On the public citation graph

Microglia Dysfunction Caused by the Loss of Rhoa Disrupts Neuronal Physiology and Leads to Neurodegeneration

https://doi.org/10.1016/j.celrep.2020.107796

0 signed · 172 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ana.24394openalex-snapshot

F yn inhibition rescues established memory and synapse loss in A lzheimer mice

inferredcites →https://doi.org/10.1002/bies.20558openalex-snapshot

GTP‐binding proteins of the Rho/Rac family: regulation, effectors and functions in vivo

inferredcites →https://doi.org/10.1002/eji.1830190815openalex-snapshot

Monokine production by microglial cell clones

inferredcites →https://doi.org/10.1002/glia.20687openalex-snapshot

Inhibition of Rho‐dependent pathways by Clostridium botulinum C3 protein induces a proinflammatory profile in microglia

inferredcites →https://doi.org/10.1002/glia.22767openalex-snapshot

c‐Src function is necessary and sufficient for triggering microglial cell activation

inferredcites →https://doi.org/10.1002/j.1460-2075.1989.tb03477.xopenalex-snapshot

The mammalian G protein rhoC is ADP‐ribosylated by Clostridium botulinum exoenzyme C3 and affects actin microfilaments in Vero cells.

inferredcites →https://doi.org/10.1002/jnr.490410210openalex-snapshot

Effect of bacterial wall lipopolysaccharide (LPS) on morphology, motility, and cytoskeletal organization of microglia in cultures

inferredcites →https://doi.org/10.1006/nbdi.2002.0530openalex-snapshot

Tumor Necrosis Factor α Increases Neuronal Vulnerability to Excitotoxic Necrosis by Inducing Expression of the AMPA–Glutamate Receptor Subunit GluR1 via an Acid Sphingomyelinase- and NF-κB-Dependent Mechanism

inferredcites →https://doi.org/10.1016/0014-5793(92)80335-eopenalex-snapshot

ADP‐ribosylation by Clostridium botulinum C3 exoenzyme increases steady‐state GTPase activities of recombinant rhoA and rhoB proteins

inferredcites →https://doi.org/10.1016/0304-3940(94)11792-hopenalex-snapshot

Establishment of human microglial cell lines after transfection of primary cultures of embryonic microglial cells with the SV40 large T antigen

inferredcites →https://doi.org/10.1016/b978-0-12-416749-0.00009-9openalex-snapshot

Inhibitors of the ROCK Serine/Threonine Kinases

inferredcites →https://doi.org/10.1016/j.bbr.2004.11.006openalex-snapshot

Detailed analysis of the behavior of Lister and Wistar rats in anxiety, object recognition and object location tasks

inferredcites →https://doi.org/10.1016/j.cell.2013.11.030openalex-snapshot

Microglia Promote Learning-Dependent Synapse Formation through Brain-Derived Neurotrophic Factor

inferredcites →https://doi.org/10.1016/j.cell.2015.01.049openalex-snapshot

TREM2 Lipid Sensing Sustains the Microglial Response in an Alzheimer’s Disease Model

inferredcites →https://doi.org/10.1016/j.cellsig.2013.05.023openalex-snapshot

Involvement of small GTPase RhoA in the regulation of superoxide production in BV2 cells in response to fibrillar Aβ peptides

inferredcites →https://doi.org/10.1016/j.cellsig.2013.08.001openalex-snapshot

Nitric oxide regulates AKT phosphorylation and nuclear translocation in cultured retinal cells

inferredcites →https://doi.org/10.1016/j.expneurol.2006.12.009openalex-snapshot

Electrical stimulation protocols for hippocampal synaptic plasticity and neuronal hyper-excitability: Are they effective or relevant?

