-
1
-
-
0033280322
-
Functional analyses of natural variation in Sp1 binding sites of a TATA-less promoter
-
Segal JA, Barnett JL, Crawford DL. Functional analyses of natural variation in Sp1 binding sites of a TATA-less promoter. J Mol Evol 1999;49:736-749.
-
(1999)
J Mol Evol
, vol.49
, pp. 736-749
-
-
Segal, J.A.1
Barnett, J.L.2
Crawford, D.L.3
-
2
-
-
0033034855
-
Evolutionary analysis of TATA-less proximal promoter function
-
Crawford DL, Segal JA, Barnett JL. Evolutionary analysis of TATA-less proximal promoter function. Mol Biol Evol 1999;16:194-207.
-
(1999)
Mol Biol Evol
, vol.16
, pp. 194-207
-
-
Crawford, D.L.1
Segal, J.A.2
Barnett, J.L.3
-
3
-
-
0037422575
-
Evidence for the widespread coupling of alternative splicing and nonsense-mediated mRNA decay in humans
-
Lewis BP, Green RE, Brenner SE. Evidence for the widespread coupling of alternative splicing and nonsense-mediated mRNA decay in humans. Proc Natl Acad Sci USA 2003;100:189-192.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 189-192
-
-
Lewis, B.P.1
Green, R.E.2
Brenner, S.E.3
-
4
-
-
0035919656
-
Haplotype variation and linkage disequilibrium in 313 human genes
-
Stephens JC, Schneider JA, Tanguay DA et al. Haplotype variation and linkage disequilibrium in 313 human genes. Science 2001;293:489-493.
-
(2001)
Science
, vol.293
, pp. 489-493
-
-
Stephens, J.C.1
Schneider, J.A.2
Tanguay, D.A.3
-
5
-
-
0037456823
-
Genetics of gene expression surveyed in maize, mouse and man
-
Schadt EE, Monks SA, Drake TA et al. Genetics of gene expression surveyed in maize, mouse and man. Nature 2003;422:297-302.
-
(2003)
Nature
, vol.422
, pp. 297-302
-
-
Schadt, E.E.1
Monks, S.A.2
Drake, T.A.3
-
6
-
-
0036648981
-
From QTL to gene: The harvest begins
-
Korstanje R, Paigen B. From QTL to gene: The harvest begins. Nat Genet 2002;31:235-236.
-
(2002)
Nat Genet
, vol.31
, pp. 235-236
-
-
Korstanje, R.1
Paigen, B.2
-
7
-
-
5944254200
-
Identification of complement factor 5 as a susceptibility locus for experimental allergic asthma
-
Karp CL, Grupe A, Schadt E et al. Identification of complement factor 5 as a susceptibility locus for experimental allergic asthma. Nat Immunol 2000;1:221-226.
-
(2000)
Nat Immunol
, vol.1
, pp. 221-226
-
-
Karp, C.L.1
Grupe, A.2
Schadt, E.3
-
9
-
-
0037312921
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
-
Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet 2003;33:177-182.
-
(2003)
Nat Genet
, vol.33
, pp. 177-182
-
-
Lohmueller, K.E.1
Pearce, C.L.2
Pike, M.3
Lander, E.S.4
Hirschhorn, J.N.5
-
10
-
-
17344362232
-
Alpha-2 macroglobulin is genetically associated with Alzheimer disease
-
Blacker D, Wilcox MA, Laird NM et al. Alpha-2 macroglobulin is genetically associated with Alzheimer disease. Nat Genet 1998;19:357-360.
-
(1998)
Nat Genet
, vol.19
, pp. 357-360
-
-
Blacker, D.1
Wilcox, M.A.2
Laird, N.M.3
-
11
-
-
15844366738
-
Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians
-
Inoue H, Ferrer J, Welling CM et al. Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians. Diabetes 1996;45:825-831.
-
(1996)
Diabetes
, vol.45
, pp. 825-831
-
-
Inoue, H.1
Ferrer, J.2
Welling, C.M.3
-
12
-
-
0026675062
-
Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction
-
Cambien F, Poirier O, Lecerf L et al. Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction. Nature 1992;359:641-644.
-
(1992)
Nature
, vol.359
, pp. 641-644
-
-
Cambien, F.1
Poirier, O.2
Lecerf, L.3
-
13
-
-
0026689561
-
Association of a polymorphism of the angiotensin I-converting enzyme gene with essential hypertension
-
Zee RY, Lou YK, Griffiths LR, Morris BJ. Association of a polymorphism of the angiotensin I-converting enzyme gene with essential hypertension. Biochem Biophys Res Commun 1992;184:9-15.
-
(1992)
Biochem Biophys Res Commun
, vol.184
, pp. 9-15
-
-
Zee, R.Y.1
Lou, Y.K.2
Griffiths, L.R.3
Morris, B.J.4
-
14
-
-
0028197681
-
Plasma angiotensin-converting enzyme activity and carotid wall thickening
-
Bonithon-Kopp C, Ducimetiere P, Touboul PJ et al. Plasma angiotensin-converting enzyme activity and carotid wall thickening. Circulation 1994;89:952-954.
-
(1994)
Circulation
, vol.89
, pp. 952-954
-
-
Bonithon-Kopp, C.1
Ducimetiere, P.2
Touboul, P.J.3
-
15
-
-
0028966390
-
Association of the alpha-adducin locus with essential hypertension
-
Casari G, Barlassina C, Cusi D et al. Association of the alpha-adducin locus with essential hypertension. Hypertension 1995;25:320-326.
-
(1995)
Hypertension
, vol.25
, pp. 320-326
-
-
Casari, G.1
Barlassina, C.2
Cusi, D.3
-
16
-
-
0031436966
-
Human beta-2 adrenoceptor gene polymorphisms are highly frequent in obesity and associate with altered adipocyte beta-2 adrenoceptor function
-
Large V, Hellstrom L, Revnisdottir S et al. Human beta-2 adrenoceptor gene polymorphisms are highly frequent in obesity and associate with altered adipocyte beta-2 adrenoceptor function. J Clin Invest 1997;100:3005-3013.
-
(1997)
J Clin Invest
, vol.100
, pp. 3005-3013
-
-
Large, V.1
Hellstrom, L.2
Revnisdottir, S.3
-
17
-
-
0029084088
-
Time of onset of non-insulin-dependent diabetes mellitus and genetic variation in the beta 3-adrenergic-receptor gene
-
Walston J, Silver K, Bogardus C et al. Time of onset of non-insulin-dependent diabetes mellitus and genetic variation in the beta 3-adrenergic-receptor gene. N Engl J Med 1995;333:343-347.
-
(1995)
N Engl J Med
, vol.333
, pp. 343-347
-
-
Walston, J.1
Silver, K.2
Bogardus, C.3
-
18
-
-
0028290165
-
Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension
-
Bonnardeaux A, Davies E, Jeunemaitre X et al. Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension. Hypertension 1994;24:63-69.
-
(1994)
Hypertension
, vol.24
, pp. 63-69
-
-
Bonnardeaux, A.1
Davies, E.2
Jeunemaitre, X.3
-
19
-
-
0022899587
-
Apolipoprotein B-gene DNA polymorphisms associated with myocardial infarction
-
Hegele RA, Huang LS, Herbert PN, et al. Apolipoprotein B-gene DNA polymorphisms associated with myocardial infarction. N Engl J Med 1986;315:1509-1515.
-
(1986)
N Engl J Med
, vol.315
, pp. 1509-1515
-
-
Hegele, R.A.1
Huang, L.S.2
Herbert, P.N.3
-
20
-
-
0031887316
-
The apolipoprotein CI A allele as a risk factor for Alzheimer's disease
-
Poduslo SE, Neal M, Herring K, Shelly J. The apolipoprotein CI A allele as a risk factor for Alzheimer's disease. Neurochem Res 1998;23:361-367.
-
(1998)
Neurochem Res
, vol.23
, pp. 361-367
-
-
Poduslo, S.E.1
Neal, M.2
Herring, K.3
Shelly, J.4
-
21
-
-
0027194791
-
Gene dose of apolipoprotein e type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder EH, Saunders AM, Strittmatter WJ et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science 1993;261:921-923.
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
-
22
-
-
0021354819
-
Polymorphism at the apoprotein-E locus in relation to risk of coronary disease
-
Cumming AM, Robertson FW. Polymorphism at the apoprotein-E locus in relation to risk of coronary disease. Clin Genet 1984;25:310-313.
-
(1984)
Clin Genet
, vol.25
, pp. 310-313
-
-
Cumming, A.M.1
Robertson, F.W.2
-
23
-
-
0027315427
-
Prevalence of apolipoprotein e phenotypes in ischemic cerebrovascular disease: A case-control study
-
Couderc R, Mahieux F, Bailleul S, Fenelon G, Mary R, Fermanian J. Prevalence of apolipoprotein E phenotypes in ischemic cerebrovascular disease: A case-control study. Stroke 1993;24:661-664.
-
(1993)
Stroke
, vol.24
, pp. 661-664
-
-
Couderc, R.1
Mahieux, F.2
Bailleul, S.3
Fenelon, G.4
Mary, R.5
Fermanian, J.6
-
24
-
-
0007691164
-
Apolipoprotein E4 allele as a predictor of cholinergic deficits and treatment outcome in Alzheimer disease
-
Poirier J, Delisle MC, Quirion R et al. Apolipoprotein E4 allele as a predictor of cholinergic deficits and treatment outcome in Alzheimer disease. Proc Natl Acad Sci USA 1995;92:12260-12264.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 12260-12264
-
-
Poirier, J.1
Delisle, M.C.2
Quirion, R.3
-
25
-
-
0028359655
-
Genetic associations with human longevity at the APOE and ACE loci
-
Schachter F, Faure-Delanef L, Guenot F et al. Genetic associations with human longevity at the APOE and ACE loci. Nat Genet 1994;6:29-32.
