On the public citation graph
High-Resolution Mechanical Imaging of Glioblastoma by Multifrequency Magnetic Resonance Elastography
0 signed · 222 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.1926.02680040056039openalex-snapshot
A Classification of the Tumors of the Glioma Group on a Histogenetic Basis with a Correlated Study of Prognosis.
inferredcites →https://doi.org/10.1002/1522-2594(200102)45:2<299::aid-mrm1039>3.0.co;2-oopenalex-snapshot
Complex-valued stiffness reconstruction for magnetic resonance elastography by algebraic inversion of the differential equation
inferredcites →https://doi.org/10.1002/jmri.22294openalex-snapshot
In vivo magnetic resonance elastography of human brain at 7 T and 1.5 T
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/mrm.21152openalex-snapshot
Fractional encoding of harmonic motions in MR elastography
inferredcites →https://doi.org/10.1002/mrm.24141openalex-snapshot
In vivo waveguide elastography of white matter tracts in the human brain
inferredcites →https://doi.org/10.1002/mrm.24473openalex-snapshot
Magnetic resonance elastography of the brain using multishot spiral readouts with self‐navigated motion correction
inferredcites →https://doi.org/10.1002/mrm.24499openalex-snapshot
In vivo measurement of volumetric strain in the human brain induced by arterial pulsation and harmonic waves
inferredcites →https://doi.org/10.1002/mrm.24674openalex-snapshot
MR Elastography of the Liver and the Spleen Using a Piezoelectric Driver, Single‐Shot Wave‐Field Acquisition, and Multifrequency Dual Parameter Reconstruction
inferredcites →https://doi.org/10.1002/nbm.1189openalex-snapshot
Non‐invasive measurement of brain viscoelasticity using magnetic resonance elastography
inferredcites →https://doi.org/10.1002/nbm.1254openalex-snapshot
In vivo brain viscoelastic properties measured by magnetic resonance elastography
inferredcites →https://doi.org/10.1002/nbm.1602openalex-snapshot
In vivo viscoelastic properties of the brain in normal pressure hydrocephalus
inferredcites →https://doi.org/10.1002/nbm.2987openalex-snapshot
MR elastography in a murine stroke model reveals correlation of macroscopic viscoelastic properties of the brain with neuronal density
inferredcites →https://doi.org/10.1007/s00234-011-0871-1openalex-snapshot
Alteration of brain viscoelasticity after shunt treatment in normal pressure hydrocephalus
inferredcites →https://doi.org/10.1007/s00330-012-2474-6openalex-snapshot
MR elastography of liver tumours: value of viscoelastic properties for tumour characterisation
inferredcites →https://doi.org/10.1007/s00330-014-3305-8openalex-snapshot
In vivo high-resolution magnetic resonance elastography of the uterine corpus and cervix
inferredcites →https://doi.org/10.1007/s00401-007-0243-4openalex-snapshot
The 2007 WHO Classification of Tumours of the Central Nervous System
inferredcites →https://doi.org/10.1016/b978-0-12-385048-5.00010-0openalex-snapshot
Nonlinear Inverse Problems
inferredcites →https://doi.org/10.1016/c2009-0-61134-xopenalex-snapshot
Parameter Estimation and Inverse Problems
inferredcites →https://doi.org/10.1016/j.neuroimage.2007.08.030openalex-snapshot
Magnetic resonance elastography of the brain
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.02.040openalex-snapshot
The impact of aging and gender on brain viscoelasticity
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.neuroimage.2013.04.089openalex-snapshot
Local mechanical properties of white matter structures in the human brain
inferredcites →https://doi.org/10.1016/j.neuroimage.2013.12.032openalex-snapshot
High-resolution mechanical imaging of the human brain by three-dimensional multifrequency magnetic resonance elastography at 7T
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/10.1016/j.nicl.2013.09.006openalex-snapshot
Cerebral magnetic resonance elastography in supranuclear palsy and idiopathic Parkinson's disease
inferredcites →https://doi.org/10.1039/c3sm50552aopenalex-snapshot
Structure-sensitive elastography: on the viscoelastic powerlaw behavior of in vivo human tissue in health and disease
inferredcites →https://doi.org/10.1056/nejmoa043330openalex-snapshot
Radiotherapy Plus Concomitant and Adjuvant Temozolomide for Glioblastoma
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/10.1080/02841850701199967openalex-snapshot
Magnetic resonance elastography of brain tumors: preliminary results
inferredcites →https://doi.org/10.1088/0031-9155/54/7/025openalex-snapshot
Scatter-based magnetic resonance elastography
inferredcites →https://doi.org/10.1088/0031-9155/57/8/2329openalex-snapshot
Multifrequency inversion in magnetic resonance elastography
inferredcites →https://doi.org/10.1088/0967-3334/34/12/1675openalex-snapshot
Statistical mapping of the effect of knee extension on thigh muscle viscoelastic properties using magnetic resonance elastography
inferredcites →https://doi.org/10.1088/1367-2630/15/8/085024openalex-snapshot
Non-invasive characterization of intracranial tumors by magnetic resonance elastography
inferredcites →https://doi.org/10.1093/neuonc/3.3.152openalex-snapshot
Prevalence estimates for primary brain tumors in the United States by behavior and major histology groups
