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Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan

Journal of human genetics, 2019-08, Vol.64 (8), p.789-794

2019

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Involvement of global coordinative structure in achieving the local pendulum swinging task

PloS one, 2022-02, Vol.17 (2), p.e0262525-e0262525

2022

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Hardness Variations and Chemical Compositional Changes in Human Cementum

Journal of Oral Tissue Engineering, 2021, Vol.19(1), pp.1-9

2021

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Study of “kakkoyosa (coolness)” as expressed by the activity of waiting in freestyle basketball battles

Cognitive Studies: Bulletin of the Japanese Cognitive Science Society, 2023/09/01, Vol.30(3), pp.358-364

2023

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Identification of unique DNA methylation sites in Kabuki syndrome using whole genome bisulfite sequencing and targeted hybridization capture followed by enzymatic methylation sequencing

Journal of human genetics, 2022-12, Vol.67 (12), p.711-720

2022

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A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency

Journal of human genetics, 2019-04, Vol.64 (4), p.341-346

2019

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The Role of RANKL and Involvement of Cementum in Orthodontic Root Resorption

Applied sciences, 2021-08, Vol.11 (16), p.7244

2021

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Interaction between global optic flow and local optic flow in visual search

Cognitive Studies: Bulletin of the Japanese Cognitive Science Society, 2023/09/01, Vol.30(3), pp.370-376

2023

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Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome

Proceedings of the National Academy of Sciences - PNAS, 2011-09, Vol.108 (36), p.14914-14919

2011

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Melatonin is a potential drug for the prevention of bone loss during space flight

Journal of pineal research, 2019-10, Vol.67 (3), p.e12594-n/a

2019

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How Does a Walker Pass Between Two People Standing in Different Configurations? Influence of Personal Space on Aperture Passing Methods

Frontiers in psychology, 2019-12, Vol.10, p.2651-2651

2019

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Optimization of lymphapheresis for manufacturing autologous CAR-T cells

International journal of hematology, 2021-10, Vol.114 (4), p.449-458

2021

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BCS1L mutations produce Fanconi syndrome with developmental disability

Journal of human genetics, 2022-03, Vol.67 (3), p.143-148

2022

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Characterization of placenta-specific microRNAs in fetal growth restriction pregnancy

Prenatal diagnosis, 2013-03, Vol.33 (3), p.214-222

2013

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Ultra–sensitive droplet digital PCR for detecting a low–prevalence somatic GNAQ mutation in Sturge–Weber syndrome

Scientific reports, 2016-03, Vol.6 (1), p.22985-22985, Article 22985

2016

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Alvocidib inhibits IRF4 expression via super‐enhancer suppression and adult T‐cell leukemia/lymphoma cell growth

Cancer science, 2022-12, Vol.113 (12), p.4092-4103

2022

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Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome

Journal of human genetics, 2019-05, Vol.64 (5), p.467-471

2019

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Target Capture/Next-Generation Sequencing for Nonsyndromic Cleft Lip and Palate in the Japanese Population

The Cleft palate-craniofacial journal, 2020-01, Vol.57 (1), p.80-87

2020

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Pregnancy-associated microRNAs in plasma as potential molecular markers of ectopic pregnancy

Fertility and sterility, 2015-05, Vol.103 (5), p.1202-1208.e1

2015

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Progressive Massive Splenomegaly in an Adult Patient with Kabuki Syndrome Complicated with Immune Thrombocytopenic Purpura

Internal Medicine, 2021/06/15, Vol.60(12), pp.1927-1933

2021

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Optical Information to Guide the Head and Handle Movements While Playing Kendama

Ecological psychology, 2018-07, Vol.30 (3), p.250-277

2018

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Evaluation of Enamel Acid Resistance and Whitening Effect of the CAP System

Dentistry journal, 2022-08, Vol.10 (9), p.161

2022

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Granulocyte collection by polymorphonuclear cell-targeting apheresis with medium-molecular-weight hydroxyethyl starch

International journal of hematology, 2021-12, Vol.114 (6), p.691-700

2021

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Rizumu-kan in embodied expression

Cognitive Studies: Bulletin of the Japanese Cognitive Science Society, 2022/12/01, Vol.29(4), pp.606-629

2022

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Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan

Involvement of global coordinative structure in achieving the local pendulum swinging task

Hardness Variations and Chemical Compositional Changes in Human Cementum

Study of “kakkoyosa (coolness)” as expressed by the activity of waiting in freestyle basketball battles

Identification of unique DNA methylation sites in Kabuki syndrome using whole genome bisulfite sequencing and targeted hybridization capture followed by enzymatic methylation sequencing

Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome

A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency

The Role of RANKL and Involvement of Cementum in Orthodontic Root Resorption

Interaction between global optic flow and local optic flow in visual search

Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome

Melatonin is a potential drug for the prevention of bone loss during space flight

How Does a Walker Pass Between Two People Standing in Different Configurations? Influence of Personal Space on Aperture Passing Methods

Optimization of lymphapheresis for manufacturing autologous CAR-T cells

BCS1L mutations produce Fanconi syndrome with developmental disability

Characterization of placenta-specific microRNAs in fetal growth restriction pregnancy

Ultra–sensitive droplet digital PCR for detecting a low–prevalence somatic GNAQ mutation in Sturge–Weber syndrome

Alvocidib inhibits IRF4 expression via super‐enhancer suppression and adult T‐cell leukemia/lymphoma cell growth

Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome

Target Capture/Next-Generation Sequencing for Nonsyndromic Cleft Lip and Palate in the Japanese Population

Pregnancy-associated microRNAs in plasma as potential molecular markers of ectopic pregnancy

Progressive Massive Splenomegaly in an Adult Patient with Kabuki Syndrome Complicated with Immune Thrombocytopenic Purpura

Optical Information to Guide the Head and Handle Movements While Playing Kendama

Evaluation of Enamel Acid Resistance and Whitening Effect of the CAP System

Granulocyte collection by polymorphonuclear cell-targeting apheresis with medium-molecular-weight hydroxyethyl starch

Rizumu-kan in embodied expression

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