-
(1994)
Nat Genet
, vol.6
, pp. 29-32
-
-
Schachter, F.1
Faure-Delanef, L.2
Guenot, F.3
-
26
-
-
0030694396
-
Long polyglutamine tracts in the androgen receptor are associated with reduced trans-activation, impaired sperm production, and male infertility
-
Tut TG, Ghadessy FJ, Trifiro MA, Pinsky L, Yong EL. Long polyglutamine tracts in the androgen receptor are associated with reduced trans-activation, impaired sperm production, and male infertility. J Clin Endocrinol Metab 1997;82:3777-3782.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3777-3782
-
-
Tut, T.G.1
Ghadessy, F.J.2
Trifiro, M.A.3
Pinsky, L.4
Yong, E.L.5
-
27
-
-
0030890995
-
Polymorphic repeats in the androgen receptor gene: Molecular markers of prostate cancer risk
-
Stanford JL, Just JJ, Gibbs M et al. Polymorphic repeats in the androgen receptor gene: molecular markers of prostate cancer risk. Cancer Res 1997;57:1194-1198.
-
(1997)
Cancer Res
, vol.57
, pp. 1194-1198
-
-
Stanford, J.L.1
Just, J.J.2
Gibbs, M.3
-
28
-
-
0030731562
-
Synergy between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset confirmed Alzheimer's disease
-
Lehmann DJ, Johnston C, Smith AD. Synergy between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset confirmed Alzheimer's disease. Hum Mol Genet 1997;6:1933-1936.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1933-1936
-
-
Lehmann, D.J.1
Johnston, C.2
Smith, A.D.3
-
29
-
-
0030861904
-
Contrasting genetic influence of CCR2 and CCR5 variants on HIV-1 infection and disease progression. Hemophilia Growth and Development Study (HGDS), Multicenter AIDS Cohort Study (MACS), Multicenter Hemophilia Cohort Study (MHCS), San Francisco City Cohort (SFCC), ALIVE Study
-
Smith MW, Dean M, Carrington M et al. Contrasting genetic influence of CCR2 and CCR5 variants on HIV-1 infection and disease progression. Hemophilia Growth and Development Study (HGDS), Multicenter AIDS Cohort Study (MACS), Multicenter Hemophilia Cohort Study (MHCS), San Francisco City Cohort (SFCC), ALIVE Study. Science 1997;277:959-965.
-
(1997)
Science
, vol.277
, pp. 959-965
-
-
Smith, M.W.1
Dean, M.2
Carrington, M.3
-
30
-
-
0029836744
-
Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene
-
Grant SF, Reid DM, Blake G, Herd R, Fogelman I, Ralston SH. Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene. Nat Genet 1996;14:203-205.
-
(1996)
Nat Genet
, vol.14
, pp. 203-205
-
-
Grant, S.F.1
Reid, D.M.2
Blake, G.3
Herd, R.4
Fogelman, I.5
Ralston, S.H.6
-
31
-
-
1842297034
-
Association analysis of the catechol O-methyltransferase gene and bipolar affective disorder
-
Gutierrez B, Bertranpetit J, Guillamat R et al. Association analysis of the catechol O-methyltransferase gene and bipolar affective disorder. Am J Psychiatry 1997;154:113-115.
-
(1997)
Am J Psychiatry
, vol.154
, pp. 113-115
-
-
Gutierrez, B.1
Bertranpetit, J.2
Guillamat, R.3
-
32
-
-
0029851636
-
Preferential transmission of the high activity allele of COMT in schizophrenia
-
Li T, Sham PC, Vallada H et al. Preferential transmission of the high activity allele of COMT in schizophrenia. Psychiatr Genet 1996;6:131-133.
-
(1996)
Psychiatr Genet
, vol.6
, pp. 131-133
-
-
Li, T.1
Sham, P.C.2
Vallada, H.3
-
33
-
-
0031014716
-
CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus
-
Donner H, Rau H, Walfish PG et al. CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus. J Clin Endocrinol Metab 1997;82:143-146.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 143-146
-
-
Donner, H.1
Rau, H.2
Walfish, P.G.3
-
34
-
-
0344718497
-
Cytotoxic T lymphocyte antigen 4 (CTLA-4) dimorphism in patients with systemic lupus erythematosus
-
Pullmann R, Jr., Lukac J, Skerenova M et al. Cytotoxic T lymphocyte antigen 4 (CTLA-4) dimorphism in patients with systemic lupus erythematosus. Clin Exp Rheumatol 1999;17:725-729.
-
(1999)
Clin Exp Rheumatol
, vol.17
, pp. 725-729
-
-
Pullmann Jr., R.1
Lukac, J.2
Skerenova, M.3
-
35
-
-
0031940241
-
Polymorphism of the NADH/NADPH oxidase p22 phox gene in patients with coronary artery disease
-
Inoue N, Kawashima S, Kanazawa K, Yamada S, Akita H, Yokoyama M. Polymorphism of the NADH/NADPH oxidase p22 phox gene in patients with coronary artery disease. Circulation 1998;97:135-137.
-
(1998)
Circulation
, vol.97
, pp. 135-137
-
-
Inoue, N.1
Kawashima, S.2
Kanazawa, K.3
Yamada, S.4
Akita, H.5
Yokoyama, M.6
-
36
-
-
0032928892
-
Genetic polymorphism of CYP11B2 gene and hypertension in Japanese
-
Tamaki S, Iwai N, Tsujita Y, Kinoshita M. Genetic polymorphism of CYP11B2 gene and hypertension in Japanese. Hypertension 1999;33:266-270.
-
(1999)
Hypertension
, vol.33
, pp. 266-270
-
-
Tamaki, S.1
Iwai, N.2
Tsujita, Y.3
Kinoshita, M.4
-
37
-
-
0029156032
-
Cytochrome P4501A1 and glutathione S-transferase (M1) genetic polymorphisms and postmenopausal breast cancer risk
-
Ambrosone CB, Freudenheim JL, Graham S et al. Cytochrome P4501A1 and glutathione S-transferase (M1) genetic polymorphisms and postmenopausal breast cancer risk. Cancer Res 1995;55:3483-34835.
-
(1995)
Cancer Res
, vol.55
, pp. 3483-34835
-
-
Ambrosone, C.B.1
Freudenheim, J.L.2
Graham, S.3
-
38
-
-
0026589459
-
Mutant debrisoquine hydroxylation genes in Parkinson's disease
-
Armstrong M, Daly AK, Cholerton S, Bateman DN, Idle JR. Mutant debrisoquine hydroxylation genes in Parkinson's disease. Lancet 1992;339:1017-1018.
-
(1992)
Lancet
, vol.339
, pp. 1017-1018
-
-
Armstrong, M.1
Daly, A.K.2
Cholerton, S.3
Bateman, D.N.4
Idle, J.R.5
-
39
-
-
0026069613
-
Association between restriction fragment length polymorphism of the human cytochrome P450IIE1 gene and susceptibility to lung cancer
-
Uematsu F, Kikuchi H, Motomiya M et al. Association between restriction fragment length polymorphism of the human cytochrome P450IIE1 gene and susceptibility to lung cancer. Jpn J Cancer Res 1991;82:254-256.
-
(1991)
Jpn J Cancer Res
, vol.82
, pp. 254-256
-
-
Uematsu, F.1
Kikuchi, H.2
Motomiya, M.3
-
40
-
-
0030933979
-
A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia
-
Arinami T, Gao M, Hamaguchi H, Toru M. A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia. Hum Mol Genet 1997;6:577-582.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 577-582
-
-
Arinami, T.1
Gao, M.2
Hamaguchi, H.3
Toru, M.4
-
41
-
-
0031594223
-
The dopamine D3 receptor (DRD3) Ser9Gly polymorphism and schizophrenia: A haplotype relative risk study and association with clozapine response
-
Malhotra AK, Goldman D, Buchanan RW et al. The dopamine D3 receptor (DRD3) Ser9Gly polymorphism and schizophrenia: a haplotype relative risk study and association with clozapine response. Mol Psychiatry 1998;3:72-75.
-
(1998)
Mol Psychiatry
, vol.3
, pp. 72-75
-
-
Malhotra, A.K.1
Goldman, D.2
Buchanan, R.W.3
-
42
-
-
0029563224
-
Association study of dopamine D3 receptor gene and schizophrenia
-
Kennedy JL, Billett EA, Macciardi FM et al. Association study of dopamine D3 receptor gene and schizophrenia. Am J Med Genet 1995;60:558-562.
-
(1995)
Am J Med Genet
, vol.60
, pp. 558-562
-
-
Kennedy, J.L.1
Billett, E.A.2
Macciardi, F.M.3
-
43
-
-
0030133840
-
Dopamine D4 receptor gene polymorphism is associated with attention deficit hyperactivity disorder
-
LaHoste GJ, Swanson JM, Wigal SB et al. Dopamine D4 receptor gene polymorphism is associated with attention deficit hyperactivity disorder. Mol Psychiatry 1996;1:121-124.
-
(1996)
Mol Psychiatry
, vol.1
, pp. 121-124
-
-
Lahoste, G.J.1
Swanson, J.M.2
Wigal, S.B.3
-
44
-
-
0033032302
-
Association of vitamin D and estrogen receptor gene polymorphism with the effect of hormone replacement therapy on bone mineral density in Japanese women
-
Kurabayashi T, Tomita M, Matsushita H et al. Association of vitamin D and estrogen receptor gene polymorphism with the effect of hormone replacement therapy on bone mineral density in Japanese women. Am J Obstet Gynecol 1999;180:1115-1120.
