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finite element method comsol multiphysics 4.3  (COMSOL Inc)

 
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    COMSOL Inc finite element method comsol multiphysics 4.3
    Finite Element Method Comsol Multiphysics 4.3, supplied by COMSOL Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/finite-element-method+numerical+software+comsol+multiphysics/comsol+multiphysics+4+3/pmc09117592-103-20-21
    Average 90 stars, based on 1 article reviews
    finite element method comsol multiphysics 4.3 - by Bioz Stars, 2026-09
    90/100 stars

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    Article Title: Hepatic tumor ablation using electric current and bioheat transfer model: a 3D numerical analysis
    Article Snippet: Regarding electrical potential, it is set at 22 volts at the electrode and 0 volts at the outer boundaries of the cylinder (Surita et al. (2012), Mellal et al. (2016), COMSOL Multiphysics 4.3).

    Article Title: Hepatic tumor ablation using electric current and bioheat transfer model: a 3D numerical analysis
    Article Snippet: The objective of this treatment is twofold: primarily, to eradicate tumor cells located at the cylinder's core, and secondarily, to avoid damaging the healthy liver cells, which are represented as a cylinder surrounding the tumor [COMSOL Multiphysics 4.3].

    Article Title: Transcranial temporal interference stimulation precisely targets deep brain regions to regulate eye movements.
    Article Snippet: COMSOL Multiphysics 4.3 (COMSOL, Inc., Burlington, MA) was used to set conductivities and calculate physics equations.

    Article Title: Hepatic tumor ablation using electric current and bioheat transfer model: a 3D numerical analysis
    Article Snippet: For these components, all the terms on the right-hand side of the equation (3) become zero: ρ∁ + ∇ ∙ (−∇T) = 0 (4) The governing equation for the conservation of electric current (Surita et al. (2012), COMSOL Multiphysics 4.3): –∇.

    Article Title: Hepatic tumor ablation using electric current and bioheat transfer model: a 3D numerical analysis
    Article Snippet: The boundary conditions for the electric current model (Surita et al. (2012), COMSOL Multiphysics 4.3): V = 0 → trocar base, liver outer boundaries, blood vessel V = V0 → electrode boundaries, trocar tip n⋅J = 0 → other boundaries Hepatic tumor ablation using electric current and bioheat transfer model: A 3D numerical analysis 57

    Article Title: Inertial microfluidic mixer for biological CubeSat missions
    Article Snippet: Numerical simulations concerning the samples mixing in the designed structures were conducted utilizing COMSOL Multiphysics 4.3 software, based on Laminar Flow module [17- 18].

    Article Title: Hepatic tumor ablation using electric current and bioheat transfer model: a 3D numerical analysis
    Article Snippet: Consequently, the governing equation can be simplified into the following form: –∇⋅(σ∇V)=0 (7) The border criteria for the bioheat model (Surita et al. (2012), Mellal et al. (2016), COMSOL Multiphysics 4.3): T = Tb → liver outer boundaries n⋅(∇T )= 0 → interior boundaries T0 = 310.15 K → initial temperature.

    Article Title: Stimulation of an entorhinal-hippocampal extinction circuit facilitates fear extinction in a post-traumatic stress disorder model
    Article Snippet: To define conductivities and compute the physics equations, COMSOL Multiphysics 4.3 (COMSOL, Inc., Burlington, MA) was employed.



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    COMSOL Inc numerical finite element method calculations using the commercial software comsol multiphysics
    ( A ) Schematic images of a cell that first invades the scaffold (1), builds up initial force in the process (2), and is later stretched by the scaffold (3). ( B ) Linear relationship of changes in displacement and changes in cellular traction forces, obtained by numerical calculations in COMSOL <t>Multiphysics.</t> Negative displacements are defined to point toward the center of the scaffold. ( C ) Exemplary images of displacements from numerical calculations before (left) and after (right) the swelling of the hydrogel. ( D ) Reaction of an exemplary cell in a scaffold as a function of time after addition of trypsin at minute 17. The black data points depict the displacement change, and the blue data points depict the change in traction force. ( E ) Optical micrographs of a cell before, during, and after addition of trypsin. The blue arrows indicate the displacement of the individual beams scaled by a factor of 10. The images below show a magnification of the left beam, with the green dashed line denoting the beam position of the initial frame and the blue dashed line denoting the position of the current frame. The numbers next to the arrow show the cellular reaction as a change in displacement and traction force relative to the first image. ( F ) Quantification of initial forces in the scaffolds for U2OS and NIH 3T3 cells. Each data point corresponds to one cell in a scaffold.
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    ( A ) Schematic images of a cell that first invades the scaffold (1), builds up initial force in the process (2), and is later stretched by the scaffold (3). ( B ) Linear relationship of changes in displacement and changes in cellular traction forces, obtained by numerical calculations in COMSOL Multiphysics. Negative displacements are defined to point toward the center of the scaffold. ( C ) Exemplary images of displacements from numerical calculations before (left) and after (right) the swelling of the hydrogel. ( D ) Reaction of an exemplary cell in a scaffold as a function of time after addition of trypsin at minute 17. The black data points depict the displacement change, and the blue data points depict the change in traction force. ( E ) Optical micrographs of a cell before, during, and after addition of trypsin. The blue arrows indicate the displacement of the individual beams scaled by a factor of 10. The images below show a magnification of the left beam, with the green dashed line denoting the beam position of the initial frame and the blue dashed line denoting the position of the current frame. The numbers next to the arrow show the cellular reaction as a change in displacement and traction force relative to the first image. ( F ) Quantification of initial forces in the scaffolds for U2OS and NIH 3T3 cells. Each data point corresponds to one cell in a scaffold.

    Journal: Science Advances

    Article Title: Mechanical stimulation of single cells by reversible host-guest interactions in 3D microscaffolds

    doi: 10.1126/sciadv.abc2648

    Figure Lengend Snippet: ( A ) Schematic images of a cell that first invades the scaffold (1), builds up initial force in the process (2), and is later stretched by the scaffold (3). ( B ) Linear relationship of changes in displacement and changes in cellular traction forces, obtained by numerical calculations in COMSOL Multiphysics. Negative displacements are defined to point toward the center of the scaffold. ( C ) Exemplary images of displacements from numerical calculations before (left) and after (right) the swelling of the hydrogel. ( D ) Reaction of an exemplary cell in a scaffold as a function of time after addition of trypsin at minute 17. The black data points depict the displacement change, and the blue data points depict the change in traction force. ( E ) Optical micrographs of a cell before, during, and after addition of trypsin. The blue arrows indicate the displacement of the individual beams scaled by a factor of 10. The images below show a magnification of the left beam, with the green dashed line denoting the beam position of the initial frame and the blue dashed line denoting the position of the current frame. The numbers next to the arrow show the cellular reaction as a change in displacement and traction force relative to the first image. ( F ) Quantification of initial forces in the scaffolds for U2OS and NIH 3T3 cells. Each data point corresponds to one cell in a scaffold.

    Article Snippet: Therefore, we used numerical finite element method calculations using the commercial software COMSOL Multiphysics.

    Techniques: