Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
about
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-pairedA Draft Sequence of the Neandertal GenomeStructural basis for the heterodimeric interaction between the acute leukaemia-associated transcription factors AML1 and CBFbetaSmad-interacting protein 1 is a repressor of liver/bone/kidney alkaline phosphatase transcription in bone morphogenetic protein-induced osteogenic differentiation of C2C12 cellsMenin is required for bone morphogenetic protein 2- and transforming growth factor beta-regulated osteoblastic differentiation through interaction with Smads and Runx2Smad6 interacts with Runx2 and mediates Smad ubiquitin regulatory factor 1-induced Runx2 degradationSrc kinase phosphorylates RUNX3 at tyrosine residues and localizes the protein in the cytoplasmHistone deacetylase 7 associates with Runx2 and represses its activity during osteoblast maturation in a deacetylation-independent mannerShort GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyInactivation of IL11 signaling causes craniosynostosis, delayed tooth eruption, and supernumerary teethProlyl isomerase Pin1 enhances osteoblast differentiation through Runx2 regulationA WW domain-containing yes-associated protein (YAP) is a novel transcriptional co-activator.Involvement of the HLXB9 homeobox gene in Currarino syndromeRunx2 (Cbfa1, AML-3) interacts with histone deacetylase 6 and represses the p21(CIP1/WAF1) promoterNovel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndromeThe gene for cherubism maps to chromosome 4p16.Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiencyThe p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in miceRandom monoallelic expression of three genes clustered within 60 kb of mouse t complex genomic DNAControl of RANKL gene expressionEndogenous Msx1 antisense transcript: in vivo and in vitro evidences, structure, and potential involvement in skeleton development in mammalsIdentification of the homeobox protein Prx1 (MHox, Prrx-1) as a regulator of osterix expression and mediator of tumor necrosis factor α action in osteoblast differentiationGeneral transcription factor IIA-gamma increases osteoblast-specific osteocalcin gene expression via activating transcription factor 4 and runt-related transcription factor 2Comparative genomics and molecular dynamics of DNA repeats in eukaryotesA RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasiaDoubly truncated FosB isoform (Delta2DeltaFosB) induces osteosclerosis in transgenic mice and modulates expression and phosphorylation of Smads in osteoblasts independent of intrinsic AP-1 activityDental eruption in afrotherian mammalsRunx3 negatively regulates Osterix expression in dental pulp cellsTranscriptional regulation of the human MIP-1alpha promoter by RUNX1 and MOZContinuous tooth generation in mouse is induced by activated epithelial Wnt/beta-catenin signalingThe life cycle of chondrocytes in the developing skeleton.Cell Fate and Differentiation of Bone Marrow Mesenchymal Stem CellsA Genetic-Pathophysiological Framework for CraniosynostosisTranscriptional regulatory cascades in Runx2-dependent bone developmentNuclear receptors in bone physiology and diseasesCritical role of activating transcription factor 4 in the anabolic actions of parathyroid hormone in boneRegulation of gene expression in osteoblasts.A mechanism of repression by acute myeloid leukemia-1, the target of multiple chromosomal translocations in acute leukemiaHuman HOX gene mutationsRegulation of the activity of the transcription factor Runx2 by two homeobox proteins, Msx2 and Dlx5
P2860
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P2860
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
description
1997 nî lūn-bûn
@nan
1997 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@ast
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@en
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@en-gb
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@nl
type
label
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@ast
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@en
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@en-gb
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@nl
prefLabel
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@ast
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@en
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@en-gb
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@nl
P2093
P3181
P1433
P1476
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
@en
P2093
A S Aylsworth
J B Mulliken
R Mertelsmann
S Albright
P304
P3181
P356
10.1016/S0092-8674(00)80260-3
P407
P577
1997-05-01T00:00:00Z