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All eyes on a phosphatase in glioma stem cells.

  • Read more about All eyes on a phosphatase in glioma stem cells.

A SHHecret target of relapsed medulloblastoma: Astrocytes.

  • Read more about A SHHecret target of relapsed medulloblastoma: Astrocytes.

A human mutation in STAT3 promotes type 1 diabetes through a defect in CD8+ T cell tolerance.

  • Read more about 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.

  • Read more about Constrained chromatin accessibility in PU.1-mutated agammaglobulinemia patients.

The epigenetic regulator ATF7ip inhibits Il2 expression, regulating Th17 responses.

  • Read more about The epigenetic regulator ATF7ip inhibits Il2 expression, regulating Th17 responses.

Impaired aVß8 and TGFß signaling lead to microglial dysmaturation and neuromotor dysfunction.

  • Read more about Impaired aVß8 and TGFß signaling lead to microglial dysmaturation and neuromotor dysfunction.

GPR56/ADGRG1 regulates development and maintenance of peripheral myelin.

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EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay.

  • Read more about 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.

  • Read more about 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.

  • Read more about Identification of a novel cis-regulatory element essential for immune tolerance.

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