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Immunodeficiency in adults a practical guide for the allergistThe multiple faces of leukocyte interstitial migrationActin cytoskeletal defects in immunodeficiencyMechanism-Based Strategies for the Management of Autoimmunity and Immune Dysregulation in Primary ImmunodeficienciesDOCK8 regulates lymphocyte shape integrity for skin antiviral immunityPrimary immunodeficiencies underlying fungal infectionsSomatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype.A 17-year old patient with DOCK8 deficiency, severe oral HSV-1 and aggressive periodontitis - a case of virally induced periodontitis?HkRP3 is a microtubule-binding protein regulating lytic granule clustering and NK cell killing.Inborn errors of human IL-17 immunity underlie chronic mucocutaneous candidiasis.Partial defects of T-cell development associated with poor T-cell function.CNS vasculitis and stroke as a complication of DOCK8 deficiency: a case reportDOCK8 deficiency in six Iranian patients.Recent Advances in DOCK8 Immunodeficiency Syndrome.Immunity to infection in IL-17-deficient mice and humansAdditional diverse findings expand the clinical presentation of DOCK8 deficiency.Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait.Hemoptysis in a Patient with Elevated Immunoglobulin E.DOCK 8 Deficiency, EBV+ Lymphomatoid Granulomatosis, and Intrafamilial Variation in Presentation.Primary Immunodeficiencies with Elevated IgE.Predispositions to Lymphoma: A Practical Review for Genetic Counselors.Atopic Dermatitis and Allergic Urticaria: Cutaneous Manifestations of Immunodeficiency.Mechanisms of Impaired Neutrophil Migration by MicroRNAs in Myelodysplastic Syndromes.Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH17 cell differentiation.Successful haploidentical donor hematopoietic stem cell transplant and restoration of STAT3 function in an adolescent with autosomal dominant hyper-IgE syndrome.Novel dedicator of cytokinesis 8 mutations identified by multiplex ligation-dependent probe amplification.Atopic dermatitis, STAT3- and DOCK8-hyper-IgE syndromes differ in IgE-based sensitization pattern.Low immunoglobulin E flags two distinct types of immune dysregulation.Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen.DOCK8 regulates fitness and function of regulatory T cells through modulation of IL-2 signaling.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
DOCK8 deficiency.
@en
DOCK8 deficiency.
@nl
type
label
DOCK8 deficiency.
@en
DOCK8 deficiency.
@nl
prefLabel
DOCK8 deficiency.
@en
DOCK8 deficiency.
@nl
P2860
P1476
DOCK8 deficiency
@en
P2093
P2860
P356
10.1111/J.1749-6632.2011.06295.X
P407
P50
P577
2011-12-01T00:00:00Z