295 related articles for article (PubMed ID: 8566949)
1. Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.
Itoh T; Cleaver JE; Yamaizumi M
Hum Genet; 1996 Feb; 97(2):176-9. PubMed ID: 8566949
[TBL] [Abstract][Full Text] [Related]
2. A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations.
Itoh T; Ono T; Yamaizumi M
Mutat Res; 1994 May; 314(3):233-48. PubMed ID: 7513056
[TBL] [Abstract][Full Text] [Related]
3. [The determination of the complementation groups for the cells of patients with xeroderma pigmentosum and the Cockayne syndrome found in Russia].
Pleskach NM; Mikhel'son VM; Raams A; Bootsma D
Tsitologiia; 1996; 38(8):863-8. PubMed ID: 9027016
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 8823375
[TBL] [Abstract][Full Text] [Related]
5. UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.
Itoh T; Fujiwara Y; Ono T; Yamaizumi M
Am J Hum Genet; 1995 Jun; 56(6):1267-76. PubMed ID: 7539208
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 1372469
[TBL] [Abstract][Full Text] [Related]
7. Cockayne syndrome and xeroderma pigmentosum.
Rapin I; Lindenbaum Y; Dickson DW; Kraemer KH; Robbins JH
Neurology; 2000 Nov; 55(10):1442-9. PubMed ID: 11185579
[TBL] [Abstract][Full Text] [Related]
8. 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; 27(14):2898-904. PubMed ID: 10390531
[TBL] [Abstract][Full Text] [Related]
9. 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
Am J Hum Genet; 1995 Jan; 56(1):167-74. PubMed ID: 7825573
[TBL] [Abstract][Full Text] [Related]
10. 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
Carcinogenesis; 1995 May; 16(5):1003-9. PubMed ID: 7767957
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 8317483
[TBL] [Abstract][Full Text] [Related]
12. 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; 243(1):22-8. PubMed ID: 9716445
[TBL] [Abstract][Full Text] [Related]
13. Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosum.
Colella S; Nardo T; Botta E; Lehmann AR; Stefanini M
Hum Mol Genet; 2000 May; 9(8):1171-5. PubMed ID: 10767341
[TBL] [Abstract][Full Text] [Related]
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; 110(3):E212-20. PubMed ID: 23267107
[TBL] [Abstract][Full Text] [Related]
15. Transcription-associated breaks in xeroderma pigmentosum group D cells from patients with combined features of xeroderma pigmentosum and Cockayne syndrome.
Theron T; Fousteri MI; Volker M; Harries LW; Botta E; Stefanini M; Fujimoto M; Andressoo JO; Mitchell J; Jaspers NG; McDaniel LD; Mullenders LH; Lehmann AR
Mol Cell Biol; 2005 Sep; 25(18):8368-78. PubMed ID: 16135823
[TBL] [Abstract][Full Text] [Related]
16. Three complementation groups in Cockayne syndrome.
Lehmann AR
Mutat Res; 1982 Dec; 106(2):347-56. PubMed ID: 6185841
[TBL] [Abstract][Full Text] [Related]
17. Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
Oh KS; Khan SG; Jaspers NG; Raams A; Ueda T; Lehmann A; Friedmann PS; Emmert S; Gratchev A; Lachlan K; Lucassan A; Baker CC; Kraemer KH
Hum Mutat; 2006 Nov; 27(11):1092-103. PubMed ID: 16947863
[TBL] [Abstract][Full Text] [Related]
18. Xeroderma pigmentosum--Cockayne syndrome complex: a further case.
Hamel BC; Raams A; Schuitema-Dijkstra AR; Simons P; van der Burgt I; Jaspers NG; Kleijer WJ
J Med Genet; 1996 Jul; 33(7):607-10. PubMed ID: 8818951
[TBL] [Abstract][Full Text] [Related]
19. Non-radioisotope method for diagnosing photosensitive genodermatoses and a new marker for xeroderma pigmentosum variant.
Hashimoto S; Egawa K; Ihn H; Tateishi S
J Dermatol; 2009 Mar; 36(3):138-43. PubMed ID: 19335687
[TBL] [Abstract][Full Text] [Related]
20. Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency.
Reid-Bayliss KS; Arron ST; Loeb LA; Bezrookove V; Cleaver JE
Proc Natl Acad Sci U S A; 2016 Sep; 113(36):10151-6. PubMed ID: 27543334
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]