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2014.11.019openalex-snapshot

c-Src deactivation by the polyphenol 3-O-caffeoylquinic acid abrogates reactive oxygen species-mediated glutamate release from microglia and neuronal excitotoxicity

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2018.02.036openalex-snapshot

Redox tuning of Ca2+ signaling in microglia drives glutamate release during hypoxia

inferredcites →https://doi.org/10.1016/j.immuni.2012.12.001openalex-snapshot

Fate Mapping Reveals Origins and Dynamics of Monocytes and Tissue Macrophages under Homeostasis

inferredcites →https://doi.org/10.1016/j.immuni.2016.02.013openalex-snapshot

Microglial Physiology and Pathophysiology: Insights from Genome-wide Transcriptional Profiling

inferredcites →https://doi.org/10.1016/j.jalz.2017.09.008openalex-snapshot

Amyloid β synaptotoxicity is Wnt‐PCP dependent and blocked by fasudil

inferredcites →https://doi.org/10.1016/j.molonc.2009.01.002openalex-snapshot

Preclinical anticancer activity of the potent, oral Src inhibitor AZD0530

inferredcites →https://doi.org/10.1016/j.neurobiolaging.2017.07.002openalex-snapshot

Transthyretin neuroprotection in Alzheimer's disease is dependent on proteolysis

inferredcites →https://doi.org/10.1016/j.neuron.2005.10.028openalex-snapshot

Synaptic Activity Regulates Interstitial Fluid Amyloid-β Levels In Vivo

inferredcites →https://doi.org/10.1016/j.neuropharm.2017.11.042openalex-snapshot

Disease-modifying benefit of Fyn blockade persists after washout in mouse Alzheimer's model

inferredcites →https://doi.org/10.1016/j.tcb.2006.11.009openalex-snapshot

Cell type-specific functions of Rho GTPases revealed by gene targeting in mice

inferredcites →https://doi.org/10.1016/j.yexcr.2004.08.012openalex-snapshot

Why three Rho proteins? RhoA, RhoB, RhoC, and cell motility

inferredcites →https://doi.org/10.1016/j.yexcr.2013.06.016openalex-snapshot

Rho GTPases in neurodegeneration diseases

inferredcites →https://doi.org/10.1016/s0165-0270(01)00374-0openalex-snapshot

The LTP Program: a data acquisition program for on-line analysis of long-term potentiation and other synaptic events

inferredcites →https://doi.org/10.1016/s0891-5849(03)00459-3openalex-snapshot

Rho a negatively regulates cytokine-mediated inducible nitric oxide synthase expression in brain-derived transformed cell lines: negative regulation of IKKα

inferredcites →https://doi.org/10.1016/s0896-6273(00)00090-8openalex-snapshot

Defective Neurogenesis in Citron Kinase Knockout Mice by Altered Cytokinesis and Massive Apoptosis

inferredcites →https://doi.org/10.1016/s0896-6273(00)80974-5openalex-snapshot

Accelerated Amyloid Deposition in the Brains of Transgenic Mice Coexpressing Mutant Presenilin 1 and Amyloid Precursor Proteins

inferredcites →https://doi.org/10.1016/s1074-7613(04)00023-8openalex-snapshot

C-Terminal Src Kinase Controls Acute Inflammation and Granulocyte Adhesion

inferredcites →https://doi.org/10.1038/351069a0openalex-snapshot

Cloning of a complementary DNA for a protein-tyrosine kinase that specifically phosphorylates a negative regulatory site of p60c-src

inferredcites →https://doi.org/10.1038/nature05289openalex-snapshot

A network dysfunction perspective on neurodegenerative diseases

inferredcites →https://doi.org/10.1038/nbt.1639openalex-snapshot

Engineered allosteric activation of kinases in living cells

inferredcites →https://doi.org/10.1038/ncomms12405openalex-snapshot

Bright monomeric near-infrared fluorescent proteins as tags and biosensors for multiscale imaging

inferredcites →https://doi.org/10.1038/ni.3423openalex-snapshot

Origin, fate and dynamics of macrophages at central nervous system interfaces

inferredcites →https://doi.org/10.1038/nmeth.3125openalex-snapshot

Neuronal morphometry directly from bitmap images

inferredcites →https://doi.org/10.1038/nmeth763openalex-snapshot

An inducible translocation strategy to rapidly activate and inhibit small GTPase signaling pathways

