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Reimagining cholinergic therapy for Alzheimer’s disease

https://doi.org/10.1093/brain/awac096
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inferredcites →https://doi.org/10.1001/archneur.1997.00550160091022openalex-snapshot
Effects of Xanomeline, a Selective Muscarinic Receptor Agonist, on Cognitive Function and Behavioral Symptoms in Alzheimer Disease
inferredcites →https://doi.org/10.1001/archneur.60.12.1745openalex-snapshot
Cortical Cholinergic Function Is More Severely Affected in Parkinsonian Dementia Than in Alzheimer Disease
inferredcites →https://doi.org/10.1001/jama.2014.3654openalex-snapshot
Pharmacological Treatment of Parkinson Disease
inferredcites →https://doi.org/10.1001/jama.2019.22360openalex-snapshot
Diagnosis and Treatment of Parkinson Disease
inferredcites →https://doi.org/10.1001/jamainternmed.2019.0677openalex-snapshot
Anticholinergic Drug Exposure and the Risk of Dementia
inferredcites →https://doi.org/10.1001/jamaneurol.2014.2757openalex-snapshot
Frequency of Cholinergic and Caudate Nucleus Dopaminergic Deficits Across the Predemented Cognitive Spectrum of Parkinson Disease and Evidence of Interaction Effects
inferredcites →https://doi.org/10.1001/jamaneurol.2015.1807openalex-snapshot
Nerve Growth Factor Gene Therapy
inferredcites →https://doi.org/10.1001/jamaneurol.2019.3606openalex-snapshot
Selective Vulnerability of the Nucleus Basalis of Meynert Among Neuropathologic Subtypes of Alzheimer Disease
inferredcites →https://doi.org/10.1002/(sici)1099-1166(199809)13:9<625::aid-gps835>3.0.co;2-2openalex-snapshot
Effect of gender and apolipoprotein E genotype on response to anticholinesterase therapy in Alzheimer's disease
inferredcites →https://doi.org/10.1002/14651858.cd001190.pub2openalex-snapshot
Donepezil for dementia due to Alzheimer's disease
inferredcites →https://doi.org/10.1002/14651858.cd006504.pub2openalex-snapshot
Cholinesterase inhibitors for dementia with Lewy bodies, Parkinson's disease dementia and cognitive impairment in Parkinson's disease
inferredcites →https://doi.org/10.1002/14651858.cd009132openalex-snapshot
Cholinesterase inhibitors for mild cognitive impairment
inferredcites →https://doi.org/10.1002/1531-8249(200009)48:3<391::aid-ana17>3.0.co;2-hopenalex-snapshot
Limited donepezil inhibition of acetylcholinesterase measured with positron emission tomography in living Alzheimer cerebral cortex
inferredcites →https://doi.org/10.1002/1531-8249(200012)48:6<913::aid-ana12>3.0.co;2-sopenalex-snapshot
The selective muscarinic M1 agonist AF102B decreases levels of total A? in cerebrospinal fluid of patients with Alzheimer's disease
inferredcites →https://doi.org/10.1002/alz.12112openalex-snapshot
Further understanding the connection between Alzheimer's disease and Down syndrome
inferredcites →https://doi.org/10.1002/alz.12229openalex-snapshot
Nerve growth factor (NGF) pathway biomarkers in Down syndrome prior to and after the onset of clinical Alzheimer's disease: A paired CSF and plasma study
inferredcites →https://doi.org/10.1002/ana.10069openalex-snapshot
Upregulation of choline acetyltransferase activity in hippocampus and frontal cortex of elderly subjects with mild cognitive impairment
inferredcites →https://doi.org/10.1002/ana.10639openalex-snapshot
Increased Alzheimer pathology in Parkinson's disease related to antimuscarinic drugs
inferredcites →https://doi.org/10.1002/ana.20100openalex-snapshot
Cholinergic nucleus basalis tauopathy emerges early in the aging‐MCI‐AD continuum
inferredcites →https://doi.org/10.1002/ana.22105openalex-snapshot
Hippocampal hyperactivation in presymptomatic familial Alzheimer's disease
inferredcites →https://doi.org/10.1002/ana.410100602openalex-snapshot
A unifying hypothesis for the cause of amyotrophic lateral sclerosis, parkinsonism, and alzheimer disease
inferredcites →https://doi.org/10.1002/ana.410170310openalex-snapshot
Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome
inferredcites →https://doi.org/10.1002/ana.410270502openalex-snapshot
Synapse loss in frontal cortex biopsies in Alzheimer's disease: Correlation with cognitive severity
inferredcites →https://doi.org/10.1002/cne.23415openalex-snapshot
Cholinergic circuitry of the human nucleus basalis and its fate in Alzheimer's disease
inferredcites →https://doi.org/10.1002/cne.902750205openalex-snapshot
Nucleus basalis (Ch4) and cortical cholinergic innervation in the human brain: Observations based on the distribution of acetylcholinesterase and choline acetyltransferase
inferredcites →https://doi.org/10.1002/ddr.10085openalex-snapshot
Talsaclidine (WAL 2014 FU), a muscarinic M1 receptor agonist for the treatment of Alzheimer's disease
inferredcites →https://doi.org/10.1002/gps.1557openalex-snapshot
Effectiveness of acetylcholinesterase inhibitors: diagnosis and severity as predictors of response in routine practice
inferredcites →https://doi.org/10.1002/gps.2195openalex-snapshot
Can CSF biomarkers or pre‐treatment progression rate predict response to cholinesterase inhibitor treatment in Alzheimer's disease?
inferredcites →https://doi.org/10.1002/gps.4043openalex-snapshot
Sex and ESR1 genotype may influence the response to treatment with donepezil and rivastigmine in patients with Alzheimer's disease
inferredcites →https://doi.org/10.1002/gps.5522openalex-snapshot
Significant effects of cholinesterase inhibitors on tau pathology in the Alzheimer's disease continuum: An in vivo positron emission tomography study
inferredcites →https://doi.org/10.1002/j.1875-9114.1998.tb03877.xopenalex-snapshot
Metrifonate: Overview of Safety and Efficacy
inferredcites →https://doi.org/10.1002/jnr.23827openalex-snapshot
Sex and the development of Alzheimer's disease
inferredcites →https://doi.org/10.1002/syn.10310openalex-snapshot
Effects of acute acetylcholinesterase inhibition on the cerebral cholinergic neuronal system and cognitive function: Functional imaging of the conscious monkey brain using animal PET in combination with microdialysis
inferredcites →https://doi.org/10.1006/clim.2001.5128openalex-snapshot
Use of Muscarinic Agonists in the Treatment of Sjögren's Syndrome
inferredcites →https://doi.org/10.1006/exnr.1994.1148openalex-snapshot
Effects of Estrogen Replacement on the Relative Levels of Choline Acetyltransferase, trkA, and Nerve Growth Factor Messenger RNAs in the Basal Forebrain and Hippocampal Formation of Adult Rats
inferredcites →https://doi.org/10.1006/exnr.1997.6504openalex-snapshot
Reduction in p140-TrkA Receptor Protein within the Nucleus Basalis and Cortex in Alzheimer's Disease
inferredcites →https://doi.org/10.1006/mcne.2001.1016openalex-snapshot
The Precursor Pro-Nerve Growth Factor Is the Predominant Form of Nerve Growth Factor in Brain and Is Increased in Alzheimer's Disease
inferredcites →https://doi.org/10.1007/978-3-0348-7218-8_24openalex-snapshot
The Pharmacology of Neurotrophic Factors
inferredcites →https://doi.org/10.1007/978-3-642-45106-5_7openalex-snapshot
Sortilins in Neurotrophic Factor Signaling
inferredcites →https://doi.org/10.1007/978-3-7091-6139-5_17openalex-snapshot
Long-term stabilizing effect of cholinesterase inhibitors in the therapy of Alzheimer’ disease
inferredcites →https://doi.org/10.1007/bf02244644openalex-snapshot
Further analysis of the cognitive effects of tetrahydroaminoacridine (THA) in Alzheimer's disease: assessment of attentional and mnemonic function using CANTAB
inferredcites →https://doi.org/10.1007/bf02257624openalex-snapshot
Nerve growth factor affects11C-nicotine binding, blood flow, EEG, and verbal episodic memory in an Alzheimer patient (Case Report)
inferredcites →https://doi.org/10.1007/s00228-013-1483-yopenalex-snapshot
A population-based study of dosing and persistence with anti-dementia medications
inferredcites →https://doi.org/10.1007/s004019900178openalex-snapshot
Evolution of Alzheimer's disease-related cytoskeletal changes in the basal nucleus of Meynert
inferredcites →https://doi.org/10.1007/s00415-009-5000-2openalex-snapshot
Cholinesterase inhibitors may increase phosphorylated tau in Alzheimer’s disease
