Mayuko Tamura
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Explore the profile of Mayuko Tamura including associated specialties, affiliations and a list of published articles.
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10
Citations
30
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Recent Articles
1.
Tanaka H, Tamura M, Muto M, Kinoshita Y, Ito N, Oka A, et al.
Horm Res Paediatr
. 2024 Mar;
PMID: 38493780
Introduction: Autosomal dominant hypophosphatemic rickets (ADHR) is caused by pathogenic variants in the fibroblast growth factor 23 (FGF23) gene, which plays a key role in the regulation of phosphorus metabolism....
2.
Nagai K, Tamura M, Murayama R, Fukuno S, Ito T, Konishi H
PLoS One
. 2023 Sep;
18(9):e0291822.
PMID: 37733713
Background: Menthol exerts relaxing, antibacterial, and anti-inflammatory activities, and is marketed as a functional food and therapeutic drug. Aim: In the present study, the effects of menthol on the expression...
3.
Nagai K, Fukuno S, Shiota M, Tamura M, Yabumoto S, Konishi H
Anticancer Res
. 2021 Dec;
41(12):6105-6112.
PMID: 34848465
Background/aim: Epirubicin (EPI), an epimer of doxorubicin (DOX), and DOX are anthracycline agents with broad-spectrum antitumor activity. The aim of the present study was to elucidate the transport characteristics of...
4.
Abali S, Tamura M, Turan S, Atay Z, Isguven P, Guran T, et al.
J Pediatr Endocrinol Metab
. 2020 Feb;
33(4):557-562.
PMID: 32049653
Background Hereditary vitamin D-resistant rickets (HVDRR) is caused by vitamin D receptor (VDR) defects. Patients with HVDRR do not respond to standard doses of calcitriol and oral calcium (Ca) treatment...
5.
Oda Y, Tamura M, Kitanaka S
Pediatr Int
. 2019 May;
61(5):520-522.
PMID: 31087584
No abstract available.
6.
Tamura M, Ishizawa M, Isojima T, Ozen S, Oka A, Makishima M, et al.
Sci Rep
. 2017 Jul;
7(1):5102.
PMID: 28698609
Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR) is a rare disorder, caused by bialellic mutations of the vitamin D receptor (VDR) gene, sometimes associated with alopecia. The aim of this study is...
7.
Itoh M, Tomio J, Toyokawa S, Tamura M, Isojima T, Kitanaka S, et al.
Glob Pediatr Health
. 2017 Jun;
4:2333794X17711342.
PMID: 28607944
Our study aimed to clarify the trend of vitamin D deficiency and rickets diagnosed in the past 10 years. This observational study used health insurance claims data from 2005 to...
8.
Tamura M, Isojima T, Kasama T, Mafune R, Shimoda K, Yasudo H, et al.
Hum Genome Var
. 2017 May;
4:17015.
PMID: 28503313
Smith-Lemli-Opitz syndrome is an autosomal recessive disease caused by mutations in 7-dehydrocholesterol reductase (), which is rarely observed in Japan. We report a Japanese case with 46,XY disorder of sex...
9.
Isojima T, Ishizawa M, Yoshimura K, Tamura M, Hirose S, Makishima M, et al.
Bone Rep
. 2017 Apr;
2:68-73.
PMID: 28377956
Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR) is caused by mutations in the gene, and its inheritance is autosomal recessive. In this report, we aimed to confirm whether HVDRR is occasionally inherited...
10.
Tamura M, Isojima T, Kawashima M, Yoshida H, Yamamoto K, Kitaoka T, et al.
PLoS One
. 2015 Jul;
10(7):e0131157.
PMID: 26153892
Context: Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR) is an autosomal recessive disease caused by biallelic mutations in the vitamin D receptor (VDR) gene. No patients have been reported with uniparental disomy...