DOCK8 Deficiency Presenting as an IPEX-Like Disorder-Reference-Cited by-同舟云学术

DOCK8 Deficiency Presenting as an IPEX-Like Disorder

Published:2017-10-23 Issue:8 Volume:37 Page:811-819
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Alroqi Fayhan J.,Charbonnier Louis-Marie,Keles Sevgi,Ghandour Fatima,Mouawad Pierre,Sabouneh Rami,Mohammed Reem,Almutairi Abduarahman,Chou Janet,Massaad Michel J.,Geha Raif S.,Baz Zeina,Chatila Talal A.

Funder

Foundation for the National Institutes of Health

Scientific and Technological Research Council of Turkey

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://link.springer.com/article/10.1007/s10875-017-0451-1/fulltext.html

Reference43 articles.

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2. McGhee SA, Chatila TA. DOCK8 immune deficiency as a model for primary cytoskeletal dysfunction. Dis Markers. 2010;29(3–4):151–6.

3. Harada Y, Tanaka Y, Terasawa M, Pieczyk M, Habiro K, Katakai T, et al. DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses. Blood. 2012;119(19):4451–61.

4. Mizesko MC, Banerjee PP, Monaco-Shawver L, Mace EM, Bernal WE, Sawalle-Belohradsky J, et al. Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol. 2013;131(3):840–8.

5. Ham H, Guerrier S, Kim J, Schoon RA, Anderson EL, Hamann MJ, et al. Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity. J Immunol. 2013;190(7):3661–9.

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