inferredcites →https://doi.org/10.1007/s00702-015-1462-9openalex-snapshot
The rationale for deep brain stimulation in Alzheimer’s disease
inferredcites →https://doi.org/10.1007/s00702-017-1775-yopenalex-snapshot
Cortical afferent inhibition abnormalities reveal cholinergic dysfunction in Parkinson’s disease: a reappraisal
inferredcites →https://doi.org/10.1007/s007020070034openalex-snapshot
Muscarinic agonists reduce tau phosphorylation in non-neuronal cells via GSK-3β inhibition and in neurons
inferredcites →https://doi.org/10.1007/s007020200090openalex-snapshot
Effect of subchronic administration of metrifonate, rivastigmine and donepezil on brain acetylcholine in aged F344 rats
inferredcites →https://doi.org/10.1007/s100720200086openalex-snapshot
Cerebrospinal fluid levels of biomarkers and activity of acetylcholinesterase (AChE) and butyrylcholinesterase in AD patients before and after treatment with different AChE inhibitors
inferredcites →https://doi.org/10.1007/s11064-006-9270-0openalex-snapshot
The Failure in NGF Maturation and its Increased Degradation as the Probable Cause for the Vulnerability of Cholinergic Neurons in Alzheimer’s Disease
inferredcites →https://doi.org/10.1007/s11910-010-0122-6openalex-snapshot
Hormonal Influences on Cognition and Risk for Alzheimer’s Disease
inferredcites →https://doi.org/10.1007/s12031-002-0025-3openalex-snapshot
AF150(S) and AF267B
inferredcites →https://doi.org/10.1007/s12031-009-9238-zopenalex-snapshot
Cholinergic Involvement in Alzheimer’s Disease. A Link with NGF Maturation and Degradation
inferredcites →https://doi.org/10.1007/s12035-020-02009-xopenalex-snapshot
Chronic Administration of Scopolamine Increased GSK3βP9, Beta Secretase, Amyloid Beta, and Oxidative Stress in the Hippocampus of Wistar Rats
inferredcites →https://doi.org/10.1007/s40264-014-0161-zopenalex-snapshot
Cardiovascular Effects of Drugs Used to Treat Alzheimer’s Disease
inferredcites →https://doi.org/10.1007/s40266-015-0273-xopenalex-snapshot
The Use of Cholinesterase Inhibitors Across All Stages of Alzheimer’s Disease
inferredcites →https://doi.org/10.1007/s40266-018-00636-7openalex-snapshot
Pharmacological Management of Dementia with Lewy Bodies
inferredcites →https://doi.org/10.1007/s40266-021-00851-9openalex-snapshot
Antipsychotic Initiation Among Older Dementia Patients Using Cholinesterase Inhibitors: A National Retrospective Cohort Study
inferredcites →https://doi.org/10.1016/0006-3223(93)90044-eopenalex-snapshot
Loss of striatal cholinergic neurons as a basis for tardive and L-dopa-induced dyskinesias, neuroleptic-induced supersensitivity psychosis and refractory schizophrenia
inferredcites →https://doi.org/10.1016/0028-3908(93)90114-iopenalex-snapshot
Cholinesterase inhibitor effects on extracellular acetylcholine in rat striatum
inferredcites →https://doi.org/10.1016/0166-2236(91)90061-xopenalex-snapshot
The basal forebrain-cortical cholinergic system: interpreting the functional consequences of excitotoxic lesions
inferredcites →https://doi.org/10.1016/0169-328x(86)90023-9openalex-snapshot
Nerve growth factor mRNA in peripheral and central rat tissues and in the human central nervous system: Lesion effects in the rat brain and levels in Alzheimer's disease
inferredcites →https://doi.org/10.1016/0169-328x(94)90159-7openalex-snapshot
NGF mRNA is not decreased in frontal cortex from Alzheimer's Disease patients
inferredcites →https://doi.org/10.1016/0197-4580(90)90059-9openalex-snapshot
Quantitative assessment of cortical synaptic density in Alzheimer's disease
inferredcites →https://doi.org/10.1016/0301-0082(95)00013-lopenalex-snapshot
The pedunculopontine tegmental nucleus: Where the striatum meets the reticular formation
inferredcites →https://doi.org/10.1016/0304-3940(83)90171-4openalex-snapshot
Loss of pigmented dopamine-β-hydroxylase positive cells from locus coeruleus in senile dementia of alzheimer's type
inferredcites →https://doi.org/10.1016/0304-3940(86)90629-4openalex-snapshot
Reduced number of [3H]nicotine and [3H]acetylcholine binding sites in the frontal cortex of Alzheimer brains
inferredcites →https://doi.org/10.1016/0304-3940(95)12256-7openalex-snapshot
Monoaminergic neurotransmitters, their precursors and metabolites in brains of Alzheimer patients
inferredcites →https://doi.org/10.1016/0306-4522(94)90285-2openalex-snapshot
Expression of neurotrophin and trk receptor genes in adult rats with fimbria transections: Effect of intraventricular nerve growth factor and brain-derived neurotrophic factor administration
inferredcites →https://doi.org/10.1016/0306-4522(95)91510-jopenalex-snapshot
Differential expression of p140trk, p75NGFR and growth-associated phosphoprotein-43 genes in nucleus basalis magnocellularis, thalamus and adjacent cortex following neocortical infarction and nerve growth factor treatment
inferredcites →https://doi.org/10.1016/0361-9230(91)90038-lopenalex-snapshot
Muscarinic cholinoceptive neurons in the frontal cortex in Alzheimer's disease
inferredcites →https://doi.org/10.1016/0893-6080(94)90053-1openalex-snapshot
Runaway synaptic modification in models of cortex: Implications for Alzheimer's disease
inferredcites →https://doi.org/10.1016/bs.apha.2019.12.003openalex-snapshot
M1 muscarinic acetylcholine receptors: A therapeutic strategy for symptomatic and disease-modifying effects in Alzheimer's disease?
inferredcites →https://doi.org/10.1016/j.ajpath.2011.04.041openalex-snapshot
Loss of Muscarinic M1 Receptor Exacerbates Alzheimer's Disease–Like Pathology and Cognitive Decline
inferredcites →https://doi.org/10.1016/j.amjopharm.2006.09.009openalex-snapshot
Sex influences on cholinesterase inhibitor treatment in elderly individuals with alzheimer's disease
inferredcites →https://doi.org/10.1016/j.biopsych.2011.06.019openalex-snapshot
Atrophy of the Cholinergic Basal Forebrain Over the Adult Age Range and in Early Stages of Alzheimer's Disease
inferredcites →https://doi.org/10.1016/j.cbi.2010.04.002openalex-snapshot
Gender-related differences in circadian rhythm of rat plasma acetyl- and butyrylcholinesterase: Effects of sex hormone withdrawal
inferredcites →https://doi.org/10.1016/j.cbi.2012.09.016openalex-snapshot
Effect of cholinesterase inhibitors on attention
inferredcites →https://doi.org/10.1016/j.celrep.2018.06.001openalex-snapshot
Longitudinal Alzheimer’s Degeneration Reflects the Spatial Topography of Cholinergic Basal Forebrain Projections
inferredcites →https://doi.org/10.1016/j.conb.2006.09.002openalex-snapshot
The role of acetylcholine in learning and memory
inferredcites →https://doi.org/10.1016/j.cub.2017.07.021openalex-snapshot
Intermittent Stimulation of the Nucleus Basalis of Meynert Improves Working Memory in Adult Monkeys
inferredcites →https://doi.org/10.1016/j.drudis.2019.08.009openalex-snapshot
Cholinergic muscarinic M1 and M4 receptors as therapeutic targets for cognitive, behavioural, and psychological symptoms in psychiatric and neurological disorders
inferredcites →https://doi.org/10.1016/j.jalz.2011.02.009openalex-snapshot
Long‐term progression of Alzheimer's disease in patients under antidementia drugs
inferredcites →https://doi.org/10.1016/j.jalz.2014.10.003openalex-snapshot
Donepezil decreases annual rate of hippocampal atrophy in suspected prodromal Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.jalz.2014.11.008openalex-snapshot
Changes in CSF cholinergic biomarkers in response to cell therapy with NGF in patients with Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.jalz.2016.05.001openalex-snapshot
An inflammatory and trophic disconnect biomarker profile revealed in Down syndrome plasma: Relation to cognitive decline and longitudinal evaluation
inferredcites →https://doi.org/10.1016/j.jalz.2017.11.009openalex-snapshot
AF710B, an M1/sigma‐1 receptor agonist with long‐lasting disease‐modifying properties in a transgenic rat model of Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.jchemneu.2010.03.005openalex-snapshot
Cortical M1 receptor concentration increases without a concomitant change in function in Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.jns.2017.03.049openalex-snapshot
