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Prospects and challenges of imaging neuroinflammation beyond TSPO in Alzheimer’s disease
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archneurol.2008.511openalex-snapshot
Carbon 11–Labeled Pittsburgh Compound B and Carbon 11–Labeled (R)-PK11195 Positron Emission Tomographic Imaging in Alzheimer Disease
inferredcites →https://doi.org/10.1001/jamaneurol.2019.1424openalex-snapshot
Association of Amyloid and Tau With Cognition in Preclinical Alzheimer Disease
inferredcites →https://doi.org/10.1002/ana.10311openalex-snapshot
Imaging the metabolic footprint of Glut1 deficiency on the brain
inferredcites →https://doi.org/10.1002/ana.410400512openalex-snapshot
Deficient glutamate tranport is associated with neurodegeneration in Alzheimer's disease
inferredcites →https://doi.org/10.1002/cne.24040openalex-snapshot
The search for true numbers of neurons and glial cells in the human brain: A review of 150 years of cell counting
inferredcites →https://doi.org/10.1002/glia.22357openalex-snapshot
Molecular imaging of microglia/macrophages in the brain
inferredcites →https://doi.org/10.1002/glia.440080208openalex-snapshot
Monoamine oxidase‐B in astrocytes
inferredcites →https://doi.org/10.1002/jnr.24075openalex-snapshot
Astrocyte dysfunction in Alzheimer disease
inferredcites →https://doi.org/10.1002/jnr.490340611openalex-snapshot
Expression of non‐adrenergic imidazoline sites in rat cerebral cortical astrocytes
inferredcites →https://doi.org/10.1002/syn.21541openalex-snapshot
Evaluation and initial in vitro and ex vivo characterization of the potential positron emission tomography ligand, BU99008 (2‐(4,5‐Dihydro‐1H‐imidazol‐2‐yl)‐1‐ methyl‐1H‐indole), for the imidazoline2 binding site
inferredcites →https://doi.org/10.1007/978-3-7091-9324-2_31openalex-snapshot
Monoamine oxidase-B in motor cortex and spinal cord in amyotrophic lateral sclerosis studied by quantitative autoradiography
inferredcites →https://doi.org/10.1007/978-3-7091-9324-2_33openalex-snapshot
Reactive gliosis and monoamine oxidase B
inferredcites →https://doi.org/10.1007/s00259-008-0908-9openalex-snapshot
Nuclear imaging of neuroinflammation: a comprehensive review of [11C]PK11195 challengers
inferredcites →https://doi.org/10.1007/s00259-010-1612-0openalex-snapshot
In vivo changes in microglial activation and amyloid deposits in brain regions with hypometabolism in Alzheimer’s disease
inferredcites →https://doi.org/10.1007/s00259-011-1895-9openalex-snapshot
In vivo imaging of astrocytosis in Alzheimer’s disease: an 11C-L-deuteriodeprenyl and PIB PET study
inferredcites →https://doi.org/10.1007/s00259-015-3047-0openalex-snapshot
Astrocytosis precedes amyloid plaque deposition in Alzheimer APPswe transgenic mouse brain: a correlative positron emission tomography and in vitro imaging study
inferredcites →https://doi.org/10.1007/s00259-016-3457-7openalex-snapshot
Decreased in vivo availability of the cannabinoid type 2 receptor in Alzheimer’s disease
inferredcites →https://doi.org/10.1007/s00259-018-4217-7openalex-snapshot
Longitudinal association between astrocyte function and glucose metabolism in autosomal dominant Alzheimer’s disease
inferredcites →https://doi.org/10.1007/s00259-019-04369-6openalex-snapshot
[11C]JNJ54173717, a novel P2X7 receptor radioligand as marker for neuroinflammation: human biodistribution, dosimetry, brain kinetic modelling and quantification of brain P2X7 receptors in patients with Parkinson’s disease and healthy volunteers
inferredcites →https://doi.org/10.1007/s00401-009-0619-8openalex-snapshot
Astrocytes: biology and pathology
inferredcites →https://doi.org/10.1007/s004010000284openalex-snapshot
Local distribution of microglia in the normal adult human central nervous system differs by up to one order of magnitude
inferredcites →https://doi.org/10.1007/s00415-019-09400-2openalex-snapshot
In vivo direct relation of tau pathology with neuroinflammation in early Alzheimer’s disease
inferredcites →https://doi.org/10.1007/s00429-017-1383-5openalex-snapshot
Human astrocytes: structure and functions in the healthy brain
inferredcites →https://doi.org/10.1016/0014-4886(95)90022-5openalex-snapshot
Early association of reactive astrocytes with senile plaques in Alzheimer's disease
inferredcites →https://doi.org/10.1016/0165-5728(89)90115-xopenalex-snapshot
Relationship of microglia and astrocytes to amyloid deposits of Alzheimer disease
inferredcites →https://doi.org/10.1016/j.ajpath.2013.02.031openalex-snapshot
A Phenotypic Change But Not Proliferation Underlies Glial Responses in Alzheimer Disease
