-
1
-
-
43049097195
-
International Society of Hypertension. Global burden of blood-pressure-related disease, 2001
-
Lawes, C. M. M., Vander Hoorn, S. & Rodgers, A. International Society of Hypertension. Global burden of blood-pressure-related disease, 2001. Lancet 371, 1513–1518 (2008)
-
(2008)
Lancet
, vol.371
, pp. 1513-1518
-
-
Lawes, C.M.M.1
Vander Hoorn, S.2
Rodgers, A.3
-
2
-
-
85010540246
-
Global burden of hypertension and systolic blood pressure of at least 110 to 115 mm Hg, 1990-2015
-
PID: 28097354
-
Forouzanfar, M. H. et al. Global burden of hypertension and systolic blood pressure of at least 110 to 115 mm Hg, 1990-2015. JAMA 317, 165–182 (2017)
-
(2017)
JAMA
, vol.317
, pp. 165-182
-
-
Forouzanfar, M.H.1
-
3
-
-
0037079309
-
Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies
-
PID: 12493255
-
Lewington, S. et al. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet 360, 1903–1913 (2002)
-
(2002)
Lancet
, vol.360
, pp. 1903-1913
-
-
Lewington, S.1
-
4
-
-
85046258129
-
ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA guideline for the prevention, detection, evaluation, and management of high blood pressure in adults: A report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines
-
Whelton, P. K. et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA guideline for the prevention, detection, evaluation, and management of high blood pressure in adults: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J. Am. Coll. Cardiol. 71, e127–e248 (2017)
-
(2017)
J. Am. Coll. Cardiol
, vol.71
, pp. e127-e248
-
-
Whelton, P.K.1
-
5
-
-
85042669063
-
Potential U.S. population impact of the 2017 ACC/AHA high blood pressure guideline
-
PID: 29146532
-
Muntner, P. et al. Potential U.S. population impact of the 2017 ACC/AHA high blood pressure guideline. J. Am. Coll. Cardiol. 71, 109–118 (2018)
-
(2018)
J. Am. Coll. Cardiol.
, vol.71
, pp. 109-118
-
-
Muntner, P.1
-
6
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
International Consortium for Blood Pressure Genome-Wide Association Studies et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 478, 103–109 (2011)
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
-
7
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
COI: 1:CAS:528:DC%2BD1MXls1Cmurk%3D, PID: 19430479
-
Levy, D. et al. Genome-wide association study of blood pressure and hypertension. Nat. Genet. 41, 677–687 (2009)
-
(2009)
Nat. Genet.
, vol.41
, pp. 677-687
-
-
Levy, D.1
-
8
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
COI: 1:CAS:528:DC%2BD1MXls1CmsbY%3D, PID: 19430483
-
Newton-Cheh, C. et al. Genome-wide association study identifies eight loci associated with blood pressure. Nat. Genet. 41, 666–676 (2009)
-
(2009)
Nat. Genet.
, vol.41
, pp. 666-676
-
-
Newton-Cheh, C.1
-
9
-
-
84883824600
-
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
-
COI: 1:CAS:528:DC%2BC3sXhsVWqsbjP, PID: 23972371
-
Franceschini, N. et al. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am. J. Hum. Genet. 93, 545–554 (2013)
-
(2013)
Am. J. Hum. Genet.
, vol.93
, pp. 545-554
-
-
Franceschini, N.1
-
10
-
-
85020170111
-
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
-
PID: 28498854
-
Liang, J. et al. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. PLoS Genet. 13, e1006728 (2017)
-
(2017)
PLoS Genet.
, vol.13
-
-
Liang, J.1
-
11
-
-
85018761807
-
Genome-wide association study meta-analysis of long-term average blood pressure in East Asians
-
COI: 1:CAS:528:DC%2BC2sXmtlamtL4%3D, PID: 28348047
-
Li, C. et al. Genome-wide association study meta-analysis of long-term average blood pressure in East Asians. Circ. Cardiovasc. Genet. 10, e001527 (2017)
-
(2017)
Circ. Cardiovasc. Genet.
, vol.10
-
-
Li, C.1
-
12
-
-
85010952930
-
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
-
COI: 1:CAS:528:DC%2BC2sXhvVeiu7g%3D, PID: 28135244
-
Warren, H. R. et al. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nat. Genet. 49, 403–415 (2017)
-
(2017)
Nat. Genet.
, vol.49
, pp. 403-415
-
-
Warren, H.R.1
-
13
-
-
85028872037
-
Genome-wide association study of blood pressure traits by Hispanic/Latino background: the Hispanic Community Health Study/Study of Latinos
-
PID: 28871152
-
Sofer, T. et al. Genome-wide association study of blood pressure traits by Hispanic/Latino background: the Hispanic Community Health Study/Study of Latinos. Sci. Rep. 7, 10348 (2017)
-
(2017)
Sci. Rep.
, vol.7
-
-
Sofer, T.1
-
14
-
-
68249107559
-
A genome-wide association study of hypertension and blood pressure in African Americans
-
PID: 19609347
-
Adeyemo, A. et al. A genome-wide association study of hypertension and blood pressure in African Americans. PLoS Genet. 5, e1000564 (2009)
-
(2009)
PLoS Genet.
, vol.5
-
-
Adeyemo, A.1
-
15
-
-
84975682930
-
International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents
-
PID: 26969751
-
Parmar, P. G. et al. International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents. Circ. Cardiovasc. Genet. 9, 266–278 (2016)
-
(2016)
Circ. Cardiovasc. Genet.
