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dc.contributor.authorPoulter, James A.
dc.contributor.authorShore, Roger C.
dc.contributor.authorZhang, Hong
dc.contributor.authorHu, Jan C. -C.
dc.contributor.authorSimmer, James P.
dc.contributor.authorAhmed, Mushtaq
dc.contributor.authorJafri, Hussain
dc.contributor.authorJohnson, Colin A.
dc.contributor.authorInglehearn, Chris F.
dc.contributor.authorMighell, Alan J.
dc.contributor.authorSeymen, Figen
dc.contributor.authorKoruyucu, Mine
dc.contributor.authorParry, David A.
dc.contributor.authorSmith, Claire E. L.
dc.contributor.authorEl-Sayed, Walid
dc.contributor.authorLogan, Clare V.
dc.contributor.authorMogi, Chihiro
dc.contributor.authorSato, Koichi
dc.contributor.authorOkajima, Fumikazu
dc.contributor.authorHarada, Akihiro
dc.date.accessioned2021-03-05T11:56:13Z
dc.date.available2021-03-05T11:56:13Z
dc.date.issued2016
dc.identifier.citationParry D. A. , Smith C. E. L. , El-Sayed W., Poulter J. A. , Shore R. C. , Logan C. V. , Mogi C., Sato K., Okajima F., Harada A., et al., "Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta", AMERICAN JOURNAL OF HUMAN GENETICS, cilt.99, sa.4, ss.984-990, 2016
dc.identifier.issn0002-9297
dc.identifier.otherav_aa9aaebe-144d-409d-b8a9-473f8c884c5e
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/113922
dc.identifier.urihttps://doi.org/10.1016/j.ajhg.2016.08.020
dc.description.abstractAmelogenesis is the process of dental enamel formation, leading to the deposition of the hardest tissue in the human body. This process requires the intricate regulation of ion transport and controlled changes to the pH of the developing enamel matrix. The means by which the enamel organ regulates pH during amelogenesis is largely unknown. We identified rare homozygous variants in GPR68 in three families with amelogenesis imperfecta, a genetically and phenotypically heterogeneous group of inherited conditions associated with abnormal enamel formation. Each of these homozygous variants (a large in-frame deletion, a frameshift deletion, and a missense variant) were predicted to result in loss of function. GPR68 encodes a proton-sensing G-protein-coupled receptor with sensitivity in the pH range that occurs in the developing enamel matrix during amelogenesis. Immunohistochemistry of rat mandibles confirmed localisation of GPR68 in the enamel organ at all stages of amelogenesis. Our data identify a role for GPR68 as a proton sensor that is required for proper enamel formation.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.titleMutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF HUMAN GENETICS
dc.contributor.departmentSaint James''s University Hospital , ,
dc.identifier.volume99
dc.identifier.issue4
dc.identifier.startpage984
dc.identifier.endpage990
dc.contributor.firstauthorID235753


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