917
-
(2003)
Diabetes
, vol.52
, pp. 910-917
-
-
Savage, D.B.1
Tan, G.D.2
Acerini, C.L.3
-
54
-
-
61749100743
-
Postreceptor insulin resistance contributes to human dyslipidemia and hepatic steatosis
-
Semple RK, Sleigh A, Murgatroyd PR, et al. Postreceptor insulin resistance contributes to human dyslipidemia and hepatic steatosis. J Clin Invest 2009;119: 315-322
-
(2009)
J Clin Invest
, vol.119
, pp. 315-322
-
-
Semple, R.K.1
Sleigh, A.2
Murgatroyd, P.R.3
|