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Increased Binding of Peripheral Benzodiazepine Receptor in Alzheimer's Disease Measured by Positron Emission Tomography with [11C]DAA1106
inferredcites →https://doi.org/10.1016/j.cell.2015.12.056openalex-snapshot
The Cellular Phase of Alzheimer’s Disease
inferredcites →https://doi.org/10.1016/j.cell.2017.05.018openalex-snapshot
A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease
inferredcites →https://doi.org/10.1016/j.celrep.2014.07.042openalex-snapshot
Microglia Modulate Wiring of the Embryonic Forebrain
inferredcites →https://doi.org/10.1016/j.celrep.2016.12.041openalex-snapshot
Coupled Proliferation and Apoptosis Maintain the Rapid Turnover of Microglia in the Adult Brain
inferredcites →https://doi.org/10.1016/j.celrep.2017.07.004openalex-snapshot
The Lifespan and Turnover of Microglia in the Human Brain
inferredcites →https://doi.org/10.1016/j.dadm.2015.09.001openalex-snapshot
Revolutionizing Alzheimer's disease and clinical trials through biomarkers
inferredcites →https://doi.org/10.1016/j.expneurol.2012.04.021openalex-snapshot
The role of astrocytes in amyloid β-protein toxicity and clearance
inferredcites →https://doi.org/10.1016/j.immuni.2013.04.004openalex-snapshot
Tissue-Resident Macrophages Self-Maintain Locally throughout Adult Life with Minimal Contribution from Circulating Monocytes
inferredcites →https://doi.org/10.1016/j.immuni.2015.06.012openalex-snapshot
Genetic Cell Ablation Reveals Clusters of Local Self-Renewing Microglia in the Mammalian Central Nervous System
inferredcites →https://doi.org/10.1016/j.immuni.2017.08.008openalex-snapshot
The TREM2-APOE Pathway Drives the Transcriptional Phenotype of Dysfunctional Microglia in Neurodegenerative Diseases
inferredcites →https://doi.org/10.1016/j.it.2019.02.001openalex-snapshot
Priming Microglia for Innate Immune Memory in the Brain
inferredcites →https://doi.org/10.1016/j.jalz.2017.09.013openalex-snapshot
Cortical microstructural changes along the Alzheimer's disease continuum
inferredcites →https://doi.org/10.1016/j.jalz.2018.06.2999openalex-snapshot
O5‐01‐05: RELATIONSHIP BETWEEN ASTROCYTE ACTIVATION USING [11C]BU99008 PET, GLUCOSE METABOLISM AND AMYLOID IN ALZHEIMER'S DISEASE: A DEMENTIA PLATFORM UK EXPERIMENTAL MEDICINE STUDY
inferredcites →https://doi.org/10.1016/j.jns.2007.01.057openalex-snapshot
Evidence for astrocytosis in ALS demonstrated by [11C](l)-deprenyl-D2 PET
inferredcites →https://doi.org/10.1016/j.nbd.2008.08.001openalex-snapshot
Microglia, amyloid, and cognition in Alzheimer's disease: An [11C](R)PK11195-PET and [11C]PIB-PET study
inferredcites →https://doi.org/10.1016/j.nbd.2018.06.004openalex-snapshot
Does inflammation precede tau aggregation in early Alzheimer's disease? A PET study
inferredcites →https://doi.org/10.1016/j.neuint.2010.10.013openalex-snapshot
Activated MAO-B in the brain of Alzheimer patients, demonstrated by [11C]-l-deprenyl using whole hemisphere autoradiography
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2012.04.021openalex-snapshot
Microglial activation in Alzheimer's disease: an (R)-[11C]PK11195 positron emission tomography study
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2012.09.012openalex-snapshot
Neuroinflammatory phenotype in early Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2015.08.024openalex-snapshot
Aging causes morphological alterations in astrocytes and microglia in human substantia nigra pars compacta
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2018.03.014openalex-snapshot
Aerobic glycolysis and tau deposition in preclinical Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.nicl.2019.101767openalex-snapshot
Quantification of white matter cellularity and damage in preclinical and early symptomatic Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.nicl.2019.101801openalex-snapshot
CSF glial biomarkers YKL40 and sTREM2 are associated with longitudinal volume and diffusivity changes in cognitively unimpaired individuals
inferredcites →https://doi.org/10.1016/j.pneurobio.2017.12.003openalex-snapshot
Functional dissection of astrocyte-secreted proteins: Implications in brain health and diseases
inferredcites →https://doi.org/10.1016/j.pscychresns.2011.08.013openalex-snapshot
Increased binding of peripheral benzodiazepine receptor in mild cognitive impairment–dementia converters measured by positron emission tomography with [11C]DAA1106
inferredcites →https://doi.org/10.1016/j.tins.2006.07.001openalex-snapshot
Microglial senescence: does the brain's immune system have an expiration date?
