-
1
-
-
0023221667
-
Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor
-
Arriza JL, Weinberger C, Cerelli G, Glaser TM, Handelin BL, Housman DE, Evans RM: Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor. Science 1987;237:268-275.
-
(1987)
Science
, vol.237
, pp. 268-275
-
-
Arriza, J.L.1
Weinberger, C.2
Cerelli, G.3
Glaser, T.M.4
Handelin, B.L.5
Housman, D.E.6
Evans, R.M.7
-
2
-
-
0037469632
-
Interdomain interactions in the mineralocorticoid receptor
-
Rogerson FM, Fuller PJ: Interdomain interactions in the mineralocorticoid receptor. Mol Cell Endocrinol 2003;200:45-55.
-
(2003)
Mol Cell Endocrinol
, vol.200
, pp. 45-55
-
-
Rogerson, F.M.1
Fuller, P.J.2
-
3
-
-
22444438401
-
Crystal structure of a mutant mineralocorticoid receptor responsible for hypertension
-
Fagart J, Huyet J, Pinon GM, Rochel M, Mayer C, Rafestin-Oblin ME: Crystal structure of a mutant mineralocorticoid receptor responsible for hypertension. Nat Struct Mol Biol 2005;12:554-555.
-
(2005)
Nat Struct Mol Biol
, vol.12
, pp. 554-555
-
-
Fagart, J.1
Huyet, J.2
Pinon, G.M.3
Rochel, M.4
Mayer, C.5
Rafestin-Oblin, M.E.6
-
4
-
-
0030945484
-
Epithelial sodium channels: function, structure, and regulation
-
Garty H, Palmer LG: Epithelial sodium channels: function, structure, and regulation. Physiol Rev 1997;77:359-396.
-
(1997)
Physiol Rev
, vol.77
, pp. 359-396
-
-
Garty, H.1
Palmer, L.G.2
-
5
-
-
34548813656
-
Structure of acid-sensing ion channel 1 at 1.9 a resolution and low pH
-
Jasti J, Furukawa H, Gonzales EB, Gouaux E: Structure of acid-sensing ion channel 1 at 1.9 a resolution and low pH. Nature 2007;449:316-323.
-
(2007)
Nature
, vol.449
, pp. 316-323
-
-
Jasti, J.1
Furukawa, H.2
Gonzales, E.B.3
Gouaux, E.4
-
6
-
-
0030731428
-
Regulation of stability and function of the epithelial Na+ channel (ENaC) by ubiquitination
-
Staub O, Gautschi I, Ishikawa T, Breitschopf K, Ciechanover A, Schild L, Rotin D: Regulation of stability and function of the epithelial Na+ channel (ENaC) by ubiquitination. EMBO J 1997;16:6325-6336.
-
(1997)
EMBO J
, vol.16
, pp. 6325-6336
-
-
Staub, O.1
Gautschi, I.2
Ishikawa, T.3
Breitschopf, K.4
Ciechanover, A.5
Schild, L.6
Rotin, D.7
-
7
-
-
31944432423
-
Mechanisms of mineralocorticoid action
-
Fuller PJ, Young MJ: Mechanisms of mineralocorticoid action. Hypertension 2005;46:1227-1235.
-
(2005)
Hypertension
, vol.46
, pp. 1227-1235
-
-
Fuller, P.J.1
Young, M.J.2
-
8
-
-
0041806574
-
Aldosterone: its receptor, target genes, and actions
-
Pearce D, Bhargava A, Cole TJ: Aldosterone: its receptor, target genes, and actions. Vitam Horm 2003;66:29-76.
-
(2003)
Vitam Horm
, vol.66
, pp. 29-76
-
-
Pearce, D.1
Bhargava, A.2
Cole, T.J.3
-
9
-
-
0037236659
-
SGK1 regulation of epithelial sodium transport
-
Pearce D: SGK1 regulation of epithelial sodium transport. Cell Physiol Biochem 2003;13:13-20.