, vol.9
, pp. 266-278
-
-
Parmar, P.G.1
-
16
-
-
84922421928
-
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
-
COI: 1:CAS:528:DC%2BC2MXhsVOhsL%2FL, PID: 25249183
-
Lu, X. et al. Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. Hum. Mol. Genet. 24, 865–874 (2015)
-
(2015)
Hum. Mol. Genet.
, vol.24
, pp. 865-874
-
-
Lu, X.1
-
17
-
-
84892418762
-
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese
-
COI: 1:CAS:528:DC%2BC3sXhvFyrtL3E, PID: 24165912
-
He, J. et al. Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese. Circ. Cardiovasc. Genet. 6, 598–607 (2013)
-
(2013)
Circ. Cardiovasc. Genet.
, vol.6
, pp. 598-607
-
-
He, J.1
-
18
-
-
79957585975
-
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
-
COI: 1:CAS:528:DC%2BC3MXmtV2hsr0%3D, PID: 21572416
-
Kato, N. et al. Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nat. Genet. 43, 531–538 (2011)
-
(2011)
Nat. Genet.
, vol.43
, pp. 531-538
-
-
Kato, N.1
-
19
-
-
84965118964
-
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
-
COI: 1:CAS:528:DC%2BC2MXhsFersL%2FJ, PID: 26390057
-
Kato, N. et al. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nat. Genet. 47, 1282–1293 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 1282-1293
-
-
Kato, N.1
-
20
-
-
84886434475
-
Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci
-
COI: 1:CAS:528:DC%2BC3sXhs1amt7jP, PID: 24001895
-
Kelly, T. N. et al. Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci. Hypertension 62, 853–859 (2013)
-
(2013)
Hypertension
, vol.62
, pp. 853-859
-
-
Kelly, T.N.1
-
21
-
-
80053383403
-
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
-
COI: 1:CAS:528:DC%2BC3MXhtFGntbfO, PID: 21909110
-
Wain, L. V. et al. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat. Genet. 43, 1005–1011 (2011)
-
(2011)
Nat. Genet.
, vol.43
, pp. 1005-1011
-
-
Wain, L.V.1
-
22
-
-
85032923056
-
New blood pressure-associated loci identified in meta-analyses of 475,000 individuals
-
COI: 1:CAS:528:DC%2BC2sXhs1KqsrjM, PID: 29030403
-
Kraja, A. T. et al. New blood pressure-associated loci identified in meta-analyses of 475,000 individuals. Circ. Cardiovasc. Genet. 10, e001778 (2017)
-
(2017)
Circ. Cardiovasc. Genet.
, vol.10
-
-
Kraja, A.T.1
-
23
-
-
84987670072
-
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
-
COI: 1:CAS:528:DC%2BC28XhsFSgurvJ, PID: 27618447
-
Surendran, P. et al. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat. Genet. 48, 1151–1161 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 1151-1161
-
-
Surendran, P.1
-
24
-
-
84987678196
-
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
-
COI: 1:CAS:528:DC%2BC28XhsFSgurvO, PID: 27618448
-
Liu, C. et al. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nat. Genet. 48, 1162–1170 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 1162-1170
-
-
Liu, C.1
-
25
-
-
85027077950
-
Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney
-
COI: 1:CAS:528:DC%2BC2sXht12iu7fO
-
Wain, L. V. et al. Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney. Hypertension 70, e4–e19 (2017)
-
(2017)
Hypertension
, vol.70
, pp. e4-e19
-
-
Wain, L.V.1
-
26
-
-
84987625495
-
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
-
COI: 1:CAS:528:DC%2BC28XhsFSgurvI, PID: 27618452
-
Ehret, G. B. et al. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat. Genet. 48, 1171–1184 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 1171-1184
-
-
Ehret, G.B.1
-
27
-
-
84995494168
-
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation
-
COI: 1:CAS:528:DC%2BC28XhvVGgtL3L, PID: 27841878
-
Hoffmann, T. J. et al. Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Nat. Genet. 49, 54–64 (2017)
-
(2017)
Nat. Genet.
, vol.49
, pp. 54-64
-
-
Hoffmann, T.J.1
-
28
-
-
84938276507
-
A method to predict the impact of regulatory variants from DNA sequence
-
COI: 1:CAS:528:DC%2BC2MXhtFeju7vM, PID: 26075791
-
Lee, D. et al. A method to predict the impact of regulatory variants from DNA sequence. Nat. Genet. 47, 955–961 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 955-961
-
-
Lee, D.1
-
29
-
-
85000443086
-
Partitioning heritability by functional annotation using genome-wide association summary statistics
-
COI: 1:CAS:528:DC%2BC2MXhsFKqu7rF, PID: 26414678
-
Finucane, H. K. et al. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nat. Genet. 47, 1228–1235 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 1228-1235
-
-
Finucane, H.K.1
-
30
-
-
84922273141
-
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
-
COI: 1:CAS:528:DC%2BC2cXhvVCkurnM, PID: 25439723
-
Gusev, A. et al. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. Am. J. Hum. Genet. 95, 535–552 (2014)
-
(2014)
Am. J. Hum. Genet.
, vol.95
, pp. 535-552
-
-
Gusev, A.1
-
31
-
-
85046840811
-
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
-
PID: 29739930
-
Barbeira, A. N. et al. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Nat. Commun. 9, 1825 (2018)
-
(2018)
Nat. Commun.