inferredcites →https://doi.org/10.1093/neuonc/nop066openalex-snapshot
Prevalence estimates for primary brain tumors in the United States by age, gender, behavior, and histology
inferredcites →https://doi.org/10.1093/neuonc/nos218openalex-snapshot
CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2005-2009
inferredcites →https://doi.org/10.1093/neuonc/not151openalex-snapshot
CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2006-2010
inferredcites →https://doi.org/10.1101/gad.1596707openalex-snapshot
Malignant astrocytic glioma: genetics, biology, and paths to treatment
inferredcites →https://doi.org/10.1109/tmi.2011.2131674openalex-snapshot
Travelling Wave Expansion: A Model Fitting Approach to the Inverse Problem of Elasticity Reconstruction
inferredcites →https://doi.org/10.1212/wnl.57.3.393openalex-snapshot
MRI features of primary central nervous system lymphomas at presentation
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.0029888openalex-snapshot
Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis
inferredcites →https://doi.org/10.1371/journal.pone.0071807openalex-snapshot
Towards an Elastographic Atlas of Brain Anatomy
inferredcites →https://doi.org/10.1371/journal.pone.0081668openalex-snapshot
Measuring the Characteristic Topography of Brain Stiffness with Magnetic Resonance Elastography
inferredcites →https://doi.org/10.2976/1.3086732openalex-snapshot
Homeostatic competition drives tumor growth and metastasis nucleation
inferredcites →https://doi.org/10.3171/2012.9.jns12519openalex-snapshot
Preoperative assessment of meningioma stiffness using magnetic resonance elastography
inferredcites →https://doi.org/10.3171/jns.1994.81.2.0165openalex-snapshot
Complications of CT-guided stereotactic biopsy of intra-axial brain lesions
inferredcites →https://doi.org/10.3174/ajnr.a2581openalex-snapshot
Differentiation of Brain Abscesses from Necrotic Glioblastomas and Cystic Metastatic Brain Tumors with Diffusion Tensor Imaging
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.4654106openalex-extracted
Low-Frequency Mr Elastography Reveals Deep Gray Matter Degradation in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1002/9781394284030.ch7openalex-snapshot
Quantitative Biomechanical Imaging via Magnetic Resonance Elastography
inferred← citeshttps://doi.org/10.1002/adfm.202100848openalex-snapshot
Viscoelastic Cell Microenvironment: Hydrogel‐Based Strategy for Recapitulating Dynamic ECM Mechanics
inferred← citeshttps://doi.org/10.1002/adfm.202419211openalex-snapshot
3D In Vitro Glioma‐Neuron‐Astrocyte Biomimetic Composites Recapitulate Key Molecular Mechanisms Linked to Glioblastoma Multiforme Pathophysiology
inferred← citeshttps://doi.org/10.1002/adhm.202202147openalex-snapshot
Dynamically Crosslinked Poly(ethylene‐glycol) Hydrogels Reveal a Critical Role of Viscoelasticity in Modulating Glioblastoma Fates and Drug Responses in 3D
inferred← citeshttps://doi.org/10.1002/adhm.71322openalex-snapshot
Forming a Precise and Reproducible Hypoxic Tumor Microenvironment in Glioblastoma by High Cell Density Bioprinting
inferred← citeshttps://doi.org/10.1002/advs.202402338openalex-snapshot
The Networking Brain: How Extracellular Matrix, Cellular Networks, and Vasculature Shape the In Vivo Mechanical Properties of the Brain
inferred← citeshttps://doi.org/10.1002/advs.77626openalex-snapshot
Longitudinal Multifrequency MR Elastography Reveals Biomechanical Signatures of Progression in a Translational Liver Tumor Model
inferred← citeshttps://doi.org/10.1002/jmri.25129openalex-snapshot
Higher‐resolution MR elastography reveals early mechanical signatures of neuroinflammation in patients with clinically isolated syndrome
inferred← citeshttps://doi.org/10.1002/jmri.25516openalex-snapshot
Increasing the spatial resolution and sensitivity of magnetic resonance elastography by correcting for subject motion and susceptibility-induced image distortions
inferred← citeshttps://doi.org/10.1002/jmri.25741openalex-snapshot
MR elastography detection of early viscoelastic response of the murine hippocampus to amyloid β accumulation and neuronal cell loss due to Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/jmri.26968openalex-snapshot
Quantitative MRI for Assessment of Treatment Outcomes in a Rabbit VX2 Hepatic Tumor Model
inferred← citeshttps://doi.org/10.1002/jmri.27475openalex-snapshot
Robustness of MR Elastography in the Healthy Brain: Repeatability, Reliability, and Effect of Different Reconstruction Methods
inferred← citeshttps://doi.org/10.1002/jmri.27833openalex-snapshot
Feasibility of Intestinal MR Elastography in Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1002/jmri.28543openalex-snapshot
Comparative Analysis of a Locally Resampling MR Elastography Reconstruction Algorithm in Liver Fibrosis
inferred← citeshttps://doi.org/10.1002/jmri.28663openalex-snapshot
Advanced MR Techniques for Preoperative Glioma Characterization: Part 2
inferred← citeshttps://doi.org/10.1002/jmri.29799openalex-snapshot
Association of In Vivo Kidney Stiffness Measured by Multifrequency MR Elastography and Long‐Term Renal Function in Transplant Recipients and Living Donors
inferred← citeshttps://doi.org/10.1002/jmri.70145openalex-snapshot
