BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

353 related articles for article (PubMed ID: 24218596)

  • 1. Repair of UV photolesions in xeroderma pigmentosum group C cells induced by translational readthrough of premature termination codons.
    Kuschal C; DiGiovanna JJ; Khan SG; Gatti RA; Kraemer KH
    Proc Natl Acad Sci U S A; 2013 Nov; 110(48):19483-8. PubMed ID: 24218596
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Readthrough of stop codons by use of aminoglycosides in cells from xeroderma pigmentosum group C patients.
    Kuschal C; Khan SG; Enk B; DiGiovanna JJ; Kraemer KH
    Exp Dermatol; 2015 Apr; 24(4):296-7. PubMed ID: 25651777
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients.
    Khan SG; Oh KS; Shahlavi T; Ueda T; Busch DB; Inui H; Emmert S; Imoto K; Muniz-Medina V; Baker CC; DiGiovanna JJ; Schmidt D; Khadavi A; Metin A; Gozukara E; Slor H; Sarasin A; Kraemer KH
    Carcinogenesis; 2006 Jan; 27(1):84-94. PubMed ID: 16081512
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effect of Readthrough Treatment in Fibroblasts of Patients Affected by Lysosomal Diseases Caused by Premature Termination Codons.
    Matalonga L; Arias Á; Tort F; Ferrer-Cortés X; Garcia-Villoria J; Coll MJ; Gort L; Ribes A
    Neurotherapeutics; 2015 Oct; 12(4):874-86. PubMed ID: 26169295
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy.
    Boyle J; Ueda T; Oh KS; Imoto K; Tamura D; Jagdeo J; Khan SG; Nadem C; Digiovanna JJ; Kraemer KH
    Hum Mutat; 2008 Oct; 29(10):1194-208. PubMed ID: 18470933
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of four novel XPC mutations in two xeroderma pigmentosum complementation group C patients and functional study of XPC Q320X mutant.
    Gu Y; Chang X; Dai S; Song Q; Zhao H; Lei P
    Gene; 2017 Sep; 628():162-169. PubMed ID: 28669926
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients.
    Nishiwaki T; Kobayashi N; Iwamoto T; Yamamoto A; Sugiura S; Liu YC; Sarasin A; Okahashi Y; Hirano M; Ueno S; Mori T
    DNA Repair (Amst); 2008 Dec; 7(12):1990-8. PubMed ID: 18817897
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Defective global genome repair in XPC mice is associated with skin cancer susceptibility but not with sensitivity to UVB induced erythema and edema.
    Berg RJ; Ruven HJ; Sands AT; de Gruijl FR; Mullenders LH
    J Invest Dermatol; 1998 Apr; 110(4):405-9. PubMed ID: 9540983
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Drug-induced readthrough of premature stop codons leads to the stabilization of laminin alpha2 chain mRNA in CMD myotubes.
    Allamand V; Bidou L; Arakawa M; Floquet C; Shiozuka M; Paturneau-Jouas M; Gartioux C; Butler-Browne GS; Mouly V; Rousset JP; Matsuda R; Ikeda D; Guicheney P
    J Gene Med; 2008 Feb; 10(2):217-24. PubMed ID: 18074402
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Toward a rationale for the PTC124 (Ataluren) promoted readthrough of premature stop codons: a computational approach and GFP-reporter cell-based assay.
    Lentini L; Melfi R; Di Leonardo A; Spinello A; Barone G; Pace A; Palumbo Piccionello A; Pibiri I
    Mol Pharm; 2014 Mar; 11(3):653-64. PubMed ID: 24483936
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Efficient repair of cyclobutane pyrimidine dimers at mutational hot spots is restored in complemented Xeroderma pigmentosum group C and trichothiodystrophy/xeroderma pigmentosum group D cells.
    Zhou NY; Bates SE; Bouziane M; Stary A; Sarasin A; O'Connor TR
    J Mol Biol; 2003 Sep; 332(2):337-51. PubMed ID: 12948486
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Properties of Non-Aminoglycoside Compounds Used to Stimulate Translational Readthrough of PTC Mutations in Primary Ciliary Dyskinesia.
    Dabrowski M; Bukowy-Bieryllo Z; Jackson CL; Zietkiewicz E
    Int J Mol Sci; 2021 May; 22(9):. PubMed ID: 34066907
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cells from XP-D and XP-D-CS patients exhibit equally inefficient repair of UV-induced damage in transcribed genes but different capacity to recover UV-inhibited transcription.
    van Hoffen A; Kalle WH; de Jong-Versteeg A; Lehmann AR; van Zeeland AA; Mullenders LH
    Nucleic Acids Res; 1999 Jul; 27(14):2898-904. PubMed ID: 10390531
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations.
    Schäfer A; Hofmann L; Gratchev A; Laspe P; Schubert S; Schürer A; Ohlenbusch A; Tzvetkov M; Hallermann C; Reichrath J; Schön MP; Emmert S
    Exp Dermatol; 2013 Jan; 22(1):24-9. PubMed ID: 23173980
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional retroviral vector for gene therapy of xeroderma pigmentosum group D patients.
    Carreau M; Quilliet X; Eveno E; Salvetti A; Danos O; Heard JM; Mezzina M; Sarasin A
    Hum Gene Ther; 1995 Oct; 6(10):1307-15. PubMed ID: 8590735
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Repair of damaged DNA by extracts from a xeroderma pigmentosum complementation group A revertant and expression of a protein absent in its parental cell line.
    Jones CJ; Cleaver JE; Wood RD
    Nucleic Acids Res; 1992 Mar; 20(5):991-5. PubMed ID: 1549511
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nucleotide excision repair proteins rapidly accumulate but fail to persist in human XP-E (DDB2 mutant) cells.
    Oh KS; Imoto K; Emmert S; Tamura D; DiGiovanna JJ; Kraemer KH
    Photochem Photobiol; 2011; 87(3):729-33. PubMed ID: 21388382
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Xeroderma Pigmentosum C: A Valuable Tool to Decipher the Signaling Pathways in Skin Cancers.
    Nasrallah A; Fayyad N; Kobaisi F; Badran B; Fayyad-Kazan H; Fayyad-Kazan M; Sève M; Rachidi W
    Oxid Med Cell Longev; 2021; 2021():6689403. PubMed ID: 34630850
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Effects of XPD mutations on ultraviolet-induced apoptosis in relation to skin cancer-proneness in repair-deficient syndromes.
    Queille S; Drougard C; Sarasin A; Daya-Grosjean L
    J Invest Dermatol; 2001 Nov; 117(5):1162-70. PubMed ID: 11710928
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Small molecule Y-320 stimulates ribosome biogenesis, protein synthesis, and aminoglycoside-induced premature termination codon readthrough.
    Hosseini-Farahabadi S; Baradaran-Heravi A; Zimmerman C; Choi K; Flibotte S; Roberge M
    PLoS Biol; 2021 May; 19(5):e3001221. PubMed ID: 33939688
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.