inferredcites →https://doi.org/10.1016/s0140-6736(01)05625-2openalex-snapshot
In-vivo measurement of activated microglia in dementia
inferredcites →https://doi.org/10.1016/s0197-4580(02)00090-8openalex-snapshot
Immune reactive cells in senile plaques and cognitive decline in Alzheimer’s disease
inferredcites →https://doi.org/10.1016/s0304-3940(99)00489-9openalex-snapshot
Chronic exposure of rat primary astrocyte cultures to manganese results in increased binding sites for the ‘peripheral-type’ benzodiazepine receptor ligand 3H-PK 11195
inferredcites →https://doi.org/10.1016/s1474-4422(15)70016-5openalex-snapshot
Neuroinflammation in Alzheimer's disease
inferredcites →https://doi.org/10.1021/acschemneuro.6b00056openalex-snapshot
In Vivo Imaging of Human Neuroinflammation
inferredcites →https://doi.org/10.1038/jcbfm.2010.63openalex-snapshot
Two Binding Sites for [ 3 H]PBR28 in Human Brain: Implications for TSPO PET Imaging of Neuroinflammation
inferredcites →https://doi.org/10.1038/nature21029openalex-snapshot
Neurotoxic reactive astrocytes are induced by activated microglia
inferredcites →https://doi.org/10.1038/ncomms13441openalex-snapshot
Mapping synaptic glutamate transporter dysfunction in vivo to regions surrounding Aβ plaques by iGluSnFR two-photon imaging
inferredcites →https://doi.org/10.1038/ni.3102openalex-snapshot
Innate immunity in Alzheimer's disease
inferredcites →https://doi.org/10.1038/nm.3639openalex-snapshot
GABA from reactive astrocytes impairs memory in mouse models of Alzheimer's disease
inferredcites →https://doi.org/10.1038/nm838openalex-snapshot
Adult mouse astrocytes degrade amyloid-β in vitro and in situ
inferredcites →https://doi.org/10.1038/nn.3554openalex-snapshot
The microglial sensome revealed by direct RNA sequencing
inferredcites →https://doi.org/10.1038/nn.3599openalex-snapshot
Identification of a unique TGF-β–dependent molecular and functional signature in microglia
inferredcites →https://doi.org/10.1038/nn.4428openalex-snapshot
Astrocytes mediate neurovascular signaling to capillary pericytes but not to arterioles
inferredcites →https://doi.org/10.1038/nn.4492openalex-snapshot
[18F]FDG PET signal is driven by astroglial glutamate transport
inferredcites →https://doi.org/10.1038/nn.4493openalex-snapshot
Identification of diverse astrocyte populations and their malignant analogs
inferredcites →https://doi.org/10.1038/nrneurol.2014.38openalex-snapshot
Microglial priming in neurodegenerative disease
inferredcites →https://doi.org/10.1038/s41467-018-02926-5openalex-snapshot
A transcriptomic atlas of aged human microglia
inferredcites →https://doi.org/10.1038/s41467-018-08279-3openalex-snapshot
Neuropathological correlates and genetic architecture of microglial activation in elderly human brain
inferredcites →https://doi.org/10.1038/s41586-018-0023-4openalex-snapshot
Innate immune memory in the brain shapes neurological disease hallmarks
inferredcites →https://doi.org/10.1038/s41593-018-0175-4openalex-snapshot
A 3D human triculture system modeling neurodegeneration and neuroinflammation in Alzheimer’s disease
inferredcites →https://doi.org/10.1038/s41593-018-0325-8openalex-snapshot
Astrocyte function from information processing to cognition and cognitive impairment
inferredcites →https://doi.org/10.1038/srep16404openalex-snapshot
Early astrocytosis in autosomal dominant Alzheimer’s disease measured in vivo by multi-tracer positron emission tomography
inferredcites →https://doi.org/10.1038/srep45496openalex-snapshot
Cortical laminar tau deposits and activated astrocytes in Alzheimer’s disease visualised by 3H-THK5117 and 3H-deprenyl autoradiography
