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Journal Abstract Search

208 related items for PubMed ID: 9973627

  • 21. Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane.
    Aamann MD, Sorensen MM, Hvitby C, Berquist BR, Muftuoglu M, Tian J, de Souza-Pinto NC, Scheibye-Knudsen M, Wilson DM, Stevnsner T, Bohr VA.
    FASEB J; 2010 Jul; 24(7):2334-46. PubMed ID: 20181933
    [Abstract] [Full Text] [Related]

  • 22. The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging.
    Stevnsner T, Muftuoglu M, Aamann MD, Bohr VA.
    Mech Ageing Dev; 2008 Jul; 129(7-8):441-8. PubMed ID: 18541289
    [Abstract] [Full Text] [Related]

  • 23. Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivity.
    Colella S, Nardo T, Mallery D, Borrone C, Ricci R, Ruffa G, Lehmann AR, Stefanini M.
    Hum Mol Genet; 1999 May; 8(5):935-41. PubMed ID: 10196384
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  • 26. Mechanistic insights into the regulation of transcription and transcription-coupled DNA repair by Cockayne syndrome protein B.
    Boetefuer EL, Lake RJ, Fan HY.
    Nucleic Acids Res; 2018 Sep 06; 46(15):7471-7479. PubMed ID: 30032309
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  • 27. Cockayne syndrome group B deficiency reduces H3K9me3 chromatin remodeler SETDB1 and exacerbates cellular aging.
    Lee JH, Demarest TG, Babbar M, Kim EW, Okur MN, De S, Croteau DL, Bohr VA.
    Nucleic Acids Res; 2019 Sep 19; 47(16):8548-8562. PubMed ID: 31276581
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  • 29. Cockayne syndrome-derived neurons display reduced synapse density and altered neural network synchrony.
    Vessoni AT, Herai RH, Karpiak JV, Leal AM, Trujillo CA, Quinet A, Agnez Lima LF, Menck CF, Muotri AR.
    Hum Mol Genet; 2016 Apr 01; 25(7):1271-80. PubMed ID: 26755826
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  • 30. Dysregulation of gene expression as a cause of Cockayne syndrome neurological disease.
    Wang Y, Chakravarty P, Ranes M, Kelly G, Brooks PJ, Neilan E, Stewart A, Schiavo G, Svejstrup JQ.
    Proc Natl Acad Sci U S A; 2014 Oct 07; 111(40):14454-9. PubMed ID: 25249633
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  • 31. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes.
    Troelstra C, van Gool A, de Wit J, Vermeulen W, Bootsma D, Hoeijmakers JH.
    Cell; 1992 Dec 11; 71(6):939-53. PubMed ID: 1339317
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  • 32. Transcription through 8-oxoguanine in DNA repair-proficient and Csb(-)/Ogg1(-) DNA repair-deficient mouse embryonic fibroblasts is dependent upon promoter strength and sequence context.
    Pastoriza-Gallego M, Armier J, Sarasin A.
    Mutagenesis; 2007 Sep 11; 22(5):343-51. PubMed ID: 17630408
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  • 33. Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition.
    van der Horst GT, van Steeg H, Berg RJ, van Gool AJ, de Wit J, Weeda G, Morreau H, Beems RB, van Kreijl CF, de Gruijl FR, Bootsma D, Hoeijmakers JH.
    Cell; 1997 May 02; 89(3):425-35. PubMed ID: 9150142
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  • 34. The cockayne syndrome group B gene product is involved in cellular repair of 8-hydroxyadenine in DNA.
    Tuo J, Jaruga P, Rodriguez H, Dizdaroglu M, Bohr VA.
    J Biol Chem; 2002 Aug 23; 277(34):30832-7. PubMed ID: 12060667
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  • 35. The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61.
    Orren DK, Dianov GL, Bohr VA.
    Nucleic Acids Res; 1996 Sep 01; 24(17):3317-22. PubMed ID: 8811084
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  • 36. Cockayne syndrome group B protein enhances elongation by RNA polymerase II.
    Selby CP, Sancar A.
    Proc Natl Acad Sci U S A; 1997 Oct 14; 94(21):11205-9. PubMed ID: 9326587
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  • 37. Formamidopyrimidine DNA glycosylase in the yeast Saccharomyces cerevisiae.
    de Oliveira R, van der Kemp PA, Thomas D, Geiger A, Nehls P, Boiteux S.
    Nucleic Acids Res; 1994 Sep 11; 22(18):3760-4. PubMed ID: 7937089
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  • 38. Cockayne syndrome group A and B proteins converge on transcription-linked resolution of non-B DNA.
    Scheibye-Knudsen M, Tseng A, Borch Jensen M, Scheibye-Alsing K, Fang EF, Iyama T, Bharti SK, Marosi K, Froetscher L, Kassahun H, Eckley DM, Maul RW, Bastian P, De S, Ghosh S, Nilsen H, Goldberg IG, Mattson MP, Wilson DM, Brosh RM, Gorospe M, Bohr VA.
    Proc Natl Acad Sci U S A; 2016 Nov 01; 113(44):12502-12507. PubMed ID: 27791127
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  • 39. Cockayne Syndrome group B protein interacts with TRF2 and regulates telomere length and stability.
    Batenburg NL, Mitchell TR, Leach DM, Rainbow AJ, Zhu XD.
    Nucleic Acids Res; 2012 Oct 01; 40(19):9661-74. PubMed ID: 22904069
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  • 40. The Cockayne syndrome group B DNA repair protein as an anti-cancer target.
    Lu Y, Mani S, Kandimalla ER, Yu D, Agrawal S, States JC, Bregman DB.
    Int J Oncol; 2001 Dec 01; 19(6):1089-97. PubMed ID: 11713576
    [Abstract] [Full Text] [Related]

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