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DOCK8 gene

Known as: FLJ00026, FLJ00152, DOCK8 
This gene may play a role in guanine nucleotide exchange
National Institutes of Health

Related topics

Related topics

2 relations
DOCK7 geneSignal Transduction

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome
To the Editor: The dedicator of cytokinesis 8 (DOCK8)1 mutation is a relatively new genetic defect discovered in a subgroup of… 
Review
2017
Review
2017
[Hyper-IgE syndromes].
A hyper-IgE syndrome is a rare immunodeficiesncy disease, often accompanied by high serum IgE. It often characterized by facial… 
2016
2016
DOCK8 eksikliği olan bir olguda aort kökü ile iliyak bifurkasyon arasında dev aort anevrizması
2014
2014
Inmunodeficiencia combinada con compromiso cutáneo asociada a mutación en DOCK8 Combined immunodeficiency with cutaneous manifestations associated with DOCK8 mutation
Different primary immunodeficiencies present increased levels of IgE and cutaneous infections of viral etiology. We report a case… 
2014
2014
Hyper Immunogobulin E Syndrome: A Report on DOCK8 Mutations in Iranian Patients
2012
2012
Management of DOCK8 deficiency by haematopoietic stem cell transplantation
Review
2012
Review
2012
Clinical Presentation and Long-Term Outcome of Dock8 Deficiency - A Survey of 134 Patients
2011
2011
DOCK 8 de ! ciency impairs CD 8 T cell survival and function in humans and mice
Abbreviations used: APC, allophycocyanin; HIES, hyperIgE syndrome; HPV, human papillomavirus; MTOC, microtubule-organizing center… 
2010
2010
Hyper-IgE syndrome: fatal progressive multifocal leukoencephalopathy in an Italian child with DOCK8 mutation
2009
2009
Immunodeficiency caused by DOCK8 mutation in primurus mice