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2021
(4)
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A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes.
Not available
S-EPMC8604862
|
biostudies-literature
Cite
Design of a targeted blood transcriptional panel for monitoring immunological changes accompanying pregnancy.
Not available
S-EPMC10861739
|
biostudies-literature
Cite
Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome.
Not available
S-EPMC7418179
|
biostudies-literature
Cite
A deep intronic splice mutation of
STAT3
underlies hyper IgE syndrome by negative dominance.
Not available
S-EPMC6697804
|
biostudies-literature
Cite
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β.
Not available
S-EPMC7014825
|
biostudies-literature
Cite
Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.
Not available
S-EPMC8409595
|
biostudies-literature
Cite
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency.
Not available
S-EPMC6170168
|
biostudies-literature
Cite
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance.
Not available
S-EPMC8217968
|
biostudies-literature
Cite
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity.
Not available
S-EPMC6141026
|
biostudies-literature
Cite
Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy.
Not available
S-EPMC8329841
|
biostudies-literature
Cite
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