, vol.9
-
-
Barbeira, A.N.1
-
32
-
-
84940780615
-
A gene-based association method for mapping traits using reference transcriptome data
-
COI: 1:CAS:528:DC%2BC2MXhtlSnurbM, PID: 26258848
-
Gamazon, E. R. et al. A gene-based association method for mapping traits using reference transcriptome data. Nat. Genet. 47, 1091–1098 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 1091-1098
-
-
Gamazon, E.R.1
-
33
-
-
84959547986
-
Integrative approaches for large-scale transcriptome-wide association studies
-
COI: 1:CAS:528:DC%2BC28Xit1ajtbc%3D, PID: 26854917
-
Gusev, A. et al. Integrative approaches for large-scale transcriptome-wide association studies. Nat. Genet. 48, 245–252 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 245-252
-
-
Gusev, A.1
-
34
-
-
84961927084
-
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets
-
COI: 1:CAS:528:DC%2BC28XkvFGrs7g%3D, PID: 27019110
-
Zhu, Z. et al. Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets. Nat. Genet. 48, 481–487 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 481-487
-
-
Zhu, Z.1
-
35
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
International Consortium for Blood Pressure Genome-Wide Association Studies et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 478, 103–109 (2011)
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
-
36
-
-
84929001104
-
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
-
GTEx Consortium. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans. Science 348, 648–660 (2015)
-
(2015)
Science
, vol.348
, pp. 648-660
-
-
-
37
-
-
85020079716
-
Genetic-variation-driven gene-expression changes highlight genes with important functions for kidney disease
-
COI: 1:CAS:528:DC%2BC2sXpt1ahtbk%3D, PID: 28575649
-
Ko, Y.-A. et al. Genetic-variation-driven gene-expression changes highlight genes with important functions for kidney disease. Am. J. Hum. Genet. 100, 940–953 (2017)
-
(2017)
Am. J. Hum. Genet.
, vol.100
, pp. 940-953
-
-
Ko, Y.A.1
-
38
-
-
84920269464
-
Tissue-based map of the human proteome
-
PID: 25613900
-
Uhlén, M. et al. Tissue-based map of the human proteome. Science 347, 1260419 (2015)
-
(2015)
Science
, vol.347
, pp. 1260419
-
-
Uhlén, M.1
-
39
-
-
84923096381
-
Biological interpretation of genome-wide association studies using predicted gene functions
-
COI: 1:CAS:528:DC%2BC2MXhtF2itrjE, PID: 25597830
-
Pers, T. H. et al. Biological interpretation of genome-wide association studies using predicted gene functions. Nat. Commun. 6, 5890 (2015)
-
(2015)
Nat. Commun.
, vol.6
-
-
Pers, T.H.1
-
40
-
-
85049149885
-
Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
-
COI: 1:CAS:528:DC%2BC1cXht1Cjt7jK, PID: 29955180
-
Gamazon, E. R. et al. Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. Nat. Genet. 50, 956–967 (2018)
-
(2018)
Nat. Genet.
, vol.50
, pp. 956-967
-
-
Gamazon, E.R.1
-
41
-
-
84928945234
-
The role of transforming growth factor β1 in the regulation of blood pressure
-
COI: 1:CAS:528:DC%2BC2MXls1alsb8%3D, PID: 25801626
-
Matsuki, K., Hathaway, C. K., Lawrence, M. G., Smithies, O. & Kakoki, M. The role of transforming growth factor β1 in the regulation of blood pressure. Curr. Hypertens. Rev. 10, 223–238 (2014)
-
(2014)
Curr. Hypertens. Rev.
, vol.10
, pp. 223-238
-
-
Matsuki, K.1
Hathaway, C.K.2
Lawrence, M.G.3
Smithies, O.4
Kakoki, M.5
-
42
-
-
29244453607
-
Neutralization of transforming growth factor-beta attenuates hypertension and prevents renal injury in uremic rats
-
COI: 1:CAS:528:DC%2BD2MXpslCmt74%3D, PID: 16148614
-
Lavoie, P. et al. Neutralization of transforming growth factor-beta attenuates hypertension and prevents renal injury in uremic rats. J. Hypertens. 23, 1895–1903 (2005)
-
(2005)
J. Hypertens.
, vol.23
, pp. 1895-1903
-
-
Lavoie, P.1
-
43
-
-
0028906190
-
Processing of transforming growth factor beta 1 precursor by human furin convertase
-
COI: 1:CAS:528:DyaK2MXlsFKktL8%3D, PID: 7737999
-
Dubois, C. M., Laprise, M. H., Blanchette, F., Gentry, L. E. & Leduc, R. Processing of transforming growth factor beta 1 precursor by human furin convertase. J. Biol. Chem. 270, 10618–10624 (1995)
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 10618-10624
-
-
Dubois, C.M.1
Laprise, M.H.2
Blanchette, F.3
Gentry, L.E.4
Leduc, R.5
-
44
-
-
77955489523
-
Associations between genetic variations in the FURIN gene and hypertension
-
COI: 1:CAS:528:DC%2BC3cXosl2gt7g%3D, PID: 20707915
-
Li, N. et al. Associations between genetic variations in the FURIN gene and hypertension. BMC Med. Genet. 11, 124 (2010)
-
(2010)
BMC Med. Genet.
