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data analysis software graphpad instat  (GraphPad Software Inc)


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    GraphPad Software Inc data analysis software graphpad instat
    Data Analysis Software Graphpad Instat, supplied by GraphPad Software 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/instat+analysis+software/graphpad+prism+software/pm40103327-336-7-7
    Average 90 stars, based on 1 article reviews
    data analysis software graphpad instat - by Bioz Stars, 2026-10
    90/100 stars

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    Software:

    Article Title: Fibrotic scar formation after cerebral ischemic stroke: Targeting the Sonic hedgehog signaling pathway for scar reduction
    Article Snippet: .. GraphPad Prism software (version 9.0.0; GraphPad Software, Boston, MA, USA; www.graphpad.com ) was used for conducting statistical analyses. ..

    other:

    Article Title: TWEAK/Fn14 axis may promote vascular smooth muscle cell senescence via p38 signaling pathway: preliminary evidence.
    Article Snippet: Graphs of statistical analyses and calculations were plotted using GraphPad Prism 8.0 (GraphPad software, inc., la Jolla, ca, Usa).

    Article Title: Mesenchymal stem cell–derived small extracellular vesicles enhance the therapeutic effect of retinal progenitor cells in retinal degenerative disease rats
    Article Snippet: Graphical representations of the data were created using GraphPad Prism 8.0.1 for Windows (GraphPad Software, Boston, MA, USA, www.graphpad.com ).

    Article Title: In vitro digestion, cellular uptake and absorption of walnut protein-based nanoparticles mediated coenzyme Q10 nanosuspensions
    Article Snippet: Oral administration of Coenzyme Q10 (CoQ10) is hindered by its low bioaccessibility, and protein-based nanoparticles, commonly used to improve this, are vulnerable to degradation by pH, salts, and enzymes.. This study examined the in vitro digestion behavior and the subsequent cellular uptake and absorption of walnut protein-based nanoparticle-stabilized CoQ10 nanosuspensions (CQ@WPNP) to investigate their potential utility in addressing these challenges.. Cryo-electron microscopy (Cryo-EM), revealed structural rearrangements of CQ@WPNP during digestion, with both WPNP and CoQ10 nanoparticles remaining stable in the gastric phase, thereby preventing premature release.

    Article Title: Non-linear oral bioavailability and clinical pharmacokinetics of high-dose Andrographis paniculata ethanolic extract: relevant dosage implications for COVID-19 treatment.
    Article Snippet: Plasma concentration-time profiles in single and repeated doses were generated using GraphPad Prism 9.3.0 (GraphPad Software, USA).

    Article Title: Patients with idiopathic pulmonary fibrosis have fatty lungs impacting respiratory physiology.
    Article Snippet: The statistical analysis was completed using GraphPad Prism V10.2.3 (GraphPad Software Inc. La Jolla, CA, USA), with a p-value ≤0.05 considered statistically significant.

    Article Title: Epigenetic regulation of thrombo-inflammation in Behçet and antiphospholipid syndrome
    Article Snippet: Statistical analyses were performed using the Graph Pad Prism V.6.0 (GraphPad Software, San Diego, California, USA) and the software STATA version 14. p-values and adjusted p-values <0.05 (in overall analysis) were considered for statistical significance.

    Article Title: Long noncoding RNA GAS5 acts as a competitive endogenous RNA to regulate GSK-3β and PTEN expression by sponging miR-23b-3p in Alzheimer’s disease
    Article Snippet: One-way analysis of variance followed by Tukey’s post hoc test was performed to analyze statistical differences between multiple groups using GraphPad Prism software, version 8.0 (GraphPad Software, San Diego, CA, USA, www.graphpad.com ).



