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The TNF family member TL1A induces IL-22 secretion in committed human T
h
17 cells via IL-9 induction.
Not available
S-EPMC6608031
|
biostudies-literature
Cite
Rare variants in <i>PRKCI</i> cause Van der Woude syndrome and other features of peridermopathy.
Not available
S-EPMC11759255
|
biostudies-literature
Cite
Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease.
Not available
S-EPMC6439872
|
biostudies-literature
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Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
Not available
S-EPMC3084597
|
biostudies-literature
Cite
Therapeutic Anticoagulation with Heparin in Noncritically Ill Patients with Covid-19.
Not available
S-EPMC8362594
|
biostudies-literature
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Baricitinib in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial and updated meta-analysis.
Not available
S-EPMC9333998
|
biostudies-literature
Cite
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosis.
Not available
S-EPMC11036449
|
biostudies-literature
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Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Not available
S-EPMC3491803
|
biostudies-literature
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Stroke genetics informs drug discovery and risk prediction across ancestries.
Not available
S-EPMC9524349
|
biostudies-literature
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Higher dose corticosteroids in patients admitted to hospital with COVID-19 who are hypoxic but not requiring ventilatory support (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC10156147
|
biostudies-literature
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