, vol.11
-
-
Li, N.1
-
45
-
-
85031679412
-
Differential blood pressure effects of ibuprofen, naproxen, and celecoxib in patients with arthritis: the PRECISION-ABPM (Prospective Randomized Evaluation of Celecoxib Integrated Safety Versus Ibuprofen or Naproxen Ambulatory Blood Pressure Measurement) Trial
-
PID: 29020251
-
Ruschitzka, F. et al. Differential blood pressure effects of ibuprofen, naproxen, and celecoxib in patients with arthritis: the PRECISION-ABPM (Prospective Randomized Evaluation of Celecoxib Integrated Safety Versus Ibuprofen or Naproxen Ambulatory Blood Pressure Measurement) Trial. Eur. Heart J. 38, 3282–3292 (2017)
-
(2017)
Eur. Heart J.
, vol.38
, pp. 3282-3292
-
-
Ruschitzka, F.1
-
46
-
-
85018280054
-
Hypertension reduces soluble guanylyl cyclase expression in the mouse aorta via the Notch signaling pathway
-
PID: 28465505
-
Rippe, C. et al. Hypertension reduces soluble guanylyl cyclase expression in the mouse aorta via the Notch signaling pathway. Sci. Rep. 7, 1334 (2017)
-
(2017)
Sci. Rep.
, vol.7
-
-
Rippe, C.1
-
47
-
-
0032029120
-
Vasodilator dysfunction in aged spontaneously hypertensive rats: changes in NO synthase III and soluble guanylyl cyclase expression, and in superoxide anion production
-
COI: 1:CAS:528:DyaK1cXivVKmt7c%3D, PID: 9659462
-
Bauersachs, J. et al. Vasodilator dysfunction in aged spontaneously hypertensive rats: changes in NO synthase III and soluble guanylyl cyclase expression, and in superoxide anion production. Cardiovasc. Res. 37, 772–779 (1998)
-
(1998)
Cardiovasc. Res.
, vol.37
, pp. 772-779
-
-
Bauersachs, J.1
-
48
-
-
0033578898
-
Downregulation of soluble guanylyl cyclase in young and aging spontaneously hypertensive rats
-
COI: 1:CAS:528:DyaK1MXmtFaqs74%3D, PID: 10488056
-
Ruetten, H., Zabel, U., Linz, W. & Schmidt, H. H. Downregulation of soluble guanylyl cyclase in young and aging spontaneously hypertensive rats. Circ. Res. 85, 534–541 (1999)
-
(1999)
Circ. Res.
, vol.85
, pp. 534-541
-
-
Ruetten, H.1
Zabel, U.2
Linz, W.3
Schmidt, H.H.4
-
49
-
-
85034843528
-
Longitudinal changes in mean and pulse pressure, and all-cause mortality: data from 71,629 untreated normotensive individuals
-
PID: 28655182
-
Protogerou, A. D. et al. Longitudinal changes in mean and pulse pressure, and all-cause mortality: data from 71,629 untreated normotensive individuals. Am. J. Hypertens. 30, 1093–1099 (2017)
-
(2017)
Am. J. Hypertens.
, vol.30
, pp. 1093-1099
-
-
Protogerou, A.D.1
-
50
-
-
77954926988
-
Is pulse pressure a predictor of new-onset diabetes in high-risk hypertensive patients?
-
PID: 20185746
-
Yasuno, S. et al. Is pulse pressure a predictor of new-onset diabetes in high-risk hypertensive patients? Diabetes Care 33, 1122–1127 (2010)
-
(2010)
Diabetes Care
, vol.33
, pp. 1122-1127
-
-
Yasuno, S.1
-
51
-
-
85040935682
-
Relationship of arterial stiffness index and pulse pressure with cardiovascular disease and mortality
-
PID: 29358193
-
Said, M. A., Eppinga, R. N., Lipsic, E., Verweij, N. & van der Harst, P. Relationship of arterial stiffness index and pulse pressure with cardiovascular disease and mortality. J. Am. Heart Assoc. 7, e007621 (2018)
-
(2018)
J. Am. Heart Assoc.
, vol.7
-
-
Said, M.A.1
Eppinga, R.N.2
Lipsic, E.3
Verweij, N.4
van der Harst, P.5
-
52
-
-
84920911189
-
Arterial stiffness in diabetes mellitus
-
COI: 1:CAS:528:DC%2BC2cXitFygtL3J, PID: 25558032
-
Prenner, S. B. & Chirinos, J. A. Arterial stiffness in diabetes mellitus. Atherosclerosis 238, 370–379 (2015)
-
(2015)
Atherosclerosis
, vol.238
, pp. 370-379
-
-
Prenner, S.B.1
Chirinos, J.A.2
-
53
-
-
84969784596
-
Diabetes and risk of arterial stiffness: a Mendelian randomization analysis
-
COI: 1:CAS:528:DC%2BC28XhslWnsrzP, PID: 26953161
-
Xu, M. et al. Diabetes and risk of arterial stiffness: a Mendelian randomization analysis. Diabetes 65, 1731–1740 (2016)
-
(2016)
Diabetes
, vol.65
, pp. 1731-1740
-
-
Xu, M.1
-
54
-
-
85048705188
-
Serum proteomic profiling to identify biomarkers of premature carotid atherosclerosis
-
PID: 29907817
-
Bhosale, S. D. et al. Serum proteomic profiling to identify biomarkers of premature carotid atherosclerosis. Sci. Rep. 8, 9209 (2018)
-
(2018)
Sci. Rep.
