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2. Cockayne syndrome: unusual neuropathological findings and review of the literature. Soffer D; Grotsky HW; Rapin I; Suzuki K Ann Neurol; 1979 Oct; 6(4):340-8. PubMed ID: 400082 [TBL] [Abstract][Full Text] [Related]
3. Cockayne syndrome with delayed recovery of RNA synthesis after ultraviolet irradiation but normal ultraviolet survival. Sugita K; Suzuki N; Kojima T; Tanabe Y; Nakajima H; Hayashi A; Arima M Pediatr Res; 1987 Jan; 21(1):34-7. PubMed ID: 2432457 [TBL] [Abstract][Full Text] [Related]
4. Use of lymphoblastoid cell lines to evaluate the hypersensitivity to ultraviolet radiation in Cockayne syndrome. Otsuka F; Tarone RE; Cayeux S; Robbins JH J Invest Dermatol; 1984 May; 82(5):480-4. PubMed ID: 6096450 [TBL] [Abstract][Full Text] [Related]
5. Host cell reactivation of plasmids containing oxidative DNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndrome fibroblasts. Spivak G; Hanawalt PC DNA Repair (Amst); 2006 Jan; 5(1):13-22. PubMed ID: 16129663 [TBL] [Abstract][Full Text] [Related]
6. Identical male twins and brother with Cockayne syndrome. Houston CS; Zaleski WA; Rozdilsky B Am J Med Genet; 1982 Oct; 13(2):211-23. PubMed ID: 6890311 [TBL] [Abstract][Full Text] [Related]
7. CAMFAK syndrome: a demyelinating inherited disease similar to Cockayne syndrome. Talwar D; Smith SA Am J Med Genet; 1989 Oct; 34(2):194-8. PubMed ID: 2554729 [TBL] [Abstract][Full Text] [Related]
8. Cockayne syndrome: magnetic resonance images of the brain in a severe form with early onset. Nishio H; Kodama S; Matsuo T; Ichihashi M; Ito H; Fujiwara Y J Inherit Metab Dis; 1988; 11(1):88-102. PubMed ID: 3128691 [TBL] [Abstract][Full Text] [Related]
9. Impaired jun-NH2-terminal kinase activation by ultraviolet irradiation in fibroblasts of patients with Cockayne syndrome complementation group B. Dhar V; Adler V; Lehmann A; Ronai Z Cell Growth Differ; 1996 Jun; 7(6):841-6. PubMed ID: 8780897 [TBL] [Abstract][Full Text] [Related]
10. Essential role of polyamines in restoration of DNA synthesis after UV radiation and expression of UV resistance in Cockayne syndrome cells. Kusano I; Hibasami H; Kawai K; Esaki K; Shiraishi T; Yatani R Biochem Biophys Res Commun; 1994 Dec; 205(2):1018-24. PubMed ID: 7802627 [TBL] [Abstract][Full Text] [Related]
11. The current evidence for defective repair of oxidatively damaged DNA in Cockayne syndrome. Frosina G Free Radic Biol Med; 2007 Jul; 43(2):165-77. PubMed ID: 17603927 [TBL] [Abstract][Full Text] [Related]
12. siRNA-mediated silencing of Cockayne Cyndrome group B gene potentiates radiation-induced apoptosis and antiproliferative effect in HeLa cells. Liu F; Yu ZJ; Sui JL; Bai B; Zhou PK Chin Med J (Engl); 2006 May; 119(9):731-9. PubMed ID: 16701013 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Hypersensitivity of Cockayne's syndrome cells to camptothecin is associated with the generation of abnormally high levels of double strand breaks in nascent DNA. Squires S; Ryan AJ; Strutt HL; Johnson RT Cancer Res; 1993 May; 53(9):2012-9. PubMed ID: 7683249 [TBL] [Abstract][Full Text] [Related]
15. Neuropathology of Cockayne syndrome: Evidence for impaired development, premature aging, and neurodegeneration. Weidenheim KM; Dickson DW; Rapin I Mech Ageing Dev; 2009 Sep; 130(9):619-36. PubMed ID: 19647012 [TBL] [Abstract][Full Text] [Related]
16. Cockayne syndrome: a cellular sensitivity to ultraviolet light. Schmickel RD; Chu EH; Trosko JE; Chang CC Pediatrics; 1977 Aug; 60(2):135-9. PubMed ID: 887325 [TBL] [Abstract][Full Text] [Related]
17. Oxidative nucleotide damage and superoxide dismutase expression in the brains of xeroderma pigmentosum group A and Cockayne syndrome. Hayashi M; Araki S; Kohyama J; Shioda K; Fukatsu R Brain Dev; 2005 Jan; 27(1):34-8. PubMed ID: 15626539 [TBL] [Abstract][Full Text] [Related]
18. A novel splice site mutation in the Cockayne syndrome group A gene in two siblings with Cockayne syndrome. Kleppa L; Kanavin ØJ; Klungland A; Strømme P Neuroscience; 2007 Apr; 145(4):1397-406. PubMed ID: 17084038 [TBL] [Abstract][Full Text] [Related]
19. Brain vascular changes in Cockayne syndrome. Hayashi M; Miwa-Saito N; Tanuma N; Kubota M Neuropathology; 2012 Apr; 32(2):113-7. PubMed ID: 21749465 [TBL] [Abstract][Full Text] [Related]
20. Cockayne syndrome in three sisters with varying clinical presentation. Mahmoud AA; Yousef GM; Al-Hifzi I; Diamandis EP Am J Med Genet; 2002 Jul; 111(1):81-5. PubMed ID: 12124741 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]