Impaired cholinergic transmission in patients with Parkinson's disease and olfactory dysfunction
inferredcites →https://doi.org/10.1016/j.mcn.2008.07.013openalex-snapshot
Isoform-specific contribution of protein kinase C to prion processing
inferredcites →https://doi.org/10.1016/j.mcn.2011.04.008openalex-snapshot
ERK1-independent α-secretase cut of β-amyloid precursor protein via M1 muscarinic receptors and PKCα/ε
inferredcites →https://doi.org/10.1016/j.nbd.2004.07.016openalex-snapshot
M1 muscarinic receptor activation protects neurons from β-amyloid toxicity. A role for Wnt signaling pathway
inferredcites →https://doi.org/10.1016/j.nbd.2017.08.019openalex-snapshot
Differential deregulation of NGF and BDNF neurotrophins in a transgenic rat model of Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2007.02.020openalex-snapshot
PET imaging of the in vivo brain acetylcholinesterase activity and nicotine binding in galantamine-treated patients with AD
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2010.11.015openalex-snapshot
Volumetric analysis of the substantia innominata in patients with Parkinson's disease according to cognitive status
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2013.05.020openalex-snapshot
Cholinergic activity correlates with reserve proxies in Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2018.01.025openalex-snapshot
Reduced substantia innominata volume mediates contributions of microvascular and macrovascular disease to cognitive deficits in Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2018.03.002openalex-snapshot
Compromise of cortical proNGF maturation causes selective retrograde atrophy in cholinergic nucleus basalis neurons
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2019.11.013openalex-snapshot
Basal forebrain metabolism in Alzheimer's disease continuum: relationship with education
inferredcites →https://doi.org/10.1016/j.neuroimage.2006.02.015openalex-snapshot
Donepezil effects on sources of cortical rhythms in mild Alzheimer's disease: Responders vs. Non-Responders
inferredcites →https://doi.org/10.1016/j.neuron.2006.01.020openalex-snapshot
M1 Receptors Play a Central Role in Modulating AD-like Pathology in Transgenic Mice
inferredcites →https://doi.org/10.1016/j.neuron.2006.05.022openalex-snapshot
Increased App Expression in a Mouse Model of Down's Syndrome Disrupts NGF Transport and Causes Cholinergic Neuron Degeneration
inferredcites →https://doi.org/10.1016/j.neuron.2016.09.006openalex-snapshot
Basal Forebrain Cholinergic Circuits and Signaling in Cognition and Cognitive Decline
inferredcites →https://doi.org/10.1016/j.neuron.2018.05.027openalex-snapshot
Muscarinic M1 Receptor Overstimulation Disrupts Working Memory Activity for Rules in Primate Prefrontal Cortex
inferredcites →https://doi.org/10.1016/j.neuropharm.2018.01.028openalex-snapshot
Current status of muscarinic M1 and M4 receptors as drug targets for neurodegenerative diseases
inferredcites →https://doi.org/10.1016/j.neuropharm.2019.107860openalex-snapshot
Modifying the progression of Alzheimer's and Parkinson's disease with deep brain stimulation
inferredcites →https://doi.org/10.1016/j.neuropharm.2020.108081openalex-snapshot
Future avenues for Alzheimer's disease detection and therapy: liquid biopsy, intracellular signaling modulation, systems pharmacology drug discovery
inferredcites →https://doi.org/10.1016/j.neuropharm.2021.108489openalex-snapshot
Aged rhesus monkeys: Cognitive performance categorizations and preclinical drug testing
inferredcites →https://doi.org/10.1016/j.neuroscience.2015.03.006openalex-snapshot
Hippocampal plasticity during the progression of Alzheimer’s disease
inferredcites →https://doi.org/10.1016/j.nurt.2008.05.002openalex-snapshot
Cholinergic Treatments with Emphasis on M1 Muscarinic Agonists as Potential Disease-Modifying Agents for Alzheimer's Disease
inferredcites →https://doi.org/10.1016/j.phrs.2010.02.009openalex-snapshot
Acetylcholinesterase inhibitors and memantine for neuroenhancement in healthy individuals: A systematic review
inferredcites →https://doi.org/10.1016/j.phrs.2016.11.035openalex-snapshot
Sex and gender differences in the treatment of Alzheimer’s disease: A systematic review of randomized controlled trials
inferredcites →https://doi.org/10.1016/j.tips.2014.04.010openalex-snapshot
Nerve growth factor metabolic dysfunction in Alzheimer's disease and Down syndrome
inferredcites →https://doi.org/10.1016/j.trci.2018.03.004openalex-snapshot
Randomized, controlled, proof‐of‐concept trial of MK‐7622 in Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0002-9440(10)62275-4openalex-snapshot
Pro-NGF Isolated from the Human Brain Affected by Alzheimer's Disease Induces Neuronal Apoptosis Mediated by p75NTR
inferredcites →https://doi.org/10.1016/s0006-8993(01)02484-2openalex-snapshot
Reduction of cerebrospinal fluid amyloid β after systemic administration of M1 muscarinic agonists
inferredcites →https://doi.org/10.1016/s0014-2999(00)00093-5openalex-snapshot
Allosteric modulation of nicotinic acetylcholine receptors as a treatment strategy for Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0028-3908(02)00378-7openalex-snapshot
Sex dimorphisms in the cognitive-enhancing action of the Alzheimer’s drug donepezil in aged Rhesus monkeys
inferredcites →https://doi.org/10.1016/s0028-3908(99)00157-4openalex-snapshot
Gender differences in the effect of rivastigmine on brain cholinesterase activity and cognitive function in rats
inferredcites →https://doi.org/10.1016/s0079-6123(03)45003-6openalex-snapshot
Muscarinic acetylcholine receptor subtypes in cerebral cortex and hippocampus
inferredcites →https://doi.org/10.1016/s0079-6123(08)62114-7openalex-snapshot
Chapter 30 New trends in cholinergic therapy for Alzheimer disease: nicotinic agonists or cholinesterase inhibitors?
inferredcites →https://doi.org/10.1016/s0079-6123(08)62408-5openalex-snapshot
Chapter 32: Trophic responses of forebrain cholinergic neurons: a discussion
inferredcites →https://doi.org/10.1016/s0140-6736(06)68350-5openalex-snapshot
Donepezil in patients with severe Alzheimer's disease: double-blind, parallel-group, placebo-controlled study
inferredcites →https://doi.org/10.1016/s0140-6736(20)30689-9openalex-snapshot
Clinical and biomarker changes of Alzheimer's disease in adults with Down syndrome: a cross-sectional study
inferredcites →https://doi.org/10.1016/s0140-6736(76)91936-xopenalex-snapshot
SELECTIVE LOSS OF CENTRAL CHOLINERGIC NEURONS IN ALZHEIMER'S DISEASE
inferredcites →https://doi.org/10.1016/s0140-6736(80)92137-6openalex-snapshot
ALZHEIMER-LIKE CHOLINERGIC DEFICIENCY IN DOWN SYNDROME
inferredcites →https://doi.org/10.1016/s0166-2236(84)80161-7openalex-snapshot
The anatomy of the CNS cholinergic neurons
inferredcites →https://doi.org/10.1016/s0169-328x(96)00193-3openalex-snapshot
Nerve growth factor mRNA and protein levels measured in the same tissue from normal and Alzheimer's disease parietal cortex
inferredcites →https://doi.org/10.1016/s0197-4580(00)83323-0openalex-snapshot
The effects of rivastigmine on behavioral symptoms in severe ad patients in a nursing home setting
inferredcites →https://doi.org/10.1016/s0304-3940(98)00019-6openalex-snapshot
Decreased trkA neurotrophin receptor expression in the parietal cortex of patients with Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0361-9230(99)00219-1openalex-snapshot
Cholinergic enhancement improves performance on working memory by modulating the functional activity in distinct brain regions: a positron emission tomography regional cerebral blood flow study in healthy humans
inferredcites →https://doi.org/10.1016/s0896-6273(04)00145-xopenalex-snapshot
Effects of Cholinergic Enhancement on Visual Stimulation, Spatial Attention, and Spatial Working Memory
inferredcites →https://doi.org/10.1016/s1474-4422(07)70109-6openalex-snapshot
Effect of rivastigmine on delay to diagnosis of Alzheimer's disease from mild cognitive impairment: the InDDEx study
inferredcites →https://doi.org/10.1016/s1474-4422(07)70113-8openalex-snapshot
MCI treatment trials: failure or not?
