-
1
-
-
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
-
Prospective Studies Collaboration Prospective Studies Collaboration
-
Lewington S, Clarke R, Qizilbash N, Peto R, Collins R, Prospective Studies Collaboration Prospective Studies Collaboration 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 2002 360 1903 1913
-
(2002)
Lancet
, vol.360
, pp. 1903-1913
-
-
Lewington, S.1
Clarke, R.2
Qizilbash, N.3
Peto, R.4
Collins, R.5
-
2
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
International Consortium for Blood Pressure Genome-Wide Association Studies International Consortium for Blood Pressure Genome-Wide Association Studies
-
Ehret GB, Munroe PB, Rice KM, International Consortium for Blood Pressure Genome-Wide Association Studies International Consortium for Blood Pressure Genome-Wide Association Studies Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 2011 478 103 109. doi: 10.1038/nature10405.
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
Ehret, G.B.1
Munroe, P.B.2
Rice, K.M.3
-
3
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
Levy D, Ehret GB, Rice K, Genome-wide association study of blood pressure and hypertension. Nat Genet 2009 41 677 687. doi: 10.1038/ng.384.
-
(2009)
Nat Genet
, vol.41
, pp. 677-687
-
-
Levy, D.1
Ehret, G.B.2
Rice, K.3
-
4
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
Wellcome Trust Case Control Consortium Wellcome Trust Case Control Consortium
-
Newton-Cheh C, Johnson T, Gateva V, Wellcome Trust Case Control Consortium Wellcome Trust Case Control Consortium Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 2009 41 666 676. doi: 10.1038/ng.361.
-
(2009)
Nat Genet
, vol.41
, pp. 666-676
-
-
Newton-Cheh, C.1
Johnson, T.2
Gateva, V.3
-
5
-
-
77951596418
-
Genetic association between intronic variants in AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10
-
Gomez-Rubio P, Meza-Montenegro MM, Cantu-Soto E, Klimecki WT., Genetic association between intronic variants in AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10. J Appl Toxicol 2010 30 260 270. doi: 10.1002/jat.1492.
-
(2010)
J Appl Toxicol
, vol.30
, pp. 260-270
-
-
Gomez-Rubio, P.1
Meza-Montenegro, M.M.2
Cantu-Soto, E.3
Klimecki, W.T.4
-
6
-
-
82955235575
-
Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in She ethnic minority of China
-
Lin Y, Lai X, Chen B, Xu Y, Huang B, Chen Z, Zhu S, Yao J, Jiang Q, Huang H, Wen J, Chen G., Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in She ethnic minority of China. Atherosclerosis 2011 219 709 714. doi: 10.1016/j.atherosclerosis.2011.09.006.
-
(2011)
Atherosclerosis
, vol.219
, pp. 709-714
-
-
Lin, Y.1
Lai, X.2
Chen, B.3
Xu, Y.4
Huang, B.5
Chen, Z.6
Zhu, S.7
Yao, J.8
Jiang, Q.9
Huang, H.10
Wen, J.11
Chen, G.12
-
7
-
-
78650810665
-
Common variants in or near FGF5, CYP17A1 and MTHFR genes are associated with blood pressure and hypertension in Chinese Hans
-
Liu C, Li H, Qi Q, Lu L, Gan W, Loos RJ, Lin X., Common variants in or near FGF5, CYP17A1 and MTHFR genes are associated with blood pressure and hypertension in Chinese Hans. J Hypertens 2011 29 70 75. doi: 10.1097/HJH.0b013e32833f60ab.
-
(2011)
J Hypertens
, vol.29
, pp. 70-75
-
-
Liu, C.1
Li, H.2
Qi, Q.3
Lu, L.4
Gan, W.5
Loos, R.J.6
Lin, X.7
-
8
-
-
84872687202
-
Recapitulation of four hypertension susceptibility genes (CSK, CYP17A1, MTHFR, and FGF5) in East Asians
-
Xi B, Shen Y, Reilly KH, Wang X, Mi J., Recapitulation of four hypertension susceptibility genes (CSK, CYP17A1, MTHFR, and FGF5) in East Asians. Metabolism 2013 62 196 203. doi: 10.1016/j.metabol.2012.07.008.
-
(2013)
Metabolism
, vol.62
, pp. 196-203
-
-
Xi, B.1
Shen, Y.2
Reilly, K.H.3
Wang, X.4
Mi, J.5
-
9
-
-
77954163950
-
Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean population
-
Hong KW, Jin HS, Lim JE, Kim S, Go MJ, Oh B., Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean population. J Hum Genet 2010 55 336 341. doi: 10.1038/jhg.2010.31.
-
(2010)
J Hum Genet
, vol.55
, pp. 336-341
-
-
Hong, K.W.1
Jin, H.S.2
Lim, J.E.3
Kim, S.4
Go, M.J.5
Oh, B.6
-
10
-
-
84938333022
-
A single nucleotide polymorphism near the CYP17A1 gene is associated with left ventricular mass in hypertensive patients under pharmacotherapy
-
Huber M, Lezius S, Reibis R, Treszl A, Kujawinska D, Jakob S, Wegscheider K, Völler H, Kreutz R., A single nucleotide polymorphism near the CYP17A1 gene is associated with left ventricular mass in hypertensive patients under pharmacotherapy. Int J Mol Sci 2015 16 17456 17468. doi: 10.3390/ijms160817456.
