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Predicting local tissue mechanics using immunohistochemistry

https://doi.org/10.1101/358119
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What this work says

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

inferredcites →https://doi.org/10.1002/cyto.a.20627openalex-snapshot
A fast, fully automated cell segmentation algorithm for high‐throughput and high‐content screening
inferredcites →https://doi.org/10.1002/glia.22309openalex-snapshot
The magnitude of the antigen‐specific T cell response is separated from the severity of spinal cord histopathology in remitting‐relapsing experimental autoimmune encephalomyelitis
inferredcites →https://doi.org/10.1002/jmri.22707openalex-snapshot
Decreased brain stiffness in Alzheimer's disease determined by magnetic resonance elastography
inferredcites →https://doi.org/10.1002/nbm.3319openalex-snapshot
Tissue structure and inflammatory processes shape viscoelastic properties of the mouse brain
inferredcites →https://doi.org/10.1007/s10237-008-0137-yopenalex-snapshot
Probing the influence of myelin and glia on the tensile properties of the spinal cord
inferredcites →https://doi.org/10.1016/bs.mcb.2014.10.005openalex-snapshot
Atomic force microscopy-based force measurements on animal cells and tissues
inferredcites →https://doi.org/10.1016/j.actbio.2016.07.040openalex-snapshot
Brain stiffness increases with myelin content
inferredcites →https://doi.org/10.1016/j.biomaterials.2014.01.038openalex-snapshot
The relationship between glial cell mechanosensitivity and foreign body reactions in the central nervous system
inferredcites →https://doi.org/10.1016/j.bpj.2015.03.039openalex-snapshot
CNS Cell Distribution and Axon Orientation Determine Local Spinal Cord Mechanical Properties
inferredcites →https://doi.org/10.1016/j.jbiomech.2010.07.002openalex-snapshot
Mechanical difference between white and gray matter in the rat cerebellum measured by scanning force microscopy
inferredcites →https://doi.org/10.1016/j.jmbbm.2015.02.024openalex-snapshot
Mechanical properties of gray and white matter brain tissue by indentation
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.06.018openalex-snapshot
MR-elastography reveals degradation of tissue integrity in multiple sclerosis
inferredcites →https://doi.org/10.1016/j.nicl.2012.09.003openalex-snapshot
Magnetic resonance elastography reveals altered brain viscoelasticity in experimental autoimmune encephalomyelitis
inferredcites →https://doi.org/10.1038/nature25742openalex-snapshot
Tissue stiffening coordinates morphogenesis by triggering collective cell migration in vivo
inferredcites →https://doi.org/10.1038/ncomms14787openalex-snapshot
The soft mechanical signature of glial scars in the central nervous system
inferredcites →https://doi.org/10.1038/nmeth.3616openalex-snapshot
Noncontact three-dimensional mapping of intracellular hydromechanical properties by Brillouin microscopy
inferredcites →https://doi.org/10.1038/nmeth.4101openalex-snapshot
In vivo quantification of spatially varying mechanical properties in developing tissues
inferredcites →https://doi.org/10.1038/nn.4394openalex-snapshot
Mechanosensing is critical for axon growth in the developing brain
inferredcites →https://doi.org/10.1054/jocn.1999.0212openalex-snapshot
Extracellular matrix and the brain: components and function
inferredcites →https://doi.org/10.1063/1.1143970openalex-snapshot
Calibration of atomic-force microscope tips
inferredcites →https://doi.org/10.1073/pnas.1200151109openalex-snapshot
Demyelination reduces brain parenchymal stiffness quantified in vivo by magnetic resonance elastography
inferredcites →https://doi.org/10.1088/1478-3975/aa6d18openalex-snapshot
The role of cell body density in ruminant retina mechanics assessed by atomic force and Brillouin microscopy
