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Rocío Pérez-González

Researcher at Nathan Kline Institute for Psychiatric Research

Publications -  35
Citations -  1464

Rocío Pérez-González is an academic researcher from Nathan Kline Institute for Psychiatric Research. The author has contributed to research in topics: Microvesicles & Neuroprotection. The author has an hindex of 16, co-authored 29 publications receiving 1083 citations. Previous affiliations of Rocío Pérez-González include New York University.

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The Exosome Secretory Pathway Transports Amyloid Precursor Protein Carboxyl-terminal Fragments from the Cell into the Brain Extracellular Space

TL;DR: It is hypothesized that the exosome secretory pathway plays a pleiotropic role in the brain:Exosome secretion is beneficial to the cell, acting as a specific releasing system of neurotoxic APP CTFs and Aβ, but the secretion of exosomes enriched with APP C TFs, neurotoxic proteins that are also a source of secreted Aβ is harmful to the brain.
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Mitovesicles are a novel population of extracellular vesicles of mitochondrial origin altered in Down syndrome.

TL;DR: Using a high-resolution density gradient separation of extracellular vesicles (EVs) isolated from murine and human DS and diploid control brains, this paper identified and characterized a previously unknown population of double-membraned EVs containing multiple mitochondrial proteins distinct from previously described EV subtypes, including microvesicles and exosomes.
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Leptin induces proliferation of neuronal progenitors and neuroprotection in a mouse model of Alzheimer's disease.

TL;DR: It is suggested that in AβPP/PS1 mice, leptin exerts changes resembling acute neurotrophic and neuroprotective effects, which could serve as the basis for the design of future treatment strategies in AD.
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Enhanced exosome secretion in Down syndrome brain - a protective mechanism to alleviate neuronal endosomal abnormalities

TL;DR: It is found that exosome secretion is enhanced in the brains of DS patients and a mouse model of the disease, and by DS fibroblasts, and increased levels of the tetraspanin CD63, a regulator ofExosome biogenesis, were observed in DS brains, suggesting the upregulation of exosomes represents a potential therapeutic goal for neurodegenerative disorders with endosomal pathology.
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The ANKK1 kinase gene and psychiatric disorders.

TL;DR: Current data show that the TaqIA polymorphism may be a marker of both DRD2 and ANKK1 genetic variants, which raises the question of whether signaling players intervene in the pathophysiology of psychiatric disorders.