, vol.8
-
-
Bhosale, S.D.1
-
55
-
-
84886473216
-
Association between CDH13 variants and cardiometabolic and vascular phenotypes in a Korean population
-
COI: 1:CAS:528:DC%2BC3sXhvVGrt73P, PID: 24142632
-
Lee, J. H. et al. Association between CDH13 variants and cardiometabolic and vascular phenotypes in a Korean population. Yonsei. Med. J. 54, 1305–1312 (2013)
-
(2013)
Yonsei. Med. J.
, vol.54
, pp. 1305-1312
-
-
Lee, J.H.1
-
56
-
-
84966930058
-
Genetic and environmental risk factors for atherosclerosis regulate transcription of phosphatase and actin regulating gene PHACTR1
-
COI: 1:CAS:528:DC%2BC28XnvFOmsbo%3D, PID: 27187934
-
Reschen, M. E., Lin, D., Chalisey, A., Soilleux, E. J. & O’Callaghan, C. A. Genetic and environmental risk factors for atherosclerosis regulate transcription of phosphatase and actin regulating gene PHACTR1. Atherosclerosis 250, 95–105 (2016)
-
(2016)
Atherosclerosis
, vol.250
, pp. 95-105
-
-
Reschen, M.E.1
Lin, D.2
Chalisey, A.3
Soilleux, E.J.4
O’Callaghan, C.A.5
-
57
-
-
84942088211
-
Disruption of phactr-1 pathway triggers pro-inflammatory and pro-atherogenic factors: new insights in atherosclerosis development
-
COI: 1:CAS:528:DC%2BC2MXhsVyjtL7J, PID: 26362351
-
Jarray, R. et al. Disruption of phactr-1 pathway triggers pro-inflammatory and pro-atherogenic factors: new insights in atherosclerosis development. Biochimie 118, 151–161 (2015)
-
(2015)
Biochimie
, vol.118
, pp. 151-161
-
-
Jarray, R.1
-
58
-
-
23444452249
-
Folic acid supplementation for 3 wk reduces pulse pressure and large artery stiffness independent of MTHFR genotype
-
COI: 1:CAS:528:DC%2BD2MXmsVSgsr4%3D, PID: 16002796
-
Williams, C., Kingwell, B. A., Burke, K., McPherson, J. & Dart, A. M. Folic acid supplementation for 3 wk reduces pulse pressure and large artery stiffness independent of MTHFR genotype. Am. J. Clin. Nutr. 82, 26–31 (2005)
-
(2005)
Am. J. Clin. Nutr.
, vol.82
, pp. 26-31
-
-
Williams, C.1
Kingwell, B.A.2
Burke, K.3
McPherson, J.4
Dart, A.M.5
-
59
-
-
0037657585
-
The interaction between MTHFR 677 C→T genotype and folate status is a determinant of coronary atherosclerosis risk
-
COI: 1:CAS:528:DC%2BD3sXjs1Oqtrk%3D, PID: 12730410
-
Girelli, D. et al. The interaction between MTHFR 677 C→T genotype and folate status is a determinant of coronary atherosclerosis risk. J. Nutr. 133, 1281–1285 (2003)
-
(2003)
J. Nutr.
, vol.133
, pp. 1281-1285
-
-
Girelli, D.1
-
60
-
-
84901808693
-
Blood pressure and incidence of twelve cardiovascular diseases: lifetime risks, healthy life-years lost, and age-specific associations in 1·25 million people
-
PID: 24881994
-
Rapsomaniki, E. et al. Blood pressure and incidence of twelve cardiovascular diseases: lifetime risks, healthy life-years lost, and age-specific associations in 1·25 million people. Lancet 383, 1899–1911 (2014)
-
(2014)
Lancet
, vol.383
, pp. 1899-1911
-
-
Rapsomaniki, E.1
-
61
-
-
0031021409
-
Relaxin: a pleiotropic hormone
-
COI: 1:CAS:528:DyaK2sXltVc%3D, PID: 9112071
-
Bani, D. Relaxin: a pleiotropic hormone. Gen. Pharmacol. 28, 13–22 (1997)
-
(1997)
Gen. Pharmacol.
, vol.28
, pp. 13-22
-
-
Bani, D.1
-
62
-
-
77958522823
-
Relaxin: a new approach for the treatment of acute congestive heart failure
-
PID: 20926940
-
Grossman, J. & Frishman, W. H. Relaxin: a new approach for the treatment of acute congestive heart failure. Cardiol. Rev. 18, 305–312 (2010)
-
(2010)
Cardiol. Rev.
, vol.18
, pp. 305-312
-
-
Grossman, J.1
Frishman, W.H.2
-
63
-
-
70449113183
-
Relaxin, a pleiotropic vasodilator for the treatment of heart failure
-
COI: 1:CAS:528:DC%2BD1MXhtlKju73O, PID: 19101795
-
Teichman, S. L. et al. Relaxin, a pleiotropic vasodilator for the treatment of heart failure. Heart. Fail. Rev. 14, 321–329 (2009)
-
(2009)
Heart. Fail. Rev.
