相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Runx2 in normal tissues and cancer cells: A developing story
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BLOOD CELLS MOLECULES AND DISEASES (2010)
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CELL AND TISSUE RESEARCH (2010)
Mutational analysis of RUNX2 gene in Chinese patients with cleidocranial dysplasia
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MUTAGENESIS (2010)
RUNX2 mutations in cleidocranial dysplasia patients
H-M Ryoo et al.
ORAL DISEASES (2010)
Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia
N. Suda et al.
ORTHODONTICS & CRANIOFACIAL RESEARCH (2010)
Cleidocranial dysplasia: clinico-radiological illustration of a rare case
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Journal of Oral Science (2010)
Perspectives on RUNX Genes: An Update
M. Michael Cohen
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)
Inhibition of the terminal differentiation of odontoblasts and their transdifferentiation into osteoblasts in Runx2 transgenic mice
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ARCHIVES OF HISTOLOGY AND CYTOLOGY (2008)
Regulation of bone development and maintenance by Runx2
Toshihisa Komori
FRONTIERS IN BIOSCIENCE-LANDMARK (2008)
Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2: Possible involvement of non-genetic or epigenetic regulation
N. Suda et al.
ORTHODONTICS & CRANIOFACIAL RESEARCH (2007)
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 with severe parietal bone dysplasia:: C-terminal RUNX2 mutations
ML Cunningham et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2006)
Cleidocranial dysplasia: Molecular genetic analysis and phenotypic-based description of a middle European patient group
U Baumert et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Overlapping expression of Runx1(Cbfa2) and Runx2(Cbfa1) transcription factors supports cooperative induction of skeletal development
N Smith et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2005)
Delayed tooth eruption and suppressed osteoclast number in the eruption pathway of heterozygous Runx2/Cbfa1 knockout mice
S Yoda et al.
ARCHIVES OF ORAL BIOLOGY (2004)
Functional analysis of RUNX2 mutations in cleidocranial dysplasia:: novel insights into genotype-phenotype correlations
T Yoshida et al.
BLOOD CELLS MOLECULES AND DISEASES (2003)
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)
Mutations in the RUNX2 gene in patients with clelidocranial dysplasia
F Otto et al.
HUMAN MUTATION (2002)
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