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Michael V. Sofroniew

Researcher at University of California, Los Angeles

Publications -  194
Citations -  39697

Michael V. Sofroniew is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: Cholinergic neuron & Astrocyte. The author has an hindex of 81, co-authored 183 publications receiving 33948 citations. Previous affiliations of Michael V. Sofroniew include University of California & Medical Research Council.

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Astrocytes: biology and pathology

TL;DR: Astrocyte functions in healthy CNS, mechanisms and functions of reactive astrogliosis and glial scar formation, and ways in which reactive astrocytes may cause or contribute to specific CNS disorders and lesions are reviewed.
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Molecular dissection of reactive astrogliosis and glial scar formation.

TL;DR: Developments in the signaling mechanisms that regulate specific aspects of reactive astrogliosis are reviewed and the potential to identify novel therapeutic molecular targets for diverse neurological disorders is highlighted.
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Reactive astrocytes protect tissue and preserve function after spinal cord injury.

TL;DR: The findings show that reactive astrocytes provide essential activities that protect tissue and preserve function after mild or moderate SCI, and suggest that identifying ways to preserve reactive astracytes, to augment their protective functions, or both, may lead to novel approaches to reducing secondary tissue degeneration and improving functional outcome after SCI.
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Astrocyte scar formation aids central nervous system axon regeneration

TL;DR: Interestingly, RNA sequencing revealed that astrocytes and non-astrocyte cells in SCI lesions express multiple axon-growth-supporting molecules, showing that contrary to the prevailing dogma, astroCyte scar formation aids rather than prevents central nervous system axon regeneration.
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Nerve growth factor signaling, neuroprotection, and neural repair

TL;DR: Expanded roles for NGF that are associated with the dynamically regulated production of NGF and its receptors that begins in development, extends throughout adult life and aging, and involves a surprising variety of neurons, glia, and nonneural cells are considered.