inferredcites →https://doi.org/10.1073/pnas.1800165115openalex-snapshot
Normal aging induces A1-like astrocyte reactivity
inferredcites →https://doi.org/10.1073/pnas.1812155116openalex-snapshot
PET imaging of microglia by targeting macrophage colony-stimulating factor 1 receptor (CSF1R)
inferredcites →https://doi.org/10.1093/brain/awt145openalex-snapshot
In vivo radioligand binding to translocator protein correlates with severity of Alzheimer’s disease
inferredcites →https://doi.org/10.1093/brain/awv404openalex-snapshot
Diverging longitudinal changes in astrocytosis and amyloid PET in autosomal dominant Alzheimer’s disease
inferredcites →https://doi.org/10.1093/brain/aww017openalex-snapshot
Early and protective microglial activation in Alzheimer’s disease: a prospective study using18F-DPA-714 PET imaging
inferredcites →https://doi.org/10.1093/brain/awx120openalex-snapshot
Brain inflammation accompanies amyloid in the majority of mild cognitive impairment cases due to Alzheimer’s disease
inferredcites →https://doi.org/10.1093/brain/awx172openalex-snapshot
Brain monoamine oxidase B and A in human parkinsonian dopamine deficiency disorders
inferredcites →https://doi.org/10.1093/brain/awy079openalex-snapshot
Distinct dynamic profiles of microglial activation are associated with progression of Alzheimer's disease
inferredcites →https://doi.org/10.1093/brain/awy188openalex-snapshot
Microglial activation correlates in vivo with both tau and amyloid in Alzheimer’s disease
inferredcites →https://doi.org/10.1097/nen.0000000000000176openalex-snapshot
Neuroinflammatory Signals in Alzheimer Disease and APP/PS1 Transgenic Mice
inferredcites →https://doi.org/10.1097/nen.0b013e318188b204openalex-snapshot
The Positron Emission Tomography Ligand DAA1106 Binds With High Affinity to Activated Microglia in Human Neurological Disorders
inferredcites →https://doi.org/10.1097/nen.0b013e3182933788openalex-snapshot
Differential Relationships of Reactive Astrocytes and Microglia to Fibrillar Amyloid Deposits in Alzheimer Disease
inferredcites →https://doi.org/10.1111/bpa.12456openalex-snapshot
Microglia show altered morphology and reduced arborization in human brain during aging and A lzheimer's disease
inferredcites →https://doi.org/10.1111/j.1365-2990.2008.01006.xopenalex-snapshot
Expression of the translocator protein of 18 kDa by microglia, macrophages and astrocytes based on immunohistochemical localization in abnormal human brain
inferredcites →https://doi.org/10.1111/j.1365-2990.2009.01030.xopenalex-snapshot
Population variation in oxidative stress and astrocyte DNA damage in relation to Alzheimer-type pathology in the ageing brain
inferredcites →https://doi.org/10.1111/j.1365-2990.2012.01306.xopenalex-snapshot
Review: Microglia of the aged brain: primed to be activated and resistant to regulation
inferredcites →https://doi.org/10.1111/j.1476-5381.1994.tb14842.xopenalex-snapshot
The effects of chronic imidazoline drug treatment on glial fibrillary acidic protein concentrations in rat brain
inferredcites →https://doi.org/10.1111/j.1749-6632.1999.tb09388.xopenalex-snapshot
Imidazoline Receptors and Human Brain Disordersa
inferredcites →https://doi.org/10.1111/nan.12009openalex-snapshot
Neuroinflammation in ageing and in neurodegenerative disease
inferredcites →https://doi.org/10.1111/nan.12011openalex-snapshot
Review: Activation patterns of microglia and their identification in the human brain
inferredcites →https://doi.org/10.1111/nan.12337openalex-snapshot
Human adult neurogenesis across the ages: An immunohistochemical study