Evaluating Measurement Stability in Glioblastomas Using Magnetic Resonance Elastography: Repeatability and Interobserver Agreement
inferred← citeshttps://doi.org/10.1002/jmri.70154openalex-snapshot
Editorial for “Evaluating Measurement Stability in Glioblastomas Using Magnetic Resonance Elastography: Repeatability and Interobserver Agreement”
inferred← citeshttps://doi.org/10.1002/mp.12372openalex-snapshot
Improving three‐dimensional mechanical imaging of breast lesions with principal component analysis
inferred← citeshttps://doi.org/10.1002/mrm.26006openalex-snapshot
In vivo wideband multifrequency MR elastography of the human brain and liver
inferred← citeshttps://doi.org/10.1002/mrm.26477openalex-snapshot
Combining rheology and MRI: Imaging healthy and tumorous brains based on mechanical properties
inferred← citeshttps://doi.org/10.1002/mrm.27672openalex-snapshot
Magnetic resonance elastography of the human brain using a multiphase DENSE acquisition
inferred← citeshttps://doi.org/10.1002/mrm.29320openalex-snapshot
Comparison of inversion methods in MR elastography: An open‐access pipeline for processing multifrequency shear‐wave data and demonstration in a phantom, human kidneys, and brain
inferred← citeshttps://doi.org/10.1002/mrm.30504openalex-snapshot
Feasibility of magnetic resonance elastography in the healthy rat heart
inferred← citeshttps://doi.org/10.1002/nbm.3388openalex-snapshot
Cerebral multifrequency MR elastography by remote excitation of intracranial shear waves
inferred← citeshttps://doi.org/10.1002/nbm.3840openalex-snapshot
Characterization of glioblastoma in an orthotopic mouse model with magnetic resonance elastography
inferred← citeshttps://doi.org/10.1002/nbm.3935openalex-snapshot
Stiffness reconstruction methods for MR elastography
inferred← citeshttps://doi.org/10.1002/nbm.70054openalex-snapshot
Improving the Accuracy and Repeatability of Renal Stiffness Measurement With Magnetic Resonance Elastography: Influence of Vibration Frequency, Acquisition Orientation, and Postprocessing—A Phantom and Volunteer Study
inferred← citeshttps://doi.org/10.1002/poh2.70027openalex-snapshot
Multifrequency Multiparameter Magnetic Resonance Elastography Applied to an In Vivo Porcine Model for Assessing Portal Hypertension
inferred← citeshttps://doi.org/10.1007/978-3-030-04996-6_4openalex-snapshot
Brain Tissue Mechanical Properties
inferred← citeshttps://doi.org/10.1007/978-4-431-56880-3_4openalex-snapshot
Stromal Barriers Within the Tumor Microenvironment and Obstacles to Nanomedicine
inferred← citeshttps://doi.org/10.1007/s00234-024-03491-zopenalex-snapshot
Mechanical properties of pediatric low-grade gliomas in children with and without neurofibromatosis type 1
inferred← citeshttps://doi.org/10.1007/s00247-023-05779-3openalex-snapshot
Clinical application of magnetic resonance elastography in pediatric neurological disorders
inferred← citeshttps://doi.org/10.1007/s00330-017-5269-yopenalex-snapshot
Progressive supranuclear palsy and idiopathic Parkinson’s disease are associated with local reduction of in vivo brain viscoelasticity
inferred← citeshttps://doi.org/10.1007/s00701-026-06898-0openalex-snapshot
Elasticity-guided tumor resection: applying biomechanical information to neurosurgical practice
inferred← citeshttps://doi.org/10.1007/s11682-019-00200-wopenalex-snapshot
Viscoelasticity of striatal brain areas reflects variations in body mass index of lean to overweight male adults
inferred← citeshttps://doi.org/10.1016/b978-0-443-30048-6.00002-4openalex-snapshot
Dynamic mechanical three-way crosstalk at the interfaces of cancer cells, immune cells, like macrophages and stromal cells
inferred← citeshttps://doi.org/10.1016/j.actbio.2019.06.034openalex-snapshot
The influence of body temperature on tissue stiffness, blood perfusion, and water diffusion in the mouse brain
inferred← citeshttps://doi.org/10.1016/j.actbio.2019.08.013openalex-snapshot
Viscoelasticity in natural tissues and engineered scaffolds for tissue reconstruction
inferred← citeshttps://doi.org/10.1016/j.actbio.2020.12.027openalex-snapshot
Superviscous Properties of the In Vivo Brain at Large Scales
inferred← citeshttps://doi.org/10.1016/j.actbio.2021.10.038openalex-snapshot
In vivo stiffness of multiple sclerosis lesions is similar to that of normal-appearing white matter
inferred← citeshttps://doi.org/10.1016/j.actbio.2022.05.048openalex-snapshot
Glioblastoma spheroid growth and chemotherapeutic responses in single and dual-stiffness hydrogels
inferred← citeshttps://doi.org/10.1016/j.addr.2022.114111openalex-snapshot
Engineering in vitro immune-competent tissue models for testing and evaluation of therapeutics
inferred← citeshttps://doi.org/10.1016/j.bioadv.2024.213860openalex-snapshot
Glioblastoma mechanobiology at multiple length scales
inferred← citeshttps://doi.org/10.1016/j.bioadv.2026.214758openalex-snapshot
Mechanical instability as a signature of viscoelastic decoupling at the tumor–brain interface
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.120903openalex-snapshot
Multiscale rheology of glioma cells
inferred← citeshttps://doi.org/10.1016/j.brain.2022.100050openalex-snapshot
Comparing the effects of linear and one-term Ogden elasticity in a model of glioblastoma invasion.
