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 *

146 related articles for article (PubMed ID: 1375035)

  • 21. The amino-terminal portion of CFTR forms a regulated Cl- channel.
    Sheppard DN; Ostedgaard LS; Rich DP; Welsh MJ
    Cell; 1994 Mar; 76(6):1091-8. PubMed ID: 7511062
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.
    Dalemans W; Barbry P; Champigny G; Jallat S; Dott K; Dreyer D; Crystal RG; Pavirani A; Lecocq JP; Lazdunski M
    Nature; 1991 Dec 19-26; 354(6354):526-8. PubMed ID: 1722027
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Regulation of the cystic fibrosis transmembrane conductance regulator chloride channel by MgATP.
    Welsh MJ; Anderson MP
    Soc Gen Physiol Ser; 1993; 48():119-27. PubMed ID: 7684867
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Some properties of sodium and chloride channels in respiratory epithelia of CF- and non-CF-patients.
    Disser J; Hazama A; Frömter E
    Adv Exp Med Biol; 1991; 290():133-41; discussion 141-4. PubMed ID: 1719754
    [No Abstract]   [Full Text] [Related]  

  • 25. Cystic fibrosis transmembrane conductance regulator. Structure and function of an epithelial chloride channel.
    Akabas MH
    J Biol Chem; 2000 Feb; 275(6):3729-32. PubMed ID: 10660517
    [No Abstract]   [Full Text] [Related]  

  • 26. Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.
    Sheppard DN; Rich DP; Ostedgaard LS; Gregory RJ; Smith AE; Welsh MJ
    Nature; 1993 Mar; 362(6416):160-4. PubMed ID: 7680769
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents.
    Sheppard DN; Welsh MJ
    J Gen Physiol; 1992 Oct; 100(4):573-91. PubMed ID: 1281220
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Functions of the cystic fibrosis transmembrane conductance regulator protein.
    Frizzell RA
    Am J Respir Crit Care Med; 1995 Mar; 151(3 Pt 2):S54-8. PubMed ID: 7533606
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cystic fibrosis transmembrane conductance regulator (CFTR).
    Higgins CF
    Br Med Bull; 1992 Oct; 48(4):754-65. PubMed ID: 1281034
    [TBL] [Abstract][Full Text] [Related]  

  • 30. GTP-binding proteins inhibit cAMP activation of chloride channels in cystic fibrosis airway epithelial cells.
    Schwiebert EM; Kizer N; Gruenert DC; Stanton BA
    Proc Natl Acad Sci U S A; 1992 Nov; 89(22):10623-7. PubMed ID: 1279687
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Novel function discovered for the cystic fibrosis gene.
    Barinaga M
    Science; 1992 Apr; 256(5056):444-5. PubMed ID: 1373905
    [No Abstract]   [Full Text] [Related]  

  • 32. CFTR expression and organ damage in cystic fibrosis.
    Tizzano EF; Buchwald M
    Ann Intern Med; 1995 Aug; 123(4):305-8. PubMed ID: 7541969
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis.
    Welsh MJ; Smith AE
    Cell; 1993 Jul; 73(7):1251-4. PubMed ID: 7686820
    [No Abstract]   [Full Text] [Related]  

  • 34. How ATP regulates the CFT regulator.
    DeFelice LJ
    Biophys J; 1994 May; 66(5):1268-9. PubMed ID: 7520288
    [No Abstract]   [Full Text] [Related]  

  • 35. Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by its R domain.
    Ostedgaard LS; Baldursson O; Welsh MJ
    J Biol Chem; 2001 Mar; 276(11):7689-92. PubMed ID: 11244086
    [No Abstract]   [Full Text] [Related]  

  • 36. Regulation of plasma membrane recycling by CFTR.
    Bradbury NA; Jilling T; Berta G; Sorscher EJ; Bridges RJ; Kirk KL
    Science; 1992 Apr; 256(5056):530-2. PubMed ID: 1373908
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Toward defining the function of the cystic fibrosis gene product.
    Forstner GG
    J Pediatr Gastroenterol Nutr; 1991 Nov; 13(4):432-3. PubMed ID: 1723427
    [No Abstract]   [Full Text] [Related]  

  • 38. A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis gene.
    Lissens W; Bonduelle M; Malfroot A; Dab I; Liebaers I
    Hum Mol Genet; 1992 Sep; 1(6):441-2. PubMed ID: 1284530
    [No Abstract]   [Full Text] [Related]  

  • 39. The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation.
    Tabcharani JA; Chang XB; Riordan JR; Hanrahan JW
    Biophys J; 1992 Apr; 62(1):1-4. PubMed ID: 1376160
    [No Abstract]   [Full Text] [Related]  

  • 40. Removal of the Fe(iii) site promotes activation of the human cystic fibrosis transmembrane conductance regulator by high-affinity Zn(ii) binding.
    Wang G
    Metallomics; 2018 Feb; 10(2):240-247. PubMed ID: 29372915
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.