-
(1999)
Am J Obstet Gynecol
, vol.180
, pp. 1115-1120
-
-
Kurabayashi, T.1
Tomita, M.2
Matsushita, H.3
-
45
-
-
0029850530
-
A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996;88:3698-3703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
46
-
-
0032525101
-
Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients
-
De Stefano V, Chiusolo P, Paciaroni K et al. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood 1998;91:3562-3565.
-
(1998)
Blood
, vol.91
, pp. 3562-3565
-
-
De Stefano, V.1
Chiusolo, P.2
Paciaroni, K.3
-
47
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BP, Koster T et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994;369:64-67.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.2
Koster, T.3
-
49
-
-
0029043899
-
Coagulation factor VII mass and activity in young men with myocardial infarction at a young age: Role of plasma lipoproteins and factor VII genotype
-
Moor E, Silveira A, van't Hooft F et al. Coagulation factor VII mass and activity in young men with myocardial infarction at a young age: Role of plasma lipoproteins and factor VII genotype. Arterioscler Thromb Vasc Biol 1995;15:655-664.
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 655-664
-
-
Moor, E.1
Silveira, A.2
Van't Hooft, F.3
-
50
-
-
0029866721
-
Fc gamma RIIA alleles are heritable risk factors for lupus nephritis in African Americans
-
Salmon JE, Millard S, Schachter LA et al. Fc gamma RIIA alleles are heritable risk factors for lupus nephritis in African Americans. J Clin Invest 1996;97:1348-1354.
-
(1996)
J Clin Invest
, vol.97
, pp. 1348-1354
-
-
Salmon, J.E.1
Millard, S.2
Schachter, L.A.3
-
51
-
-
0028848010
-
A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus
-
Hager J, Hansen L, Vaisse C et al. A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus. Nat Genet 1995;9:299-304.
-
(1995)
Nat Genet
, vol.9
, pp. 299-304
-
-
Hager, J.1
Hansen, L.2
Vaisse, C.3
-
52
-
-
0026583193
-
Linkage of type 2 diabetes to the glucokinase gene
-
Hattersley AT, Turner RC, Permutt MA et al. Linkage of type 2 diabetes to the glucokinase gene. Lancet 1992;339:1307-1310.
-
(1992)
Lancet
, vol.339
, pp. 1307-1310
-
-
Hattersley, A.T.1
Turner, R.C.2
Permutt, M.A.3
-
53
-
-
17344366286
-
Association of a human G-protein beta3 subunit variant with hypertension
-
Siffert W, Rosskopf D, Siffert G et al. Association of a human G-protein beta3 subunit variant with hypertension. Nat Genet 1998;18:45-48.
-
(1998)
Nat Genet
, vol.18
, pp. 45-48
-
-
Siffert, W.1
Rosskopf, D.2
Siffert, G.3
-
54
-
-
0032079569
-
Inherited platelet glycoprotein polymorphisms and a risk for coronary heart disease in young central Europeans
-
Sperr WR, Huber K, Roden M, et al. Inherited platelet glycoprotein polymorphisms and a risk for coronary heart disease in young central Europeans. Thromb Res 1998;90:117-123.
-
(1998)
Thromb Res
, vol.90
, pp. 117-123
-
-
Sperr, W.R.1
Huber, K.2
Roden, M.3
-
55
-
-
0027306050
-
Genetic risk and carcinogen exposure: A common inherited defect of the carcinogen-metabolism gene glutathione S-transferase M1 (GSTM1) that increases susceptibility to bladder cancer
-
Bell DA, Taylor JA, Paulson DF, Robertson CN, Mohler JL, Lucier GW. Genetic risk and carcinogen exposure: a common inherited defect of the carcinogen-metabolism gene glutathione S-transferase M1 (GSTM1) that increases susceptibility to bladder cancer. J Natl Cancer Inst 1993;85:1159-1164.
-
(1993)
J Natl Cancer Inst
, vol.85
, pp. 1159-1164
-
-
Bell, D.A.1
Taylor, J.A.2
Paulson, D.F.3
Robertson, C.N.4
Mohler, J.L.5
Lucier, G.W.6
-
56
-
-
0028283887
-
Combined effect of CYP1A1 inducibility and GSTM1 polymorphism on histological type of lung cancer
-
Anttila S, Hirvonen A, Husgafvel-Pursiainen K, Karjalainen A, Nurminen T, Vainio H. Combined effect of CYP1A1 inducibility and GSTM1 polymorphism on histological type of lung cancer. Carcinogenesis 1994;15:1133-1135.
-
(1994)
Carcinogenesis
, vol.15
, pp. 1133-1135
-
-
Anttila, S.1
Hirvonen, A.2
Husgafvel-Pursiainen, K.3
Karjalainen, A.4
Nurminen, T.5
Vainio, H.6
-
57
-
-
0027511164
-
Association between polymorphism of the glycogen synthase gene and non-insulin-dependent diabetes mellitus
-
Groop LC, Kankuri M, Schalin-Jantti C, et al. Association between polymorphism of the glycogen synthase gene and non-insulin-dependent diabetes mellitus. N Engl J Med 1993;328:10-14.
-
(1993)
N Engl J Med
, vol.328
, pp. 10-14
-
-
Groop, L.C.1
Kankuri, M.2
Schalin-Jantti, C.3
-
58
-
-
0031560096
-
5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity
-
Hinney A, Ziegler A, Nothen MM, Remschmidt H, Hebebrand J. 5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity. Lancet 1997;350:1324-1325.
-
(1997)
Lancet
, vol.350
, pp. 1324-1325
-
-
Hinney, A.1
Ziegler, A.2
Nothen, M.M.3
Remschmidt, H.4
Hebebrand, J.5
-
59
-
-
0029100429
-
Association between clozapine response and allelic variation in 5-HT2A receptor gene
-
Arranz M, Collier D, Sodhi M et al. Association between clozapine response and allelic variation in 5-HT2A receptor gene. Lancet 1995;346:281-282.
-
(1995)
Lancet
, vol.346
, pp. 281-282
-
-
Arranz, M.1
Collier, D.2
Sodhi, M.3
-
60
-
-
0029988749
-
Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia
-
Inayama Y, Yoneda H, Sakai T et al. Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia. Am J Med Genet 1996;67:103-105.
-
(1996)
Am J Med Genet
, vol.67
, pp. 103-105
-
-
Inayama, Y.1
Yoneda, H.2
Sakai, T.3
-
61
-
-
0034006946
-
Osteoporotic fractures are associated with an 86-base pair repeat polymorphism in the interleukin-1-receptor antagonist gene but not with polymorphisms in the interleukin-1beta gene
-
Langdahl BL, Lokke E, Carstens M, Stenkjaer LL, Eriksen EF. Osteoporotic fractures are associated with an 86-base pair repeat polymorphism in the interleukin-1-receptor antagonist gene but not with polymorphisms in the interleukin-1beta gene. J Bone Miner Res 2000;15:402-414.
-
(2000)
J Bone Miner Res
, vol.15
, pp. 402-414
-
-
Langdahl, B.L.1
Lokke, E.2
Carstens, M.3
Stenkjaer, L.L.4
Eriksen, E.F.5
-
62
-
-
0034068817
-
Polymorphisms of the 1L-4, TNF-alpha, and Fcepsilon RIbeta genes and the risk of allergic disorders in at-risk infants
-
Zhu S, Chan-Yeung M, Becker AB et al. Polymorphisms of the 1L-4, TNF-alpha, and Fcepsilon RIbeta genes and the risk of allergic disorders in at-risk infants. Am J Respir Crit Care Med 2000;161:1655-1659.
-
(2000)
Am J Respir Crit Care Med
, vol.161
, pp. 1655-1659
-
-
Zhu, S.1
Chan-Yeung, M.2
Becker, A.B.3
-
63
-
-
0001325237
-
The association of atopy with a gain-of-function mutation in the alpha subunit of the interleukin-4 receptor
-
Hershey GK, Friedrich MF, Esswein LA, Thomas ML, Chatila TA. The association of atopy with a gain-of-function mutation in the alpha subunit of the interleukin-4 receptor. N Engl J Med 1997;337:1720-1725.
-
(1997)
N Engl J Med
, vol.337
, pp. 1720-1725
-
-
Hershey, G.K.1
Friedrich, M.F.2
Esswein, L.A.3
Thomas, M.L.4
Chatila, T.A.5
-
64
-
-
0032951341
-
Association of radial bone mineral density with CA repeat polymorphism at the interleukin 6 locus in postmenopausal Japanese women
-
Tsukamoto K, Yoshida H, Watanabe S et al. Association of radial bone mineral density with CA repeat polymorphism at the interleukin 6 locus in postmenopausal Japanese women. J Hum Genet 1999;44:148-151.
-
(1999)
J Hum Genet
, vol.44
, pp. 148-151
-
-
Tsukamoto, K.1
Yoshida, H.2
Watanabe, S.3
-
65
-
-
0021343570
-
A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus
-
Bell GI, Horita S, Karam JH. A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus. Diabetes 1984;33:176-183.
-
(1984)
Diabetes
, vol.33
, pp. 176-183
-
-
Bell, G.I.1
Horita, S.2
Karam, J.H.3
-
66
-
-
0021348199
-
Polymorphisms in the 5′-flanking region of the insulin gene and non-insulin-dependent diabetes
-
Hitman GA, Jowett NI, Williams LG, Humphries S, Winter RM, Galton DJ. Polymorphisms in the 5′-flanking region of the insulin gene and non-insulin-dependent diabetes. Clin Sci (Lond) 1984;66:383-388.