inferredcites →https://doi.org/10.1016/s1474-4422(15)00258-6openalex-snapshot
Nursing home placement in the Donepezil and Memantine in Moderate to Severe Alzheimer's Disease (DOMINO-AD) trial: secondary and post-hoc analyses
inferredcites →https://doi.org/10.1016/s1474-4422(15)00389-0openalex-snapshot
Rivastigmine for gait stability in patients with Parkinson's disease (ReSPonD): a randomised, double-blind, placebo-controlled, phase 2 trial
inferredcites →https://doi.org/10.1016/s1569-7339(08)00237-3openalex-snapshot
Handbook Of Behavioral Neuroscience
inferredcites →https://doi.org/10.1017/s1092852900020174openalex-snapshot
Selective Benefit of Donepezil on Oral Naming in Alzheimer's Disease in Men Compared to Women
inferredcites →https://doi.org/10.1021/acs.jmedchem.7b00597openalex-snapshot
Design and Synthesis of γ- and δ-Lactam M 1 Positive Allosteric Modulators (PAMs): Convulsion and Cholinergic Toxicity of an M 1 -Selective PAM with Weak Agonist Activity
inferredcites →https://doi.org/10.1021/acschemneuro.6b00278openalex-snapshot
Disease-Modifying Effects of M1 Muscarinic Acetylcholine Receptor Activation in an Alzheimer’s Disease Mouse Model
inferredcites →https://doi.org/10.1038/177185a0openalex-snapshot
Quantitative Determination of Acetylcholinesterase Activity in Individual Nerve Cells
inferredcites →https://doi.org/10.1038/4571090aopenalex-snapshot
A prion protein connection
inferredcites →https://doi.org/10.1038/mp.2017.183openalex-snapshot
Quantification of brain cholinergic denervation in Alzheimer’s disease using PET imaging with [18F]-FEOBV
inferredcites →https://doi.org/10.1038/nature07761openalex-snapshot
Cellular prion protein mediates impairment of synaptic plasticity by amyloid-β oligomers
inferredcites →https://doi.org/10.1038/ncomms13249openalex-snapshot
Basal forebrain degeneration precedes and predicts the cortical spread of Alzheimer’s pathology
inferredcites →https://doi.org/10.1038/nrneurol.2013.223openalex-snapshot
Alzheimer disease therapy—moving from amyloid-β to tau
inferredcites →https://doi.org/10.1038/s41380-020-0797-2openalex-snapshot
The human brain NGF metabolic pathway is impaired in the pre-clinical and clinical continuum of Alzheimers disease
inferredcites →https://doi.org/10.1038/s41386-018-0033-9openalex-snapshot
M1-positive allosteric modulators lacking agonist activity provide the optimal profile for enhancing cognition
inferredcites →https://doi.org/10.1038/s41401-020-00565-5openalex-snapshot
New therapeutics beyond amyloid-β and tau for the treatment of Alzheimer’s disease
inferredcites →https://doi.org/10.1038/s41582-018-0032-9openalex-snapshot
Sex differences in Alzheimer disease — the gateway to precision medicine
inferredcites →https://doi.org/10.1038/s41582-018-0132-6openalex-snapshot
Dementia in Down syndrome: unique insights for Alzheimer disease research
inferredcites →https://doi.org/10.1038/s41598-017-09780-3openalex-snapshot
Reduced basal forebrain atrophy progression in a randomized Donepezil trial in prodromal Alzheimer’s disease
inferredcites →https://doi.org/10.1038/sj.cdd.4400713openalex-snapshot
M1 muscarinic receptors block caspase activation by phosphoinositide 3-kinase- and MAPK/ERK-independent pathways
inferredcites →https://doi.org/10.1038/srep29266openalex-snapshot
Association between acetylcholinesterase inhibitors and risk of stroke in patients with dementia
inferredcites →https://doi.org/10.1042/bj0262056openalex-snapshot
Choline-esterase. An enzyme present in the blood-serum of the horse
inferredcites →https://doi.org/10.1046/j.1365-2125.1998.0460s1007.xopenalex-snapshot
Pharmacokinetic and pharmacodynamic profile of donepezil HCl following multiple oral doses
inferredcites →https://doi.org/10.1046/j.1471-4159.1996.66020877.xopenalex-snapshot
Activation of m 1 Muscarinic Acetylcholine Receptor Regulates τ Phosphorylation in Transfected PC12 Cells
inferredcites →https://doi.org/10.1046/j.1471-4159.1998.70051991.xopenalex-snapshot
M1 Muscarinic Agonist Treatment Reverses Cognitive and Cholinergic Impairments of Apolipoprotein E‐Deficient Mice
inferredcites →https://doi.org/10.1046/j.1471-4159.1998.71052094.xopenalex-snapshot
Mitogen‐Activated Protein Kinase‐Dependent and Protein Kinase C‐Dependent Pathways Link the m1 Muscarinic Receptor to β‐Amyloid Precursor Protein Secretion
inferredcites →https://doi.org/10.1046/j.1471-4159.1999.0720206.xopenalex-snapshot
Site‐Specific Dephosphorylation of Tau of Apolipoprotein E‐Deficient and Control Mice by M1 Muscarinic Agonist Treatment
inferredcites →https://doi.org/10.1046/j.1471-4159.2000.740777.xopenalex-snapshot
Increased Levels of Tau Protein in SH‐SY5Y Cells After Treatment with Cholinesterase Inhibitors and Nicotinic Agonists
inferredcites →https://doi.org/10.1055/s-0031-1296432openalex-snapshot
Gender Differences in the Pharmacokinetics of Rivastigmine in Rats
inferredcites →https://doi.org/10.1055/s-0031-1296941openalex-snapshot
Pharmacokinetics and Tissue Distribution of Galantamine and Galantamine-related Radioactivity after Single Intravenous and Oral Administration in the Rat
inferredcites →https://doi.org/10.1055/s-0039-1678579openalex-snapshot
Parkinson's Disease Dementia and Lewy Body Disease
inferredcites →https://doi.org/10.1055/s-2007-1014631openalex-snapshot
Neuronotrophic Factors in Cellular Functional and Cognitive Repair of Adult Brain
inferredcites →https://doi.org/10.1056/nejm198611133152001openalex-snapshot
Oral Tetrahydroaminoacridine in Long-Term Treatment of Senile Dementia, Alzheimer Type
inferredcites →https://doi.org/10.1056/nejmoa050151openalex-snapshot
Vitamin E and Donepezil for the Treatment of Mild Cognitive Impairment
inferredcites →https://doi.org/10.1056/nejmoa2017015openalex-snapshot
Muscarinic Cholinergic Receptor Agonist and Peripheral Antagonist for Schizophrenia
inferredcites →https://doi.org/10.1073/pnas.0408500102openalex-snapshot
Chronic nicotine administration exacerbates tau pathology in a transgenic model of Alzheimer's disease
inferredcites →https://doi.org/10.1073/pnas.0510645103openalex-snapshot
Activity-dependent release of precursor nerve growth factor, conversion to mature nerve growth factor, and its degradation by a protease cascade
inferredcites →https://doi.org/10.1073/pnas.181219298openalex-snapshot
Failed retrograde transport of NGF in a mouse model of Down's syndrome: Reversal of cholinergic neurodegenerative phenotypes following NGF infusion
inferredcites →https://doi.org/10.1073/pnas.93.24.13541openalex-snapshot
Muscarinic acetylcholine receptor expression in memory circuits: Implications for treatment of Alzheimer disease
inferredcites →https://doi.org/10.1073/pnas.95.19.11465openalex-snapshot
Activation of the genetically defined m1 muscarinic receptor potentiates N -methyl- d -aspartate (NMDA) receptor currents in hippocampal pyramidal cells
inferredcites →https://doi.org/10.1073/pnas.96.7.4067openalex-snapshot
A nerve growth factor mimetic TrkA antagonist causes withdrawal of cortical cholinergic boutons in the adult rat
inferredcites →https://doi.org/10.1073/pnas.97.19.10424openalex-snapshot
Identification of diverse nerve growth factor-regulated genes by serial analysis of gene expression (SAGE) profiling
inferredcites →https://doi.org/10.1074/jbc.m109.051086openalex-snapshot
The α-Secretase-derived N-terminal Product of Cellular Prion, N1, Displays Neuroprotective Function in Vitro and in Vivo
inferredcites →https://doi.org/10.1074/jbc.m209892200openalex-snapshot
Activation of Muscarinic Receptors Inhibits औ-Amyloid Peptide-induced Signaling in Cortical Slices
inferredcites →https://doi.org/10.1074/jbc.m212532200openalex-snapshot
α7 Nicotinic Acetylcholine Receptors Mediate β-Amyloid Peptide-induced Tau Protein Phosphorylation
inferredcites →https://doi.org/10.1080/19420889.2017.1389359openalex-snapshot
Potential for intermittent stimulation of nucleus basalis of Meynert to impact treatment of alzheimer's disease
inferredcites →https://doi.org/10.1093/brain/99.3.459openalex-snapshot
NEUROTRANSMITTER-RELATED ENZYMES AND INDICES OF HYPOXIA IN SENILE DEMENTIA AND OTHER ABIOTROPHIES
inferredcites →https://doi.org/10.1093/brain/awab111openalex-snapshot
The role of noradrenaline in cognition and cognitive disorders
inferredcites →https://doi.org/10.1093/brain/awh067openalex-snapshot
The cognitive ability of an incident cohort of Parkinson’s patients in the UK. The CamPaIGN study
inferredcites →https://doi.org/10.1093/brain/awp176openalex-snapshot
Modulation of fusiform cortex activity by cholinesterase inhibition predicts effects on subsequent memory
