Runx2 control of organization, assembly and activity of the regulatory machinery for skeletal gene expression. - Wikidata - awgldk - TriplyDB

Runx2 control of organization, assembly and activity of the regulatory machinery for skeletal gene expression.

Runx2 control of organization, assembly and activity of the regulatory machinery for skeletal gene expression.

http://www.wikidata.org/entity/Q35779750

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Histone deacetylase 7 associates with Runx2 and represses its activity during osteoblast maturation in a deacetylation-independent manner Prolyl isomerase Pin1 enhances osteoblast differentiation through Runx2 regulation CHIP promotes Runx2 degradation and negatively regulates osteoblast differentiation Cell Fate and Differentiation of Bone Marrow Mesenchymal Stem Cells Effects of anti-tumor necrosis factor α agents on bone Regulation of gene expression in osteoblasts.Osteoblasts Are the Centerpiece of the Metastatic Bone Microenvironment Multiple levels of epigenetic control for bone biology and pathology Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study Bone morphogenic protein 2 activates protein kinase D to regulate histone deacetylase 7 localization and repression of Runx2 Parathyroid hormone-responsive Smad3-related factor, Tmem119, promotes osteoblast differentiation and interacts with the bone morphogenetic protein-Runx2 pathway Osteogenesis and neurogenesis: a robust link also for language evolution Possible functional links among brain- and skull-related genes selected in modern humans FOXP2, retinoic acid, and language: a promising direction The shape of the human language-ready brain Snail1 controls bone mass by regulating Runx2 and VDR expression during osteoblast differentiation.A novel RUNX2 missense mutation predicted to disrupt DNA binding causes cleidocranial dysplasia in a large Chinese family with hyperplastic nails.A mouse embryonic stem cell bank for inducible overexpression of human chromosome 21 genes.Digital expression profiling identifies RUNX2, CDC5L, MDM2, RECQL4, and CDK4 as potential predictive biomarkers for neo-adjuvant chemotherapy response in paediatric osteosarcoma.FGF2-activated ERK mitogen-activated protein kinase enhances Runx2 acetylation and stabilization.The gene for aromatase, a rate-limiting enzyme for local estrogen biosynthesis, is a downstream target gene of Runx2 in skeletal tissues.Subnuclear targeting of the Runx3 tumor suppressor and its epigenetic association with mitotic chromosomes.The bone-specific expression of Runx2 oscillates during the cell cycle to support a G1-related antiproliferative function in osteoblasts.T-box 3 negatively regulates osteoblast differentiation by inhibiting expression of osterix and runx2 Spatial segregation of BMP/Smad signaling affects osteoblast differentiation in C2C12 cells.A functional N-terminal domain in C/EBPβ-LAP* is required for interacting with SWI/SNF and to repress Ric-8B gene transcription in osteoblasts Increased bone adiposity and peroxisomal proliferator-activated receptor-gamma2 expression in type I diabetic mice.Epigenetic landscape during osteoblastogenesis defines a differentiation-dependent Runx2 promoter region.The bone-specific Runx2-P1 promoter displays conserved three-dimensional chromatin structure with the syntenic Supt3h promoter.Assessment of transmission distortion on chromosome 6p in healthy individuals using tagSNPs.Selective Runx2-II deficiency leads to low-turnover osteopenia in adult mice.Osteogenic differentiation of human mesenchymal stem cells synergistically enhanced by biomimetic peptide amphiphiles combined with conditioned medium.Targeted apc;twist double-mutant mice: a new model of spontaneous osteosarcoma that mimics the human disease The Role of RUNX2 in Osteosarcoma Oncogenesis.Zfp521 controls bone mass by HDAC3-dependent attenuation of Runx2 activity.Common fragile site tumor suppressor genes and corresponding mouse models of cancer.The human SWI/SNF complex associates with RUNX1 to control transcription of hematopoietic target genes The osteogenic or adipogenic lineage commitment of human mesenchymal stem cells is determined by protein kinase C delta Actin microfilament mediates osteoblast Cbfa1 responsiveness to BMP2 under simulated microgravity TGF-beta mediated Dlx5 signaling plays a crucial role in osteo-chondroprogenitor cell lineage determination during mandible development

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Runx2 control of organization, assembly and activity of the regulatory machinery for skeletal gene expression.

http://www.wikidata.org/entity/Q35779750

description

2004 nî lūn-bûn

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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2004年论文

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2004年论文

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name

Runx2 control of organization, ...... for skeletal gene expression.

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Runx2 control of organization, ...... for skeletal gene expression.

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Runx2 control of organization, ...... for skeletal gene expression.

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Runx2 control of organization, ...... for skeletal gene expression.

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Amjad Javed

http://www.w3.org/2001/XMLSchema#string

Andre J van Wijnen

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Daniel W Young

http://www.w3.org/2001/XMLSchema#string

Gary S Stein

http://www.w3.org/2001/XMLSchema#string

Jane B Lian

http://www.w3.org/2001/XMLSchema#string

Janet L Stein

http://www.w3.org/2001/XMLSchema#string

Je-Yong Choi

http://www.w3.org/2001/XMLSchema#string

Martin Montecino

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Sayyed K Zaidi

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Shirwin M Pockwinse

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P2860

Transcriptional repression by AML1 and LEF-1 is mediated by the TLE/Groucho corepressors

Interaction and functional cooperation of PEBP2/CBF with Smads. Synergistic induction of the immunoglobulin germline Calpha promoter

Physical interaction of the activator protein-1 factors c-Fos and c-Jun with Cbfa1 for collagenase-3 promoter activation

Mitotic partitioning and selective reorganization of tissue-specific transcription factors in progeny cells

Targeting of the YY1 transcription factor to the nucleolus and the nuclear matrix in situ: The C-terminus is a principal determinant for nuclear trafficking

Spatial and temporal dynamics of DNA replication sites in mammalian cells

The nuclear matrix protein NMP-1 is the transcription factor YY1.

Histone acetylation in vivo at the osteocalcin locus is functionally linked to vitamin D-dependent, bone tissue-specific transcription.

CCAAT/enhancer-binding protein beta is required for mitotic clonal expansion during adipogenesis.

Transcription factor TFIIB and the vitamin D receptor cooperatively activate ligand-dependent transcription.

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4315-4329

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10.1038/SJ.ONC.1207676

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24

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23

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2004-05-01T00:00:00Z

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8550541

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1004071585

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15156188

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