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Sureni V. Mullegama et al.
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Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities
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A cryptic microdeletion including MBD5 occurring within the breakpoint of a reciprocal translocation between chromosomes 2 and 5 in a patient with developmental delay and obesity
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The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1
Holly N. Cukier et al.
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2q23.1 microdeletion of the MBD5 gene in a female with seizures, developmental delay and distinct dysmorphic features
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Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder
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2q23 De Novo Microdeletion Involving the MBD5 Gene in a Patient With Developmental Delay, Postnatal Microcephaly and Distinct Facial Features
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Two to Tango: Regulation of Mammalian Iron Metabolism
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Intestinal Ferritin H Is Required for an Accurate Control of Iron Absorption
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Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures
Stephen R. Williams et al.
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The Human Proteins MBD5 and MBD6 Associate with Heterochromatin but They Do Not Bind Methylated DNA
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Iron regulates phosphorylation of Smad1/5/8 and gene expression of Bmp6, Smad7, Id1, and Atoh8 in the mouse liver
Leon Kautz et al.
BLOOD (2008)
GCN5 acetyltransferase complex controls glucose metabolism through transcriptional repression of PGC-1α
Caries Lerin et al.
CELL METABOLISM (2006)
The methyl-CpG binding protein MBD1 is required for PML-RARα function
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TACC3 mediates the association of MBD2 with histone acetyltransferases and relieves transcriptional repression of methylated promoters
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Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload
V Niederkofler et al.
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The thymine DNA glycosylase MBD4 represses transcription and is associated with methylated p16INK4a and hMLH1 genes
E Kondo et al.
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Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization
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The mCpG-binding domain of human MBD3 does not bind to mCpG but interacts with NuRD/Mi2 components HDAC1 and MTA2
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cis elements of the villin gene control expression in restricted domains of the vertical (crypt) and horizontal (duodenum, cecum) axes of the intestine
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Coordinate transcriptional and translational regulation of ferritin in response to oxidative stress
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Mechanism of transcriptional regulation by methyl-CpG binding protein MBD1
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MOLECULAR AND CELLULAR BIOLOGY (2000)
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
A Donovan et al.
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Early embryonic lethality of H ferritin gene deletion in mice
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JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation
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