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All eyes on a phosphatase in glioma stem cells.
A SHHecret target of relapsed medulloblastoma: Astrocytes.
A human mutation in STAT3 promotes type 1 diabetes through a defect in CD8+ T cell tolerance.
Constrained chromatin accessibility in PU.1-mutated agammaglobulinemia patients.
The epigenetic regulator ATF7ip inhibits Il2 expression, regulating Th17 responses.
Impaired aVß8 and TGFß signaling lead to microglial dysmaturation and neuromotor dysfunction.
GPR56/ADGRG1 regulates development and maintenance of peripheral myelin.
EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay.
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70.
Identification of a novel cis-regulatory element essential for immune tolerance.