-
(1984)
Clin Sci (Lond)
, vol.66
, pp. 383-388
-
-
Hitman, G.A.1
Jowett, N.I.2
Williams, L.G.3
Humphries, S.4
Winter, R.M.5
Galton, D.J.6
-
67
-
-
0028557255
-
Variant sequences of insulin receptor substrate-1 in patients with noninsulin-dependent diabetes mellitus
-
Imai Y, Fusco A, Suzuki Y et al. Variant sequences of insulin receptor substrate-1 in patients with noninsulin-dependent diabetes mellitus. J Clin Endocrinol Metab 1994;79:1655-1658.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 1655-1658
-
-
Imai, Y.1
Fusco, A.2
Suzuki, Y.3
-
68
-
-
0029798832
-
Platelet glycoprotein IIIa PlA polymorphism and myocardial infarction
-
author reply 1073-1074
-
Marian AJ, Brugada R, Kleiman NS. Platelet glycoprotein IIIa PlA polymorphism and myocardial infarction. N Engl J Med 1996;335:1071-1072; author reply 1073-1074.
-
(1996)
N Engl J Med
, vol.335
, pp. 1071-1072
-
-
Marian, A.J.1
Brugada, R.2
Kleiman, N.S.3
-
69
-
-
7144262383
-
Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia
-
Bowen T, Guy CA, Craddock N et al. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Mol Psychiatry 1998;3:266-269.
-
(1998)
Mol Psychiatry
, vol.3
, pp. 266-269
-
-
Bowen, T.1
Guy, C.A.2
Craddock, N.3
-
70
-
-
0032871802
-
Sequence variants in the 5′ flanking region of the leptin gene are associated with obesity in women
-
Li WD, Reed DR, Lee JH et al. Sequence variants in the 5′ flanking region of the leptin gene are associated with obesity in women. Ann Hum Genet 1999;63:227-234.
-
(1999)
Ann Hum Genet
, vol.63
, pp. 227-234
-
-
Li, W.D.1
Reed, D.R.2
Lee, J.H.3
-
71
-
-
0025241155
-
Lipoprotein and hepatic lipase gene variants in coronary atherosclerosis
-
Thorn JA, Chamberlain JC, Alcolado JC et al. Lipoprotein and hepatic lipase gene variants in coronary atherosclerosis. Atherosclerosis 1990;85:55-60.
-
(1990)
Atherosclerosis
, vol.85
, pp. 55-60
-
-
Thorn, J.A.1
Chamberlain, J.C.2
Alcolado, J.C.3
-
72
-
-
0028170324
-
Polymorphism of the tumour necrosis factor beta gene in multiple sclerosis and rheumatoid arthritis
-
Vandevyver C, Raus P, Stinissen P, Philippaerts L, Cassiman JJ, Raus J. Polymorphism of the tumour necrosis factor beta gene in multiple sclerosis and rheumatoid arthritis. Eur J Immunogenet 1994;21:377-382.
-
(1994)
Eur J Immunogenet
, vol.21
, pp. 377-382
-
-
Vandevyver, C.1
Raus, P.2
Stinissen, P.3
Philippaerts, L.4
Cassiman, J.J.5
Raus, J.6
-
73
-
-
0030447092
-
Mannose-binding protein genetic polymorphisms in black patients with systemic lupus erythematosus
-
Sullivan KE, Wooten C, Goldman D, Petri M. Mannose-binding protein genetic polymorphisms in black patients with systemic lupus erythematosus. Arthritis Rheum 1996;39:2046-2051.
-
(1996)
Arthritis Rheum
, vol.39
, pp. 2046-2051
-
-
Sullivan, K.E.1
Wooten, C.2
Goldman, D.3
Petri, M.4
-
74
-
-
0025317768
-
DNA length polymorphism 5′ to the myelin basic protein gene is associated with multiple sclerosis
-
Boylan KB, Takahashi N, Paty DW et al. DNA length polymorphism 5′ to the myelin basic protein gene is associated with multiple sclerosis. Ann Neurol 1990;27:291-297.
-
(1990)
Ann Neurol
, vol.27
, pp. 291-297
-
-
Boylan, K.B.1
Takahashi, N.2
Paty, D.W.3
-
75
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995;10:111-113.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
76
-
-
0030610090
-
The mutation Ala677->Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis
-
Arruda VR, von Zuben PM, Chiaparini LC, Annichino-Bizzacchi JM, Costa FF. The mutation Ala677->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis. Thromb Haemost 1997;77:818-821.
-
(1997)
Thromb Haemost
, vol.77
, pp. 818-821
-
-
Arruda, V.R.1
Von Zuben, P.M.2
Chiaparini, L.C.3
Annichino-Bizzacchi, J.M.4
Costa, F.F.5
-
77
-
-
0030048029
-
A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene
-
Wang XL, Sim AS, Badenhop RF, McCredie RM, Wilcken DE. A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene. Nat Med 1996;2:41-45.
-
(1996)
Nat Med
, vol.2
, pp. 41-45
-
-
Wang, X.L.1
Sim, A.S.2
Badenhop, R.F.3
McCredie, R.M.4
Wilcken, D.E.5
-
78
-
-
0031915397
-
DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease
-
Sanghera DK, Aston CE, Saha N, Kamboh MI. DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease. Am J Hum Genet 1998;62:36-44.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 36-44
-
-
Sanghera, D.K.1
Aston, C.E.2
Saha, N.3
Kamboh, M.I.4
-
79
-
-
0031595923
-
A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity
-
Deeb SS, Fajas L, Nemoto M et al. A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nat Genet 1998;20:284-287.
-
(1998)
Nat Genet
, vol.20
, pp. 284-287
-
-
Deeb, S.S.1
Fajas, L.2
Nemoto, M.3
-
80
-
-
0025820942
-
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease
-
Palmer MS, Dryden AJ, Hughes JT, Collinge J. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 1991;352:340-342.
-
(1991)
Nature
, vol.352
, pp. 340-342
-
-
Palmer, M.S.1
Dryden, A.J.2
Hughes, J.T.3
Collinge, J.4
-
81
-
-
0030028429
-
Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease
-
Alzheimer's Disease Collaborative Group
-
Wragg M, Hutton M, Talbot C. Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease. Alzheimer's Disease Collaborative Group. Lancet 1996;347:509-512.
-
(1996)
Lancet
, vol.347
, pp. 509-512
-
-
Wragg, M.1
Hutton, M.2
Talbot, C.3
-
82
-
-
0036075274
-
Human resistin gene: Molecular scanning and evaluation of association with insulin sensitivity and type 2 diabetes in Caucasians
-
Wang H, Chu WS, Hemphill C, Elbein SC. Human resistin gene: molecular scanning and evaluation of association with insulin sensitivity and type 2 diabetes in Caucasians. J Clin Endocrinol Metab 2002;87:2520-2524.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 2520-2524
-
-
Wang, H.1
Chu, W.S.2
Hemphill, C.3
Elbein, S.C.4
-
83
-
-
0023228997
-
Deoxyribonucleic acid (DNA) polymorphism of the alpha 1-antitrypsin gene in chronic lung disease
-
Kalsheker NA, Hodgson IJ, Watkins GL, White JP, Morrison HM, Stockley RA. Deoxyribonucleic acid (DNA) polymorphism of the alpha 1-antitrypsin gene in chronic lung disease. BMJ (Clin Res Ed) 1987;294:1511-1514.
-
(1987)
BMJ (Clin Res Ed)
, vol.294
, pp. 1511-1514
-
-
Kalsheker, N.A.1
Hodgson, I.J.2
Watkins, G.L.3
White, J.P.4
Morrison, H.M.5
Stockley, R.A.6
-
84
-
-
0031060710
-
Microsatellite polymorphism of the alpha 1-antichymotrypsin gene locus associated with sporadic Alzheimer's disease
-
Morgan K, Morgan L, Carpenter K, et al. Microsatellite polymorphism of the alpha 1-antichymotrypsin gene locus associated with sporadic Alzheimer's disease. Hum Genet 1997;99:27-31.
-
(1997)
Hum Genet
, vol.99
, pp. 27-31
-
-
Morgan, K.1
Morgan, L.2
Carpenter, K.3
-
85
-
-
0028934522
-
Molecular variant of angiotensinogen gene is associated with coronary atherosclerosis
-
Ishigami T, Umemura S, Iwamoto T et al. Molecular variant of angiotensinogen gene is associated with coronary atherosclerosis. Circulation 1995;91:951-954.
-
(1995)
Circulation
, vol.91
, pp. 951-954
-
-
Ishigami, T.1
Umemura, S.2
Iwamoto, T.3
-
86
-
-
0026669336
-
Molecular basis of human hypertension: Role of angiotensinogen
-
Jeunemaitre X, Soubrier F, Kotelevtsev YV et al. Molecular basis of human hypertension: role of angiotensinogen. Cell 1992;71:169-180.
-
(1992)
Cell
, vol.71
, pp. 169-180
-
-
Jeunemaitre, X.1
Soubrier, F.2
Kotelevtsev, Y.V.3
-
87
-
-
0028901713
-
Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction
-
Eriksson P, Kallin B, van't Hooft FM, Bavenholm P, Hamsten A. Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction. Proc Natl Acad Sci USA 1995;92:1851-1855.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 1851-1855
-
-
Eriksson, P.1
Kallin, B.2
Van't Hooft, F.M.3
Bavenholm, P.4
Hamsten, A.5
-
88
-
-
0023759159
-
Association of genetic variant of the glucose transporter with non-insulin-dependent diabetes mellitus
-
Li SR, Baroni MG, Oelbaum RS, Stock J, Galton DJ. Association of genetic variant of the glucose transporter with non-insulin-dependent diabetes mellitus. Lancet 1988;2:368-370.
