Takakazu Yoshioka

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early‐onset sarcoidosis

Ikuo Okafuji, Ryuta Nishikomori, Nobuo Kanazawa et al. · Arthritis & Rheumatism · 2008 · 163 citations · Full text

Life Sciences, Dermatology, Immunology +15

Disease-associated CIAS1 mutations induce monocyte death, revealing low-level mosaicism in mutation-negative cryopyrin-associated periodic syndrome patients

Megumu K. Saito, Ryuta Nishikomori, Naotomo Kambe et al. · Blood · 2007 · 148 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Somatic mosaicism of <i>CIAS1</i> in a patient with chronic infantile neurologic, cutaneous, articular syndrome

Megumu K. Saito, Akihiro Fujisawa, Ryuta Nishikomori et al. · Arthritis & Rheumatism · 2005 · 138 citations

Life Sciences, Immunology, Molecular Genetics +13

Autosomal Dominant Anhidrotic Ectodermal Dysplasia with Immunodeficiency Caused by a Novel NFKBIA Mutation, p.Ser36Tyr, Presents with Mild Ectodermal Dysplasia and Non-Infectious Systemic Inflammation

Takakazu Yoshioka, Ryuta Nishikomori, Junichi Hara et al. · Journal of Clinical Immunology · 2013 · 44 citations

Life Sciences, Genetics, Molecular Genetics +16

Differential Requirement for the CD40-CD154 Costimulatory Pathway during Th Cell Priming by CD8α+ and CD8α− Murine Dendritic Cell Subsets

Takahiro Yasumi, Kenji Katamura, Takakazu Yoshioka et al. · The Journal of Immunology · 2004 · 32 citations · Full text

Life Sciences, Cell Biology, Immunology +17