Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells
暂无分享,去创建一个
D. Gisselsson | M. Ehrlich | D. Smeets | E. Pålsson | Chunbo Shao | C. Tuck-Muller | Suzana Sogorovic
[1] D. Gisselsson,et al. Telomere‐mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma , 2005, Genes, chromosomes & cancer.
[2] Keith D Robertson,et al. Isolation and characterization of a novel DNA methyltransferase complex linking DNMT3B with components of the mitotic chromosome condensation machinery. , 2004, Nucleic acids research.
[3] M. Milili,et al. Defective B-cell-negative selection and terminal differentiation in the ICF syndrome. , 2004, Blood.
[4] A. T. Sumner,et al. ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome , 1995, Human Genetics.
[5] D. Smeets,et al. ICF syndrome: a new case and review of the literature , 1994, Human Genetics.
[6] C. Romano,et al. Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency , 1979, Human Genetics.
[7] M. Ehrlich. The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease. , 2003, Clinical immunology.
[8] D. Gisselsson. Chromosome instability in cancer: how, when, and why? , 2003, Advances in cancer research.
[9] Albert Jeltsch,et al. Molecular Enzymology of the Catalytic Domains of the Dnmt3a and Dnmt3b DNA Methyltransferases* 210 , 2002, The Journal of Biological Chemistry.
[10] R. Reddel,et al. Comparison of human mammary epithelial cells immortalized by simian virus 40 T-Antigen or by the telomerase catalytic subunit , 2002, Oncogene.
[11] David E. Misek,et al. DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes. , 2001, Human molecular genetics.
[12] D. Gisselsson,et al. Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[13] T. Ide,et al. Clonal chromosomal aberrations accompanied by strong telomerase activity in immortalization of human B-lymphoblastoid cell lines transformed by Epstein-Barr virus. , 2001, Cancer genetics and cytogenetics.
[14] C. Wijmenga,et al. Genetic variation in ICF syndrome: Evidence for genetic heterogeneity , 2000, Human mutation.
[15] M. Ehrlich,et al. Hypersensitivity to radiation-induced non-apoptotic and apoptotic death in cell lines from patients with the ICF chromosome instability syndrome. , 2000, Mutation research.
[16] D. Gisselsson,et al. Locus‐specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia , 2000, Genes, chromosomes & cancer.
[17] M. Ehrlich,et al. DNA hypomethylation and unusual chromosome instability in cell lines fromICF syndrome patients , 2000, Cytogenetic and Genome Research.
[18] R. Kuick,et al. Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2. , 2000, Human molecular genetics.
[19] C. Schmoor,et al. Measurement of telomere length in haematopoietic cells using in situ hybridization techniques. , 2000, Biochemical Society transactions.
[20] G. Henze,et al. Non-Hodgkin's lymphoma in pediatric patients with chromosomal breakage syndromes (AT and NBS): experience from the BFM trials. , 2000, Annals of oncology : official journal of the European Society for Medical Oncology.
[21] C. Wijmenga,et al. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[22] N. Tommerup,et al. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene , 1999, Nature.
[23] C. Papadopoulos,et al. Nanoelectronics: Growing Y-junction carbon nanotubes , 1999, Nature.
[24] D. Haber,et al. DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development , 1999, Cell.
[25] M. Ehrlich,et al. Preferential induction of chromosome 1 multibranched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidine. , 1997, Cytogenetics and cell genetics.
[26] H. Tanke,et al. Heterogeneity in telomere length of human chromosomes. , 1996, Human molecular genetics.
[27] M. Stacey,et al. FISH analysis on spontaneously arising micronuclei in the ICF syndrome. , 1995, Journal of medical genetics.
[28] J. Sawyer,et al. Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization. , 1995, American journal of medical genetics.
[29] F. Ledeist,et al. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. , 1993, Human molecular genetics.
[30] E. Viégas-Péquignot,et al. Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin. , 1993, Cytogenetics and cell genetics.
[31] R. Tupler,et al. Interphase cytogenetics of the ICF syndrome , 1992, Annals of human genetics.
[32] P. Lorenz,et al. [ICF syndrome. Immunodeficiency, chromosomal centromere instability, facial anomalies. Case report and literature review]. , 1992, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde.
[33] G. Holmgren,et al. Fragility of the Centromeric Region of Chromosome 1 Associated with Combined Immunodeficiency in Siblings A Recessively Inherited Entity? , 1990, Acta paediatrica Scandinavica.
[34] F. Ledeist,et al. Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies. , 1989, American journal of medical genetics.
[35] R. Blaese,et al. Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9, and 16. , 1988, The Journal of pediatrics.
[36] O. Zuffardi,et al. Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome. , 1988, Journal of medical genetics.
[37] M. Schmid,et al. A direct demonstration of somatically paired heterochromatin of human chromosomes. , 1983, Cytogenetics and cell genetics.
[38] C. Shaw,et al. Observations of radiation-induced chromosome fragment loss in live mammalian cells in culture, and its effect on colony-forming ability. , 1981, International journal of radiation biology and related studies in physics, chemistry, and medicine.
[39] R. Bumsted,et al. Case Report and Literature Review , 1980 .