Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma
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R. Gascoyne | J. Connors | A. Brooks-Wilson | J. Spinelli | R. Gallagher | Amy C. MacArthur | S. Leach | Johanna M. Schuetz | Amy C Macarthur | A. Lai
[1] I. Ionita-Laza,et al. Estimating the number of unseen variants in the human genome , 2009, Proceedings of the National Academy of Sciences.
[2] Y. Pommier,et al. Bloom's syndrome helicase and Mus81 are required to induce transient double-strand DNA breaks in response to DNA replication stress. , 2008, Journal of molecular biology.
[3] R. Gascoyne,et al. Organochlorines and risk of non‐Hodgkin lymphoma , 2007, International journal of cancer.
[4] R. Gascoyne,et al. A systematic evaluation of the ataxia telangiectasia mutated gene does not show an association with non‐Hodgkin lymphoma , 2007, International journal of cancer.
[5] Weidong Wang. Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins , 2007, Nature Reviews Genetics.
[6] Joseph M. Connors,et al. Genetic Variation in H2AFX Contributes to Risk of Non–Hodgkin Lymphoma , 2007, Cancer Epidemiology Biomarkers & Prevention.
[7] D. Januszkiewicz-Lewandowska,et al. Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia , 2006, Leukemia.
[8] Päivi Heikkilä,et al. Evaluation of RAD50 in familial breast cancer predisposition , 2006, International journal of cancer.
[9] K. Chrzanowska,et al. Carrier frequency of mutation 657del5 in the NBS1 gene in a population of polish pediatric patients with sporadic lymphoid malignancies , 2006, International journal of cancer.
[10] Paul Scheet,et al. Automating sequence-based detection and genotyping of SNPs from diploid samples , 2006, Nature Genetics.
[11] G. Morgan,et al. Haplotypic variation in MRE11, RAD50 and NBS1 and risk of non-Hodgkin's lymphoma , 2006, Leukemia & lymphoma.
[12] M. Kastan,et al. The Rad50S allele promotes ATM-dependent DNA damage responses and suppresses ATM deficiency: implications for the Mre11 complex as a DNA damage sensor. , 2005, Genes & development.
[13] Arto Mannermaa,et al. RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability. , 2005, Carcinogenesis.
[14] Mark Daly,et al. Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..
[15] J. Yokota,et al. First case of aplastic anemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability , 2004, Human Genetics.
[16] Karl Sperling,et al. Increased cancer risk of heterozygotes with NBS1 germline mutations in poland , 2004, International journal of cancer.
[17] W. Foulkes,et al. Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria , 2004, Journal of Medical Genetics.
[18] Lior Pachter,et al. VISTA: computational tools for comparative genomics , 2004, Nucleic Acids Res..
[19] R. Winqvist,et al. Mutation screening of Mre11 complex genes: indication of RAD50 involvement in breast and ovarian cancer susceptibility , 2003, Journal of medical genetics.
[20] Z. Herceg,et al. Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis. , 2003, Cancer research.
[21] Peter Donnelly,et al. A comparison of bayesian methods for haplotype reconstruction from population genotype data. , 2003, American journal of human genetics.
[22] Yair Andegeko,et al. Requirement of the MRN complex for ATM activation by DNA damage , 2003, The EMBO journal.
[23] Christopher A. Haiman,et al. Choosing Haplotype-Tagging SNPS Based on Unphased Genotype Data Using a Preliminary Sample of Unrelated Subjects with an Example from the Multiethnic Cohort Study , 2003, Human Heredity.
[24] O. Evgrafov,et al. 657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls , 2003, American journal of medical genetics. Part A.
[25] David Gordon,et al. Viewing and Editing Assembled Sequences Using Consed , 2003, Current protocols in bioinformatics.
[26] A. Børresen-Dale,et al. Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin , 2003, European Journal of Human Genetics.
[27] S. Gallinger,et al. Heterozygosity for the BLMAsh Mutation and Cancer Risk , 2003 .
[28] Shinya Matsuura,et al. Nijmegen breakage syndrome gene, NBS1, and molecular links to factors for genome stability , 2002, Oncogene.
