Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections.
by Dobbs, Kerry

The New England journal of medicine, June 18, 2015, Vol.372(25), pp.2409-2422


Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency
by Pai, Sung-Yun

The Journal of Allergy and Clinical Immunology, July 2014, Vol.134(1), pp.221-223.e7


A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton.
by Janssen, Erin

The Journal of clinical investigation, October 3, 2016, Vol.126(10), pp.3837-3851


A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency
by Jabara, Haifa H.

Jabara, H. H., S. E. Boyden, J. Chou, N. Ramesh, M. J. Massaad, H. Benson, W. Bainter, et al. 2015. “A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency.” Nature genetics 48 (1): 74-78. doi:10.1038/ng.3465.


DOCK8 Functions as an Adaptor that Links TLR–MyD88 Signaling to B Cell Activation
by Rauter, Ingrid

Jabara, Haifa Halim, Douglas Ray McDonald, Erin Margaret Janssen, Michel Massaad, Narayanaswamy Ramesh, Arturo Borzutzky, Ingrid Rauter, et al. 2012. DOCK8 functions as an adaptor that links TLR–MyD88 signaling to B cell activation. Nature immunology 13(6): 612-620.


DOCK8 Deficiency Presenting as an IPEX-Like Disorder
by Alroqi, Fayhan

Journal of Clinical Immunology, Nov 2017, Vol.37(8), pp.811-819


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