-
1
-
-
12344282783
-
Global burden of hypertension: analysis of worldwide data
-
Kearney P.M., Whelton M., Reynolds K., Muntner P., Whelton P.K., He J. Global burden of hypertension: analysis of worldwide data. Lancet 2005, 365:217-223.
-
(2005)
Lancet
, vol.365
, pp. 217-223
-
-
Kearney, P.M.1
Whelton, M.2
Reynolds, K.3
Muntner, P.4
Whelton, P.K.5
He, J.6
-
2
-
-
43049097195
-
Global burden of blood-pressure-related disease, 2001
-
Lawes C.M., Vander H.S., Rodgers A. Global burden of blood-pressure-related disease, 2001. Lancet 2008, 371:1513-1518.
-
(2008)
Lancet
, vol.371
, pp. 1513-1518
-
-
Lawes, C.M.1
Vander, H.S.2
Rodgers, A.3
-
3
-
-
34250350040
-
Guidelines for the management of arterial hypertension: the Task Force for the Management of Arterial Hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC)
-
Mancia G., De Backer G., Dominiczak A., Cifkova R., Fagard R., Germano G., Grassi G., Heagerty A.M., Kjeldsen S.E., Laurent S., Narkiewicz K., Ruilope L., Rynkiewicz A., Schmieder R.E., Boudier H.A., Zanchetti A., Vahanian A., Camm J., De Caterina R., Dean V., Dickstein K., Filippatos G., Funck-Brentano C., Hellemans I., Kristensen S.D., McGregor K., Sechtem U., Silber S., Tendera M., Widimsky P., Zamorano J.L., Erdine S., Kiowski W., Agabiti-Rosei E., Ambrosioni E., Lindholm L.H., Viigimaa M., Adamopoulos S., Agabiti-Rosei E., Ambrosioni E., Bertomeu V., Clement D., Erdine S., Farsang C., Gaita D., Lip G., Mallion J.M., Manolis A.J., Nilsson P.M., O'Brien E., Ponikowski P., Redon J., Ruschitzka F., Tamargo J., van Zwieten P., Waeber B., Williams B. Guidelines for the management of arterial hypertension: the Task Force for the Management of Arterial Hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). J. Hypertens. 2007, 25(2007):1105-1187.
-
(2007)
J. Hypertens.
, vol.25
, Issue.2007
, pp. 1105-1187
-
-
Mancia, G.1
De Backer, G.2
Dominiczak, A.3
Cifkova, R.4
Fagard, R.5
Germano, G.6
Grassi, G.7
Heagerty, A.M.8
Kjeldsen, S.E.9
Laurent, S.10
Narkiewicz, K.11
Ruilope, L.12
Rynkiewicz, A.13
Schmieder, R.E.14
Boudier, H.A.15
Zanchetti, A.16
Vahanian, A.17
Camm, J.18
De Caterina, R.19
Dean, V.20
Dickstein, K.21
Filippatos, G.22
Funck-Brentano, C.23
Hellemans, I.24
Kristensen, S.D.25
McGregor, K.26
Sechtem, U.27
Silber, S.28
Tendera, M.29
Widimsky, P.30
Zamorano, J.L.31
Erdine, S.32
Kiowski, W.33
Agabiti-Rosei, E.34
Ambrosioni, E.35
Lindholm, L.H.36
Viigimaa, M.37
Adamopoulos, S.38
Agabiti-Rosei, E.39
Ambrosioni, E.40
Bertomeu, V.41
Clement, D.42
Erdine, S.43
Farsang, C.44
Gaita, D.45
Lip, G.46
Mallion, J.M.47
Manolis, A.J.48
Nilsson, P.M.49
O'Brien, E.50
Ponikowski, P.51
Redon, J.52
Ruschitzka, F.53
Tamargo, J.54
van Zwieten, P.55
Waeber, B.56
Williams, B.57
more..
-
4
-
-
0347423198
-
Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure
-
Chobanian A.V., Bakris G.L., Black H.R., Cushman W.C., Green L.A., Izzo J.L., Jones D.W., Materson B.J., Oparil S., Wright J.T., Roccella E.J. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension 2003, 42:1206-1252.
-
(2003)
Hypertension
, vol.42
, pp. 1206-1252
-
-
Chobanian, A.V.1
Bakris, G.L.2
Black, H.R.3
Cushman, W.C.4
Green, L.A.5
Izzo, J.L.6
Jones, D.W.7
Materson, B.J.8
Oparil, S.9
Wright, J.T.10
Roccella, E.J.11
-
5
-
-
0037079309
-
Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for onemillion adults in 61 prospective studies
-
Lewington S., Clarke R., Qizilbash N., Peto R., Collins R. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for onemillion 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
-
7
-
-
0034711753
-
Essential hypertension. Part I: definition and etiology
-
Carretero O.A., Oparil S. Essential hypertension. Part I: definition and etiology. Circulation 2000, 101:329-335.
-
(2000)
Circulation
, vol.101
, pp. 329-335
-
-
Carretero, O.A.1
Oparil, S.2
-
8
-
-
0017761036
-
The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results
-
Feinleib M., Garrison R.J., Fabsitz R., Christian J.C., Hrubec Z., Borhani N.O., Kannel W.B., Rosenman R., Schwartz J.T., Wagner J.O. The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results. Am. J. Epidemiol. 1977, 106:284-285.
-
(1977)
Am. J. Epidemiol.
, vol.106
, pp. 284-285
-
-
Feinleib, M.1
Garrison, R.J.2
Fabsitz, R.3
Christian, J.C.4
Hrubec, Z.5
Borhani, N.O.6
Kannel, W.B.7
Rosenman, R.8
Schwartz, J.T.9
Wagner, J.O.10
-
9
-
-
0022502168
-
The influence of genetics and household environment upon the variability of normal blood pressure: the Montreal Adoption Survey
-
Mongeau J.G., Biron P., Sing C.F. The influence of genetics and household environment upon the variability of normal blood pressure: the Montreal Adoption Survey. Clin. Exp. Hypertens. A 1986, 8:653-660.
-
(1986)
Clin. Exp. Hypertens. A
, vol.8
, pp. 653-660
-
-
Mongeau, J.G.1
Biron, P.2
Sing, C.F.3
-
10
-
-
0037906525
-
Essential hypertension
-
Staessen J.A., Wang J., Bianchi G., Birkenhager W.H. Essential hypertension. Lancet 2003, 361:1629-1641.
-
(2003)
Lancet
, vol.361
, pp. 1629-1641
-
-
Staessen, J.A.1
Wang, J.2
Bianchi, G.3
Birkenhager, W.H.4
-
11
-
-
0038375052
-
Genome-wide mapping of human loci for essential hypertension
-
Caulfield M., Munroe P., Pembroke J., Samani N., Dominiczak A., Brown M., Benjamin N., Webster J., Ratcliffe P., O'Shea S., Papp J., Taylor E., Dobson R., Knight J., Newhouse S., Hooper J., Lee W., Brain N., Clayton D., Lathrop G.M., Farrall M., Connell J. Genome-wide mapping of human loci for essential hypertension. Lancet 2003, 361:2118-2123.
-
(2003)
Lancet
, vol.361
, pp. 2118-2123
-
-
Caulfield, M.1
Munroe, P.2
Pembroke, J.3
Samani, N.4
Dominiczak, A.5
Brown, M.6
Benjamin, N.7
Webster, J.8
Ratcliffe, P.9
O'Shea, S.10
Papp, J.11
Taylor, E.12
Dobson, R.13
Knight, J.14
Newhouse, S.15
Hooper, J.16
Lee, W.17
Brain, N.18
Clayton, D.19
Lathrop, G.M.20
Farrall, M.21
Connell, J.22
more..
-
12
-
-
0021230230
-
Blood pressure and its correlates in an African tribe in urban and rural environments
-
Poulter N., Khaw K.T., Hopwood B.E., Mugambi M., Peart W.S., Rose G., Sever P.S. Blood pressure and its correlates in an African tribe in urban and rural environments. J. Epidemiol. Community Health 1984, 38:181-185.
-
(1984)
J. Epidemiol. Community Health
, vol.38
, pp. 181-185
-
-
Poulter, N.1
Khaw, K.T.2
Hopwood, B.E.3
Mugambi, M.4
Peart, W.S.5
Rose, G.6
Sever, P.S.7
-
13
-
-
0019200575
-
Is the renin system necessary?
-
Brunner H.R., Gavras H. Is the renin system necessary?. Am. J. Med. 1980, 69:739-745.
-
(1980)
Am. J. Med.
, vol.69
, pp. 739-745
-
-
Brunner, H.R.1
Gavras, H.2
-
14
-
-
0033755028
-
Genetics of hypertension: from experimental models to clinical applications
-
Lee W.K., Padmanabhan S., Dominiczak A.F. Genetics of hypertension: from experimental models to clinical applications. J. Hum. Hypertens. 2000, 14:631-647.
-
(2000)
J. Hum. Hypertens.
, vol.14
, pp. 631-647
-
-
Lee, W.K.1
Padmanabhan, S.2
Dominiczak, A.F.3
-
15
-
-
0033979807
-
Genetic analysis of inherited hypertension in the rat
-
Rapp J.P. Genetic analysis of inherited hypertension in the rat. Physiol. Rev. 2000, 80:135-172.
-
(2000)
Physiol. Rev.
, vol.80
, pp. 135-172
-
-
Rapp, J.P.1
-
16
-
-
0346294232
-
Application of chromosomal substitution techniques in gene-function discovery
-
Cowley A.W., Roman R.J., Jacob H.J. Application of chromosomal substitution techniques in gene-function discovery. J. Physiol. 2004, 554:46-55.
-
(2004)