[29] D. Schild,et al. Recombinational DNA repair and human disease. , 2002, Mutation research.
[30] V. A. Morrison,et al. Mutations and molecular variants of the NBS1 gene in non‐Hodgkin lymphoma , 2002, Genes, chromosomes & cancer.
[31] P. Gregersen,et al. BLM Heterozygosity and the Risk of Colorectal Cancer , 2002, Science.
[32] G. Boivin,et al. Enhanced Tumor Formation in Mice Heterozygous for Blm Mutation , 2002, Science.
[33] M. L. Le Beau,et al. Cancer predisposition and hematopoietic failure in Rad50(S/S) mice. , 2002, Genes & development.
[34] P. Bork,et al. Human non-synonymous SNPs: server and survey. , 2002, Nucleic acids research.
[35] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[36] Alessandra Viel,et al. Human MRE11 is inactivated in mismatch repair‐deficient cancers , 2002, EMBO reports.
[37] C. Gilbert,et al. Checkpoint activation in response to double-strand breaks requires the Mre11/Rad50/Xrs2 complex , 2001, Nature Cell Biology.
[38] R. DePinho,et al. Rescue of a telomere length defect of Nijmegen breakage syndrome cells requires NBS and telomerase catalytic subunit , 2001, Current Biology.
[39] John A. Tainer,et al. Structural Biochemistry and Interaction Architecture of the DNA Double-Strand Break Repair Mre11 Nuclease and Rad50-ATPase , 2001, Cell.
[40] H. G. Einsiedel,et al. Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). , 2001, Cancer research.
[41] P. Donnelly,et al. A new statistical method for haplotype reconstruction from population data. , 2001, American journal of human genetics.
[42] P. Bismarck,et al. The common deletion 657del5 in the Nibrin gene is not a major risk factor for B or T cell non-Hodgkin lymphoma in a pediatric population , 2000, Leukemia.
[43] M. Schrappe,et al. No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non‐Hodgkin's lymphoma of childhood and adolescence , 2000, British journal of haematology.
[44] John R Yates,et al. The hMre11/hRad50 Protein Complex and Nijmegen Breakage Syndrome: Linkage of Double-Strand Break Repair to the Cellular DNA Damage Response , 1998, Cell.
[45] P. Green,et al. Base-calling of automated sequencer traces using phred. I. Accuracy assessment. , 1998, Genome research.
[46] P Green,et al. Base-calling of automated sequencer traces using phred. II. Error probabilities. , 1998, Genome research.
[47] D. Weaver,et al. Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells. , 1997, Nucleic acids research.
[48] K. Chrzanowska,et al. Nijmegen breakage syndrome. , 1996, Journal of medical genetics.
[49] K. Chrzanowska,et al. Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome. , 1995, American journal of medical genetics.
[50] J. Groden,et al. Bloom's syndrome , 1992, Human Genetics.
[51] J. Opitz,et al. Familial microcephaly with normal intelligence, immunodeficiency, and risk for lymphoreticular malignancies: a new autosomal recessive disorder. , 1985, American journal of medical genetics.
[52] P. Nowell,et al. Cloning of the chromosome breakpoint of neoplastic B cells with the t(14;18) chromosome translocation. , 1984, Science.
[53] E. Seemanová,et al. [Mutations in tumor suppressor gene NBS1 in adult patients with malignancies]. , 2006, Casopis lekaru ceskych.
[54] E. Seemanová,et al. [Increased risk of malignancies in heterozygotes in families of patients with Nijmegen breakage syndrome]. , 2006, Casopis lekaru ceskych.
[55] Theodore R Holford,et al. Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium. , 2006, The Lancet. Oncology.
[56] J. Pincheira,et al. Human syndromes with genomic instability and multiprotein machines that repair DNA double-strand breaks. , 2003, Histology and histopathology.
[57] S. Gallinger,et al. Heterozygosity for the BLM(Ash) mutation and cancer risk. , 2003, Cancer research.
[58] S. Matsuura. [Nijmegen breakage syndrome]. , 2001, Ryoikibetsu shokogun shirizu.
[59] S Rozen,et al. Primer3 on the WWW for general users and for biologist programmers. , 2000, Methods in molecular biology.
[60] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .