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SCI Abstract
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Epigenetic Regulation of OLIG2 in Glioblastoma: Mechanisms and Therapeutic Targets to Combat Treatment Resistance
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Loss of COL20A1 in Schwann Cells Alters Regeneration of the Neuromuscular Junction and Locomotor Activity in Mice
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Ketogenic Diet Mitigates Age-Related Cognitive Decline and Neuroinflammation in Rats, While Antibiotics Exacerbate Brain Health Risks
The ketogenic diet (KD), a high-fat, low-carbohydrate regimen, has been shown to exert neuroprotective effects in various ...
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Exploring Ciliary Mechanisms in the Causation of Hydrocephalus in Humans—Similarities and Differences from Animal Models
Hydrocephalus is a condition defined by excessive cerebrospinal fluid (CSF) relative to the brain volume. Congenital and i...
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Serum Metabolomic Profiling in Possible Early-Stage Multiple Sclerosis: A Targeted H-NMR Comparison of OCB Type 1 and Type 2 Patterns
Oligoclonal band (OCB) analysis in cerebrospinal fluid (CSF) remains a cornerstone for the early diagnosis of multiple scl...
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Antiepileptic and Neuroprotective Biochemical Actions of Sabinene Prevent the Development of Pentylenetetrazol-Induced Seizures and Neuropsychiatric Comorbidities in Mice
Epilepsy is a long-term neurological disorder that leads to disability with neuropsychiatric comorbidities. Studies have s...
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Cognitive and Behavioral Effects of Chronic Tartrazine Use in vivo: An Assessment Within and Above the Acceptable Daily Intake
The use of dyes is a common practice in several industrial sectors to increase the attractiveness of the merchandise. Tart...
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Correction: Urolithin A Enhances Tight Junction Protein Expression in Endothelial Cells Cultured In Vitro via Pink1-Parkin-Mediated Mitophagy in Irradiated Astrocytes
Department of Neurology, The First Affiliated Hospital, Sun Yat-Sen University, No.58 Zhongshan Road 2, Guangzhou, 510080,...
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Integrin CD11b Alleviates Cerebral Ischemia/Reperfusion Injury via a Mechanism Involving Microglia/Macrophage Polarization
The polarization of microglia/macrophages is crucial for maintaining the neuroinflammatory response during cerebral ischem...
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Salivary Circadian Gene Expression as a Molecular Indicator of Early Cognitive Impairment in Shift Workers: A Cross-Sectional Study of 300 Adults
This cross-sectional study explored the potential utility of salivary circadian gene expression as a non-invasive biomarke...
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Therapeutic Potential of products derived from for Alzheimer’s Disease Treatment
AD is a neurodegenerative disorder and is associated with the presence of amyloid-β plaques and neurofibrillary tangl...
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RGS2-Related Non-coding Interaction Network Modulates the NF-Kappa B Signaling Pathway in MS Patients: A Systems Biology Investigation
Multiple sclerosis (MS) is the most common chronic inflammatory disease affecting the brain and spinal cord, with approxim...
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miR-146A and miR-146B Promoter Methylation and Common Sequence Variations Are Not Likely to Be Involved in Autism Spectrum Disorder
One of the well-studied epigenetic regulators is miRNA (miRNA) which plays critical roles in gene regulation and has been ...
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Comprehensive in Silico Reclassification of MECP2 Variants of Uncertain Significance in Rett Syndrome: Performance Evaluation and Structural Analysis
Rett syndrome (RTT) is a severe neurodevelopmental disorder primarily caused by missense variants in the MECP2 gene. Howev...
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Iron and Ferritin Dyshomeostasis Intersect with Sex, Age, and Disease Severity in Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease, characterized by progressive loss of motor neuro...
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The Impact of Glutamatergic Excitotoxicity on the Differentiation of Cerebellar Neural Stem Cells
The adult cerebellum retains a small Sox2/prominin-1 NSC pool whose fate is shaped by developmental cues and the glutamate...
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Higher Serum Aspartate May be Associated with Better Cognitive Function as Mediated by Reduced Aβ Accumulation in Frontal and Temporal Lobes in Mild Cognitive Impairment
Aspartate, a key excitatory neurotransmitter, has shown conflicting links to cognitive disorders like Alzheimer’s di...
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Spinocerebellar Ataxia Type 1 (SCA1) Cell Models Display Widespread Mitochondrial and Extra-Nuclear Alterations
Ataxin-1 (ATXN1) is a nuclear-cytoplasmic shuttling protein, which, when expanded in its polyglutamine coding stretch, cau...
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Regulation of Hippocamposeptal Synaptic Transmission by GABABRs Is Altered in 5XFAD Mice in a Sex- and Age-Dependent Manner
Hippocamposeptal (HS) neurons send GABAergic projections from the hippocampus to the medial septum/diagonal band of Broca ...
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Sedative Effects of Daidzin, Possibly Through the GABAA Receptor Interaction Pathway: In Vivo Approach with Molecular Dynamic Simulations
The soy isoflavone daidzin (DZN) has been considered a hopeful bioactive compound having diverse biological activities, in...
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REV-ERBα Mitigates Astrocyte Activation and Protects Dopaminergic Neurons from Damage
Parkinson’s disease (PD) is characterized by astrocyte activation and disruptions in circadian rhythm. Within the as...
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Sex-Specific ADNP/NAP (Davunetide) Regulation of Cocaine-Induced Plasticity
Cocaine use disorder (CUD) is a chronic neuropsychiatric disorder estimated to effect 1–3% of the population. Activi...
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Involvement of CXCL10 rs4256246, CXCR4 rs2228014, CCR2 rs1799864 and CXCL16 rs2277680 in the Predisposition to Schizophrenia
Chemokine ligands and their receptors have acquired less attention than pro- and anti-inflammatory cytokines in schizophre...
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Identification and Validation of Endoplasmic Reticulum Stress-Related Gene in Traumatic Brain Injury
Endoplasmic reticulum stress (ERS) plays an essential role in the development of traumatic brain injury (TBI). We aimed to...
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An early Transcriptomic Investigation in Adult Patients with Spinal Muscular Atrophy Under Treatment with Nusinersen
Spinal muscular atrophy (SMA) is a rare degenerative disorder with loss of motor neurons caused by mutations in the SMN1 g...
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The Role of Thioredoxin System in Shank3 Mouse Model of Autism
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder characterized by difficulties in social interactio...
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Genomic Validation in the UK Biobank Cohort Suggests a Role of C8B and MFG-E8 in the Pathogenesis of Trigeminal Neuralgia
Trigeminal neuralgia (TN) is a severe facial pain disease of uncertain pathophysiology and unclear genetic background. Alt...
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Investigating the Genetic Association of 40 Biochemical Indicators with Parkinson’s Disease
The mechanisms of Parkinson’s disease (PD) are not fully understood, which hinders the development of effective ther...
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Clinical and Molecular Profiles of a Cohort of Egyptian Patients with Collagen VI-Related Dystrophy
Collagen VI-related dystrophies (COL6-RD) display a wide spectrum of disease severity and genetic variability ranging from...
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Identification of Pathogenic Missense Mutations of NF1 Using Computational Approaches
Neurofibromatosis type 1 (NF1) is a prevalent autosomal dominant disorder caused by mutations in the NF1 gene, leading to ...
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