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Year Number of Results
1967 1
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1975 2
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1985 1
1989 1
1990 3
1991 1
1992 3
1993 1
1994 1
1995 2
1997 3
1998 6
1999 3
2000 3
2001 8
2002 1
2003 4
2005 5
2006 7
2007 3
2008 3
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102 results

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Page 1
Cleidocranial Dysplasia: A Review of Clinical, Radiological, Genetic Implications and a Guidelines Proposal.
Farrow E, Nicot R, Wiss A, Laborde A, Ferri J. Farrow E, et al. J Craniofac Surg. 2018 Mar;29(2):382-389. doi: 10.1097/SCS.0000000000004200. J Craniofac Surg. 2018. PMID: 29189406 Review.
In this review, we aimed to depict the clinical, radiological, and genetic features of cleidocranial dysplasia (CCD) and to suggest management guidelines, based on our experience of 8 cases, with an emphasis given to dental complications.The most common craniofacial …
In this review, we aimed to depict the clinical, radiological, and genetic features of cleidocranial dysplasia (CCD) and to su …
Molecular Mechanism of Runx2-Dependent Bone Development.
Komori T. Komori T. Mol Cells. 2020 Feb 29;43(2):168-175. doi: 10.14348/molcells.2019.0244. Mol Cells. 2020. PMID: 31896233 Free PMC article. Review.
Furthermore, Runx2 induces the proliferation of mesenchymal cells and their commitment into osteoblast-lineage cells through the induction of hedgehog (Gli1, Ptch1, Ihh), Fgf (Fgfr2, Fgfr3), Wnt (Tcf7, Wnt10b), and Pthlh (Pth1r) signaling pathway gene expression in calvaria, and …
Furthermore, Runx2 induces the proliferation of mesenchymal cells and their commitment into osteoblast-lineage cells through the induction o …
Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.
Jaruga A, Hordyjewska E, Kandzierski G, Tylzanowski P. Jaruga A, et al. Clin Genet. 2016 Nov;90(5):393-402. doi: 10.1111/cge.12812. Epub 2016 Jun 30. Clin Genet. 2016. PMID: 27272193 Review.
It is located on chromosome 6p21 and has two functional isoforms (type I and type II) under control of two alternate promoters (P1 and P2). Mutations within RUNX2 are linked to Cleidocranial dysplasia syndrome (CCD) in humans. CCD is an autosomal skeletal disorder c …
It is located on chromosome 6p21 and has two functional isoforms (type I and type II) under control of two alternate promoters (P1 and P2). …
Teeth Impaction and Structural Teeth Anomalies.
Haba D, Decolli Y, Marciuc E, Sîrghe AE. Haba D, et al. Semin Musculoskelet Radiol. 2020 Oct;24(5):523-534. doi: 10.1055/s-0040-1709210. Epub 2020 Oct 9. Semin Musculoskelet Radiol. 2020. PMID: 33036040 Review.
Thus it has become the imaging modality of choice for many clinical situations, such as the assessment of dental impaction and structural teeth anomalies or other associated diseases and disorders (e.g., Gardner's syndrome, cleidocranial dysplasia). This article rev …
Thus it has become the imaging modality of choice for many clinical situations, such as the assessment of dental impaction and structural te …
Developmental disorders of the dentition: an update.
Klein OD, Oberoi S, Huysseune A, Hovorakova M, Peterka M, Peterkova R. Klein OD, et al. Am J Med Genet C Semin Med Genet. 2013 Nov;163C(4):318-32. doi: 10.1002/ajmg.c.31382. Epub 2013 Oct 4. Am J Med Genet C Semin Med Genet. 2013. PMID: 24124058 Free PMC article. Review.
Finally, isolated and syndromic causes of supernumerary teeth are considered, including cleidocranial dysplasia and Gardner syndrome....
Finally, isolated and syndromic causes of supernumerary teeth are considered, including cleidocranial dysplasia and Gardner sy …
Genetic craniofacial aberrations.
Pirinen S. Pirinen S. Acta Odontol Scand. 1998 Dec;56(6):356-9. doi: 10.1080/000163598428310. Acta Odontol Scand. 1998. PMID: 10066116 Review.
This article reviews the most recent molecular findings related to Turner syndrome, Beckwith-Wiedemann syndrome, Marfan syndrome, Treacher Collins syndrome, cleidocranial dysplasia, and cleft lip and palate....
This article reviews the most recent molecular findings related to Turner syndrome, Beckwith-Wiedemann syndrome, Marfan syndrome, Treacher C …
Cleidocranial dysplasia: etiology and stomatognathic and craniofacial abnormalities.
D'Alessandro G, Tagariello T, Piana G. D'Alessandro G, et al. Minerva Stomatol. 2010 Mar;59(3):117-27. Minerva Stomatol. 2010. PMID: 20357738 Review. English, Italian.
Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic trait. ...
Cleidocranial dysplasia (CCD) is a rare disorder which is inherited as an autosomal genetic trait. ...
Biology of RUNX2 and Cleidocranial Dysplasia.
Cohen MM Jr. Cohen MM Jr. J Craniofac Surg. 2013 Jan;24(1):130-3. doi: 10.1097/SCS.0b013e3182636b7e. J Craniofac Surg. 2013. PMID: 23348269 Review.
Three features of cleidocranial dysplasia that are not always appreciated are hypoplastic iliac wings, short stature, and brachydactyly. ...Two sections follow: the biology of RUNX2 and the nature of haploinsufficiency in RUNX2 mutations for cleidocranial
Three features of cleidocranial dysplasia that are not always appreciated are hypoplastic iliac wings, short stature, and brac …
RUNX2-modifying enzymes: therapeutic targets for bone diseases.
Kim WJ, Shin HL, Kim BS, Kim HJ, Ryoo HM. Kim WJ, et al. Exp Mol Med. 2020 Aug;52(8):1178-1184. doi: 10.1038/s12276-020-0471-4. Epub 2020 Aug 13. Exp Mol Med. 2020. PMID: 32788656 Free PMC article. Review.
Genetic defects in RUNX2 itself or in its PTM regulatory pathways result in craniofacial malformations. Haploinsufficiency in RUNX2 causes cleidocranial dysplasia (CCD), which is characterized by open fontanelle and hypoplastic clavicles. ...
Genetic defects in RUNX2 itself or in its PTM regulatory pathways result in craniofacial malformations. Haploinsufficiency in RUNX2 causes …
102 results