Characterization of a nuclear deformed epidermal autoregulatory factor-1 (DEAF-1)-related (NUDR) transcriptional regulator protein
about
Cloning and characterization of hGMEB1, a novel glucocorticoid modulatory element binding proteinTwo new members of the emerging KDWK family of combinatorial transcription modulators bind as a heterodimer to flexibly spaced PuCGPy half-sitesMutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problemsInteractome mapping of the phosphatidylinositol 3-kinase-mammalian target of rapamycin pathway identifies deformed epidermal autoregulatory factor-1 as a new glycogen synthase kinase-3 interactorDeaf-1 regulates epithelial cell proliferation and side-branching in the mammary glandDeaf1 isoforms control the expression of genes encoding peripheral tissue antigens in the pancreatic lymph nodes during type 1 diabetesGenomic organization of human GMEB-1 and rat GMEB-2: structural conservation of two multifunctional proteinsPDCD2 is a negative regulator of HCF-1 (C1)Ubc9 is a novel modulator of the induction properties of glucocorticoid receptorsMouse deformed epidermal autoregulatory factor 1 recruits a LIM domain factor, LMO-4, and CLIM coregulatorsDefective neural tube closure and anteroposterior patterning in mice lacking the LIM protein LMO4 or its interacting partner Deaf-1Cloning of a mouse glucocorticoid modulatory element binding protein, a new member of the KDWK familyDEAF1 binds unmethylated and variably spaced CpG dinucleotide motifs.Transcriptional expression of serotonergic regulators in laser-captured microdissected dorsal raphe neurons of subjects with major depressive disorder: sex-specific differences.Coupling clinical exome sequencing with functional characterization studies to diagnose a patient with familial Mediterranean fever and MED13L haploinsufficiency syndromes5-HT1A gene promoter polymorphism and [18F]MPPF binding potential in healthy subjects: a PET study.Dynamic association of NUP98 with the human genome.The identification of trans-acting factors that regulate the expression of GDF5 via the osteoarthritis susceptibility SNP rs143383.Autoimmune regulator: from loss of function to autoimmunity.Transcriptional dysregulation of 5-HT1A autoreceptors in mental illness.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.Increased serotonin-1A (5-HT1A) autoreceptor expression and reduced raphe serotonin levels in deformed epidermal autoregulatory factor-1 (Deaf-1) gene knock-out miceDeformed epidermal autoregulatory factor-1 (DEAF1) interacts with the Ku70 subunit of the DNA-dependent protein kinase complex.Stress-induced alterations in 5-HT1A receptor transcriptional modulators NUDR and Freud-1The Arginine/Lysine-Rich Element within the DNA-Binding Domain Is Essential for Nuclear Localization and Function of the Intracellular Pathogen Resistance 1Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brainReduced DEAF1 function during type 1 diabetes inhibits translation in lymph node stromal cells by suppressing Eif4g3.DEAF-1 regulates immunity gene expression in DrosophilaGender-specific decrease in NUDR and 5-HT1A receptor proteins in the prefrontal cortex of subjects with major depressive disorder.Proprotein convertase subtilisin/kexin type 4 in mammalian fertility: a review.Type 1 diabetes in mice and men: gene expression profiling to investigate disease pathogenesis.DEAF1 is a Pellino1-interacting protein required for interferon production by Sendai virus and double-stranded RNA.The sickness unto DeafBackbone and side-chain assignments of a tethered complex between LMO4 and DEAF-1.Identification of a nuclear export signal and protein interaction domains in deformed epidermal autoregulatory factor-1 (DEAF-1).DEAF-1 function is essential for the early embryonic development of Drosophila.Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype.Nuclear DEAF-1-related (NUDR) protein contains a novel DNA binding domain and represses transcription of the heterogeneous nuclear ribonucleoprotein A2/B1 promoter.Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsy.
P2860
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P2860
Characterization of a nuclear deformed epidermal autoregulatory factor-1 (DEAF-1)-related (NUDR) transcriptional regulator protein
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Characterization of a nuclear ...... nscriptional regulator protein
@ast
Characterization of a nuclear ...... nscriptional regulator protein
@en
Characterization of a nuclear ...... nscriptional regulator protein
@en-gb
Characterization of a nuclear ...... nscriptional regulator protein
@nl
type
label
Characterization of a nuclear ...... nscriptional regulator protein
@ast
Characterization of a nuclear ...... nscriptional regulator protein
@en
Characterization of a nuclear ...... nscriptional regulator protein
@en-gb
Characterization of a nuclear ...... nscriptional regulator protein
@nl
prefLabel
Characterization of a nuclear ...... nscriptional regulator protein
@ast
Characterization of a nuclear ...... nscriptional regulator protein
@en
Characterization of a nuclear ...... nscriptional regulator protein
@en-gb
Characterization of a nuclear ...... nscriptional regulator protein
@nl
P2093
P3181
P1476
Characterization of a nuclear ...... nscriptional regulator protein
@en
P2093
A J Ziemba
J I Huggenvik
M W Collard
R J Michelson
P304
P3181
P356
10.1210/ME.12.10.1619
10.1210/MEND.12.10.0181
P407
P577
1998-10-01T00:00:00Z