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Concentration‐dependent effects of proinflammatory cytokines on barrier function and tight junction protein expression in brain microvascular endothelial cells and the hypothermic and hyperthermic effects on tight junction protein expression

Clinical & experimental neuroimmunology, 2023-02, Vol.14 (1), p.52-60

2023

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Carrier transport properties in highly ordered smectic liquid crystal phase

Electrical engineering in Japan, 2021-03, Vol.214 (1), p.10-17

2021

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Mutation of mtDNA ND1 Gene in 20 Type 2 Diabetes Mellitus Patients of Gorontalonese and Javanese Ethnicity

Hayati : journal of biosciences, 2014-12, Vol.21 (4), p.159-165

2014

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Filipino-type β0-thalassemia has 116 kb Deletion : Its Correct Breakpoints and Five Cases Found in Japan

The Bulletin of the Yamaguchi Medical School, 2012-12, Vol.59 (3/4), p.53-59

2012

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The interference by HbF on HbA1c (BM Test HbA1c) measurement in enzymatic method

Annals of clinical biochemistry, 2015-09, Vol.52 (5), p.569-575

2015

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A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin

Hemoglobin, 2018-01, Vol.42 (1), p.1-6

2018

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Origin of Charge Carrier Transport Properties in Smectic E Phase

Denki Gakkai ronbunshi. A, Kiso zairyÅ, 2020-05, Vol.140 (5), p.292-298

2020

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Carrier Transport Properties in Highly Ordered Smectic Liquid Crystal Phase

Denki Gakkai ronbunshi. A, Kiso zairyÅ, 2020-04, Vol.140 (4), p.253-258

2020

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A New Krüppel-Like Factor 1 Mutation (c.947G > A or p.C316Y) in Humans Causes β-Thalassemia Minor

Hemoglobin, 2015-01, Vol.39 (2), p.121-126

2015

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Oxidation Status of β-Thalassemia Minor and Hb H Disease, and Its Association with Glycerol Lysis Time (GLT50)

Hemoglobin, 2014-01, Vol.38 (3), p.169-172

2014

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A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon gene

Hemoglobin, 2013, Vol.37 (3), p.227-240

2013

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The +1,506 (A>C) Mutation in the 3′ Untranslated Region Affects β-Globin Expression

Hemoglobin, 2012-08, Vol.36 (4), p.399-406

2012

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Identification of a Novel Mutation in the β-Globin Gene 3′ Untranslated Region [+1,506 (A>C)] in a Japanese Male with a Heterozygous β-Thalassemia Phenotype

Hemoglobin, 2012-04, Vol.36 (2), p.170-176

2012

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A New β0-Thalassemia Mutation (codon 102, AAC>ATCAC) in Coexistence with a Heterozygous P4.2 Nippon Gene

Hemoglobin, 2013-06, Vol.37 (3), p.227-240

2013

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A New β 0 -Thalassemia Mutation (codon 102, AAC>A TC AC) in Coexistence with a Heterozygous P4.2 Nippon Gene

Hemoglobin, 2013-06, Vol.37 (3), p.227-240

2013

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Establishment of multiplex hybri-probe method--analysis using the polymorphism of UGT1A1 gene

Rinsho byori. The Japanese journal of clinical pathology, 2012-06, Vol.60 (6), p.523

2012

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Analysis of Hypervariable Region 1D-Loop mtDNA Mutation in Diabetes Mellitus Type 2 Patients

Advanced science, engineering and medicine, 2014-01, Vol.6 (1), p.114-118

2014

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Internet-based approach to population screening for common hemoglobinopathies in United Arab Emirates

Nursing & health sciences, 2011-06, Vol.13 (2), p.105-113

2011

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“Hazamaru Kobo” in KOSEN: Workshop to Realize Self-Learning to Cultivate Their Creative Manufacturing as an Extracurricular Activity