inferredcites →https://doi.org/10.1038/nn.3318openalex-snapshot

Microglia emerge from erythromyeloid precursors via Pu.1- and Irf8-dependent pathways

inferredcites →https://doi.org/10.1038/nn.3531openalex-snapshot

A new type of microglia gene targeting shows TAK1 to be pivotal in CNS autoimmune inflammation

inferredcites →https://doi.org/10.1038/nprot.2013.155openalex-snapshot

Object recognition test in mice

inferredcites →https://doi.org/10.1038/nrd1719openalex-snapshot

Rho kinase, a promising drug target for neurological disorders

inferredcites →https://doi.org/10.1038/nrm.2016.67openalex-snapshot

Regulating Rho GTPases and their regulators

inferredcites →https://doi.org/10.1038/nrm1128openalex-snapshot

ROCKs: multifunctional kinases in cell behaviour

inferredcites →https://doi.org/10.1038/nrn2038openalex-snapshot

Microglia-mediated neurotoxicity: uncovering the molecular mechanisms

inferredcites →https://doi.org/10.1038/nrn3722openalex-snapshot

Microglia and brain macrophages in the molecular age: from origin to neuropsychiatric disease

inferredcites →https://doi.org/10.1038/s41593-018-0145-xopenalex-snapshot

Microglial immune checkpoint mechanisms

inferredcites →https://doi.org/10.1073/pnas.0403954101openalex-snapshot

Cre-lox-regulated conditional RNA interference from transgenes

inferredcites →https://doi.org/10.1073/pnas.0503274102openalex-snapshot

Detection of glutamate release from neurons by genetically encoded surface-displayed FRET nanosensors

inferredcites →https://doi.org/10.1074/jbc.m110.169342openalex-snapshot

S100B Protein Stimulates Microglia Migration via RAGE-dependent Up-regulation of Chemokine Expression and Release

inferredcites →https://doi.org/10.1074/jbc.m112.353961openalex-snapshot

Calcium-permeable α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Receptors Trigger Neuronal Nitric-oxide Synthase Activation to Promote Nerve Cell Death in an Src Kinase-dependent Fashion

inferredcites →https://doi.org/10.1074/jbc.m600504200openalex-snapshot

Tumor Necrosis Factor-α Induces Neurotoxicity via Glutamate Release from Hemichannels of Activated Microglia in an Autocrine Manner

inferredcites →https://doi.org/10.1074/jbc.r113.515486openalex-snapshot

Cell Type-specific Signaling Function of RhoA GTPase: Lessons from Mouse Gene Targeting

inferredcites →https://doi.org/10.1083/jcb.200212049openalex-snapshot

Activity of Rho-family GTPases during cell division as visualized with FRET-based probes

inferredcites →https://doi.org/10.1091/mbc.e09-10-0859openalex-snapshot

RhoA is dispensable for skin development, but crucial for contraction and directed migration of keratinocytes

inferredcites →https://doi.org/10.1093/brain/aww016openalex-snapshot

Eliminating microglia in Alzheimer’s mice prevents neuronal loss without modulating amyloid-β pathology

inferredcites →https://doi.org/10.1096/fj.09-141754openalex-snapshot

Massive gliosis induced by interleukin‐6 suppresses Aβ deposition in vivo: evidence against inflammation as a driving force for amyloid deposition

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.1219179openalex-snapshot

A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells

inferredcites →https://doi.org/10.1126/scisignal.aal2005openalex-snapshot

Caveolin-1–mediated internalization of the vitamin C transporter SVCT2 in microglia triggers an inflammatory phenotype

inferredcites →https://doi.org/10.1128/mcb.20.11.4106-4114.2000openalex-snapshot

Analysis of Fractalkine Receptor CX3CR1 Function by Targeted Deletion and Green Fluorescent Protein Reporter Gene Insertion

inferredcites →https://doi.org/10.1128/mcb.23.12.4219-4229.2003openalex-snapshot

RhoE Binds to ROCK I and Inhibits Downstream Signaling

inferredcites →https://doi.org/10.1186/1750-1326-6-16openalex-snapshot

Hippocampal expression of murine TNFα results in attenuation of amyloid deposition in vivo

inferredcites →https://doi.org/10.1242/jcs.113.17.3073openalex-snapshot

Involvement of Iba1 in membrane ruffling and phagocytosis of macrophages/microglia

inferredcites →https://doi.org/10.1517/13543784.2013.778242openalex-snapshot

Fasudil and its analogs: a new powerful weapon in the long war against central nervous system disorders?

