-
1
-
-
39549093148
-
General cardiovascular risk profile for use in primary care: The Framingham Heart Study
-
R.B. D'Agostino Sr., R.S. Vasan, and M.J. Pencina et al. General cardiovascular risk profile for use in primary care: the Framingham Heart Study Circulation 117 2008 743 753
-
(2008)
Circulation
, vol.117
, pp. 743-753
-
-
D'Agostino, Sr.R.B.1
Vasan, R.S.2
Pencina, M.J.3
-
3
-
-
33646147809
-
Emergence of novel genetic effects on blood pressure and hemodynamics in adolescence: The Georgia Cardiovascular Twin Study
-
N. Kupper, D. Ge, F.A. Treiber, and H. Snieder Emergence of novel genetic effects on blood pressure and hemodynamics in adolescence: the Georgia Cardiovascular Twin Study Hypertension 47 2006 948 954
-
(2006)
Hypertension
, vol.47
, pp. 948-954
-
-
Kupper, N.1
Ge, D.2
Treiber, F.A.3
Snieder, H.4
-
4
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
T.A. Manolio, F.S. Collins, and N.J. Cox et al. Finding the missing heritability of complex diseases Nature 461 2009 747 753
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
-
5
-
-
0035936780
-
Molecular mechanisms of human hypertension
-
R.P. Lifton, A.G. Gharavi, and D.S. Geller Molecular mechanisms of human hypertension Cell 104 2001 545 556
-
(2001)
Cell
, vol.104
, pp. 545-556
-
-
Lifton, R.P.1
Gharavi, A.G.2
Geller, D.S.3
-
6
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
G.B. Ehret, P.B. Munroe, and K.M. Rice et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk Nature 478 2011 103 109
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
Ehret, G.B.1
Munroe, P.B.2
Rice, K.M.3
-
7
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
N. Risch, and K. Merikangas The future of genetic studies of complex human diseases Science 273 1996 1516 1517
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
8
-
-
56749149825
-
Replication of the Wellcome Trust genome-wide association study of essential hypertension: The Family Blood Pressure Program
-
G.B. Ehret, A.C. Morrison, and A.A. O'Connor et al. Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program Eur J Hum Genet 16 2008 1507 1511
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 1507-1511
-
-
Ehret, G.B.1
Morrison, A.C.2
O'Connor, A.A.3
-
9
-
-
33847609151
-
Population-based sample reveals gene-gender interactions in blood pressure in White Americans
-
B.K. Rana, P.A. Insel, and S.H. Payne et al. Population-based sample reveals gene-gender interactions in blood pressure in White Americans Hypertension 49 2007 96 106
-
(2007)
Hypertension
, vol.49
, pp. 96-106
-
-
Rana, B.K.1
Insel, P.A.2
Payne, S.H.3
-
10
-
-
33845994780
-
Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies
-
J.V. Pearson, M.J. Huentelman, and R. Halperin et al. Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies Am J Hum Genet 80 2007 126 139
-
(2007)
Am J Hum Genet
, vol.80
, pp. 126-139
-
-
Pearson, J.V.1
Huentelman, M.J.2
Halperin, R.3
-
11
-
-
0033759719
-
Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects
-
N.J. Schork, S.K. Nath, D. Fallin, and A. Chakravarti Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects Am J Hum Genet 67 2000 1208 1218
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1208-1218
-
-
Schork, N.J.1
Nath, S.K.2
