These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 9261995)

  • 1. Lose salt and gain a friend! A tribute to Gerhard Giebisch.
    Rossier BC
    Wien Klin Wochenschr; 1997 Jun; 109(12-13):504-6. PubMed ID: 9261995
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function.
    Derst C; Konrad M; Köckerling A; Károlyi L; Deschenes G; Daut J; Karschin A; Seyberth HW
    Biochem Biophys Res Commun; 1997 Jan; 230(3):641-5. PubMed ID: 9015377
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.
    Simon DB; Karet FE; Rodriguez-Soriano J; Hamdan JH; DiPietro A; Trachtman H; Sanjad SA; Lifton RP
    Nat Genet; 1996 Oct; 14(2):152-6. PubMed ID: 8841184
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Bartter's syndrome].
    Daniluk U; Kaczmarski M; Wasilewska J; Matuszewska E; Semeniuk J; Sidor K; Krasnow A
    Pol Merkur Lekarski; 2004 May; 16(95):484-9. PubMed ID: 15518434
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome.
    Finer G; Shalev H; Birk OS; Galron D; Jeck N; Sinai-Treiman L; Landau D
    J Pediatr; 2003 Mar; 142(3):318-23. PubMed ID: 12640382
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Epithelial sodium channel and the control of sodium balance: interaction between genetic and environmental factors.
    Rossier BC; Pradervand S; Schild L; Hummler E
    Annu Rev Physiol; 2002; 64():877-97. PubMed ID: 11826291
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Aldosterone resistance: structural and functional considerations and new perspectives.
    Zennaro MC; Hubert EL; Fernandes-Rosa FL
    Mol Cell Endocrinol; 2012 Mar; 350(2):206-15. PubMed ID: 21664233
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heterozygous mutations of the gene for Kir 1.1 (ROMK) in antenatal Bartter syndrome presenting with transient hyperkalemia, evolving to a benign course.
    Cho JT; Guay-Woodford LM
    J Korean Med Sci; 2003 Feb; 18(1):65-8. PubMed ID: 12589089
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The epithelial sodium channel: from molecule to disease.
    Schild L
    Rev Physiol Biochem Pharmacol; 2004; 151():93-107. PubMed ID: 15146350
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mutation of the epithelial Na+ channel causes type 1 pseudohypoaldosteronism.
    Bonny O; Knoers N; Monnens L; Rossier BC
    Pediatr Nephrol; 2002 Oct; 17(10):804-8. PubMed ID: 12376807
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Central role for ENaC in development of hypertension.
    Pratt JH
    J Am Soc Nephrol; 2005 Nov; 16(11):3154-9. PubMed ID: 16192416
    [TBL] [Abstract][Full Text] [Related]  

  • 12. New roles for renal potassium channels.
    Wagner CA
    J Nephrol; 2010; 23(1):5-8. PubMed ID: 20091480
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Blood pressure variation in healthy humans: a possible interaction with beta-2 adrenergic receptor genotype and renal epithelial sodium channels.
    Snyder EM; Joyner MJ; Turner ST; Johnson BD
    Med Hypotheses; 2005; 65(2):296-9. PubMed ID: 15922102
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Characterization of the epithelial sodium channel in human pre-eclampsia syncytiotrophoblast].
    del Monaco S; Assef Y; Damiano A; Zotta E; Ibarra C; Kotsias BA
    Medicina (B Aires); 2006; 66(1):31-5. PubMed ID: 16555725
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Neonatal Bartter disease diagnosed with the detection of a mutation of the KCNJ1 gene which codifies the synthesis of the renal ROMK1 potassium channel].
    García Nieto V; Müller D; van der Vliet W; Claverie-Martín F
    Nefrologia; 2001; 21(5):448-55. PubMed ID: 11795013
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Thiazolidinediones expand body fluid volume through PPARgamma stimulation of ENaC-mediated renal salt absorption.
    Guan Y; Hao C; Cha DR; Rao R; Lu W; Kohan DE; Magnuson MA; Redha R; Zhang Y; Breyer MD
    Nat Med; 2005 Aug; 11(8):861-6. PubMed ID: 16007095
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hypokalemia and the pathology of ion transport molecules.
    Antes LM; Kujubu DA; Fernandez PC
    Semin Nephrol; 1998 Jan; 18(1):31-45. PubMed ID: 9459287
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism.
    Edelheit O; Hanukoglu I; Gizewska M; Kandemir N; Tenenbaum-Rakover Y; Yurdakök M; Zajaczek S; Hanukoglu A
    Clin Endocrinol (Oxf); 2005 May; 62(5):547-53. PubMed ID: 15853823
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome.
    Vollmer M; Koehrer M; Topaloglu R; Strahm B; Omran H; Hildebrandt F
    Pediatr Nephrol; 1998 Jan; 12(1):69-71. PubMed ID: 9502574
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comparative roles of the renal apical sodium transport systems in blood pressure control.
    Meneton P
    J Am Soc Nephrol; 2000 Nov; 11 Suppl 16():S135-9. PubMed ID: 11065345
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.