Source:http://linkedlifedata.com/resource/pubmed/id/19960292
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2009-12-4
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pubmed:abstractText |
The clinical appearance of patients with cleidocranial dysplasia (CCD), which is caused by mutations in the RUNX2 gene, is characterized by anomalies of the clavicles, thorax, spine, pelvis and extremities and by disturbances of the skull and tooth development. Of orthodontic relevance are multiple supernumerary teeth associated with delayed tooth eruption. The present investigation is based on the hypothesis that an altered phenotypic expression of periodontal ligament (PDL) cells from CCD patients and a reduced ability of those cells to support the differentiation of bone-resorbing osteoclasts might contribute to delayed tooth eruption.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
D
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1615-6714
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
70
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
495-510
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pubmed:meshHeading |
pubmed-meshheading:19960292-Cell Differentiation,
pubmed-meshheading:19960292-Cells, Cultured,
pubmed-meshheading:19960292-Cleidocranial Dysplasia,
pubmed-meshheading:19960292-Core Binding Factor Alpha 1 Subunit,
pubmed-meshheading:19960292-Female,
pubmed-meshheading:19960292-Humans,
pubmed-meshheading:19960292-Male,
pubmed-meshheading:19960292-Osteoclasts,
pubmed-meshheading:19960292-Periodontal Ligament,
pubmed-meshheading:19960292-Polymorphism, Single Nucleotide,
pubmed-meshheading:19960292-Tooth, Unerupted,
pubmed-meshheading:19960292-Tooth Eruption
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pubmed:year |
2009
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pubmed:articleTitle |
The role of periodontal ligament cells in delayed tooth eruption in patients with cleidocranial dysostosis.
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pubmed:affiliation |
Department of Orthodontics, University of Bonn, Germany. s.lossdoerfer@gmx.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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