Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability
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Title
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability
Authors
Keywords
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Journal
NATURE GENETICS
Volume 46, Issue 4, Pages 385-388
Publisher
Springer Nature
Online
2014-03-10
DOI
10.1038/ng.2917
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Related references
Note: Only part of the references are listed.- Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height
- (2015) Katrina Tatton-Brown et al. Oncotarget
- Molecular Mechanisms of Childhood Overgrowth
- (2013) KATRINA TATTON-BROWN et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- The NSD 1 and EZH 2 Overgrowth Genes, Similarities and Differences
- (2013) KATRINA TATTON-BROWN et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Mutations in epigenetic modifiers in the pathogenesis and therapy of acute myeloid leukemia
- (2013) O. Abdel-Wahab et al. BLOOD
- A DNMT3A mutation common in AML exhibits dominant-negative effects in murine ES cells
- (2013) S. J. Kim et al. BLOOD
- EZH2 in normal and malignant hematopoiesis
- (2013) K Lund et al. LEUKEMIA
- Height matters—from monogenic disorders to normal variation
- (2013) Claudia Durand et al. Nature Reviews Endocrinology
- Mutations in epigenetic regulators in myelodysplastic syndromes
- (2012) Gorica Nikoloski et al. INTERNATIONAL JOURNAL OF HEMATOLOGY
- Age-Related Prognostic Impact of Different Types ofDNMT3AMutations in Adults With Primary Cytogenetically Normal Acute Myeloid Leukemia
- (2012) Guido Marcucci et al. JOURNAL OF CLINICAL ONCOLOGY
- Structural insights into the regulation and the recognition of histone marks by the SET domain of NSD1
- (2011) Masayo Morishita et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome
- (2011) Alexander Hoischen et al. NATURE GENETICS
- Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia
- (2011) Xiao-Jing Yan et al. NATURE GENETICS
- De novo DNA methylation: a germ cell perspective
- (2011) Sébastien A. Smallwood et al. TRENDS IN GENETICS
- Structure and Function of Mammalian DNA Methyltransferases
- (2010) Renata Zofia Jurkowska et al. CHEMBIOCHEM
- Targeting of EZH2 to a defined genomic site is sufficient for recruitment of Dnmt3a but not de novo DNA methylation
- (2010) Margaret Rush et al. Epigenetics
- Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads
- (2010) G. Lunter et al. GENOME RESEARCH
- DNMT3AMutations in Acute Myeloid Leukemia
- (2010) Timothy J. Ley et al. NEW ENGLAND JOURNAL OF MEDICINE
- Structural basis for recognition of H3K4 methylation status by the DNA methyltransferase 3A ATRX–DNMT3–DNMT3L domain
- (2009) Junji Otani et al. EMBO REPORTS
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