BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 17191107)

  • 1. Gene expression profile study in CFTR mutated bronchial cell lines.
    Gambardella S; Biancolella M; D'Apice MR; Amati F; Sangiuolo F; Farcomeni A; Chillemi G; Bueno S; Desideri A; Novelli G
    Clin Exp Med; 2006 Dec; 6(4):157-65. PubMed ID: 17191107
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis.
    Hamosh A; Trapnell BC; Zeitlin PL; Montrose-Rafizadeh C; Rosenstein BJ; Crystal RG; Cutting GR
    J Clin Invest; 1991 Dec; 88(6):1880-5. PubMed ID: 1721624
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Reduced expression of Tis7/IFRD1 protein in murine and human cystic fibrosis airway epithelial cell models homozygous for the F508del-CFTR mutation.
    Blanchard E; Marie S; Riffault L; Bonora M; Tabary O; Clement A; Jacquot J
    Biochem Biophys Res Commun; 2011 Aug; 411(3):471-6. PubMed ID: 21723850
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Isolation of CF cell lines corrected at DeltaF508-CFTR locus by SFHR-mediated targeting.
    Bruscia E; Sangiuolo F; Sinibaldi P; Goncz KK; Novelli G; Gruenert DC
    Gene Ther; 2002 Jun; 9(11):683-5. PubMed ID: 12032687
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Suitability of oligonucleotide-mediated cystic fibrosis gene repair in airway epithelial cells.
    de Semir D; Nadal M; González JR; Larriba S; Avinyó A; Nunes V; Casals T; Estivill X; Aran JM
    J Gene Med; 2003 Jul; 5(7):625-39. PubMed ID: 12825202
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Abnormal spatial diffusion of Ca2+ in F508del-CFTR airway epithelial cells.
    Antigny F; Norez C; Cantereau A; Becq F; Vandebrouck C
    Respir Res; 2008 Oct; 9(1):70. PubMed ID: 18973672
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Anti-inflammatory effect of miglustat in bronchial epithelial cells.
    Dechecchi MC; Nicolis E; Norez C; Bezzerri V; Borgatti M; Mancini I; Rizzotti P; Ribeiro CM; Gambari R; Becq F; Cabrini G
    J Cyst Fibros; 2008 Nov; 7(6):555-65. PubMed ID: 18815075
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nonsense mutation R1162X of the cystic fibrosis transmembrane conductance regulator gene does not reduce messenger RNA expression in nasal epithelial tissue.
    Rolfini R; Cabrini G
    J Clin Invest; 1993 Dec; 92(6):2683-7. PubMed ID: 7504691
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145, -223, and -494 is altered in ΔF508 cystic fibrosis airway epithelium.
    Oglesby IK; Chotirmall SH; McElvaney NG; Greene CM
    J Immunol; 2013 Apr; 190(7):3354-62. PubMed ID: 23436935
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cystic fibrosis patients with the 3272-26A-->G mutation have mild disease, leaky alternative mRNA splicing, and CFTR protein at the cell membrane.
    Beck S; Penque D; Garcia S; Gomes A; Farinha C; Mata L; Gulbenkian S; Gil-Ferreira K; Duarte A; Pacheco P; Barreto C; Lopes B; Cavaco J; Lavinha J; Amaral MD
    Hum Mutat; 1999; 14(2):133-44. PubMed ID: 10425036
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Strain-dependent pulmonary gene expression profiles of a cystic fibrosis mouse model.
    Haston CK; Cory S; Lafontaine L; Dorion G; Hallett MT
    Physiol Genomics; 2006 Apr; 25(2):336-45. PubMed ID: 16614460
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R; Kianishirazi R; Cassiman JJ; Zamani M; Cuppens H
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Altered terminal glycosylation and the pathophysiology of CF lung disease.
    Rhim AD; Stoykova LI; Trindade AJ; Glick MC; Scanlin TF
    J Cyst Fibros; 2004 Aug; 3 Suppl 2():95-6. PubMed ID: 15463936
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The study of cystic fibrosis transmembrane conductance regulator gene mutations in a group of patients from Romania.
    Frenţescu L; Brownsell E; Hinks J; Malone G; Shaw H; Budişan L; Bulman M; Schwarz M; Pop L; Filip M; Tomescu E; Moşescu S; Popa I; Benga G
    J Cyst Fibros; 2008 Sep; 7(5):423-8. PubMed ID: 18467194
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cystic fibrosis: molecular update and clinical implications].
    Orozco L; Chávez M; Saldaña Y; Velázquez R; Carnevale A; González-del Angel A; Jiménez S
    Rev Invest Clin; 2006; 58(2):139-52. PubMed ID: 16827266
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial correction of endogenous DeltaF508 CFTR in human cystic fibrosis airway epithelia by spliceosome-mediated RNA trans-splicing.
    Liu X; Jiang Q; Mansfield SG; Puttaraju M; Zhang Y; Zhou W; Cohn JA; Garcia-Blanco MA; Mitchell LG; Engelhardt JF
    Nat Biotechnol; 2002 Jan; 20(1):47-52. PubMed ID: 11753361
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes.
    Salvatore F; Scudiero O; Castaldo G
    Am J Med Genet; 2002 Jul; 111(1):88-95. PubMed ID: 12124743
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Modifier genes in cystic fibrosis lung disease.
    Merlo CA; Boyle MP
    J Lab Clin Med; 2003 Apr; 141(4):237-41. PubMed ID: 12677168
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maintaining low Ca2+ level in the endoplasmic reticulum restores abnormal endogenous F508del-CFTR trafficking in airway epithelial cells.
    Norez C; Antigny F; Becq F; Vandebrouck C
    Traffic; 2006 May; 7(5):562-73. PubMed ID: 16643279
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Regulated expression of the human CFTR gene in epithelial cells.
    Ye L; Chan S; Chow YH; Tsui LC; Hu J
    Mol Ther; 2001 May; 3(5 Pt 1):723-33. PubMed ID: 11356077
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.