-
1
-
-
0035936780
-
Molecular mechanisms of human hypertension
-
Lifton RP, Gharavi AG, Geller DS. 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
-
2
-
-
0025817650
-
Blood pressure control-special role of the kidneys and body fluids
-
Jun 28
-
Guyton AC. Blood pressure control-special role of the kidneys and body fluids. Science. Jun 28. 1991;252:1813-1816.
-
(1991)
Science
, vol.252
, pp. 1813-1816
-
-
Guyton, A.C.1
-
3
-
-
0742322637
-
Present status of genetic mechanisms in hypertension
-
Jan
-
Luft FC. Present status of genetic mechanisms in hypertension. Med Clin North Am. Jan 2004;88:1-18, vii.
-
(2004)
Med Clin North Am
, vol.88
, pp. 1-18
-
-
Luft, F.C.1
-
4
-
-
12444257322
-
Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p
-
Gong M, Zhang H, Schulz H, Lee YA, Sun K, Bahring S, Luft FC, Nurnberg P, Reis A, Rohde K, Ganten D, Hui R, Hubner N. Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p. Hum Mol Genet. 2003;12:1273-1277.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1273-1277
-
-
Gong, M.1
Zhang, H.2
Schulz, H.3
Lee, Y.A.4
Sun, K.5
Bahring, S.6
Luft, F.C.7
Nurnberg, P.8
Reis, A.9
Rohde, K.10
Ganten, D.11
Hui, R.12
Hubner, N.13
-
5
-
-
0033770421
-
Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study
-
Levy D, DeStefano AL, Larson MG, O'Donnell CJ, Lifton RP, Gavras H, Cupples LA, Myers RH. Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study. Hypertension. 2000;36:477-483.
-
(2000)
Hypertension
, vol.36
, pp. 477-483
-
-
Levy, D.1
DeStefano, A.L.2
Larson, M.G.3
O'Donnell, C.J.4
Lifton, R.P.5
Gavras, H.6
Cupples, L.A.7
Myers, R.H.8
-
6
-
-
17944373014
-
Human hypertension caused by mutations in WNK kinases
-
Wilson FH, Disse-Nicodeme S, Choate KA, Ishikawa K, Nelson-Williams C, Desitter I, Gunel M, Milford DV, Lipkin GW, Achard JM, Feely MP, Dussol B, Berland Y, Unwin RJ, Mayan H, Simon DB, Farfel Z, Jeunemaitre X, Lifton RP. 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
-
7
-
-
0030140024
-
Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12
-
Schuster H, Wienker TE, Bahring S, Bilginturan N, Toka HR, Neitzel H, Jeschke E, Toka O, Gilbert D, Lowe A, Ott J, Haller H, Luft FC. Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12. Nat Genet. 1996;13:98-100.
-
(1996)
Nat Genet
, vol.13
, pp. 98-100
-
-
Schuster, H.1
Wienker, T.E.2
Bahring, S.3
Bilginturan, N.4
Toka, H.R.5
Neitzel, H.6
Jeschke, E.7
Toka, O.8
Gilbert, D.9
Lowe, A.10
Ott, J.11
Haller, H.12
Luft, F.C.13
-
8
-
-
19244386918
-
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21
-
Mansfield TA, Simon DB, Farfel Z, Bia M, Tucci JR, Lebel M, Gutkin M, Vialettes B, Christofilis MA, Kauppinen-Makelin R, Mayan H, Risch N, Lifton RP. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21. Nature Genetics. 1997;16:202-205.
-
(1997)
Nature Genetics
, vol.16
, pp. 202-205
-
-
Mansfield, T.A.1
Simon, D.B.2
Farfel, Z.3
Bia, M.4
Tucci, J.R.5
Lebel, M.6
Gutkin, M.7
Vialettes, B.8
Christofilis, M.A.9
Kauppinen-Makelin, R.10
Mayan, H.11
Risch, N.12
Lifton, R.P.13
-
9
-
-
2542446285
-
Activating mutation of the renal epithelial chloride channel ClC-Kb predisposing to hypertension
-
Jeck N, Waldegger S, Lampert A, Boehmer C, Waldegger P, Lang PA, Wissinger B, Friedrich B, Risler T, Moehle R, Lang UE, Zill P, Bondy B, Schaeffeler E, Schwab M, Seyberth H, Lang F. Activating mutation of the renal epithelial chloride channel ClC-Kb predisposing to hypertension. Hypertension. 2004;43:1175-1181.
-
(2004)
Hypertension
, vol.43
, pp. 1175-1181
-
-
Jeck, N.1
Waldegger, S.2
Lampert, A.3
Boehmer, C.4
Waldegger, P.5
Lang, P.A.6
Wissinger, B.7
Friedrich, B.8
Risler, T.9
Moehle, R.10
Lang, U.E.11
Zill, P.12
Bondy, B.13
Schaeffeler, E.14
Schwab, M.15
Seyberth, H.16
Lang, F.17
-
10
-
-
16944366243
-
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
-
Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, Stone R, Schurman S, Nayir A, Alpay H, Bakkaloglu A, Rodriguez-Soriano J, Morales JM, Sanjad SA, Taylor CM, Pilz D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP. 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..
-
11
-
-
0347362500
-
A common sequence variation of the CLCNKB gene strongly activates ClC-Kb chloride channel activity
-
Jeck N, Waldegger P, Doroszewicz J, Seyberth H, Waldegger S. A common sequence variation of the CLCNKB gene strongly activates ClC-Kb chloride channel activity. Kidney Int. 2004;65:190-197.
-
(2004)
Kidney Int
, vol.65
, pp. 190-197
-
-
Jeck, N.1
Waldegger, P.2
Doroszewicz, J.3
Seyberth, H.4
Waldegger, S.5
-
12
-
-
0037312921
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
-
Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet. 2003;33: 177-182.
-
(2003)
Nat Genet
, vol.33
, pp. 177-182
-
-
Lohmueller, K.E.1
Pearce, C.L.2
Pike, M.3
Lander, E.S.4
Hirschhorn, J.N.5
-
13
-
-
12144285594
-
Assessing the impact of population stratification on genetic association studies
-
Freedman ML, Reich D, Penney KL, McDonald GJ, Mignault AA, Patterson N, Gabriel SB, Topol EJ, Smoller JW, Pato CN, Pato MT, Petryshen TL, Kolonel LN, Lander ES, Sklar P, Henderson B, Hirschhorn JN, Altshuler D. Assessing the impact of population stratification on genetic association studies. Nat Genet. 2004;36:388-393.
-
(2004)
Nat Genet
, vol.36
, pp. 388-393
-
-
Freedman, M.L.1
Reich, D.2
Penney, K.L.3
McDonald, G.J.4
Mignault, A.A.5
Patterson, N.6
Gabriel, S.B.7
Topol, E.J.8
Smoller, J.W.9
Pato, C.N.10
Pato, M.T.11
Petryshen, T.L.12
Kolonel, L.N.13
Lander, E.S.14
Sklar, P.15
Henderson, B.16
Hirschhorn, J.N.17
Altshuler, D.18
-
14
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
Pritchard JK, Stephens M, Donnelly P. Inference of population structure using multilocus genotype data. Genetics. 2000;155:945-959.
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
15
-
-
0035528928
-
Case-control studies of association in structured or admixed populations
-
Pritchard JK, Donnelly P. Case-control studies of association in structured or admixed populations. Theor Popul Biol. 2001;60:227-237.
-
(2001)
Theor Popul Biol
, vol.60
, pp. 227-237
-
-
Pritchard, J.K.1
Donnelly, P.2
|