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particle image velocimetry piv tool  (MathWorks Inc)


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    MathWorks Inc particle image velocimetry piv tool
    Particle Image Velocimetry Piv Tool, supplied by MathWorks 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/particle+image+velocimetry+(piv)+tool/pm36418198-245-16-22
    Average 90 stars, based on 1 article reviews
    particle image velocimetry piv tool - by Bioz Stars, 2026-09
    90/100 stars

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    other:

    Article Title: CRISPR-mediated correction of skeletal muscle Ca 2+ handling in a novel DMD patient-derived pluripotent stem cell model.
    Article Snippet: To do his, we measured the velocity of myotube contraction in response o acetylcholine stimulation using particle image velocimetry (PIV) ool in MATLAB, PIVlab [24] .

    Article Title: In-situ optical assessment of rat epicardial kinematic parameters reveals frequency-dependent mechanic heterogeneity related to gender.
    Article Snippet: Background: Gender-related cardiac mechanics following the electrical activity has been investigated from basic to clinical research, but results are still controversial.. The aim of this work is to study the gender related cardiac mechanics and to focus on its heart rate dependency.. Methods: We employed 12 Sprague Dawley rats (5 males and 7 females) of the same age and, through a novel high resolution artificial vision contactless approach, we evaluated in-situ cardiac kinematic.



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    (A) Time-course expression levels of genes within HALLMARK_MYOGENESIS that regulate muscle contraction, including TNNC2 , TNNI1 , TNNI2 , TNNT1 , TNNT3 and TPM2 . Wald test with Benjamini-Hochberg method for multiple comparison adjustment (* padj < 0.05, ** padj < 0.01, *** padj < 0.001). TPM, Transcripts Per Million. Each condition has 4 biological replicates. (B-D) Analysis of myotube contraction velocity using Particle Image <t>Velocimetry.</t> In response to acetylcholine (Ach) stimulation, DMD-K2957fs myotubes had significantly slower velocity magnitude than BIONi010-C (B) or CORR-K2957fs (C) myotubes, whereas no significant difference of velocity between BIONi010-C and CORR-K2957fs myotubes (D). Data represent mean ± SEM (n= 9; at least three independent experiments). Two-way ANOVA, Sidak test (** p < 0.01; *** p < 0.001).
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    (A) Time-course expression levels of genes within HALLMARK_MYOGENESIS that regulate muscle contraction, including TNNC2 , TNNI1 , TNNI2 , TNNT1 , TNNT3 and TPM2 . Wald test with Benjamini-Hochberg method for multiple comparison adjustment (* padj < 0.05, ** padj < 0.01, *** padj < 0.001). TPM, Transcripts Per Million. Each condition has 4 biological replicates. (B-D) Analysis of myotube contraction velocity using Particle Image <t>Velocimetry.</t> In response to acetylcholine (Ach) stimulation, DMD-K2957fs myotubes had significantly slower velocity magnitude than BIONi010-C (B) or CORR-K2957fs (C) myotubes, whereas no significant difference of velocity between BIONi010-C and CORR-K2957fs myotubes (D). Data represent mean ± SEM (n= 9; at least three independent experiments). Two-way ANOVA, Sidak test (** p < 0.01; *** p < 0.001).
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    (A) Time-course expression levels of genes within HALLMARK_MYOGENESIS that regulate muscle contraction, including TNNC2 , TNNI1 , TNNI2 , TNNT1 , TNNT3 and TPM2 . Wald test with Benjamini-Hochberg method for multiple comparison adjustment (* padj < 0.05, ** padj < 0.01, *** padj < 0.001). TPM, Transcripts Per Million. Each condition has 4 biological replicates. (B-D) Analysis of myotube contraction velocity using Particle Image <t>Velocimetry.</t> In response to acetylcholine (Ach) stimulation, DMD-K2957fs myotubes had significantly slower velocity magnitude than BIONi010-C (B) or CORR-K2957fs (C) myotubes, whereas no significant difference of velocity between BIONi010-C and CORR-K2957fs myotubes (D). Data represent mean ± SEM (n= 9; at least three independent experiments). Two-way ANOVA, Sidak test (** p < 0.01; *** p < 0.001).
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    (A) Time-course expression levels of genes within HALLMARK_MYOGENESIS that regulate muscle contraction, including TNNC2 , TNNI1 , TNNI2 , TNNT1 , TNNT3 and TPM2 . Wald test with Benjamini-Hochberg method for multiple comparison adjustment (* padj < 0.05, ** padj < 0.01, *** padj < 0.001). TPM, Transcripts Per Million. Each condition has 4 biological replicates. (B-D) Analysis of myotube contraction velocity using Particle Image <t>Velocimetry.</t> In response to acetylcholine (Ach) stimulation, DMD-K2957fs myotubes had significantly slower velocity magnitude than BIONi010-C (B) or CORR-K2957fs (C) myotubes, whereas no significant difference of velocity between BIONi010-C and CORR-K2957fs myotubes (D). Data represent mean ± SEM (n= 9; at least three independent experiments). Two-way ANOVA, Sidak test (** p < 0.01; *** p < 0.001).
    Pivlab—Time Resolved Digital Particle Image Velocimetry (Piv) Tool For Matlab Version: 1.4, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Time-course expression levels of genes within HALLMARK_MYOGENESIS that regulate muscle contraction, including TNNC2 , TNNI1 , TNNI2 , TNNT1 , TNNT3 and TPM2 . Wald test with Benjamini-Hochberg method for multiple comparison adjustment (* padj < 0.05, ** padj < 0.01, *** padj < 0.001). TPM, Transcripts Per Million. Each condition has 4 biological replicates. (B-D) Analysis of myotube contraction velocity using Particle Image Velocimetry. In response to acetylcholine (Ach) stimulation, DMD-K2957fs myotubes had significantly slower velocity magnitude than BIONi010-C (B) or CORR-K2957fs (C) myotubes, whereas no significant difference of velocity between BIONi010-C and CORR-K2957fs myotubes (D). Data represent mean ± SEM (n= 9; at least three independent experiments). Two-way ANOVA, Sidak test (** p < 0.01; *** p < 0.001).

    Journal: bioRxiv

    Article Title: CRISPR-mediated correction of skeletal muscle Ca 2+ handling in a novel DMD patient-derived pluripotent stem cell model

    doi: 10.1101/2022.02.17.480850

    Figure Lengend Snippet: (A) Time-course expression levels of genes within HALLMARK_MYOGENESIS that regulate muscle contraction, including TNNC2 , TNNI1 , TNNI2 , TNNT1 , TNNT3 and TPM2 . Wald test with Benjamini-Hochberg method for multiple comparison adjustment (* padj < 0.05, ** padj < 0.01, *** padj < 0.001). TPM, Transcripts Per Million. Each condition has 4 biological replicates. (B-D) Analysis of myotube contraction velocity using Particle Image Velocimetry. In response to acetylcholine (Ach) stimulation, DMD-K2957fs myotubes had significantly slower velocity magnitude than BIONi010-C (B) or CORR-K2957fs (C) myotubes, whereas no significant difference of velocity between BIONi010-C and CORR-K2957fs myotubes (D). Data represent mean ± SEM (n= 9; at least three independent experiments). Two-way ANOVA, Sidak test (** p < 0.01; *** p < 0.001).

    Article Snippet: To do this, we measured the velocity of myotube contraction in response to acetylcholine stimulation using particle image velocimetry (PIV) tool in MATLAB, PIVlab [ ].

    Techniques: Expressing