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Emily R. Rosario

Researcher at University of Southern California

Publications -  31
Citations -  2929

Emily R. Rosario is an academic researcher from University of Southern California. The author has contributed to research in topics: Androgen & Estrogen. The author has an hindex of 20, co-authored 24 publications receiving 2637 citations.

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β-Amyloid Oligomers Induce Phosphorylation of Tau and Inactivation of Insulin Receptor Substrate via c-Jun N-Terminal Kinase Signaling: Suppression by Omega-3 Fatty Acids and Curcumin

TL;DR: Data indicate JNK mediates Aβ oligomer inactivation of IRS-1 and phospho-tau pathology and that dietary treatment with fish oil/DHA, curcumin, or a combination of both has the potential to improve insulin/trophic signaling and cognitive deficits in AD.
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Protective actions of sex steroid hormones in Alzheimer's disease.

TL;DR: The successful use of hormone therapies in aging men and women to delay, prevent, and or treat AD will require additional research to optimize key parameters of hormone therapy and may benefit from the continuing development of selective estrogen and androgen receptor modulators.
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Progesterone and Estrogen Regulate Alzheimer-Like Neuropathology in Female 3xTg-AD Mice

TL;DR: It is demonstrated that estrogen and progesterone independently and interactively regulate AD-like neuropathology and suggest that an optimized hormone therapy may be useful in reducing the risk of AD in postmenopausal women.
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Brain levels of sex steroid hormones in men and women during normal aging and in Alzheimer's disease

TL;DR: Sex-specific relationships between normal, age-related depletion of androgens and estrogens in men and women, which may be relevant to development of AD, are demonstrated.
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Sex differences in β-amyloid accumulation in 3xTg-AD mice: Role of neonatal sex steroid hormone exposure

TL;DR: Compared progression of β-amyloid pathology in male and female triple transgenic mice is compared to demonstrate significant sex differences in pathology in 3xTg-AD mice and suggest that these differences may be mediated by organizational actions of sex steroid hormones during development.