Michael Greenberg

Michael Greenberg, Ph.D.

Nathan Marsh Pusey Professor of Neurobiology, Harvard Medical School
Professor of Neurology, Boston Children's Hospital
Director of the Hock E. Tan and K. Lisa Yang Center for Autism Research, Harvard Medical School

Michael Greenberg, Ph.D. – Faculty Profile

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Title: Nathan Marsh Pusey Professor of Neurobiology, Harvard Medical School; Director of the Hock E. Tan and K. Lisa Yang Center for Autism Research, Harvard Medical School; Professor of Neurology, Boston Children's Hospital.

The Aim

The Greenberg Lab studies how life experiences turn genes on or off to shape learning and brain development. The lab focuses on the molecular mechanisms by which sensory experiences regulate gene expression in the brain.

The Impact

This research has illuminated how the brain rewires itself in response to experience, a process essential for learning, memory, and behavior. Several of the genes and pathways the lab has identified are mutated in autism and other neurodevelopmental disorders, positioning this work as foundational for developing new therapies for these conditions.

A Closer Look

Article: State of Stasis , Harvard Medical School / Harvard Gazette, June 2020. This piece describes how Mike Greenberg and colleagues identified a tiny cluster of hypothalamic neurons that can flip mice into and out of a hibernation‑like state, or torpor, revealing brain circuits that dial down body temperature and metabolism and opening avenues for understanding suspended animation and its medical uses.

Article: Decoding Brain Evolution , Harvard Medical School, December 2021. This article highlights Mike Greenberg’s co‑leadership of the Allen Discovery Center for Human Brain Evolution, which links evolutionary genetic variants to their effects in neurons to explain how human brains acquired uniquely human cognitive and behavioral capacities.

Contact

Email: michael_greenberg@hms.harvard.edu
Lab website: greenberg.hms.harvard.edu

Publications View
A defect in nurturing in mice lacking the immediate early gene fosB.
Authors: Authors: Brown JR, Ye H, Bronson RT, Dikkes P, Greenberg ME.
Cell
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E2F-1 functions in mice to promote apoptosis and suppress proliferation.
Authors: Authors: Field SJ, Tsai FY, Kuo F, Zubiaga AM, Kaelin WG, Livingston DM, Orkin SH, Greenberg ME.
Cell
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Stimulation of growth factor receptor signal transduction by activation of voltage-sensitive calcium channels.
Authors: Authors: Rosen LB, Greenberg ME.
Proc Natl Acad Sci U S A
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Ca(2+)-dependent routes to Ras: mechanisms for neuronal survival, differentiation, and plasticity?
Authors: Authors: Finkbeiner S, Greenberg ME.
Neuron
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Light entrainment and activation of signal transduction pathways in the SCN.
Authors: Authors: Kornhauser JM, Ginty DD, Greenberg ME, Mayo KE, Takahashi JS.
Prog Brain Res
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Intracellular signaling pathways activated by neurotrophic factors.
Authors: Authors: Segal RA, Greenberg ME.
Annu Rev Neurosci
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Signal transduction pathways activated by ciliary neurotrophic factor and related cytokines.
Authors: Authors: Frank DA, Greenberg ME.
Perspect Dev Neurobiol
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Opposing effects of ERK and JNK-p38 MAP kinases on apoptosis.
Authors: Authors: Xia Z, Dickens M, Raingeaud J, Davis RJ, Greenberg ME.
Science
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Induction of a nerve growth factor-sensitive kinase that phosphorylates the DNA-binding domain of the orphan nuclear receptor NGFI-B.
Authors: Authors: Hirata Y, Whalin M, Ginty DD, Xing J, Greenberg ME, Milbrandt J, Guroff G.
J Neurochem
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Interleukin 2 signaling involves the phosphorylation of Stat proteins.
Authors: Authors: Frank DA, Robertson MJ, Bonni A, Ritz J, Greenberg ME.
Proc Natl Acad Sci U S A
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