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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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IMAGING SCIENCE IN DENTISTRY (2015)
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Novel complex disease allele mutations in cleidocranial dysplasia patients
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JOURNAL OF ORAL PATHOLOGY & MEDICINE (2014)
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EUROPEAN CELLS & MATERIALS (2014)
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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GENETICS AND MOLECULAR RESEARCH (2013)
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 CELLULAR PHYSIOLOGY (2013)
Transcriptional Regulatory Cascades in Runx2-Dependent Bone Development
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JOURNAL OF BIOCHEMISTRY (2012)
Cleidocranial dysplasia: oral features and genetic analysis of 11 patients
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ORAL DISEASES (2012)
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
C. Y. Fang et al.
GENETICS AND MOLECULAR RESEARCH (2011)
Runx2 Protein Expression Utilizes the Runx2 P1 Promoter to Establish Osteoprogenitor Cell Number for Normal Bone Formation
Julie C. Liu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Deletions of the RUNX2 Gene Are Present in About 10% of Individuals with Cleidocranial Dysplasia
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HUMAN MUTATION (2010)
Effect of Cleidocranial Dysplasia-Related Novel Mutation of RUNX2 on Characteristics of Dental Pulp Cells and Tooth Development
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JOURNAL OF CELLULAR BIOCHEMISTRY (2010)
Mutational analysis of RUNX2 gene in Chinese patients with cleidocranial dysplasia
Chenying Zhang et al.
MUTAGENESIS (2010)
Runx2 association with progression of prostate cancer in patients: mechanisms mediating bone osteolysis and osteoblastic metastatic lesions
J. Akech et al.
ONCOGENE (2010)
RUNX2 mutations in cleidocranial dysplasia patients
H-M Ryoo et al.
ORAL DISEASES (2010)
Perspectives on RUNX Genes: An Update
M. Michael Cohen
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)
A Runx2 threshold for the cleidocranial dysplasia phenotype
Yang Lou et al.
HUMAN MOLECULAR GENETICS (2009)
Two of four alternatively spliced isoforms of RUNX2 control osteocalcin gene expression in human osteoblast cells
Naoyuki Makita et al.
GENE (2008)
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.
CLINICAL GENETICS (2007)
Regulatory roles of Runx2 in metastatic tumor and cancer cell interactions with bone
J. Pratap et al.
CANCER AND METASTASIS REVIEWS (2006)
Runx2 and dental development
Simon Camilleri et al.
EUROPEAN JOURNAL OF ORAL SCIENCES (2006)
Cbfβ regulates Runx2 function isoform-dependently in postnatal bone development
Naoko Kanatani et al.
DEVELOPMENTAL BIOLOGY (2006)
Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype
HJ Kim et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2006)
Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF
K Izumi et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Cleidocranial dysplasia with severe parietal bone dysplasia:: C-terminal RUNX2 mutations
ML Cunningham et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2006)
The Runx2 osteogenic transcription factor regulates matrix metalloproteinase 9 in bone metastatic cancer cells and controls cell invasion
J Pratap et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of Indian hedgehog
CA Yoshida et al.
GENES & DEVELOPMENT (2004)
Duplicate zebrafish runx2 orthologues are expressed in developing skeletal elements
MV Flores et al.
GENE EXPRESSION PATTERNS (2004)
Conservation and expression of an alternative 3′ exon of Runx2 encoding a novel proline-rich C-terminal domain
A Terry et al.
GENE (2004)
Functional and hierarchical interactions among zebrafish vox/vent homeobox genes
CN Gilardelli et al.
DEVELOPMENTAL DYNAMICS (2004)
Structure and regulated expression of mammalian RUNX genes
D Levanon et al.
ONCOGENE (2004)
Runx2 control of organization, assembly and activity of the regulatory machinery for skeletal gene expression
GS Stein et al.
ONCOGENE (2004)
Selective deficiency of the bone-related Runx2-II unexpectedly preserves osteoblast-mediated skeletogenesis
ZS Xiao et al.
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
MH Lee et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo
QP Zheng et al.
JOURNAL OF CELL BIOLOGY (2003)
Functional analysis of RUNX2 mutations in cleidocranial dysplasia:: novel insights into genotype-phenotype correlations
T Yoshida et al.
BLOOD CELLS MOLECULES AND DISEASES (2003)
Regulation of the osteoblast-specific transcription factor, runx2: Responsiveness to multiple signal transduction pathways
RT Franceschi et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2003)
Runx2 expression and action in chondrocytes are regulated by retinoid signaling and parathyroid hormone-related peptide (PTHrP)
M Iwamoto et al.
OSTEOARTHRITIS AND CARTILAGE (2003)
Spatio-temporal expression patterns of Runx2 isoforms in early skeletogenesis
KY Choi et al.
EXPERIMENTAL AND MOLECULAR MEDICINE (2002)
Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations
T Yoshida et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia
L Machuca-Tzili et al.
CLINICAL GENETICS (2002)
Causal relationship between the loss of RUNX3 expression and gastric cancer
QL Li et al.
CELL (2002)
The novel zinc finger-containing transcription factor Osterix is required for osteoblast differentiation and bone formation
K Nakashima et al.
CELL (2002)
Mutations in the RUNX2 gene in patients with clelidocranial dysplasia
F Otto et al.
HUMAN MUTATION (2002)
Overexpression of Cbfa1 in osteoblasts inhibits osteoblast maturation and causes osteopenia with multiple fractures
WG Liu et al.
JOURNAL OF CELL BIOLOGY (2001)
Differential expression patterns of Runx2 isoforms in cranial suture morphogenesis
MH Park et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2001)
Characterization of the upstream mouse Cbfa1/Runx2 promoter
ZS Xiao et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2001)
Cbfa1 is a positive regulatory factor in chondrocyte maturation
H Enomoto et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)