inferredcites →https://doi.org/10.1523/jneurosci.0336-15.2015openalex-snapshot

Elimination of Microglia Improves Functional Outcomes Following Extensive Neuronal Loss in the Hippocampus

inferredcites →https://doi.org/10.1523/jneurosci.0849-05.2005openalex-snapshot

NMDA Receptor Activation Inhibits α-Secretase and Promotes Neuronal Amyloid-β Production

inferredcites →https://doi.org/10.1523/jneurosci.4440-12.2013openalex-snapshot

Regulation of Microglial Proliferation during Chronic Neurodegeneration

inferredcites →https://doi.org/10.1523/jneurosci.4807-10.2011openalex-snapshot

The Small GTPase RhoA Is Required to Maintain Spinal Cord Neuroepithelium Organization and the Neural Stem Cell Pool

inferredcites →https://doi.org/10.1523/jneurosci.5966-09.2010openalex-snapshot

Rett Syndrome Microglia Damage Dendrites and Synapses by the Elevated Release of Glutamate

inferredcites →https://doi.org/10.1679/aohc.60.453openalex-snapshot

Effects of Colchicine on Amoeboid Microglial Cells in the Postnatal Rat Brain.

inferredcites →https://doi.org/10.2174/1389450117666160401123825openalex-snapshot

ROCK in CNS: Different Roles of Isoforms and Therapeutic Target for Neurodegenerative Disorders

inferredcites →https://doi.org/10.3389/fncel.2014.00282openalex-snapshot

The emerging role of guanine nucleotide exchange factors in ALS and other neurodegenerative diseases

inferredcites →https://doi.org/10.3389/fncel.2014.00314openalex-snapshot

Rho family GTPases: key players in neuronal development, neuronal survival, and neurodegeneration

inferredcites →https://doi.org/10.4161/sgtp.29846openalex-snapshot

Rho-associated coiled-coil containing kinases (ROCK)

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.4646303openalex-extracted

Actin And Microtubules: A Tale of Two Cytoskeletons in Microglial Function

inferred← citeshttps://doi.org/10.1002/glia.24067openalex-snapshot

Morphofunctional programming of microglia requires distinct roles of type II myosins

inferred← citeshttps://doi.org/10.1002/glia.24323openalex-snapshot

Movers and shakers: Microglial dynamics and modulation of neural networks

inferred← citeshttps://doi.org/10.1002/glia.70207openalex-snapshot

CX3CR1 Modulates Migration of Resident Microglia Towards Cortical Laser‐Induced Lesions

inferred← citeshttps://doi.org/10.1002/iid3.900openalex-snapshot

Melatonin regulates microglial polarization to M2 cell via RhoA/ROCK signaling pathway in epilepsy

inferred← citeshttps://doi.org/10.1002/wrna.1678openalex-snapshot

Microexon alternative splicing of small GTPase regulators: Implication in central nervous system diseases

inferred← citeshttps://doi.org/10.1007/s00018-025-05648-2openalex-snapshot

Microglia regulate myelin clearance and cholesterol metabolism after demyelination via interferon regulatory factor 5

inferred← citeshttps://doi.org/10.1007/s10571-021-01060-zopenalex-snapshot

TTC3-Mediated Protein Quality Control, A Potential Mechanism for Cognitive Impairment

inferred← citeshttps://doi.org/10.1007/s11011-021-00689-5openalex-snapshot

Cellular and molecular pathophysiology in the progression of Parkinson’s disease

inferred← citeshttps://doi.org/10.1007/s12035-025-05144-5openalex-snapshot

Quaking Protein in Myelin Maintenance and Regeneration in the Central Nervous System

inferred← citeshttps://doi.org/10.1016/bs.apcsb.2025.10.018openalex-snapshot

G-protein coupled receptor regulates cytoskeletal remodelling of extracellular Tau in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2025.07.018openalex-snapshot

