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miR-361-5p contributes to the pathogenesis of Alzheimer’s disease
by
Rezazadeh, Maryam
, Talebi, Mahnaz
, Jalaiei, Abbas
, Arsang-Jang, Shahram
, Ghafouri-Fard, Soudeh
, Gharesouran, Jalal
in
631/80
/ 692/617/375
/ Aged
/ Aged, 80 and over
/ Alzheimer Disease - genetics
/ Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ ATAD1
/ Bioinformatics
/ Biomarkers
/ Brain - metabolism
/ Brain - pathology
/ Cognitive ability
/ Cytokines
/ Disease
/ DNA-Binding Proteins - genetics
/ DNA-Binding Proteins - metabolism
/ Endocytosis
/ Female
/ Gene expression
/ Gene Expression Regulation
/ Glutamatergic synapses
/ Glutamatergic transmission
/ Homer Scaffolding Proteins - genetics
/ Homer Scaffolding Proteins - metabolism
/ HOMER1
/ Humanities and Social Sciences
/ Humans
/ Male
/ Membrane Proteins - genetics
/ Membrane Proteins - metabolism
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Middle Aged
/ MIR-361
/ multidisciplinary
/ Neurodegenerative diseases
/ Pathogenesis
/ Polymerase chain reaction
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Thermal cycling
2025
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miR-361-5p contributes to the pathogenesis of Alzheimer’s disease
by
Rezazadeh, Maryam
, Talebi, Mahnaz
, Jalaiei, Abbas
, Arsang-Jang, Shahram
, Ghafouri-Fard, Soudeh
, Gharesouran, Jalal
in
631/80
/ 692/617/375
/ Aged
/ Aged, 80 and over
/ Alzheimer Disease - genetics
/ Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ ATAD1
/ Bioinformatics
/ Biomarkers
/ Brain - metabolism
/ Brain - pathology
/ Cognitive ability
/ Cytokines
/ Disease
/ DNA-Binding Proteins - genetics
/ DNA-Binding Proteins - metabolism
/ Endocytosis
/ Female
/ Gene expression
/ Gene Expression Regulation
/ Glutamatergic synapses
/ Glutamatergic transmission
/ Homer Scaffolding Proteins - genetics
/ Homer Scaffolding Proteins - metabolism
/ HOMER1
/ Humanities and Social Sciences
/ Humans
/ Male
/ Membrane Proteins - genetics
/ Membrane Proteins - metabolism
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Middle Aged
/ MIR-361
/ multidisciplinary
/ Neurodegenerative diseases
/ Pathogenesis
/ Polymerase chain reaction
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Thermal cycling
2025
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miR-361-5p contributes to the pathogenesis of Alzheimer’s disease
by
Rezazadeh, Maryam
, Talebi, Mahnaz
, Jalaiei, Abbas
, Arsang-Jang, Shahram
, Ghafouri-Fard, Soudeh
, Gharesouran, Jalal
in
631/80
/ 692/617/375
/ Aged
/ Aged, 80 and over
/ Alzheimer Disease - genetics
/ Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ ATAD1
/ Bioinformatics
/ Biomarkers
/ Brain - metabolism
/ Brain - pathology
/ Cognitive ability
/ Cytokines
/ Disease
/ DNA-Binding Proteins - genetics
/ DNA-Binding Proteins - metabolism
/ Endocytosis
/ Female
/ Gene expression
/ Gene Expression Regulation
/ Glutamatergic synapses
/ Glutamatergic transmission
/ Homer Scaffolding Proteins - genetics
/ Homer Scaffolding Proteins - metabolism
/ HOMER1
/ Humanities and Social Sciences
/ Humans
/ Male
/ Membrane Proteins - genetics
/ Membrane Proteins - metabolism
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Middle Aged
/ MIR-361
/ multidisciplinary
/ Neurodegenerative diseases
/ Pathogenesis
/ Polymerase chain reaction
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Thermal cycling
2025
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miR-361-5p contributes to the pathogenesis of Alzheimer’s disease
Journal Article
miR-361-5p contributes to the pathogenesis of Alzheimer’s disease
2025
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Overview
Alzheimer’s disease (AD) is a progressive neurodegenerative disorder. This study investigated the roles of HOMER1, ATAD1, and miR-361 in AD pathogenesis using microarray (GSE106241, GSE157239; n = 60) and RT-PCR (n = 100; 50 AD patients, 50 controls from Northwest Iran) analyses. Decreased expression of HOMER1 and ATAD1, key regulators of glutamatergic synapses, and miR-361, a potential regulator of both, was observed in AD brain tissue (GSE106241, categorized into seven Braak stages), suggesting a link between their dysregulation, impaired synaptic function, and increased neuroinflammation. However, blood-based RT-PCR showed no significant difference in HOMER1 or ATAD1. miR-361 was significantly lower in AD patients (adjusted p < 0.043). These findings, limited by sample size and lacking a formal power analysis, require further investigation to validate their potential as peripheral biomarkers for AD. Future studies with larger sample sizes are warranted.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ Aged
/ Alzheimer Disease - genetics
/ Alzheimer Disease - metabolism
/ Alzheimer Disease - pathology
/ ATAD1
/ Disease
/ DNA-Binding Proteins - genetics
/ DNA-Binding Proteins - metabolism
/ Female
/ Homer Scaffolding Proteins - genetics
/ Homer Scaffolding Proteins - metabolism
/ HOMER1
/ Humanities and Social Sciences
/ Humans
/ Male
/ Membrane Proteins - genetics
/ Membrane Proteins - metabolism
/ MIR-361
/ Proteins
/ Science
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