inferredcites →https://doi.org/10.1089/neu.2006.0169openalex-snapshot
Mechanical Heterogeneity of the Rat Hippocampus Measured by Atomic Force Microscope Indentation
inferredcites →https://doi.org/10.1089/neu.2008-0727openalex-snapshot
MECHANICALLY INDUCED REACTIVE GLIOSIS CAUSES ATP-MEDIATED ALTERATIONS IN ASTROCYTE STIFFNESS
inferredcites →https://doi.org/10.1089/neu.2008.0727openalex-snapshot
Mechanically Induced Reactive Gliosis Causes ATP-Mediated Alterations in Astrocyte Stiffness
inferredcites →https://doi.org/10.1096/fj.10-163790openalex-snapshot
Reactive glial cells: increased stiffness correlates with increased intermediate filament expression
inferredcites →https://doi.org/10.1111/j.1460-9568.2008.06108.xopenalex-snapshot
Distribution and synthesis of extracellular matrix proteoglycans, hyaluronan, link proteins and tenascin‐R in the rat spinal cord
inferredcites →https://doi.org/10.1126/science.1240104openalex-snapshot
Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation
inferredcites →https://doi.org/10.1146/annurev-bioeng-071811-150045openalex-snapshot
Mechanics in Neuronal Development and Repair
inferredcites →https://doi.org/10.1152/jn.00558.2011openalex-snapshot
An in vitro spinal cord slice preparation for recording from lumbar motoneurons of the adult mouse
inferredcites →https://doi.org/10.1177/0006355x2007044001003openalex-snapshot
Towards a reliable characterisation of the mechanical behaviour of brain tissue: The effects of post-mortem time and sample preparation
inferredcites →https://doi.org/10.1186/s12859-015-0617-xopenalex-snapshot
Robust and automated three-dimensional segmentation of densely packed cell nuclei in different biological specimens with Lines-of-Sight decomposition
inferredcites →https://doi.org/10.1242/dev.079145openalex-snapshot
The mechanical control of nervous system development
inferredcites →https://doi.org/10.1242/dev.109637openalex-snapshot
Systematic profiling of spatiotemporal tissue and cellular stiffness in the developing brain
inferredcites →https://doi.org/10.1371/journal.pone.0023451openalex-snapshot
The Influence of Physiological Aging and Atrophy on Brain Viscoelastic Properties in Humans
inferredcites →https://doi.org/10.1371/journal.pone.0092582openalex-snapshot
Enhanced Adult Neurogenesis Increases Brain Stiffness: In Vivo Magnetic Resonance Elastography in a Mouse Model of Dopamine Depletion
inferredcites →https://doi.org/10.1523/jneurosci.4605-08.2009openalex-snapshot
Axial Diffusivity Is the Primary Correlate of Axonal Injury in the Experimental Autoimmune Encephalomyelitis Spinal Cord: A Quantitative Pixelwise Analysis
inferredcites →https://doi.org/10.7554/elife.39356openalex-snapshot
Rapid changes in tissue mechanics regulate cell behaviour in the developing embryonic brain

What points at this work

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

inferred← citeshttps://doi.org/10.1007/s11831-019-09352-wopenalex-snapshot
Fifty Shades of Brain: A Review on the Mechanical Testing and Modeling of Brain Tissue
inferred← citeshttps://doi.org/10.1016/j.bpj.2019.10.044openalex-snapshot
Zebrafish Spinal Cord Repair Is Accompanied by Transient Tissue Stiffening
inferred← citeshttps://doi.org/10.1016/j.ijmecsci.2020.105914openalex-snapshot
Topological features dictate the mechanics of the mammalian brains
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2020.104159openalex-snapshot
Viscoelastic mapping of mouse brain tissue: Relation to structure and age
inferred← citeshttps://doi.org/10.1016/j.neulet.2019.134673openalex-snapshot
Mechanical regulation of oligodendrocyte biology
inferred← citeshttps://doi.org/10.1111/ejn.14766openalex-snapshot
Mechanobiology of the brain in ageing and Alzheimer's disease
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