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Results: 1 to 20 of 38

Cited In for PubMed (Select 14639525)

1.

Identification of Novel Proteins Co-Purifying with Cockayne Syndrome Group B (CSB) Reveals Potential Roles for CSB in RNA Metabolism and Chromatin Dynamics.

Nicolai S, Filippi S, Caputo M, Cipak L, Gregan J, Ammerer G, Frontini M, Willems D, Prantera G, Balajee AS, Proietti-De-Santis L.

PLoS One. 2015 Jun 1;10(6):e0128558. doi: 10.1371/journal.pone.0128558. eCollection 2015.

2.

Regulation of the Rhp26ERCC6/CSB chromatin remodeler by a novel conserved leucine latch motif.

Wang L, Limbo O, Fei J, Chen L, Kim B, Luo J, Chong J, Conaway RC, Conaway JW, Ranish JA, Kadonaga JT, Russell P, Wang D.

Proc Natl Acad Sci U S A. 2014 Dec 30;111(52):18566-71. doi: 10.1073/pnas.1420227112. Epub 2014 Dec 15.

3.

A new mutation in the CSB gene in a Chinese patient with mild Cockayne syndrome.

Luo Y, Ling Y, Chen J, Xu X, Chen C, Leng F, Cheng J, Chen M, Lu Z.

Clin Case Rep. 2014 Apr;2(2):33-6. doi: 10.1002/ccr3.47. Epub 2014 Feb 7.

4.

ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination.

Shehata L, Simeonov DR, Raams A, Wolfe L, Vanderver A, Li X, Huang Y, Garner S, Boerkoel CF, Thurm A, Herman GE, Tifft CJ, He M, Jaspers NG, Gahl WA.

Am J Med Genet A. 2014 Nov;164A(11):2892-900. doi: 10.1002/ajmg.a.36709. Epub 2014 Sep 22.

PMID:
25251875
5.

The cockayne syndrome B protein is essential for neuronal differentiation and neuritogenesis.

Ciaffardini F, Nicolai S, Caputo M, Canu G, Paccosi E, Costantino M, Frontini M, Balajee AS, Proietti-De-Santis L.

Cell Death Dis. 2014 May 29;5:e1268. doi: 10.1038/cddis.2014.228.

6.

ERCC6L2 mutations link a distinct bone-marrow-failure syndrome to DNA repair and mitochondrial function.

Tummala H, Kirwan M, Walne AJ, Hossain U, Jackson N, Pondarre C, Plagnol V, Vulliamy T, Dokal I.

Am J Hum Genet. 2014 Feb 6;94(2):246-56. doi: 10.1016/j.ajhg.2014.01.007.

7.

Multiple interaction partners for Cockayne syndrome proteins: implications for genome and transcriptome maintenance.

Aamann MD, Muftuoglu M, Bohr VA, Stevnsner T.

Mech Ageing Dev. 2013 May-Jun;134(5-6):212-24. doi: 10.1016/j.mad.2013.03.009. Epub 2013 Apr 9. Review.

8.

Genetic variability in DNA repair proteins in age-related macular degeneration.

Blasiak J, Synowiec E, Salminen A, Kaarniranta K.

Int J Mol Sci. 2012 Oct 18;13(10):13378-97. doi: 10.3390/ijms131013378. Review.

9.

Evidence for premature aging due to oxidative stress in iPSCs from Cockayne syndrome.

Andrade LN, Nathanson JL, Yeo GW, Menck CF, Muotri AR.

Hum Mol Genet. 2012 Sep 1;21(17):3825-34. doi: 10.1093/hmg/dds211. Epub 2012 Jun 1.

10.

Dysmyelination not demyelination causes neurological symptoms in preweaned mice in a murine model of Cockayne syndrome.

Revet I, Feeney L, Tang AA, Huang EJ, Cleaver JE.

Proc Natl Acad Sci U S A. 2012 Mar 20;109(12):4627-32. doi: 10.1073/pnas.1202621109. Epub 2012 Mar 5.

11.

Interaction between the Cockayne syndrome B and p53 proteins: implications for aging.

Frontini M, Proietti-De-Santis L.

Aging (Albany NY). 2012 Feb;4(2):89-97. Review.

12.

Rad26p regulates the occupancy of histone H2A-H2B dimer at the active genes in vivo.

Malik S, Chaurasia P, Lahudkar S, Uprety B, Bhaumik SR.

Nucleic Acids Res. 2012 Apr;40(8):3348-63. doi: 10.1093/nar/gkr1244. Epub 2011 Dec 22.

13.

Testicular nuclear receptor 4 (TR4) regulates UV light-induced responses via Cockayne syndrome B protein-mediated transcription-coupled DNA repair.

Liu S, Yan SJ, Lee YF, Liu NC, Ting HJ, Li G, Wu Q, Chen LM, Chang C.

J Biol Chem. 2011 Nov 4;286(44):38103-8. doi: 10.1074/jbc.M111.259523. Epub 2011 Sep 14.

14.

Reciprocally regulated chromatin association of Cockayne syndrome protein B and p53 protein.

Lake RJ, Basheer A, Fan HY.

J Biol Chem. 2011 Oct 7;286(40):34951-8. doi: 10.1074/jbc.M111.252643. Epub 2011 Aug 18.

15.

DNA repair deficiency in neurodegeneration.

Jeppesen DK, Bohr VA, Stevnsner T.

Prog Neurobiol. 2011 Jul;94(2):166-200. doi: 10.1016/j.pneurobio.2011.04.013. Epub 2011 Apr 30. Review.

16.

DNA damage and base excision repair in mitochondria and their role in aging.

Gredilla R.

J Aging Res. 2010 Dec 30;2011:257093. doi: 10.4061/2011/257093.

17.

Cockayne syndrome B protects against methamphetamine-enhanced oxidative DNA damage in murine fetal brain and postnatal neurodevelopmental deficits.

McCallum GP, Wong AW, Wells PG.

Antioxid Redox Signal. 2011 Mar 1;14(5):747-56. doi: 10.1089/ars.2009.2946. Epub 2011 Jan 5.

18.

Involvement of oxidatively damaged DNA and repair in cancer development and aging.

Tudek B, Winczura A, Janik J, Siomek A, Foksinski M, OliƄski R.

Am J Transl Res. 2010 May 15;2(3):254-84.

19.

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.

20.

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 3rd, Stevnsner T, Bohr VA.

FASEB J. 2010 Jul;24(7):2334-46. doi: 10.1096/fj.09-147991. Epub 2010 Feb 24.

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