K. Shirao

Polycomb-group complex 1 acts as an E3 ubiquitin ligase for Geminin to sustain hematopoietic stem cell activity

M. Ohtsubo, M. Tsumura, Masao Kobayashi, 2008, Proceedings of the National Academy of Sciences.

Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene

M. Ohtsubo, S. Okada, M. Tsumura, 2008, Journal of Medical Genetics.

"Bitter sweet": a child case of erythritol-induced anaphylaxis.

M. Nagao, T. Fujisawa, M. Yamaguchi, 2013, Allergology international : official journal of the Japanese Society of Allergology.

Development of a New Enzymatic Diagnosis Method for Very-long-chain Acyl-CoA Dehydrogenase Deficiency by Detecting 2-Hexadecenoyl-CoA Production and its Application in Tandem Mass Spectrometry-based Selective Screening and Newborn Screening in Japan

E. Naito, S. Okada, M. Tsumura, 2008, Pediatric Research.

The novel IFNGR1 mutation 774del4 produces a truncated form of interferon-γ receptor 1 and has a dominant-negative effect on interferon-γ signal transduction

M. Ohtsubo, S. Okada, M. Tsumura, 2007, Journal of Medical Genetics.

The novel IFNGR1 mutation 774del4 produces a truncated form of interferon-gamma receptor 1 and has a dominant-negative effect on interferon-gamma signal transduction.

M. Ohtsubo, S. Okada, M. Tsumura, 2007, Journal of medical genetics.

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency

M. Ohtsubo, S. Okada, M. Tsumura, 2010, Human Genetics.

Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15.

S. Okada, M. Tsumura, Masao Kobayashi, 2009, Rheumatology.

Optimal step-down approach for pediatric asthma controlled by salmeterol/fluticasone: A randomized, controlled trial (OSCAR study).

H. Mezawa, K. Akashi, T. Fujisawa, 2016, Allergology international : official journal of the Japanese Society of Allergology.