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Results: 1-16 |
Results: 16
Mutations in the Na-Cl cotransporter reduce blood pressure in humans
Authors: Cruz, DN Simon, DB Nelson-Williams, C Farhi, A Finberg, K Burleson, L Gill, JR Lifton, RP
Citation: Dn. Cruz et al., Mutations in the Na-Cl cotransporter reduce blood pressure in humans, HYPERTENSIO, 37(6), 2001, pp. 1458-1464
Molecular mechanisms of human hypertension
Authors: Lifton, RP Gharavi, AG Geller, DS
Citation: Rp. Lifton et al., Molecular mechanisms of human hypertension, CELL, 104(4), 2001, pp. 545-556
Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life
Authors: Cruz, DN Shaer, AJ Bia, MJ Lifton, RP Simon, DB
Citation: Dn. Cruz et al., Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life, KIDNEY INT, 59(2), 2001, pp. 710-717
Human hypertension caused by mutations in WNK kinases
Authors: Wilson, FH Disse-Nicodeme, S Choate, KA Ishikawa, K Nelson-Willams, 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
Citation: Fh. Wilson et al., Human hypertension caused by mutations in WNK kinases, SCIENCE, 293(5532), 2001, pp. 1107-1112
Molecular cloning and characterization of Atp6n1b - A novel fourth murine vacuolar H+-ATPase a-subunit gene
Authors: Smith, AN Finberg, KE Wagner, CA Lifton, RP Devonald, MAJ Su, Y Karet, FE
Citation: An. Smith et al., Molecular cloning and characterization of Atp6n1b - A novel fourth murine vacuolar H+-ATPase a-subunit gene, J BIOL CHEM, 276(45), 2001, pp. 42382-42388
IgA nephropathy, the most common cause of glomerulonephritis, is linked to6q22-23
Authors: Gharavi, AG Yan, Y Scolari, F Schena, FP Frasca, GM Ghiggeri, GM Cooper, K Amoroso, A Viola, BF Battini, G Caridi, G Canova, C Farhi, A Subramanian, V Nelson-Williams, C Woodford, S Julian, BA Wyatt, RJ Lifton, RP
Citation: Ag. Gharavi et al., IgA nephropathy, the most common cause of glomerulonephritis, is linked to6q22-23, NAT GENET, 26(3), 2000, pp. 354-357
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing
Authors: Smith, AN Skaug, J Choate, KA Nayir, A Bakkaloglu, A Ozen, S Hulton, SA Sanjad, SA Al-Sabban, EA Lifton, RP Scherer, SW Karet, FE
Citation: An. Smith et al., Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing, NAT GENET, 26(1), 2000, pp. 71-75
Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases
Authors: Su, IH Frank, R Gauthier, BG Valderrama, E Simon, DB Lifton, RP Trachtman, H
Citation: Ih. Su et al., Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases, PED NEPHROL, 14(10-11), 2000, pp. 970-972
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
Authors: Levy, D DeStefano, AL Larson, MG O'Donnell, CJ Lifton, RP Gavras, H Cupples, LA Myers, RH
Citation: D. Levy et al., 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, HYPERTENSIO, 36(4), 2000, pp. 477-483
Glucocorticoid-remediable aldosteronism and pregnancy
Authors: Wyckoff, JA Seely, EW Hurwitz, S Anderson, BF Lifton, RP Dluhy, RG
Citation: Ja. Wyckoff et al., Glucocorticoid-remediable aldosteronism and pregnancy, HYPERTENSIO, 35(2), 2000, pp. 668-672
Activating mineralocorticoid receptor mutation in hypertension exacerbatedby pregnancy
Authors: Geller, DS Farhi, A Pinkerton, N Fradley, M Moritz, M Spitzer, A Meinke, G Tsai, FTF Sigler, PB Lifton, RP
Citation: Ds. Geller et al., Activating mineralocorticoid receptor mutation in hypertension exacerbatedby pregnancy, SCIENCE, 289(5476), 2000, pp. 119-123
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubularacidosis with sensorineural deafness
Authors: Karet, FE Finberg, KE Nelson, RD Nayir, A Mocan, H Sanjad, SA Rodriguez-Soriano, J Santos, F Cremers, CWRJ Di Pietro, A Hoffbrand, BI Winiarski, J Bakkaloglu, A Ozen, S Dusunsel, R Goodyer, P Hulton, SA Wu, DK Skvorak, AB Morton, CC Cunningham, MJ Jha, V Lifton, RP
Citation: Fe. Karet et al., Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubularacidosis with sensorineural deafness, NAT GENET, 21(1), 1999, pp. 84-90
Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption
Authors: Simon, DB Lu, Y Choate, KA Velazquez, H Al-Sabban, E Praga, M Casari, C Bettinelli, A Colussi, C Rodriguez-Soriano, J McCredie, D Milford, D Sanjad, S Lifton, RP
Citation: Db. Simon et al., Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption, SCIENCE, 285(5424), 1999, pp. 103-106
Absence of amiloride-sensitive sodium absorption in the airway of an infant with pseudohypoaldosteronism
Authors: Prince, LS Launspach, JL Geller, DS Lifton, RP Pratt, JH Zabner, J Welsh, MJ
Citation: Ls. Prince et al., Absence of amiloride-sensitive sodium absorption in the airway of an infant with pseudohypoaldosteronism, J PEDIAT, 135(6), 1999, pp. 786-789
Commentary - Glucocorticoid-remediable aldosteronism
Authors: Dluhy, RG Lifton, RP
Citation: Rg. Dluhy et Rp. Lifton, Commentary - Glucocorticoid-remediable aldosteronism, J CLIN END, 84(12), 1999, pp. 4341-4344
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34
Authors: Karet, FE Finberg, KE Nayir, A Bakkaloglu, A Ozen, S Hulton, SA Sanjad, SA Al-Sabban, EA Medina, JF Lifton, RP
Citation: Fe. Karet et al., Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34, AM J HU GEN, 65(6), 1999, pp. 1656-1665
Risultati: 1-16 |