inferredcites →https://doi.org/10.1111/nan.12408openalex-snapshot
Age‐associated changes in the blood‐brain barrier: comparative studies in human and mouse
inferredcites →https://doi.org/10.1111/neup.12235openalex-snapshot
TMEM119 marks a subset of microglia in the human brain
inferredcites →https://doi.org/10.1126/science.1110647openalex-snapshot
Resting Microglial Cells Are Highly Dynamic Surveillants of Brain Parenchyma in Vivo
inferredcites →https://doi.org/10.1126/science.1194637openalex-snapshot
Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
inferredcites →https://doi.org/10.1126/science.1202529openalex-snapshot
Synaptic Pruning by Microglia Is Necessary for Normal Brain Development
inferredcites →https://doi.org/10.1126/science.aat4104openalex-snapshot
Cell-autonomous clock of astrocytes drives circadian behavior in mammals
inferredcites →https://doi.org/10.1155/2014/693851openalex-snapshot
Proliferation in the Alzheimer Hippocampus Is due to Microglia, Not Astroglia, and Occurs at Sites of Amyloid Deposition
inferredcites →https://doi.org/10.1159/000017324openalex-snapshot
Evidence Supporting the Existence of an Activity-Dependent Astrocyte-Neuron Lactate Shuttle
inferredcites →https://doi.org/10.1159/000337115openalex-snapshot
Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity
inferredcites →https://doi.org/10.1177/1073858413504466openalex-snapshot
Multiple Roles for Astrocytes as Effectors of Cytokines and Inflammatory Mediators
inferredcites →https://doi.org/10.1177/1536012118792317openalex-snapshot
Emerging PET Radiotracers and Targets for Imaging of Neuroinflammation in Neurodegenerative Diseases: Outlook Beyond TSPO
inferredcites →https://doi.org/10.1186/1742-2094-10-90openalex-snapshot
3H-Deprenyl and 3H-PIB autoradiography show different laminar distributions of astroglia and fibrillar β-amyloid in Alzheimer brain
inferredcites →https://doi.org/10.1186/1742-2094-9-179openalex-snapshot
Extensive innate immune gene activation accompanies brain aging, increasing vulnerability to cognitive decline and neurodegeneration: a microarray study
inferredcites →https://doi.org/10.1186/1750-1326-6-55openalex-snapshot
Age-dependent decrease in glutamine synthetase expression in the hippocampal astroglia of the triple transgenic Alzheimer's disease mouse model: mechanism for deficient glutamatergic transmission?
inferredcites →https://doi.org/10.1186/s12974-016-0601-zopenalex-snapshot
Microglial immunophenotype in dementia with Alzheimer’s pathology
inferredcites →https://doi.org/10.1186/s12974-017-0893-7openalex-snapshot
YKL-40 (Chitinase 3-like I) is expressed in a subset of astrocytes in Alzheimer’s disease and other tauopathies
inferredcites →https://doi.org/10.1186/s13024-017-0192-xopenalex-snapshot
Glial contributions to neurodegeneration in tauopathies
inferredcites →https://doi.org/10.1186/s13024-018-0244-xopenalex-snapshot
Early long-term administration of the CSF1R inhibitor PLX3397 ablates microglia and reduces accumulation of intraneuronal amyloid, neuritic plaque deposition and pre-fibrillar oligomers in 5XFAD mouse model of Alzheimer’s disease
inferredcites →https://doi.org/10.1186/s13064-018-0104-yopenalex-snapshot
Astrocytes, neurons, synapses: a tripartite view on cortical circuit development
inferredcites →https://doi.org/10.1186/s40478-018-0592-3openalex-snapshot
Systemic infection modifies the neuroinflammatory response in late stage Alzheimer’s disease
inferredcites →https://doi.org/10.1212/01.wnl.0000338622.27876.0dopenalex-snapshot
Microglial activation and amyloid deposition in mild cognitive impairment