-
(2015)
Int J Mol Sci
, vol.16
, pp. 17456-17468
-
-
Huber, M.1
Lezius, S.2
Reibis, R.3
Treszl, A.4
Kujawinska, D.5
Jakob, S.6
Wegscheider, K.7
Völler, H.8
Kreutz, R.9
-
11
-
-
79951665862
-
The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders
-
Miller WL, Auchus RJ., The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. Endocr Rev 2011 32 81 151. doi: 10.1210/er.2010-0013.
-
(2011)
Endocr Rev
, vol.32
, pp. 81-151
-
-
Miller, W.L.1
Auchus, R.J.2
-
12
-
-
18844367746
-
Minireview: Regulation of steroidogenesis by electron transfer
-
Miller WL., Minireview: regulation of steroidogenesis by electron transfer. Endocrinology 2005 146 2544 2550. doi: 10.1210/en.2005-0096.
-
(2005)
Endocrinology
, vol.146
, pp. 2544-2550
-
-
Miller, W.L.1
-
13
-
-
84962554401
-
CYP17A1 enzyme activity is linked to ambulatory blood pressure in a family-based population study
-
published online ahead of print August 20, 2015]. Accessed February 12, 2016
-
Ackermann D, Pruijm M, Ponte B, CYP17A1 enzyme activity is linked to ambulatory blood pressure in a family-based population study [published online ahead of print August 20, 2015]. Am J Hypertens. doi: 10.1093/ajh/hpv138. http://ajh.oxfordjournals.org/content/early/2015/08/19/ajh.hpv138. Accessed February 12, 2016
-
Am J Hypertens
-
-
Ackermann, D.1
Pruijm, M.2
Ponte, B.3
-
14
-
-
0013979505
-
17-hydroxylation deficiency in man
-
Biglieri EG, Herron MA, Brust N., 17-hydroxylation deficiency in man. J Clin Invest 1966 45 1946 1954. doi: 10.1172/JCI105499.
-
(1966)
J Clin Invest
, vol.45
, pp. 1946-1954
-
-
Biglieri, E.G.1
Herron, M.A.2
Brust, N.3
-
15
-
-
66149160385
-
Genetics of congenital adrenal hyperplasia
-
Krone N, Arlt W., Genetics of congenital adrenal hyperplasia. Best Pract Res Clin Endocrinol Metab 2009 23 181 192. doi: 10.1016/j.beem.2008.10.014.
-
(2009)
Best Pract Res Clin Endocrinol Metab
, vol.23
, pp. 181-192
-
-
Krone, N.1
Arlt, W.2
-
16
-
-
84863720397
-
APEX1 regulation of aldosterone synthase gene transcription is disrupted by a common polymorphism in humans
-
McManus F, Sands W, Diver L, MacKenzie SM, Fraser R, Davies E, Connell JM., APEX1 regulation of aldosterone synthase gene transcription is disrupted by a common polymorphism in humans. Circ Res 2012 111 212 219. doi: 10.1161/CIRCRESAHA.111.262931.
-
(2012)
Circ Res
, vol.111
, pp. 212-219
-
-
McManus, F.1
Sands, W.2
Diver, L.3
MacKenzie, S.M.4
Fraser, R.5
Davies, E.6
Connell, J.M.7
-
17
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ., Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005 21 263 265. doi: 10.1093/bioinformatics/bth457.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
18
-
-
33847644921
-
Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency
-
Barr M, MacKenzie SM, Friel EC, Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency. Hypertension 2007 49 113 119. doi: 10.1161/01.HYP.0000249904.93940.7a.
-
(2007)
Hypertension
, vol.49
, pp. 113-119
-
-
Barr, M.1
MacKenzie, S.M.2
Friel, E.C.3
-
19
-
-
0038375052
-
Genome-wide mapping of human loci for essential hypertension
-
MRC British Genetics of Hypertension Study MRC British Genetics of Hypertension Study
-
Caulfield M, Munroe P, Pembroke J, MRC British Genetics of Hypertension Study MRC British Genetics of Hypertension Study Genome-wide mapping of human loci for essential hypertension. Lancet 2003 361 2118 2123. doi: 10.1016/S0140-6736(03)13722-1.
-
(2003)
Lancet
, vol.361
, pp. 2118-2123
-
-
Caulfield, M.1
Munroe, P.2
Pembroke, J.3
-
20
-
-
36248979113
-
Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: Data from the MRC BRIGHT Study
-
Freel EM, Ingram M, Friel EC, Fraser R, Brown M, Samani NJ, Caulfield M, Munroe P, Farrall M, Webster J, Clayton D, Dominiczak AF, Davies E, Connell JM., Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study. Clin Endocrinol (Oxf) 2007 67 832 838. doi: 10.1111/j.1365-2265.2007.02971.x.
