研究者学術情報データベース

イナヅ　テツヤ
稲津　哲也
INAZU Tetsuya

所属薬学部薬学科

職名教授

論文
1.	2024/07	Role of plant homeodomain finger protein 8 in P19 embryonic carcinoma cells revealed by genome editing and specific inhibitor │ Biochemistry and Biophysics Reports │ 38 (101670) (共著)
2.	2024/02/29	Possibility of active vitamin D treatment to prevent sarcopenia in adults with prediabetes: DPVD ancillary study: a randomized controlled trial │ The Lancet Healthy Longevity │ S2666-7568(24)00009-6. (共著)
3.	2023/02/07	Total colectomy for poorly controlled hypokalemia due to Gitelman syndrome │ BMJ Case Rep │ 16 (2),e252916 (共著)
4.	2022/11/12	HDAC8 is implicated in embryoid body formation via canonical Hedgehog signaling and regulates neuronal differentiation │ Biochem. Biophys. Res. Commun. │ 629,78-85頁 (共著)
5.	2022/10/14	Comprehensive in silico functional prediction analysis of CDKL5 by single amino acid substitution in the catalytic domain │ Int. J. Mol. Sci. │ 23 (20),12281 (共著)
6.	2022/05/25	Effect of active vitamin D treatment on development of type 2 diabetes: DPVD randomized controlled trial in Japanese population │ BMJ │ May 25 (377:e066222) (共著)
7.	2021/12	p.Asn77Lys homozygous CLN6 mutation in two unrelated Japanese patients with Kufs disease, an adult onset neuronal ceroid lipofuscinosis │ Clinica Chimica Acta │ 523,191-195頁 (共著)
8.	2021/09	Zinc finger protein 483 (ZNF483) regulates neuronal differentiation and methyl-CpG-binding protein 2 (MeCP2) intracellular localization │ Biochem. Biophys. Res. Commun. │ 568,68-75頁 (共著)
9.	2020/07	Establishment of a simple method for inducing neuronal differentiation of P19 EC cells without embryoid body formation and analysis of the role of histone deacetylase 8 activity in this differentiation │ Biol.Pharm.Bull. │ 43 (7),1096–1103 (共著)
10.	2020/06	Cyclin-dependent kinase-like 5 (CDKL5): Possible cellular signaling targets and involvement in CDKL5 deficiency disorder │ Neural Plasticity │ volume 2020,Article ID 6970190 (共著)
11.	2019/11	In silico study of Rett syndrome treatment-related genes, MECP2, CDKL5, and FOXG1 by evolutionary classification and disordered region assessment │ International Journal of Molecular Sciences │ 20 (22),5593 (共著)
12.	2019/10	Yokukansan, a Kampo medicine, enhances the level of neuronal lineage markers in differentiated P19 embryonic carcinoma cells │ Heliyon │ 5 (10),e02662 (共著)
13.	2019/02	Straightforward and rapid method for detection of cyclin-dependent kinase-like 5 activity │ Analytical Biochemistry │ 566,58-61 (共著)
14.	2018/03	HDAC8 regulates neural differentiation through embryoid bodies formation in P19 cells │ Biochemical and Biophysical Research Communications │ 498 (1),45-51 (共著)
15.	2016/07	Rationale and design of Diabetes Prevention with active Vitamin D (DPVD): a randomized, double-blind, placebo-controlled study │ BMJ Open │ 6 (7),e011183 (共著)
16.	2016/06	A novel CDKL5 mutation in a Japanese patient with atypical Rett syndrome │ Clinica Chimica Acta │ 459,132-136 (共著)
17.	2015/04	Incidence of type 2 diabetes in pre-diabetic Japanese individuals categorized by HbA1c levels: a Historical Cohort Study │ PLoS One │ 10 (4),e0122698 (共著)
18.	2015/03	A Novel PHEX Mutation in Japanese Patients with X-linked Hypophosphatemic Rickets │ Case Reports in Genetics │ 2015:301264 (共著)
19.	2015/01	Allele-specific real time polymerase chain reaction as a tool for urate transporter 1 mutation detection │ Methods in Molecular Biology │ ,1275, 117-125 (共著)
20.	2015/01	Generation of rat induced pluripotent cells using a plasmid vector and possible application of a keratan sulfate glycan recognizing antibody in discriminating teratoma formation phenotypes │ Biol.Pharm.Bull. │ 38 (1),127-133 (共著)
21.	2013/08	Idursulfase enzyme replacement therapy in an adult patient with severe Hunter syndrome having a novel mutation of iduronate-2-sulfatase gene │ Clinica Chimica Acta │ 423,66-68 (共著)
22.	2013/07	Atorvastatin, Etidronate, or Both in Patients at High Risk for Atherosclerotic Aortic Plaques: a Randomized Controlled Trial │ Circulation │ 127 (23),2327-2335 (共著)
23.	2013/01	Simple and rapid detection method for the mutations in SLC22A12 that cause hypouricemia by allele-specific real-time polymerase chain reaction │ Clinica Chimica Acta │ 415,330-333 (共著)
24.	2011/11	Tandem configurations of variably duplicated segments of 22q11.2 confirmed by fiber-FISH analysis. │ J Hum Genet. │ 56 (11),810-2 (共著)
25.	2011/05	Effect of atorvastatin and etidronate combination therapy on regression of aortic atherosclerotic plaques evaluated by magnetic resonance imaging │ Journal of Atherosclerosis and Thrombosis │ 18 (5),384-95 (共著)
26.	2009/12	Cardiovascular event rates in patients with cerebrovascular disease and atherothrombosis at other vascular locations: Results from 1-year outcomes in the Japanese REACH Registry │ J Neurol Sci. │ 287 (1-2),45-51 (共著)