J. Physiol.
, vol.554
, pp. 46-55
-
-
Cowley, A.W.1
Roman, R.J.2
Jacob, H.J.3
-
17
-
-
1842684068
-
Genome sequence of the Brown Norway rat yields insights into mammalian evolution
-
Gibbs R.A., Weinstock G.M., Metzker M.L., Muzny D.M., Sodergren E.J., Scherer S., Scott G., Steffen D., Worley K.C., Burch P.E., Okwuonu G., Hines S., Lewis L., DeRamo C., Delgado O., Dugan-Rocha S., Miner G., Morgan M., Hawes A., Gill R., Celera, Holt R.A., Adams M.D., Amanatides P.G., Baden-Tillson H., Barnstead M., Chin S., Evans C.A., Ferriera S., Fosler C., Glodek A., Gu Z., Jennings D., Kraft C.L., Nguyen T., Pfannkoch C.M., Sitter C., Sutton G.G., Venter J.C., Woodage T., Smith D., Lee H.M., Gustafson E., Cahill P., Kana A., Doucette-Stamm L., Weinstock K., Fechtel K., Weiss R.B., Dunn D.M., Green E.D., Blakesley R.W., Bouffard G.G., De Jong P.J., Osoegawa K., Zhu B., Marra M., Schein J., Bosdet I., Fjell C., Jones S., Krzywinski M., Mathewson C., Siddiqui A., Wye N., McPherson J., Zhao S., Fraser C.M., Shetty J., Shatsman S., Geer K., Chen Y., Abramzon S., Nierman W.C., Havlak P.H., Chen R., Durbin K.J., Egan A., Ren Y., Song X.Z., Li B., Liu Y., Qin X., Cawley S., Worley K.C., Cooney A.J., D'Souza L.M., Martin K., Wu J.Q., Gonzalez-Garay M.L., Jackson A.R., Kalafus K.J., McLeod M.P., Milosavljevic A., Virk D., Volkov A., Wheeler D.A., Zhang Z., Bailey J.A., Eichler E.E., Tuzun E., Birney E., Mongin E., Ureta-Vidal A., Woodwark C., Zdobnov E., Bork P., Suyama M., Torrents D., Alexandersson M., Trask B.J., Young J.M., Huang H., Wang H., Xing H., Daniels S., Gietzen D., Schmidt J., Stevens K., Vitt U., Wingrove J., Camara F., Mar A.M., Abril J.F., Guigo R., Smit A., Dubchak I., Rubin E.M., Couronne O., Poliakov A., Hubner N., Ganten D., Goesele C., Hummel O., Kreitler T., Lee Y.A., Monti J., Schulz H., Zimdahl H., Himmelbauer H., Lehrach H., Jacob H.J., Bromberg S., Gullings-Handley J., Jensen-Seaman M.I., Kwitek A.E., Lazar J., Pasko D., Tonellato P.J., Twigger S., Ponting C.P., Duarte J.M., Rice S., Goodstadt L., Beatson S.A., Emes R.D., Winter E.E., Webber C., Brandt P., Nyakatura G., Adetobi M., Chiaromonte F., Elnitski L., Eswara P., Hardison R.C., Hou M., Kolbe D., Makova K., Miller W., Nekrutenko A., Riemer C., Schwartz S., Taylor J., Yang S., Zhang Y., Lindpaintner K., Andrews T.D., Caccamo M., Clamp M., Clarke L., Curwen V., Durbin R., Eyras E., Searle S.M., Cooper G.M., Batzoglou S., Brudno M., Sidow A., Stone E.A., Venter J.C., Payseur B.A., Bourque G., Lopez-Otin C., Puente X.S., Chakrabarti K., Chatterji S., Dewey C., Pachter L., Bray N., Yap V.B., Caspi A., Tesler G., Pevzner P.A., Haussler D., Roskin K.M., Baertsch R., Clawson H., Furey T.S., Hinrichs A.S., Karolchik D., Kent W.J., Rosenbloom K.R., Trumbower H., Weirauch M., Cooper D.N., Stenson P.D., Ma B., Brent M., Arumugam M., Shteynberg D., Copley R.R., Taylor M.S., Riethman H., Mudunuri U., Peterson J., Guyer M., Felsenfeld A., Old S., Mockrin S., Collins F. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature 2004, 428:493-521.
-
(2004)
Nature
, vol.428
, pp. 493-521
-
-
Gibbs, R.A.1
Weinstock, G.M.2
Metzker, M.L.3
Muzny, D.M.4
Sodergren, E.J.5
Scherer, S.6
Scott, G.7
Steffen, D.8
Worley, K.C.9
Burch, P.E.10
Okwuonu, G.11
Hines, S.12
Lewis, L.13
DeRamo, C.14
Delgado, O.15
Dugan-Rocha, S.16
Miner, G.17
Morgan, M.18
Hawes, A.19
Gill, R.20
Celera21
Holt, R.A.22
Adams, M.D.23
Amanatides, P.G.24
Baden-Tillson, H.25
Barnstead, M.26
Chin, S.27
Evans, C.A.28
Ferriera, S.29
Fosler, C.30
Glodek, A.31
Gu, Z.32
Jennings, D.33
Kraft, C.L.34
Nguyen, T.35
Pfannkoch, C.M.36
Sitter, C.37
Sutton, G.G.38
Venter, J.C.39
Woodage, T.40
Smith, D.41
Lee, H.M.42
Gustafson, E.43
Cahill, P.44
Kana, A.45
Doucette-Stamm, L.46
Weinstock, K.47
Fechtel, K.48
Weiss, R.B.49
Dunn, D.M.50
Green, E.D.51
Blakesley, R.W.52
Bouffard, G.G.53
De Jong, P.J.54
Osoegawa, K.55
Zhu, B.56
Marra, M.57
Schein, J.58
Bosdet, I.59
Fjell, C.60
Jones, S.61
Krzywinski, M.62
Mathewson, C.63
Siddiqui, A.64
Wye, N.65
McPherson, J.66
Zhao, S.67
Fraser, C.M.68
Shetty, J.69
Shatsman, S.70
Geer, K.71
Chen, Y.72
Abramzon, S.73
Nierman, W.C.74
Havlak, P.H.75
Chen, R.76
Durbin, K.J.77
Egan, A.78
Ren, Y.79
Song, X.Z.80
Li, B.81
Liu, Y.82
Qin, X.83
Cawley, S.84
Worley, K.C.85
Cooney, A.J.86
D'Souza, L.M.87
Martin, K.88
Wu, J.Q.89
Gonzalez-Garay, M.L.90
Jackson, A.R.91
Kalafus, K.J.92
McLeod, M.P.93
Milosavljevic, A.94
Virk, D.95
Volkov, A.96
Wheeler, D.A.97
Zhang, Z.98
Bailey, J.A.99
more..
-
18
-
-
70349883935
-
Inferring meta-covariates in classification
-
Springer, New York, V. Kadirkamanathan, G. Sanguinetti, M. Girolami, M. Niranjan, J. Noirel (Eds.)
-
Harris K., McMillan L., Girolami M. Inferring meta-covariates in classification. Pattern recognition in bioinformatics, Lecture Notes in Bioinformatics Volume 5780 2009, 150-161. Springer, New York. V. Kadirkamanathan, G. Sanguinetti, M. Girolami, M. Niranjan, J. Noirel (Eds.).
-
(2009)
Pattern recognition in bioinformatics, Lecture Notes in Bioinformatics Volume 5780
, pp. 150-161
-
-
Harris, K.1
McMillan, L.2
Girolami, M.3
-
19
-
-
13844267011
-
The visual language of synteny
-
Hunt E., Hanlon N., Leader D.P., Bryce H., Dominiczak A.F. The visual language of synteny. OMICS 2004, 8:289-305.
-
(2004)
OMICS
, vol.8
, pp. 289-305
-
-
Hunt, E.1
Hanlon, N.2
Leader, D.P.3
Bryce, H.4
Dominiczak, A.F.5
-
20
-
-
0037440746
-
Interaction between blood pressure quantitative trait loci in rats in which trait variation at chromosome 1 is conditional upon a specific allele at chromosome 10
-
Monti J., Plehm R., Schulz H., Ganten D., Kreutz R., Hubner N. Interaction between blood pressure quantitative trait loci in rats in which trait variation at chromosome 1 is conditional upon a specific allele at chromosome 10. Hum. Mol. Genet. 2003, 12:435-439.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 435-439
-
-
Monti, J.1
Plehm, R.2
Schulz, H.3
Ganten, D.4
Kreutz, R.5
Hubner, N.6
-
21
-
-
33750202275
-
The genetic dissection of essential hypertension
-
Cowley A.W. The genetic dissection of essential hypertension. Nat. Rev. Genet. 2006, 7:829-840.
-
(2006)
Nat. Rev. Genet.
, vol.7
, pp. 829-840
-
-
Cowley, A.W.1
-
22
-
-
0037146578
-
Finding genes that underlie complex traits
-
Glazier A.M., Nadeau J.H., Aitman T.J. Finding genes that underlie complex traits. Science 2002, 298:2345-2349.
-
(2002)
Science
, vol.298
, pp. 2345-2349
-
-
Glazier, A.M.1
Nadeau, J.H.2
Aitman, T.J.3
-
23
-
-
3843052401
-
Dissecting quantitative trait loci into opposite blood pressure effects on Dahl rat chromosome 8 by congenic strains
-
Ariyarajah A., Palijan A., Dutil J., Prithiviraj K., Deng Y., Deng A.Y. Dissecting quantitative trait loci into opposite blood pressure effects on Dahl rat chromosome 8 by congenic strains. J. Hypertens. 2004, 22:1495-1502.
-
(2004)
J. Hypertens.
, vol.22
, pp. 1495-1502
-
-
Ariyarajah, A.1
Palijan, A.2
Dutil, J.3
Prithiviraj, K.4
Deng, Y.5
Deng, A.Y.6
-
24
-
-
15744384640
-
Multiple quantitative trait loci for blood pressure interacting epistatically and additively on Dahl rat chromosome 2
-
Dutil J., Eliopoulos V., Tremblay J., Hamet P., Charron S., Deng A.Y. Multiple quantitative trait loci for blood pressure interacting epistatically and additively on Dahl rat chromosome 2. Hypertension 2005, 45:557-564.
-
(2005)
Hypertension
, vol.45
, pp. 557-564
-
-
Dutil, J.1
Eliopoulos, V.2
Tremblay, J.3
Hamet, P.4
Charron, S.5
Deng, A.Y.6
-
25
-
-
25144452252
-
Severe hypertension caused by alleles from normotensive Lewis for a quantitative trait locus on chromosome 2
-
Eliopoulos V., Dutil J., Deng Y., Grondin M., Deng A.Y. Severe hypertension caused by alleles from normotensive Lewis for a quantitative trait locus on chromosome 2. Physiol. Genomics 2005, 22:70-75.
-
(2005)
Physiol. Genomics
, vol.22
, pp. 70-75
-
-
Eliopoulos, V.1
Dutil, J.2
Deng, Y.3
Grondin, M.4
Deng, A.Y.5
-
26
-
-
18244377271
-
Complete and overlapping congenics proving the existence of a quantitative trait locus for blood pressure on Dahl rat chromosome 17
-
Grondin M., Eliopoulos V., Lambert R., Deng Y., Ariyarajah A., Moujahidine M., Dutil J., Charron S., Deng A.Y. Complete and overlapping congenics proving the existence of a quantitative trait locus for blood pressure on Dahl rat chromosome 17. Physiol. Genomics 2005, 21:112-116.
-
(2005)
Physiol. Genomics
, vol.21
, pp. 112-116
-
-
Grondin, M.1
Eliopoulos, V.2
Lambert, R.3
Deng, Y.4
Ariyarajah, A.5
Moujahidine, M.6
Dutil, J.7
Charron, S.8
Deng, A.Y.9
-
27
-
-
0141997247
-
Comprehensive congenic coverage revealing multiple blood pressure quantitative trait loci on Dahl rat chromosome 10
-
Palijan A., Lambert R., Dutil J., Sivo Z., Deng A.Y. Comprehensive congenic coverage revealing multiple blood pressure quantitative trait loci on Dahl rat chromosome 10. Hypertension 2003, 42:515-522.
-
(2003)
Hypertension
, vol.42
, pp. 515-522
-
-
Palijan, A.1
Lambert, R.2
Dutil, J.3
Sivo, Z.4
Deng, A.Y.5
-
28
-
-
0347133175
-
Quantitative trait loci with opposing blood pressure effects demonstrating epistasis on Dahl rat chromosome 3
-
Palijan A., Dutil J., Deng A.Y. Quantitative trait loci with opposing blood pressure effects demonstrating epistasis on Dahl rat chromosome 3. Physiol. Genomics 2003, 15:1-8.
-
(2003)
Physiol. Genomics
, vol.15
, pp. 1-8
-
-
Palijan, A.1
Dutil, J.2
Deng, A.Y.3
-
29
-
-
5144230654
-
Effect of Add1 gene transfer on blood pressure in reciprocal congenic strains of Milan rats
-
Tripodi G., Florio M., Ferrandi M., Modica R., Zimdahl H., Hubner N., Ferrari P., Bianchi G. Effect of Add1 gene transfer on blood pressure in reciprocal congenic strains of Milan rats. Biochem. Biophys. Res. Commun. 2004, 324:562-568.
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.324
, pp. 562-568
-
-
Tripodi, G.1
Florio, M.2
Ferrandi, M.3
Modica, R.4
Zimdahl, H.5
Hubner, N.6
Ferrari, P.7
Bianchi, G.8
-
30
-
-
15744384640
-
Multiple quantitative trait loci for blood pressure interacting epistatically and additively on Dahl rat chromosome 2
-
Dutil J., Eliopoulos V., Tremblay J., Hamet P., Charron S., Deng A.Y. Multiple quantitative trait loci for blood pressure interacting epistatically and additively on Dahl rat chromosome 2. Hypertension 2005, 45:557-564.