Journal of JSEE, 2021, Vol.69(1), pp.1_45-1_48

2021

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“Hazamaru Kobo” in KOSEN: Workshop to Realize Self-Learning to Cultivate Their Creative Manufacturing as an Extracurricular Activity

Journal of JSEE, 2021, Vol.69 (1), p.1-1_48

2021

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はざまる工房: ものづくりを創造的に実践するファブスペース

工学教育, 2021, Vol.69(1), pp.1_45-1_48

2021

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Behavioral impairment in SHATI/NAT8L knockout mice via dysfunction of myelination development

Scientific reports, 2017-12, Vol.7 (1), p.16872-10, Article 16872

2017

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CD47 promotes peripheral T cell survival by preventing dendritic cell-mediated T cell necroptosis

Proceedings of the National Academy of Sciences - PNAS, 2023-08, Vol.120 (33), p.e2304943120-e2304943120

2023

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Efficacy of Anti-Tachycardia Pacing for Terminating Fast Ventricular Tachycardia in Japanese Implantable Cardioverter Defibrillator Patients: Primary Results of the SATISFACTION Study

Circulation Journal, 2014/10/24, Vol.78(11), pp.2643-2650

2014

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Complexity Perspectives on Researching Language Learner and Teacher Psychology

1st, 2020

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Concentration‐dependent effects of proinflammatory cytokines on barrier function and tight junction protein expression in brain microvascular endothelial cells and the hypothermic and hyperthermic effects on tight junction protein expression

Carrier transport properties in highly ordered smectic liquid crystal phase

Mutation of mtDNA ND1 Gene in 20 Type 2 Diabetes Mellitus Patients of Gorontalonese and Javanese Ethnicity

Filipino-type β0-thalassemia has 116 kb Deletion : Its Correct Breakpoints and Five Cases Found in Japan

The interference by HbF on HbA1c (BM Test HbA1c) measurement in enzymatic method

A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin

Origin of Charge Carrier Transport Properties in Smectic E Phase

Carrier Transport Properties in Highly Ordered Smectic Liquid Crystal Phase

A New Krüppel-Like Factor 1 Mutation (c.947G > A or p.C316Y) in Humans Causes β-Thalassemia Minor

Oxidation Status of β-Thalassemia Minor and Hb H Disease, and Its Association with Glycerol Lysis Time (GLT50)

A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon gene

The +1,506 (A>C) Mutation in the 3′ Untranslated Region Affects β-Globin Expression

Identification of a Novel Mutation in the β-Globin Gene 3′ Untranslated Region [+1,506 (A>C)] in a Japanese Male with a Heterozygous β-Thalassemia Phenotype

A New β0-Thalassemia Mutation (codon 102, AAC>ATCAC) in Coexistence with a Heterozygous P4.2 Nippon Gene

A New β 0 -Thalassemia Mutation (codon 102, AAC>A TC AC) in Coexistence with a Heterozygous P4.2 Nippon Gene

Establishment of multiplex hybri-probe method--analysis using the polymorphism of UGT1A1 gene

Analysis of Hypervariable Region 1D-Loop mtDNA Mutation in Diabetes Mellitus Type 2 Patients

Internet-based approach to population screening for common hemoglobinopathies in United Arab Emirates

“Hazamaru Kobo” in KOSEN: Workshop to Realize Self-Learning to Cultivate Their Creative Manufacturing as an Extracurricular Activity

“Hazamaru Kobo” in KOSEN: Workshop to Realize Self-Learning to Cultivate Their Creative Manufacturing as an Extracurricular Activity

はざまる工房: ものづくりを創造的に実践するファブスペース

Behavioral impairment in SHATI/NAT8L knockout mice via dysfunction of myelination development

CD47 promotes peripheral T cell survival by preventing dendritic cell-mediated T cell necroptosis

Efficacy of Anti-Tachycardia Pacing for Terminating Fast Ventricular Tachycardia in Japanese Implantable Cardioverter Defibrillator Patients: Primary Results of the SATISFACTION Study

Complexity Perspectives on Researching Language Learner and Teacher Psychology

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