The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease
- 23 October 2003
- journal article
- review article
- Published by Elsevier in Clinical Immunology
- Vol. 109 (1) , 17-28
- https://doi.org/10.1016/s1521-6616(03)00201-8
Abstract
No abstract availableKeywords
This publication has 80 references indexed in Scilit:
- DNA methylation in cancer: too much, but also too littleOncogene, 2002
- Three novel DNMT3B mutations in Japanese patients with ICF syndromeAmerican Journal of Medical Genetics, 2002
- DNMT1 and DNMT3b cooperate to silence genes in human cancer cellsNature, 2002
- Dnmt3b, de Novo DNA Methyltransferase, Interacts with SUMO-1 and Ubc9 through Its N-Terminal Region and Is Subject to Modification by SUMO-1Biochemical and Biophysical Research Communications, 2001
- α-Satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissuesHuman Genetics, 1997
- Preferential induction of chromosome 1 multibranched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidineCytogenetic and Genome Research, 1997
- Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndromeEuropean Journal of Pediatrics, 1995
- Chromosome instability in ICF syndrome: Formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridizationAmerican Journal of Medical Genetics, 1995
- Targeted mutation of the DNA methyltransferase gene results in embryonic lethalityPublished by Elsevier ,1992
- Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9, and 16The Journal of Pediatrics, 1988