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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

304 related items for PubMed ID: 25810436

  • 1. ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
    Andrini O, Keck M, Briones R, Lourdel S, Vargas-Poussou R, Teulon J.
    Am J Physiol Renal Physiol; 2015 Jun 15; 308(12):F1324-34. PubMed ID: 25810436
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Novel CLCNKB mutations causing Bartter syndrome affect channel surface expression.
    Keck M, Andrini O, Lahuna O, Burgos J, Cid LP, Sepúlveda FV, L'hoste S, Blanchard A, Vargas-Poussou R, Lourdel S, Teulon J.
    Hum Mutat; 2013 Sep 15; 34(9):1269-78. PubMed ID: 23703872
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype.
    Jeck N, Konrad M, Peters M, Weber S, Bonzel KE, Seyberth HW.
    Pediatr Res; 2000 Dec 15; 48(6):754-8. PubMed ID: 11102542
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.
    Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M.
    J Med Genet; 2008 Mar 15; 45(3):182-6. PubMed ID: 18310267
    [Abstract] [Full Text] [Related]

  • 12. 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.
    Kidney Int; 2004 Jan 15; 65(1):190-7. PubMed ID: 14675050
    [Abstract] [Full Text] [Related]

  • 13. CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca2+ dependence of ClC-Kb channels.
    Andrini O, Keck M, L'Hoste S, Briones R, Mansour-Hendili L, Grand T, Sepúlveda FV, Blanchard A, Lourdel S, Vargas-Poussou R, Teulon J.
    Pflugers Arch; 2014 Sep 15; 466(9):1713-23. PubMed ID: 24271511
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene.
    Hayama A, Rai T, Sasaki S, Uchida S.
    Histochem Cell Biol; 2003 Jun 15; 119(6):485-93. PubMed ID: 12761627
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Barttin increases surface expression and changes current properties of ClC-K channels.
    Waldegger S, Jeck N, Barth P, Peters M, Vitzthum H, Wolf K, Kurtz A, Konrad M, Seyberth HW.
    Pflugers Arch; 2002 Jun 15; 444(3):411-8. PubMed ID: 12111250
    [Abstract] [Full Text] [Related]

  • 20. [Progress of research on the role of CLCNKB gene in classical Bartter syndrome].
    Zhou J, Wang C, Bao H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May 10; 37(5):573-577. PubMed ID: 32335890
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.