BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 23270647)

  • 21. Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers.
    LeSimple P; Liao J; Robert R; Gruenert DC; Hanrahan JW
    J Physiol; 2010 Apr; 588(Pt 8):1195-209. PubMed ID: 20156845
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A defective flexible loop contributes to the processing and gating defects of the predominant cystic fibrosis-causing mutation.
    Chen X; Zhu S; Zhenin M; Xu W; Bose SJ; Wong MP; Leung GPH; Senderowitz H; Chen JH
    FASEB J; 2019 Apr; 33(4):5126-5142. PubMed ID: 30668920
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast.
    Teem JL; Berger HA; Ostedgaard LS; Rich DP; Tsui LC; Welsh MJ
    Cell; 1993 Apr; 73(2):335-46. PubMed ID: 7682896
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.
    French PJ; van Doorninck JH; Peters RH; Verbeek E; Ameen NA; Marino CR; de Jonge HR; Bijman J; Scholte BJ
    J Clin Invest; 1996 Sep; 98(6):1304-12. PubMed ID: 8823295
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cystic fibrosis transmembrane regulator regulates uptake of sphingoid base phosphates and lysophosphatidic acid: modulation of cellular activity of sphingosine 1-phosphate.
    Boujaoude LC; Bradshaw-Wilder C; Mao C; Cohn J; Ogretmen B; Hannun YA; Obeid LM
    J Biol Chem; 2001 Sep; 276(38):35258-64. PubMed ID: 11443135
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Comparative processing and function of human and ferret cystic fibrosis transmembrane conductance regulator.
    Fisher JT; Liu X; Yan Z; Luo M; Zhang Y; Zhou W; Lee BJ; Song Y; Guo C; Wang Y; Lukacs GL; Engelhardt JF
    J Biol Chem; 2012 Jun; 287(26):21673-85. PubMed ID: 22570484
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Potentiators of Defective ΔF508-CFTR Gating that Do Not Interfere with Corrector Action.
    Phuan PW; Veit G; Tan JA; Finkbeiner WE; Lukacs GL; Verkman AS
    Mol Pharmacol; 2015 Oct; 88(4):791-9. PubMed ID: 26245207
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Sequential quality-control checkpoints triage misfolded cystic fibrosis transmembrane conductance regulator.
    Younger JM; Chen L; Ren HY; Rosser MF; Turnbull EL; Fan CY; Patterson C; Cyr DM
    Cell; 2006 Aug; 126(3):571-82. PubMed ID: 16901789
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Diffusional mobility of the cystic fibrosis transmembrane conductance regulator mutant, delta F508-CFTR, in the endoplasmic reticulum measured by photobleaching of GFP-CFTR chimeras.
    Haggie PM; Stanton BA; Verkman AS
    J Biol Chem; 2002 May; 277(19):16419-25. PubMed ID: 11877404
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment.
    Yang Y; Janich S; Cohn JA; Wilson JM
    Proc Natl Acad Sci U S A; 1993 Oct; 90(20):9480-4. PubMed ID: 7692448
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Functional stability of rescued delta F508 cystic fibrosis transmembrane conductance regulator in airway epithelial cells.
    Jurkuvenaite A; Chen L; Bartoszewski R; Goldstein R; Bebok Z; Matalon S; Collawn JF
    Am J Respir Cell Mol Biol; 2010 Mar; 42(3):363-72. PubMed ID: 19502384
    [TBL] [Abstract][Full Text] [Related]  

  • 32. VAMP-associated Proteins (VAP) as Receptors That Couple Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Proteostasis with Lipid Homeostasis.
    Ernst WL; Shome K; Wu CC; Gong X; Frizzell RA; Aridor M
    J Biol Chem; 2016 Mar; 291(10):5206-20. PubMed ID: 26740627
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive.
    Denning GM; Anderson MP; Amara JF; Marshall J; Smith AE; Welsh MJ
    Nature; 1992 Aug; 358(6389):761-4. PubMed ID: 1380673
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mammalian osmolytes and S-nitrosoglutathione promote Delta F508 cystic fibrosis transmembrane conductance regulator (CFTR) protein maturation and function.
    Howard M; Fischer H; Roux J; Santos BC; Gullans SR; Yancey PH; Welch WJ
    J Biol Chem; 2003 Sep; 278(37):35159-67. PubMed ID: 12837761
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Derlin-1 promotes the efficient degradation of the cystic fibrosis transmembrane conductance regulator (CFTR) and CFTR folding mutants.
    Sun F; Zhang R; Gong X; Geng X; Drain PF; Frizzell RA
    J Biol Chem; 2006 Dec; 281(48):36856-63. PubMed ID: 16954204
    [TBL] [Abstract][Full Text] [Related]  

  • 36. SYVN1, NEDD8, and FBXO2 Proteins Regulate ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Ubiquitin-mediated Proteasomal Degradation.
    Ramachandran S; Osterhaus SR; Parekh KR; Jacobi AM; Behlke MA; McCray PB
    J Biol Chem; 2016 Dec; 291(49):25489-25504. PubMed ID: 27756846
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dendrimer-based selective autophagy-induction rescues ΔF508-CFTR and inhibits Pseudomonas aeruginosa infection in cystic fibrosis.
    Brockman SM; Bodas M; Silverberg D; Sharma A; Vij N
    PLoS One; 2017; 12(9):e0184793. PubMed ID: 28902888
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene.
    Dörk T; Wulbrand U; Richter T; Neumann T; Wolfes H; Wulf B; Maass G; Tümmler B
    Hum Genet; 1991 Aug; 87(4):441-6. PubMed ID: 1715308
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Correcting the F508del-CFTR variant by modulating eukaryotic translation initiation factor 3-mediated translation initiation.
    Hutt DM; Loguercio S; Roth DM; Su AI; Balch WE
    J Biol Chem; 2018 Aug; 293(35):13477-13495. PubMed ID: 30006345
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Rescue of DeltaF508-CFTR (cystic fibrosis transmembrane conductance regulator) by curcumin: involvement of the keratin 18 network.
    Lipecka J; Norez C; Bensalem N; Baudouin-Legros M; Planelles G; Becq F; Edelman A; Davezac N
    J Pharmacol Exp Ther; 2006 May; 317(2):500-5. PubMed ID: 16424149
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.