inferredcites →https://doi.org/10.1093/brain/awt372openalex-snapshot
RETRACTED AND REPLACED: Nerve growth factor metabolic dysfunction in Down’s syndrome brains
inferredcites →https://doi.org/10.1093/brain/awx310openalex-snapshot
In vivo cholinergic basal forebrain atrophy predicts cognitive decline in de novo Parkinson’s disease
inferredcites →https://doi.org/10.1093/brain/awx333openalex-snapshot
Early nucleus basalis of Meynert degeneration predicts cognitive decline in Parkinson’s disease
inferredcites →https://doi.org/10.1093/brain/awx356openalex-snapshot
Effect of cholinergic treatment depends on cholinergic integrity in early Alzheimer’s disease
inferredcites →https://doi.org/10.1093/brain/awy072openalex-snapshot
Nucleus basalis of Meynert degeneration precedes and predicts cognitive impairment in Parkinson’s disease
inferredcites →https://doi.org/10.1093/brain/awy132openalex-snapshot
The cholinergic system in the pathophysiology and treatment of Alzheimer’s disease
inferredcites →https://doi.org/10.1093/braincomms/fcaa058openalex-snapshot
M1 muscarinic acetylcholine receptor dysfunction in moderate Alzheimer’s disease pathology
inferredcites →https://doi.org/10.1093/cercor/bhv227openalex-snapshot
Activation of Muscarinic M1 Acetylcholine Receptors Induces Long-Term Potentiation in the Hippocampus
inferredcites →https://doi.org/10.1093/cercor/bhw177openalex-snapshot
Cholinergic Surveillance over Hippocampal RNA Metabolism and Alzheimer's-Like Pathology
inferredcites →https://doi.org/10.1093/cercor/bhw195openalex-snapshot
Volume Loss of the Nucleus Basalis of Meynert is Associated with Atrophy of Innervated Regions in Mild Cognitive Impairment
inferredcites →https://doi.org/10.1093/eurheartj/eht182openalex-snapshot
The use of cholinesterase inhibitors and the risk of myocardial infarction and death: a nationwide cohort study in subjects with Alzheimer's disease
inferredcites →https://doi.org/10.1093/gerona/57.3.m173openalex-snapshot
Prevalence and Impact of Medical Comorbidity in Alzheimer's Disease
inferredcites →https://doi.org/10.1093/jnen/59.4.308openalex-snapshot
The Cholinergic Deficit Coincides with Aβ Deposition at the Earliest Histopathologic Stages of Alzheimer Disease
inferredcites →https://doi.org/10.1093/jnen/63.6.641openalex-snapshot
Increased proNGF Levels in Subjects with Mild Cognitive Impairment and Mild Alzheimer Disease
inferredcites →https://doi.org/10.1093/ntr/nty116openalex-snapshot
Nicotinic Acetylcholine Receptor Agonists for the Treatment of Alzheimer’s Dementia: An Update
inferredcites →https://doi.org/10.1093/sleep/32.8.999openalex-snapshot
Donepezil Improves Episodic Memory in Young Individuals Vulnerable to the Effects of Sleep Deprivation
showing the first 200 of 315

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4633265openalex-extracted
Carltonine-Derived Compounds for Targeted Butyrylcholinesterase Inhibition
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Sex‐specific declines in cholinergic‐targeting tRNA fragments in the nucleus accumbens in Alzheimer's disease
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Sex‐dependent cholinergic effects on amyloid pathology: A translational study
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Evidence for a novel neuronal mechanism driving Alzheimer's disease, upstream of amyloid
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The impact of cholinesterase inhibitors on cognitive trajectories in mild cognitive impairment patients based on amyloid beta status
inferred← citeshttps://doi.org/10.1002/alz.70445openalex-snapshot
Single‐nucleus analysis reveals oxidative stress in Down syndrome basal forebrain neurons at birth
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New Peripheral Pyridine‐Substituted Cobalt, Copper, and Manganese Phthalocyanines as Potential In Vitro Acetyl/Butyrylcholinesterase Inhibitors in the Treatment of Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/cbdv.202403401openalex-snapshot
Serotonergic Modulators in Alzheimer's Disease: A Hope in the Hopeless Condition
inferred← citeshttps://doi.org/10.1002/cns.71151openalex-snapshot
Advances in Targeting Central Cholinergic Dysfunction for Neurodegenerative Diseases: From Pharmacotherapy to Neuromodulation
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Amyloid accumulation, brain atrophy, and cognitive decline in emergent Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/hipo.23622openalex-snapshot
Cholinergic and behavior‐dependent beta and gamma waves are coupled between olfactory bulb and hippocampus
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Rapid identification of chemical components and screening of acetylcholinesterase inhibitors from Dalbergia odorifera based on mass defect and diagnostic ion filtering strategy, affinity ultrafiltration, and liquid chromatography‐tandem mass spectrometry
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Multi‐Target Drug Design in Alzheimer's Disease Treatment: Emerging Technologies, Advantages, Challenges, and Limitations
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Role of Pyrazole Moiety in the Treatment of Alzheimer's Disease: A Comprehensive Review of Various Synthetic Routes and Probable Mechanisms of Action
inferred← citeshttps://doi.org/10.1007/978-1-0716-3311-3_1openalex-snapshot
Recent Progress in the Treatment Strategies for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-981-95-7121-5_3openalex-snapshot
Management of Alzheimer’s Disease-Associated Cognitive Disabilities
inferred← citeshttps://doi.org/10.1007/s00044-025-03484-4openalex-snapshot
Novel diazepine-carbamate derivatives as dual-acting butyrylcholinesterase inhibitors and antioxidants for Alzheimer’s disease
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The Janus face of CaMKII: from memory consolidation to neurotoxic switch in Alzheimer’s disease
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Nanozyme-based dual-signal sensing system for colorimetric and photothermal detection of AChE activity in the blood of liver-injured mice
inferred← citeshttps://doi.org/10.1007/s00702-025-02887-2openalex-snapshot
Cholinergic neurotransmission in the brain of streptozotocin-induced rat model of sporadic Alzheimer’s disease: long-term follow up
inferred← citeshttps://doi.org/10.1007/s10722-026-02756-1openalex-snapshot
Botany, phytochemistry, pharmacology, phytotoxicity and industrial applications of Grewia tiliifolia Vahl: a comprehensive review
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Ameliorative effects of thiamin on learning behavior and memory dysfunction in a rat model of hypothyroidism: implication of oxidative stress and acetylcholinesterase
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α-Synuclein as a molecular link between Parkinson’s disease and chronic kidney disease: insights into the kidney-brain axis
inferred← citeshttps://doi.org/10.1007/s11030-026-11725-wopenalex-snapshot
Computational discovery and dynamic profiling of dual acetylcholinesterase and monoacylglycerol lipase inhibitors for Alzheimer’s disease
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Mechanisms of the Pathogenesis of Alzheimer’s Disease: The Role of the Basal Forebrain
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Flavonoids as a phytobiotic agent: sources, classifications, biological benefits, and useful impacts on broilers and layers
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Synergistic Neuroprotection in Tauopathic Mice via Green-Synthesized Silver Nanoparticles Co-delivering Methylene Blue and Moringa oleifera
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Environmental Factors Drive Neurodegenerative Diseases Through Glutamate Excitotoxicity: A Convergent Mechanistic Pathway
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Lipid metabolism, neuroinflammation, and oxidative stress in Alzheimer disease: an integrated mechanistic review
inferred← citeshttps://doi.org/10.1007/s40263-023-01017-4openalex-snapshot
Turning the Spotlight to Cholinergic Pharmacotherapy of the Human Language System
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Analysis of the mitochondrial status of murine neuronal N2a cells treated with resveratrol and synthetic isomeric resveratrol analogs: aza-stilbenes
inferred← citeshttps://doi.org/10.1016/b978-0-443-15596-3.16001-1openalex-snapshot
Literature cited
inferred← citeshttps://doi.org/10.1016/b978-0-443-15702-8.00033-6openalex-snapshot
Why do we need new therapies for neurodegenerative disorders?