inferredcites →https://doi.org/10.1212/wnl.0000000000006082openalex-snapshot
CSF biomarkers of neuroinflammation and cerebrovascular dysfunction in early Alzheimer disease
inferredcites →https://doi.org/10.1212/wnl.0000000000007133openalex-snapshot
Microglial activation in early Alzheimer trajectory is associated with higher gray matter volume
inferredcites →https://doi.org/10.1371/journal.pbio.1000527openalex-snapshot
Microglial Interactions with Synapses Are Modulated by Visual Experience
inferredcites →https://doi.org/10.1371/journal.pone.0013950openalex-snapshot
Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease
inferredcites →https://doi.org/10.14283/jpad.2019.11openalex-snapshot
Advancing Alzheimer's Disease Treatment: Lessons from CTAD 2018
inferredcites →https://doi.org/10.1523/eneuro.0088-18.2018openalex-snapshot
Microglia Enhance Synapse Activity to Promote Local Network Synchronization
inferredcites →https://doi.org/10.1523/jneurosci.1487-12.2012openalex-snapshot
Reactive Astrocytes Overexpress TSPO and Are Detected by TSPO Positron Emission Tomography Imaging
inferredcites →https://doi.org/10.1523/jneurosci.3441-12.2013openalex-snapshot
Microglia Regulate the Number of Neural Precursor Cells in the Developing Cerebral Cortex
inferredcites →https://doi.org/10.1523/jneurosci.4037-13.2014openalex-snapshot
Phenotypic Heterogeneity and Plasticity of Isocortical and Hippocampal Astrocytes in the Human Brain
inferredcites →https://doi.org/10.1523/jneurosci.4363-08.2009openalex-snapshot
Resting Microglia Directly Monitor the Functional State of Synapses In Vivo and Determine the Fate of Ischemic Terminals
inferredcites →https://doi.org/10.1523/jneurosci.4707-08.2009openalex-snapshot
Uniquely Hominid Features of Adult Human Astrocytes
inferredcites →https://doi.org/10.1523/jneurosci.5098-09.2010openalex-snapshot
Amyloid-β Aggregates Cause Alterations of Astrocytic Metabolic Phenotype: Impact on Neuronal Viability
inferredcites →https://doi.org/10.1523/jneurosci.6221-11.2012openalex-snapshot
Genomic Analysis of Reactive Astrogliosis
inferredcites →https://doi.org/10.2967/jnumed.110.079459openalex-snapshot
Mixed-Affinity Binding in Humans with 18-kDa Translocator Protein Ligands
inferredcites →https://doi.org/10.2967/jnumed.110.087031openalex-snapshot
Evidence for Astrocytosis in Prodromal Alzheimer Disease Provided by 11 C-Deuterium-L-Deprenyl: A Multitracer PET Paradigm Combining 11 C-Pittsburgh Compound B and 18 F-FDG
inferredcites →https://doi.org/10.2967/jnumed.112.108258openalex-snapshot
Imaging Imidazoline-I2Binding Sites in Porcine Brain Using11C-BU99008
inferredcites →https://doi.org/10.2967/jnumed.113.131854openalex-snapshot
Evaluation of 11C-BU99008, a PET Ligand for the Imidazoline2 Binding Sites in Rhesus Brain
inferredcites →https://doi.org/10.2967/jnumed.118.208009openalex-snapshot
Evaluation of 11C-BU99008, a PET Ligand for the Imidazoline2 Binding Site in Human Brain
inferredcites →https://doi.org/10.3109/13813455.2010.539616openalex-snapshot
Astrocytes and energy metabolism
inferredcites →https://doi.org/10.3389/fnint.2016.00008openalex-snapshot
The Role of Astrocytic Aquaporin-4 in Synaptic Plasticity and Learning and Memory
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Cortical Gray to White Matter Signal Intensity Ratio as an Early Sign of Cognitive Decline in Alzheimer's Dementia and Mild Cognitive Impairment
inferred← citeshttps://doi.org/10.1001/jamapsychiatry.2023.0664openalex-snapshot
Does Microglial Activation Lead to Cognitive Changes After COVID-19 Infection?
