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UnknownSystematic screening for primary immunodeficiencies in patients hospitalized for severe infection in pediatric intensive care unit.
Not available
S-EPMC12214530 | biostudies-literature
UnknownDominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.
Not available
S-EPMC7971136 | biostudies-literature
UnknownGermline-activating mutations in PIK3CD compromise B cell development and function.
Not available
S-EPMC6080914 | biostudies-literature
UnknownHomozygous NLRP1 gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosis.
Not available
S-EPMC6754618 | biostudies-literature
UnknownActivating mutations in PIK3CD disrupt the differentiation and function of human and murine CD4+ T cells.
Not available
S-EPMC6612302 | biostudies-literature
UnknownIFN-γ and CD25 drive distinct pathologic features during hemophagocytic lymphohistiocytosis.
Not available
S-EPMC7117880 | biostudies-literature
UnknownFactors associated with and kinetics of anti-IFN-α autoantibodies in <i>RAG1/2</i> deficiency.
Not available
S-EPMC12281840 | biostudies-literature
UnknownAutoantibodies against type I IFNs in patients with critical influenza pneumonia.
Not available
S-EPMC9485705 | biostudies-literature
UnknownA loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes.
Not available
S-EPMC9026234 | biostudies-literature
UnknownHuman germline heterozygous gain-of-function STAT6 variants cause severe allergic disease.
Not available
S-EPMC10037107 | biostudies-literature
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