Biallelic mutations in the ATM gene in T-prolymphocytic leukemia (original) (raw)
Sedgewick, R.P. & Boder, E., Ataxia-talangiectasia. in Handbook of Clinical Neurology, vol. 16 (eds. Vinken, G.B.P. and Klawans, H.) 347–123 (Elsevier Scientific Publishers, New York, 1991). Google Scholar
Meyn, M.S. Ataxia-telangiectasia and cellular responses to DNA damage. Cancer Res.55, 5991–6001 (1995). CASPubMed Google Scholar
Taylor, A.M.R., Metcatfe, J.A., Thick, J. & Mak, Y.F. Leukemia and lymphoma in ataxia telangiectasia. Blood87, 423–438 (1996). CASPubMed Google Scholar
Savitsky, K. et al. A single ataxia telangiectasia gene with a product similar to Pl-3 kinase. Science268, 1749–1753 (1995). ArticleCASPubMed Google Scholar
Savitsky, K. et al. The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species. Hum. Mol Genet.4, 2025–2032 (1995). ArticleCASPubMed Google Scholar
Chen, G., Lee, E.Y.-H.P. The product of the ATM gene is a 370-kDa nuclear phospho-protein. J. Biol. Chem.271, 33693–33697 (1996). ArticleCASPubMed Google Scholar
Lakin, N.D. et al. Analysis of the ATM protein in wild-type and ataxia telangiectasia cells. Oncogene13, 2707–2716 (1996). CASPubMed Google Scholar
Brown, K.D. et al. The ataxia telangiectasia gene product, a constitutively expressed nuclear protein that is not up-regulated following genome damage. Proc. Natl. Acad. Sci. USA94, 1840–1845 (1997). ArticleCASPubMedPubMed Central Google Scholar
Nowak, R. Discovery of AT gene sparks biomedical research bonanza. Science268, 1700–1701 (1995). ArticleCASPubMed Google Scholar
Athma, P., Rappaport, R. & Swift, M. Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer. Cancer Genet. Cytogenet.92, 130–134 (1996). ArticleCASPubMed Google Scholar
FitzGerald, M.G. et al. Heterozygous ATM mutations do not contribute to early onset of breast cancer. Nature Genet.15, 307–310 (1997). ArticleCASPubMed Google Scholar
Vorechovsky, I. et al. The ATM gene and susceptibility to breast cancer: Combined mutation analysis of 38 consecutive breast tumors reveals no evidence for somatic mutations and constitutional AT heterozygosity. Cancer Res.56, 2726–2732 (1996). CASPubMed Google Scholar
Kerangueven, F. et al. Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions. Oncogene14, 339–347 (1997). ArticleCASPubMed Google Scholar
Matutes, E. et al. Clinical and laboratory features of 78 cases of T-prolymphocytic leukemia. Blood78, 3269–3274 (1991). CASPubMed Google Scholar
Harris, N.L. et al. A revised European-American classification of lymphoid neoplasms: A proposal from the international lymphoma study group. Blood84, 1361–1392 (1994). CASPubMed Google Scholar
Dohner, H. et al. Pentostatin in prolymphocytic leukemia: Phase II trial of the European organization for research and treatment of cancer leukemia cooperative study group. J. Natl. Cancer Inst.85, 658–662 (1993). ArticleCASPubMed Google Scholar
Brito-Babapulle, V., Pomfret, M., Matutes, E. & Catovsky, D. Cytogenetic studies on prolymphocytic leukemia. II. T-cell prolymphocytic leukemia. Blood70, 926–931 (1987). CASPubMed Google Scholar
Finan Daniele, R., Rowlands, D. & Nowell, P. Cytogenetics of chronic T cell leukemia, including two patients with a 14q+ translocation. Virchows Arch. Biol. Cell Pathol.29, 121–127 (1978). Google Scholar
Zech, L. et al. Inversion of chromosome 14 marks human T-cell chronic lymphocytic leukemia. Nature308, 858–860 (1984). ArticleCASPubMed Google Scholar
