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Journal Abstract Search
135 related items for PubMed ID: 9580660
21. Xeroderma pigmentosum and molecular cloning of DNA repair genes. Boulikas T. Anticancer Res; 1996; 16(2):693-708. PubMed ID: 8687116 [Abstract] [Full Text] [Related]
22. A 10-year follow-up of a child with mild case of xeroderma pigmentosum complementation group D diagnosed by whole-genome sequencing. Ono R, Masaki T, Mayca Pozo F, Nakazawa Y, Swagemakers SM, Nakano E, Sakai W, Takeuchi S, Kanda F, Ogi T, van der Spek PJ, Sugasawa K, Nishigori C. Photodermatol Photoimmunol Photomed; 2016 Jul; 32(4):174-80. PubMed ID: 26993158 [Abstract] [Full Text] [Related]
23. A low content of ERCC1 and a 120 kDa protein is a frequent feature of group F xeroderma pigmentosum fibroblast cells. Yagi T, Wood RD, Takebe H. Mutagenesis; 1997 Jan; 12(1):41-4. PubMed ID: 9025096 [Abstract] [Full Text] [Related]
24. Defining the function of xeroderma pigmentosum group F protein in psoralen interstrand cross-link-mediated DNA repair and mutagenesis. Chen Z, Xu XS, Harrison J, Wang G. Biochem J; 2004 Apr 01; 379(Pt 1):71-8. PubMed ID: 14728600 [Abstract] [Full Text] [Related]
25. A truncated human xeroderma pigmentosum complementation group A protein expressed from an adenovirus sensitizes human tumor cells to ultraviolet light and cisplatin. Rosenberg E, Taher MM, Kuemmerle NB, Farnsworth J, Valerie K. Cancer Res; 2001 Jan 15; 61(2):764-70. PubMed ID: 11212280 [Abstract] [Full Text] [Related]
26. Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene. Frederick GD, Amirkhan RH, Schultz RA, Friedberg EC. Hum Mol Genet; 1994 Oct 15; 3(10):1783-8. PubMed ID: 7849702 [Abstract] [Full Text] [Related]
27. Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patients. Amr K, Messaoud O, El Darouti M, Abdelhak S, El-Kamah G. Gene; 2014 Jan 01; 533(1):52-6. PubMed ID: 24135642 [Abstract] [Full Text] [Related]
28. Roles of XPG and XPF/ERCC1 endonucleases in UV-induced immunostaining of PCNA in fibroblasts. Miura M, Nakamura S, Sasaki T, Takasaki Y, Shiomi T, Yamaizumi M. Exp Cell Res; 1996 Jul 10; 226(1):126-32. PubMed ID: 8660947 [Abstract] [Full Text] [Related]
29. A nonsense mutation in the Xeroderma pigmentosum complementation group F (XPF) gene is associated with gastric carcinogenesis. Wei ZH, Guo WH, Wu J, Suo WH, Fu GH. Gene; 2014 Mar 10; 537(2):238-44. PubMed ID: 24412486 [Abstract] [Full Text] [Related]
30. Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF. Popp I, Punekar M, Telford N, Stivaros S, Chandler K, Minnis M, Castleton A, Higham C, Hopewell L, Gareth Evans D, Raams A, Theil AF, Meyer S, Schindler D. BMC Med Genet; 2018 Jan 11; 19(1):7. PubMed ID: 29325523 [Abstract] [Full Text] [Related]
31. Functional Comparison of XPF Missense Mutations Associated to Multiple DNA Repair Disorders. Marín M, Ramírez MJ, Carmona MA, Jia N, Ogi T, Bogliolo M, Surrallés J. Genes (Basel); 2019 Jan 17; 10(1):. PubMed ID: 30658521 [Abstract] [Full Text] [Related]
32. Interstrand crosslink repair: can XPF-ERCC1 be let off the hook? Bergstralh DT, Sekelsky J. Trends Genet; 2008 Feb 17; 24(2):70-6. PubMed ID: 18192062 [Abstract] [Full Text] [Related]
33. Clinical symptoms and DNA repair characteristics of xeroderma pigmentosum patients from Germany. Thielmann HW, Popanda O, Edler L, Jung EG. Cancer Res; 1991 Jul 01; 51(13):3456-70. PubMed ID: 2054785 [Abstract] [Full Text] [Related]
34. Mutations in the XPD gene in xeroderma pigmentosum group D cell strains: confirmation of genotype-phenotype correlation. Kobayashi T, Uchiyama M, Fukuro S, Tanaka K. Am J Med Genet; 2002 Jul 01; 110(3):248-52. PubMed ID: 12116233 [Abstract] [Full Text] [Related]
35. Growth retardation, early death, and DNA repair defects in mice deficient for the nucleotide excision repair enzyme XPF. Tian M, Shinkura R, Shinkura N, Alt FW. Mol Cell Biol; 2004 Feb 01; 24(3):1200-5. PubMed ID: 14729965 [Abstract] [Full Text] [Related]
36. Multiple roles of the ERCC1-XPF endonuclease in DNA repair and resistance to anticancer drugs. Kirschner K, Melton DW. Anticancer Res; 2010 Sep 01; 30(9):3223-32. PubMed ID: 20944091 [Abstract] [Full Text] [Related]
37. Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells. Mezzina M, Eveno E, Chevallier-Lagente O, Benoit A, Carreau M, Vermeulen W, Hoeijmakers JH, Stefanini M, Lehmann AR, Weber CA. Carcinogenesis; 1994 Aug 01; 15(8):1493-8. PubMed ID: 8055625 [Abstract] [Full Text] [Related]
38. Diagnosis of eight groups of xeroderma pigmentosum by genetic complementation using recombinant adenovirus vectors. Yamashita T, Okura M, Ishii-Osai Y, Hida T. J Dermatol; 2016 Oct 01; 43(10):1167-1173. PubMed ID: 26971583 [Abstract] [Full Text] [Related]
39. Quantitative determination of the expression of xeroderma pigmentosum F gene in human nonmelanoma skin cancers. Chang LC, Sheu HM, Huang YS, Kuo KW. Biochem Biophys Res Commun; 2000 Jul 05; 273(2):454-8. PubMed ID: 10873627 [Abstract] [Full Text] [Related]
40. Functional complementation of xeroderma pigmentosum complementation group E by replication protein A in an in vitro system. Kazantsev A, Mu D, Nichols AF, Zhao X, Linn S, Sancar A. Proc Natl Acad Sci U S A; 1996 May 14; 93(10):5014-8. PubMed ID: 8643521 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]