Fallin, D.3
Chakravarti, A.4
-
12
-
-
9144232544
-
The genetics of coronary heart disease: The contribution of twin studies
-
A. Evans, G.C. Van Baal, and P. McCarron et al. The genetics of coronary heart disease: the contribution of twin studies Twin Res 6 2003 432 441
-
(2003)
Twin Res
, vol.6
, pp. 432-441
-
-
Evans, A.1
Van Baal, G.C.2
McCarron, P.3
-
13
-
-
11244321599
-
Heritability of daytime ambulatory blood pressure in an extended twin design
-
N. Kupper, G. Willemsen, H. Riese, D. Posthuma, D.I. Boomsma, and E.J. de Geus Heritability of daytime ambulatory blood pressure in an extended twin design Hypertension 45 2005 80 85
-
(2005)
Hypertension
, vol.45
, pp. 80-85
-
-
Kupper, N.1
Willemsen, G.2
Riese, H.3
Posthuma, D.4
Boomsma, D.I.5
De Geus, E.J.6
-
14
-
-
0038458878
-
Heritability of blood pressure and hemodynamics in African- and European-American youth
-
H. Snieder, G.A. Harshfield, and F.A. Treiber Heritability of blood pressure and hemodynamics in African- and European-American youth Hypertension 41 2003 1196 1201
-
(2003)
Hypertension
, vol.41
, pp. 1196-1201
-
-
Snieder, H.1
Harshfield, G.A.2
Treiber, F.A.3
-
15
-
-
16244398035
-
Mapping quantitative trait loci using linkage disequilibrium: Marker- versus trait-based methods
-
A. Tenesa, P.M. Visscher, A.D. Carothers, and S.A. Knott Mapping quantitative trait loci using linkage disequilibrium: marker- versus trait-based methods Behav Genet 35 2005 219 228
-
(2005)
Behav Genet
, vol.35
, pp. 219-228
-
-
Tenesa, A.1
Visscher, P.M.2
Carothers, A.D.3
Knott, S.A.4
-
16
-
-
34548202734
-
Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: Discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo
-
F. Rao, L. Zhang, and J. Wessel et al. Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo Circulation 116 2007 993 1006
-
(2007)
Circulation
, vol.116
, pp. 993-1006
-
-
Rao, F.1
Zhang, L.2
Wessel, J.3
-
17
-
-
33646164662
-
Rho kinase polymorphism influences blood pressure and systemic vascular resistance in human twins: Role of heredity
-
T.M. Seasholtz, J. Wessel, and F. Rao et al. Rho kinase polymorphism influences blood pressure and systemic vascular resistance in human twins: role of heredity Hypertension 47 2006 937 947
-
(2006)
Hypertension
, vol.47
, pp. 937-947
-
-
Seasholtz, T.M.1
Wessel, J.2
Rao, F.3
-
18
-
-
37349070985
-
Development and validation of a noninvasive method to estimate cardiac output using cuff sphygmomanometry
-
S.S. Chio, J.J. Tsai, and Y.M. Hsu et al. Development and validation of a noninvasive method to estimate cardiac output using cuff sphygmomanometry Clin Cardiol 30 2007 615 620
-
(2007)
Clin Cardiol
, vol.30
, pp. 615-620
-
-
Chio, S.S.1
Tsai, J.J.2
Hsu, Y.M.3
-
19
-
-
0036628754
-
Early decline in the catecholamine release-inhibitory peptide catestatin in humans at genetic risk of hypertension
-
D.T. O'Connor, M.T. Kailasam, B.P. Kennedy, M.G. Ziegler, N. Yanaihara, and R.J. Parmer Early decline in the catecholamine release-inhibitory peptide catestatin in humans at genetic risk of hypertension J Hypertens 20 2002 1335 1345
-
(2002)
J Hypertens
, vol.20
, pp. 1335-1345
-
-
O'Connor, D.T.1
Kailasam, M.T.2
Kennedy, B.P.3
Ziegler, M.G.4
Yanaihara, N.5
Parmer, R.J.6
-
20
-
-
