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Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay
ML Weber, HY Hsin, E Kalay, DS BroZkova, T Shimizu, M Bayram, K Deeley, EC Kuchler, J Forella, TD Ruff, VM Trombetta, RC Sencak, M Hummel, J Briseno-Ruiz, SK Revu, JM Granjeiro, LS Antunes, LA Antunes, FV Abreu, MC Costa, PN Tannure, M Koruyucu,...
Jazyk angličtina Země Velká Británie
Grantová podpora
NT14348
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
BioMedCentral
od 2000-12-01 do 2020-12-31
BioMedCentral Open Access
od 2000
Directory of Open Access Journals
od 2000
Free Medical Journals
od 2000
PubMed Central
od 2000 do 2020
Europe PubMed Central
od 2000
ProQuest Central
od 2009-01-01 do 2021-01-31
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2000-11-01
Open Access Digital Library
od 2000-01-01
Medline Complete (EBSCOhost)
od 2000-01-01 do 2021-03-12
Health & Medicine (ProQuest)
od 2009-01-01 do 2021-01-31
ROAD: Directory of Open Access Scholarly Resources
od 2000
Springer Nature OA/Free Journals
od 2000-12-01 do 2020-12-31
PubMed
25023176
DOI
10.1186/1471-2350-15-81
Knihovny.cz E-zdroje
- MeSH
- demineralizace zubů * genetika MeSH
- dítě MeSH
- dospělí MeSH
- genetické asociační studie MeSH
- jednonukleotidový polymorfismus MeSH
- lidé MeSH
- lidské chromozomy, pár 14 MeSH
- mladiství MeSH
- mladý dospělý MeSH
- myši MeSH
- nádorové buněčné linie MeSH
- percepční nedoslýchavost genetika patologie MeSH
- předškolní dítě MeSH
- receptory pro estrogeny fyziologie genetika MeSH
- rodokmen MeSH
- vazebná nerovnováha MeSH
- zubní kaz * genetika MeSH
- zubní sklovina růst a vývoj MeSH
- zvířata MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- myši MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- zvířata MeSH
BACKGROUND: Congenital forms of hearing impairment can be caused by mutations in the estrogen related receptor beta (ESRRB) gene. Our initial linkage studies suggested the ESRRB locus is linked to high caries experience in humans. METHODS: We tested for association between the ESRRB locus and dental caries in 1,731 subjects, if ESRRB was expressed in whole saliva, if ESRRB was associated with the microhardness of the dental enamel, and if ESRRB was expressed during enamel development of mice. RESULTS: Two families with recessive ESRRB mutations and DFNB35 hearing impairment showed more extensive dental destruction by caries. Expression levels of ESRRB in whole saliva samples showed differences depending on sex and dental caries experience. CONCLUSIONS: The common etiology of dental caries and hearing impairment provides a venue to assist in the identification of individuals at risk to either condition and provides options for the development of new caries prevention strategies, if the associated ESRRB genetic variants are correlated with efficacy.
Citace poskytuje Crossref.org
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