-
(1988)
Lancet
, vol.2
, pp. 368-370
-
-
Li, S.R.1
Baroni, M.G.2
Oelbaum, R.S.3
Stock, J.4
Galton, D.J.5
-
89
-
-
0028931804
-
Primary structure of the serotonin transporter in unipolar depression and bipolar disorder
-
Lesch KP, Gross J, Franzek E, Wolozin BL, Riederer P, Murphy DL. Primary structure of the serotonin transporter in unipolar depression and bipolar disorder. Biol Psychiatry 1995;37:215-223.
-
(1995)
Biol Psychiatry
, vol.37
, pp. 215-223
-
-
Lesch, K.P.1
Gross, J.2
Franzek, E.3
Wolozin, B.L.4
Riederer, P.5
Murphy, D.L.6
-
90
-
-
0030942229
-
Tumour necrosis factor haplotypes and asthma
-
Moffatt MF, Cookson WO. Tumour necrosis factor haplotypes and asthma. Hum Mol Genet 1997;6:551-554.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 551-554
-
-
Moffatt, M.F.1
Cookson, W.O.2
-
91
-
-
15444348298
-
Polymorphisms of the tumour necrosis factor-alpha gene, coronary heart disease and obesity
-
Herrmann SM, Ricard S, Nicaud V et al. Polymorphisms of the tumour necrosis factor-alpha gene, coronary heart disease and obesity. Eur J Clin Invest 1998;28:59-66.
-
(1998)
Eur J Clin Invest
, vol.28
, pp. 59-66
-
-
Herrmann, S.M.1
Ricard, S.2
Nicaud, V.3
-
92
-
-
0030766567
-
A TNF-alpha promoter polymorphism is associated with juvenile onset psoriasis and psoriatic arthritis
-
Hohler T, Kruger A, Schneider PM et al. A TNF-alpha promoter polymorphism is associated with juvenile onset psoriasis and psoriatic arthritis. J Invest Dermatol 1997;109:562-565.
-
(1997)
J Invest Dermatol
, vol.109
, pp. 562-565
-
-
Hohler, T.1
Kruger, A.2
Schneider, P.M.3
-
93
-
-
0026443678
-
Tumour necrosis factor-beta gene RFLP alleles in Finnish IDDM haplotypes
-
The Childhood Diabetes in Finland (DiMe) Study Group
-
Ilonen J, Merivuori H, Reijonen H et al. Tumour necrosis factor-beta gene RFLP alleles in Finnish IDDM haplotypes. The Childhood Diabetes in Finland (DiMe) Study Group. Scand J Immunol 1992;36:779-783.
-
(1992)
Scand J Immunol
, vol.36
, pp. 779-783
-
-
Ilonen, J.1
Merivuori, H.2
Reijonen, H.3
-
94
-
-
0036616916
-
Association of the tumour necrosis factor alpha-308G/A polymorphism with the risk of diabetes in an elderly population-based cohort
-
Heijmans BT, Westendorp RG, Droog S, Kluft C, Knook DL, Slagboom PE. Association of the tumour necrosis factor alpha-308G/A polymorphism with the risk of diabetes in an elderly population-based cohort. Genes Immun 2002;3:225-228.
-
(2002)
Genes Immun
, vol.3
, pp. 225-228
-
-
Heijmans, B.T.1
Westendorp, R.G.2
Droog, S.3
Kluft, C.4
Knook, D.L.5
Slagboom, P.E.6
-
95
-
-
7144250518
-
Role of a p53 polymorphism in the development of human papillomavirus-associated cancer
-
Storey A, Thomas M, Kalita A et al. Role of a p53 polymorphism in the development of human papillomavirus-associated cancer. Nature 1998;393:229-234.
-
(1998)
Nature
, vol.393
, pp. 229-234
-
-
Storey, A.1
Thomas, M.2
Kalita, A.3
-
96
-
-
0031957513
-
Uncoupling protein-1 mRNA expression in obese human subjects: The role of sequence variations at the uncoupling protein-1 gene locus
-
Esterbauer H, Oberkofler H, Liu YM et al. Uncoupling protein-1 mRNA expression in obese human subjects: the role of sequence variations at the uncoupling protein-1 gene locus. J Lipid Res 1998;39:834-844.
-
(1998)
J Lipid Res
, vol.39
, pp. 834-844
-
-
Esterbauer, H.1
Oberkofler, H.2
Liu, Y.M.3
-
97
-
-
0032989496
-
An uncoupling protein 2 gene variant is associated with a raised body mass index but not Type II diabetes
-
Cassell PG, Neverova M, Janmohamed S, et al. An uncoupling protein 2 gene variant is associated with a raised body mass index but not Type II diabetes. Diabetologia 1999;42:688-692.
-
(1999)
Diabetologia
, vol.42
, pp. 688-692
-
-
Cassell, P.G.1
Neverova, M.2
Janmohamed, S.3
-
98
-
-
0034434968
-
Evidence that single nucleotide polymorphism in the uncoupling protein 3 (UCP3) gene influences fat distribution in women of European and Asian origin
-
Cassell PG, Saker PJ, Huxtable SJ et al. Evidence that single nucleotide polymorphism in the uncoupling protein 3 (UCP3) gene influences fat distribution in women of European and Asian origin. Diabetologia 2000;43:1558-1564.
-
(2000)
Diabetologia
, vol.43
, pp. 1558-1564
-
-
Cassell, P.G.1
Saker, P.J.2
Huxtable, S.J.3
-
99
-
-
23444460542
-
Prediction of bone density from vitamin D receptor alleles
-
Morrison NA, Qi JC, Tokita A et al. Prediction of bone density from vitamin D receptor alleles. Nature 1994;367:284-287.
-
(1994)
Nature
, vol.367
, pp. 284-287
-
-
Morrison, N.A.1
Qi, J.C.2
Tokita, A.3
-
100
-
-
0029118873
-
Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease
-
Okuizumi K, Onodera O, Namba Y et al. Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease. Nat Genet 1995;11:207-209.
-
(1995)
Nat Genet
, vol.11
, pp. 207-209
-
-
Okuizumi, K.1
Onodera, O.2
Namba, Y.3
-
101
-
-
0034969427
-
Activation of cardiac renin-angiotensin system in unstable angina
-
Neri Serneri GG, Boddi M, Poggesi L et al. Activation of cardiac renin-angiotensin system in unstable angina. J Am Coll Cardiol 2001;38:49-55.
-
(2001)
J Am Coll Cardiol
, vol.38
, pp. 49-55
-
-
Neri Serneri, G.G.1
Boddi, M.2
Poggesi, L.3
-
102
-
-
0035660423
-
Apolipoprotein C-I expression in the brain in Alzheimer's disease
-
Petit-Turcotte C, Stohl SM, Beffert U,et al. Apolipoprotein C-I expression in the brain in Alzheimer's disease. Neurobiol Dis 2001;8:953-963.
-
(2001)
Neurobiol Dis
, vol.8
, pp. 953-963
-
-
Petit-Turcotte, C.1
Stohl, S.M.2
Beffert, U.3
-
103
-
-
0030010322
-
Apolipoprotein e in patients with dementia of the Alzheimer type and vascular dementia
-
Isoe K, Urakami K, Sato K, Takahashi K. Apolipoprotein E in patients with dementia of the Alzheimer type and vascular dementia. Acta Neurol Scand 1996;93:133-137.
-
(1996)
Acta Neurol Scand
, vol.93
, pp. 133-137
-
-
Isoe, K.1
Urakami, K.2
Sato, K.3
Takahashi, K.4
-
104
-
-
0035127966
-
High expression of apolipoprotein e mRNA in the brains with sporadic Alzheimer's disease
-
Yamagata K, Urakami K, Ikeda K et al. High expression of apolipoprotein E mRNA in the brains with sporadic Alzheimer's disease. Dement Geriatr Cogn Disord 2001;12:57-62.
-
(2001)
Dement Geriatr Cogn Disord
, vol.12
, pp. 57-62
-
-
Yamagata, K.1
Urakami, K.2
Ikeda, K.3
-
105
-
-
0031911126
-
Increased apolipoprotein E mRNA in the hippocampus in Alzheimer disease and in rats after entorhinal cortex lesioning
-
Zarow C, Victoroff J. Increased apolipoprotein E mRNA in the hippocampus in Alzheimer disease and in rats after entorhinal cortex lesioning. Exp Neurol 1998;149:79-86.
-
(1998)
Exp Neurol
, vol.149
, pp. 79-86
-
-
Zarow, C.1
Victoroff, J.2
-
106
-
-
0030897885
-
Abnormal expression of serotonin transporter mRNA in the frontal and temporal cortex of schizophrenics
-
Hernandez I, Sokolov BP. Abnormal expression of serotonin transporter mRNA in the frontal and temporal cortex of schizophrenics. Mol Psychiatry 1997;2:57-64.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 57-64
-
-
Hernandez, I.1
Sokolov, B.P.2
-
107
-
-
0028334453
-
The abundance of mRNA for dopamine D2 receptor isoforms in brain tissue from controls and schizophrenics
-
Roberts DA, Balderson D, Pickering-Brown SM, Deakin JF, Owen F. The abundance of mRNA for dopamine D2 receptor isoforms in brain tissue from controls and schizophrenics. Brain Res Mol Brain Res 1994;25:173-175.