34247617824
-
Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): Naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension
-
F. Rao, G. Wen, and J.R. Gayen et al. Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension Circulation 115 2007 2271 2281
-
(2007)
Circulation
, vol.115
, pp. 2271-2281
-
-
Rao, F.1
Wen, G.2
Gayen, J.R.3
-
21
-
-
68949191193
-
Neuropeptide Y(1) Receptor NPY1R discovery of naturally occurring human genetic variants governing gene expression in cella as well as pleiotropic effects on autonomic activity and blood pressure in vivo
-
L. Wang, F. Rao, and K. Zhang et al. Neuropeptide Y(1) Receptor NPY1R discovery of naturally occurring human genetic variants governing gene expression in cella as well as pleiotropic effects on autonomic activity and blood pressure in vivo J Am Coll Cardiol 54 2009 944 954
-
(2009)
J Am Coll Cardiol
, vol.54
, pp. 944-954
-
-
Wang, L.1
Rao, F.2
Zhang, K.3
-
22
-
-
44349093638
-
Measurements of secretogranins II, III, v and proconvertases 1/3 and 2 in plasma from patients with neuroendocrine tumours
-
M. Stridsberg, B. Eriksson, and E.T. Janson Measurements of secretogranins II, III, V and proconvertases 1/3 and 2 in plasma from patients with neuroendocrine tumours Regul Pept 148 2008 95 98
-
(2008)
Regul Pept
, vol.148
, pp. 95-98
-
-
Stridsberg, M.1
Eriksson, B.2
Janson, E.T.3
-
23
-
-
0037317663
-
Antihypertensive treatments obscure familial contributions to blood pressure variation
-
J.S. Cui, J.L. Hopper, and S.B. Harrap Antihypertensive treatments obscure familial contributions to blood pressure variation Hypertension 41 2003 207 210
-
(2003)
Hypertension
, vol.41
, pp. 207-210
-
-
Cui, J.S.1
Hopper, J.L.2
Harrap, S.B.3
-
24
-
-
0034657115
-
Genetic analysis of the age at menopause by using estimating equations and Bayesian random effects models
-
K.A. Do, B.M. Broom, and P. Kuhnert et al. Genetic analysis of the age at menopause by using estimating equations and Bayesian random effects models Stat Med 19 2000 1217 1235
-
(2000)
Stat Med
, vol.19
, pp. 1217-1235
-
-
Do, K.A.1
Broom, B.M.2
Kuhnert, P.3
-
25
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
L. Almasy, and J. Blangero Multipoint quantitative-trait linkage analysis in general pedigrees Am J Hum Genet 62 1998 1198 1211
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
26
-
-
0031732094
-
A computer program for aligning a cDNA sequence with a genomic DNA sequence
-
L. Florea, G. Hartzell, Z. Zhang, G.M. Rubin, and W. Miller A computer program for aligning a cDNA sequence with a genomic DNA sequence Genome Res 8 1998 967 974
-
(1998)
Genome Res
, vol.8
, pp. 967-974
-
-
Florea, L.1
Hartzell, G.2
Zhang, Z.3
Rubin, G.M.4
Miller, W.5
-
27
-
-
0030861452
-
Independent and tight regulation of transcriptional units in Escherichia coli via the LacR/O, the TetR/O and AraC/I1-I2 regulatory elements
-
R. Lutz, and H. Bujard Independent and tight regulation of transcriptional units in Escherichia coli via the LacR/O, the TetR/O and AraC/I1-I2 regulatory elements Nucleic Acids Res 25 1997 1203 1210
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 1203-1210
-
-
Lutz, R.1
Bujard, H.2
-
28
-
-
0041657693
-