, vol.14
, pp. 321-329
-
-
Teichman, S.L.1
-
64
-
-
65249190276
-
Relaxin for the treatment of patients with acute heart failure (Pre-RELAX-AHF): a multicentre, randomised, placebo-controlled, parallel-group, dose-finding phase IIb study
-
COI: 1:CAS:528:DC%2BD1MXltVCqtbk%3D, PID: 19329178
-
Teerlink, J. R. et al. Relaxin for the treatment of patients with acute heart failure (Pre-RELAX-AHF): a multicentre, randomised, placebo-controlled, parallel-group, dose-finding phase IIb study. Lancet 373, 1429–1439 (2009)
-
(2009)
Lancet
, vol.373
, pp. 1429-1439
-
-
Teerlink, J.R.1
-
65
-
-
84872314588
-
Relaxin family peptides and their receptors
-
COI: 1:CAS:528:DC%2BC3sXhvFKnsL8%3D, PID: 23303914
-
Bathgate, Ra. D. et al. Relaxin family peptides and their receptors. Physiol. Rev. 93, 405–480 (2013)
-
(2013)
Physiol. Rev.
, vol.93
, pp. 405-480
-
-
Bathgate, R.D.1
-
66
-
-
0031584835
-
Cloning and expression of the adenosine kinase gene from rat and human tissues
-
COI: 1:CAS:528:DyaK2sXhsFWkt7w%3D, PID: 9070863
-
McNally, T. et al. Cloning and expression of the adenosine kinase gene from rat and human tissues. Biochem. Biophys. Res. Commun. 231, 645–650 (1997)
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.231
, pp. 645-650
-
-
McNally, T.1
-
67
-
-
0030847083
-
Adenosine and adenosine receptors in the cardiovascular system: biochemistry, physiology, and pharmacology
-
COI: 1:CAS:528:DyaK2sXltFChtro%3D, PID: 9223356
-
Shryock, J. C. & Belardinelli, L. Adenosine and adenosine receptors in the cardiovascular system: biochemistry, physiology, and pharmacology. Am. J. Cardiol. 79, 2–10 (1997)
-
(1997)
Am. J. Cardiol.
, vol.79
, pp. 2-10
-
-
Shryock, J.C.1
Belardinelli, L.2
-
68
-
-
0023358574
-
Cardiac effects of adenosine. Mechanism of action, pathophysiologic and clinical significance
-
PID: 2441109
-
Böhm, M. Cardiac effects of adenosine. Mechanism of action, pathophysiologic and clinical significance. Klin. Wochenschr. 65, 487–499 (1987)
-
(1987)
Klin. Wochenschr.
, vol.65
, pp. 487-499
-
-
Böhm, M.1
-
69
-
-
84900431481
-
Low coronary microcirculatory resistance associated with profound hypotension during intravenous adenosine infusion: implications for the functional assessment of coronary stenoses
-
PID: 24399244
-
Echavarría-Pinto, M. et al. Low coronary microcirculatory resistance associated with profound hypotension during intravenous adenosine infusion: implications for the functional assessment of coronary stenoses. Circ. Cardiovasc. Interv. 7, 35–42 (2014)
-
(2014)
Circ. Cardiovasc. Interv.
, vol.7
, pp. 35-42
-
-
Echavarría-Pinto, M.1
-
70
-
-
0026417567
-
Adenosine and supraventricular tachycardia
-
COI: 1:STN:280:DyaK38%2FkvFKjsg%3D%3D, PID: 1944450
-
Camm, A. J. & Garratt, C. J. Adenosine and supraventricular tachycardia. N. Engl. J. Med. 325, 1621–1629 (1991)
-
(1991)
N. Engl. J. Med.
, vol.325
, pp. 1621-1629
-
-
Camm, A.J.1
Garratt, C.J.2
-
71
-
-
0033760331
-
The effect of adenosine on blood pressure variability in sinoaortic denervated rats is mediated by adenosine A2a-receptor
-
COI: 1:CAS:528:DC%2BD3cXnslKjsLs%3D, PID: 11065230
-
Shen, F. M. & Su, D. F. The effect of adenosine on blood pressure variability in sinoaortic denervated rats is mediated by adenosine A2a-receptor. J. Cardiovasc. Pharmacol. 36, 681–686 (2000)
-
(2000)
J. Cardiovasc. Pharmacol.
, vol.36
, pp. 681-686
-
-
Shen, F.M.1
Su, D.F.2
-
72
-
-
84930065286
-
PDE3A mutations cause autosomal dominant hypertension with brachydactyly
-
COI: 1:CAS:528:DC%2BC2MXht1Wltb7F, PID: 25961942
-
Maass, P. G. et al. PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nat. Genet. 47, 647–653 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 647-653
-
-
Maass, P.G.1
-
73
-
-
84930067097
-
Hypertension linked to PDE3A activation
-
COI: 1:CAS:528:DC%2BC2MXht1WltLfE, PID: 26018892
-
Houslay, M. Hypertension linked to PDE3A activation. Nat. Genet. 47, 562–563 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 562-563
-
-
Houslay, M.1
-
74
-
-
6844242322
-
A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly
-
COI: 1:CAS:528:DyaK1cXnsFCitg%3D%3D, PID: 9453014
-
Schuster, H. et al. A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly. Kidney Int. 53, 167–172 (1998)
-
(1998)
Kidney Int.
, vol.53
, pp. 167-172
-
-
Schuster, H.1
-
75
-
-
17544388677
-
Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly
-
COI: 1:STN:280:DyaK2svkvVKqtw%3D%3D, PID: 9303020
-
Naraghi, R. et al. Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly. Stroke 28, 1749–1754 (1997)
-
(1997)
Stroke
, vol.28
, pp. 1749-1754
-
-
Naraghi, R.1
-
76
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
-
COI: 1:CAS:528:DC%2BC3MXivVSntLg%3D, PID: 21378990
-
Schunkert, H. et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat. Genet. 43, 333–338 (2011)
-
(2011)
Nat. Genet.