inferred← citeshttps://doi.org/10.1016/j.ceb.2021.04.002openalex-snapshot
The extracellular matrix viscoelasticity as a regulator of cell and tissue dynamics
inferred← citeshttps://doi.org/10.1016/j.ceca.2019.03.007openalex-snapshot
Mechanosensitive ion channels push cancer progression
inferred← citeshttps://doi.org/10.1016/j.cell.2025.05.019openalex-snapshot
MT-125 inhibits non-muscle myosin IIA and IIB and prolongs survival in glioblastoma
inferred← citeshttps://doi.org/10.1016/j.clineuro.2021.106531openalex-snapshot
Shear wave elastography for intracranial epidermoid tumors
inferred← citeshttps://doi.org/10.1016/j.coche.2016.01.011openalex-snapshot
Mechanotransduction in cancer
inferred← citeshttps://doi.org/10.1016/j.coisb.2017.04.005openalex-snapshot
Genome variation across cancers scales with tissue stiffness – An invasion-mutation mechanism and implications for immune cell infiltration
inferred← citeshttps://doi.org/10.1016/j.drup.2026.101470openalex-snapshot
Extracellular matrix stiffness and mechanotransduction in cancer drug resistance
inferred← citeshttps://doi.org/10.1016/j.ebiom.2025.105808openalex-snapshot
Mechanotransduction as a therapeutic target for brain tumours
inferred← citeshttps://doi.org/10.1016/j.ejrad.2021.110136openalex-snapshot
Decreased tissue stiffness in glioblastoma by MR elastography is associated with increased cerebral blood flow
inferred← citeshttps://doi.org/10.1016/j.jbior.2019.100658openalex-snapshot
Three dimensional in vitro models of cancer: Bioprinting multilineage glioblastoma models
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2021.104645openalex-snapshot
Influence of fibrosis progression on the viscous properties of in vivo liver tissue elucidated by shear wave dispersion in multifrequency MR elastography
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2022.105302openalex-snapshot
The effects of geometry on stiffness measurements in high-field magnetic resonance elastography: A study on rodent cardiac phantoms
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2022.105599openalex-snapshot
Comparison of Macroscale and Microscale Mechanical Properties of Fresh and Fixed-Frozen Porcine Colonic Tissue
inferred← citeshttps://doi.org/10.1016/j.matbio.2019.06.002openalex-snapshot
Transcriptomic analysis reveals that BMP4 sensitizes glioblastoma tumor-initiating cells to mechanical cues
inferred← citeshttps://doi.org/10.1016/j.media.2016.01.001openalex-snapshot
Tomoelastography by multifrequency wave number recovery from time-harmonic propagating shear waves
inferred← citeshttps://doi.org/10.1016/j.media.2016.05.012openalex-snapshot
Nonlinear multiscale regularisation in MR elastography: Towards fine feature mapping
inferred← citeshttps://doi.org/10.1016/j.media.2018.03.003openalex-snapshot
Heterogeneous Multifrequency Direct Inversion (HMDI) for magnetic resonance elastography with application to a clinical brain exam
inferred← citeshttps://doi.org/10.1016/j.media.2020.101710openalex-snapshot
Artificial neural networks for magnetic resonance elastography stiffness estimation in inhomogeneous materials
inferred← citeshttps://doi.org/10.1016/j.mri.2026.110746openalex-snapshot
The clinical utility of magnetic resonance elastography in differentiating tumor recurrence from pseudoprogression in glioblastoma
inferred← citeshttps://doi.org/10.1016/j.mtbio.2026.103390openalex-snapshot
Nanomedicine targeting ECM stiffness: restoring mechanical homeostasis for cancer immunotherapy
inferred← citeshttps://doi.org/10.1016/j.neuron.2023.10.005openalex-snapshot
Mechanics in the nervous system: From development to disease
inferred← citeshttps://doi.org/10.1016/j.nicl.2017.12.023openalex-snapshot
Combining viscoelasticity, diffusivity and volume of the hippocampus for the diagnosis of Alzheimer's disease based on magnetic resonance imaging
inferred← citeshttps://doi.org/10.1016/j.nicl.2019.102109openalex-snapshot
REVIEW: MR elastography of brain tumors
inferred← citeshttps://doi.org/10.1016/j.nicl.2021.102579openalex-snapshot
MR Elastography demonstrates reduced white matter shear stiffness in early-onset hydrocephalus
inferred← citeshttps://doi.org/10.1016/j.nicl.2024.103606openalex-snapshot