-
(1994)
Brain Res Mol Brain Res
, vol.25
, pp. 173-175
-
-
Roberts, D.A.1
Balderson, D.2
Pickering-Brown, S.M.3
Deakin, J.F.4
Owen, F.5
-
108
-
-
0035809776
-
Schizophrenia: Elevated mRNA for dopamine D2 (Longer) receptors in frontal cortex
-
Tallerico T, Novak G, Liu IS, Ulpian C, Seeman P. Schizophrenia: elevated mRNA for dopamine D2 (Longer) receptors in frontal cortex. Brain Res Mol Brain Res 2001;87:160-165.
-
(2001)
Brain Res Mol Brain Res
, vol.87
, pp. 160-165
-
-
Tallerico, T.1
Novak, G.2
Liu, I.S.3
Ulpian, C.4
Seeman, P.5
-
109
-
-
0035895251
-
A peripheral marker for schizophrenia: Increased levels of D3 dopamine receptor mRNA in blood lymphocytes
-
Ilani T, Ben-Shachar D, Strous RD et al. A peripheral marker for schizophrenia: Increased levels of D3 dopamine receptor mRNA in blood lymphocytes. Proc Natl Acad Sci U S A 2001;98:625-628.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 625-628
-
-
Ilani, T.1
Ben-Shachar, D.2
Strous, R.D.3
-
110
-
-
0002624569
-
Change of dopamine receptor mRNA expression in lymphocyte of schizophrenic patients
-
Kwak YT, Koo MS, Choi CH, Sunwoo I. Change of dopamine receptor mRNA expression in lymphocyte of schizophrenic patients. BMC Med Genet 2001;2:3.
-
(2001)
BMC Med Genet
, vol.2
, pp. 3
-
-
Kwak, Y.T.1
Koo, M.S.2
Choi, C.H.3
Sunwoo, I.4
-
111
-
-
0034075898
-
Regulation of gene expression during severe caloric restriction: Lack of induction of p85 alpha phosphatidylinositol 3-kinase mRNA in skeletal muscle of patients with type II (non-insulin-dependent) diabetes mellitus
-
Andreelli F, Laville M, Vega N, Riou JP, Vidal H. Regulation of gene expression during severe caloric restriction: lack of induction of p85 alpha phosphatidylinositol 3-kinase mRNA in skeletal muscle of patients with type II (non-insulin-dependent) diabetes mellitus. Diabetologia 2000;43:356-363.
-
(2000)
Diabetologia
, vol.43
, pp. 356-363
-
-
Andreelli, F.1
Laville, M.2
Vega, N.3
Riou, J.P.4
Vidal, H.5
-
112
-
-
0035029812
-
Regulation by insulin of gene expression in human skeletal muscle and adipose tissue. Evidence for specific defects in type 2 diabetes
-
Ducluzeau PH, Perretti N, Laville M et al. Regulation by insulin of gene expression in human skeletal muscle and adipose tissue. Evidence for specific defects in type 2 diabetes. Diabetes 2001;50:1134-1142.
-
(2001)
Diabetes
, vol.50
, pp. 1134-1142
-
-
Ducluzeau, P.H.1
Perretti, N.2
Laville, M.3
-
113
-
-
0029739976
-
Glycogen synthase activity is reduced in cultured skeletal muscle cells of non-insulin-dependent diabetes mellitus subjects. Biochemical and molecular mechanisms
-
Henry RR, Ciaraldi TP, Abrams-Carter L, Mudaliar S, Park KS, Nikoulina SE. Glycogen synthase activity is reduced in cultured skeletal muscle cells of non-insulin-dependent diabetes mellitus subjects. Biochemical and molecular mechanisms. J Clin Invest 1996;98:1231-126.
-
(1996)
J Clin Invest
, vol.98
, pp. 1231-2126
-
-
Henry, R.R.1
Ciaraldi, T.P.2
Abrams-Carter, L.3
Mudaliar, S.4
Park, K.S.5
Nikoulina, S.E.6
-
114
-
-
0034457043
-
Impaired insulin-stimulated expression of the glycogen synthase gene in skeletal muscle of type 2 diabetic patients is acquired rather than inherited
-
Huang X, Vaag A, Hansson M, Weng J, Laurila E, Groop L. Impaired insulin-stimulated expression of the glycogen synthase gene in skeletal muscle of type 2 diabetic patients is acquired rather than inherited. J Clin Endocrinol Metab 2000;85:1584-1590.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 1584-1590
-
-
Huang, X.1
Vaag, A.2
Hansson, M.3
Weng, J.4
Laurila, E.5
Groop, L.6
-
115
-
-
0028858765
-
Increased concentrations of glycogen synthase protein in skeletal muscle of patients with NIDDM
-
Lofman M, Yki-Jarvinen H, Parkkonen M et al. Increased concentrations of glycogen synthase protein in skeletal muscle of patients with NIDDM. Am J Physiol 1995;269:E27-E32.
-
(1995)
Am J Physiol
, vol.269
-
-
Lofman, M.1
Yki-Jarvinen, H.2
Parkkonen, M.3
-
116
-
-
0026315717
-
Impaired expression of glycogen synthase mRNA in skeletal muscle of NIDDM patients
-
Vestergaard H, Bjorbaek C, Andersen PH, Bak JF, Pedersen O. Impaired expression of glycogen synthase mRNA in skeletal muscle of NIDDM patients. Diabetes 1991;40:1740-1745.
-
(1991)
Diabetes
, vol.40
, pp. 1740-1745
-
-
Vestergaard, H.1
Bjorbaek, C.2
Andersen, P.H.3
Bak, J.F.4
Pedersen, O.5
-
117
-
-
0027325287
-
Glycogen synthase and phosphofructokinase protein and mRNA levels in skeletal muscle from insulin-resistant patients with non-insulin-dependent diabetes mellitus
-
Vestergaard H, Lund S, Larsen FS, Bjerrum OJ, Pedersen O. Glycogen synthase and phosphofructokinase protein and mRNA levels in skeletal muscle from insulin-resistant patients with non-insulin-dependent diabetes mellitus. J Clin Invest 1993;91:2342-50.
-
(1993)
J Clin Invest
, vol.91
, pp. 2342-2350
-
-
Vestergaard, H.1
Lund, S.2
Larsen, F.S.3
Bjerrum, O.J.4
Pedersen, O.5
-
118
-
-
0030273870
-
5-HT1A and 5-HT2A receptor mRNAs and binding site densities are differentially altered in schizophrenia
-
Burnet PW, Eastwood SL, Harrison PJ. 5-HT1A and 5-HT2A receptor mRNAs and binding site densities are differentially altered in schizophrenia. Neuropsychopharmacology 1996;15:442-455.
-
(1996)
Neuropsychopharmacology
, vol.15
, pp. 442-455
-
-
Burnet, P.W.1
Eastwood, S.L.2
Harrison, P.J.3
-
119
-
-
0034650980
-
Abnormalities in 5-HT2A receptor mRNA expression in frontal cortex of chronic elderly schizophrenics with varying histories of neuroleptic treatment
-
Hernandez I, Sokolov BP. Abnormalities in 5-HT2A receptor mRNA expression in frontal cortex of chronic elderly schizophrenics with varying histories of neuroleptic treatment. J Neurosci Res 2000;59:218-225.
-
(2000)
J Neurosci Res
, vol.59
, pp. 218-225
-
-
Hernandez, I.1
Sokolov, B.P.2
-
120
-
-
0032713057
-
Asthmatic airway biopsy specimens are more likely to express the IL-4 alternative splice variant IL-4delta2
-
Glare EM, Divjak M, Rolland JM, Walters EH. Asthmatic airway biopsy specimens are more likely to express the IL-4 alternative splice variant IL-4delta2. J Allergy Clin Immunol 1999;104:978-982.
-
(1999)
J Allergy Clin Immunol
, vol.104
, pp. 978-982
-
-
Glare, E.M.1
Divjak, M.2
Rolland, J.M.3
Walters, E.H.4
-
121
-
-
10544256182
-
IL-4 and IL-5 mRNA and protein in bronchial biopsies from patients with atopic and nonatopic asthma: Evidence against "intrinsic" asthma being a distinct immunopathologic entity
-
Humbert M, Durham SR, Ying S et al. IL-4 and IL-5 mRNA and protein in bronchial biopsies from patients with atopic and nonatopic asthma: evidence against "intrinsic" asthma being a distinct immunopathologic entity. Am J Respir Crit Care Med 1996;154:1497-1504.
-
(1996)
Am J Respir Crit Care Med
, vol.154
, pp. 1497-1504
-
-
Humbert, M.1
Durham, S.R.2
Ying, S.3
-
122
-
-
0030228818
-
Interleukin-13 and interkukin-4 are coexpressed in atopic asthma
-
Kotsimbos TC, Ernst P, Hamid QA. Interleukin-13 and interkukin-4 are coexpressed in atopic asthma. Proc Assoc Am Physicians 1996;108:368-373.
-
(1996)
Proc Assoc Am Physicians
, vol.108
, pp. 368-373
-
-
Kotsimbos, T.C.1
Ernst, P.2
Hamid, Q.A.3
-
123
-
-
0031944825
-
Cytokine mRNA expression in asthma is not restricted to the large airways
-
Minshall EM, Hogg JC, Hamid QA. Cytokine mRNA expression in asthma is not restricted to the large airways. J Allergy Clin Immunol 1998;101:386-390.