inferred← citeshttps://doi.org/10.1002/alz.12341openalex-snapshot
Acute systemic inflammation exacerbates neuroinflammation in Alzheimer's disease: IL‐1β drives amplified responses in primed astrocytes and neuronal network dysfunction
inferred← citeshttps://doi.org/10.1002/alz.12342openalex-snapshot
Knowledge gaps in Alzheimer's disease immune biomarker research
inferred← citeshttps://doi.org/10.1002/ana.25911openalex-snapshot
Neuroinflammation and Tau Colocalize in vivo in Progressive Supranuclear Palsy
inferred← citeshttps://doi.org/10.1002/ddr.22040openalex-snapshot
Evaluation of advanced, pathophysiologic new targets for imaging of CNS
inferred← citeshttps://doi.org/10.1002/glia.24311openalex-snapshot
Piezo1 channel‐mediated C a2+ signaling inhibits lipopolysaccharide‐induced activation of the NF‐κB inflammatory signaling pathway and generation of TNF ‐α and IL ‐6 in microglial cells
inferred← citeshttps://doi.org/10.1002/hlca.202400014openalex-snapshot
Potential of miRNA as Imaging Targets for PET
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Imaging Neuroinflammation: Quantification of Astrocytosis in a Multitracer PET Approach
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PET Imaging of Monoamine Oxidase B
inferred← citeshttps://doi.org/10.1007/978-3-030-53176-8_17openalex-snapshot
Neuroinflammation: From Target Selection to Preclinical and Clinical Studies
inferred← citeshttps://doi.org/10.1007/978-3-031-68237-7_45openalex-snapshot
Bioimaging of Neuroimmune Disorders: Physical Principles of Neuroimaging Modalities and Clinical Applications
inferred← citeshttps://doi.org/10.1007/978-981-19-7376-5_14openalex-snapshot
Molecular Imaging of Neuroinflammation in Alzheimer’s Disease and Mild Cognitive Impairment
inferred← citeshttps://doi.org/10.1007/s00259-019-04394-5openalex-snapshot
Connectomics and molecular imaging in neurodegeneration
inferred← citeshttps://doi.org/10.1007/s00259-019-04562-7openalex-snapshot
From molecules to system failure: translational frontiers of multimodal imaging in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1007/s00259-021-05601-yopenalex-snapshot
Imaging translocator protein expression with positron emission tomography
inferred← citeshttps://doi.org/10.1007/s00259-021-05640-5openalex-snapshot
PET imaging of reactive astrocytes in neurological disorders
inferred← citeshttps://doi.org/10.1007/s12264-026-01656-9openalex-snapshot
A Humanized Knock-in Mouse Model of the PSEN1 V97L Mutation from a Major Chinese Alzheimer’s Disease Pedigree Reveals Early Neuroinflammation
inferred← citeshttps://doi.org/10.1016/b978-0-323-85841-0.00015-8openalex-snapshot
Immune dysregulation and neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.bbi.2021.07.017openalex-snapshot
Immune environment of the brain in schizophrenia and during the psychotic episode: A human post-mortem study
inferred← citeshttps://doi.org/10.1016/j.cpet.2020.12.003openalex-snapshot
Preclinical Evaluation of TSPO and MAO-B PET Radiotracers in an LPS Model of Neuroinflammation
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104813openalex-snapshot
A microengineered Brain-Chip to model neuroinflammation in humans
inferred← citeshttps://doi.org/10.1016/j.lmd.2024.100031openalex-snapshot
Advances in radiopharmaceuticals for precision medicine: A global and Chinese perspective
inferred← citeshttps://doi.org/10.1016/j.nbd.2022.105698openalex-snapshot
Inflammation in dementia with Lewy bodies
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2026.109084openalex-snapshot
Neurotheranostics in Alzheimer's Disease: Current concepts and experimental strategies
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2020.109858openalex-snapshot
The role of microglia in neuroprogressive disorders: mechanisms and possible neurotherapeutic effects of induced ketosis
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2026.111816openalex-snapshot
Beyond gray matter: unveiling the critical role of white matter in Alzheimer's disease
inferred← citeshttps://doi.org/10.1021/acsomega.2c00588openalex-snapshot
The 18-kDa Translocator Protein PET Tracers as a Diagnostic Marker for Neuroinflammation: Development and Current Standing
inferred← citeshttps://doi.org/10.1021/acsptsci.3c00213openalex-snapshot
