文献
J-GLOBAL ID:202002254196665037
整理番号:20A1075916
家族性エナメル質形成不全症において発見されたOGR1のLeu74Proのミスセンス変異はpH感知機構の消失を実際的に引き起こす【JST・京大機械翻訳】
A missense mutation of Leu74Pro of OGR1 found in familial amelogenesis imperfecta actually causes the loss of the pH-sensing mechanism
著者 (4件):
Sato Koichi
(Laboratory of Signal Transduction, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, 371-8512, Japan)
,
Mogi Chihiro
(Laboratory of Integrated Signaling System, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, 371-8512, Japan)
,
Mighell Alan J.
(Department of Oral Biology, School of Dentistry, St James’s University Hospital, University of Leeds, Leeds, LS9 7TF, UK)
,
Okajima Fumikazu
(Laboratory of Signal Transduction, Faculty of Pharmaceutical Sciences, Aomori University, Aomori, 030-0943, Japan)
資料名:
Biochemical and Biophysical Research Communications
(Biochemical and Biophysical Research Communications)
巻:
526
号:
4
ページ:
920-926
発行年:
2020年
JST資料番号:
B0118A
ISSN:
0006-291X
資料種別:
逐次刊行物 (A)
記事区分:
短報
発行国:
オランダ (NLD)
言語:
英語 (EN)