-
(2005)
Hypertension
, vol.45
, pp. 557-564
-
-
Dutil, J.1
Eliopoulos, V.2
Tremblay, J.3
Hamet, P.4
Charron, S.5
Deng, A.Y.6
-
31
-
-
5144230654
-
Effect of Add1 gene transfer on blood pressure in reciprocal congenic strains of Milan rats
-
Tripodi G., Florio M., Ferrandi M., Modica R., Zimdahl H., Hubner N., Ferrari P., Bianchi G. Effect of Add1 gene transfer on blood pressure in reciprocal congenic strains of Milan rats. Biochem. Biophys. Res. Commun. 2004, 324:562-568.
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.324
, pp. 562-568
-
-
Tripodi, G.1
Florio, M.2
Ferrandi, M.3
Modica, R.4
Zimdahl, H.5
Hubner, N.6
Ferrari, P.7
Bianchi, G.8
-
32
-
-
0032958470
-
Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats
-
Aitman T.J., Glazier A.M., Wallace C.A., Cooper L.D., Norsworthy P.J., Wahid F.N., Al Majali K.M., Trembling P.M., Mann C.J., Shoulders C.C., Graf D., St Lezin E., Kurtz T.W., Kren V., Pravenec M., Ibrahimi A., Abumrad N.A., Stanton L.W., Scott J. Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats. Nat. Genet. 1999, 21:76-83.
-
(1999)
Nat. Genet.
, vol.21
, pp. 76-83
-
-
Aitman, T.J.1
Glazier, A.M.2
Wallace, C.A.3
Cooper, L.D.4
Norsworthy, P.J.5
Wahid, F.N.6
Al Majali, K.M.7
Trembling, P.M.8
Mann, C.J.9
Shoulders, C.C.10
Graf, D.11
St Lezin, E.12
Kurtz, T.W.13
Kren, V.14
Pravenec, M.15
Ibrahimi, A.16
Abumrad, N.A.17
Stanton, L.W.18
Scott, J.19
-
33
-
-
0347131011
-
Transgenic expression of CD36 in the spontaneously hypertensive rat is associated with amelioration of metabolic disturbances but has no effect on hypertension
-
Pravenec M., Landa V., Zidek V., Musilova A., Kazdova L., Qi N., Wang J., St Lezin E., Kurtz T.W. Transgenic expression of CD36 in the spontaneously hypertensive rat is associated with amelioration of metabolic disturbances but has no effect on hypertension. Physiol. Res. 2003, 52:681-688.
-
(2003)
Physiol. Res.
, vol.52
, pp. 681-688
-
-
Pravenec, M.1
Landa, V.2
Zidek, V.3
Musilova, A.4
Kazdova, L.5
Qi, N.6
Wang, J.7
St Lezin, E.8
Kurtz, T.W.9
-
34
-
-
10644230208
-
Genetic study of the CD36 gene in a French diabetic population
-
Lepretre F., Linton K.J., Lacquemant C., Vatin V., Samson C., Dina C., Chikri M., Ali S., Scherer P., Seron K., Vasseur F., Aitman T., Froguel P. Genetic study of the CD36 gene in a French diabetic population. Diabetes Metab. 2004, 30:459-463.
-
(2004)
Diabetes Metab.
, vol.30
, pp. 459-463
-
-
Lepretre, F.1
Linton, K.J.2
Lacquemant, C.3
Vatin, V.4
Samson, C.5
Dina, C.6
Chikri, M.7
Ali, S.8
Scherer, P.9
Seron, K.10
Vasseur, F.11
Aitman, T.12
Froguel, P.13
-
35
-
-
0035799118
-
CD36 deficiency associated with insulin resistance
-
Miyaoka K., Kuwasako T., Hirano K., Nozaki S., Yamashita S., Matsuzawa Y. CD36 deficiency associated with insulin resistance. Lancet 2001, 357:686-687.
-
(2001)
Lancet
, vol.357
, pp. 686-687
-
-
Miyaoka, K.1
Kuwasako, T.2
Hirano, K.3
Nozaki, S.4
Yamashita, S.5
Matsuzawa, Y.6
-
36
-
-
48349142758
-
Identification of renal Cd36 as a determinant of blood pressure and risk for hypertension
-
Pravenec M., Churchill P.C., Churchill M.C., Viklicky O., Kazdova L., Aitman T.J., Petretto E., Hubner N., Wallace C.A., Zimdahl H., Zidek V., Landa V., Dunbar J., Bidani A., Griffin K., Qi N., Maxova M., Kren V., Mlejnek P., Wang J., Kurtz T.W. Identification of renal Cd36 as a determinant of blood pressure and risk for hypertension. Nat. Genet. 2008, 40:952-954.
-
(2008)
Nat. Genet.
, vol.40
, pp. 952-954
-
-
Pravenec, M.1
Churchill, P.C.2
Churchill, M.C.3
Viklicky, O.4
Kazdova, L.5
Aitman, T.J.6
Petretto, E.7
Hubner, N.8
Wallace, C.A.9
Zimdahl, H.10
Zidek, V.11
Landa, V.12
Dunbar, J.13
Bidani, A.14
Griffin, K.15
Qi, N.16
Maxova, M.17
Kren, V.18
Mlejnek, P.19
Wang, J.20
Kurtz, T.W.21
more..
-
37
-
-
10344259145
-
Quantitative trait loci in genetically hypertensive rats. Possible sex specificity
-
Clark J.S., Jeffs B., Davidson A.O., Lee W.K., Anderson N.H., Bihoreau M.T., Brosnan M.J., Devlin A.M., Kelman A.W., Lindpaintner K., Dominiczak A.F. Quantitative trait loci in genetically hypertensive rats. Possible sex specificity. Hypertension 1996, 28:898-906.
-
(1996)
Hypertension
, vol.28
, pp. 898-906
-
-
Clark, J.S.1
Jeffs, B.2
Davidson, A.O.3
Lee, W.K.4
Anderson, N.H.5
Bihoreau, M.T.6
Brosnan, M.J.7
Devlin, A.M.8
Kelman, A.W.9
Lindpaintner, K.10
Dominiczak, A.F.11
-
38
-
-
0033966178
-
Applicability of a "speed" congenic strategy to dissect blood pressure quantitative trait loci on rat chromosome 2
-
Jeffs B., Negrin C.D., Graham D., Clark J.S., Anderson N.H., Gauguier D., Dominiczak A.F. Applicability of a "speed" congenic strategy to dissect blood pressure quantitative trait loci on rat chromosome 2. Hypertension 2000, 35:179-187.
-
(2000)
Hypertension
, vol.35
, pp. 179-187
-
-
Jeffs, B.1
Negrin, C.D.2
Graham, D.3
Clark, J.S.4
Anderson, N.H.5
Gauguier, D.6
Dominiczak, A.F.7
-
39
-
-
0345893762
-
Further chromosomal mapping of a blood pressure QTL in Dahl rats on chromosome 2 using congenic strains
-
Dutil J., Deng A.Y. Further chromosomal mapping of a blood pressure QTL in Dahl rats on chromosome 2 using congenic strains. Physiol. Genomics 2001, 6:3-9.
-
(2001)
Physiol. Genomics
, vol.6
, pp. 3-9
-
-
Dutil, J.1
Deng, A.Y.2
-
40
-
-
42649111665
-
Progress and prospects in rat genetics: a community view
-
Aitman T.J., Critser J.K., Cuppen E., Dominiczak A., Fernandez-Suarez X.M., Flint J., Gauguier D., Geurts A.M., Gould M., Harris P.C., Holmdahl R., Hubner N., Izsvak Z., Jacob H.J., Kuramoto T., Kwitek A.E., Marrone A., Mashimo T., Moreno C., Mullins J., Mullins L., Olsson T., Pravenec M., Riley L., Saar K., Serikawa T., Shull J.D., Szpirer C., Twigger S.N., Voigt B., Worley K. Progress and prospects in rat genetics: a community view. Nat. Genet. 2008, 40:516-522.
-
(2008)
Nat. Genet.
, vol.40
, pp. 516-522
-
-
Aitman, T.J.1
Critser, J.K.2
Cuppen, E.3
Dominiczak, A.4
Fernandez-Suarez, X.M.5
Flint, J.6
Gauguier, D.7
Geurts, A.M.8
Gould, M.9
Harris, P.C.10
Holmdahl, R.11
Hubner, N.12
Izsvak, Z.13
Jacob, H.J.14
Kuramoto, T.15
Kwitek, A.E.16
Marrone, A.17
Mashimo, T.18
Moreno, C.19
Mullins, J.20
Mullins, L.21
Olsson, T.22
Pravenec, M.23
Riley, L.24
Saar, K.25
Serikawa, T.26
Shull, J.D.27
Szpirer, C.28
Twigger, S.N.29
Voigt, B.30
Worley, K.31
more..
-
41
-
-
0037340133
-
Microarray analysis of rat chromosome 2 congenic strains
-
McBride M.W., Carr F.J., Graham D., Anderson N.H., Clark J.S., Lee W.K., Charchar F.J., Brosnan M.J., Dominiczak A.F. Microarray analysis of rat chromosome 2 congenic strains. Hypertension 2003, 41:847-853.
-
(2003)
Hypertension
, vol.41
, pp. 847-853
-
-
McBride, M.W.1
Carr, F.J.2
Graham, D.3
Anderson, N.H.4
Clark, J.S.5
Lee, W.K.6
Charchar, F.J.7
Brosnan, M.J.8
Dominiczak, A.F.9
-
42
-
-
20144373060
-
Reduction of Gstm1 expression in the stroke-prone spontaneously hypertension rat contributes to increased oxidative stress
-
McBride M.W., Brosnan M.J., Mathers J., McLellan L.I., Miller W.H., Graham D., Hanlon N., Hamilton C.A., Polke J.M., Lee W.K., Dominiczak A.F. Reduction of Gstm1 expression in the stroke-prone spontaneously hypertension rat contributes to increased oxidative stress. Hypertension 2005, 45:786-792.
-
(2005)
Hypertension
, vol.45
, pp. 786-792
-
-
McBride, M.W.1
Brosnan, M.J.2
Mathers, J.3
McLellan, L.I.4
Miller, W.H.5
Graham, D.6
Hanlon, N.7
Hamilton, C.A.8
Polke, J.M.9
Lee, W.K.10
Dominiczak, A.F.11
-
43
-
-
36448963043
-
Candidate genes that determine response to salt in the stroke-prone spontaneously hypertensive rat: congenic analysis
-
Graham D., McBride M.W., Gaasenbeek M., Gilday K., Beattie E., Miller W.H., McClure J.D., Polke J.M., Montezano A., Touyz R.M., Dominiczak A.F. Candidate genes that determine response to salt in the stroke-prone spontaneously hypertensive rat: congenic analysis. Hypertension 2007, 50:1134-1141.
-
(2007)
Hypertension
, vol.50
, pp. 1134-1141
-
-
Graham, D.1
McBride, M.W.2
Gaasenbeek, M.3
Gilday, K.4
Beattie, E.5
Miller, W.H.6
McClure, J.D.7
Polke, J.M.8
Montezano, A.9
Touyz, R.M.10
Dominiczak, A.F.11
-
44
-
-
0037385533
-
Defining the blood pressure QTL on chromosome 7 in Dahl rats by a 177-kb congenic segment containing Cyp11b1
-
Garrett M.R., Rapp J.P. Defining the blood pressure QTL on chromosome 7 in Dahl rats by a 177-kb congenic segment containing Cyp11b1. Mamm. Genome 2003, 14:268-273.
