software version 7.10 Search Results


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MetaMorph Inc commercial software package metamorph version 7.10.5
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SCANCO USA INC software version 7.10.1.1
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Bluesky Medical Group Inc statistics version 7.10 software
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Scimedia Ltd bv workbench 2.6.1
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Charles River Laboratories endosafe portable testing system endosafe pts reader, integrated software version 7.10, service pack 2.0, and printer
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De Novo Software Inc fcs express 7 flow version 7.10.0007
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MetaMorph Inc software version 7.10.1.161
Software Version 7.10.1.161, supplied by MetaMorph 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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MetaMorph Inc software version 7.10.3
Systemic administration of iPS-MSCs improves cardiac function in a rat ischemic cardiomyopathy model. (a) Representative images of M-mode echocardiography in the control group, iPS-MSC group, and siAlix-MSC group. (b) Ejection fraction (EF), left <t>ventricular</t> end-diastolic diameter (LVDd), and left ventricular end-diastolic diameter (LVD) before and 1 week after sequential administration of cells in each group (control group, n = 10; iPS-MSC group, n = 12; siAlix-MSC group; n = 9). Data are presented as mean ± SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001 between groups, by one-way analysis of variance with post hoc Turkey's multiple comparisons.
Software Version 7.10.3, supplied by MetaMorph 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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Brookhaven Instruments nanobrookzetapluszeta potential analyzer brookhaveninstruments software-zetapals particlesizing software version number 7.10
Systemic administration of iPS-MSCs improves cardiac function in a rat ischemic cardiomyopathy model. (a) Representative images of M-mode echocardiography in the control group, iPS-MSC group, and siAlix-MSC group. (b) Ejection fraction (EF), left <t>ventricular</t> end-diastolic diameter (LVDd), and left ventricular end-diastolic diameter (LVD) before and 1 week after sequential administration of cells in each group (control group, n = 10; iPS-MSC group, n = 12; siAlix-MSC group; n = 9). Data are presented as mean ± SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001 between groups, by one-way analysis of variance with post hoc Turkey's multiple comparisons.
Nanobrookzetapluszeta Potential Analyzer Brookhaveninstruments Software Zetapals Particlesizing Software Version Number 7.10, supplied by Brookhaven Instruments, 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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Tekscan Inc associated software footmat research version 7.10-14
Systemic administration of iPS-MSCs improves cardiac function in a rat ischemic cardiomyopathy model. (a) Representative images of M-mode echocardiography in the control group, iPS-MSC group, and siAlix-MSC group. (b) Ejection fraction (EF), left <t>ventricular</t> end-diastolic diameter (LVDd), and left ventricular end-diastolic diameter (LVD) before and 1 week after sequential administration of cells in each group (control group, n = 10; iPS-MSC group, n = 12; siAlix-MSC group; n = 9). Data are presented as mean ± SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001 between groups, by one-way analysis of variance with post hoc Turkey's multiple comparisons.
Associated Software Footmat Research Version 7.10 14, supplied by Tekscan 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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Applied Maths bionumerics version 7.10 fingerprinting software
Systemic administration of iPS-MSCs improves cardiac function in a rat ischemic cardiomyopathy model. (a) Representative images of M-mode echocardiography in the control group, iPS-MSC group, and siAlix-MSC group. (b) Ejection fraction (EF), left <t>ventricular</t> end-diastolic diameter (LVDd), and left ventricular end-diastolic diameter (LVD) before and 1 week after sequential administration of cells in each group (control group, n = 10; iPS-MSC group, n = 12; siAlix-MSC group; n = 9). Data are presented as mean ± SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001 between groups, by one-way analysis of variance with post hoc Turkey's multiple comparisons.
Bionumerics Version 7.10 Fingerprinting Software, supplied by Applied Maths, 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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Biotechnology Information dnastart biological software version 7.10
Systemic administration of iPS-MSCs improves cardiac function in a rat ischemic cardiomyopathy model. (a) Representative images of M-mode echocardiography in the control group, iPS-MSC group, and siAlix-MSC group. (b) Ejection fraction (EF), left <t>ventricular</t> end-diastolic diameter (LVDd), and left ventricular end-diastolic diameter (LVD) before and 1 week after sequential administration of cells in each group (control group, n = 10; iPS-MSC group, n = 12; siAlix-MSC group; n = 9). Data are presented as mean ± SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001 between groups, by one-way analysis of variance with post hoc Turkey's multiple comparisons.
Dnastart Biological Software Version 7.10, supplied by Biotechnology Information, 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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Image Search Results


Systemic administration of iPS-MSCs improves cardiac function in a rat ischemic cardiomyopathy model. (a) Representative images of M-mode echocardiography in the control group, iPS-MSC group, and siAlix-MSC group. (b) Ejection fraction (EF), left ventricular end-diastolic diameter (LVDd), and left ventricular end-diastolic diameter (LVD) before and 1 week after sequential administration of cells in each group (control group, n = 10; iPS-MSC group, n = 12; siAlix-MSC group; n = 9). Data are presented as mean ± SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001 between groups, by one-way analysis of variance with post hoc Turkey's multiple comparisons.

Journal: Regenerative Therapy

Article Title: Systemic administration of induced pluripotent stem cell-derived mesenchymal stem cells improves cardiac function through extracellular vesicle-mediated tissue repair in a rat model of ischemic cardiomyopathy

doi: 10.1016/j.reth.2024.12.008

Figure Lengend Snippet: Systemic administration of iPS-MSCs improves cardiac function in a rat ischemic cardiomyopathy model. (a) Representative images of M-mode echocardiography in the control group, iPS-MSC group, and siAlix-MSC group. (b) Ejection fraction (EF), left ventricular end-diastolic diameter (LVDd), and left ventricular end-diastolic diameter (LVD) before and 1 week after sequential administration of cells in each group (control group, n = 10; iPS-MSC group, n = 12; siAlix-MSC group; n = 9). Data are presented as mean ± SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001 between groups, by one-way analysis of variance with post hoc Turkey's multiple comparisons.

Article Snippet: The fibrotic area was calculated as the ratio of the total fibrotic area to the total left ventricular area using the MetaMorph software (version 7.10.3).

Techniques: Control