inferred← citeshttps://doi.org/10.1016/b978-0-443-19088-9.00005-6openalex-snapshot
The involvement of the cholinergic system in Alzheimer disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-19088-9.00007-xopenalex-snapshot
NGF-based cholinergic therapies in Alzheimer disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-19088-9.00011-1openalex-snapshot
A brief history of the CNS cholinergic transmission
inferred← citeshttps://doi.org/10.1016/b978-0-443-19088-9.00012-3openalex-snapshot
Cognition and modulation of the cholinergic system
inferred← citeshttps://doi.org/10.1016/b978-0-443-19088-9.00014-7openalex-snapshot
Memory network and cognitive reserve are associated with preserved and stimulated cholinergic neurotransmission
inferred← citeshttps://doi.org/10.1016/b978-0-443-19088-9.00015-9openalex-snapshot
Cholinergic therapy in Alzheimer disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-19088-9.00016-0openalex-snapshot
CNS muscarinic receptors and muscarinic receptor agonists in Alzheimer disease treatment
inferred← citeshttps://doi.org/10.1016/j.apsb.2025.02.030openalex-snapshot
Discovery of novel butyrylcholinesterase inhibitors for treating Alzheimer's disease
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β-Sitosterol ameliorates the cognitive deficits and neuropathological hallmarks in an Alzheimer’s disease model
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Determinants of approved acetylcholinesterase inhibitor response outcomes in Alzheimer’s disease: relevance for precision medicine in neurodegenerative diseases
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Structural and functional remodeling of neural networks in β-amyloid driven hippocampal hyperactivity
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The new perspective of Alzheimer's Disease Research: Mechanism and therapeutic strategy of neuronal senescence
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The potential role of aryl hydrocarbon receptor in Alzheimer's disease: Protective or detrimental
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The therapeutic potential of early exercise in Alzheimer's disease: Focus on the brain-spleen axis
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Design, synthesis, and biological evaluation of novel capsaicin-tacrine hybrids as multi-target agents for the treatment of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107877openalex-snapshot
Development of novel aza-stilbenes as a new class of selective MAO-B inhibitors for the treatment of Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109894openalex-snapshot
Carltonine B derivatives: Synthesis and structure-activity relationship insights for selective butyrylcholinesterase inhibition
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116754openalex-snapshot
Neuroprotective effects of Anshen Bunao Syrup on cognitive dysfunction in Alzheimer's disease rat models
inferred← citeshttps://doi.org/10.1016/j.bios.2024.117078openalex-snapshot
Triple-mode sensing platform for acetylcholinesterase activity monitoring and anti-Alzheimer's drug screening based on a highly stable Cu (I) compound
inferred← citeshttps://doi.org/10.1016/j.cbi.2023.110667openalex-snapshot
Solvents and detergents compatible with enzyme kinetic studies of cholinesterases
inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111703openalex-snapshot
Photochemistry-driven design of small molecule cholinesterase ligands
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.110964openalex-snapshot
Artificial intelligence-driven development of natural multi-target derivatives with BuChE inhibitory activity for treating Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2026.111765openalex-snapshot
An integrated in silico approach to identify pyridine-based AChE and BChE inhibitors for Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.dscb.2024.100125openalex-snapshot
The promising role of bioactive congeners present in Cassytha filiformis in Alzheimer's disease: An explicative review
inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.118961openalex-snapshot
Leveraging multitargeting BChE-MAO B inhibitors against microglia-related neuroinflammation: in vitro biological evaluation, structure-activity relationships, drug-like properties, and X-ray crystal complexes
inferred← citeshttps://doi.org/10.1016/j.fhfh.2025.100215openalex-snapshot
Emulsion-enhanced synergy of walnut-derived hexapeptide (EPEVLR) and DHA in mitigating D-galactose-induced cognitive decline in mice
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e37702openalex-snapshot
Interactions of memantine and rivastigmine with graphene oxide nanocarrier and beta-amyloid protein using molecular docking and in-silico methods
inferred← citeshttps://doi.org/10.1016/j.ibneur.2024.11.004openalex-snapshot
Exploring the potential of probiotics in Alzheimer's disease and gut dysbiosis
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2026.113334openalex-snapshot
Testing effects of paced breathing on plasma Aβ and brain perivascular spaces
inferred← citeshttps://doi.org/10.1016/j.insi.2026.100247openalex-snapshot
Network pharmacology-guided identification and molecular validation of multi-target phytoconstituents from Gmelina arborea against Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.111786openalex-snapshot
Up-regulation of GPR139 in the medial septum ameliorates cognitive impairment in two mouse models of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.jep.2024.117731openalex-snapshot
The potential anti-Alzheimer's activity of Oxalis corniculata Linn. Methanolic extract in experimental rats: Role of APOE4/LRP1, TLR4/NF-κβ/NLRP3, Wnt 3/β-catenin/GSK-3β, autophagy and apoptotic cues
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Dihuang Yinzi improves scopolamine-induced learning and memory impairment by regulating plasma exosome-derived BDNF
inferred← citeshttps://doi.org/10.1016/j.jgr.2025.05.002openalex-snapshot
Structure−activity relationship of ginsenoside derivatives with different glycosides and double bond position on anti-aging bioactivities
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2023.109397openalex-snapshot
Insights into prevention mechanisms of bioactive components from healthy diets against Alzheimer's disease
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AChE/BuChE inhibitory, DNA nuclease and cytotoxic properties of axially 5-[6-(benzyloxy)-2H-1,3-benzoxazin-3(4H)-yl]pentanoxy and 5-[6-(hexyloxy)-2H-1,3-benzoxazin-3(4H)-yl]pentanoxy substituted silicon phthalocyanines
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Imidazopyridine–coumarin derivatives as novel multi-target directed ligands (MTDLs): Balancing acetylcholinesterase inhibition and antioxidant activity for neuroprotection
inferred← citeshttps://doi.org/10.1016/j.mtcomm.2023.106322openalex-snapshot
Cyclic β-hairpin peptide loaded PLGA nanoparticles: A potential anti-amyloid therapeutic
inferred← citeshttps://doi.org/10.1016/j.nbd.2023.106132openalex-snapshot
Adrenergic regulation of astroglial aerobic glycolysis and lipid metabolism: Towards a noradrenergic hypothesis of neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.neuarg.2024.08.005openalex-snapshot
Demencias. ¿Qué hacemos hoy y qué podríamos hacer? Análisis de una cohorte en el mundo real de pacientes con trastornos cognitivos y conductuales
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2023.105167openalex-snapshot
Noradrenergic and cholinergic systems take centre stage in neuropsychiatric diseases of ageing
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2026.106790openalex-snapshot
Rethinking early Alzheimer’s disease: An impaired internal model updating disorder?
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2023.09.010openalex-snapshot
Early treatment with an M1 and sigma-1 receptor agonist prevents cognitive decline in a transgenic rat model displaying Alzheimer-like amyloid pathology
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2025.03.006openalex-snapshot
Long-term nucleus basalis cholinergic lesions alter the structure of cortical vasculature, astrocytic density and microglial activity in Wistar rats
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Cell-type-specific optogenetic fMRI on basal forebrain reveals functional network basis of behavioral preference
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Action of the Purinergic and Cholinergic Anti-inflammatory Pathways on Oxidative Stress in Patients with Alzheimer’s Disease in the Context of the COVID-19 Pandemic
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.11.029openalex-snapshot
Comparison of the efficacy of updated drugs for the treatment on the improvement of cognitive function in patients with Alzheimer ’s disease: A systematic review and network meta- analysis
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2026.08.008openalex-snapshot
Early functional disconnection of the basal forebrain–hippocampal system predicts memory impairment in amnestic mild cognitive impairment
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Therapeutic potential of proline-rich peptide-1 (PRP-1) in counteracting amyloid-β-mediated cortical and hippocampal neurodegeneration in a rat model
inferred← citeshttps://doi.org/10.1016/j.nlm.2022.107686openalex-snapshot
Dissociating the involvement of muscarinic and nicotinic cholinergic receptors in object memory destabilization and reconsolidation
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Dual inhibition of butyrylcholinesterase and p38α mitogen-activated protein kinase: A new approach for the treatment of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2025.111334openalex-snapshot
Neochlorogenic acid ameliorates Alzheimer's disease-like pathology via scavenging oxidative stress and restoring blood-brain barrier function in zebrafish
inferred← citeshttps://doi.org/10.1016/j.psc.2022.07.003openalex-snapshot
Pathophysiology of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1016/j.snb.2025.138511openalex-snapshot
Simultaneous profiling of cholinesterases and NAD(P)H in murine hippocampus via a dual-responsive indicator to investigate cholinergic impairment in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.talanta.2025.128086openalex-snapshot
Rapid and simple sensing of acetylcholinesterase and inhibition activity by utilizing a portable Raman spectrometer
inferred← citeshttps://doi.org/10.1016/j.trac.2023.117369openalex-snapshot
Application of biomarker-derived fluorescent probes for the detection of Alzheimer's disease
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c00933openalex-snapshot
Targeting Neuroinflammation and Cognitive Decline: First-in-Class Dual Butyrylcholinesterase and p38α Mitogen-Activated Protein Kinase Inhibitors
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.5c00630openalex-snapshot
Functional Evaluation of Tetrahydroisoquinoline-Derived Ligands Reveals Distinct Modulatory Profiles at the Muscarinic M1 Receptor
inferred← citeshttps://doi.org/10.1021/acsomega.5c12400openalex-snapshot
N- Salicyloyl Tryptamine Derivatives Improve Mitochondrial Function To Treat Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1021/acsomega.6c01108openalex-snapshot
“Behavioral and Neuroinflammatory Evaluation of a Novel Isoxazole-5-One Derivative in Animal Models of Alzheimer’s Disease via TNF-α, COX-2, IL-6, and NF-κB Modulation”
inferred← citeshttps://doi.org/10.1038/s41392-024-01911-3openalex-snapshot
Recent advances in Alzheimer’s disease: mechanisms, clinical trials and new drug development strategies
inferred← citeshttps://doi.org/10.1038/s41467-024-50042-4openalex-snapshot
Histamine H1 receptors in dentate gyrus-projecting cholinergic neurons of the medial septum suppress contextual fear retrieval in mice
inferred← citeshttps://doi.org/10.1038/s41598-024-80102-0openalex-snapshot
The novel orthosteric agonist M1 muscarinic acetylcholine receptor reveals anti-Alzheimer’s disease activity
inferred← citeshttps://doi.org/10.1039/d3cp01480kopenalex-snapshot
Interactions with amyloid beta peptide and acetylcholinesterase increase alkaline phosphatase activity
inferred← citeshttps://doi.org/10.1039/d4md00060aopenalex-snapshot
Carltonine-derived compounds for targeted butyrylcholinesterase inhibition
inferred← citeshttps://doi.org/10.1039/d5tb02633dopenalex-snapshot
Advances in ultrasensitive detection technologies for blood-based biomarkers of Alzheimer's disease
inferred← citeshttps://doi.org/10.1039/d6ay01083kopenalex-snapshot
Engineering a nanocluster-immobilized MOF@MOF architecture-based ratiometric fluorescence bioassay for sensing neurodegenerative disease-related acetylcholinesterase and inhibitor drugs
inferred← citeshttps://doi.org/10.1080/07391102.2025.2458327openalex-snapshot
Pharmacophore-based virtual screening of the chromone derivatives as potential therapeutic for Alzheimer’s disease
inferred← citeshttps://doi.org/10.1080/14737175.2024.2313557openalex-snapshot
Are pharmacotherapeutics effective for treating aphasia?
