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Journal Abstract Search
600 related items for PubMed ID: 12567255
1. [Xeroderma pigmentosum and related syndromes]. Berneburg M, Krutmann J. Hautarzt; 2003 Jan; 54(1):33-40. PubMed ID: 12567255 [Abstract] [Full Text] [Related]
2. Xeroderma pigmentosum. Norgauer J, Idzko M, Panther E, Hellstern O, Herouy Y. Eur J Dermatol; 2003 Jan; 13(1):4-9. PubMed ID: 12609773 [Abstract] [Full Text] [Related]
3. The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect. Berneburg M, Clingen PH, Harcourt SA, Lowe JE, Taylor EM, Green MH, Krutmann J, Arlett CF, Lehmann AR. Cancer Res; 2000 Jan 15; 60(2):431-8. PubMed ID: 10667598 [Abstract] [Full Text] [Related]
4. A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. Cleaver JE, Thompson LH, Richardson AS, States JC. Hum Mutat; 1999 Jan 15; 14(1):9-22. PubMed ID: 10447254 [Abstract] [Full Text] [Related]
5. Human cancer and DNA repair-deficient diseases. Sarasin A, Stary A. Cancer Detect Prev; 1997 Jan 15; 21(5):406-11. PubMed ID: 9307843 [Abstract] [Full Text] [Related]
6. [Ocular manifestations in xeroderma pigmentosum]. Süsskind D, Berneburg M, Rohrbach JM. Klin Monbl Augenheilkd; 2011 Mar 15; 228(3):239-44. PubMed ID: 20799158 [Abstract] [Full Text] [Related]
7. Trichothiodystrophy and the relationship between DNA repair and cancer. Lehmann AR. Bioessays; 1989 Dec 15; 11(6):168-70. PubMed ID: 2695082 [Abstract] [Full Text] [Related]
8. Multiple involvement of nucleotide excision repair enzymes: clinical manifestations of molecular intricacies. Jaspers NG. Cytokines Mol Ther; 1996 Jun 15; 2(2):115-9. PubMed ID: 9384696 [Abstract] [Full Text] [Related]
9. 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 15; 36(3):138-43. PubMed ID: 19335687 [Abstract] [Full Text] [Related]
10. [Trichothiodystrophy: progresssive manifestations]. Foulc P, Jumbou O, David A, Sarasin A, Stalder JF. Ann Dermatol Venereol; 1999 Oct 15; 126(10):703-7. PubMed ID: 10604009 [Abstract] [Full Text] [Related]
11. The genetic basis of xeroderma pigmentosum and trichothiodystrophy syndromes. Stary A, Sarasin A. Cancer Surv; 1996 Oct 15; 26():155-71. PubMed ID: 8783572 [No Abstract] [Full Text] [Related]
12. [DNA repair and related diseases]. Sarasin A, Robert-Knebelmann C, Stary A. Pathol Biol (Paris); 1992 Feb 15; 40(2):169-77. PubMed ID: 1608657 [Abstract] [Full Text] [Related]
13. A temperature-sensitive disorder in basal transcription and DNA repair in humans. Vermeulen W, Rademakers S, Jaspers NG, Appeldoorn E, Raams A, Klein B, Kleijer WJ, Hansen LK, Hoeijmakers JH. Nat Genet; 2001 Mar 15; 27(3):299-303. PubMed ID: 11242112 [Abstract] [Full Text] [Related]
14. Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy: do the genes explain the diseases? Chu G, Mayne L. Trends Genet; 1996 May 15; 12(5):187-92. PubMed ID: 8984734 [Abstract] [Full Text] [Related]
15. [Repair of DNA damage using nucleotide excision repair (NER)--relationship with cancer risk]. Butkiewicz D, Rusin M, Pawlas M, Czarny M, Chorazy M. Postepy Hig Med Dosw; 2002 May 15; 56(4):485-98. PubMed ID: 12418414 [Abstract] [Full Text] [Related]
16. DNA repair. Seven genes for three diseases. Wood RD. Nature; 1991 Mar 21; 350(6315):190. PubMed ID: 2005975 [No Abstract] [Full Text] [Related]
17. Xeroderma pigmentosum group E and DDB2, a smaller subunit of damage-specific DNA binding protein: proposed classification of xeroderma pigmentosum, Cockayne syndrome, and ultraviolet-sensitive syndrome. Itoh T. J Dermatol Sci; 2006 Feb 21; 41(2):87-96. PubMed ID: 16325378 [Abstract] [Full Text] [Related]
18. [Trichothiodystrophies: anomalies of the repair and transcription of genes]. Robert C, Sarasin A. Ann Dermatol Venereol; 1999 Oct 21; 126(10):669-71. PubMed ID: 10604001 [No Abstract] [Full Text] [Related]
19. Xeroderma pigmentosum genes: functions inside and outside DNA repair. Sugasawa K. Carcinogenesis; 2008 Mar 21; 29(3):455-65. PubMed ID: 18174245 [Abstract] [Full Text] [Related]
20. Recent advances in chromosome breakage syndromes and their diagnosis. Mathur R, Chowdhury MR, Singh G. Indian Pediatr; 2000 Jun 21; 37(6):615-25. PubMed ID: 10869141 [Abstract] [Full Text] [Related] Page: [Next] [New Search]