Localised delivery of interleukin-13 from a PLGA microparticle embedded GelMA hydrogel improves functional and histopathological recovery in a mouse contusion spinal cord injury model

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2022.121690openalex-snapshot

Blood-brain barrier Permeable nanoparticles for Alzheimer's disease treatment by selective mitophagy of microglia

inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108560openalex-snapshot

QUAKING Regulates Microexon Alternative Splicing of the Rho GTPase Pathway and Controls Microglia Homeostasis

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112624openalex-snapshot

ArhGAP11A mediates amyloid-β generation and neuropathology in an Alzheimer’s disease-like mouse model

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113447openalex-snapshot

Microglial Rac1 is essential for experience-dependent brain plasticity and cognitive performance

inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117150openalex-snapshot

Optogenetic mediated contractility enables reversible control of microglial morphology and migration in vivo

inferred← citeshttps://doi.org/10.1016/j.ejcb.2022.151247openalex-snapshot

Mechanical actuators in microglia dynamics and function

inferred← citeshttps://doi.org/10.1016/j.foodres.2020.109548openalex-snapshot

Cytotoxic activity of poly-ɛ-caprolactone lipid-core nanocapsules loaded with lycopene-rich extract from red guava (Psidium guajava L.) on breast cancer cells

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.11.039openalex-snapshot

Activation of adenosine A3 receptors regulates vitamin C transport and redox balance in neurons

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2022.02.012openalex-snapshot

Visualizing physiological parameters in cells and tissues using genetically encoded indicators for metabolites

inferred← citeshttps://doi.org/10.1016/j.isci.2024.108921openalex-snapshot

Parkinson’s disease risk enhancers in microglia

inferred← citeshttps://doi.org/10.1016/j.jep.2026.121920openalex-snapshot

Uncovering the quality markers and mechanisms of Gastrodia elata against LPS-induced neuroinflammation via network pharmacology and experimental verification

inferred← citeshttps://doi.org/10.1016/j.jneuroim.2021.577688openalex-snapshot

Disrupting RhoA activity by blocking Arhgef3 expression mitigates microglia-induced neuroinflammation post spinal cord contusion

inferred← citeshttps://doi.org/10.1016/j.mocell.2025.100265openalex-snapshot

Rationale and emerging evidence for microglial replacement in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.neuron.2021.08.014openalex-snapshot

RhoA drives actin compaction to restrict axon regeneration and astrocyte reactivity after CNS injury

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2024.102586openalex-snapshot

A cytoskeleton symphony: Actin and microtubules in microglia dynamics and aging

inferred← citeshttps://doi.org/10.1016/j.redox.2025.103851openalex-snapshot

Enhancing microglial antioxidant capacity via the ascorbate transporter SVCT2 delays onset and modifies disease progression in mouse models of Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.xpro.2020.100147openalex-snapshot

A Protocol for FRET-Based Live-Cell Imaging in Microglia

inferred← citeshttps://doi.org/10.1021/acsami.5c09843openalex-snapshot

Engineered Stem Cell Membrane-Coated Nanodrugs for Targeted Therapy of Alzheimer’s Disease

inferred← citeshttps://doi.org/10.1038/s41386-021-01139-7openalex-snapshot

Astrocyte-derived TNF and glutamate critically modulate microglia activation by methamphetamine

inferred← citeshttps://doi.org/10.1038/s41419-023-06217-wopenalex-snapshot

RhoA balances microglial reactivity and survival during neuroinflammation

inferred← citeshttps://doi.org/10.1038/s41419-025-07947-9openalex-snapshot

Loss of RhoA in microglia disables glycolytic adaptation and impairs spinal cord injury recovery through Arhgap25/HIF-1α pathway

inferred← citeshttps://doi.org/10.1038/s41423-021-00751-3openalex-snapshot

Microglia as hackers of the matrix: sculpting synapses and the extracellular space

