Related references
Note: Only part of the references are listed.Somatic reversion of pathogenic DOCK8 variants alters lymphocyte differentiation and function to effectively cure DOCK8 deficiency
Bethany A. Pillay et al.
JOURNAL OF CLINICAL INVESTIGATION (2021)
Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome
Zahra Aryan et al.
PEDIATRIC BLOOD & CANCER (2020)
Clinical, immunological features and follow up of 20 patients with dedicator of cytokinesis 8 (DOCK8) deficiency
Sule Haskologlu et al.
PEDIATRIC ALLERGY AND IMMUNOLOGY (2020)
B Cell Reconstitution and Influencing Factors After Hematopoietic Stem Cell Transplantation in Children
Nicolaas G. van der Maas et al.
FRONTIERS IN IMMUNOLOGY (2019)
Wiskott-Aldrich Syndrome (WAS) and Dedicator of Cytokinesis 8-(DOCK8) Deficiency
Michael H. Albert et al.
FRONTIERS IN PEDIATRICS (2019)
Metabolomics Distinguishes DOCK8 Deficiency from Atopic Dermatitis: Towards a Biomarker Discovery
Minnie Jacob et al.
METABOLITES (2019)
Peripheral eosinophilia in primary immunodeficiencies of actin dysregulation: A case series of Wiskott-Aldrich syndrome, CARMIL2 and DOCK8 deficiency and review of the literature
David Kim et al.
ANNALS OF DIAGNOSTIC PATHOLOGY (2019)
Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency
Susanne E. Aydin et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE (2019)
Hematopoietic stem cell transplant effectively rescues lymphocyte differentiation and function in DOCK8-deficient patients
Bethany A. Pillay et al.
JCI INSIGHT (2019)
Dedicator of cytokinesis 8-deficient CD4+ T cells are biased to a TH2 effector fate at the expense of TH1 and TH17 cells
Stuart G. Tangye et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2017)
A human immunodeficiency syndrome caused by mutations in CARMIL2
T. Schober et al.
NATURE COMMUNICATIONS (2017)
DOCK8 deficiency: Insights into pathophysiology, clinical features and management
Catherine M. Biggs et al.
CLINICAL IMMUNOLOGY (2017)
Haploidentical Related Donor Hematopoietic Stem Cell Transplantation for Dedicator-of-Cytokinesis 8 Deficiency Using Post-Transplantation Cyclophosphamide
Nirali N. Shah et al.
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION (2017)
The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis
Bernd Hartz et al.
BLOOD (2016)
Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE
Anne-Kathrin Kienzler et al.
CLINICAL IMMUNOLOGY (2016)
Food allergies can persist after myeloablative hematopoietic stem cell transplantation in dedicator of cytokinesis 8-deficient patients
Corinne S. Happel et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2016)
Hematopoietic stem cell transplantation outcomes for 11 patients with dedicator of cytokinesis 8 deficiency
Waleed Al-Herz et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2016)
Recent Advances in DOCK8 Immunodeficiency Syndrome
Qian Zhang et al.
JOURNAL OF CLINICAL IMMUNOLOGY (2016)
Treosulfan-based conditioning regimens for allogeneic haematopoietic stem cell transplantation in children with non-malignant diseases
M. A. Slatter et al.
BONE MARROW TRANSPLANTATION (2015)
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
Karin R. Engelhardt et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2015)
DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
Susanne E. Aydin et al.
JOURNAL OF CLINICAL IMMUNOLOGY (2015)
STAT3 is a central regulator of lymphocyte differentiation and function
Alisa Kane et al.
CURRENT OPINION IN IMMUNOLOGY (2014)
Dedicator of cytokinesis 8-deficient patients have a breakdown in peripheral B-cell tolerance and defective regulatory T cells
Erin Janssen et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2014)
Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype
Huie Jing et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2014)
Dedicator of Cytokinesis 8 Interacts with Talin and Wiskott-Aldrich Syndrome Protein To Regulate NK Cell Cytotoxicity
Hyoungjun Ham et al.
JOURNAL OF IMMUNOLOGY (2013)
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation
Haifa H. Jabara et al.
NATURE IMMUNOLOGY (2012)
Successful bone marrow transplantation for DOCK8 deficient hyper IgE syndrome
Ayse Metin et al.
PEDIATRIC TRANSPLANTATION (2012)
IL-21 is the primary common γ chain-binding cytokine required for human B-cell differentiation in vivo
Mike Recher et al.
BLOOD (2011)
Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study
Daniele Moratto et al.
BLOOD (2011)
DOCK8 is essential for T-cell survival and the maintenance of CD8+ T-cell memory
Teresa Lambe et al.
EUROPEAN JOURNAL OF IMMUNOLOGY (2011)
Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency
Vincent Barlogis et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2011)
DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice
Katrina L. Randall et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2011)
Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency
Douglas R. McDonald et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2010)
Successful Long-Term Correction of Autosomal Recessive Hyper-IgE Syndrome due to DOCK8 Deficiency by Hematopoietic Stem Cell Transplantation
T. C. Bittner et al.
KLINISCHE PADIATRIE (2010)
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
Karin R. Engelhardt et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2009)
Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production
Katrina L. Randall et al.
NATURE IMMUNOLOGY (2009)
Combined Immunodeficiency Associated with DOCK8 Mutations
Qian Zhang et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)