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1. ディジョージ（22q11.2欠失）症候群：臨床的特徴および診断 digeorge 22q11 2 deletion syndrome clinical features and diagnosis
2. ディジョージ症候群（22q11.2欠失）：疫学および病因 digeorge 22q11 2 deletion syndrome epidemiology and pathogenesis
3. ディジョージ症候群（22q11.2欠失）：マネージメントおよび予後 digeorge 22q11 2 deletion syndrome management and prognosis
4. 総動脈幹 truncus arteriosus
5. 同種造血細胞移植後の免疫再構築のための戦略 strategies for immune reconstitution following allogeneic hematopoietic cell transplantation

Ground-based assessment of JAXA mouse habitat cage unit by mouse phenotypic studies.

Shimbo M1, Kudo T, Hamada M, Jeon H, Imamura Y, Asano K, Okada R, Tsunakawa Y, Mizuno S, Yagami K, Ishikawa C, Li H, Shiga T, Ishida J, Hamada J, Murata K, Ishimaru T, Hashimoto M, Fukamizu A, Yamane M, Ikawa M, Morita H, Shinohara M, Asahara H, Akiyama T, Akiyama N, Sasanuma H, Yoshida N, Zhou R, Wang YY, Ito T, Kokubu Y, Noguchi TA, Ishimine H, Kurisaki A, Shiba D, Mizuno H, Shirakawa M, Ito N, Takeda S, Takahashi S.
Experimental animals / Japanese Association for Laboratory Animal Science.Exp Anim.2016 May 20;65(2):175-87. doi: 10.1538/expanim.15-0077. Epub 2016 Jan 28.
The Japan Aerospace Exploration Agency developed the mouse Habitat Cage Unit (HCU) for installation in the Cell Biology Experiment Facility (CBEF) onboard the Japanese Experimental Module ("Kibo") on the International Space Station. The CBEF provides "space-based controls" by generating artificial g
PMID 26822934

Skin Barrier Recovery by the Protease-Activated Receptor-2 Antagonist Lobaric Acid.

Joo YA1, Chung H1, Yoon S1, Park JI1, Lee JE1, Myung CH1, Hwang JS1.
Biomolecules & therapeutics.Biomol Ther (Seoul).2016 May 13. doi: 10.4062/biomolther.2016.011. [Epub ahead of print]
Atopic dermatitis (AD) results from gene and environment interactions that lead to a range of immunological abnormalities and breakdown of the skin barrier. Protease-activated receptor 2 (PAR2) belongs to a family of G-protein coupled receptors and is expressed in suprabasal layers of the epidermis.
PMID 27169822

Shiloh Y1, Lederman HM2.
Ageing research reviews.Ageing Res Rev.2016 May 12. pii: S1568-1637(16)30078-2. doi: 10.1016/j.arr.2016.05.002. [Epub ahead of print]
A-T is a prototype genome instability syndrome and a multifaceted disease. A-T leads to neurodegeneration - primarily cerebellar atrophy, immunodeficiency, oculocutaneous telangiectasia (dilated blood vessels), vestigial thymus and gonads, endocrine abnormalities, cancer predisposition and varying s
PMID 27181190

Postmortem Molecular Screening for Cardiac Ryanodine Receptor Type 2 Mutations in Sudden Unexplained Death : R420W Mutated Case With Characteristics of Status Thymico-Lymphaticus

Circulation journal : official journal of the Japanese Circulation Society 70(11), 1402-1406, 2006-10-20
NAID 110004858627