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Publisher Correction: TGFβ signaling mediates microglial resilience to spatiotemporally restricted myelin degeneration.

  • Read more about Publisher Correction: TGFβ signaling mediates microglial resilience to spatiotemporally restricted myelin degeneration.

A generalizable foundation model for analysis of human brain MRI.

  • Read more about A generalizable foundation model for analysis of human brain MRI.

TGFß signaling mediates microglial resilience to spatiotemporally restricted myelin degeneration.

  • Read more about TGFß signaling mediates microglial resilience to spatiotemporally restricted myelin degeneration.

Proinflammatory immune cells disrupt angiogenesis and promote germinal matrix hemorrhage in prenatal human brain.

  • Read more about Proinflammatory immune cells disrupt angiogenesis and promote germinal matrix hemorrhage in prenatal human brain.

CRISPRi screens in human iPSC-derived astrocytes elucidate regulators of distinct inflammatory reactive states.

  • Read more about CRISPRi screens in human iPSC-derived astrocytes elucidate regulators of distinct inflammatory reactive states.

Developmental dynamics of RNA translation in the human brain.

  • Read more about Developmental dynamics of RNA translation in the human brain.

CNS fibroblasts form a fibrotic scar in response to immune cell infiltration.

  • Read more about CNS fibroblasts form a fibrotic scar in response to immune cell infiltration.

Microglial Gi-dependent dynamics regulate brain network hyperexcitability.

  • Read more about Microglial Gi-dependent dynamics regulate brain network hyperexcitability.

Aberrant oligodendroglial-vascular interactions disrupt the blood-brain barrier, triggering CNS inflammation.

  • Read more about Aberrant oligodendroglial-vascular interactions disrupt the blood-brain barrier, triggering CNS inflammation.

Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.

  • Read more about Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.

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