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Expression of the Hutchinson-Gilford Progeria Mutation Leads to Aberrant Dentin Formation
Hutchinson-Gilford progeria syndrome (HGPS) is a rare accelerated senescence disease, manifesting dental abnormalities and several symptoms suggestive of premature aging. Although irregular secondary dentin formation in HGPS patients has been reported, pathological mechanisms underlying aberrant den...
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| Vydáno v: | Sci Rep |
|---|---|
| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group UK
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6193977/ https://ncbi.nlm.nih.gov/pubmed/30337599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-33764-6 |
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