PathMap Literature Based Discovery Engine
Share your Discovery:
Guaranteed to find unpublished literature based discoveries.
Discovery: Considering PubMed #41177462, intranasal S-GEVs co-functionalized with ApoE peptides may bypass the cribriform plate and target astrocytic LRP1 receptors in order to suppress NF-κB and may resolve some neuroinflammation in Alzheimer's and ALS.


Administration, Intranasal
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Blood-Brain Barrier
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Apolipoproteins E
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Low Density Lipoprotein Receptor-Related Protein-1
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Signal Transduction
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Neuroinflammatory astrocyte subtypes in the mouse brain


Pathologic Processes
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Gene Expression Regulation
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Biological Phenomena
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_gates_from_biological_phenomena
Neuroinflammatory Diseases
_gates_to_neuroinflammatory_diseases
Karyoptosis mediates cell death and neurodegeneration upon proteotoxic stress.


Hypothesis: If Botox were injected into the nerve ending on the third toe on the left foot, the toxin can "climb" retrograde from toe through motor neurons eventually to the brain and temporarily inhibit vesicular docking "from toe to head", potentially allowing a timed pharmacological therapeutic window for toxic EV clearance through the lymph system instead of docking and seeding.


Botulinum Toxins, Type A
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Axonal Transport
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_gates_from_axonal_transport
SNARE Proteins
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_gates_from_snare_proteins
Lymphatic Vessel Endothelial Hyaluronan Receptor-1
_gates_to_lymphatic_vessel_endothelial_hyaluronan_receptor_1
Ferroptosis


Use of MBTPS1 inhibitors is a plausible strategy to prevent the terminal phase of nuclear death in specific cellular contexts.


Membrane-Bound Transcription Factor Peptidase, Site 1
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SREBP Activation
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_gates_from_srebp_activation
Cellular Lipid Homeostasis
_gates_to_cellular_lipid_homeostasis
_gates_from_cellular_lipid_homeostasis
Terminal Cell Death
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Stabilizing the CREB3 tether via S1P/S2P protease inhibition represents a novel mechanism to prevent the terminal phase of neuronal death.


Endoplasmic Reticulum Stress
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Proteolysis
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Cyclic AMP-Response Element-Binding Protein
_gates_to_cyclic_amp_response_element_binding_protein
_gates_from_cyclic_amp_response_element_binding_protein
Nuclear Envelope
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Parkinson's Disease versus Alzheimer's Disease: Shared and Exclusive Pathways


Pathologic Processes
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Mitochondrial Diseases
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Lipid Metabolism Disorders
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Lipid Droplet Accumulation
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Lysosomal Storage Diseases
apo-SOD1 research, July 2026


SOD1 Research July 2026


What types of infections might cause a high C-Reactive Protein result?


ALS; FUS; STMN2; TDP-43; protein translation; stress granule


Frontotemporal dementia; Splicing; TDP-43; Transcriptomics.


Sarcopenia and Amyotrophic Lateral Sclerosis: Biological Pathways and Analysis


Is TDP-43 proteinopathy associated with toxoplasmosis?


The ALS-T2D comorbidity is driven by a bidirectional, exosome-mediated proteostatic collapse. Peripheral tissues (muscle, pancreas) dictate CNS TDP-43 stability via exosomal miRNAs (miR-126a-5p) and glucose-dependent modifications (O-GlcNAcylation). Conversely, pharmacological activation of ubiquitin-peptidases (e.g., Acarbose targeting USP46) or restitution of glycolytic cofactors (F2,6BP) represent novel, cross-disciplinary therapeutic targets capable of halting systemic proteinopathy.


Diabetes Mellitus, Type 2
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Extracellular Vesicles
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DNA-Binding Proteins
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_gates_from_dna_binding_proteins
Amyotrophic Lateral Sclerosis
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#PITRM1 #ALS #Microglia #Mitochondria


What is Karyoptosis and how does it align with past and present neurodegenerative disease research? Does Karyoptosis provide a new context in which a new class of repurposed therapeutics is formed?


Proteotoxic Stress
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Cyclic AMP-Response Element Binding Protein
_gates_to_cyclic_amp_response_element_binding_protein
_gates_from_cyclic_amp_response_element_binding_protein
Nuclear Envelope
_gates_to_nuclear_envelope
_gates_from_nuclear_envelope
Apoptosis
_gates_to_apoptosis
Why are frontotemporal dementia and c9orf72 ALS considered different diseases if they are both driven by the same abnormal expansion of a GGGGCC (G₄C₂) sequence in the first intron of the C9orf72 gene? Is it logical to think that CRISPR therapeutics for FTD potentially be used for ALS as well?


C9orf72 expansion
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Gene Expression Regulation
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_gates_from_gene_expression_regulation
Protein Aggregation, Pathological
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_gates_from_protein_aggregation__pathological
CRISPR-Cas Systems
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