Blau syndrome NOD2 mutations result in loss of NOD2 cross-regulatory function

The studies described here provide an analysis of the pathogenesis of Blau syndrome and thereby the function of NOD2 as seen through the lens of its dysfunction resulting from Blau-associated NOD2 mutations in its nucleotide-binding domain (NBD). As such, this analysis also sheds light on the role o...

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Detalles Bibliográficos
Autores principales: Mao, Liming, Dhar, Atika, Meng, Guangxun, Fuss, Ivan, Montgomery-Recht, Kim, Yang, Zhiqiong, Xu, Qiuyun, Kitani, Atsushi, Strober, Warren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520668/
https://www.ncbi.nlm.nih.gov/pubmed/36189261
http://dx.doi.org/10.3389/fimmu.2022.988862

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520668/
https://www.ncbi.nlm.nih.gov/pubmed/36189261
http://dx.doi.org/10.3389/fimmu.2022.988862

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