Low-frequency MR elastography reveals altered deep gray matter viscoelasticity in multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.optlastec.2026.114763openalex-snapshot
Characterizing brain tissue viscoelasticity using air-coupled ultrasound transducer-based optical coherence elastography with power-law-constrained Kelvin-Voigt fractional derivative model☆★
inferred← citeshttps://doi.org/10.1016/j.plrev.2023.01.017openalex-snapshot
Mechanotransduction in tumor dynamics modeling
inferred← citeshttps://doi.org/10.1016/j.pnmrs.2024.05.002openalex-snapshot
Magnetic resonance elastography in a nutshell: Tomographic imaging of soft tissue viscoelasticity for detecting and staging disease with a focus on inflammation
inferred← citeshttps://doi.org/10.1016/j.tips.2021.02.006openalex-snapshot
Channeling Force in the Brain: Mechanosensitive Ion Channels Choreograph Mechanics and Malignancies
inferred← citeshttps://doi.org/10.1016/j.ultrasmedbio.2021.03.030openalex-snapshot
Shear Wave Elastography: A Review on the Confounding Factors and Their Potential Mitigation in Detecting Chronic Kidney Disease
inferred← citeshttps://doi.org/10.1016/j.zemedi.2026.08.001openalex-snapshot
Magnetic resonance elastography of brain tumors
inferred← citeshttps://doi.org/10.1021/acs.biomac.7b00324openalex-snapshot
Soft Substrates Containing Hyaluronan Mimic the Effects of Increased Stiffness on Morphology, Motility, and Proliferation of Glioma Cells
inferred← citeshttps://doi.org/10.1021/acsami.3c12514openalex-snapshot
Hyaluronic Acid Hydrogels with Phototunable Supramolecular Cross-Linking for Spatially Controlled Lymphatic Tube Formation
inferred← citeshttps://doi.org/10.1021/acsami.4c16993openalex-snapshot
Matrix Stiffness Regulates GBM Migration and Chemoradiotherapy Responses via Chromatin Condensation in 3D Viscoelastic Matrices
inferred← citeshttps://doi.org/10.1021/acsomega.3c04064openalex-snapshot
Developing Bovine Brain-Derived Extracellular Matrix Hydrogels: a Screen of Decellularization Methods for Their Impact on Biochemical and Mechanical Properties
inferred← citeshttps://doi.org/10.1038/s41388-023-02844-xopenalex-snapshot
Biophysics in tumor growth and progression: from single mechano-sensitive molecules to mechanomedicine
inferred← citeshttps://doi.org/10.1038/s41551-019-0370-yopenalex-snapshot
Compressive tumours cause neuronal damage
inferred← citeshttps://doi.org/10.1038/s41551-025-01369-wopenalex-snapshot
Water and ions binding to extracellular matrix drives stress relaxation, aiding MRI detection of swelling-associated pathology
inferred← citeshttps://doi.org/10.1038/s41551-025-01446-0openalex-snapshot
Mechanical regulation of extracellular vesicle activity during tumour progression
inferred← citeshttps://doi.org/10.1038/s41563-022-01400-4openalex-snapshot
Matrix viscoelasticity controls spatiotemporal tissue organization
inferred← citeshttps://doi.org/10.1038/s41580-023-00583-1openalex-snapshot
Cell–extracellular matrix mechanotransduction in 3D
inferred← citeshttps://doi.org/10.1038/s41586-020-2612-2openalex-snapshot
Effects of extracellular matrix viscoelasticity on cellular behaviour
inferred← citeshttps://doi.org/10.1038/s41592-024-02564-4openalex-snapshot
Probing the physical hallmarks of cancer
inferred← citeshttps://doi.org/10.1038/s41598-022-05878-5openalex-snapshot
Fully automated quantification of in vivo viscoelasticity of prostate zones using magnetic resonance elastography with Dense U-net segmentation
inferred← citeshttps://doi.org/10.1038/s42254-022-00543-2openalex-snapshot
Magnetic resonance elastography from fundamental soft-tissue mechanics to diagnostic imaging
inferred← citeshttps://doi.org/10.1039/d1sm01291fopenalex-snapshot
Whole tissue and single cell mechanics are correlated in human brain tumors
inferred← citeshttps://doi.org/10.1063/5.0277950openalex-snapshot
The glioblastoma biomechanical landscape: A systematic review of magnetic resonance elastography (MRE) of brain tumors and healthy brain
inferred← citeshttps://doi.org/10.1073/pnas.1902847116openalex-snapshot
Myosin IIA suppresses glioblastoma development in a mechanically sensitive manner
inferred← citeshttps://doi.org/10.1073/pnas.1913511116openalex-snapshot
How tissue fluidity influences brain tumor progression
inferred← citeshttps://doi.org/10.1080/01616412.2020.1796381openalex-snapshot
