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Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I-DNA covalent complex.

Horibata K, Saijo M, Bay MN, Lan L, Kuraoka I, Brooks PJ, Honma M, Nohmi T, Yasui A, Tanaka K.

Genes Cells. 2011 Jan;16(1):101-14. doi: 10.1111/j.1365-2443.2010.01467.x. Epub 2010 Dec 9.


Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells.

Selzer RR, Nyaga S, Tuo J, May A, Muftuoglu M, Christiansen M, Citterio E, Brosh RM Jr, Bohr VA.

Nucleic Acids Res. 2002 Feb 1;30(3):782-93.


The transcriptional response after oxidative stress is defective in Cockayne syndrome group B cells.

Kyng KJ, May A, Brosh RM Jr, Cheng WH, Chen C, Becker KG, Bohr VA.

Oncogene. 2003 Feb 27;22(8):1135-49.


The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair.

Brosh RM Jr, Balajee AS, Selzer RR, Sunesen M, Proietti De Santis L, Bohr VA.

Mol Biol Cell. 1999 Nov;10(11):3583-94.


Downregulation of Cockayne syndrome B protein reduces human 8-oxoguanine DNA glycosylase-1 expression and repair of UV radiation-induced 8-oxo-7,8-dihydro-2'-deoxyguanine.

Javeri A, Lyons JG, Huang XX, Halliday GM.

Cancer Sci. 2011 Sep;102(9):1651-8. doi: 10.1111/j.1349-7006.2011.02005.x. Epub 2011 Jul 18.


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.


Functional crosstalk between hOgg1 and the helicase domain of Cockayne syndrome group B protein.

Tuo J, Chen C, Zeng X, Christiansen M, Bohr VA.

DNA Repair (Amst). 2002 Nov 3;1(11):913-27.


Disruption of the Cockayne syndrome B gene impairs spontaneous tumorigenesis in cancer-predisposed Ink4a/ARF knockout mice.

Lu Y, Lian H, Sharma P, Schreiber-Agus N, Russell RG, Chin L, van der Horst GT, Bregman DB.

Mol Cell Biol. 2001 Mar;21(5):1810-8.


Role of the ATPase domain of the Cockayne syndrome group B protein in UV induced apoptosis.

Balajee AS, Proietti De Santis L, Brosh RM Jr, Selzer R, Bohr VA.

Oncogene. 2000 Jan 27;19(4):477-89.


Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome.

Horibata K, Iwamoto Y, Kuraoka I, Jaspers NG, Kurimasa A, Oshimura M, Ichihashi M, Tanaka K.

Proc Natl Acad Sci U S A. 2004 Oct 26;101(43):15410-5. Epub 2004 Oct 14.


The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA.

Tuo J, Müftüoglu M, Chen C, Jaruga P, Selzer RR, Brosh RM Jr, Rodriguez H, Dizdaroglu M, Bohr VA.

J Biol Chem. 2001 Dec 7;276(49):45772-9. Epub 2001 Oct 1.


Deletion of 5' sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome.

Laugel V, Dalloz C, Stary A, Cormier-Daire V, Desguerre I, Renouil M, Fourmaintraux A, Velez-Cruz R, Egly JM, Sarasin A, Dollfus H.

Eur J Hum Genet. 2008 Mar;16(3):320-7. doi: 10.1038/sj.ejhg.5201991. Epub 2008 Jan 9.


The conserved Cockayne syndrome B-piggyBac fusion protein (CSB-PGBD3) affects DNA repair and induces both interferon-like and innate antiviral responses in CSB-null cells.

Bailey AD, Gray LT, Pavelitz T, Newman JC, Horibata K, Tanaka K, Weiner AM.

DNA Repair (Amst). 2012 May 1;11(5):488-501. doi: 10.1016/j.dnarep.2012.02.004. Epub 2012 Apr 6.


The relationship between benzo[a]pyrene-induced mutagenesis and carcinogenesis in repair-deficient Cockayne syndrome group B mice.

Wijnhoven SW, Kool HJ, van Oostrom CT, Beems RB, Mullenders LH, van Zeeland AA, van der Horst GT, Vrieling H, van Steeg H.

Cancer Res. 2000 Oct 15;60(20):5681-7.


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. Epub 2002 Jun 11.


Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.

Itoh T, Cleaver JE, Yamaizumi M.

Hum Genet. 1996 Feb;97(2):176-9.


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.


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 Jr, 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. Epub 2001 Jul 3.

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