RUNX2 mutations in cleidocranial dysplasia

scientific article published on 15 October 2013

RUNX2 mutations in cleidocranial dysplasia is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.4238/2013.OCTOBER.15.5
P698PubMed publication ID24222232

P2093author name stringJ-W Kim
J Ko
K-E Lee
E B Tuna
F Seymen
K Gencay
M Yildirim
P433issue4
P304page(s)4567-4574
P577publication date2013-10-15
P1433published inGenetics and Molecular ResearchQ15762471
P1476titleRUNX2 mutations in cleidocranial dysplasia
P478volume12

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cites work (P2860)
Q36240998A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review
Q47602200A novel gene mutation of Runx2 in cleidocranial dysplasia
Q57588039Acute myeloid leukemia in a 3 years old child with cleidocranial dysplasia
Q92704944Autophagy drives osteogenic differentiation of human gingival mesenchymal stem cells
Q35187603Bovine collagen peptides compounds promote the proliferation and differentiation of MC3T3-E1 pre-osteoblasts
Q38858036Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation
Q92514294Craniofacial features of cleidocranial dysplasia
Q47394908Exploring molecular mechanism of bone-forming capacity of Eurycoma longifolia: Evidence of enhanced expression of bone-related biomarkers.
Q47373153Mechanism of NF-κB signaling pathway and autophagy in the regulation of osteoblast differentiation
Q41822489Mitogen-activated protein kinase (MAPK)-regulated interactions between Osterix and Runx2 are critical for the transcriptional osteogenic program
Q37615559Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case
Q42505084Osteogenic differentiation of human gingival mesenchymal stem cells by Aristolochia bracteolata supplementation through enhanced Runx2 expression
Q54165255Patients with isolated oligo/hypodontia caused by RUNX2 duplication.
Q34809860Prevalence, etiology, diagnosis, treatment and complications of supernumerary teeth
Q93043682Structural Genome Variations Related to Craniosynostosis

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