Mechanical properties of human glioma
inferred← citeshttps://doi.org/10.1088/0031-9155/61/24/r401openalex-snapshot
Magnetic resonance elastography (MRE) of the human brain: technique, findings and clinical applications
inferred← citeshttps://doi.org/10.1088/1361-6560/ab9a84openalex-snapshot
A heterogenous, time harmonic, nearly incompressible transverse isotropic finite element brain simulation platform for MR elastography
inferred← citeshttps://doi.org/10.1088/1361-6560/ac145aopenalex-snapshot
MR elastography inversion by compressive recovery
inferred← citeshttps://doi.org/10.1093/braincomms/fcae424openalex-snapshot
The contributions of relative brain viscosity to brain function and health
inferred← citeshttps://doi.org/10.1097/rli.0000000000000685openalex-snapshot
In Vivo Quantification of Water Diffusion, Stiffness, and Tissue Fluidity in Benign Prostatic Hyperplasia and Prostate Cancer
inferred← citeshttps://doi.org/10.1097/rli.0000000000000971openalex-snapshot
MR Elastography in Cancer
inferred← citeshttps://doi.org/10.1097/rmr.0000000000000181openalex-snapshot
Quantifying Tumor Stiffness With Magnetic Resonance Elastography
inferred← citeshttps://doi.org/10.1097/rmr.0000000000000292openalex-snapshot
Magnetic Resonance Elastography in Intracranial Neoplasms: A Scoping Review
inferred← citeshttps://doi.org/10.1098/rstb.2018.0215openalex-snapshot
Tissue mechanics, an important regulator of development and disease
inferred← citeshttps://doi.org/10.1101/2020.07.16.207233openalex-snapshot
Patient-derived glioblastoma cells (GBM) exhibit distinct biomechanical profiles associated with altered activity in the cytoskeleton regulatory pathway
inferred← citeshttps://doi.org/10.1101/2020.09.02.279794openalex-snapshot
Intracellular stiffening competes with cortical softening in glioblastoma cells
inferred← citeshttps://doi.org/10.1101/2020.11.21.352724openalex-snapshot
Sex Differences in MRI-Based Metrics of Glioma Invasion and Brain Mechanics
inferred← citeshttps://doi.org/10.1101/2024.04.27.591399openalex-snapshot
MT-125 Inhibits Non-Muscle Myosin IIA and IIB, Synergizes with Oncogenic Kinase Inhibitors, and Prolongs Survival in Glioblastoma
inferred← citeshttps://doi.org/10.1101/2024.06.16.599204openalex-snapshot
Isolating Poroelastic and Viscoelastic Mechanisms of Soft Tissues and Hydrogels Through Sequential Microscale Indentation Testing: New Applications of Indentation Theory for Microscale Characterization
inferred← citeshttps://doi.org/10.1109/ojemb.2021.3075569openalex-snapshot
Ultrasound Shear Wave Elastography and Transient Optical Coherence Elastography: Side-by-Side Comparison of Repeatability and Accuracy
inferred← citeshttps://doi.org/10.1109/ojemb.2025.3528194openalex-snapshot
Non-Invasive Measurement of Elasticity in Glioblastoma Multiforme Validates Decreased TMZ Sensitivity in Astrocyte Co-Culture
inferred← citeshttps://doi.org/10.1109/tbme.2022.3171287openalex-snapshot
Electromechanical Characterization of Human Brain Tissues: A Potential Biomarker for Tumor Delineation
inferred← citeshttps://doi.org/10.1109/tbme.2024.3381708openalex-snapshot
Indirect Shear Wave Excitation for Brain Magnetic Resonance Elastography With Minimal Cerebral Blood Flow Alteration
inferred← citeshttps://doi.org/10.1109/tmi.2023.3261346openalex-snapshot
MR Elastography With Optimization-Based Phase Unwrapping and Traveling Wave Expansion-Based Neural Network (TWENN)
inferred← citeshttps://doi.org/10.1109/tuffc.2016.2583785openalex-snapshot
Ultrasound Shear Wave Viscoelastography: Model-Independent Quantification of the Complex Shear Modulus
inferred← citeshttps://doi.org/10.1111/cns.14809openalex-snapshot
Mechanobiological insight into brain diseases based on mechanosensitive channels: Common mechanisms and clinical potential
inferred← citeshttps://doi.org/10.1117/12.2287553openalex-snapshot
Viscoelastic characterization of dispersive media by inversion of a general wave propagation model in optical coherence elastography
inferred← citeshttps://doi.org/10.1117/12.2515946openalex-snapshot
Perspectives and advances in optical elastography
inferred← citeshttps://doi.org/10.1126/sciadv.aef7087openalex-snapshot
Matrix stress relaxation drives glioblastoma cell response in viscoelastic biomaterials