, vol.43
, pp. 333-338
-
-
Schunkert, H.1
-
77
-
-
0026693041
-
The human gene encoding acetylcholinesterase is located on the long arm of chromosome 7
-
COI: 1:CAS:528:DyaK38XlsVClsrk%3D, PID: 1609795
-
Getman, D. K., Eubanks, J. H., Camp, S., Evans, G. A. & Taylor, P. The human gene encoding acetylcholinesterase is located on the long arm of chromosome 7. Am. J. Hum. Genet. 51, 170–177 (1992)
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 170-177
-
-
Getman, D.K.1
Eubanks, J.H.2
Camp, S.3
Evans, G.A.4
Taylor, P.5
-
78
-
-
0141674889
-
Acetylcholinesterase inhibition: a novel approach in the treatment of neurogenic orthostatic hypotension
-
COI: 1:STN:280:DC%2BD3szps1WqtQ%3D%3D, PID: 12933939
-
Singer, W. et al. Acetylcholinesterase inhibition: a novel approach in the treatment of neurogenic orthostatic hypotension. J. Neurol. Neurosurg. Psychiatry 74, 1294–1298 (2003)
-
(2003)
J. Neurol. Neurosurg. Psychiatry
, vol.74
, pp. 1294-1298
-
-
Singer, W.1
-
79
-
-
79953104103
-
Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster
-
Del Greco, M. F. et al. Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. Hum. Mol. Genet. 20, 1660–1671 (2011)
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 1660-1671
-
-
Del Greco, M.F.1
-
80
-
-
84888132259
-
Identifying multiple causative genes at a single GWAS locus
-
COI: 1:CAS:528:DC%2BC3sXhvFCisLvM, PID: 24006081
-
Flister, M. J. et al. Identifying multiple causative genes at a single GWAS locus. Genome Res. 23, 1996–2002 (2013)
-
(2013)
Genome Res.
, vol.23
, pp. 1996-2002
-
-
Flister, M.J.1
-
81
-
-
61749091170
-
Natriuretic peptides: Their structures, receptors, physiologic functions and therapeutic applications
-
Potter, L. R., Yoder, A. R., Flora, D. R., Antos, L. K. & Dickey, D. M. Natriuretic peptides: their structures, receptors, physiologic functions and therapeutic applications. Handb. Exp. Pharmacol. 341–366 (2009)
-
(2009)
Handb. Exp. Pharmacol.
, pp. 341-366
-
-
Potter, L.R.1
Yoder, A.R.2
Flora, D.R.3
Antos, L.K.4
Dickey, D.M.5
-
82
-
-
0029589606
-
ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family
-
COI: 1:CAS:528:DyaK2MXhtVSgtr7J, PID: 8543009
-
Brandt, S. & Jentsch, T. J. ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family. FEBS Lett. 377, 15–20 (1995)
-
(1995)
FEBS Lett.
, vol.377
, pp. 15-20
-
-
Brandt, S.1
Jentsch, T.J.2
-
84
-
-
78149265272
-
Robust relationship inference in genome-wide association studies
-
COI: 1:CAS:528:DC%2BC3cXhsVSlt7bK, PID: 20926424
-
Manichaikul, A. et al. Robust relationship inference in genome-wide association studies. Bioinformatics 26, 2867–2873 (2010)
-
(2010)
Bioinformatics
, vol.26
, pp. 2867-2873
-
-
Manichaikul, A.1
-
85
-
-
84943171338
-
A global reference for human genetic variation
-
PID: 4750478
-
The 1000 Genomes Project Consortium. A global reference for human genetic variation. Nature 526, 68–74 (2015)
-
(2015)
Nature
, vol.526
, pp. 68-74
-
-
-
86
-
-
84989838868
-
Reference-based phasing using the Haplotype Reference Consortium panel
-
COI: 1:CAS:528:DC%2BC28Xhs1SltLzF, PID: 27694958
-
Loh, P.-R. et al. Reference-based phasing using the Haplotype Reference Consortium panel. Nat. Genet. 48, 1443–1448 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 1443-1448
-
-
Loh, P.R.1
-
87
-
-
84984598118
-
Next-generation genotype imputation service and methods
-
COI: 1:CAS:528:DC%2BC28XhsVWksL%2FK, PID: 27571263
-
Das, S. et al. Next-generation genotype imputation service and methods. Nat. Genet. 48, 1284–1287 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 1284-1287
-
-
Das, S.1
-
88
-
-
84899513456
-
Fast principal component analysis of large-scale genome-wide data
-
PID: 24718290
-
Abraham, G. & Inouye, M. Fast principal component analysis of large-scale genome-wide data. PLoS One 9, e93766 (2014)
-
(2014)
PLoS One
, vol.9
-
-
Abraham, G.1
Inouye, M.2
-
89
-
-
6544294068
-
Effect of pain and nonsteroidal analgesics on blood pressure
-
COI: 1:STN:280:DC%2BD3c%2FntlaktQ%3D%3D, PID: 10605351, 29
-
Chawla, P. S. & Kochar, M. S. Effect of pain and nonsteroidal analgesics on blood pressure. WMJ 98, 22–25 (1999). 29
-
(1999)
WMJ
, vol.98
, pp. 22-25
-
-
Chawla, P.S.1
Kochar, M.S.2
-
90
-
-
0025650953
-
Cardiovascular and sensory responses to forearm ischemia and dynamic hand exercise
-
COI: 1:STN:280:DyaK3M%2FotlSqsg%3D%3D, PID: 2260726
-
Maixner, W., Gracely, R. H., Zuniga, J. R., Humphrey, C. B. & Bloodworth, G. R. Cardiovascular and sensory responses to forearm ischemia and dynamic hand exercise. Am. J. Physiol. 259, R1156–R1163 (1990)
-
(1990)
Am. J. Physiol.
