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 *

169 related articles for article (PubMed ID: 8294433)

  • 1. The COOH terminus of suppressor of stem loop (SSL2/RAD25) in yeast is essential for overall genomic excision repair and transcription-coupled repair.
    Sweder KS; Hanawalt PC
    J Biol Chem; 1994 Jan; 269(3):1852-7. PubMed ID: 8294433
    [TBL] [Abstract][Full Text] [Related]  

  • 2. RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability.
    Park E; Guzder SN; Koken MH; Jaspers-Dekker I; Weeda G; Hoeijmakers JH; Prakash S; Prakash L
    Proc Natl Acad Sci U S A; 1992 Dec; 89(23):11416-20. PubMed ID: 1333609
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The requirement of yeast Ssl2 (Rad25) for the repair of cisplatin-damaged DNA.
    Yang WL; Cvijic ME; Ishii K; Chin KV
    Biochem Biophys Res Commun; 1998 Sep; 250(3):593-7. PubMed ID: 9784390
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SSL2, a suppressor of a stem-loop mutation in the HIS4 leader encodes the yeast homolog of human ERCC-3.
    Gulyas KD; Donahue TF
    Cell; 1992 Jun; 69(6):1031-42. PubMed ID: 1318786
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast.
    Wang Z; Svejstrup JQ; Feaver WJ; Wu X; Kornberg RD; Friedberg EC
    Nature; 1994 Mar; 368(6466):74-6. PubMed ID: 8107888
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2.
    Scherly D; Nouspikel T; Corlet J; Ucla C; Bairoch A; Clarkson SG
    Nature; 1993 May; 363(6425):182-5. PubMed ID: 8483504
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
    Oh KS; Khan SG; Jaspers NG; Raams A; Ueda T; Lehmann A; Friedmann PS; Emmert S; Gratchev A; Lachlan K; Lucassan A; Baker CC; Kraemer KH
    Hum Mutat; 2006 Nov; 27(11):1092-103. PubMed ID: 16947863
    [TBL] [Abstract][Full Text] [Related]  

  • 8. RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6.
    van Gool AJ; Verhage R; Swagemakers SM; van de Putte P; Brouwer J; Troelstra C; Bootsma D; Hoeijmakers JH
    EMBO J; 1994 Nov; 13(22):5361-9. PubMed ID: 7957102
    [TBL] [Abstract][Full Text] [Related]  

  • 9. DNA repair deficiencies associated with mutations in genes encoding subunits of transcription initiation factor TFIIH in yeast.
    Sweder KS; Chun R; Mori T; Hanawalt PC
    Nucleic Acids Res; 1996 Apr; 24(8):1540-6. PubMed ID: 8628689
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. RAD25 is a DNA helicase required for DNA repair and RNA polymerase II transcription.
    Guzder SN; Sung P; Bailly V; Prakash L; Prakash S
    Nature; 1994 Jun; 369(6481):578-81. PubMed ID: 8202161
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.
    Vermeulen W; Scott RJ; Rodgers S; Müller HJ; Cole J; Arlett CF; Kleijer WJ; Bootsma D; Hoeijmakers JH; Weeda G
    Am J Hum Genet; 1994 Feb; 54(2):191-200. PubMed ID: 8304337
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
    Riou L; Zeng L; Chevallier-Lagente O; Stary A; Nikaido O; Taïeb A; Weeda G; Mezzina M; Sarasin A
    Hum Mol Genet; 1999 Jun; 8(6):1125-33. PubMed ID: 10332046
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
    Weeda G; Eveno E; Donker I; Vermeulen W; Chevallier-Lagente O; Taïeb A; Stary A; Hoeijmakers JH; Mezzina M; Sarasin A
    Am J Hum Genet; 1997 Feb; 60(2):320-9. PubMed ID: 9012405
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.
    Moriwaki S; Stefanini M; Lehmann AR; Hoeijmakers JH; Robbins JH; Rapin I; Botta E; Tanganelli B; Vermeulen W; Broughton BC; Kraemer KH
    J Invest Dermatol; 1996 Oct; 107(4):647-53. PubMed ID: 8823375
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evidence for defective repair of cyclobutane pyrimidine dimers with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cells.
    Barrett SF; Robbins JH; Tarone RE; Kraemer KH
    Mutat Res; 1991 Nov; 255(3):281-91. PubMed ID: 1719400
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The rem mutations in the ATP-binding groove of the Rad3/XPD helicase lead to Xeroderma pigmentosum-Cockayne syndrome-like phenotypes.
    Herrera-Moyano E; Moriel-Carretero M; Montelone BA; Aguilera A
    PLoS Genet; 2014 Dec; 10(12):e1004859. PubMed ID: 25500814
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Yeast DNA-repair gene RAD14 encodes a zinc metalloprotein with affinity for ultraviolet-damaged DNA.
    Guzder SN; Sung P; Prakash L; Prakash S
    Proc Natl Acad Sci U S A; 1993 Jun; 90(12):5433-7. PubMed ID: 8516285
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene.
    Mounkes LC; Jones RS; Liang BC; Gelbart W; Fuller MT
    Cell; 1992 Dec; 71(6):925-37. PubMed ID: 1458540
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.
    Broughton BC; Thompson AF; Harcourt SA; Vermeulen W; Hoeijmakers JH; Botta E; Stefanini M; King MD; Weber CA; Cole J
    Am J Hum Genet; 1995 Jan; 56(1):167-74. PubMed ID: 7825573
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.