-
(1998)
J Allergy Clin Immunol
, vol.101
, pp. 386-390
-
-
Minshall, E.M.1
Hogg, J.C.2
Hamid, Q.A.3
-
124
-
-
0032972804
-
IL-4 and IL-5 mRNA expression in induced sputum of asthmatic subjects: Comparison with bronchial wash
-
Olivenstein R, Taha R, Minshall EM, Hamid QA. IL-4 and IL-5 mRNA expression in induced sputum of asthmatic subjects: comparison with bronchial wash. J Allergy Clin Immunol 1999;103:238-245.
-
(1999)
J Allergy Clin Immunol
, vol.103
, pp. 238-245
-
-
Olivenstein, R.1
Taha, R.2
Minshall, E.M.3
Hamid, Q.A.4
-
125
-
-
0026610142
-
Predominant TH2-like bronchoalveolar T-lymphocyte population in atopic asthma
-
Robinson DS, Hamid Q, Ying S et al. Predominant TH2-like bronchoalveolar T-lymphocyte population in atopic asthma. N Engl J Med 1992;326:298-304.
-
(1992)
N Engl J Med
, vol.326
, pp. 298-304
-
-
Robinson, D.S.1
Hamid, Q.2
Ying, S.3
-
126
-
-
0031723763
-
Expression of the IL-4 receptor alpha-subunit is increased in bronchial biopsy specimens from atopic and nonatopic asthmatic subjects
-
Kotsimbos TC, Ghaffar O, Minshall EM et al. Expression of the IL-4 receptor alpha-subunit is increased in bronchial biopsy specimens from atopic and nonatopic asthmatic subjects. J Allergy Clin Immunol 1998;102:859-866.
-
(1998)
J Allergy Clin Immunol
, vol.102
, pp. 859-866
-
-
Kotsimbos, T.C.1
Ghaffar, O.2
Minshall, E.M.3
-
127
-
-
0029083859
-
Increased obese mRNA expression in omental fat cells from massively obese humans
-
Hamilton BS, Paglia D, Kwan AY, Deitel M. Increased obese mRNA expression in omental fat cells from massively obese humans. Nat Med 1995;1:953-956.
-
(1995)
Nat Med
, vol.1
, pp. 953-956
-
-
Hamilton, B.S.1
Paglia, D.2
Kwan, A.Y.3
Deitel, M.4
-
128
-
-
0033960706
-
Leptin, peroxisome proliferator-activated receptor-gamma, and CCAAT/enhancer binding protein-alpha mRNA expression in adipose tissue of humans and their relation to cardiovascular risk factors
-
Krempler F, Breban D, Oberkofler H et al. Leptin, peroxisome proliferator-activated receptor-gamma, and CCAAT/enhancer binding protein-alpha mRNA expression in adipose tissue of humans and their relation to cardiovascular risk factors. Arteriosder Thromb Vasc Biol 2000;20:443-449.
-
(2000)
Arteriosder Thromb Vasc Biol
, vol.20
, pp. 443-449
-
-
Krempler, F.1
Breban, D.2
Oberkofler, H.3
-
129
-
-
0031054698
-
Depot- and sex-specific differences in human leptin mRNA expression: Implications for the control of regional fat distribution
-
Montague CT, Prins JB, Sanders L, Digby JE, O'Rahilly S. Depot- and sex-specific differences in human leptin mRNA expression: implications for the control of regional fat distribution. Diabetes 1997;46:342-7.
-
(1997)
Diabetes
, vol.46
, pp. 342-347
-
-
Montague, C.T.1
Prins, J.B.2
Sanders, L.3
Digby, J.E.4
O'Rahilly, S.5
-
130
-
-
0029020677
-
Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity
-
Considine RV, Considine EL, Williams CJ et al. Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity. J Clin Invest 1995;95:2986-2988.
-
(1995)
J Clin Invest
, vol.95
, pp. 2986-2988
-
-
Considine, R.V.1
Considine, E.L.2
Williams, C.J.3
-
131
-
-
13344295079
-
Serum immunoreactive-leptin concentrations in normal-weight and obese humans
-
Considine RV, Sinha MK, Heiman ML et al. Serum immunoreactive-leptin concentrations in normal-weight and obese humans. N Engl J Med 1996;334:292-295.
-
(1996)
N Engl J Med
, vol.334
, pp. 292-295
-
-
Considine, R.V.1
Sinha, M.K.2
Heiman, M.L.3
-
132
-
-
0029050937
-
Overexpression of the obese (ob) gene in adipose tissue of human obese subjects
-
Lonnqvist F, Arner P, Nordfors L, Schalling M. Overexpression of the obese (ob) gene in adipose tissue of human obese subjects. Nat Med 1995;1:950-953.
-
(1995)
Nat Med
, vol.1
, pp. 950-953
-
-
Lonnqvist, F.1
Arner, P.2
Nordfors, L.3
Schalling, M.4
-
133
-
-
0030055611
-
The expression of ob gene is not acutely regulated by insulin and fasting in human abdominal subcutaneous adipose tissue
-
Vidal H, Auboeuf D, De Vos P et al. The expression of ob gene is not acutely regulated by insulin and fasting in human abdominal subcutaneous adipose tissue. J Clin Invest 1996;98:251-255.
-
(1996)
J Clin Invest
, vol.98
, pp. 251-255
-
-
Vidal, H.1
Auboeuf, D.2
De Vos, P.3
-
134
-
-
0034174922
-
Molecular cloning, sequencing and expression of obese gene in the Chinese
-
Xu M, Zhong G, Fu Z et al. Molecular cloning, sequencing and expression of obese gene in the Chinese. Chin Med J (Engl) 2000;113:350-353.
-
(2000)
Chin Med J (Engl)
, vol.113
, pp. 350-353
-
-
Xu, M.1
Zhong, G.2
Fu, Z.3
-
135
-
-
0030747895
-
Tissue distribution and quantification of the expression of mRNAs of peroxisome proliferator-activated receptors and liver X receptor-alpha in humans: No alteration in adipose tissue of obese and NIDDM patients
-
Auboeuf D, Rieusset J, Fajas L, et al. Tissue distribution and quantification of the expression of mRNAs of peroxisome proliferator-activated receptors and liver X receptor-alpha in humans: no alteration in adipose tissue of obese and NIDDM patients. Diabetes 1997;46:1319-27.
-
(1997)
Diabetes
, vol.46
, pp. 1319-1327
-
-
Auboeuf, D.1
Rieusset, J.2
Fajas, L.3
-
136
-
-
0032006547
-
Skeletal muscle peroxisome proliferator- Activated receptor-gamma expression in obesity and non- insulin-dependent diabetes mellitus
-
Kruszynska YT, Mukherjee R, Jow L, Dana S, Paterniti JR, Olefsky JM. Skeletal muscle peroxisome proliferator- activated receptor-gamma expression in obesity and non- insulin-dependent diabetes mellitus. J Clin Invest 1998;101:543-548.
-
(1998)
J Clin Invest
, vol.101
, pp. 543-548
-
-
Kruszynska, Y.T.1
Mukherjee, R.2
Jow, L.3
Dana, S.4
Paterniti, J.R.5
Olefsky, J.M.6
-
137
-
-
0004473133
-
PPAR-gamma gene expression is elevated in skeletal muscle of obese and type II diabetic subjects
-
Park KS, Ciaraldi TP, Abrams-Carter L, Mudaliar S, Nikoulina SE, Henry RR. PPAR-gamma gene expression is elevated in skeletal muscle of obese and type II diabetic subjects. Diabetes 1997;46:1230-1234.
-
(1997)
Diabetes
, vol.46
, pp. 1230-1234
-
-
Park, K.S.1
Ciaraldi, T.P.2
Abrams-Carter, L.3
Mudaliar, S.4
Nikoulina, S.E.5
Henry, R.R.6
-
138
-
-
0036736813
-
Differential effects of adiposity on peroxisomal proliferator-activated receptor gamma1 and gamma2 messenger ribonucleic acid expression in human adipocytes
-
Sewter C, Blows F, Considine R, Vidal-Puig A, O'Rahilly S. Differential effects of adiposity on peroxisomal proliferator-activated receptor gamma1 and gamma2 messenger ribonucleic acid expression in human adipocytes. J Clin Endocrinol Metab 2002;87:4203-4207.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 4203-4207
-
-
Sewter, C.1
Blows, F.2
Considine, R.3
Vidal-Puig, A.4
O'Rahilly, S.5
-
139
-
-
0030977450
-
Peroxisome proliferator-activated receptor gene expression in human tissues. Effects of obesity, weight loss, and regulation by insulin and glucocorticoids
-
Vidal-Puig AJ, Considine RV, Jimenez-Linan M et al. Peroxisome proliferator-activated receptor gene expression in human tissues. Effects of obesity, weight loss, and regulation by insulin and glucocorticoids. J Clin Invest 1997;99:2416-2422.
-
(1997)
J Clin Invest
, vol.99
, pp. 2416-2422
-
-
Vidal-Puig, A.J.1
Considine, R.V.2
Jimenez-Linan, M.3
-
140
-
-
0030574051
-
Quantification of presenilin-1 mRNA in Alzheimer's disease brains
-
Johnston JA, Froelich S, Lannfelt L, Cowburn RF. Quantification of presenilin-1 mRNA in Alzheimer's disease brains. FEBS Lett 1996;394:279-284.
-
(1996)
FEBS Lett
, vol.394
, pp. 279-284
-
-
Johnston, J.A.1
Froelich, S.2
Lannfelt, L.3
Cowburn, R.F.4
-
141
-
-
0031939135
-
The expression of presenilin-1 mRNA in skin fibroblasts from Alzheimer's disease
-
Ikeda K, Urakami K, Isoe K, Ohno K, Nakashima K. The expression of presenilin-1 mRNA in skin fibroblasts from Alzheimer's disease. Dement Geriatr Cogn Disord 1998;9:145-148.