Candidate Tracers for Imaging Colony-Stimulating Factor 1 Receptor in Neuroinflammation with Positron Emission Tomography: Issues and Progress
inferred← citeshttps://doi.org/10.1038/s41582-021-00549-xopenalex-snapshot
Peripheral and central immune system crosstalk in Alzheimer disease — a research prospectus
inferred← citeshttps://doi.org/10.1039/d1md00035gopenalex-snapshot
Synthesis and pharmacological evaluation of [ 18 F]PBR316: a novel PET ligand targeting the translocator protein 18 kDa (TSPO) with low binding sensitivity to human single nucleotide polymorphism rs6971
inferred← citeshttps://doi.org/10.1093/brain/awaa457openalex-snapshot
Glial cells and adaptive immunity in frontotemporal dementia with tau pathology
inferred← citeshttps://doi.org/10.1093/braincomms/fcac134openalex-snapshot
Brain alterations in the early Alzheimer’s continuum with amyloid-β, tau, glial and neurodegeneration CSF markers
inferred← citeshttps://doi.org/10.1111/bpa.13232openalex-snapshot
The post‐stroke young adult brain has limited capacity to re‐express the gene expression patterns seen during early postnatal brain development
inferred← citeshttps://doi.org/10.1111/ejn.15613openalex-snapshot
Neuroinflammation PET imaging of the translocator protein (TSPO) in Alzheimer's disease: An update
inferred← citeshttps://doi.org/10.1111/nan.12642openalex-snapshot
Invited Review – Understanding cause and effect in Alzheimer's pathophysiology: Implications for clinical trials
inferred← citeshttps://doi.org/10.1136/jnnp-2020-325549openalex-snapshot
Neuroinflammation predicts disease progression in progressive supranuclear palsy
inferred← citeshttps://doi.org/10.1136/jnnp-2020-325980openalex-snapshot
Does increased microglial activation lead to faster progression in PSP?
inferred← citeshttps://doi.org/10.1148/radiol.2020200028openalex-snapshot
Molecular Imaging Approaches in Dementia
inferred← citeshttps://doi.org/10.1186/s12974-023-02869-9openalex-snapshot
The mitochondrial protein TSPO in Alzheimer’s disease: relation to the severity of AD pathology and the neuroinflammatory environment
inferred← citeshttps://doi.org/10.1212/wnl.0000000000208090openalex-snapshot
White Matter Neuroinflammation Matters in Early Alzheimer Disease
inferred← citeshttps://doi.org/10.14283/jpad.2019.11openalex-snapshot
Advancing Alzheimer's Disease Treatment: Lessons from CTAD 2018
inferred← citeshttps://doi.org/10.1631/bdm.2400107openalex-snapshot
Engineered inflammation-induced neurodevelopmental disorders using a neurovascular-unit-on-a-chip
inferred← citeshttps://doi.org/10.2147/jpr.s246883openalex-snapshot
The Role of Neuro-Immune Interactions in Chronic Pain: Implications for Clinical Practice
inferred← citeshttps://doi.org/10.31083/j.fbl2711318openalex-snapshot
Quo vadis PGRMC? Grand-Scale Biology in Human Health and Disease
inferred← citeshttps://doi.org/10.3233/jad-201344openalex-snapshot
In vitro Characterization of the Regional Binding Distribution of Amyloid PET Tracer Florbetaben and the Glia Tracers Deprenyl and PK11195 in Autopsy Alzheimer’s Brain Tissue
inferred← citeshttps://doi.org/10.3233/jad-215680openalex-snapshot
Combination Therapy in Alzheimer’s Disease: Is It Time?
inferred← citeshttps://doi.org/10.3389/fimmu.2021.620698openalex-snapshot
The Immune System's Role in the Consequences of Mild Traumatic Brain Injury (Concussion)
inferred← citeshttps://doi.org/10.3389/fnins.2022.807435openalex-snapshot
Imaging of Reactive Astrogliosis by Positron Emission Tomography
inferred← citeshttps://doi.org/10.3389/fnins.2022.824888openalex-snapshot
Microglia and Astrocyte Function and Communication: What Do We Know in Humans?
inferred← citeshttps://doi.org/10.3390/genes16050590openalex-snapshot
Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy
inferred← citeshttps://doi.org/10.3390/ijms231810572openalex-snapshot
Glial Cell-Mediated Neuroinflammation in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/ph15030276openalex-snapshot
Synthesis and Evaluation of a 18F-Labeled Ligand for PET Imaging of Colony-Stimulating Factor 1 Receptor
inferred← citeshttps://doi.org/10.37349/en.2023.00012openalex-snapshot
The effect of the tumour necrosis factor-alpha-inhibitor etanercept on microglial activation patients with mild cognitive impairment—a PET study
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