inferred← citeshttps://doi.org/10.1038/s41588-026-02619-6openalex-snapshot

Decoding common and rare noncoding variant effects across cellular and developmental contexts

inferred← citeshttps://doi.org/10.1084/jem.20222105openalex-snapshot

A novel molecular class that recruits HDAC/MECP2 complexes to PU.1 motifs reduces neuroinflammation

inferred← citeshttps://doi.org/10.1089/neu.2023.0284openalex-snapshot

Exposure to Low-Intensity Blast Increases Clearance of Brain Amyloid Beta

inferred← citeshttps://doi.org/10.1093/brain/awad184openalex-snapshot

Cdc42GAP deficiency contributes to the Alzheimer’s disease phenotype

inferred← citeshttps://doi.org/10.1096/fj.202101633ropenalex-snapshot

The clock modulator Nobiletin mitigates astrogliosis‐associated neuroinflammation and disease hallmarks in an Alzheimer’s disease model

inferred← citeshttps://doi.org/10.1101/2020.04.08.031567openalex-snapshot

The Alzheimer’s disease-associated protective Plcγ2 -P522R variant promotes beneficial microglial functions

inferred← citeshttps://doi.org/10.1101/2020.11.02.365841openalex-snapshot

Comparative gene pathway analysis during adolescent binge-EtOH exposure, withdrawal, and following abstinence

inferred← citeshttps://doi.org/10.1101/2021.06.17.448790openalex-snapshot

Alzheimer’s disease-associated P460L mutation in ephrin receptor type A1 (EphA1) leads to dysregulated Rho-GTPase signaling

inferred← citeshttps://doi.org/10.1101/2021.09.06.459142openalex-snapshot

CHAS, a deconvolution tool, infers cell type-specific signatures in bulk brain histone acetylation studies of neurological and psychiatric disorders

inferred← citeshttps://doi.org/10.1101/2021.10.18.464802openalex-snapshot

Rac1 signaling in microglia is essential for synaptic proteome plasticity and experience-dependent cognitive performance

inferred← citeshttps://doi.org/10.1101/2023.08.14.553274openalex-snapshot

IRF5 regulates microglial myelin clearance and cholesterol metabolism after demyelination

inferred← citeshttps://doi.org/10.1101/2023.11.16.567220openalex-snapshot

Dynamic neuroinflammatory profiles predict Alzheimer’s disease pathology in microglia-containing cerebral organoids

inferred← citeshttps://doi.org/10.1101/2024.02.29.582679openalex-snapshot

Increasing the vitamin C transporter SVCT2 in microglia improves synaptic plasticity and restrains memory impairments in Alzheimer’s disease models

inferred← citeshttps://doi.org/10.1101/2024.09.23.614458openalex-snapshot

CX3CR1 modulates migration of resident microglia towards brain injury

inferred← citeshttps://doi.org/10.1101/2024.09.27.615114openalex-snapshot

Deficiency of actin depolymerizing factors ADF/Cfl1 in microglia decreases motility and impairs memory

inferred← citeshttps://doi.org/10.1101/2025.02.18.638922openalex-snapshot

Mapping the regulatory effects of common and rare non-coding variants across cellular and developmental contexts in the brain and heart

inferred← citeshttps://doi.org/10.1111/ejn.15662openalex-snapshot

Diverse pathways to neuronal necroptosis in Alzheimer's disease

inferred← citeshttps://doi.org/10.1111/febs.16197openalex-snapshot

Src family kinases (SFKs): critical regulators of microglial homeostatic functions and neurodegeneration in Parkinson's and Alzheimer's diseases

inferred← citeshttps://doi.org/10.1111/gtc.13088openalex-snapshot

IMPDH2 forms spots at branching sites and distal ends of astrocyte stem processes

inferred← citeshttps://doi.org/10.1126/sciadv.abm2545openalex-snapshot

Microglial GPR56 is the molecular target of maternal immune activation-induced parvalbumin-positive interneuron deficits