-
(2007)
Clin Endocrinol (Oxf
, vol.67
, pp. 832-838
-
-
Freel, E.M.1
Ingram, M.2
Friel, E.C.3
Fraser, R.4
Brown, M.5
Samani, N.J.6
Caulfield, M.7
Munroe, P.8
Farrall, M.9
Webster, J.10
Clayton, D.11
Dominiczak, A.F.12
Davies, E.13
Connell, J.M.14
-
21
-
-
0034909430
-
NF-1C, Sp1, and Sp3 are essential for transcription of the human gene for P450c17 (steroid 17alpha-hydroxylase/17,20 lyase) in human adrenal NCI-H295A cells
-
Lin CJ, Martens JW, Miller WL., NF-1C, Sp1, and Sp3 are essential for transcription of the human gene for P450c17 (steroid 17alpha-hydroxylase/17,20 lyase) in human adrenal NCI-H295A cells. Mol Endocrinol 2001 15 1277 1293. doi: 10.1210/mend.15.8.0679.
-
(2001)
Mol Endocrinol
, vol.15
, pp. 1277-1293
-
-
Lin, C.J.1
Martens, J.W.2
Miller, W.L.3
-
22
-
-
33644926096
-
Deoxycorticosterone inactivation by AKR1C3 in human mineralocorticoid target tissues
-
Sharma KK, Lindqvist A, Zhou XJ, Auchus RJ, Penning TM, Andersson S., Deoxycorticosterone inactivation by AKR1C3 in human mineralocorticoid target tissues. Mol Cell Endocrinol 2006 248 79 86. doi: 10.1016/j.mce.2005.10.024.
-
(2006)
Mol Cell Endocrinol
, vol.248
, pp. 79-86
-
-
Sharma, K.K.1
Lindqvist, A.2
Zhou, X.J.3
Auchus, R.J.4
Penning, T.M.5
Andersson, S.6
-
23
-
-
0029003101
-
Mildly raised corticosterone excretion rates in patients with essential hypertension
-
Soro A, Ingram MC, Tonolo G, Glorioso N, Fraser R., Mildly raised corticosterone excretion rates in patients with essential hypertension. J Hum Hypertens 1995 9 391 393
-
(1995)
J Hum Hypertens
, vol.9
, pp. 391-393
-
-
Soro, A.1
Ingram, M.C.2
Tonolo, G.3
Glorioso, N.4
Fraser, R.5
-
24
-
-
0035017246
-
Multidrug resistance P-glycoprotein hampers the access of cortisol but not of corticosterone to mouse and human brain
-
Karssen AM, Meijer OC, van der Sandt IC, Lucassen PJ, de Lange EC, de Boer AG, de Kloet ER., Multidrug resistance P-glycoprotein hampers the access of cortisol but not of corticosterone to mouse and human brain. Endocrinology 2001 142 2686 2694. doi: 10.1210/endo.142.6.8213.
-
(2001)
Endocrinology
, vol.142
, pp. 2686-2694
-
-
Karssen, A.M.1
Meijer, O.C.2
Van Der Sandt, I.C.3
Lucassen, P.J.4
De Lange, E.C.5
De Boer, A.G.6
De Kloet, E.R.7
-
25
-
-
33745224303
-
The role of corticosterone in human hypothalamic-pituitary-Adrenal axis feedback
-
Raubenheimer PJ, Young EA, Andrew R, Seckl JR., The role of corticosterone in human hypothalamic-pituitary-Adrenal axis feedback. Clin Endocrinol (Oxf) 2006 65 22 26. doi: 10.1111/j.1365-2265.2006.02540.x.
-
(2006)
Clin Endocrinol (Oxf
, vol.65
, pp. 22-26
-
-
Raubenheimer, P.J.1
Young, E.A.2
Andrew, R.3
Seckl, J.R.4
-
26
-
-
0014435596
-
Selective retention of corticosterone by limbic structures in rat brain
-
McEwen BS, Weiss JM, Schwartz LS., Selective retention of corticosterone by limbic structures in rat brain. Nature 1968 220 911 912
-
(1968)
Nature
, vol.220
, pp. 911-912
-
-
McEwen, B.S.1
Weiss, J.M.2
Schwartz, L.S.3
-
27
-
-
84936946445
-
Why do humans have two glucocorticoids: A question of intestinal fortitude
-
Morris DJ., Why do humans have two glucocorticoids: a question of intestinal fortitude. Steroids 2015 102 32 38. doi: 10.1016/j.steroids.2015.06.017.
-
(2015)
Steroids
, vol.102
, pp. 32-38
-
-
Morris, D.J.1
-
28
-
-
0345401521
-
Multiple comparison procedures: The practical solution
-
Saville DJ., Multiple comparison procedures: the practical solution. Am Stat 1990 44 174 180
-
(1990)
Am Stat
, vol.44
, pp. 174-180
-
-
Saville, D.J.1
-
29
-
-
0345401521
-
Multiple comparison procedures: The practical solution
-
Saville DJ., Multiple comparison procedures: the practical solution. Am Stat 1990 44 174 180
-
(1990)
Am Stat
, vol.44
, pp. 174-180
-
-
Saville, D.J.1
|