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Natalia V. Gulyaeva

Researcher at Russian Academy of Sciences

Publications -  267
Citations -  2897

Natalia V. Gulyaeva is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Hippocampus & Hippocampal formation. The author has an hindex of 24, co-authored 241 publications receiving 2334 citations. Previous affiliations of Natalia V. Gulyaeva include Russian Academy & Moscow State University.

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Phosphorylated neurofilament heavy subunits as a marker of neurodegeneration in demyelinating diseases of the CNS

TL;DR: It is concluded that neurodegeneration occurs in RMS, ADEM, and ALS and the pNFH content should be studied in larger cohorts of patients and at strictly defined time points.
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Exosomes secretion and autophagy in long-term protection of neurons from excitotoxic damage

TL;DR: It is suggested that the long-term effects of preconditioning may be mediated by exosome secretion, as shown by dot blot of extracellular fluid using anti-CD63 antibody.
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The Neurochemistry of Stress: the Chemistry of the Stress Response and Stress Vulnerability

TL;DR: The stress response may have to be measured; important goals of translational studies include validation of animal models of depression and unification of physiological and biochemical indices of the stress response for comparative analysis of different models and data from depressive patients, as well as elaboration of valid indices of The neurochemistry of depression is the essence of most stress-related mental and neurologic diseases.
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7,8-DHF enhances SHH in the hippocampus and striatum during early abstinence but has minor effects on alcohol intake in IA2BC paradigm and abstinence-related anxiety-like behavior in rats

TL;DR: In this article , the effect of 7,8-DHF on drinking pattern, anxiety-like behavior and expression of SHH and a downstream transcription factor, GLI, in the limbic brain structures during early abstinence after voluntary alcohol intake was investigated.
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Good guys from a shady family.

TL;DR: Effects of b-carbolines seem to be highly dependent on modifying substituents, providing a promising potential for the design of useful synthetic analogs of natural substances by rearing good guys in the shady b-carboline family.