Croce, C.M. et al. Gene for alpha-chain of human T-cell receptor: Location on chromosome 14 region involved in T-cell neoplasms. Science227, 1044–1047 (1985). ArticleCASPubMed Google Scholar
Virgilio, L. et al. Identification of the TCL1 gene involved in T-cell malignancies. Proc. Natl. Acad. Sci. USA91, 12530–12534 (1994). ArticleCAS Google Scholar
Narducci, M.G. et al. TCL1 oncogene activation in preleukemic T cells from a case of ataxia-telangiectasia. Blood86, 2358–2364 (1995). CASPubMed Google Scholar
Thick, J. et al. Expression of either the TCL1 oncogene, or transcripts from its homologue MTCP1/c6.1B, in leukaemic and non-leukaemic T cells from ataxia telangiectasia patients. Oncogene12, 379–386 (1996). CASPubMed Google Scholar
Gilad, S. etal. Predominance of null mutations in ataxia-telangiectasia. Hum. Mol. Genet.5, 433–439 (1996). ArticleCASPubMed Google Scholar
Imai, T. et al. Identification and characterization of a new gene physically linked to the ATM gene. Genome Res.6, 439–447 (1996). ArticleCASPubMed Google Scholar
Pittman, S., Morilla, R. & Catovsky, D., T-cell leukemias II. Cytogenetic studies. Leukocyte Res.6, 33–42 (1982). ArticleCAS Google Scholar
Hoda Maljaie, S.H. et al. Expression of c-myc oncoprotein in chronic T cell leukemias. Leukemia9, 1694–1699 (1995). Google Scholar
James, M.R. et al. A radiation hybrid map of 506 STS markers spanning human chromosome 11. Nature Genet.8, 70–76 (1994). ArticleCASPubMed Google Scholar
Zakian, V.A. ATM-related genes: What do they tell us about function of the human gene? Cell82, 685–687 (1995). ArticleCASPubMed Google Scholar
Shafman, T. et al. Interaction between ATM protein and c-Abl in response to DNA damage. Nature387, 520–523 (1997). ArticleCASPubMed Google Scholar
Barlow, C. et al. Atm-deficient mice: A paradigm of ataxia telangiectasia. Cell86, 159–171 (1996). ArticleCASPubMed Google Scholar
Elson, A. et al. Pleiotropic defects in ataxia-telangiectasia protein deficient mice. Proc. Natl. Acad. Sci. USA93, 13084–13089 (1996). ArticleCASPubMedPubMed Central Google Scholar
Xu, Y. et al. Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma. Genes Dev.10, 2411–2422 (1996). ArticleCASPubMed Google Scholar
Lichter, P. et al. High resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science247, 64–69 (1990). ArticleCASPubMed Google Scholar
Stilgenbauer, S. et al. Molecular Cytogenetic delineation of a novel critical genomic region in chromosome bands 11 q22.3-q23.1 in lymphoproliferative disorders. Proc. Natl. Acad. Sci. USA93, 11837–11841 (1996). ArticleCAS Google Scholar
Stilgenbauer, S. et al. High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics. Blood81, 2118–2124 (1993). CASPubMed Google Scholar
Herz, J. et al. Surface localization and high affinity for calcium of a 500-kD liver membrane protein closely related to the LDL-receptor suggest a physiological role as lipopro-tein receptor. EMBO J.7, 4119–4127 (1988). ArticleCASPubMedPubMed Central Google Scholar
Van Leuven, F. et al. Structure of the gene (LRP1) coding for the human alpha 2-macro-globulin receptor lipoprotein receptor-related protein. Genomics24, 78–89 (1994). ArticleCASPubMed Google Scholar
Beaudet, A.L. & Tsui, L.-C. A suggested nomenclature for designating mutations. Hum. Mutat.2, 245–248 (1993). ArticleCASPubMed Google Scholar