inferred← citeshttps://doi.org/10.1126/sciadv.ads9181openalex-snapshot

The chloride intracellular channel 1 (CLIC1) is essential for microglial morphodynamics and neuroinflammation

inferred← citeshttps://doi.org/10.1126/science.abo7649openalex-snapshot

Transforming the understanding of brain immunity

inferred← citeshttps://doi.org/10.1126/scisignal.aba5754openalex-snapshot

Daily alcohol intake triggers aberrant synaptic pruning leading to synapse loss and anxiety-like behavior

inferred← citeshttps://doi.org/10.1186/s12974-025-03588-zopenalex-snapshot

Profilin 1 controls a microglial cytoskeleton checkpoint to prevent senescence and premature synaptic decline

inferred← citeshttps://doi.org/10.1186/s13024-020-00402-7openalex-snapshot

The Alzheimer’s disease-associated protective Plcγ2-P522R variant promotes immune functions

inferred← citeshttps://doi.org/10.1186/s13036-024-00449-wopenalex-snapshot

Microglia morphological response to mesenchymal stromal cell extracellular vesicles demonstrates EV therapeutic potential for modulating neuroinflammation

inferred← citeshttps://doi.org/10.1186/s13041-025-01271-1openalex-snapshot

Mycophenolate mofetil reduces the branching of microglial processes

inferred← citeshttps://doi.org/10.1186/s13073-025-01586-7openalex-snapshot

Aligned cross-modal integration and regulatory heterogeneity characterization of single-cell multiomic data with deep contrastive learning

inferred← citeshttps://doi.org/10.1186/s40035-026-00590-0openalex-snapshot

Fyn kinase: a key mechanistic regulator and therapeutic target in tauopathy and neurodegenerative diseases

inferred← citeshttps://doi.org/10.1186/s40478-021-01264-wopenalex-snapshot

TNF-mediated neuroinflammation is linked to neuronal necroptosis in Alzheimer's disease hippocampus

inferred← citeshttps://doi.org/10.1242/jcs.264117openalex-snapshot

GAK antagonises ROCK-dependent regulation of actomyosin dynamics

inferred← citeshttps://doi.org/10.1371/journal.pone.0293301openalex-snapshot

CD11c is not required by microglia to convey neuroprotection after prion infection

inferred← citeshttps://doi.org/10.18097/pbmcr1705openalex-snapshot

MicroRNA: role in pathogenesis, problems of microRNA therapy, and future prospects

inferred← citeshttps://doi.org/10.2217/epi-2022-0096openalex-snapshot

The Role of H3K9 Acetylation and Gene Expression in Different Brain Regions of Alzheimer’s Disease Patients

inferred← citeshttps://doi.org/10.3233/jad-221113openalex-snapshot

Genome-Wide Mapping Implicates 5-Hydroxymethylcytosines in Diabetes Mellitus and Alzheimer’s Disease

inferred← citeshttps://doi.org/10.3233/jad-230408openalex-snapshot

RhoA-LIMK Signaling Axis Reveals Rostral-Caudal Plane and Spatial Dysregulation in the Brain of Alzheimer’s Disease Mouse Models

inferred← citeshttps://doi.org/10.3389/fimmu.2021.683026openalex-snapshot

Microglial Morphology Across Distantly Related Species: Phylogenetic, Environmental and Age Influences on Microglia Reactivity and Surveillance States

inferred← citeshttps://doi.org/10.3389/fimmu.2024.1412699openalex-snapshot

The microglial innate immune receptor TREM2 participates in fear memory formation through excessive prelimbic cortical synaptic pruning

inferred← citeshttps://doi.org/10.3389/fncel.2021.661612openalex-snapshot

Pharmacological Modulators of Small GTPases of Rho Family in Neurodegenerative Diseases

inferred← citeshttps://doi.org/10.3389/fnins.2024.1362239openalex-snapshot

Role of microbiota-gut-brain axis in natural aging-related alterations in behavior

inferred← citeshttps://doi.org/10.3389/fnmol.2021.744942openalex-snapshot

MicroRNAs Play a Role in Parkinson’s Disease by Regulating Microglia Function: From Pathogenetic Involvement to Therapeutic Potential