inferred← citeshttps://doi.org/10.1142/s1793545817420081openalex-snapshot
An approach to viscoelastic characterization of dispersive media by inversion of a general wave propagation model
inferred← citeshttps://doi.org/10.1148/radiol.252429openalex-snapshot
MR Elastography Characterization of Biomechanical Properties to Enhance Enterographic Fibrosis Diagnosis
inferred← citeshttps://doi.org/10.1177/0271678x17691530openalex-snapshot
Perfusion alters stiffness of deep gray matter
inferred← citeshttps://doi.org/10.1177/0271678x19850936openalex-snapshot
Cardiac-gated steady-state multifrequency magnetic resonance elastography of the brain: Effect of cerebral arterial pulsation on brain viscoelasticity
inferred← citeshttps://doi.org/10.1186/s40644-020-00314-1openalex-snapshot
Magnetic Resonance Elastography reveals effects of anti-angiogenic glioblastoma treatment on tumor stiffness and captures progression in an orthotopic mouse model
inferred← citeshttps://doi.org/10.1186/s41747-026-00713-2openalex-snapshot
Feasibility of multifrequency MR elastography of the seminal vesicles in healthy men, benign prostatic hyperplasia, and prostate cancer
inferred← citeshttps://doi.org/10.1242/jcs.191742openalex-snapshot
Tissue mechanics regulate brain development, homeostasis and disease
inferred← citeshttps://doi.org/10.1259/bjr.20200265openalex-snapshot
Harnessing brain waves: a review of brain magnetic resonance elastography for clinicians and scientists entering the field
inferred← citeshttps://doi.org/10.1371/journal.pone.0161179openalex-snapshot
Dopaminergic Neurodegeneration in the Mouse Is Associated with Decrease of Viscoelasticity of Substantia Nigra Tissue
inferred← citeshttps://doi.org/10.1371/journal.pone.0191919openalex-snapshot
Quantitative characterization of viscoelastic behavior in tissue-mimicking phantoms and ex vivo animal tissues
inferred← citeshttps://doi.org/10.1586/17446651.2016.1151784openalex-snapshot
Current imaging techniques for the diagnosis of pituitary adenoma
inferred← citeshttps://doi.org/10.21037/qims-24-101openalex-snapshot
Effects of oral contrast agent on the viscoelastic properties of the terminal ileum investigated using magnetic resonance elastography
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10569219/v1openalex-snapshot
Piezo1 Knockdown Sensitizes Brain Cancer Cells to Focused Ultrasound-Induced Apoptosis
inferred← citeshttps://doi.org/10.2463/mrms.mp.2022-0149openalex-snapshot
A Versatile MR Elastography Research Tool with a Modified Motion Signal-to-noise Ratio Approach
inferred← citeshttps://doi.org/10.3171/2018.2.spine171195openalex-snapshot
In vivo assessment of spinal cord elasticity using shear wave ultrasound in dogs
inferred← citeshttps://doi.org/10.3174/ajnr.a4832openalex-snapshot
Shear Stiffness of 4 Common Intracranial Tumors Measured Using MR Elastography: Comparison with Intraoperative Consistency Grading
inferred← citeshttps://doi.org/10.3174/ajnr.a5415openalex-snapshot
MR Elastography Analysis of Glioma Stiffness andIDH1-Mutation Status
inferred← citeshttps://doi.org/10.3389/fbioe.2021.666456openalex-snapshot
Real-Time Multifrequency MR Elastography of the Human Brain Reveals Rapid Changes in Viscoelasticity in Response to the Valsalva Maneuver
inferred← citeshttps://doi.org/10.3389/fbioe.2023.1236949openalex-snapshot
Effects of kidney perfusion on renal stiffness and tissue fluidity measured with tomoelastography in an MRI-compatible ex vivo model
inferred← citeshttps://doi.org/10.3389/fcell.2026.1849535openalex-snapshot
Mechanotransduction in glioma stem cell fate determination: from niche mechanics to therapeutic vulnerability and state plasticity
inferred← citeshttps://doi.org/10.3389/fncel.2018.00025openalex-snapshot
Glial Tissue Mechanics and Mechanosensing by Glial Cells
inferred← citeshttps://doi.org/10.3389/fneur.2018.01010openalex-snapshot
Magnetic Resonance Elastography of Rodent Brain
inferred← citeshttps://doi.org/10.3389/fonc.2021.701336openalex-snapshot
Rectal Tumor Stiffness Quantified by In Vivo Tomoelastography and Collagen Content Estimated by Histopathology Predict Tumor Aggressiveness
inferred← citeshttps://doi.org/10.3389/fonc.2021.805628openalex-snapshot
