Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E
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Title
Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E
Authors
Keywords
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Journal
Epigenetics
Volume 9, Issue 8, Pages 1184-1193
Publisher
Informa UK Limited
Online
2014-07-18
DOI
10.4161/epi.29676
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- (2014) Keivan Kaveh Moghadam et al. BRAIN
- Epigenetic regulation: Basic concepts and relevance to neurologic disease
- (2014) C. J. Klein et al. NEUROLOGY
- DNA methylation dynamics in health and disease
- (2013) Yehudit Bergman et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss
- (2013) C. J. Klein et al. NEUROLOGY
- Global Epigenomic Reconfiguration During Mammalian Brain Development
- (2013) R. Lister et al. SCIENCE
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- (2012) Zhifu Sun et al. BIOINFORMATICS
- Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
- (2012) Holger Heyn et al. Epigenetics
- Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
- (2012) Juliane Winkelmann et al. HUMAN MOLECULAR GENETICS
- Epigenetic mechanisms governing the process of neurodegeneration
- (2012) Irfan A. Qureshi et al. MOLECULAR ASPECTS OF MEDICINE
- A unique regulatory phase of DNA methylation in the early mammalian embryo
- (2012) Zachary D. Smith et al. NATURE
- pcaGoPromoter - An R Package for Biological and Regulatory Interpretation of Principal Components in Genome-Wide Gene Expression Data
- (2012) Morten Hansen et al. PLoS One
- Advances in Epigenetics and Epigenomics for Neurodegenerative Diseases
- (2011) Irfan A. Qureshi et al. Current Neurology and Neuroscience Reports
- Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
- (2011) Christopher J Klein et al. NATURE GENETICS
- DNA excision repair proteins and Gadd45 as molecular players for active DNA demethylation
- (2010) Dengke K. Ma et al. CELL CYCLE
- Epigenetics in neurodegeneration: A new layer of complexity
- (2010) Sueli C.F. Marques et al. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
- Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development
- (2008) R. Hirasawa et al. GENES & DEVELOPMENT
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