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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Sci Rep
Egile Nagusiak: Choi, Hwajung, Kim, Tak-Heun, Jeong, Ju-Kyeong, Strandgren, Charlotte, Eriksson, Maria, Cho, Eui-Sic
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Nature Publishing Group UK 2018
Gaiak:
Sarrera elektronikoa: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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