Mechanical Properties in the Glioma Microenvironment: Emerging Insights and Theranostic Opportunities
inferred← citeshttps://doi.org/10.3389/fonc.2024.1402578openalex-snapshot
In vivo characterization of brain tumor biomechanics: magnetic resonance elastography in intracranial B16 melanoma and GL261 glioma mouse models
inferred← citeshttps://doi.org/10.3389/fphy.2021.633848openalex-snapshot
Actuators for MRE: New Perspectives With Flexible Electroactive Materials
inferred← citeshttps://doi.org/10.3389/fphy.2021.666192openalex-snapshot
Viscoelasticity Imaging of Biological Tissues and Single Cells Using Shear Wave Propagation
inferred← citeshttps://doi.org/10.3389/fphy.2021.670571openalex-snapshot
Existing and Potential Applications of Elastography for Measuring the Viscoelasticity of Biological Tissues In Vivo
inferred← citeshttps://doi.org/10.3389/fphy.2022.910036openalex-snapshot
Magnetic resonance elastography of malignant tumors
inferred← citeshttps://doi.org/10.3390/biom14020184openalex-snapshot
Phenotypic Heterogeneity, Bidirectionality, Universal Cues, Plasticity, Mechanics, and the Tumor Microenvironment Drive Cancer Metastasis
inferred← citeshttps://doi.org/10.3390/biomedicines14010205openalex-snapshot
The Extracellular Matrix, the Silent ‘Architect’ of Glioma
inferred← citeshttps://doi.org/10.3390/brainsci12070927openalex-snapshot
Mechanical Properties of the Extracellular Environment of Human Brain Cells Drive the Effectiveness of Drugs in Fighting Central Nervous System Cancers
inferred← citeshttps://doi.org/10.3390/cancers13184539openalex-snapshot
Atomic Force Microscope Nanoindentation Analysis of Diffuse Astrocytic Tumor Elasticity: Relation with Tumor Histopathology
inferred← citeshttps://doi.org/10.3390/cancers14071725openalex-snapshot
Quantification of Tissue Compression Identifies High-Grade Glioma Patients with Reduced Survival
inferred← citeshttps://doi.org/10.3390/cancers14143401openalex-snapshot
Advanced Neuroimaging Approaches to Pediatric Brain Tumors
inferred← citeshttps://doi.org/10.3390/cells14211707openalex-snapshot
Impact of the ECM on the Mechanical Memory of Cancer Cells
inferred← citeshttps://doi.org/10.3390/cells15100876openalex-snapshot
The Biomechanics of Glioblastoma: Why Glioblastoma Models and Clinical Reality Diverge
inferred← citeshttps://doi.org/10.3390/gels8080496openalex-snapshot
Biomimetic Hydrogels in the Study of Cancer Mechanobiology: Overview, Biomedical Applications, and Future Perspectives
inferred← citeshttps://doi.org/10.3390/ijms22062962openalex-snapshot
Advanced Spheroid, Tumouroid and 3D Bioprinted In-Vitro Models of Adult and Paediatric Glioblastoma
inferred← citeshttps://doi.org/10.3390/nano13060963openalex-snapshot
Investigation of Soft Matter Nanomechanics by Atomic Force Microscopy and Optical Tweezers: A Comprehensive Review
inferred← citeshttps://doi.org/10.51926/iste.9160.ch1openalex-snapshot
Biomécanique du foie : caractérisations, modélisations et applications cliniques
inferred← citeshttps://doi.org/10.64898/2026.04.17.719181openalex-snapshot
Challenges in Brillouin microscopy: Addressing heterogeneity and contamination for reliable biomechanical mapping of fresh brain tumors
inferred← citeshttps://doi.org/10.64898/2026.05.06.26352294openalex-snapshot
Directional interface mechanics using magnetic resonance elastography predicts focal tumor recurrence in glioblastomas
inferred← citeshttps://doi.org/10.64898/2026.06.07.730664openalex-snapshot
Extracellular Matrix Mechanobiology in Pancreatic Ductal Adenocarcinoma: Correlating In Vivo Patient Magnetic Resonance Elastography with Ex Vivo Tissue Mechanics and Histopathology
inferred← citeshttps://doi.org/10.64898/2026.09.29.755236openalex-snapshot
Human cerebral assembloids as a model to study the interaction of glioblastoma with resident glial cells
inferred← citeshttps://doi.org/10.70675/8295b051z541cz4fa9z833ezf06b80b85bffopenalex-snapshot
Conditions optimales et sensibilité de l'ERM cérébrale : milieux homogènes à hétérogènes
inferred← citeshttps://doi.org/10.70675/98801c9bzbcbcz492dz8be0z209572f81f51openalex-snapshot
Elastographie par Résonance Magnétique : Contrôle optimal pour l’encodage du mouvement à temps d’écho court et acquisitions multifréquence simultanée
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.