inferred← citeshttps://doi.org/10.1080/14756366.2024.2313682openalex-snapshot
Novel anti-neuroinflammatory pyranone-carbamate derivatives as selective butyrylcholinesterase inhibitors for treating Alzheimer’s disease
inferred← citeshttps://doi.org/10.1093/braincomms/fcae204openalex-snapshot
Chronic inflammation with microglia senescence at basal forebrain: impact on cholinergic deficit in Alzheimer’s brain haemodynamics
inferred← citeshttps://doi.org/10.1093/ndt/gfaf029openalex-snapshot
Cholinergic system in patients with chronic kidney disease: cognitive and renal implications
inferred← citeshttps://doi.org/10.1097/md.0000000000040726openalex-snapshot
Exploring the potential mechanism of Polygonatum sibiricum for Alzheimer’s disease based on network pharmacology and molecular docking: An observational study
inferred← citeshttps://doi.org/10.1101/2024.06.19.598824openalex-snapshot
Interaction between mitochondrial translocator protein and aging in inflammatory responses in mouse hippocampus
inferred← citeshttps://doi.org/10.1109/jstqe.2025.3564366openalex-snapshot
Photobiomodulation Ameliorates Neuronal Damage in an Amyloid-Beta Induced Rat Model
inferred← citeshttps://doi.org/10.1111/acel.70039openalex-snapshot
Age‐Dependent Regulation of Hippocampal Inflammation by the Mitochondrial Translocator Protein in Mice
inferred← citeshttps://doi.org/10.1111/jnc.15683openalex-snapshot
Long‐term nucleus basalis cholinergic depletion induces attentional deficits and impacts cortical neurons and BDNF levels without affecting the NGF synthesis
inferred← citeshttps://doi.org/10.1111/jnc.16027openalex-snapshot
Recent advances in cholinergic mechanisms: A preface for the ISCM2022 special issue
inferred← citeshttps://doi.org/10.1111/jnc.16032openalex-snapshot
Brain energy metabolism: A roadmap for future research
inferred← citeshttps://doi.org/10.1111/jnc.70081openalex-snapshot
Evaluation of the Alterations in Central Cholinergic Neurotransmission in Aging and Amyloid Precursor Protein Knock‐In Mice
inferred← citeshttps://doi.org/10.1111/joim.70096openalex-snapshot
Co‐pathologies and biological processes beyond amyloid‐beta and tau in people with Alzheimer's disease: Evidence from clinical cohort studies
inferred← citeshttps://doi.org/10.1111/nan.12835openalex-snapshot
Early loss of locus coeruleus innervation promotes cognitive and neuropathological changes before amyloid plaque deposition in a transgenic rat model of Alzheimer's disease
inferred← citeshttps://doi.org/10.1126/sciadv.ado1508openalex-snapshot
Distinct septo-hippocampal cholinergic projections separately mediate stress-induced emotional and cognitive deficits
inferred← citeshttps://doi.org/10.1134/s0012500823700179openalex-snapshot
Ammonium Amphiphiles Based on Natural Compounds: Design, Synthesis, Properties, and Biomedical Applications. A Review
inferred← citeshttps://doi.org/10.1152/jn.00476.2024openalex-snapshot
Cortical acetylcholine response to deep brain stimulation of the basal forebrain in mice
inferred← citeshttps://doi.org/10.1155/2023/9935942openalex-snapshot
[Retracted] The Effective Components, Core Targets, and Key Pathways of Ginseng against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1159/000537883openalex-snapshot
LINC00472 Regulates Ferroptosis of Neurons in Alzheimer’s Disease via FOXO1
inferred← citeshttps://doi.org/10.1177/13872877251325891openalex-snapshot
The unsafe profile of lecanemab
inferred← citeshttps://doi.org/10.1177/13872877251400667openalex-snapshot
Dysregulated mTOR signaling in Alzheimer's disease: Linking pathogenic mechanisms to emerging therapeutic strategies
inferred← citeshttps://doi.org/10.1177/13872877261417548openalex-snapshot
Serious doubts about amyloid-β (Aβ) biomarkers and anti-Aβ immunotherapy
inferred← citeshttps://doi.org/10.1186/s13195-024-01536-2openalex-snapshot
Effects of strategic white matter hyperintensities of cholinergic pathways on basal forebrain volume in patients with amyloid-negative neurocognitive disorders
inferred← citeshttps://doi.org/10.1186/s13195-026-02051-2openalex-snapshot
Aging alters the vulnerability pattern to amyloid-beta oligomers in wild-type mice: a behavioral and neurobiological study
inferred← citeshttps://doi.org/10.1248/bpb.b22-00797openalex-snapshot
Plantainoside B in Bacopa monniera Binds to Aβ Aggregates Attenuating Neuronal Damage and Memory Deficits Induced by Aβ
inferred← citeshttps://doi.org/10.1248/bpb.b25-00308openalex-snapshot
Stimulation of α7 Nicotinic Acetylcholine Receptors by PNU282987 Demonstrates Efferocytosis-Like Activation and Neuroprotection in Human Models of Microglia and Cholinergic Neurons under the Pathophysiological Conditions of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1523/jneurosci.2148-24.2025openalex-snapshot
MiR-153 Prevents NRF2 Nuclear Translocation to Drive Hypoperfusion-Related Cognitive Deficits by Targeting KPNA5
inferred← citeshttps://doi.org/10.1590/1980-5764-dn-2025-0290openalex-snapshot
Non-pharmacological strategies for the management of Alzheimer's disease
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4225413/v1openalex-snapshot
Exploring the potential mechanism of Polygonatum sibiricum for Alzheimer's disease based on network pharmacology and molecular docking
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7399280/v1openalex-snapshot
Network Pharmacology-guided Identification and Molecular Validation of Multi-Target Phytoconstituents from Gmelina arborea against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7399280/v2openalex-snapshot
Network Pharmacology-guided Identification and Molecular Validation of Multi-Target Phytoconstituents from Gmelina arborea against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7521725/v1openalex-snapshot
Exploring potential inhibitors from Eriobotrya japonica targeting AChE and BChE in Alzheimer's Disease through docking, ADMET profiling, and DFT analysis
inferred← citeshttps://doi.org/10.2174/0115734080401748250711113148openalex-snapshot
In Vitro Investigation of Acetylcholinesterase Inhibition by Methanolic Extract of Muntingia calabura Bark
inferred← citeshttps://doi.org/10.2174/0118715249302264240715060630openalex-snapshot
Targeting Adenylate Cyclase: A Novel Concept for Stimulation of Neurogenesis and Pharmacotherapy of Alzheimer's Disease
inferred← citeshttps://doi.org/10.2174/1567205020666230309113749openalex-snapshot
Effect of APOE4 Allele and Gender on the Rate of Atrophy in the Hippocampus, Entorhinal Cortex, and Fusiform Gyrus in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.2174/1573408019666230816143357openalex-snapshot
Insight into JNK Inhibition-based Strategy for the Treatment of Alzheimer's Disease
inferred← citeshttps://doi.org/10.2174/9798898812553125010009openalex-snapshot
The Role of Nutraceuticals in the Treatment of Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.2174/9798898815646126010005openalex-snapshot
Tau Protein in Alzheimer's Disease
inferred← citeshttps://doi.org/10.22533/at.ed.15934123010610openalex-snapshot
PHARMACOLOGICAL TREATMENT OF ALZHEIMER'S DISEASE: AN INTEGRATIVE REVIEW ON THE EFFECTIVENESS OF CHOLINESTERASE AND MEMANTINE INHIBITORS
inferred← citeshttps://doi.org/10.31083/jin23090openalex-snapshot
Current Status of Plant-Based Bioactive Compounds as Therapeutics in Alzheimer’s Diseases
