Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
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N. Tommerup | J. Russo | C. Hsieh | T. Bestor | D. Bourc’his | Guo-liang Xu | M. Bugge | M. Hultén | Xiaoyan Qu | E. Viégas-Péquignot | Guo-Liang Xu
[1] D. Higgs,et al. Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome) , 1995, Cell.
[2] B. Erlanger,et al. Localization of 5-methylcytosine in human metaphase chromosomes by immunoelectron microscopy , 1976, Cell.
[3] R J Roberts,et al. Predictive motifs derived from cytosine methyltransferases. , 1989, Nucleic acids research.
[4] R. Roberts,et al. Hhal methyltransferase flips its target base out of the DNA helix , 1994, Cell.
[5] G. Schuler. Pieces of the puzzle: expressed sequence tags and the catalog of human genes , 1997, Journal of Molecular Medicine.
[6] F. Ledeist,et al. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. , 1993, Human molecular genetics.
[7] R Holliday,et al. DNA modification mechanisms and gene activity during development , 1975, Science.
[8] C. Wijmenga,et al. Localization of the ICF syndrome to chromosome 20 by homozygosity mapping. , 1998, American journal of human genetics.
[9] M. Jeanpierre. Human satellites 2 and 3. , 1994, Annales de genetique.
[10] D. Bourc’his,et al. Abnormal methylation does not prevent X inactivation in ICF patients , 1999, Cytogenetic and Genome Research.
[11] C. Walsh,et al. Cytosine methylation and the ecology of intragenomic parasites. , 1997, Trends in genetics : TIG.
[12] T. Trautner,et al. Cytosine-specific type II DNA methyltransferases. A conserved enzyme core with variable target-recognizing domains. , 1989, Journal of molecular biology.
[13] T. Bestor. The host defence function of genomic methylation patterns. , 1998, Novartis Foundation symposium.
[14] A. T. Sumner,et al. A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves. , 1998, Journal of medical genetics.
[15] C. Hsieh. In Vivo Activity of Murine De Novo Methyltransferases, Dnmt3a and Dnmt3b , 1999, Molecular and Cellular Biology.
[16] A. Moorman,et al. WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma. , 1998, Human molecular genetics.
[17] A. Niveleau,et al. Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients. , 1994, Human molecular genetics.
[18] K. Robertson,et al. The human DNA methyltransferases (DNMTs) 1, 3a and 3b: coordinate mRNA expression in normal tissues and overexpression in tumors. , 1999, Nucleic acids research.
[19] Matthias Merkenschlager,et al. Association of Transcriptionally Silent Genes with Ikaros Complexes at Centromeric Heterochromatin , 1997, Cell.
[20] C. Hsieh,et al. Dependence of transcriptional repression on CpG methylation density , 1994, Molecular and cellular biology.
[21] E. Li,et al. Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases , 1998, Nature Genetics.
[22] A. Niveleau,et al. Monitoring of urinary excretion of modified nucleosides in cancer patients using a set of six monoclonal antibodies. , 1992, Cancer letters.
[23] 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.
[24] R. Tupler,et al. Interphase cytogenetics of the ICF syndrome , 1992, Annals of human genetics.
[25] Rudolf Jaenisch,et al. DNA hypomethylation leads to elevated mutation rates , 1998, Nature.
[26] J. Jeddeloh,et al. Maintenance of genomic methylation requires a SWI2/SNF2-like protein , 1999, Nature Genetics.