BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 25651777)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. Stop codon context influences genome-wide stimulation of termination codon readthrough by aminoglycosides.
    Wangen JR; Green R
    Elife; 2020 Jan; 9():. PubMed ID: 31971508
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: molecular genetic evidence for a common ancestor.
    Gozukara EM; Khan SG; Metin A; Emmert S; Busch DB; Shahlavi T; Coleman DM; Miller M; Chinsomboon N; Stefanini M; Kraemer KH
    J Invest Dermatol; 2001 Aug; 117(2):197-204. PubMed ID: 11511294
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Aminoglycosides are efficient reagents to induce readthrough of premature termination codon in mutant B4GALNT1 genes found in families of hereditary spastic paraplegia.
    Yesmin F; Bhuiyan RH; Ohmi Y; Ohkawa Y; Tajima O; Okajima T; Furukawa K; Furukawa K
    J Biochem; 2020 Aug; 168(2):103-112. PubMed ID: 32282910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The minor gentamicin complex component, X2, is a potent premature stop codon readthrough molecule with therapeutic potential.
    Friesen WJ; Johnson B; Sierra J; Zhuo J; Vazirani P; Xue X; Tomizawa Y; Baiazitov R; Morrill C; Ren H; Babu S; Moon YC; Branstrom A; Mollin A; Hedrick J; Sheedy J; Elfring G; Weetall M; Colacino JM; Welch EM; Peltz SW
    PLoS One; 2018; 13(10):e0206158. PubMed ID: 30359426
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia.
    Bukowy-Bieryllo Z; Dabrowski M; Witt M; Zietkiewicz E
    RNA Biol; 2016 Oct; 13(10):1041-1050. PubMed ID: 27618201
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Readthrough of ACTN3 577X nonsense mutation produces full-length α-actinin-3 protein.
    Harada N; Hatakeyama A; Okuyama M; Miyatake Y; Nakagawa T; Kuroda M; Masumoto S; Tsutsumi R; Nakaya Y; Sakaue H
    Biochem Biophys Res Commun; 2018 Jul; 502(3):422-428. PubMed ID: 29857001
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of new-generation aminoglycoside promoting premature termination codon readthrough in cancer cells.
    Bidou L; Bugaud O; Belakhov V; Baasov T; Namy O
    RNA Biol; 2017 Mar; 14(3):378-388. PubMed ID: 28145797
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patients.
    Amr K; Messaoud O; El Darouti M; Abdelhak S; El-Kamah G
    Gene; 2014 Jan; 533(1):52-6. PubMed ID: 24135642
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A unique chromosomal in-frame deletion identified among seven XP-C patients.
    Schubert S; Rieper P; Ohlenbusch A; Seebode C; Lehmann J; Gratchev A; Emmert S
    Photodermatol Photoimmunol Photomed; 2016 Sep; 32(5-6):276-283. PubMed ID: 27387384
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stop codons and the +4 nucleotide may influence the efficiency of G418 in rescuing nonsense mutations of the HERG gene.
    Yu H; Meng Y; Zhang S; Tian C; Wu F; Li N; Li Q; Jin Y; Pu J
    Int J Mol Med; 2019 Dec; 44(6):2037-2046. PubMed ID: 31573043
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life.
    Slor H; Batko S; Khan SG; Sobe T; Emmert S; Khadavi A; Frumkin A; Busch DB; Albert RB; Kraemer KH
    J Invest Dermatol; 2000 Dec; 115(6):974-80. PubMed ID: 11121128
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel small molecules potentiate premature termination codon readthrough by aminoglycosides.
    Baradaran-Heravi A; Balgi AD; Zimmerman C; Choi K; Shidmoossavee FS; Tan JS; Bergeaud C; Krause A; Flibotte S; Shimizu Y; Anderson HJ; Mouly V; Jan E; Pfeifer T; Jaquith JB; Roberge M
    Nucleic Acids Res; 2016 Aug; 44(14):6583-98. PubMed ID: 27407112
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels.
    Chavanne F; Broughton BC; Pietra D; Nardo T; Browitt A; Lehmann AR; Stefanini M
    Cancer Res; 2000 Apr; 60(7):1974-82. PubMed ID: 10766188
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.