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Richard J. Smeyne

Researcher at Thomas Jefferson University

Publications -  130
Citations -  13895

Richard J. Smeyne is an academic researcher from Thomas Jefferson University. The author has contributed to research in topics: Substantia nigra & MPTP. The author has an hindex of 55, co-authored 122 publications receiving 12857 citations. Previous affiliations of Richard J. Smeyne include University of Medicine and Dentistry of New Jersey & Hoffmann-La Roche.

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Severe sensory and sympathetic neuropathies in mice carrying a disrupted Trk/NGF receptor gene

TL;DR: These findings demonstrate that Trk is the primary mediator of the trophic actions of NGF in vivo and that this signalling pathway plays a crucial role in the development of both the peripheral and the central nervous systems.
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Continuous c-fos expression precedes programmed cell death in vivo

TL;DR: Evidence is provided showing that the continuous expression of Fos, beginning hours or days before the morphological demise of the cell, appears to be a hallmark of terminal differentiation and a harbinger of death.
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Targeted disruption of the trkB neurotrophin receptor gene results in nervous system lesions and neonatal death

TL;DR: Neuroanatomical examination of trkBTK (-/-) mice revealed neuronal deficiencies in the central and peripheral nervous systems, illustrating the role of the gp145trkB protein-tyrosine kinase receptor in the ontogeny of the mammalian nervous system.
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Disruption of the neurotrophin-3 receptor gene trkC eliminates la muscle afferents and results in abnormal movements

TL;DR: It is shown that homozygous mice defective for TrkC tyrosine protein kinase receptors lack la muscle afferent projections to spinal motor neurons and have fewer large myelinated axons in the dorsal root and posterior columns of the spinal cord, indicating that NT3/TrkC-dependent sensory neurons may play a primary role in proprioception, the sense of position and movement of the limbs.
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Nrf2-mediated neuroprotection in the MPTP mouse model of Parkinson's disease : Critical role for the astrocyte

TL;DR: Stark results indicate that Nrf2 expression restricted to astrocytes is sufficient to protect against MPTP andAstrocytic modulation of the NRF2-ARE pathway is a promising target for therapeutics aimed at reducing or preventing neuronal death in PD.