-
(2003)
Mamm. Genome
, vol.14
, pp. 268-273
-
-
Garrett, M.R.1
Rapp, J.P.2
-
45
-
-
16444377442
-
Identification of hypertension-related genes through an integrated genomic-transcriptomic approach
-
Yagil C., Hubner N., Monti J., Schulz H., Sapojnikov M., Luft F.C., Ganten D., Yagil Y. Identification of hypertension-related genes through an integrated genomic-transcriptomic approach. Circ. Res. 2005, 96:617-625.
-
(2005)
Circ. Res.
, vol.96
, pp. 617-625
-
-
Yagil, C.1
Hubner, N.2
Monti, J.3
Schulz, H.4
Sapojnikov, M.5
Luft, F.C.6
Ganten, D.7
Yagil, Y.8
-
46
-
-
14644437750
-
Locating a blood pressure quantitative trait locus within 117kb on the rat genome: substitution mapping and renal expression analysis
-
Garrett M.R., Meng H., Rapp J.P., Joe B. Locating a blood pressure quantitative trait locus within 117kb on the rat genome: substitution mapping and renal expression analysis. Hypertension 2005, 45:451-459.
-
(2005)
Hypertension
, vol.45
, pp. 451-459
-
-
Garrett, M.R.1
Meng, H.2
Rapp, J.P.3
Joe, B.4
-
47
-
-
78049300896
-
Mapping genetic determinants of blood pressure that are different between Dahl salt-sensitive and spontaneously hypertensive rats
-
Toland E.J., Yerga-Woolwine S., Farms P.K., Joe B. Mapping genetic determinants of blood pressure that are different between Dahl salt-sensitive and spontaneously hypertensive rats. Hypertension 2009, 54:E61-E62.
-
(2009)
Hypertension
, vol.54
-
-
Toland, E.J.1
Yerga-Woolwine, S.2
Farms, P.K.3
Joe, B.4
-
48
-
-
67749106611
-
Knockout rats via embryo microinjection of zinc-finger nucleases
-
Geurts A.M., Cost G.J., Freyvert Y., Zeitler B., Miller J.C., Choi V.M., Jenkins S.S., Wood A., Cui X., Meng X., Vincent A., Lam S., Michalkiewicz M., Schilling R., Foeckler J., Kalloway S., Weiler H., Menoret S., Anegon I., Davis G.D., Zhang L., Rebar E.J., Gregory P.D., Urnov F.D., Jacob H.J., Buelow R. Knockout rats via embryo microinjection of zinc-finger nucleases. Science 2009, 325:433.
-
(2009)
Science
, vol.325
, pp. 433
-
-
Geurts, A.M.1
Cost, G.J.2
Freyvert, Y.3
Zeitler, B.4
Miller, J.C.5
Choi, V.M.6
Jenkins, S.S.7
Wood, A.8
Cui, X.9
Meng, X.10
Vincent, A.11
Lam, S.12
Michalkiewicz, M.13
Schilling, R.14
Foeckler, J.15
Kalloway, S.16
Weiler, H.17
Menoret, S.18
Anegon, I.19
Davis, G.D.20
Zhang, L.21
Rebar, E.J.22
Gregory, P.D.23
Urnov, F.D.24
Jacob, H.J.25
Buelow, R.26
more..
-
49
-
-
0037224772
-
Positional identification of Ncf1 as a gene that regulates arthritis severity in rats
-
Olofsson P., Holmberg J., Tordsson J., Lu S., Akerstrom B., Holmdahl R. Positional identification of Ncf1 as a gene that regulates arthritis severity in rats. Nat. Genet. 2003, 33:25-32.
-
(2003)
Nat. Genet.
, vol.33
, pp. 25-32
-
-
Olofsson, P.1
Holmberg, J.2
Tordsson, J.3
Lu, S.4
Akerstrom, B.5
Holmdahl, R.6
-
50
-
-
32844460938
-
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
-
Aitman T.J., Dong R., Vyse T.J., Norsworthy P.J., Johnson M.D., Smith J., Mangion J., Roberton-Lowe C., Marshall A.J., Petretto E., Hodges M.D., Bhangal G., Patel S.G., Sheehan-Rooney K., Duda M., Cook P.R., Evans D.J., Domin J., Flint J., Boyle J.J., Pusey C.D., Cook H.T. Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Nature 2006, 439:851-855.
-
(2006)
Nature
, vol.439
, pp. 851-855
-
-
Aitman, T.J.1
Dong, R.2
Vyse, T.J.3
Norsworthy, P.J.4
Johnson, M.D.5
Smith, J.6
Mangion, J.7
Roberton-Lowe, C.8
Marshall, A.J.9
Petretto, E.10
Hodges, M.D.11
Bhangal, G.12
Patel, S.G.13
Sheehan-Rooney, K.14
Duda, M.15
Cook, P.R.16
Evans, D.J.17
Domin, J.18
Flint, J.19
Boyle, J.J.20
Pusey, C.D.21
Cook, H.T.22
more..
-
51
-
-
42649106487
-
Jund is a determinant of macrophage activation and is associated with glomerulonephritis susceptibility
-
Behmoaras J., Bhangal G., Smith J., McDonald K., Mutch B., Lai P.C., Domin J., Game L., Salama A., Foxwell B.M., Pusey C.D., Cook H.T., Aitman T.J. Jund is a determinant of macrophage activation and is associated with glomerulonephritis susceptibility. Nat. Genet. 2008, 40:553-559.
-
(2008)
Nat. Genet.
, vol.40
, pp. 553-559
-
-
Behmoaras, J.1
Bhangal, G.2
Smith, J.3
McDonald, K.4
Mutch, B.5
Lai, P.C.6
Domin, J.7
Game, L.8
Salama, A.9
Foxwell, B.M.10
Pusey, C.D.11
Cook, H.T.12
Aitman, T.J.13
-
52
-
-
47249097572
-
Molecular networks in Dahl salt-sensitive hypertension based on transcriptome analysis of a panel of consomic rats
-
Liang M., Lee N.H., Wang H., Greene A.S., Kwitek A.E., Kaldunski M.L., Luu T.V., Frank B.C., Bugenhagen S., Jacob H.J., Cowley A.W. Molecular networks in Dahl salt-sensitive hypertension based on transcriptome analysis of a panel of consomic rats. Physiol. Genomics 2008, 34:54-64.
-
(2008)
Physiol. Genomics
, vol.34
, pp. 54-64
-
-
Liang, M.1
Lee, N.H.2
Wang, H.3
Greene, A.S.4
Kwitek, A.E.5
Kaldunski, M.L.6
Luu, T.V.7
Frank, B.C.8
Bugenhagen, S.9
Jacob, H.J.10
Cowley, A.W.11
-
53
-
-
42049087447
-
Renal regional proteomes in young Dahl salt-sensitive rats
-
Tian Z., Greene A.S., Usa K., Matus I.R., Bauwens J., Pietrusz J.L., Cowley A.W., Liang M. Renal regional proteomes in young Dahl salt-sensitive rats. Hypertension 2008, 51:899-904.
-
(2008)
Hypertension
, vol.51
, pp. 899-904
-
-
Tian, Z.1
Greene, A.S.2
Usa, K.3
Matus, I.R.4
Bauwens, J.5
Pietrusz, J.L.6
Cowley, A.W.7
Liang, M.8
-
54
-
-
4043089215
-
Consomic rat model systems for physiological genomics
-
Cowley A.W., Liang M., Roman R.J., Greene A.S., Jacob H.J. Consomic rat model systems for physiological genomics. Acta Physiol. Scand. 2004, 181:585-592.
-
(2004)
Acta Physiol. Scand.
, vol.181
, pp. 585-592
-
-
Cowley, A.W.1
Liang, M.2
Roman, R.J.3
Greene, A.S.4
Jacob, H.J.5
-
55
-
-
61449224751
-
A resource for the simultaneous high-resolution mapping of multiple quantitative trait loci in rats: the NIH heterogeneous stock
-
Johannesson M., Lopez-Aumatell R., Stridh P., Diez M., Tuncel J., Blazquez G., Martinez-Membrives E., Canete T., Vicens-Costa E., Graham D., Copley R.R., Hernandez-Pliego P., Beyeen A.D., Ockinger J., Fernandez-Santamaria C., Gulko P.S., Brenner M., Tobena A., Guitart-Masip M., Gimenez-Llort L., Dominiczak A., Holmdahl R., Gauguier D., Olsson T., Mott R., Valdar W., Redei E.E., Fernandez-Teruel A., Flint J. A resource for the simultaneous high-resolution mapping of multiple quantitative trait loci in rats: the NIH heterogeneous stock. Genome Res. 2009, 19:150-158.
-
(2009)
Genome Res.
, vol.19
, pp. 150-158
-
-
Johannesson, M.1
Lopez-Aumatell, R.2
Stridh, P.3
Diez, M.4
Tuncel, J.5
Blazquez, G.6
Martinez-Membrives, E.7
Canete, T.8
Vicens-Costa, E.9
Graham, D.10
Copley, R.R.11
Hernandez-Pliego, P.12
Beyeen, A.D.13
Ockinger, J.14
Fernandez-Santamaria, C.15
Gulko, P.S.16
Brenner, M.17
Tobena, A.18
Guitart-Masip, M.19
Gimenez-Llort, L.20
Dominiczak, A.21
Holmdahl, R.22
Gauguier, D.23
Olsson, T.24
Mott, R.25
Valdar, W.26
Redei, E.E.27
Fernandez-Teruel, A.28
Flint, J.29
more..
-
56
-
-
33746540478
-
Genome-wide genetic association of complex traits in heterogeneous stock mice
-
Valdar W., Solberg L.C., Gauguier D., Burnett S., Klenerman P., Cookson W.O., Taylor M.S., Rawlins J.N., Mott R., Flint J. Genome-wide genetic association of complex traits in heterogeneous stock mice. Nat. Genet. 2006, 38:879-887.
-
(2006)
Nat. Genet.
, vol.38
, pp. 879-887
-
-
Valdar, W.1
Solberg, L.C.2
Gauguier, D.3
Burnett, S.4
Klenerman, P.5
Cookson, W.O.6
Taylor, M.S.7
Rawlins, J.N.8
Mott, R.9
Flint, J.10
-
57
-
-
20144377218
-
Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease
-
Hubner N., Wallace C.A., Zimdahl H., Petretto E., Schulz H., Maciver F., Mueller M., Hummel O., Monti J., Zidek V., Musilova A., Kren V., Causton H., Game L., Born G., Schmidt S., Muller A., Cook S.A., Kurtz T.W., Whittaker J., Pravenec M., Aitman T.J. Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease. Nat. Genet. 2005, 37:243-253.
-
(2005)
Nat. Genet.
, vol.37
, pp. 243-253
-
-
Hubner, N.1
Wallace, C.A.2
Zimdahl, H.3
Petretto, E.4
Schulz, H.5
Maciver, F.6
Mueller, M.7
Hummel, O.8
Monti, J.9
Zidek, V.10
Musilova, A.11
Kren, V.12
Causton, H.13
Game, L.14
Born, G.15
Schmidt, S.16
Muller, A.17
Cook, S.A.18
Kurtz, T.W.19
Whittaker, J.20
Pravenec, M.21
Aitman, T.J.22
more..
-
58
-
-
42649105447
-
Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease
-
Monti J., Fischer J., Paskas S., Heinig M., Schulz H., Gosele C., Heuser A., Fischer R., Schmidt C., Schirdewan A., Gross V., Hummel O., Maatz H., Patone G., Saar K., Vingron M., Weldon S.M., Lindpaintner K., Hammock B.D., Rohde K., Dietz R., Cook S.A., Schunck W.H., Luft F.C., Hubner N. Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease. Nat. Genet. 2008, 40:529-537.
