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Results: 1 to 20 of 33

Cited In for PubMed (Select 9565609)


Molecular regulation of UV-induced DNA repair.

Shah P, He YY.

Photochem Photobiol. 2015 Mar-Apr;91(2):254-64. doi: 10.1111/php.12406. Epub 2015 Jan 14.


CSB interacts with SNM1A and promotes DNA interstrand crosslink processing.

Iyama T, Lee SY, Berquist BR, Gileadi O, Bohr VA, Seidman MM, McHugh PJ, Wilson DM 3rd.

Nucleic Acids Res. 2015 Jan;43(1):247-58. doi: 10.1093/nar/gku1279. Epub 2014 Dec 10.


Identification of two missense mutations of ERCC6 in three Chinese sisters with Cockayne syndrome by whole exome sequencing.

Yu S, Chen L, Ye L, Fei L, Tang W, Tian Y, Geng Q, Yi X, Xie J.

PLoS One. 2014 Dec 2;9(12):e113914. doi: 10.1371/journal.pone.0113914. eCollection 2014.


Mitochondrial reactive oxygen species are scavenged by Cockayne syndrome B protein in human fibroblasts without nuclear DNA damage.

Cleaver JE, Brennan-Minnella AM, Swanson RA, Fong KW, Chen J, Chou KM, Chen YW, Revet I, Bezrookove V.

Proc Natl Acad Sci U S A. 2014 Sep 16;111(37):13487-92. doi: 10.1073/pnas.1414135111. Epub 2014 Aug 18.


The sequence-specific transcription factor c-Jun targets Cockayne syndrome protein B to regulate transcription and chromatin structure.

Lake RJ, Boetefuer EL, Tsai PF, Jeong J, Choi I, Won KJ, Fan HY.

PLoS Genet. 2014 Apr 17;10(4):e1004284. doi: 10.1371/journal.pgen.1004284. eCollection 2014 Apr.


DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae.

Boiteux S, Jinks-Robertson S.

Genetics. 2013 Apr;193(4):1025-64. doi: 10.1534/genetics.112.145219. Review.


Structure, function and regulation of CSB: a multi-talented gymnast.

Lake RJ, Fan HY.

Mech Ageing Dev. 2013 May-Jun;134(5-6):202-11. doi: 10.1016/j.mad.2013.02.004. Epub 2013 Feb 16. Review.


Human Cockayne syndrome B protein reciprocally communicates with mitochondrial proteins and promotes transcriptional elongation.

Berquist BR, Canugovi C, Sykora P, Wilson DM 3rd, Bohr VA.

Nucleic Acids Res. 2012 Sep 1;40(17):8392-405. Epub 2012 Jun 28.


ATP-dependent chromatin remodeling in the DNA-damage response.

Lans H, Marteijn JA, Vermeulen W.

Epigenetics Chromatin. 2012 Jan 30;5:4. doi: 10.1186/1756-8935-5-4.


A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair.

Anindya R, Mari PO, Kristensen U, Kool H, Giglia-Mari G, Mullenders LH, Fousteri M, Vermeulen W, Egly JM, Svejstrup JQ.

Mol Cell. 2010 Jun 11;38(5):637-48. doi: 10.1016/j.molcel.2010.04.017.


UV-induced association of the CSB remodeling protein with chromatin requires ATP-dependent relief of N-terminal autorepression.

Lake RJ, Geyko A, Hemashettar G, Zhao Y, Fan HY.

Mol Cell. 2010 Jan 29;37(2):235-46. doi: 10.1016/j.molcel.2009.10.027.


Deletion of the Chd6 exon 12 affects motor coordination.

Lathrop MJ, Chakrabarti L, Eng J, Rhodes CH, Lutz T, Nieto A, Liggitt HD, Warner S, Fields J, Stöger R, Fiering S.

Mamm Genome. 2010 Apr;21(3-4):130-42. doi: 10.1007/s00335-010-9248-8. Epub 2010 Jan 29.


Nucleic acid binding activity of human Cockayne syndrome B protein and identification of Ca(2+) as a novel metal cofactor.

Berquist BR, Wilson DM 3rd.

J Mol Biol. 2009 Sep 4;391(5):820-32. doi: 10.1016/j.jmb.2009.06.078. Epub 2009 Jul 4.


An abundant evolutionarily conserved CSB-PiggyBac fusion protein expressed in Cockayne syndrome.

Newman JC, Bailey AD, Fan HY, Pavelitz T, Weiner AM.

PLoS Genet. 2008 Mar 21;4(3):e1000031. doi: 10.1371/journal.pgen.1000031.


Cockayne syndrome B protein stimulates apurinic endonuclease 1 activity and protects against agents that introduce base excision repair intermediates.

Wong HK, Muftuoglu M, Beck G, Imam SZ, Bohr VA, Wilson DM 3rd.

Nucleic Acids Res. 2007;35(12):4103-13. Epub 2007 Jun 12.


A new connection of mRNP biogenesis and export with transcription-coupled repair.

Gaillard H, Wellinger RE, Aguilera A.

Nucleic Acids Res. 2007;35(12):3893-906. Epub 2007 May 30.


Functional TFIIH is required for UV-induced translocation of CSA to the nuclear matrix.

Saijo M, Hirai T, Ogawa A, Kobayashi A, Kamiuchi S, Tanaka K.

Mol Cell Biol. 2007 Apr;27(7):2538-47. Epub 2007 Jan 22.


Cockayne syndrome exhibits dysregulation of p21 and other gene products that may be independent of transcription-coupled repair.

Cleaver JE, Hefner E, Laposa RR, Karentz D, Marti T.

Neuroscience. 2007 Apr 14;145(4):1300-8. Epub 2006 Oct 19.


Cockayne syndrome group B protein (CSB) plays a general role in chromatin maintenance and remodeling.

Newman JC, Bailey AD, Weiner AM.

Proc Natl Acad Sci U S A. 2006 Jun 20;103(25):9613-8. Epub 2006 Jun 13.


CSA-dependent degradation of CSB by the ubiquitin-proteasome pathway establishes a link between complementation factors of the Cockayne syndrome.

Groisman R, Kuraoka I, Chevallier O, Gaye N, Magnaldo T, Tanaka K, Kisselev AF, Harel-Bellan A, Nakatani Y.

Genes Dev. 2006 Jun 1;20(11):1429-34.

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