A transporter of Escherichia coli specific for L- and D-methionine is the prototype for a new family within the ABC superfamily
-
Z. Zhang, J.N. Feige, and A.B. Chang et al. A transporter of Escherichia coli specific for L- and D-methionine is the prototype for a new family within the ABC superfamily Arch Microbiol 180 2003 88 100
-
(2003)
Arch Microbiol
, vol.180
, pp. 88-100
-
-
Zhang, Z.1
Feige, J.N.2
Chang, A.B.3
-
29
-
-
70449266733
-
Plate assay of thiamine. I. Using Kloeckera brevis
-
A. Jones, and M. Finch Plate assay of thiamine. I. Using Kloeckera brevis Appl Microbiol 7 1959 309 311
-
(1959)
Appl Microbiol
, vol.7
, pp. 309-311
-
-
Jones, A.1
Finch, M.2
-
30
-
-
70449325180
-
Plate assay of thiamine. II. Using Lactobacillus fermenti
-
B.J. Hughes, and A. Jones Plate assay of thiamine. II. Using Lactobacillus fermenti Appl Microbiol 7 1959 311 314
-
(1959)
Appl Microbiol
, vol.7
, pp. 311-314
-
-
Hughes, B.J.1
Jones, A.2
-
31
-
-
77954763156
-
Genome-wide allele-specific analysis: Insights into regulatory variation
-
T. Pastinen Genome-wide allele-specific analysis: insights into regulatory variation Nat Rev Genet 11 2010 533 538
-
(2010)
Nat Rev Genet
, vol.11
, pp. 533-538
-
-
Pastinen, T.1
-
32
-
-
70350651269
-
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis
-
B. Ge, D.K. Pokholok, and T. Kwan et al. Global patterns of cis variation in human cells revealed by high-density allelic expression analysis Nat Genet 41 2009 1216 1222
-
(2009)
Nat Genet
, vol.41
, pp. 1216-1222
-
-
Ge, B.1
Pokholok, D.K.2
Kwan, T.3
-
33
-
-
79851479498
-
Global analysis of the impact of environmental perturbation on cis-regulation of gene expression
-
E. Grundberg, V. Adoue, and T. Kwan et al. Global analysis of the impact of environmental perturbation on cis-regulation of gene expression PLoS Genet 7 2011 e1001279
-
(2011)
PLoS Genet
, vol.7
, pp. 1001279
-
-
Grundberg, E.1
Adoue, V.2
Kwan, T.3
-
34
-
-
69549102945
-
A customized and versatile high-density genotyping array for the mouse
-
H. Yang, Y. Ding, and L.N. Hutchins et al. A customized and versatile high-density genotyping array for the mouse Nat Methods 6 2009 663 666
-
(2009)
Nat Methods
, vol.6
, pp. 663-666
-
-
Yang, H.1
Ding, Y.2
Hutchins, L.N.3
-
35
-
-
33750738372
-
Thiamin
-
M.E. Shils, M. Shike, A.C. Ross, B. Caballero, R.J. Cousins, 10th edition Lippincott Williams & Wilkins Baltimore
-
R. Butterworth Thiamin M.E. Shils, M. Shike, A.C. Ross, B. Caballero, R.J. Cousins, Modern Nutrition in Health and Disease 10th edition 2006 Lippincott Williams & Wilkins Baltimore
-
(2006)
Modern Nutrition in Health and Disease
-
-
Butterworth, R.1
-
36
-
-
0028090414
-
Genetic dissection of complex traits
-
E.S. Lander, and N.J. Schork Genetic dissection of complex traits Science 265 1994 2037 2048
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
37
-
-
77952553812
-
Genome-wide case/control studies in hypertension: Only the 'tip of the iceberg'
-
K. Zhang, A.B. Weder, E. Eskin, and D.T. O'Connor Genome-wide case/control studies in hypertension: only the 'tip of the iceberg' J Hypertens 28 2010 1115 1123
-
(2010)
J Hypertens
, vol.28
, pp. 1115-1123
-
-
Zhang, K.1
Weder, A.B.2
Eskin, E.3
O'Connor, D.T.4
-
38
-
-
34248664706
-