-
(2008)
Nat. Genet.
, vol.40
, pp. 529-537
-
-
Monti, J.1
Fischer, J.2
Paskas, S.3
Heinig, M.4
Schulz, H.5
Gosele, C.6
Heuser, A.7
Fischer, R.8
Schmidt, C.9
Schirdewan, A.10
Gross, V.11
Hummel, O.12
Maatz, H.13
Patone, G.14
Saar, K.15
Vingron, M.16
Weldon, S.M.17
Lindpaintner, K.18
Hammock, B.D.19
Rohde, K.20
Dietz, R.21
Cook, S.A.22
Schunck, W.H.23
Luft, F.C.24
Hubner, N.25
more..
-
59
-
-
42649125570
-
Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular mass
-
Petretto E., Sarwar R., Grieve I., Lu H., Kumaran M.K., Muckett P.J., Mangion J., Schroen B., Benson M., Punjabi P.P., Prasad S.K., Pennell D.J., Kiesewetter C., Tasheva E.S., Corpuz L.M., Webb M.D., Conrad G.W., Kurtz T.W., Kren V., Fischer J., Hubner N., Pinto Y.M., Pravenec M., Aitman T.J., Cook S.A. Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular mass. Nat. Genet. 2008, 40:546-552.
-
(2008)
Nat. Genet.
, vol.40
, pp. 546-552
-
-
Petretto, E.1
Sarwar, R.2
Grieve, I.3
Lu, H.4
Kumaran, M.K.5
Muckett, P.J.6
Mangion, J.7
Schroen, B.8
Benson, M.9
Punjabi, P.P.10
Prasad, S.K.11
Pennell, D.J.12
Kiesewetter, C.13
Tasheva, E.S.14
Corpuz, L.M.15
Webb, M.D.16
Conrad, G.W.17
Kurtz, T.W.18
Kren, V.19
Fischer, J.20
Hubner, N.21
Pinto, Y.M.22
Pravenec, M.23
Aitman, T.J.24
Cook, S.A.25
more..
-
60
-
-
0033828113
-
Glutathione S-transferase polymorphisms and their biological consequences
-
Hayes J.D., Strange R.C. Glutathione S-transferase polymorphisms and their biological consequences. Pharmacology 2000, 61:154-166.
-
(2000)
Pharmacology
, vol.61
, pp. 154-166
-
-
Hayes, J.D.1
Strange, R.C.2
-
61
-
-
18844370620
-
Common genetic mechanisms of blood pressure elevation in two independent rodent models of human essential hypertension
-
Friese R.S., Mahboubi P., Mahapatra N.R., Mahata S.K., Schork N.J., Schmid-Schonbein G.W., O'Connor D.T. Common genetic mechanisms of blood pressure elevation in two independent rodent models of human essential hypertension. Am. J. Hypertens. 2005, 18:633-652.
-
(2005)
Am. J. Hypertens.
, vol.18
, pp. 633-652
-
-
Friese, R.S.1
Mahboubi, P.2
Mahapatra, N.R.3
Mahata, S.K.4
Schork, N.J.5
Schmid-Schonbein, G.W.6
O'Connor, D.T.7
-
62
-
-
53649091022
-
Glutathione S-transferase variants and hypertension
-
Delles C., Padmanabhan S., Lee W.K., Miller W.H., McBride M.W., McClure J.D., Brain N.J., Wallace C., Marcano A.C., Schmieder R.E., Brown M.J., Caulfield M.J., Munroe P.B., Farrall M., Webster J., Connell J.M., Dominiczak A.F. Glutathione S-transferase variants and hypertension. J. Hypertens. 2008, 26:1343-1352.
-
(2008)
J. Hypertens.
, vol.26
, pp. 1343-1352
-
-
Delles, C.1
Padmanabhan, S.2
Lee, W.K.3
Miller, W.H.4
McBride, M.W.5
McClure, J.D.6
Brain, N.J.7
Wallace, C.8
Marcano, A.C.9
Schmieder, R.E.10
Brown, M.J.11
Caulfield, M.J.12
Munroe, P.B.13
Farrall, M.14
Webster, J.15
Connell, J.M.16
Dominiczak, A.F.17
-
63
-
-
43449087893
-
Genetics of the human renin angiotensin system
-
Jeunemaitre X. Genetics of the human renin angiotensin system. J. Mol. Med. 2008, 86:637-641.
-
(2008)
J. Mol. Med.
, vol.86
, pp. 637-641
-
-
Jeunemaitre, X.1
-
64
-
-
65649108517
-
Significance of genetic polymorphisms of the renin-angiotensin-aldosterone system in cardiovascular and renal disease
-
Rudnicki M., Mayer G. Significance of genetic polymorphisms of the renin-angiotensin-aldosterone system in cardiovascular and renal disease. Pharmacogenomics 2009, 10:463-476.
-
(2009)
Pharmacogenomics
, vol.10
, pp. 463-476
-
-
Rudnicki, M.1
Mayer, G.2
-
65
-
-
39749113160
-
Meta-analysis of the association of 4 angiotensinogen polymorphisms with essential hypertension: a role beyond M235T?
-
Pereira T.V., Nunes A.C., Rudnicki M., Yamada Y., Pereira A.C., Krieger J.E. Meta-analysis of the association of 4 angiotensinogen polymorphisms with essential hypertension: a role beyond M235T?. Hypertension 2008, 51:778-783.
-
(2008)
Hypertension
, vol.51
, pp. 778-783
-
-
Pereira, T.V.1
Nunes, A.C.2
Rudnicki, M.3
Yamada, Y.4
Pereira, A.C.5
Krieger, J.E.6
-
66
-
-
33646047704
-
Update on G-protein polymorphisms in hypertension
-
Zhu H., Wang X., Lu Y., Poola J., Momin Z., Harshfield G.A., Snieder H., Dong Y. Update on G-protein polymorphisms in hypertension. Curr. Hypertens. Rep. 2006, 8:23-29.
-
(2006)
Curr. Hypertens. Rep.
, vol.8
, pp. 23-29
-
-
Zhu, H.1
Wang, X.2
Lu, Y.3
Poola, J.4
Momin, Z.5
Harshfield, G.A.6
Snieder, H.7
Dong, Y.8
-
67
-
-
14644401770
-
Adducin polymorphism: detection and impact on hypertension and related disorders
-
Bianchi G., Ferrari P., Staessen J.A. Adducin polymorphism: detection and impact on hypertension and related disorders. Hypertension 2005, 45:331-340.
-
(2005)
Hypertension
, vol.45
, pp. 331-340
-
-
Bianchi, G.1
Ferrari, P.2
Staessen, J.A.3
-
68
-
-
34547890304
-
Functional genomics of the oxidative stress pathway
-
Delles C., Moreno M.U., Padmanabhan S., Graham D., McBride M.W., Dominiczak A.F. Functional genomics of the oxidative stress pathway. Curr. Hypertens. Rev. 2009, 3:156-165.
-
(2009)
Curr. Hypertens. Rev.
, vol.3
, pp. 156-165
-
-
Delles, C.1
Moreno, M.U.2
Padmanabhan, S.3
Graham, D.4
McBride, M.W.5
Dominiczak, A.F.6
-
69
-
-
38949165231
-
NADPH oxidase CYBA polymorphisms, oxidative stress and cardiovascular diseases
-
San Jose G., Fortuno A., Beloqui O., Diez J., Zalba G. NADPH oxidase CYBA polymorphisms, oxidative stress and cardiovascular diseases. Clin. Sci. (Lond) 2008, 114:173-182.
-
(2008)
Clin. Sci. (Lond)
, vol.114
, pp. 173-182
-
-
San Jose, G.1
Fortuno, A.2
Beloqui, O.3
Diez, J.4
Zalba, G.5
-
70
-
-
3042731163
-
Serum aldosterone and the incidence of hypertension in nonhypertensive persons
-
Vasan R.S., Evans J.C., Larson M.G., Wilson P.W., Meigs J.B., Rifai N., Benjamin E.J., Levy D. Serum aldosterone and the incidence of hypertension in nonhypertensive persons. N. Engl. J. Med. 2004, 351:33-41.
-
(2004)
N. Engl. J. Med.
, vol.351
, pp. 33-41
-
-
Vasan, R.S.1
Evans, J.C.2
Larson, M.G.3
Wilson, P.W.4
Meigs, J.B.5
Rifai, N.6
Benjamin, E.J.7
Levy, D.8
-
71
-
-
67049117543
-
Programming of hypertension: associations of plasma aldosterone in adult men and women with birthweight, cortisol, and blood pressure
-
Reynolds R.M., Walker B.R., Phillips D.I., Dennison E.M., Fraser R., Mackenzie S.M., Davies E., Connell J.M. Programming of hypertension: associations of plasma aldosterone in adult men and women with birthweight, cortisol, and blood pressure. Hypertension 2009, 53:932-936.
-
(2009)
Hypertension
, vol.53
, pp. 932-936
-
-
Reynolds, R.M.1
Walker, B.R.2
Phillips, D.I.3
Dennison, E.M.4
Fraser, R.5
Mackenzie, S.M.6
Davies, E.7
Connell, J.M.8
-
72
-
-
59649090400
-
Altered corticosteroid biosynthesis in essential hypertension: a digenic phenomenon
-
Davies E., Mackenzie S.M., Freel E.M., Alvarez-Madrazo S., Fraser R., Connell J.M. Altered corticosteroid biosynthesis in essential hypertension: a digenic phenomenon. Mol. Cell Endocrinol. 2009, 300:185-191.
-
(2009)
Mol. Cell Endocrinol.
, vol.300
, pp. 185-191
-
-
Davies, E.1
Mackenzie, S.M.2
Freel, E.M.3
Alvarez-Madrazo, S.4
Fraser, R.5
Connell, J.M.6
-
73
-
-
60349127030
-
Effects of genetic variation in the aldosterone synthase (CYP11B2) gene on enzyme function
-
Holloway C.D., Mackenzie S.M., Fraser R., Miller S., Barr M., Wilkinson D., Forbes G.H., Friel E., Connell J.M., Davies E. Effects of genetic variation in the aldosterone synthase (CYP11B2) gene on enzyme function. Clin. Endocrinol. (Oxf) 2009, 70:363-371.
-
(2009)
Clin. Endocrinol. (Oxf)
, vol.70
, pp. 363-371
-
-
Holloway, C.D.1
Mackenzie, S.M.2
Fraser, R.3
Miller, S.4
Barr, M.5
Wilkinson, D.6
Forbes, G.H.7
Friel, E.8
Connell, J.M.9
Davies, E.10
-
74
-
-
33845355513
-
Association of the C-344T aldosterone synthase gene variant with essential hypertension: a meta-analysis
-
Sookoian S., Gianotti T.F., Gonzalez C.D., Pirola C.J. Association of the C-344T aldosterone synthase gene variant with essential hypertension: a meta-analysis. J. Hypertens. 2007, 25:5-13.
-
(2007)
J. Hypertens.
, vol.25
, pp. 5-13
-
-
Sookoian, S.1
Gianotti, T.F.2
Gonzalez, C.D.3
Pirola, C.J.4
-
75
-
-
67650665283
-
Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array
-
Sober S., Org E., Kepp K., Juhanson P., Eyheramendy S., Gieger C., Lichtner P., Klopp N., Veldre G., Viigimaa M., Doring A., Putku M., Kelgo P., Shaw-Hawkins S., Howard P., Onipinla A., Dobson R.J., Newhouse S.J., Brown M., Dominiczak A., Connell J., Samani N., Farrall M., Caulfield M.J., Munroe P.B., Illig T., Wichmann H.E., Meitinger T., Laan M. Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array. PLoS. One 2009, 4:e6034.
