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UnknownGermline-activating mutations in PIK3CD compromise B cell development and function.
Not available
S-EPMC6080914 | biostudies-literature
UnknownAutoantibodies against type I IFNs in patients with critical influenza pneumonia.
Not available
S-EPMC9485705 | biostudies-literature
UnknownHuman germline heterozygous gain-of-function STAT6 variants cause severe allergic disease.
Not available
S-EPMC10037107 | biostudies-literature
UnknownWhole-genome sequencing of a sporadic primary immunodeficiency cohort.
Not available
S-EPMC7334047 | biostudies-literature
UnknownRecessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia.
Not available
S-EPMC9206114 | biostudies-literature
UnknownRespiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
Not available
S-EPMC9178406 | biostudies-literature
UnknownRare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
Not available
S-EPMC10074346 | biostudies-literature
UnknownQuality of life after pharmacomechanical catheter-directed thrombolysis for proximal deep venous thrombosis.
Not available
S-EPMC7681916 | biostudies-literature
UnknownThe risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies.
Not available
S-EPMC9173764 | biostudies-literature
UnknownX-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.
Not available
S-EPMC8532080 | biostudies-literature
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