Thiamine attenuates the hypertension and metabolic abnormalities in CD36-defective SHR: Uncoupling of glucose oxidation from cellular entry accompanied with enhanced protein O-GlcNAcylation in CD36 deficiency
-
T. Tanaka, K. Sohmiya, and T. Kono et al. Thiamine attenuates the hypertension and metabolic abnormalities in CD36-defective SHR: uncoupling of glucose oxidation from cellular entry accompanied with enhanced protein O-GlcNAcylation in CD36 deficiency Mol Cell Biochem 299 2007 23 35
-
(2007)
Mol Cell Biochem
, vol.299
, pp. 23-35
-
-
Tanaka, T.1
Sohmiya, K.2
Kono, T.3
-
39
-
-
34548083742
-
Whole-genome analysis of sporadic amyotrophic lateral sclerosis
-
T. Dunckley, M.J. Huentelman, and D.W. Craig et al. Whole-genome analysis of sporadic amyotrophic lateral sclerosis N Engl J Med 357 2007 775 788
-
(2007)
N Engl J Med
, vol.357
, pp. 775-788
-
-
Dunckley, T.1
Huentelman, M.J.2
Craig, D.W.3
-
40
-
-
33750334020
-
Common Kibra alleles are associated with human memory performance
-
A. Papassotiropoulos, D.A. Stephan, and M.J. Huentelman et al. Common Kibra alleles are associated with human memory performance Science 314 2006 475 478
-
(2006)
Science
, vol.314
, pp. 475-478
-
-
Papassotiropoulos, A.1
Stephan, D.A.2
Huentelman, M.J.3
-
41
-
-
34147181052
-
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms
-
S. Melquist, D.W. Craig, and M.J. Huentelman et al. Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms Am J Hum Genet 80 2007 769 778
-
(2007)
Am J Hum Genet
, vol.80
, pp. 769-778
-
-
Melquist, S.1
Craig, D.W.2
Huentelman, M.J.3
-
42
-
-
55849139823
-
Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms
-
M. Comabella, D.W. Craig, and M. Camina-Tato et al. Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms PLoS One 3 2008 e3490
-
(2008)
PLoS One
, vol.3
, pp. 3490
-
-
Comabella, M.1
Craig, D.W.2
Camina-Tato, M.3
-
43
-
-
45549095449
-
Common sequence variants on 20q11.22 confer melanoma susceptibility
-
K.M. Brown, S. Macgregor, and G.W. Montgomery et al. Common sequence variants on 20q11.22 confer melanoma susceptibility Nat Genet 40 2008 838 840
-
(2008)
Nat Genet
, vol.40
, pp. 838-840
-
-
Brown, K.M.1
Macgregor, S.2
Montgomery, G.W.3
-
44
-
-
0032990411
-
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness
-
V. Labay, T. Raz, and D. Baron et al. Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness Nat Genet 22 1999 300 304
-
(1999)
Nat Genet
, vol.22
, pp. 300-304
-
-
Labay, V.1
Raz, T.2
Baron, D.3
-
45
-
-
74949104831
-
Biotin-responsive basal ganglia disease in ethnic Europeans with novel SLC19A3 mutations
-
R. Debs, C. Depienne, and A. Rastetter et al. Biotin-responsive basal ganglia disease in ethnic Europeans with novel SLC19A3 mutations Arch Neurol 67 2010 126 130
-
(2010)
Arch Neurol
, vol.67
, pp. 126-130
-
-
Debs, R.1
Depienne, C.2
Rastetter, A.3
-
46
-
-
0028863507
-
Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains
-
M. Pravenec, D. Gauguier, and J.J. Schott et al. Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains J Clin Invest 96 1995 1973 1978
-
(1995)
J Clin Invest
, vol.96
, pp. 1973-1978
-
-
Pravenec, M.1
Gauguier, D.2
Schott, J.J.3
-
47
-
-
33845611513
-
Thiamine (vitamin B1) improves endothelium-dependent vasodilatation in the presence of hyperglycemia