-
(2009)
PLoS. One
, vol.4
-
-
Sober, S.1
Org, E.2
Kepp, K.3
Juhanson, P.4
Eyheramendy, S.5
Gieger, C.6
Lichtner, P.7
Klopp, N.8
Veldre, G.9
Viigimaa, M.10
Doring, A.11
Putku, M.12
Kelgo, P.13
Shaw-Hawkins, S.14
Howard, P.15
Onipinla, A.16
Dobson, R.J.17
Newhouse, S.J.18
Brown, M.19
Dominiczak, A.20
Connell, J.21
Samani, N.22
Farrall, M.23
Caulfield, M.J.24
Munroe, P.B.25
Illig, T.26
Wichmann, H.E.27
Meitinger, T.28
Laan, M.29
more..
-
76
-
-
0021957675
-
A comparison of sib-pair linkage tests for disease susceptibility loci
-
Blackwelder W.C., Elston R.C. A comparison of sib-pair linkage tests for disease susceptibility loci. Genet. Epidemiol. 1985, 2:85-97.
-
(1985)
Genet. Epidemiol.
, vol.2
, pp. 85-97
-
-
Blackwelder, W.C.1
Elston, R.C.2
-
77
-
-
78049306477
-
Recruitment of families for a study into the genetics of hypertension (InGenious HyperCare). A single centre experience
-
Neisius U., Taurino C., Padmanabhan S., Zanchetti A., Delles C., Dominiczak A.F. Recruitment of families for a study into the genetics of hypertension (InGenious HyperCare). A single centre experience. J. Hypertens. 2009, 27:S165.
-
(2009)
J. Hypertens.
, vol.27
-
-
Neisius, U.1
Taurino, C.2
Padmanabhan, S.3
Zanchetti, A.4
Delles, C.5
Dominiczak, A.F.6
-
78
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007, 447:661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
79
-
-
34147216956
-
A review of the genetics of essential hypertension
-
Binder A. A review of the genetics of essential hypertension. Curr. Opin. Cardiol. 2007, 22:176-184.
-
(2007)
Curr. Opin. Cardiol.
, vol.22
, pp. 176-184
-
-
Binder, A.1
-
80
-
-
5444222846
-
Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3
-
Koivukoski L., Fisher S.A., Kanninen T., Lewis C.M., von Wowern F., Hunt S., Kardia S.L., Levy D., Perola M., Rankinen T., Rao D.C., Rice T., Thiel B.A., Melander O. Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3. Hum. Mol. Genet. 2004, 13:2325-2332.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2325-2332
-
-
Koivukoski, L.1
Fisher, S.A.2
Kanninen, T.3
Lewis, C.M.4
von Wowern, F.5
Hunt, S.6
Kardia, S.L.7
Levy, D.8
Perola, M.9
Rankinen, T.10
Rao, D.C.11
Rice, T.12
Thiel, B.A.13
Melander, O.14
-
81
-
-
33644980079
-
Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study
-
Padmanabhan S., Wallace C., Munroe P.B., Dobson R., Brown M., Samani N., Clayton D., Farrall M., Webster J., Lathrop M., Caulfield M., Dominiczak A.F., Connell J.M. Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study. Hypertension 2006, 47:603-608.
-
(2006)
Hypertension
, vol.47
, pp. 603-608
-
-
Padmanabhan, S.1
Wallace, C.2
Munroe, P.B.3
Dobson, R.4
Brown, M.5
Samani, N.6
Clayton, D.7
Farrall, M.8
Webster, J.9
Lathrop, M.10
Caulfield, M.11
Dominiczak, A.F.12
Connell, J.M.13
-
82
-
-
0842332610
-
Positional identification of hypertension susceptibility genes on chromosome 2
-
Barkley R.A., Chakravarti A., Cooper R.S., Ellison R.C., Hunt S.C., Province M.A., Turner S.T., Weder A.B., Boerwinkle E. Positional identification of hypertension susceptibility genes on chromosome 2. Hypertension 2004, 43:477-482.
-
(2004)
Hypertension
, vol.43
, pp. 477-482
-
-
Barkley, R.A.1
Chakravarti, A.2
Cooper, R.S.3
Ellison, R.C.4
Hunt, S.C.5
Province, M.A.6
Turner, S.T.7
Weder, A.B.8
Boerwinkle, E.9
-
83
-
-
33746497751
-
Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension
-
Wallace C., Xue M.Z., Newhouse S.J., Marcano A.C., Onipinla A.K., Burke B., Gungadoo J., Dobson R.J., Brown M., Connell J.M., Dominiczak A., Lathrop G.M., Webster J., Farrall M., Mein C., Samani N.J., Caulfield M.J., Clayton D.G., Munroe P.B. Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension. Am. J. Hum. Genet. 2006, 79:323-331.
-
(2006)
Am. J. Hum. Genet.
, vol.79
, pp. 323-331
-
-
Wallace, C.1
Xue, M.Z.2
Newhouse, S.J.3
Marcano, A.C.4
Onipinla, A.K.5
Burke, B.6
Gungadoo, J.7
Dobson, R.J.8
Brown, M.9
Connell, J.M.10
Dominiczak, A.11
Lathrop, G.M.12
Webster, J.13
Farrall, M.14
Mein, C.15
Samani, N.J.16
Caulfield, M.J.17
Clayton, D.G.18
Munroe, P.B.19
-
84
-
-
20844455582
-
Genotyping over 100, 000 SNPs on a pair of oligonucleotide arrays
-
Matsuzaki H., Dong S., Loi H., Di X., Liu G., Hubbell E., Law J., Berntsen T., Chadha M., Hui H., Yang G., Kennedy G.C., Webster T.A., Cawley S., Walsh P.S., Jones K.W., Fodor S.P., Mei R. Genotyping over 100, 000 SNPs on a pair of oligonucleotide arrays. Nat. Methods 2004, 1:109-111.
-
(2004)
Nat. Methods
, vol.1
, pp. 109-111
-
-
Matsuzaki, H.1
Dong, S.2
Loi, H.3
Di, X.4
Liu, G.5
Hubbell, E.6
Law, J.7
Berntsen, T.8
Chadha, M.9
Hui, H.10
Yang, G.11
Kennedy, G.C.12
Webster, T.A.13
Cawley, S.14
Walsh, P.S.15
Jones, K.W.16
Fodor, S.P.17
Mei, R.18
-
85
-
-
18144425478
-
A genome-wide scalable SNP genotyping assay using microarray technology
-
Gunderson K.L., Steemers F.J., Lee G., Mendoza L.G., Chee M.S. A genome-wide scalable SNP genotyping assay using microarray technology. Nat. Genet. 2005, 37:549-554.
-
(2005)
Nat. Genet.
, vol.37
, pp. 549-554
-
-
Gunderson, K.L.1
Steemers, F.J.2
Lee, G.3
Mendoza, L.G.4
Chee, M.S.5
-
86
-
-
35748962317
-
Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
-
Levy D., Larson M.G., Benjamin E.J., Newton-Cheh C., Wang T.J., Hwang S.J., Vasan R.S., Mitchell G.F. Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. BMC Med. Genet. 2007, 8(Suppl 1):S3.
-
(2007)
BMC Med. Genet.
, vol.8
, Issue.SUPPL 1
-
-
Levy, D.1
Larson, M.G.2
Benjamin, E.J.3
Newton-Cheh, C.4
Wang, T.J.5
Hwang, S.J.6
Vasan, R.S.7
Mitchell, G.F.8
-
87
-
-
77953425627
-
Dissecting complex traits: recent advances in hypertension genomics
-
O'Shaughnessy K.M. Dissecting complex traits: recent advances in hypertension genomics. Genome Med. 2009, 1:43.
-
(2009)
Genome Med.
, vol.1
, pp. 43
-
-
O'Shaughnessy, K.M.1
-
88
-
-
67349188883
-
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
-
Cho Y.S., Go M.J., Kim Y.J., Heo J.Y., Oh J.H., Ban H.J., Yoon D., Lee M.H., Kim D.J., Park M., Cha S.H., Kim J.W., Han B.G., Min H., Ahn Y., Park M.S., Han H.R., Jang H.Y., Cho E.Y., Lee J.E., Cho N.H., Shin C., Park T., Park J.W., Lee J.K., Cardon L., Clarke G., McCarthy M.I., Lee J.Y., Lee J.K., Oh B., Kim H.L. A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Nat. Genet. 2009, 41:527-534.
-
(2009)
Nat. Genet.
, vol.41
, pp. 527-534
-
-
Cho, Y.S.1
Go, M.J.2
Kim, Y.J.3
Heo, J.Y.4
Oh, J.H.5
Ban, H.J.6
Yoon, D.7
Lee, M.H.8
Kim, D.J.9
Park, M.10
Cha, S.H.11
Kim, J.W.12
Han, B.G.13
Min, H.14
Ahn, Y.15
Park, M.S.16
Han, H.R.17
Jang, H.Y.18
Cho, E.Y.19
Lee, J.E.20
Cho, N.H.21
Shin, C.22
Park, T.23
Park, J.W.24
Lee, J.K.25
Cardon, L.26
Clarke, G.27
McCarthy, M.I.28
Lee, J.Y.29
Lee, J.K.30
Oh, B.31
Kim, H.L.32
more..
-
89
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
Newton-Cheh C., Johnson T., Gateva V., Tobin M.D., Bochud M., Coin L., Najjar S.S., Zhao J.H., Heath S.C., Eyheramendy S., Papadakis K., Voight B.F., Scott L.J., Zhang F., Farrall M., Tanaka T., Wallace C., Chambers J.C., Khaw K.T., Nilsson P., van der H.P., Polidoro S., Grobbee D.E., Onland-Moret N.C., Bots M.L., Wain L.V., Elliott K.S., Teumer A., Luan J., Lucas G., Kuusisto J., Burton P.R., Hadley D., McArdle W.L., Brown M., Dominiczak A., Newhouse S.J., Samani N.J., Webster J., Zeggini E., Beckmann J.S., Bergmann S., Lim N., Song K., Vollenweider P., Waeber G., Waterworth D.M., Yuan X., Groop L., Orho-Melander M., Allione A., Di Gregorio A., Guarrera S., Panico S., Ricceri F., Romanazzi V., Sacerdote C., Vineis P., Barroso I., Sandhu M.S., Luben R.N., Crawford G.J., Jousilahti P., Perola M., Boehnke M., Bonnycastle L.L., Collins F.S., Jackson A.U., Mohlke K.L., Stringham H.M., Valle T.T., Willer C.J., Bergman R.N., Morken M.A., Doring A., Gieger C., Illig T., Meitinger T., Org E., Pfeufer A., Wichmann H.E., Kathiresan S., Marrugat J., O'Donnell C.J., Schwartz S.M., Siscovick D.S., Subirana I., Freimer N.B., Hartikainen A.L., McCarthy M.I., O'Reilly P.F., Peltonen L., Pouta A., de Jong P.E., Snieder H., van Gilst W.H., Clarke R., Goel A., Hamsten A., Peden J.F., Seedorf U., Syvanen A.C., Tognoni G., Lakatta E.G., Sanna S., Scheet P., Schlessinger D., Scuteri A., Dorr M., Ernst F., Felix S.B., Homuth G., Lorbeer R., Reffelmann T., Rettig R., Volker U., Galan P., Gut I.G., Hercberg S., Lathrop G.M., Zelenika D., Deloukas P., Soranzo N., Williams F.M., Zhai G., Salomaa V., Laakso M., Elosua R., Forouhi N.G., Volzke H., Uiterwaal C.S., van der Schouw Y.T., Numans M.E., Matullo G., Navis G., Berglund G., Bingham S.A., Kooner J.S., Connell J.M., Bandinelli S., Ferrucci L., Watkins H., Spector T.D., Tuomilehto J., Altshuler D., Strachan D.P., Laan M., Meneton P., Wareham N.J., Uda M., Jarvelin M.R., Mooser V., Melander O., Loos R.J., Elliott P., Abecasis G.R., Caulfield M., Munroe P.B. Genome-wide association study identifies eight loci associated with blood pressure. Nat. Genet. 2009, 41:666-676.