-
(2003)
Cell Physiol Biochem
, vol.13
, pp. 13-20
-
-
Pearce, D.1
-
10
-
-
0033047937
-
Aldosterone action: induction of p21(ras) and fra-2 and transcription-independent decrease in myc, jun, and fos
-
Spindler B, Verrey F: Aldosterone action: induction of p21(ras) and fra-2 and transcription-independent decrease in myc, jun, and fos. Am J Physiol 1999; 276:C1154-C1161.
-
(1999)
Am J Physiol
, vol.276
, pp. C1154-C1161
-
-
Spindler, B.1
Verrey, F.2
-
11
-
-
0033151832
-
Serum and glucocorticoidinducible kinase (SGK) is a target of the PI 3-kinase-stimulated signaling pathway
-
Park J, Leong ML, Buse P, Maiyar AC, Firestone GL, Hemmings BA: Serum and glucocorticoidinducible kinase (SGK) is a target of the PI 3-kinase-stimulated signaling pathway. EMBO J 1999;18:3024-3033.
-
(1999)
EMBO J
, vol.18
, pp. 3024-3033
-
-
Park, J.1
Leong, M.L.2
Buse, P.3
Maiyar, A.C.4
Firestone, G.L.5
Hemmings, B.A.6
-
12
-
-
28144436789
-
Serum-and glucocorticoid-regulated kinase 1 regulates ubiquitin ligase neural precursor cell-expressed, developmentally down-regulated protein 4-2 by inducing interaction with 14-3-3
-
Bhalla V, Daidie D, Li H, Pao AC, LaGrange LP, Wang J, Vandewalle A, Stockand JD, Staub O, Pearce D: Serum-and glucocorticoid-regulated kinase 1 regulates ubiquitin ligase neural precursor cell-expressed, developmentally down-regulated protein 4-2 by inducing interaction with 14-3-3. Mol Endocrinol 2005;19:3073-3084.
-
(2005)
Mol Endocrinol
, vol.19
, pp. 3073-3084
-
-
Bhalla, V.1
Daidie, D.2
Li, H.3
Pao, A.C.4
LaGrange, L.P.5
Wang, J.6
Vandewalle, A.7
Stockand, J.D.8
Staub, O.9
Pearce, D.10
-
13
-
-
0001601125
-
A salt wasting syndrome in infancy
-
Cheek D, Perry J: A salt wasting syndrome in infancy. Arch Dis Child 1958;33:252-256.
-
(1958)
Arch Dis Child
, vol.33
, pp. 252-256
-
-
Cheek, D.1
Perry, J.2
-
15
-
-
0033565228
-
Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism
-
Kerem E, Bistritzer T, Hanukoglu A, Hofmann T, Zhou Z, Bennett W, MacLaughlin E, Barker P, Nash M, Quittell L, Boucher R, Knowles MR: Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism. N Engl J Med 1999;341:156-162.
-
(1999)
N Engl J Med
, vol.341
, pp. 156-162
-
-
Kerem, E.1
Bistritzer, T.2
Hanukoglu, A.3
Hofmann, T.4
Zhou, Z.5
Bennett, W.6
MacLaughlin, E.7
Barker, P.8
Nash, M.9
Quittell, L.10
Boucher, R.11
Knowles, M.R.12
-
16
-
-
13344295074
-
Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1
-
Chang SS, Grunder S, Hanukoglu A, Rosler A, Mathew PM, Hanukoglu I, Schild L, Lu Y, Shimkets RA, Nelson-Williams C, Rossier BC, Lifton RP: 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
-
17
-
-
80052052102
-
A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1
-
Dirlewanger M, Huser D, Zennaro MC, Girardin E, Schild L, Schwitzgebel VM: A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1. Am J Physiol Endocrinol Metab 2011; 301:E467-E473.
-
(2011)
Am J Physiol Endocrinol Metab
, vol.301
, pp. E467-E473
-
-
Dirlewanger, M.1
Huser, D.2
Zennaro, M.C.3
Girardin, E.4
Schild, L.5
Schwitzgebel, V.M.6
-
18
-
-
18444397746
-
Mineralocorticoid resistance
-
Geller DS: Mineralocorticoid resistance. Clin Endocrinol (Oxf) 2005;62:513-520.
