Mutation of the uracil DNA glycosylase gene detected in glioblastoma.

[1]  I. Pogribny,et al.  Presence and consequence of uracil in preneoplastic DNA from folate/methyl-deficient rats. , 1997, Carcinogenesis.

[2]  T. Jorgensen,et al.  Identification of defective illegitimate recombinational repair of oxidatively-induced DNA double-strand breaks in ataxia-telangiectasia cells. , 1997, Mutation research.

[3]  B. Ames,et al.  Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[4]  K. Kvaløy,et al.  Human uracil-DNA glycosylase gene: sequence organization, methylation pattern, and mapping to chromosome 12q23-q24.1. , 1996, Genomics.

[5]  J. Tainer,et al.  Excision of cytosine and thymine from DNA by mutants of human uracil‐DNA glycosylase. , 1996, The EMBO journal.

[6]  A. Yang,et al.  HhaI and HpaII DNA methyltransferases bind DNA mismatches, methylate uracil and block DNA repair. , 1995, Nucleic acids research.

[7]  K. Kinzler,et al.  The molecular basis of Turcot's syndrome. , 1995, The New England journal of medicine.

[8]  J. Tainer,et al.  Crystal structure and mutational analysis of human uracil-DNA glycosylase: Structural basis for specificity and catalysis , 1995, Cell.

[9]  M. Walsh,et al.  E2F-1 and a Cyclin-like DNA Repair Enzyme, Uracil-DNA Glycosylase, Provide Evidence for an Autoregulatory Mechanism for Transcription (*) , 1995, The Journal of Biological Chemistry.

[10]  L. Liotta,et al.  A microdissection technique for archival DNA analysis of specific cell populations in lesions < 1 mm in size. , 1995, The American journal of pathology.

[11]  L. Liotta,et al.  Identical allelic loss on chromosome 11q13 in microdissected in situ and invasive human breast cancer. , 1995, Cancer research.

[12]  C. Harris,et al.  Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis. , 1994, Cancer research.

[13]  N. Copeland,et al.  The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer , 1993, Cell.

[14]  B. Ames,et al.  Oxidants, antioxidants, and the degenerative diseases of aging. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[15]  L. Rorke,et al.  Relation between maternal diet and subsequent primitive neuroectodermal brain tumors in young children. , 1993, The New England journal of medicine.

[16]  M. Rosenblum,et al.  Patterns of proto‐oncogene expression in human glioma cell lines , 1989, Journal of neuroscience research.

[17]  T. Sekiya,et al.  Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[18]  A. Walker,et al.  Epidemiology of brain tumors , 1985, Neurology.

[19]  G. Stein.  T98G: An anchorage‐independent human tumor cell line that exhibits stationary phase G1 arrest in vitro , 1979, Journal of cellular physiology.

[20]  J. Pontén,et al.  Properties of human malignant glioma cells in vitro. , 1978, Medical biology.

[21]  P. Kleihues,et al.  Tumors associated with p53 germline mutations: a synopsis of 91 families. , 1997, The American journal of pathology.

[22]  Lei Li,et al.  Characterization of molecular defects in xeroderma pigmentosum group C , 1993, Nature Genetics.

[23]  M. Apuzzo.  Malignant cerebral glioma , 1990 .