-
(2009)
Nat. Genet.
, vol.41
, pp. 666-676
-
-
Newton-Cheh, C.1
Johnson, T.2
Gateva, V.3
Tobin, M.D.4
Bochud, M.5
Coin, L.6
Najjar, S.S.7
Zhao, J.H.8
Heath, S.C.9
Eyheramendy, S.10
Papadakis, K.11
Voight, B.F.12
Scott, L.J.13
Zhang, F.14
Farrall, M.15
Tanaka, T.16
Wallace, C.17
Chambers, J.C.18
Khaw, K.T.19
Nilsson, P.20
van der, H.P.21
Polidoro, S.22
Grobbee, D.E.23
Onland-Moret, N.C.24
Bots, M.L.25
Wain, L.V.26
Elliott, K.S.27
Teumer, A.28
Luan, J.29
Lucas, G.30
Kuusisto, J.31
Burton, P.R.32
Hadley, D.33
McArdle, W.L.34
Brown, M.35
Dominiczak, A.36
Newhouse, S.J.37
Samani, N.J.38
Webster, J.39
Zeggini, E.40
Beckmann, J.S.41
Bergmann, S.42
Lim, N.43
Song, K.44
Vollenweider, P.45
Waeber, G.46
Waterworth, D.M.47
Yuan, X.48
Groop, L.49
Orho-Melander, M.50
Allione, A.51
Di Gregorio, A.52
Guarrera, S.53
Panico, S.54
Ricceri, F.55
Romanazzi, V.56
Sacerdote, C.57
Vineis, P.58
Barroso, I.59
Sandhu, M.S.60
Luben, R.N.61
Crawford, G.J.62
Jousilahti, P.63
Perola, M.64
Boehnke, M.65
Bonnycastle, L.L.66
Collins, F.S.67
Jackson, A.U.68
Mohlke, K.L.69
Stringham, H.M.70
Valle, T.T.71
Willer, C.J.72
Bergman, R.N.73
Morken, M.A.74
Doring, A.75
Gieger, C.76
Illig, T.77
Meitinger, T.78
Org, E.79
Pfeufer, A.80
Wichmann, H.E.81
Kathiresan, S.82
Marrugat, J.83
O'Donnell, C.J.84
Schwartz, S.M.85
Siscovick, D.S.86
Subirana, I.87
Freimer, N.B.88
Hartikainen, A.L.89
McCarthy, M.I.90
O'Reilly, P.F.91
Peltonen, L.92
Pouta, A.93
de Jong, P.E.94
Snieder, H.95
van Gilst, W.H.96
Clarke, R.97
Goel, A.98
Hamsten, A.99
more..
-
90
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
Levy D., Ehret G.B., Rice K., Verwoert G.C., Launer L.J., Dehghan A., Glazer N.L., Morrison A.C., Johnson A.D., Aspelund T., Aulchenko Y., Lumley T., Kottgen A., Vasan R.S., Rivadeneira F., Eiriksdottir G., Guo X., Arking D.E., Mitchell G.F., Mattace-Raso F.U., Smith A.V., Taylor K., Scharpf R.B., Hwang S.J., Sijbrands E.J., Bis J., Harris T.B., Ganesh S.K., O'Donnell C.J., Hofman A., Rotter J.I., Coresh J., Benjamin E.J., Uitterlinden A.G., Heiss G., Fox C.S., Witteman J.C., Boerwinkle E., Wang T.J., Gudnason V., Larson M.G., Chakravarti A., Psaty B.M., van Duijn C.M. Genome-wide association study of blood pressure and hypertension. Nat. Genet. 2009, 41:677-687.
-
(2009)
Nat. Genet.
, vol.41
, pp. 677-687
-
-
Levy, D.1
Ehret, G.B.2
Rice, K.3
Verwoert, G.C.4
Launer, L.J.5
Dehghan, A.6
Glazer, N.L.7
Morrison, A.C.8
Johnson, A.D.9
Aspelund, T.10
Aulchenko, Y.11
Lumley, T.12
Kottgen, A.13
Vasan, R.S.14
Rivadeneira, F.15
Eiriksdottir, G.16
Guo, X.17
Arking, D.E.18
Mitchell, G.F.19
Mattace-Raso, F.U.20
Smith, A.V.21
Taylor, K.22
Scharpf, R.B.23
Hwang, S.J.24
Sijbrands, E.J.25
Bis, J.26
Harris, T.B.27
Ganesh, S.K.28
O'Donnell, C.J.29
Hofman, A.30
Rotter, J.I.31
Coresh, J.32
Benjamin, E.J.33
Uitterlinden, A.G.34
Heiss, G.35
Fox, C.S.36
Witteman, J.C.37
Boerwinkle, E.38
Wang, T.J.39
Gudnason, V.40
Larson, M.G.41
Chakravarti, A.42
Psaty, B.M.43
van Duijn, C.M.44
more..
-
91
-
-
0035936780
-
Molecular mechanisms of human hypertension
-
Lifton R.P., Gharavi A.G., Geller D.S. Molecular mechanisms of human hypertension. Cell 2001, 104:545-556.
-
(2001)
Cell
, vol.104
, pp. 545-556
-
-
Lifton, R.P.1
Gharavi, A.G.2
Geller, D.S.3
-
92
-
-
0027218610
-
Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients
-
Mitsuuchi Y., Kawamoto T., Miyahara K., Ulick S., Morton D.H., Naiki Y., Kuribayashi I., Toda K., Hara T., Orii T. Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients. Biochem. Biophys. Res. Commun. 1993, 190:864-869.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.190
, pp. 864-869
-
-
Mitsuuchi, Y.1
Kawamoto, T.2
Miyahara, K.3
Ulick, S.4
Morton, D.H.5
Naiki, Y.6
Kuribayashi, I.7
Toda, K.8
Hara, T.9
Orii, T.10
-
93
-
-
0026543990
-
Congenitally defective aldosterone biosynthesis in humans: the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients
-
Mitsuuchi Y., Kawamoto T., Naiki Y., Miyahara K., Toda K., Kuribayashi I., Orii T., Yasuda K., Miura K., Nakao K. Congenitally defective aldosterone biosynthesis in humans: the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients. Biochem. Biophys. Res. Commun. 1992, 182:974-979.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.182
, pp. 974-979
-
-
Mitsuuchi, Y.1
Kawamoto, T.2
Naiki, Y.3
Miyahara, K.4
Toda, K.5
Kuribayashi, I.6
Orii, T.7
Yasuda, K.8
Miura, K.9
Nakao, K.10
-
94
-
-
0026771282
-
Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency
-
Pascoe L., Curnow K.M., Slutsker L., Rosler A., White P.C. Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency. Proc. Natl. Acad. Sci. U. S. A. 1992, 89:4996-5000.
-
(1992)
Proc. Natl. Acad. Sci. U. S. A.
, vol.89
, pp. 4996-5000
-
-
Pascoe, L.1
Curnow, K.M.2
Slutsker, L.3
Rosler, A.4
White, P.C.5
-
96
-
-
51149104842
-
WNK kinases, renal ion transport and hypertension
-
San Cristobal P., de los H.P., Ponce-Coria J., Moreno E., Gamba G. WNK kinases, renal ion transport and hypertension. Am. J. Nephrol. 2008, 28:860-870.
-
(2008)
Am. J. Nephrol.
, vol.28
, pp. 860-870
-
-
San Cristobal, P.1
de los, H.P.2
Ponce-Coria, J.3
Moreno, E.4
Gamba, G.5
-
97
-
-
39149129333
-
Cotransporters, WNKs and hypertension: an update
-
Flatman P.W. Cotransporters, WNKs and hypertension: an update. Curr. Opin. Nephrol. Hypertens. 2008, 17:186-192.
-
(2008)
Curr. Opin. Nephrol. Hypertens.
, vol.17
, pp. 186-192
-
-
Flatman, P.W.1
-
98
-
-
17944373014
-
Human hypertension caused by mutations in WNK kinases
-
Wilson F.H., Disse-Nicodeme S., Choate K.A., Ishikawa K., Nelson-Williams C., Desitter I., Gunel M., Milford D.V., Lipkin G.W., Achard J.M., Feely M.P., Dussol B., Berland Y., Unwin R.J., Mayan H., Simon D.B., Farfel Z., Jeunemaitre X., Lifton R.P. Human hypertension caused by mutations in WNK kinases. Science 2001, 293:1107-1112.
-
(2001)
Science
, vol.293
, pp. 1107-1112
-
-
Wilson, F.H.1
Disse-Nicodeme, S.2
Choate, K.A.3
Ishikawa, K.4
Nelson-Williams, C.5
Desitter, I.6
Gunel, M.7
Milford, D.V.8
Lipkin, G.W.9
Achard, J.M.10
Feely, M.P.11
Dussol, B.12
Berland, Y.13
Unwin, R.J.14
Mayan, H.15
Simon, D.B.16
Farfel, Z.17
Jeunemaitre, X.18
Lifton, R.P.19
-
99
-
-
26444443132
-
Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study
-
Newhouse S.J., Wallace C., Dobson R., Mein C., Pembroke J., Farrall M., Clayton D., Brown M., Samani N., Dominiczak A., Connell J.M., Webster J., Lathrop G.M., Caulfield M., Munroe P.B. Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study. Hum. Mol. Genet. 2005, 14:1805-1814.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 1805-1814
-
-
Newhouse, S.J.1
Wallace, C.2
Dobson, R.3
Mein, C.4
Pembroke, J.5
Farrall, M.6
Clayton, D.7
Brown, M.8
Samani, N.9
Dominiczak, A.10
Connell, J.M.11
Webster, J.12
Lathrop, G.M.13
Caulfield, M.14
Munroe, P.B.15
-
100
-
-
33644874530
-
Association of WNK1 gene polymorphisms and haplotypes with ambulatory blood pressure in the general population
-
Tobin M.D., Raleigh S.M., Newhouse S., Braund P., Bodycote C., Ogleby J., Cross D., Gracey J., Hayes S., Smith T., Ridge C., Caulfield M., Sheehan N.A., Munroe P.B., Burton P.R., Samani N.J. Association of WNK1 gene polymorphisms and haplotypes with ambulatory blood pressure in the general population. Circulation 2005, 112:3423-3429.
-
(2005)
Circulation
, vol.112
, pp. 3423-3429
-
-
Tobin, M.D.1
Raleigh, S.M.2
Newhouse, S.3
Braund, P.4
Bodycote, C.5
Ogleby, J.6
Cross, D.7
Gracey, J.8
Hayes, S.9
Smith, T.10
Ridge, C.11
Caulfield, M.12
Sheehan, N.A.13
Munroe, P.B.14
Burton, P.R.15
Samani, N.J.16
-
101
-
-
45849115433
-
Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population
-
Tobin M.D., Tomaszewski M., Braund P.S., Hajat C., Raleigh S.M., Palmer T.M., Caulfield M., Burton P.R., Samani N.J. Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension 2008, 51:1658-1664.
-
(2008)
Hypertension
, vol.51
, pp. 1658-1664
-
-
Tobin, M.D.1
Tomaszewski, M.2
Braund, P.S.3
Hajat, C.4
Raleigh, S.M.5
Palmer, T.M.6
Caulfield, M.7
Burton, P.R.8
Samani, N.J.9
-
102
-
-
42649084334
-
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
-
Ji W., Foo J.N., O'Roak B.J., Zhao H., Larson M.G., Simon D.B., Newton-Cheh C., State M.W., Levy D., Lifton R.P. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat. Genet. 2008, 40:592-599.