-
S. Arora, A. Lidor, and C.J. Abularrage et al. Thiamine (vitamin B1) improves endothelium-dependent vasodilatation in the presence of hyperglycemia Ann Vasc Surg 20 2006 653 658
-
(2006)
Ann Vasc Surg
, vol.20
, pp. 653-658
-
-
Arora, S.1
Lidor, A.2
Abularrage, C.J.3
-
48
-
-
0017293299
-
Effect of thiamine bromide on cerebral circulation and arterial pressure (an experimental and clinical study)
-
E.V. Romanova, and M.D. Gaevyi [Effect of thiamine bromide on cerebral circulation and arterial pressure (an experimental and clinical study)] Farmakol Toksikol 39 1976 173 176
-
(1976)
Farmakol Toksikol
, vol.39
, pp. 173-176
-
-
Romanova, E.V.1
Gaevyi, M.D.2
-
49
-
-
0030770404
-
The response to treatment of subclinical thiamine deficiency in the elderly
-
T.J. Wilkinson, H.C. Hanger, J. Elmslie, P.M. George, and R. Sainsbury The response to treatment of subclinical thiamine deficiency in the elderly Am J Clin Nutr 66 1997 925 928
-
(1997)
Am J Clin Nutr
, vol.66
, pp. 925-928
-
-
Wilkinson, T.J.1
Hanger, H.C.2
Elmslie, J.3
George, P.M.4
Sainsbury, R.5
-
50
-
-
0033650190
-
Diuretic use: A risk for subclinical thiamine deficiency in elderly patients
-
P.M. Suter, J. Haller, A. Hany, and W. Vetter Diuretic use: a risk for subclinical thiamine deficiency in elderly patients J Nutr Health Aging 4 2000 69 71
-
(2000)
J Nutr Health Aging
, vol.4
, pp. 69-71
-
-
Suter, P.M.1
Haller, J.2
Hany, A.3
Vetter, W.4
-
51
-
-
2542470632
-
Neuroendocrine transcriptome in genetic hypertension: Multiple changes in diverse adrenal physiological systems
-
R.S. Fries, P. Mahboubi, and N.R. Mahapatra et al. Neuroendocrine transcriptome in genetic hypertension: multiple changes in diverse adrenal physiological systems Hypertension 43 2004 1301 1311
-
(2004)
Hypertension
, vol.43
, pp. 1301-1311
-
-
Fries, R.S.1
Mahboubi, P.2
Mahapatra, N.R.3
-
52
-
-
76549133916
-
Global metabolic consequences of the chromogranin A-null model of hypertension: Transcriptomic detection, pathway identification, and experimental verification
-
R.S. Friese, J.R. Gayen, N.R. Mahapatra, G.W. Schmid-Schonbein, D.T. O'Connor, and S.K. Mahata Global metabolic consequences of the chromogranin A-null model of hypertension: transcriptomic detection, pathway identification, and experimental verification Physiol Genomics 40 2010 195 207
-
(2010)
Physiol Genomics
, vol.40
, pp. 195-207
-
-
Friese, R.S.1
Gayen, J.R.2
Mahapatra, N.R.3
Schmid-Schonbein, G.W.4
O'Connor, D.T.5
Mahata, S.K.6
-
53
-
-
84868618810
-
Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome
-
R.S. Friese, C. Ye, and C.M. Nievergelt et al. Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome Circ Cardiovasc Genet 5 2012 430 440
-
(2012)
Circ Cardiovasc Genet
, vol.5
, pp. 430-440
-
-
Friese, R.S.1
Ye, C.2
Nievergelt, C.M.3
-
54
-
-
67649386565
-
Tissue-specific mRNA expression profiles of human solute carrier 35 transporters
-
M. Nishimura, S. Suzuki, T. Satoh, and S. Naito Tissue-specific mRNA expression profiles of human solute carrier 35 transporters Drug Metab Pharmacokinet 24 2009 91 99
-
(2009)
Drug Metab Pharmacokinet
, vol.24
, pp. 91-99
-
-
Nishimura, M.1
Suzuki, S.2
Satoh, T.3
Naito, S.4
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