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Items: 1 to 20 of 165

3.

Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.

Itoh T, Cleaver JE, Yamaizumi M.

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

PMID:
8566949
4.

DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.

Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH.

J Invest Dermatol. 1996 Oct;107(4):647-53.

5.

Cells from XP-D and XP-D-CS patients exhibit equally inefficient repair of UV-induced damage in transcribed genes but different capacity to recover UV-inhibited transcription.

van Hoffen A, Kalle WH, de Jong-Versteeg A, Lehmann AR, van Zeeland AA, Mullenders LH.

Nucleic Acids Res. 1999 Jul 15;27(14):2898-904.

6.
7.

Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.

Vermeulen W, Jaeken J, Jaspers NG, Bootsma D, Hoeijmakers JH.

Am J Hum Genet. 1993 Jul;53(1):185-92.

8.

Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers.

Spivak G, Itoh T, Matsunaga T, Nikaido O, Hanawalt P, Yamaizumi M.

DNA Repair (Amst). 2002 Aug 6;1(8):629-43.

PMID:
12509286
9.

Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes.

Carreau M, Eveno E, Quilliet X, Chevalier-Lagente O, Benoit A, Tanganelli B, Stefanini M, Vermeulen W, Hoeijmakers JH, Sarasin A, et al.

Carcinogenesis. 1995 May;16(5):1003-9.

PMID:
7767957
11.

Clinical characteristics of three patients with UVs syndrome, a photosensitive disorder with defective DNA repair.

Itoh T, Yamaizumi M, Ichihashi M, Hiro-Oka M, Matsui T, Matsuno M, Ono T.

Br J Dermatol. 1996 Jun;134(6):1147-50.

PMID:
8763445
13.

Cockayne syndrome without typical clinical manifestations including neurologic abnormalities.

Miyauchi-Hashimoto H, Akaeda T, Maihara T, Ikenaga M, Horio T.

J Am Acad Dermatol. 1998 Oct;39(4 Pt 1):565-70.

PMID:
9777763
14.

Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells.

VĂ©lez-Cruz R, Zadorin AS, Coin F, Egly JM.

Proc Natl Acad Sci U S A. 2013 Jan 15;110(3):E212-20. doi: 10.1073/pnas.1213076110. Epub 2012 Dec 24.

15.

Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A.

Itoh T, Shiomi T, Shiomi N, Harada Y, Wakasugi M, Matsunaga T, Nikaido O, Friedberg EC, Yamaizumi M.

Mutat Res. 1996 Feb 15;362(2):167-74.

PMID:
8596535
16.

Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.

Greenhaw GA, Hebert A, Duke-Woodside ME, Butler IJ, Hecht JT, Cleaver JE, Thomas GH, Horton WA.

Am J Hum Genet. 1992 Apr;50(4):677-89.

17.

Cockayne syndrome in two adult siblings.

Miyauchi H, Horio T, Akaeda T, Asada Y, Chang HR, Ishizaki K, Ikenaga M.

J Am Acad Dermatol. 1994 Feb;30(2 Pt 2):329-35.

PMID:
8294592
18.

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, et al.

Am J Hum Genet. 1995 Jan;56(1):167-74. Review.

20.

Complementation of transformed fibroblasts from patients with combined xeroderma pigmentosum-Cockayne syndrome.

Ellison AR, Nouspikel T, Jaspers NG, Clarkson SG, Gruenert DC.

Exp Cell Res. 1998 Aug 25;243(1):22-8.

PMID:
9716445
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