about
DOCK8 deficiency impairs CD8 T cell survival and function in humans and miceCTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferationAutoimmune lymphoproliferative syndrome with somatic Fas mutationsFAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of functionAge-related prevalence and antibiotic resistance of pathogenic staphylococci and streptococci in children with infected atopic dermatitis at a single-specialty center.Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease.B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans.Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type IMutations in STAT3 and diagnostic guidelines for hyper-IgE syndromeSTAT1 hyperphosphorylation and defective IL12R/IL23R signaling underlie defective immunity in autosomal dominant chronic mucocutaneous candidiasis.G6PC3 mutations cause non-syndromic severe congenital neutropenia.Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulationMulticenter experience in hematopoietic stem cell transplantation for serious complications of common variable immunodeficiency.Autoimmunity in human primary immunodeficiency diseases.C1q deficiency leads to the defective suppression of IFN-alpha in response to nucleoprotein containing immune complexes.Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency.TGF-beta(1) genotype and accelerated decline in lung function of patients with cystic fibrosisSTAT3 is a critical cell-intrinsic regulator of human unconventional T cell numbers and functionThe extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.Functional STAT3 deficiency compromises the generation of human T follicular helper cells.X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and Hepatitis.IMMUNODEFICIENCIES. Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations.Suppression of allogeneic reactivity in vitro by the syncytiotrophoblast membrane glycocalyx of the human term placenta is carbohydrate dependent.Recently identified factors predisposing children to infectious diseases.DOCK8 is critical for the survival and function of NKT cellsSignal transducer and activator of transcription 3 (STAT3) mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8(+) T-cell memory formation and function.Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficienciesNaive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cells.IL-21 signalling via STAT3 primes human naive B cells to respond to IL-2 to enhance their differentiation into plasmablasts.Atopic dermatitis in children.Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.Skin pH Is the Master Switch of Kallikrein 5-Mediated Skin Barrier Destruction in a Murine Atopic Dermatitis Model.Clinical features that identify children with primary immunodeficiency diseases.Mycobacterium vaccae reduces scratching behavior but not the rash in NC mice with eczema: a randomized, blinded, placebo-controlled trial.Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD).Fas stimulation of T lymphocytes promotes rapid intercellular exchange of death signals via membrane nanotubes.Human complete Stat-1 deficiency is associated with defective type I and II IFN responses in vitro but immunity to some low virulence viruses in vivo.Haptoglobin is synthesized during granulocyte differentiation, stored in specific granules, and released by neutrophils in response to activation.Differential cytokine secretion results from p65 and c-Rel NF-κB subunit signaling in peripheral blood mononuclear cells of TNF receptor-associated periodic syndrome patients.
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description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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type
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Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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Peter Arkwright
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Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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Peter D Arkwright
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P106
P21
P31
P496
0000-0002-7411-5375