inferred← citeshttps://doi.org/10.3390/biomedicines10020237openalex-snapshot

Profiling Microglia in a Mouse Model of Machado–Joseph Disease

inferred← citeshttps://doi.org/10.3390/biomedicines11123198openalex-snapshot

Rhamnetin Prevents Bradykinin-Induced Expression of Matrix Metalloproteinase-9 in Rat Brain Astrocytes by Suppressing Protein Kinase-Dependent AP-1 Activation

inferred← citeshttps://doi.org/10.3390/cells11132022openalex-snapshot

Microglial Depletion Has No Impact on Disease Progression in a Mouse Model of Machado–Joseph Disease

inferred← citeshttps://doi.org/10.3390/cells11172753openalex-snapshot

Na,K-ATPase Acts as a Beta-Amyloid Receptor Triggering Src Kinase Activation

inferred← citeshttps://doi.org/10.3390/cells12101367openalex-snapshot

The RhoA-ROCK1/ROCK2 Pathway Exacerbates Inflammatory Signaling in Immortalized and Primary Microglia

inferred← citeshttps://doi.org/10.3390/cells9091926openalex-snapshot

Conventional and Non-Conventional Roles of Non-Muscle Myosin II-Actin in Neuronal Development and Degeneration

inferred← citeshttps://doi.org/10.3390/ijms21186676openalex-snapshot

Deleterious Alteration of Glia in the Brain of Alzheimer’s Disease

inferred← citeshttps://doi.org/10.3390/ijms231810432openalex-snapshot

p27kip1 Modulates the Morphology and Phagocytic Activity of Microglia

inferred← citeshttps://doi.org/10.3390/ijms24021599openalex-snapshot

Astrocytic Neuroimmunological Roles Interacting with Microglial Cells in Neurodegenerative Diseases

inferred← citeshttps://doi.org/10.3390/ijms252212391openalex-snapshot

Structure of Full-Length Src Kinase and Its Key Phosphorylated States: Molecular Dynamics Study

inferred← citeshttps://doi.org/10.3390/ijms26199458openalex-snapshot

Utilizing Network Toxicology and Molecular Dynamics Simulations to Efficiently Evaluate the Neurotoxicity and Underlying Mechanisms of the Endocrine-Disrupting Chemical Triclosan

inferred← citeshttps://doi.org/10.3390/ijms27031492openalex-snapshot

Altered Microglia-Neuron Crosstalk and Regional Heterogeneity in Alzheimer’s Disease Revealed by Single-Nucleus RNA Sequencing

inferred← citeshttps://doi.org/10.3390/molecules28155846openalex-snapshot

Elucidation of Pharmacological Mechanism Underlying the Anti-Alzheimer’s Disease Effects of Evodia rutaecarpa and Discovery of Novel Lead Molecules: An In Silico Study

inferred← citeshttps://doi.org/10.3892/etm.2022.11405openalex-snapshot

Ketamine administration ameliorates anesthesia and surgery‑induced cognitive dysfunction via activation of TRPV4 channel opening

inferred← citeshttps://doi.org/10.4103/nrr.nrr-d-24-00284openalex-snapshot

Neuroinflammation revisited through the microglial lens

inferred← citeshttps://doi.org/10.48130/targetome-0026-0035openalex-snapshot

From molecular markers to architectural control: cytoskeletal checkpoints as the decisive state-access layer of the aging microglial targetome

inferred← citeshttps://doi.org/10.6084/m9.figshare.16778487openalex-snapshot

Additional file 7 of TNF-mediated neuroinflammation is linked to neuronal necroptosis in Alzheimer's disease hippocampus

inferred← citeshttps://doi.org/10.6084/m9.figshare.16778490openalex-snapshot

Additional file 8 of TNF-mediated neuroinflammation is linked to neuronal necroptosis in Alzheimer's disease hippocampus

inferred← citeshttps://doi.org/10.64898/2025.12.10.693462openalex-snapshot

Reconstructing developmental and disease progression with sample-level embeddings

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.