Výsledky vyhledávání - "Shervin, Gholizadeh"

Akademický článek

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Interregulation between fragile X mental retardation protein and methyl CpG binding protein 2 in the mouse posterior cerebral cortex

Autor: Lu-Yang Wang, Tian Kong, David R. Hampson, Enea Koxhioni, Yosuke Niibori, James H. Eubanks, Alexander W.M. Hooper, Shervin Gholizadeh, Jason Arsenault, Laura K. K. Pacey

Publikováno v: Human Molecular Genetics

Several X-linked neurodevelopmental disorders including Rett syndrome, induced by mutations in the MECP2 gene, and fragile X syndrome (FXS), caused by mutations in the FMR1 gene, share autism-related features. The mRNA coding for methyl CpG binding p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5597bf9877fb975144e909fff1b7f96
https://doi.org/10.1093/hmg/ddaa226

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Akademický článek

Early versus late-phase consolidation of opiate reward memories requires distinct molecular and temporal mechanisms in the amygdala-prefrontal cortical pathway.

Autor: Shervin Gholizadeh, Ninglei Sun, Xavier De Jaeger, Melanie Bechard, Lique Coolen, Steven R Laviolette

Publikováno v: PLoS ONE, Vol 8, Iss 5, p e63612 (2013)

The consolidation of newly acquired memories involves the temporal transition from a recent, less stable trace to a more permanent consolidated form. Opiates possess potent rewarding effects and produce powerful associative memories. The activation o

Externí odkaz: https://doaj.org/article/bd56ea9cc4b64adcbc39b8b1ebdd1ba6

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Burden and cost of comorbidities in patients with neuromyelitis optica spectrum disorder

Autor: Fabio Magrini, Lawrence J. Cook, Alex Exuzides, Andy Surinach, Craig S. Meyer, Daniel Sheinson, Shervin Gholizadeh, Michael R. Yeaman, Paris Sidiropoulos

Publikováno v: Journal of the Neurological Sciences. 427:117530

Neuromyelitis optica spectrum disorder (NMOSD) is associated with various comorbidities, including non-autoimmune and autoimmune conditions. The burden and cost of illness for NMOSD are unclear, particularly in the context of comorbidities.Claims dat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f4e59c84fefce20208a5e6f878943f8
https://doi.org/10.1016/j.jns.2021.117530

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The costs of care from a US claims database in patients with neuromyelitis optica spectrum disorder

Autor: Andy Surinach, Paris Sidiropoulos, Daniel Sheinson, Alex Exuzides, Michael R. Yeaman, Fabio Magrini, Lawrence J. Cook, Craig S. Meyer, Shervin Gholizadeh

Publikováno v: Journal of the Neurological Sciences. 427:117553

Background Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disease of the central nervous system that often leads to severe disability. Patients with highly active NMOSD have approximately a 10-times higher hospital inpatient admi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::558cc8a0cbf7898d2413c370570e1365
https://doi.org/10.1016/j.jns.2021.117553

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Melatonin reverses H-89 induced spatial memory deficit: Involvement of oxidative stress and mitochondrial function

Autor: Ghorban Taghizadeh, Gelareh Vakilzadeh, Tina Khorshidahmad, Mehdi Gharghabi, Mehdi Sanati, Mehdi Aghsami, Mohammad Sharifzadeh, Shervin Gholizadeh, Hajar Mehdizadeh, Rojin Sharif

Publikováno v: Behavioural Brain Research. 316:115-124

Oxidative stress and mitochondrial dysfunction play indispensable role in memory and learning impairment. Growing evidences have shed light on anti-oxidative role for melatonin in memory deficit. We have previously reported that inhibition of protein

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad221488e85205b4c1d010fafa5430d2
https://doi.org/10.1016/j.bbr.2016.08.040

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Expression of fragile X mental retardation protein in neurons and glia of the developing and adult mouse brain

Autor: David R. Hampson, Shervin Gholizadeh, Sebok Kumar Halder

Publikováno v: Brain Research. 1596:22-30

Fragile X syndrome is the most common inherited form of mental retardation and autism. It is caused by a reduction or elimination of the expression of fragile X mental retardation protein (FMRP). Because fragile X syndrome is a neurodevelopmental dis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b86913f76a874ef97d62450b5aa84366
https://doi.org/10.1016/j.brainres.2014.11.023

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