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Monte J. Radeke

Researcher at University of California, Santa Barbara

Publications -  43
Citations -  5655

Monte J. Radeke is an academic researcher from University of California, Santa Barbara. The author has contributed to research in topics: Neurotrophin & Retinal pigment epithelium. The author has an hindex of 29, co-authored 42 publications receiving 5289 citations.

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Differential regulation of mRNA encoding nerve growth factor and its receptor in rat sciatic nerve during development, degeneration, and regeneration: role of macrophages.

TL;DR: Taniuchi et al. as discussed by the authors found that the levels of nerve growth factor (NGF) mRNA (mRNANGF) and NGF receptor mRNA(mRNA(rec)) in the sciatic nerve were 10 and 120 times higher, respectively, than in adult animals.
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The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis re-visited.

TL;DR: This article revisits the original hypothesis that chronic local inflammatory and immune-mediated events at the level of Bruch's membrane play critical roles in drusen biogenesis and, by extension, in the pathobiology of AMD, and identifies and characterize the local complement system in the RPE-choroid complex.
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Immunocytochemical localization of TrkB in the central nervous system of the adult rat.

TL;DR: The detection of TrkB immunoreactivity on cell bodies and dendrites is consistent with recent models suggesting that neurotrophins may be derived from presynaptic and/or autocrine sources in addition to the classical postsynaptic target.
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The Alzheimer's Aβ-peptide is deposited at sites of complement activation in pathologic deposits associated with aging and age-related macular degeneration

TL;DR: It is shown that Aβ is associated with a substructural vesicular component within drusen, which could be an important component of the local inflammatory events that contribute to atrophy of the retinal pigmented epithelium, Drusen biogenesis, and the pathogenesis of AMD.
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Developmental and mature expression of full-length and truncated TrkB receptors in the rat forebrain.

TL;DR: The dendritic localization of trkB receptors supports the hypothesis that dendrites, as well as axons, are important sites for neurotrophin actions in the central nervous system.