Concepedia

Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the NOD2 mutation

Tomoko Matsuda, Naotomo Kambe, Yoko Ueki, Nobuo Kanazawa, Kazushi Izawa, Yoshitaka Honda, Atsushi Kawakami, Syuji Takei, Kyoko Tonomura, Masami Inoue,

Annals of the Rheumatic Diseases · 2020 · 84 citations · 27 references

DOI

Concepts

References

27

Nod2 Is a General Sensor of Peptidoglycan through Muramyl Dipeptide (MDP) Detection

Stephen E. Girardin, Ivo G. Boneca, Jérôme Viala et al. · Journal of Biological Chemistry · 2003 · 2.4K citations · Full text

, , +17

Host Recognition of Bacterial Muramyl Dipeptide Mediated through NOD2

Naohiro Inohara, Yasunori Ogura, Ana Fontalba et al. · Journal of Biological Chemistry · 2003 · 1.7K citations · Full text

, , +17

Nod2, a Nod1/Apaf-1 Family Member That Is Restricted to Monocytes and Activates NF-κB

Yasunori Ogura, Naohiro Inohara, Adalberto Benito et al. · Journal of Biological Chemistry · 2001 · 1.4K citations · Full text

, , +17

CARD15 mutations in Blau syndrome

Corinne Miceli‐Richard, Suzanne Lesage, M. Rybojad et al. · Nature Genetics · 2001 · 966 citations

, , +6

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor- B activation: common genetic etiology with Blau syndrome

Nobuo Kanazawa · Blood · 2004 · 482 citations · Full text

, , +9