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A Runx2 threshold for the cleidocranial dysplasia phenotype.
Runx2 deficiency and defective subnuclear targeting bypass senescence to promote immortalization and tumorigenic potential.
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A Runx2 threshold for the cleidocranial dysplasia phenotype.
A Runx2 threshold for the cleidocranial dysplasia phenotype. Hum Mol Genet. 2009 Feb 01; 18(3):556-68.
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PubMed
subject areas
Animals
Bone Development
Cells, Cultured
Clavicle
Cleidocranial Dysplasia
Core Binding Factor Alpha 1 Subunit
Female
Growth Plate
Humans
Male
Mice
Mice, Inbred C57BL
Mice, Transgenic
Osteoblasts
Phenotype
Skull
authors with profiles
Jitesh Pratap