-
(1998)
Dement Geriatr Cogn Disord
, vol.9
, pp. 145-148
-
-
Ikeda, K.1
Urakami, K.2
Isoe, K.3
Ohno, K.4
Nakashima, K.5
-
142
-
-
0033844395
-
The expression of presenilin 1 mRNA in skin fibroblasts and brains from sporadic Alzheimer's disease
-
Ikeda K, Urakami K, Arai H et al. The expression of presenilin 1 mRNA in skin fibroblasts and brains from sporadic Alzheimer's disease. Dement Geriatr Cogn Disord 2000;11:245-250.
-
(2000)
Dement Geriatr Cogn Disord
, vol.11
, pp. 245-250
-
-
Ikeda, K.1
Urakami, K.2
Arai, H.3
-
143
-
-
0036590319
-
Angiotensinogen genotype, plasma protein and mRNA concentration in isolated systolic hypertension
-
Davis D, Liyou N, Lockwood D, Johnson A. Angiotensinogen genotype, plasma protein and mRNA concentration in isolated systolic hypertension. Clin Genet 2002;61:363-368.
-
(2002)
Clin Genet
, vol.61
, pp. 363-368
-
-
Davis, D.1
Liyou, N.2
Lockwood, D.3
Johnson, A.4
-
144
-
-
0034982912
-
Serial analysis of gene expression in the frontal cortex of patients with bipolar disorder
-
Sun Y, Zhang L, Johnston NL, Torrey EF, Yolken RH. Serial analysis of gene expression in the frontal cortex of patients with bipolar disorder. Br J Psychiatry Suppl 2001;41:s137-s141.
-
(2001)
Br J Psychiatry Suppl
, vol.41
-
-
Sun, Y.1
Zhang, L.2
Johnston, N.L.3
Torrey, E.F.4
Yolken, R.H.5
-
145
-
-
0032811118
-
Expression pattern of tumour necrosis factor receptors in subcutaneous and omental human adipose tissue: Role of obesity and non-insulin-dependent diabetes mellitus
-
Hube F, Birgel M, Lee YM, Hauner H. Expression pattern of tumour necrosis factor receptors in subcutaneous and omental human adipose tissue: role of obesity and non-insulin-dependent diabetes mellitus. Eur J Clin Invest 1999;29:672-678.
-
(1999)
Eur J Clin Invest
, vol.29
, pp. 672-678
-
-
Hube, F.1
Birgel, M.2
Lee, Y.M.3
Hauner, H.4
-
146
-
-
0028931724
-
Increased adipose tissue expression of tumor necrosis factor-alpha in human obesity and insulin resistance
-
Hotamisligil GS, Arner P, Caro JF, Atkinson RL, Spiegelman BM. Increased adipose tissue expression of tumor necrosis factor-alpha in human obesity and insulin resistance. J Clin Invest 1995;95:2409-2415.
-
(1995)
J Clin Invest
, vol.95
, pp. 2409-2415
-
-
Hotamisligil, G.S.1
Arner, P.2
Caro, J.F.3
Atkinson, R.L.4
Spiegelman, B.M.5
-
147
-
-
0028968879
-
The expression of tumor necrosis factor in human adipose tissue: Regulation by obesity, weight loss, and relationship to lipoprotein lipase
-
Kern PA, Saghizadeh M, Ong JM, Bosch RJ, Deem R, Simsolo RB. The expression of tumor necrosis factor in human adipose tissue: Regulation by obesity, weight loss, and relationship to lipoprotein lipase. J Clin Invest 1995;95:2111-2119.
-
(1995)
J Clin Invest
, vol.95
, pp. 2111-2119
-
-
Kern, P.A.1
Saghizadeh, M.2
Ong, J.M.3
Bosch, R.J.4
Deem, R.5
Simsolo, R.B.6
-
148
-
-
0035023128
-
Adipose tissue tumor necrosis factor and interleukin-6 expression in human obesity and insulin resistance
-
Kern PA, Ranganathan S, Li C, Wood L, Ranganathan G. Adipose tissue tumor necrosis factor and interleukin-6 expression in human obesity and insulin resistance. Am J Physiol Endocrinol Metab 2001;280:E745-E751.
-
(2001)
Am J Physiol Endocrinol Metab
, vol.280
-
-
Kern, P.A.1
Ranganathan, S.2
Li, C.3
Wood, L.4
Ranganathan, G.5
-
149
-
-
0006597145
-
Subcutaneous adipose tissue expression of tumour necrosis factor-alpha is not associated with whole body insulin resistance in obese nondiabetic or in type-2 diabetic subjects
-
Koistinen HA, Bastard JP, Dusserre E, et al. Subcutaneous adipose tissue expression of tumour necrosis factor-alpha is not associated with whole body insulin resistance in obese nondiabetic or in type-2 diabetic subjects. Eur J Clin Invest 2000;30:302-310.
-
(2000)
Eur J Clin Invest
, vol.30
, pp. 302-310
-
-
Koistinen, H.A.1
Bastard, J.P.2
Dusserre, E.3
-
150
-
-
0030717887
-
Uncoupling protein gene: Quantification of expression levels in adipose tissues of obese and non-obese humans
-
Oberkofler H, Dallinger G, Liu YM, Hell E, Krempler F, Patsch W. Uncoupling protein gene: quantification of expression levels in adipose tissues of obese and non-obese humans. J Lipid Res 1997;38:2125-2133.
-
(1997)
J Lipid Res
, vol.38
, pp. 2125-2133
-
-
Oberkofler, H.1
Dallinger, G.2
Liu, Y.M.3
Hell, E.4
Krempler, F.5
Patsch, W.6
-
151
-
-
0031816020
-
Uncoupling protein-2 gene: Reduced mRNA expression in intraperitoneal adipose tissue of obese humans
-
Oberkofler H, Liu YM, Esterbauer H, Hell E, Krempler F, Patsch W. Uncoupling protein-2 gene: reduced mRNA expression in intraperitoneal adipose tissue of obese humans. Diabetologia 1998;41:940-946.
-
(1998)
Diabetologia
, vol.41
, pp. 940-946
-
-
Oberkofler, H.1
Liu, Y.M.2
Esterbauer, H.3
Hell, E.4
Krempler, F.5
Patsch, W.6
-
152
-
-
0031437096
-
Increased uncoupling protein-2 and -3 mRNA expression during fasting in obese and lean humans
-
Millet L, Vidal H, Andreelli F et al. Increased uncoupling protein-2 and -3 mRNA expression during fasting in obese and lean humans. J Clin Invest 1997;100:2665-2670.
-
(1997)
J Clin Invest
, vol.100
, pp. 2665-2670
-
-
Millet, L.1
Vidal, H.2
Andreelli, F.3
-
153
-
-
0031844583
-
Reduced gene expression of UCP2 but not UCP3 in skeletal muscle of human obese subjects
-
Nordfors L, Hoffstedt J, Nyberg B et al. Reduced gene expression of UCP2 but not UCP3 in skeletal muscle of human obese subjects. Diabetologia 1998;41:935-939.
-
(1998)
Diabetologia
, vol.41
, pp. 935-939
-
-
Nordfors, L.1
Hoffstedt, J.2
Nyberg, B.3
-
154
-
-
0036373929
-
Relationship between plasma free fatty acids and uncoupling protein-3 gene expression in skeletal muscle of obese subjects: In vitro evidence of a causal link
-
Sbraccia P, D'Adamo M, Leonetti F, et al. Relationship between plasma free fatty acids and uncoupling protein-3 gene expression in skeletal muscle of obese subjects: in vitro evidence of a causal link. Clin Endocrinol (Oxf) 2002;57:199-207.
-
(2002)
Clin Endocrinol (Oxf)
, vol.57
, pp. 199-207
-
-
Sbraccia, P.1
D'Adamo, M.2
Leonetti, F.3
-
155
-
-
0033087317
-
Effects of obesity and stable weight reduction on UCP2 and UCP3 gene expression in humans
-
Vidal-Puig A, Rosenbaum M, Considine RC, Leibel RL, Dohm GL, Lowell BB. Effects of obesity and stable weight reduction on UCP2 and UCP3 gene expression in humans. Obes Res 1999;7:133-140.
-
(1999)
Obes Res
, vol.7
, pp. 133-140
-
-
Vidal-Puig, A.1
Rosenbaum, M.2
Considine, R.C.3
Leibel, R.L.4
Dohm, G.L.5
Lowell, B.B.6
-
156
-
-
0001439521
-
Uncoupling protein-3 gene expression: Reduced skeletal muscle mRNA in obese humans during pronounced weight loss
-
Esterbauer H, Oberkofler H, Dallinger G et al. Uncoupling protein-3 gene expression: reduced skeletal muscle mRNA in obese humans during pronounced weight loss. Diabetologia 1999;42:302-309.
-
(1999)
Diabetologia
, vol.42
, pp. 302-309
-
-
Esterbauer, H.1
Oberkofler, H.2
Dallinger, G.3
-
157
-
-
0031809715
-
mRNA expression of the long and short forms of uncoupling protein-3 in obese and lean humans
-
Millet L, Vidal H, Larrouy D, Andreelli F, Laville M, Langin D. mRNA expression of the long and short forms of uncoupling protein-3 in obese and lean humans. Diabetologia 1998;41:829-832.
-
(1998)
Diabetologia
, vol.41
, pp. 829-832
-
-
Millet, L.1
Vidal, H.2
Larrouy, D.3
Andreelli, F.4
Laville, M.5
Langin, D.6
|