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 *

202 related articles for article (PubMed ID: 16943574)

  • 1. Mutation analysis of SCNN1B in a family with Liddle's syndrome.
    Wang W; Zhou W; Jiang L; Cui B; Ye L; Su T; Wang J; Li X; Ning G
    Endocrine; 2006 Jun; 29(3):385-90. PubMed ID: 16943574
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel mutation in the beta-subunit of the epithelial sodium channel gene (SCNN1B) in a Thai family with Liddle's syndrome.
    Sawathiparnich P; Sumboonnanonda A; Weerakulwattana P; Limwongse C
    J Pediatr Endocrinol Metab; 2009 Jan; 22(1):85-9. PubMed ID: 19344079
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Liddle's syndrome associated with a point mutation in the extracellular domain of the epithelial sodium channel gamma subunit.
    Hiltunen TP; Hannila-Handelberg T; Petäjäniemi N; Kantola I; Tikkanen I; Virtamo J; Gautschi I; Schild L; Kontula K
    J Hypertens; 2002 Dec; 20(12):2383-90. PubMed ID: 12473862
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Liddle's syndrome caused by a novel mutation in the proline-rich PY motif of the epithelial sodium channel beta-subunit.
    Furuhashi M; Kitamura K; Adachi M; Miyoshi T; Wakida N; Ura N; Shikano Y; Shinshi Y; Sakamoto K; Hayashi M; Satoh N; Nishitani T; Tomita K; Shimamoto K
    J Clin Endocrinol Metab; 2005 Jan; 90(1):340-4. PubMed ID: 15483078
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome.
    Abriel H; Loffing J; Rebhun JF; Pratt JH; Schild L; Horisberger JD; Rotin D; Staub O
    J Clin Invest; 1999 Mar; 103(5):667-73. PubMed ID: 10074483
    [TBL] [Abstract][Full Text] [Related]  

  • 6. WW domains of Nedd4 bind to the proline-rich PY motifs in the epithelial Na+ channel deleted in Liddle's syndrome.
    Staub O; Dho S; Henry P; Correa J; Ishikawa T; McGlade J; Rotin D
    EMBO J; 1996 May; 15(10):2371-80. PubMed ID: 8665844
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of the epithelial sodium channel in Liddle's syndrome.
    Uehara Y; Sasaguri M; Kinoshita A; Tsuji E; Kiyose H; Taniguchi H; Noda K; Ideishi M; Inoue J; Tomita K; Arakawa K
    J Hypertens; 1998 Aug; 16(8):1131-5. PubMed ID: 9794716
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Liddle's syndrome mutations increase Na+ transport through dual effects on epithelial Na+ channel surface expression and proteolytic cleavage.
    Knight KK; Olson DR; Zhou R; Snyder PM
    Proc Natl Acad Sci U S A; 2006 Feb; 103(8):2805-8. PubMed ID: 16477034
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family.
    Wang LP; Gao LG; Zhou XL; Wu HY; Zhang L; Wen D; Li YH; Liu YX; Tian T; Fan XH; Jiang XJ; Zhang HM; Hui RT
    Chin Med J (Engl); 2012 Apr; 125(8):1401-4. PubMed ID: 22613642
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Conservation of pH sensitivity in the epithelial sodium channel (ENaC) with Liddle's syndrome mutation.
    Konstas AA; Mavrelos D; Korbmacher C
    Pflugers Arch; 2000 Dec; 441(2-3):341-50. PubMed ID: 11211122
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Disorders of the epithelial Na(+) channel in Liddle's syndrome and autosomal recessive pseudohypoaldosteronism type 1.
    Oh YS; Warnock DG
    Exp Nephrol; 2000; 8(6):320-5. PubMed ID: 11014928
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations and variants of the epithelial sodium channel gene in Liddle's syndrome and primary hypertension.
    Melander O; Orho M; Fagerudd J; Bengtsson K; Groop PH; Mattiasson I; Groop L; Hulthén UL
    Hypertension; 1998 May; 31(5):1118-24. PubMed ID: 9576123
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A family with Liddle's syndrome caused by a new missense mutation in the beta subunit of the epithelial sodium channel.
    Inoue J; Iwaoka T; Tokunaga H; Takamune K; Naomi S; Araki M; Takahama K; Yamaguchi K; Tomita K
    J Clin Endocrinol Metab; 1998 Jun; 83(6):2210-3. PubMed ID: 9626162
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular genetics of Liddle's syndrome.
    Yang KQ; Xiao Y; Tian T; Gao LG; Zhou XL
    Clin Chim Acta; 2014 Sep; 436():202-6. PubMed ID: 24882431
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A study of mutation(s) of the epithelial sodium channel gene in a Liddle's syndrome family].
    Ma X; Tian Y; Gao Y; Guo X
    Zhonghua Nei Ke Za Zhi; 2001 Jun; 40(6):390-3. PubMed ID: 11798604
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two sporadic cases of Liddle's syndrome caused by De novo ENaC mutations.
    Yamashita Y; Koga M; Takeda Y; Enomoto N; Uchida S; Hashimoto K; Yamano S; Dohi K; Marumo F; Sasaki S
    Am J Kidney Dis; 2001 Mar; 37(3):499-504. PubMed ID: 11228173
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regulation of the epithelial Na+ channel by Nedd4 and ubiquitination.
    Staub O; Abriel H; Plant P; Ishikawa T; Kanelis V; Saleki R; Horisberger JD; Schild L; Rotin D
    Kidney Int; 2000 Mar; 57(3):809-15. PubMed ID: 10720933
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype-phenotype analysis of a newly discovered family with Liddle's syndrome.
    Jeunemaitre X; Bassilana F; Persu A; Dumont C; Champigny G; Lazdunski M; Corvol P; Barbry P
    J Hypertens; 1997 Oct; 15(10):1091-100. PubMed ID: 9350583
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Aldosterone responsiveness of the epithelial sodium channel (ENaC) in colon is increased in a mouse model for Liddle's syndrome.
    Bertog M; Cuffe JE; Pradervand S; Hummler E; Hartner A; Porst M; Hilgers KF; Rossier BC; Korbmacher C
    J Physiol; 2008 Jan; 586(2):459-75. PubMed ID: 18006588
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Vasopressin-stimulated CFTR Cl- currents are increased in the renal collecting duct cells of a mouse model of Liddle's syndrome.
    Chang CT; Bens M; Hummler E; Boulkroun S; Schild L; Teulon J; Rossier BC; Vandewalle A
    J Physiol; 2005 Jan; 562(Pt 1):271-84. PubMed ID: 15513933
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.