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Journal Abstract Search


113 related items for PubMed ID: 11065344

  • 1. Scnn1 sodium channel gene family in genetically engineered mice.
    Hummler E, Beermann F.
    J Am Soc Nephrol; 2000 Nov; 11 Suppl 16():S129-34. PubMed ID: 11065344
    [Abstract] [Full Text] [Related]

  • 2. Conditional gene targeting of the ENaC subunit genes Scnn1b and Scnn1g.
    Mérillat AM, Charles RP, Porret A, Maillard M, Rossier B, Beermann F, Hummler E.
    Am J Physiol Renal Physiol; 2009 Feb; 296(2):F249-56. PubMed ID: 19036848
    [Abstract] [Full Text] [Related]

  • 3. Cloning, chromosomal localization, and physical linkage of the beta and gamma subunits (SCNN1B and SCNN1G) of the human epithelial amiloride-sensitive sodium channel.
    Voilley N, Bassilana F, Mignon C, Merscher S, Mattéi MG, Carle GF, Lazdunski M, Barbry P.
    Genomics; 1995 Aug 10; 28(3):560-5. PubMed ID: 7490094
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  • 4. Epithelial sodium channel genes Scnn1b and Scnn1g are closely linked on distal mouse chromosome 7.
    Brooker DR, Kozak CA, Kleyman TR.
    Genomics; 1995 Oct 10; 29(3):784-6. PubMed ID: 8575777
    [Abstract] [Full Text] [Related]

  • 5. A novel splice-site mutation in the gamma subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families.
    Strautnieks SS, Thompson RJ, Gardiner RM, Chung E.
    Nat Genet; 1996 Jun 10; 13(2):248-50. PubMed ID: 8640238
    [Abstract] [Full Text] [Related]

  • 6. Lessons from mouse mutants of epithelial sodium channel and its regulatory proteins.
    Hummler E, Vallon V.
    J Am Soc Nephrol; 2005 Nov 10; 16(11):3160-6. PubMed ID: 16192419
    [Abstract] [Full Text] [Related]

  • 7. 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 10; 62(5):547-53. PubMed ID: 15853823
    [Abstract] [Full Text] [Related]

  • 8. Interpretation of phenotype in genetically engineered mice.
    Doetschman T.
    Lab Anim Sci; 1999 Apr 10; 49(2):137-43. PubMed ID: 10331542
    [Abstract] [Full Text] [Related]

  • 9. Defective respiratory amiloride-sensitive sodium transport predisposes to pulmonary oedema and delays its resolution in mice.
    Egli M, Duplain H, Lepori M, Cook S, Nicod P, Hummler E, Sartori C, Scherrer U.
    J Physiol; 2004 Nov 01; 560(Pt 3):857-65. PubMed ID: 15308680
    [Abstract] [Full Text] [Related]

  • 10. Revealing a subclinical salt-losing phenotype in heterozygous carriers of the novel S562P mutation in the alpha subunit of the epithelial sodium channel.
    Riepe FG, van Bemmelen MX, Cachat F, Plendl H, Gautschi I, Krone N, Holterhus PM, Theintz G, Schild L.
    Clin Endocrinol (Oxf); 2009 Feb 01; 70(2):252-8. PubMed ID: 18547339
    [Abstract] [Full Text] [Related]

  • 11. Genetic engineering in the mouse: tuning TNF/TNFR expression.
    Douni E, Alexiou M, Kollias G.
    Methods Mol Med; 2004 Feb 01; 98():137-70. PubMed ID: 15064438
    [Abstract] [Full Text] [Related]

  • 12. Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome.
    Sheridan MB, Fong P, Groman JD, Conrad C, Flume P, Diaz R, Harris C, Knowles M, Cutting GR.
    Hum Mol Genet; 2005 Nov 15; 14(22):3493-8. PubMed ID: 16207733
    [Abstract] [Full Text] [Related]

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  • 14. 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 15; 11(8):861-6. PubMed ID: 16007095
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  • 18. An AvaII PCR/RFLP in an exon of the canine gene for the beta subunit of the amiloride-sensitive sodium channel (SCNN1B).
    Zhou T, Nonneman D, Shibuya H, Khan S, Liu PC, Johnson GS.
    Anim Genet; 1998 Jun 15; 29(3):239. PubMed ID: 9720188
    [No Abstract] [Full Text] [Related]

  • 19. SCNN1, an epithelial cell sodium channel gene in the conserved linkage group on mouse chromosome 6 and human chromosome 12.
    Meisler MH, Barrow LL, Canessa CM, Rossier BC.
    Genomics; 1994 Nov 01; 24(1):185-6. PubMed ID: 7896277
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