, vol.259
, pp. R1156-R1163
-
-
Maixner, W.1
Gracely, R.H.2
Zuniga, J.R.3
Humphrey, C.B.4
Bloodworth, G.R.5
-
91
-
-
84954053117
-
A genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction
-
COI: 1:CAS:528:DC%2BC28XnsFOluw%3D%3D, PID: 26752167
-
Taylor, J. Y. et al. A genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction. Sci. Rep. 6, 18812 (2016)
-
(2016)
Sci. Rep.
, vol.6
-
-
Taylor, J.Y.1
-
92
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
COI: 1:CAS:528:DC%2BD2sXmvFKlsLY%3D, PID: 17572673
-
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. 39, 906–913 (2007)
-
(2007)
Nat. Genet.
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
93
-
-
84923946495
-
LD score regression distinguishes confounding from polygenicity in genome-wide association studies
-
COI: 1:CAS:528:DC%2BC2MXhvFCntb8%3D, PID: 25642630
-
Bulik-Sullivan, B. K. et al. LD score regression distinguishes confounding from polygenicity in genome-wide association studies. Nat. Genet. 47, 291–295 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 291-295
-
-
Bulik-Sullivan, B.K.1
-
94
-
-
77955894071
-
METAL: fast and efficient meta-analysis of genomewide association scans
-
COI: 1:CAS:528:DC%2BC3cXhtVGru73F, PID: 20616382
-
Willer, C. J., Li, Y. & Abecasis, G. R. METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26, 2190–2191 (2010)
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
95
-
-
78650856517
-
GCTA: a tool for genome-wide complex trait analysis
-
COI: 1:CAS:528:DC%2BC3MXktVejtg%3D%3D, PID: 21167468
-
Yang, J., Lee, S. H., Goddard, M. E. & Visscher, P. M. GCTA: a tool for genome-wide complex trait analysis. Am. J. Hum. Genet. 88, 76–82 (2011)
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 76-82
-
-
Yang, J.1
Lee, S.H.2
Goddard, M.E.3
Visscher, P.M.4
-
96
-
-
77952822074
-
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations
-
COI: 1:CAS:528:DC%2BC3cXlt1equ7w%3D, PID: 20335276
-
Denny, J. C. et al. PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations. Bioinformatics 26, 1205–1210 (2010)
-
(2010)
Bioinformatics
, vol.26
, pp. 1205-1210
-
-
Denny, J.C.1
-
97
-
-
84906273890
-
PheWAS: data analysis and plotting tools for phenome-wide association studies in the Renvironment
-
COI: 1:CAS:528:DC%2BC2cXhtlSrtbbO, PID: 24733291
-
Carroll, R. J., Bastarache, L. & Denny, J. C. R. PheWAS: data analysis and plotting tools for phenome-wide association studies in the Renvironment. Bioinformatics 30, 2375–2376 (2014)
-
(2014)
Bioinformatics
, vol.30
, pp. 2375-2376
-
-
Carroll, R.J.1
Bastarache, L.2
Denny, J.C.R.3
-
98
-
-
84979503522
-
The SIDER database of drugs and side effects
-
COI: 1:CAS:528:DC%2BC2sXhtV2gu7fK, PID: 26481350
-
Kuhn, M., Letunic, I., Jensen, L. J. & Bork, P. The SIDER database of drugs and side effects. Nucleic Acids Res. 44, D1075–D1079 (2016)
-
(2016)
Nucleic Acids Res.
, vol.44
, pp. D1075-D1079
-
-
Kuhn, M.1
Letunic, I.2
Jensen, L.J.3
Bork, P.4
-
99
-
-
84893076281
-
Lessons learned from developing a drug evidence base to support pharmacovigilance
-
COI: 1:STN:280:DC%2BC2czosleqsw%3D%3D, PID: 24454585
-
Smith, J. C. et al. Lessons learned from developing a drug evidence base to support pharmacovigilance. Appl. Clin. Inform. 4, 596–617 (2013)
-
(2013)
Appl. Clin. Inform.
, vol.4
, pp. 596-617
-
-
Smith, J.C.1
-
100
-
-
85070670869
-
DGIdb 3.0: a redesign and expansion of the drug-gene interaction database
-
Cotto, K. C. et al. DGIdb 3.0: a redesign and expansion of the drug-gene interaction database. Nucleic Acids Res. 46, D1068–D1073 (2017)
-
(2017)
Nucleic Acids Res.
, vol.46
, pp. D1068-D1073
-
-
Cotto, K.C.1
-
101
-
-
85040867496
-
Therapeutic target database update 2018: enriched resource for facilitating bench-to-clinic research of targeted therapeutics
-
COI: 1:CAS:528:DC%2BC1cXitlGitr%2FI, PID: 29140520
-
Li, Y. H. et al. Therapeutic target database update 2018: enriched resource for facilitating bench-to-clinic research of targeted therapeutics. Nucleic Acids Res. 46, D1121–D1127 (2018)
-
(2018)
Nucleic Acids Res.
, vol.46
, pp. D1121-D1127
-
-
Li, Y.H.1
|