inferred← citeshttps://doi.org/10.31083/jin26903openalex-snapshot
5-Fluorouracil Impairs Transmission of Acetylcholine in the Hippocampus and Induces Cognitive Impairments in Mice
inferred← citeshttps://doi.org/10.31857/s0044467724050026openalex-snapshot
The role of the basal forebrain in the pathogenesis of Alzheimer’s disease
inferred← citeshttps://doi.org/10.31857/s2686953522600544openalex-snapshot
AMMONIUM AMPHIPHILES BASED ON NATURAL COMPOUNDS: DESIGN, SYNTHESIS, PROPERTIES AND BIOMEDICAL APPLICATIONS. A REVIEW
inferred← citeshttps://doi.org/10.3233/adr-240035openalex-snapshot
Caring for Individuals with Alzheimer’s Disease: A Spotlight on Hispanic Caregivers
inferred← citeshttps://doi.org/10.3389/fchem.2025.1479763openalex-snapshot
dyphAI dynamic pharmacophore modeling with AI: a tool for efficient screening of new acetylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1722477openalex-snapshot
Nerve growth factor responsive elements modulate immune cell inflammation and are dysregulated in an Alzheimer’s disease mouse model
inferred← citeshttps://doi.org/10.3389/fnagi.2022.876019openalex-snapshot
Phenotypic Displays of Cholinergic Enzymes Associate With Markers of Inflammation, Neurofibrillary Tangles, and Neurodegeneration in Pre- and Early Symptomatic Dementia Subjects
inferred← citeshttps://doi.org/10.3389/fnagi.2025.1518198openalex-snapshot
Associations between peripheral nerve stimulation and cognitive performance: insights from healthy individuals and various disease pathologies
inferred← citeshttps://doi.org/10.3389/fneur.2025.1505739openalex-snapshot
Evaluation of vascular cognitive impairment and identification of imaging markers using machine learning: a multimodal MRI study
inferred← citeshttps://doi.org/10.3389/fnins.2022.998224openalex-snapshot
Predictors of response to acetylcholinesterase inhibitors in dementia: A systematic review
inferred← citeshttps://doi.org/10.3389/fnmol.2022.941467openalex-snapshot
Altered levels of variant cholinesterase transcripts contribute to the imbalanced cholinergic signaling in Alzheimer’s and Parkinson’s disease
inferred← citeshttps://doi.org/10.3389/fphar.2022.941656openalex-snapshot
Landscape of immune infiltration in entorhinal cortex of patients with Alzheimerʼs disease
inferred← citeshttps://doi.org/10.3389/fphar.2023.1276100openalex-snapshot
Impairment of exocytotic transmitter release by decynium-22 through an inhibition of ion channels
inferred← citeshttps://doi.org/10.3389/fphar.2025.1694610openalex-snapshot
From heart to brain: cognitive potential of propranolol and diltiazem through cholinergic enhancement via butyrylcholinesterase inhibition
inferred← citeshttps://doi.org/10.3389/fphar.2026.1929468openalex-snapshot
Adult-onset hippocampal α7 nicotinic acetylcholine receptor loss rapidly drives Alzheimer-like neuropathology in mice
inferred← citeshttps://doi.org/10.3390/biology14091114openalex-snapshot
Mulberroside A: A Multi-Target Neuroprotective Agent in Alzheimer’s Disease via Cholinergic Restoration and PI3K/AKT Pathway Activation
inferred← citeshttps://doi.org/10.3390/biom15010110openalex-snapshot
Anxiolytic, Antidepressant, and Anticholinesterase Effects of Essential Oil from Myrcia sylvatica (G.Mey.) DC
inferred← citeshttps://doi.org/10.3390/biom15081188openalex-snapshot
Apelin-13-Mediated Upregulation of METTL3 Ameliorates Alzheimer’s Disease via Inhibiting Neuroinflammation Through m6A-Dependent Regulation of lncRNA BDNF-AS
inferred← citeshttps://doi.org/10.3390/biom16050726openalex-snapshot
Akkermansia muciniphila and Alzheimer’s Disease: Mechanisms, Evidence and Translational Potential
inferred← citeshttps://doi.org/10.3390/brainsci14060590openalex-snapshot
Research Progress on the Pathogenesis, Diagnosis, and Drug Therapy of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/cimb46070407openalex-snapshot
Muscarinic Receptors and Alzheimer’s Disease: New Perspectives and Mechanisms
inferred← citeshttps://doi.org/10.3390/ijms24010507openalex-snapshot
Modulation of Muscarinic Signalling in the Central Nervous System by Steroid Hormones and Neurosteroids
inferred← citeshttps://doi.org/10.3390/ijms24021340openalex-snapshot
Mechanistic Insights, Treatment Paradigms, and Clinical Progress in Neurological Disorders: Current and Future Prospects
inferred← citeshttps://doi.org/10.3390/ijms24076598openalex-snapshot
Δ8-THC Protects against Amyloid Beta Toxicity Modulating ER Stress In Vitro: A Transcriptomic Analysis
inferred← citeshttps://doi.org/10.3390/ijms241512025openalex-snapshot
The Sigma Receptors in Alzheimer’s Disease: New Potential Targets for Diagnosis and Therapy
inferred← citeshttps://doi.org/10.3390/ijms25073892openalex-snapshot
Alzheimer’s Amyloid Hypothesis and Antibody Therapy: Melting Glaciers?
inferred← citeshttps://doi.org/10.3390/ijms26031234openalex-snapshot
Deciphering the Functions of Raphe–Hippocampal Serotonergic and Glutamatergic Circuits and Their Deficits in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/ijms26146980openalex-snapshot
Alzheimer’s Disease Etiology Hypotheses and Therapeutic Strategies: A Perspective
inferred← citeshttps://doi.org/10.3390/ijms26199444openalex-snapshot
Alzheimer’s Disease: From Molecular Mechanisms to Promising Therapeutic Strategies
inferred← citeshttps://doi.org/10.3390/ijms26199670openalex-snapshot
The Central Cholinergic Synapse: A Primer
inferred← citeshttps://doi.org/10.3390/ijms27104556openalex-snapshot
Network Pharmacology Reveals the Therapeutic Potential of BBB-Permeable Compounds from Lonicera caerulea for Alzheimer’s Disease and Lipid Metabolism Disorders
inferred← citeshttps://doi.org/10.3390/life13010221openalex-snapshot
Involvement of an Aberrant Vascular System in Neurodevelopmental, Neuropsychiatric, and Neuro-Degenerative Diseases
inferred← citeshttps://doi.org/10.3390/md23030091openalex-snapshot
The Advancements of Marine Natural Products in the Treatment of Alzheimer’s Disease: A Study Based on Cell and Animal Experiments
inferred← citeshttps://doi.org/10.3390/medsci14040426openalex-snapshot
Concurrent Use of Anticholinergic and Antidementia Medicines in Older Adults with Dementia: A Systematic Review of Prevalence, Predictors and Clinical Outcomes
inferred← citeshttps://doi.org/10.3390/molecules29215131openalex-snapshot
Recent Advances in Therapeutics for the Treatment of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/nu16081232openalex-snapshot
L-Carnitine in the Treatment of Psychiatric and Neurological Manifestations: A Systematic Review
inferred← citeshttps://doi.org/10.3390/ph15101214openalex-snapshot
Synthesis, Biological Evaluation and Machine Learning Prediction Model for Fluorinated Cinchona Alkaloid-Based Derivatives as Cholinesterase Inhibitors
inferred← citeshttps://doi.org/10.3390/ph18121871openalex-snapshot
Pharmacokinetic and Pharmacodynamic Evaluation of PZ-2891, an Anti-Alzheimer’s Disease Agonist of PANK2
inferred← citeshttps://doi.org/10.62993/cmed.2024.2.1openalex-snapshot
Dementia. Specifics of its manifestations. Clinical patterns of dementia in Alzheimer's disease
inferred← citeshttps://doi.org/10.7759/cureus.31065openalex-snapshot
Conventional Versus New Treatment: Comparing the Effects of Acetylcholinesterase Inhibitors and N-Methyl-D-Aspartate Receptor Antagonist With Aducanumab
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