Identification of the in vivo casein kinase II phosphorylation site within the homeodomain of the cardiac tisue-specifying homeobox gene product Csx/Nkx2.5
about
Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathwaysCK2 phosphorylation of the PRH/Hex homeodomain functions as a reversible switch for DNA bindingRegulation of cardiac specific nkx2.5 gene activity by small ubiquitin-like modifierPhosphorylation of murine homeodomain protein Dlx3 by protein kinase C.Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart diseaseCrystal Structure of the Human NKX2.5 Homeodomain in Complex with DNA TargetThe paired-like homeodomain protein, Arix, mediates protein kinase A-stimulated dopamine beta-hydroxylase gene transcription through its phosphorylation statusComplex SUMO-1 regulation of cardiac transcription factor Nkx2-5Characterization of homo- and heterodimerization of cardiac Csx/Nkx2.5 homeoproteinPrediction of cardiac transcription networks based on molecular data and complex clinical phenotypes.Expression of sumoylation deficient Nkx2.5 mutant in Nkx2.5 haploinsufficient mice leads to congenital heart defects.The Dlx3 protein harbors basic residues required for nuclear localization, transcriptional activity and binding to Msx1.Ischemia-reperfusion injury and pregnancy initiate time-dependent and robust signs of up-regulation of cardiac progenitor cells.Cardiac transcription factor Nkx2.5 is downregulated under excessive O-GlcNAcylation condition.Role for Hes1-induced phosphorylation in Groucho-mediated transcriptional repression.NKX3.1 is regulated by protein kinase CK2 in prostate tumor cellsPhosphorylation of Shox2 is required for its function to control sinoatrial node formation.NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity.Thrombopoietin induces HOXA9 nuclear transport in immature hematopoietic cells: potential mechanism by which the hormone favorably affects hematopoietic stem cells.Assessment of embryonic myocardial cell differentiation using a dual fluorescent reporter system.NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets.Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoproteinKaryopherins in nuclear transport of homeodomain proteins during development.Sumoylation and regulation of cardiac gene expression.Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy.Protein kinase CK2 in health and disease: CK2 and its role in Wnt and NF-kappaB signaling: linking development and cancer.From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases.DNA-binding sequence of the human prostate-specific homeodomain protein NKX3.1.Stem cells transform into a cardiac phenotype with remodeling of the nuclear transport machinery.The representation of heart development in the gene ontologyNovel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations.Ser¹¹⁹ phosphorylation modulates the activity and conformation of PRRXL1, a homeodomain transcription factor.Activation of HLXB9 by juxtaposition with MYB via formation of t(6;7)(q23;q36) in an AML-M4 cell line (GDM-1).The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes.Protein kinase C-mediated phosphorylation of the leukemia-associated HOXA9 protein impairs its DNA binding ability and induces myeloid differentiation.Phosphorylation of HOX11/TLX1 on Threonine-247 during mitosis modulates expression of cyclin B1.Fractal heterogeneity in minimal matrix models of scars modulates stiff-niche stem-cell responses via nuclear exit of a mechanorepressor.Expression of Hex homeobox gene during skin development: Increase in epidermal cell proliferation by transfecting the Hex to the dermis.Mutation of a CK2 phosphorylation site in cdc25C impairs importin alpha/beta binding and results in cytoplasmic retention.Molecular characterization, expression patterns and polymorphism analysis of porcine Six1 gene.
P2860
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P2860
Identification of the in vivo casein kinase II phosphorylation site within the homeodomain of the cardiac tisue-specifying homeobox gene product Csx/Nkx2.5
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@ast
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@en
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@en-gb
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@nl
type
label
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@ast
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@en
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@en-gb
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@nl
prefLabel
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@ast
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@en
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@en-gb
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@nl
P2860
P921
P356
P1476
Identification of the in vivo ...... meobox gene product Csx/Nkx2.5
@en
P2093
P2860
P304
P356
10.1128/MCB.19.1.526
P407
P577
1999-01-01T00:00:00Z