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Runx2
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NextBio Summary
General Info
Body Atlas
Most Correlated Tissues
Ciliary ganglion
Parotid gland
Superior cervical ganglion
Atrioventricular node
Granulocyte-macrophage progenitor cell of bone marrow
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Disease Atlas
Most Correlated Diseases
Dysostosis
Disease of mouth
Bacterial infection of skin
Viral infections of the central nervous system
Skeletal dysplasia
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Pharmaco Atlas
Most Correlated Compounds
PF 03084014
Gonadotropins, Equine
iron(III) meso-tetramesitylporphyrin
GA 101
Ifna protein, mouse
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Knockdown Atlas
Most Correlated Gene Perturbations
BAG3
TIMP2
MLLT1
MAPK14
INHA
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
A BK channel-targeted peptide induces age-dependent improvement in behavioral and neural sound repre…
Structure and Origin of the White Cap Locus and Its Role in Evolution of Grain Color in Maize.
Identification of a novel RUNX2 gene mutation in an Italian family with cleidocranial dysplasia.
Thrap3 promotes osteogenesis by inhibiting the degradation of Runx2.
NaF reduces KLK4 expression by decreasing Foxo1/Runx2 expression in LS8 cells.
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Clinical Trials
Most Relevant Clinical Trials
Transcription Factor Runx2 in Necrotic Femoral Head Tissue
Cleidocranial Dysplasia (CCD): From Genotype to Phenotype and Considerations for Care
Effects of Dehydroepiandrosterone Supplementation on Cumulus Cells Gene Expression Under Controlled …
Roles of microRNAs in the Development of Osteoporosis in Men - Preliminary Study
Effect of Baricitinib Treatment on Peripheral Bone in RA
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