-
(2008)
Nat. Genet.
, vol.40
, pp. 592-599
-
-
Ji, W.1
Foo, J.N.2
O'Roak, B.J.3
Zhao, H.4
Larson, M.G.5
Simon, D.B.6
Newton-Cheh, C.7
State, M.W.8
Levy, D.9
Lifton, R.P.10
-
103
-
-
9044235777
-
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
-
Simon D.B., Nelson-Williams C., Bia M.J., Ellison D., Karet F.E., Molina A.M., Vaara I., Iwata F., Cushner H.M., Koolen M., Gainza F.J., Gitleman H.J., Lifton R.P. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat. Genet. 1996, 12:24-30.
-
(1996)
Nat. Genet.
, vol.12
, pp. 24-30
-
-
Simon, D.B.1
Nelson-Williams, C.2
Bia, M.J.3
Ellison, D.4
Karet, F.E.5
Molina, A.M.6
Vaara, I.7
Iwata, F.8
Cushner, H.M.9
Koolen, M.10
Gainza, F.J.11
Gitleman, H.J.12
Lifton, R.P.13
-
104
-
-
0026512508
-
Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes
-
Bettinelli A., Bianchetti M.G., Girardin E., Caringella A., Cecconi M., Appiani A.C., Pavanello L., Gastaldi R., Isimbaldi C., Lama G. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes. J. Pediatr. 1992, 120:38-43.
-
(1992)
J. Pediatr.
, vol.120
, pp. 38-43
-
-
Bettinelli, A.1
Bianchetti, M.G.2
Girardin, E.3
Caringella, A.4
Cecconi, M.5
Appiani, A.C.6
Pavanello, L.7
Gastaldi, R.8
Isimbaldi, C.9
Lama, G.10
-
105
-
-
0030032699
-
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2
-
Simon D.B., Karet F.E., Hamdan J.M., DiPietro A., Sanjad S.A., Lifton R.P. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nat. Genet. 1996, 13:183-188.
-
(1996)
Nat. Genet.
, vol.13
, pp. 183-188
-
-
Simon, D.B.1
Karet, F.E.2
Hamdan, J.M.3
DiPietro, A.4
Sanjad, S.A.5
Lifton, R.P.6
-
106
-
-
0029794875
-
+ channel, ROMK
-
+ channel, ROMK. Nat. Genet. 1996, 14:152-156.
-
(1996)
Nat. Genet.
, vol.14
, pp. 152-156
-
-
Simon, D.B.1
Karet, F.E.2
Rodriguez-Soriano, J.3
Hamdan, J.H.4
DiPietro, A.5
Trachtman, H.6
Sanjad, S.A.7
Lifton, R.P.8
-
107
-
-
16944366243
-
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
-
Simon D.B., Bindra R.S., Mansfield T.A., Nelson-Williams C., Mendonca E., Stone R., Schurman S., Nayir A., Alpay H., Bakkaloglu A., Rodriguez-Soriano J., Morales J.M., Sanjad S.A., Taylor C.M., Pilz D., Brem A., Trachtman H., Griswold W., Richard G.A., John E., Lifton R.P. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat. Genet. 1997, 17:171-178.
-
(1997)
Nat. Genet.
, vol.17
, pp. 171-178
-
-
Simon, D.B.1
Bindra, R.S.2
Mansfield, T.A.3
Nelson-Williams, C.4
Mendonca, E.5
Stone, R.6
Schurman, S.7
Nayir, A.8
Alpay, H.9
Bakkaloglu, A.10
Rodriguez-Soriano, J.11
Morales, J.M.12
Sanjad, S.A.13
Taylor, C.M.14
Pilz, D.15
Brem, A.16
Trachtman, H.17
Griswold, W.18
Richard, G.A.19
John, E.20
Lifton, R.P.21
more..
-
108
-
-
33646695396
-
Type IV Bartter syndrome: report of two new cases
-
Zaffanello M., Taranta A., Palma A., Bettinelli A., Marseglia G.L., Emma F. Type IV Bartter syndrome: report of two new cases. Pediatr. Nephrol. 2006, 21:766-770.
-
(2006)
Pediatr. Nephrol.
, vol.21
, pp. 766-770
-
-
Zaffanello, M.1
Taranta, A.2
Palma, A.3
Bettinelli, A.4
Marseglia, G.L.5
Emma, F.6
-
109
-
-
37849188852
-
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome
-
Vezzoli G., Arcidiacono T., Paloschi V., Terranegra A., Biasion R., Weber G., Mora S., Syren M.L., Coviello D., Cusi D., Bianchi G., Soldati L. Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome. J. Nephrol. 2006, 19:525-528.
-
(2006)
J. Nephrol.
, vol.19
, pp. 525-528
-
-
Vezzoli, G.1
Arcidiacono, T.2
Paloschi, V.3
Terranegra, A.4
Biasion, R.5
Weber, G.6
Mora, S.7
Syren, M.L.8
Coviello, D.9
Cusi, D.10
Bianchi, G.11
Soldati, L.12
-
110
-
-
0025789561
-
Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects
-
Hanukoglu A. Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects. J. Clin. Endocrinol. Metab. 1991, 73:936-944.
-
(1991)
J. Clin. Endocrinol. Metab.
, vol.73
, pp. 936-944
-
-
Hanukoglu, A.1
-
111
-
-
0031861245
-
Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
-
Geller D.S., Rodriguez-Soriano J., Vallo B.A., Schifter S., Bayer M., Chang S.S., Lifton R.P. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I. Nat. Genet. 1998, 19:279-281.
-
(1998)
Nat. Genet.
, vol.19
, pp. 279-281
-
-
Geller, D.S.1
Rodriguez-Soriano, J.2
Vallo, B.A.3
Schifter, S.4
Bayer, M.5
Chang, S.S.6
Lifton, R.P.7
-
112
-
-
13344295074
-
Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1
-
Chang S.S., Grunder S., Hanukoglu A., Rosler A., Mathew P.M., Hanukoglu I., Schild L., Lu Y., Shimkets R.A., Nelson-Williams C., Rossier B.C., Lifton R.P. Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nat. Genet. 1996, 12:248-253.
-
(1996)
Nat. Genet.
, vol.12
, pp. 248-253
-
-
Chang, S.S.1
Grunder, S.2
Hanukoglu, A.3
Rosler, A.4
Mathew, P.M.5
Hanukoglu, I.6
Schild, L.7
Lu, Y.8
Shimkets, R.A.9
Nelson-Williams, C.10
Rossier, B.C.11
Lifton, R.P.12
-
113
-
-
0014029230
-
Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone
-
Sutherland D.J., Ruse J.L., Laidlaw J.C. Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone. Can. Med. Assoc. J. 1966, 95:1109-1119.
-
(1966)
Can. Med. Assoc. J.
, vol.95
, pp. 1109-1119
-
-
Sutherland, D.J.1
Ruse, J.L.2
Laidlaw, J.C.3
-
114
-
-
0026580019
-
A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
-
Lifton R.P., Dluhy R.G., Powers M., Rich G.M., Cook S., Ulick S., Lalouel J.M. A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature 1992, 355:262-265.
-
(1992)
Nature
, vol.355
, pp. 262-265
-
-
Lifton, R.P.1
Dluhy, R.G.2
Powers, M.3
Rich, G.M.4
Cook, S.5
Ulick, S.6
Lalouel, J.M.7
-
115
-
-
0026919361
-
Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase
-
Lifton R.P., Dluhy R.G., Powers M., Rich G.M., Gutkin M., Fallo F., Gill J.R., Feld L., Ganguly A., Laidlaw J.C. Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase. Nat. Genet. 1992, 2:66-74.
-
(1992)
Nat. Genet.
, vol.2
, pp. 66-74
-
-
Lifton, R.P.1
Dluhy, R.G.2
Powers, M.3
Rich, G.M.4
Gutkin, M.5
Fallo, F.6
Gill, J.R.7
Feld, L.8
Ganguly, A.9
Laidlaw, J.C.10
-
116
-
-
0026701168
-
Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2
-
Pascoe L., Curnow K.M., Slutsker L., Connell J.M., Speiser P.W., New M.I., White P.C. Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2. Proc. Natl. Acad. Sci. U. S. A. 1992, 89:8327-8331.
-
(1992)
Proc. Natl. Acad. Sci. U. S. A.
, vol.89
, pp. 8327-8331
-
-
Pascoe, L.1
Curnow, K.M.2
Slutsker, L.3
Connell, J.M.4
Speiser, P.W.5
New, M.I.6
White, P.C.7
-
117
-
-
0029160972
-
Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase
-
Mune T., Rogerson F.M., Nikkila H., Agarwal A.K., White P.C. Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase. Nat. Genet. 1995, 10:394-399.
-
(1995)
Nat. Genet.
, vol.10
, pp. 394-399
-
-
Mune, T.1
Rogerson, F.M.2
Nikkila, H.3
Agarwal, A.K.4
White, P.C.5
-
118
-
-
0030049329
-
Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene
-
Stewart P.M., Krozowski Z.S., Gupta A., Milford D.V., Howie A.J., Sheppard M.C., Whorwood C.B. Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene. Lancet 1996, 347:88-91.
-
(1996)
Lancet
, vol.347
, pp. 88-91
-
-
Stewart, P.M.1
Krozowski, Z.S.2
Gupta, A.3
Milford, D.V.4
Howie, A.J.5
Sheppard, M.C.6
Whorwood, C.B.7
-
119
-
-
0034617130
-
Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy
-
Geller D.S., Farhi A., Pinkerton N., Fradley M., Moritz M., Spitzer A., Meinke G., Tsai F.T., Sigler P.B., Lifton R.P. Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy. Science 2000, 289:119-123.
-
(2000)
Science
, vol.289
, pp. 119-123
-
-
Geller, D.S.1
Farhi, A.2
Pinkerton, N.3
Fradley, M.4
Moritz, M.5
Spitzer, A.6
Meinke, G.7
Tsai, F.T.8
Sigler, P.B.9
Lifton, R.P.10
-
120
-
-
0027946089
-
Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel
-
Shimkets R.A., Warnock D.G., Bositis C.M., Nelson-Williams C., Hansson J.H., Schambelan M., Gill J.R., Ulick S., Milora R.V., Findling J.W. Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel. Cell 1994, 79:407-414.
-
(1994)
Cell
, vol.79
, pp. 407-414
-
-
Shimkets, R.A.1
Warnock, D.G.2
Bositis, C.M.3
Nelson-Williams, C.4
Hansson, J.H.5
Schambelan, M.6
Gill, J.R.7
Ulick, S.8
Milora, R.V.9
Findling, J.W.10
-
121
-
-
0029092801
-
Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome
-
Hansson J.H., Nelson-Williams C., Suzuki H., Schild L., Shimkets R., Lu Y., Canessa C., Iwasaki T., Rossier B., Lifton R.P. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome. Nat. Genet. 1995, 11:76-82.
-
(1995)
Nat. Genet.
, vol.11
, pp. 76-82
-
-
Hansson, J.H.1
Nelson-Williams, C.2
Suzuki, H.3
Schild, L.4
Shimkets, R.5
Lu, Y.6
Canessa, C.7
Iwasaki, T.8
Rossier, B.9
Lifton, R.P.10
-
122
-
-
0029046975
-
A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system
-
Schild L., Canessa C.M., Shimkets R.A., Gautschi I., Lifton R.P., Rossier B.C. A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system. Proc. Natl. Acad. Sci. U.S.A. 1995, 92:5699-5703.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 5699-5703
-
-
Schild, L.1
Canessa, C.M.2
Shimkets, R.A.3
Gautschi, I.4
Lifton, R.P.5
Rossier, B.C.6
|