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 *

211 related articles for article (PubMed ID: 25431422)

  • 61. TFIIH mutations can impact on translational fidelity of the ribosome.
    Khalid F; Phan T; Qiang M; Maity P; Lasser T; Wiese S; Penzo M; Alupei M; Orioli D; Scharffetter-Kochanek K; Iben S
    Hum Mol Genet; 2023 Mar; 32(7):1102-1113. PubMed ID: 36308430
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Common pathways for ultraviolet skin carcinogenesis in the repair and replication defective groups of xeroderma pigmentosum.
    Cleaver JE
    J Dermatol Sci; 2000 May; 23(1):1-11. PubMed ID: 10699759
    [TBL] [Abstract][Full Text] [Related]  

  • 63. The Drosophila melanogaster homologue of the Xeroderma pigmentosum D gene product is located in euchromatic regions and has a dynamic response to UV light-induced lesions in polytene chromosomes.
    Reynaud E; Lomelí H; Vázquez M; Zurita M
    Mol Biol Cell; 1999 Apr; 10(4):1191-203. PubMed ID: 10198066
    [TBL] [Abstract][Full Text] [Related]  

  • 64. 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]  

  • 65. TFIIH controls developmentally-regulated cell cycle progression as a holocomplex.
    Matsuno M; Kose H; Okabe M; Hiromi Y
    Genes Cells; 2007 Nov; 12(11):1289-300. PubMed ID: 17986012
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Isolation and characterization of two human transcription factor IIH (TFIIH)-related complexes: ERCC2/CAK and TFIIH.
    Reardon JT; Ge H; Gibbs E; Sancar A; Hurwitz J; Pan ZQ
    Proc Natl Acad Sci U S A; 1996 Jun; 93(13):6482-7. PubMed ID: 8692841
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Competent transcription initiation by RNA polymerase II in cell-free extracts from xeroderma pigmentosum groups B and D in an optimized RNA transcription assay.
    Satoh MS; Hanawalt PC
    Biochim Biophys Acta; 1997 Nov; 1354(3):241-51. PubMed ID: 9427533
    [TBL] [Abstract][Full Text] [Related]  

  • 68. 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]  

  • 69. 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]  

  • 70. ARCH domain of XPD, an anchoring platform for CAK that conditions TFIIH DNA repair and transcription activities.
    Abdulrahman W; Iltis I; Radu L; Braun C; Maglott-Roth A; Giraudon C; Egly JM; Poterszman A
    Proc Natl Acad Sci U S A; 2013 Feb; 110(8):E633-42. PubMed ID: 23382212
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Nucleotide excision repair/transcription gene defects in the fetus and impaired TFIIH-mediated function in transcription in placenta leading to preeclampsia.
    Moslehi R; Ambroggio X; Nagarajan V; Kumar A; Dzutsev A
    BMC Genomics; 2014 May; 15():373. PubMed ID: 24885447
    [TBL] [Abstract][Full Text] [Related]  

  • 72. TFIIH: A multi-subunit complex at the cross-roads of transcription and DNA repair.
    Kolesnikova O; Radu L; Poterszman A
    Adv Protein Chem Struct Biol; 2019; 115():21-67. PubMed ID: 30798933
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Defective transcription/repair factor IIH recruitment to specific UV lesions in trichothiodystrophy syndrome.
    Chiganças V; Lima-Bessa KM; Stary A; Menck CF; Sarasin A
    Cancer Res; 2008 Aug; 68(15):6074-83. PubMed ID: 18676829
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genes.
    Dumaz N; Duthu A; Ehrhart JC; Drougard C; Appella E; Anderson CW; May P; Sarasin A; Daya-Grosjean L
    Mol Carcinog; 1997 Dec; 20(4):340-7. PubMed ID: 9433478
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells.
    Marionnet C; Benoit A; Benhamou S; Sarasin A; Stary A
    J Mol Biol; 1995 Oct; 252(5):550-62. PubMed ID: 7563073
    [TBL] [Abstract][Full Text] [Related]  

  • 76. 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]  

  • 77. Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2).
    Emmert S; Ueda T; Zumsteg U; Weber P; Khan SG; Oh KS; Boyle J; Laspe P; Zachmann K; Boeckmann L; Kuschal C; Bircher A; Kraemer KH
    Exp Dermatol; 2009 Jan; 18(1):64-8. PubMed ID: 18637129
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
    Graham JM; Anyane-Yeboa K; Raams A; Appeldoorn E; Kleijer WJ; Garritsen VH; Busch D; Edersheim TG; Jaspers NG
    Am J Hum Genet; 2001 Aug; 69(2):291-300. PubMed ID: 11443545
    [TBL] [Abstract][Full Text] [Related]  

  • 79. UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum.
    Madzak C; Armier J; Stary A; Daya-Grosjean L; Sarasin A
    Carcinogenesis; 1993 Jul; 14(7):1255-60. PubMed ID: 8392442
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.
    Takayama K; Salazar EP; Lehmann A; Stefanini M; Thompson LH; Weber CA
    Cancer Res; 1995 Dec; 55(23):5656-63. PubMed ID: 7585650
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.