DEAF-1 function is essential for the early embryonic development of Drosophila.
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Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problemsDeaf-1 regulates epithelial cell proliferation and side-branching in the mammary glandStructural and Functional Profiling of the Human Histone Methyltransferase SMYD3Structural and Functional Analysis of the DEAF-1 and BS69 MYND DomainsIdentification and characterization of Smyd2: a split SET/MYND domain-containing histone H3 lysine 36-specific methyltransferase that interacts with the Sin3 histone deacetylase complexDefective neural tube closure and anteroposterior patterning in mice lacking the LIM protein LMO4 or its interacting partner Deaf-1C-terminal domain of SMYD3 serves as a unique HSP90-regulated motif in oncogenesisDEAF1 binds unmethylated and variably spaced CpG dinucleotide motifs.Modifiers of notch transcriptional activity identified by genome-wide RNAi.Molecular genetic analysis of Chd3 and polytene chromosome region 76B-D in Drosophila melanogaster.The structure of an LIM-only protein 4 (LMO4) and Deformed epidermal autoregulatory factor-1 (DEAF1) complex reveals a common mode of binding to LMO4.Activation of Ftz-F1-Responsive Genes through Ftz/Ftz-F1 Dependent Enhancers.Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brainDEAF-1 regulates immunity gene expression in DrosophilaSET/MYND Lysine Methyltransferases Regulate Gene Transcription and Protein Activity.Residual expression of SMYD2 and SMYD3 is associated with the acquisition of complex karyotype in chronic lymphocytic leukemia.AIRE is a critical spindle-associated protein in embryonic stem cells.The sickness unto DeafIdentification of a nuclear export signal and protein interaction domains in deformed epidermal autoregulatory factor-1 (DEAF-1).Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype.Role of the Red Ginseng in Defense against the Environmental Heat Stress in Sprague Dawley Rats.Identification of a syndrome comprising microcephaly and intellectual disability but not white matter disease associated with a homozygous c.676C>T p.R226W DEAF1 mutation.DNA methylation mediates BmDeaf1-regulated tissue- and stage-specific expression of BmCHSA-2b in the silkworm, Bombyx mori.
P2860
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P248
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P2860
DEAF-1 function is essential for the early embryonic development of Drosophila.
description
2002 nî lūn-bûn
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2002年の論文
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2002年学术文章
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2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
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2002年學術文章
@zh-hant
name
DEAF-1 function is essential for the early embryonic development of Drosophila.
@en
DEAF-1 function is essential for the early embryonic development of Drosophila.
@nl
type
label
DEAF-1 function is essential for the early embryonic development of Drosophila.
@en
DEAF-1 function is essential for the early embryonic development of Drosophila.
@nl
prefLabel
DEAF-1 function is essential for the early embryonic development of Drosophila.
@en
DEAF-1 function is essential for the early embryonic development of Drosophila.
@nl
P2093
P2860
P356
P1433
P1476
DEAF-1 function is essential for the early embryonic development of Drosophila.
@en
P2093
Alexey Veraksa
James Kennison
William McGinnis
P2860
P356
10.1002/GENE.10090
P577
2002-06-01T00:00:00Z