-
(2005)
Clin Endocrinol (Oxf)
, vol.62
, pp. 513-520
-
-
Geller, D.S.1
-
19
-
-
0031861245
-
Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
-
Geller DS, Rodriguez-Soriano J, Vallo Boado A, Schifter S, Bayer M, Chang SS, Lifton RP: 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 Boado, A.3
Schifter, S.4
Bayer, M.5
Chang, S.S.6
Lifton, R.P.7
-
20
-
-
0343247729
-
Pseudohypoaldosteronism due to renal and multisystem resistance to mineralocorticoids respond differently to carbenoxolone
-
Hanukoglu A, Joy O, Steinitz M, Rosler A, Hanukoglu I: Pseudohypoaldosteronism due to renal and multisystem resistance to mineralocorticoids respond differently to carbenoxolone. J Steroid Biochem Mol Biol 1997;60:105-112.
-
(1997)
J Steroid Biochem Mol Biol
, vol.60
, pp. 105-112
-
-
Hanukoglu, A.1
Joy, O.2
Steinitz, M.3
Rosler, A.4
Hanukoglu, I.5
-
21
-
-
33751512003
-
Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1
-
Riepe FG, Finkeldei J, de Sanctis L, Einaudi S, Testa A, Karges B, Peter M, Viemann M, Grotzinger J, Sippell WG, Fejes-Toth G, Krone N: Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1. J Clin Endocrinol Metab 2006;91:4552-4561.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 4552-4561
-
-
Riepe, F.G.1
Finkeldei, J.2
de Sanctis, L.3
Einaudi, S.4
Testa, A.5
Karges, B.6
Peter, M.7
Viemann, M.8
Grotzinger, J.9
Sippell, W.G.10
Fejes-Toth, G.11
Krone, N.12
-
22
-
-
33646357245
-
Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults
-
Geller DS, Zhang J, Zennaro MC, Vallo-Boado A, Rodriguez-Soriano J, Furu L, Haws R, Metzger D, Botelho B, Karaviti L, Haqq AM, Corey H, Janssens S, Corvol P, Lifton RP: Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults. J Am Soc Nephrol 2006;17: 1429-1436.
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 1429-1436
-
-
Geller, D.S.1
Zhang, J.2
Zennaro, M.C.3
Vallo-Boado, A.4
Rodriguez-Soriano, J.5
Furu, L.6
Haws, R.7
Metzger, D.8
Botelho, B.9
Karaviti, L.10
Haqq, A.M.11
Corey, H.12
Janssens, S.13
Corvol, P.14
Lifton, R.P.15
-
23
-
-
2442462008
-
Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene
-
Riepe FG, Krone N, Morlot M, Peter M, Sippell WG, Partsch CJ: Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene. J Clin Endocrinol Metab 2004;89:2150-2152.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 2150-2152
-
-
Riepe, F.G.1
Krone, N.2
Morlot, M.3
Peter, M.4
Sippell, W.G.5
Partsch, C.J.6
-
24
-
-
0023039605
-
Syndrome of hypertension and hyperkalemia with normal glomerular filtration rate
-
Gordon RD: Syndrome of hypertension and hyperkalemia with normal glomerular filtration rate. Hypertension 1986;8:93-102.
-
(1986)
Hypertension
, vol.8
, pp. 93-102
-
-
Gordon, R.D.1
-
25
-
-
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
-
26
-
-
0034839813
-
Transient pseudohypoaldosteronism secondary to posterior urethral valves-a case report and review of the literature
-
Bulchmann G, Schuster T, Heger A, Kuhnle U, Joppich I, Schmidt H: Transient pseudohypoaldosteronism secondary to posterior urethral valves-a case report and review of the literature. Eur J Pediatr Surg 2001;11:277-279.
-
(2001)
Eur J Pediatr Surg
, vol.11
, pp. 277-279
-
-
Bulchmann, G.1
Schuster, T.2
Heger, A.3
Kuhnle, U.4
Joppich, I.5
Schmidt, H.6
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