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    GraphPad Software Inc one-way analysis of variance (anova) using tukey-kramer multiple comparisons test graphpad instat software
    Translational stop codons within transcribed M. leprae pseudogenes . These graphs show M. leprae transcribed pseudogenes containing translational stop codons (UAA, UGA, or UAG). The number of in-frame (5'3' frame 1) stop codons/pseudogene was identified in silico by translation of the DNA sequence for each pseudogene . using (ExPasy Translate Tool: ): Panel A shows the % of transcribed pseudogenes containing the specified number of stop codons/pseudogene (e.g. 1–5, 6–10, etc), obtained by dividing the number of transcribed pseudogenes within each group by that of the total number of transcribed pseudogenes with stop codons; Panel B shows the % transcribed pseudogenes in each group containing translational start codons, obtained by dividing the number of transcribed pseudogenes within each group containing translational start codons by that of the total # pseudogenes with stop codons and translational started codons; Panel C, shows the # of stop codons/group as a function of gene length in base pairs (bp). The mean and standard deviation of the of the gene length (bp) from each group were compared to that of the other groups <t>using</t> <t>GraphPad</t> <t>InStat</t> software and all groups were significantly different ( p < 0.001) from all other groups except for 21–25 vs 26–40.
    One Way Analysis Of Variance (Anova) Using Tukey Kramer Multiple Comparisons Test Graphpad Instat Software, supplied by GraphPad Software 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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    Translational stop codons within transcribed M. leprae pseudogenes . These graphs show M. leprae transcribed pseudogenes containing translational stop codons (UAA, UGA, or UAG). The number of in-frame (5'3' frame 1) stop codons/pseudogene was identified in silico by translation of the DNA sequence for each pseudogene . using (ExPasy Translate Tool: ): Panel A shows the % of transcribed pseudogenes containing the specified number of stop codons/pseudogene (e.g. 1–5, 6–10, etc), obtained by dividing the number of transcribed pseudogenes within each group by that of the total number of transcribed pseudogenes with stop codons; Panel B shows the % transcribed pseudogenes in each group containing translational start codons, obtained by dividing the number of transcribed pseudogenes within each group containing translational start codons by that of the total # pseudogenes with stop codons and translational started codons; Panel C, shows the # of stop codons/group as a function of gene length in base pairs (bp). The mean and standard deviation of the of the gene length (bp) from each group were compared to that of the other groups <t>using</t> <t>GraphPad</t> <t>InStat</t> software and all groups were significantly different ( p < 0.001) from all other groups except for 21–25 vs 26–40.
    Instat Data Analysis Software, supplied by GraphPad Software 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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    Translational stop codons within transcribed M. leprae pseudogenes . These graphs show M. leprae transcribed pseudogenes containing translational stop codons (UAA, UGA, or UAG). The number of in-frame (5'3' frame 1) stop codons/pseudogene was identified in silico by translation of the DNA sequence for each pseudogene . using (ExPasy Translate Tool: ): Panel A shows the % of transcribed pseudogenes containing the specified number of stop codons/pseudogene (e.g. 1–5, 6–10, etc), obtained by dividing the number of transcribed pseudogenes within each group by that of the total number of transcribed pseudogenes with stop codons; Panel B shows the % transcribed pseudogenes in each group containing translational start codons, obtained by dividing the number of transcribed pseudogenes within each group containing translational start codons by that of the total # pseudogenes with stop codons and translational started codons; Panel C, shows the # of stop codons/group as a function of gene length in base pairs (bp). The mean and standard deviation of the of the gene length (bp) from each group were compared to that of the other groups using GraphPad InStat software and all groups were significantly different ( p < 0.001) from all other groups except for 21–25 vs 26–40.

    Journal: BMC Genomics

    Article Title: Implications of high level pseudogene transcription in Mycobacterium leprae

    doi: 10.1186/1471-2164-10-397

    Figure Lengend Snippet: Translational stop codons within transcribed M. leprae pseudogenes . These graphs show M. leprae transcribed pseudogenes containing translational stop codons (UAA, UGA, or UAG). The number of in-frame (5'3' frame 1) stop codons/pseudogene was identified in silico by translation of the DNA sequence for each pseudogene . using (ExPasy Translate Tool: ): Panel A shows the % of transcribed pseudogenes containing the specified number of stop codons/pseudogene (e.g. 1–5, 6–10, etc), obtained by dividing the number of transcribed pseudogenes within each group by that of the total number of transcribed pseudogenes with stop codons; Panel B shows the % transcribed pseudogenes in each group containing translational start codons, obtained by dividing the number of transcribed pseudogenes within each group containing translational start codons by that of the total # pseudogenes with stop codons and translational started codons; Panel C, shows the # of stop codons/group as a function of gene length in base pairs (bp). The mean and standard deviation of the of the gene length (bp) from each group were compared to that of the other groups using GraphPad InStat software and all groups were significantly different ( p < 0.001) from all other groups except for 21–25 vs 26–40.

    Article Snippet: Statistical analysis of data for this study was obtained from the comparison of means and standard deviations of raw data and performed using One-way Analysis of Variance (ANOVA) using Tukey-Kramer Multiple Comparisons Test GraphPad InStat software.

    Techniques: In Silico, Sequencing, Standard Deviation, Software