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 *

315 related articles for article (PubMed ID: 19153657)

  • 21. [Advance in research on causative genes of xeroderma pigmentosum and related diseases].
    Sun Z; Guo Y; Zhang J; Zhuang Y; Li M; Yao Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):708-12. PubMed ID: 27577229
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Understanding photodermatoses associated with defective DNA repair: Photosensitive syndromes without associated cancer predisposition.
    Yew YW; Giordano CN; Spivak G; Lim HW
    J Am Acad Dermatol; 2016 Nov; 75(5):873-882. PubMed ID: 27745642
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [DNA lesions: mechanisms of recognition and repair].
    Sarasin A
    Bull Cancer; 1997 May; 84(5):467-72. PubMed ID: 9295859
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Repair of DNA damage using nucleotide excision repair (NER)--relationship with cancer risk].
    Butkiewicz D; Rusin M; Pawlas M; Czarny M; Chorazy M
    Postepy Hig Med Dosw; 2002; 56(4):485-98. PubMed ID: 12418414
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Transcription-Coupled Nucleotide Excision Repair and the Transcriptional Response to UV-Induced DNA Damage.
    Nieto Moreno N; Olthof AM; Svejstrup JQ
    Annu Rev Biochem; 2023 Jun; 92():81-113. PubMed ID: 37040775
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity.
    Cleaver JE; Lam ET; Revet I
    Nat Rev Genet; 2009 Nov; 10(11):756-68. PubMed ID: 19809470
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Cell type-specific hypersensitivity to oxidative damage in CSB and XPA mice.
    de Waard H; de Wit J; Gorgels TG; van den Aardweg G; Andressoo JO; Vermeij M; van Steeg H; Hoeijmakers JH; van der Horst GT
    DNA Repair (Amst); 2003 Jan; 2(1):13-25. PubMed ID: 12509265
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G.
    Cooper PK; Nouspikel T; Clarkson SG; Leadon SA
    Science; 1997 Feb; 275(5302):990-3. PubMed ID: 9020084
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A disease-associated XPA allele interferes with TFIIH binding and primarily affects transcription-coupled nucleotide excision repair.
    van den Heuvel D; Kim M; Wondergem AP; van der Meer PJ; Witkamp M; Lambregtse F; Kim HS; Kan F; Apelt K; Kragten A; González-Prieto R; Vertegaal ACO; Yeo JE; Kim BG; van Doorn R; Schärer OD; Luijsterburg MS
    Proc Natl Acad Sci U S A; 2023 Mar; 120(11):e2208860120. PubMed ID: 36893274
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The "Dutch DNA Repair Group", in retrospect.
    Bootsma D
    Mutat Res; 2001 Feb; 485(1):37-41. PubMed ID: 11341992
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum.
    Brooks PJ
    Neuroscience; 2007 Apr; 145(4):1407-17. PubMed ID: 17184928
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The nucleotide excision repair proteins through the lens of molecular dynamics simulations.
    Pinto ÉSM; Krause MJ; Dorn M; Feltes BC
    DNA Repair (Amst); 2023 Jul; 127():103510. PubMed ID: 37148846
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Unraveling DNA repair in human: molecular mechanisms and consequences of repair defect.
    Tuteja N; Tuteja R
    Crit Rev Biochem Mol Biol; 2001; 36(3):261-90. PubMed ID: 11450971
    [TBL] [Abstract][Full Text] [Related]  

  • 35. DNA Repair Dysfunction and Neurodegeneration: Lessons From Rare Pediatric Disorders.
    Shabbir SH
    J Child Neurol; 2016 Mar; 31(3):392-6. PubMed ID: 26116382
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Cockayne syndrome--an inherited multisystem disorder with cutaneous photosensitivity and defective repair of DNA. Comparison with xeroderma pigmentosum.
    Otsuka F; Robbins JH
    Am J Dermatopathol; 1985 Aug; 7(4):387-92. PubMed ID: 3842793
    [No Abstract]   [Full Text] [Related]  

  • 37. Heterogeneity and overlaps in nucleotide excision repair disorders.
    Ferri D; Orioli D; Botta E
    Clin Genet; 2020 Jan; 97(1):12-24. PubMed ID: 30919937
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.
    Cleaver JE; Thompson LH; Richardson AS; States JC
    Hum Mutat; 1999; 14(1):9-22. PubMed ID: 10447254
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 16.