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注意：仅列出部分参考文献，下载原文获取全部文献信息。Runx2: Structure, function, and phosphorylation in osteoblast differentiation
S. Vimalraj et al.
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES (2015)
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JOURNAL OF ORAL PATHOLOGY & MEDICINE (2014)
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Novel RUNX2 frameshift mutations in Chinese patients with cleidocranial dysplasia
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EUROPEAN JOURNAL OF ORAL SCIENCES (2013)
RUNX2 mutations in cleidocranial dysplasia
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Oncogenic cooperation between PI3K/Akt signaling and transcription factor Runx2 promotes the invasive properties of metastatic breast cancer cells
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JOURNAL OF BIOCHEMISTRY (2012)
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RUNX2 analysis of Danish cleidocranial dysplasia families
L. Hansen et al.
CLINICAL GENETICS (2011)
A novel single-base deletion mutation of the RUNX2 gene in a Chinese family with cleidocranial dysplasia
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GENETICS AND MOLECULAR RESEARCH (2011)
Runx2 Protein Expression Utilizes the Runx2 P1 Promoter to Establish Osteoprogenitor Cell Number for Normal Bone Formation
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Deletions of the RUNX2 Gene Are Present in About 10% of Individuals with Cleidocranial Dysplasia
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Effect of Cleidocranial Dysplasia-Related Novel Mutation of RUNX2 on Characteristics of Dental Pulp Cells and Tooth Development
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J. Akech et al.
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RUNX2 mutations in cleidocranial dysplasia patients
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AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)
A Runx2 threshold for the cleidocranial dysplasia phenotype
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HUMAN MOLECULAR GENETICS (2009)
Two of four alternatively spliced isoforms of RUNX2 control osteocalcin gene expression in human osteoblast cells
Naoyuki Makita et al.
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Analysis of the Runx2 promoter in osseous and non-osseous cells and identification of HIF2A as a potent transcription activator
Hiroyuki Tamiya et al.
GENE (2008)
Osteogenic transcription factor Runx2 is a maternal determinant of dorsoventral patterning in zebrafish
Maria Vega C. Flores et al.
NATURE CELL BIOLOGY (2008)
A novel RUNX2 missense mutation predicted to disrupt DNA binding causes cleidocranial dysplasia in a large Chinese family with hyperplastic nails
Shaohua Tang et al.
BMC MEDICAL GENETICS (2007)
The presence of germ line mosaicism in cleidocranial dysplasia
T. Pal et al.
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Regulatory roles of Runx2 in metastatic tumor and cancer cell interactions with bone
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Runx2 and dental development
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EUROPEAN JOURNAL OF ORAL SCIENCES (2006)
Cbfβ regulates Runx2 function isoform-dependently in postnatal bone development
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Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype
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JOURNAL OF CELLULAR PHYSIOLOGY (2006)
Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF
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AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Cleidocranial dysplasia with severe parietal bone dysplasia:: C-terminal RUNX2 mutations
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The Runx2 osteogenic transcription factor regulates matrix metalloproteinase 9 in bone metastatic cancer cells and controls cell invasion
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Duplicate zebrafish runx2 orthologues are expressed in developing skeletal elements
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Conservation and expression of an alternative 3′ exon of Runx2 encoding a novel proline-rich C-terminal domain
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Structure and regulated expression of mammalian RUNX genes
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ONCOGENE (2004)
Runx2 control of organization, assembly and activity of the regulatory machinery for skeletal gene expression
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ONCOGENE (2004)
Selective deficiency of the bone-related Runx2-II unexpectedly preserves osteoblast-mediated skeletogenesis
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JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
BMP-2-induced Runx2 expression is mediated by Dlx5, and TGF-β1 opposes the BMP-2-induced osteoblast differentiation by suppression of Dlx5 expression
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JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo
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JOURNAL OF CELL BIOLOGY (2003)
Functional analysis of RUNX2 mutations in cleidocranial dysplasia:: novel insights into genotype-phenotype correlations
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Regulation of the osteoblast-specific transcription factor, runx2: Responsiveness to multiple signal transduction pathways
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JOURNAL OF CELLULAR BIOCHEMISTRY (2003)
Runx2 expression and action in chondrocytes are regulated by retinoid signaling and parathyroid hormone-related peptide (PTHrP)
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OSTEOARTHRITIS AND CARTILAGE (2003)
Spatio-temporal expression patterns of Runx2 isoforms in early skeletogenesis
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Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations
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AMERICAN JOURNAL OF HUMAN GENETICS (2002)
New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia
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Causal relationship between the loss of RUNX3 expression and gastric cancer
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The novel zinc finger-containing transcription factor Osterix is required for osteoblast differentiation and bone formation
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Overexpression of Cbfa1 in osteoblasts inhibits osteoblast maturation and causes osteopenia with multiple fractures
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Differential expression patterns of Runx2 isoforms in cranial suture morphogenesis
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JOURNAL OF BONE AND MINERAL RESEARCH (2001)
Characterization of the upstream mouse Cbfa1/Runx2 promoter
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Cbfa1 is a positive regulatory factor in chondrocyte maturation
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