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 *

400 related articles for article (PubMed ID: 22902621)

  • 21. Cystic fibrosis transmembrane conductance regulator protein repair as a therapeutic strategy in cystic fibrosis.
    Sloane PA; Rowe SM
    Curr Opin Pulm Med; 2010 Nov; 16(6):591-7. PubMed ID: 20829696
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Unravelling the Regions of Mutant F508del-CFTR More Susceptible to the Action of Four Cystic Fibrosis Correctors.
    Amico G; Brandas C; Moran O; Baroni D
    Int J Mol Sci; 2019 Nov; 20(21):. PubMed ID: 31683989
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The cystic fibrosis-causing mutation deltaF508 affects multiple steps in cystic fibrosis transmembrane conductance regulator biogenesis.
    Thibodeau PH; Richardson JM; Wang W; Millen L; Watson J; Mendoza JL; Du K; Fischman S; Senderowitz H; Lukacs GL; Kirk K; Thomas PJ
    J Biol Chem; 2010 Nov; 285(46):35825-35. PubMed ID: 20667826
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator.
    Bartoszewski R; Króliczewski J; Piotrowski A; Jasiecka AJ; Bartoszewska S; Vecchio-Pagan B; Fu L; Sobolewska A; Matalon S; Cutting GR; Rowe SM; Collawn JF
    Cell Mol Biol Lett; 2016; 21():23. PubMed ID: 28536625
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Restoration of R117H CFTR folding and function in human airway cells through combination treatment with VX-809 and VX-770.
    Gentzsch M; Ren HY; Houck SA; Quinney NL; Cholon DM; Sopha P; Chaudhry IG; Das J; Dokholyan NV; Randell SH; Cyr DM
    Am J Physiol Lung Cell Mol Physiol; 2016 Sep; 311(3):L550-9. PubMed ID: 27402691
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Human heat shock protein 105/110 kDa (Hsp105/110) regulates biogenesis and quality control of misfolded cystic fibrosis transmembrane conductance regulator at multiple levels.
    Saxena A; Banasavadi-Siddegowda YK; Fan Y; Bhattacharya S; Roy G; Giovannucci DR; Frizzell RA; Wang X
    J Biol Chem; 2012 Jun; 287(23):19158-70. PubMed ID: 22505710
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Analysis of CFTR folding and degradation in transiently transfected cells.
    Grove DE; Rosser MF; Watkins RL; Cyr DM
    Methods Mol Biol; 2011; 741():219-32. PubMed ID: 21594788
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Localization and suppression of a kinetic defect in cystic fibrosis transmembrane conductance regulator folding.
    Qu BH; Strickland EH; Thomas PJ
    J Biol Chem; 1997 Jun; 272(25):15739-44. PubMed ID: 9188468
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Enhancement of premature stop codon readthrough in the CFTR gene by Ataluren (PTC124) derivatives.
    Pibiri I; Lentini L; Melfi R; Gallucci G; Pace A; Spinello A; Barone G; Di Leonardo A
    Eur J Med Chem; 2015 Aug; 101():236-44. PubMed ID: 26142488
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Investigation of folding and degradation of in vitro synthesized mutant proteins in microsomes.
    Cuthbert AW; Fuller W
    Methods Mol Biol; 2003; 232():265-83. PubMed ID: 12840556
    [No Abstract]   [Full Text] [Related]  

  • 31. An overview on chemical structures as ΔF508-CFTR correctors.
    Spanò V; Montalbano A; Carbone A; Scudieri P; Galietta LJV; Barraja P
    Eur J Med Chem; 2019 Oct; 180():430-448. PubMed ID: 31326599
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Restoration of CFTR function in patients with cystic fibrosis carrying the F508del-CFTR mutation.
    De Stefano D; Villella VR; Esposito S; Tosco A; Sepe A; De Gregorio F; Salvadori L; Grassia R; Leone CA; De Rosa G; Maiuri MC; Pettoello-Mantovani M; Guido S; Bossi A; Zolin A; Venerando A; Pinna LA; Mehta A; Bona G; Kroemer G; Maiuri L; Raia V
    Autophagy; 2014; 10(11):2053-74. PubMed ID: 25350163
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Aggregates of mutant CFTR fragments in airway epithelial cells of CF lungs: new pathologic observations.
    Du K; Karp PH; Ackerley C; Zabner J; Keshavjee S; Cutz E; Yeger H
    J Cyst Fibros; 2015 Mar; 14(2):182-93. PubMed ID: 25453871
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Co-Translational Folding of the First Transmembrane Domain of ABC-Transporter CFTR is Supported by Assembly with the First Cytosolic Domain.
    Kleizen B; van Willigen M; Mijnders M; Peters F; Grudniewska M; Hillenaar T; Thomas A; Kooijman L; Peters KW; Frizzell R; van der Sluijs P; Braakman I
    J Mol Biol; 2021 Jun; 433(13):166955. PubMed ID: 33771570
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A microRNA network regulates expression and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulator.
    Ramachandran S; Karp PH; Jiang P; Ostedgaard LS; Walz AE; Fisher JT; Keshavjee S; Lennox KA; Jacobi AM; Rose SD; Behlke MA; Welsh MJ; Xing Y; McCray PB
    Proc Natl Acad Sci U S A; 2012 Aug; 109(33):13362-7. PubMed ID: 22853952
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Non-native Conformers of Cystic Fibrosis Transmembrane Conductance Regulator NBD1 Are Recognized by Hsp27 and Conjugated to SUMO-2 for Degradation.
    Gong X; Ahner A; Roldan A; Lukacs GL; Thibodeau PH; Frizzell RA
    J Biol Chem; 2016 Jan; 291(4):2004-2017. PubMed ID: 26627832
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Control of cystic fibrosis transmembrane conductance regulator membrane trafficking: not just from the endoplasmic reticulum to the Golgi.
    Farinha CM; Matos P; Amaral MD
    FEBS J; 2013 Sep; 280(18):4396-406. PubMed ID: 23773658
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Impact of the deltaF508 mutation in first nucleotide-binding domain of human cystic fibrosis transmembrane conductance regulator on domain folding and structure.
    Lewis HA; Zhao X; Wang C; Sauder JM; Rooney I; Noland BW; Lorimer D; Kearins MC; Conners K; Condon B; Maloney PC; Guggino WB; Hunt JF; Emtage S
    J Biol Chem; 2005 Jan; 280(2):1346-53. PubMed ID: 15528182
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein.
    Brown CR; Hong-Brown LQ; Biwersi J; Verkman AS; Welch WJ
    Cell Stress Chaperones; 1996 Jun; 1(2):117-25. PubMed ID: 9222597
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Expression and degradation of the cystic fibrosis transmembrane conductance regulator in Saccharomyces cerevisiae.
    Kiser GL; Gentzsch M; Kloser AK; Balzi E; Wolf DH; Goffeau A; Riordan JR
    Arch Biochem Biophys; 2001 Jun; 390(2):195-205. PubMed ID: 11396922
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.