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one-way anova with a tukey's post-hoc test  (GraphPad Software Inc)


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    GraphPad Software Inc one-way anova with a tukey's post-hoc test
    One Way Anova With A Tukey's Post Hoc Test, 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/anova+of+tukey%E2%80%99s+test+or+t-test+provided+by+graphpad+prism+program+iv+version/one+way+anova+with+tukey%E2%80%99s+post+hoc+test/pmc12143723-111-12-4
    Average 90 stars, based on 1 article reviews
    one-way anova with a tukey's post-hoc test - by Bioz Stars, 2026-10
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    Article Title: Microbial and histopathological study of the vibriosis caused by Vibrio vulnificus serovar E in eels: the metalloprotease Vvp is not an essential lesional factor.
    Article Snippet: Vibrio vulnificus biotype 2 serovar E (Bt2-serE) is a zoonotic pathogen that causes a haemorrhagic septicaemia in eels, called warm water vibriosis.. The main objective of the present work was to study the onset of the eel vibriosis from the microbiological and histopathological viewpoint, as well as to ascertain the role of the protease Vvp as a lesional factor by comparing the histopathological lesions caused by the wild strain and its vvp deficient derivative.. The wild-type strain was observed to attach to the gills, where it multiplied following saturation dynamics, subsequently invading the blood stream and reaching the internal organs.



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    Bone loss and cortical porosity in Sp7 R342C knock-in mice. a R342C mutation does not affect femur length of 8-week-old mice. b H&E-stained paraffin-embedded sections from the tibia show no growth plate morphological differences between Sp7 R342C/R342C mice and wild-type littermates. Scale bars are shown in the images. c μCT images from the femoral metaphysis and diaphysis of 8-week-old mice show bone loss and increased cortical porosity in Sp7 R342C/R342C mice compared to wild-type littermates. Scale bars are shown in the images. d Quantification of metaphysis parameters. e Quantification of midshaft diaphysis. BMD: bone mineral density, BV/TV: bone volume fraction, Ct. TMD: cortical bone tissue mineral density, Ct. porosity: cortical porosity. Two-way <t>ANOVA</t> analysis followed by post <t>hoc</t> <t>Tukey–Kramer</t> test was performed (* P < 0.05; ** P < 0.01, *** P < 0.001, **** P < 0.000 1)
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    Bone loss and cortical porosity in Sp7 R342C knock-in mice. a R342C mutation does not affect femur length of 8-week-old mice. b H&E-stained paraffin-embedded sections from the tibia show no growth plate morphological differences between Sp7 R342C/R342C mice and wild-type littermates. Scale bars are shown in the images. c μCT images from the femoral metaphysis and diaphysis of 8-week-old mice show bone loss and increased cortical porosity in Sp7 R342C/R342C mice compared to wild-type littermates. Scale bars are shown in the images. d Quantification of metaphysis parameters. e Quantification of midshaft diaphysis. BMD: bone mineral density, BV/TV: bone volume fraction, Ct. TMD: cortical bone tissue mineral density, Ct. porosity: cortical porosity. Two-way <t>ANOVA</t> analysis followed by post <t>hoc</t> <t>Tukey–Kramer</t> test was performed (* P < 0.05; ** P < 0.01, *** P < 0.001, **** P < 0.000 1)
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    Bone loss and cortical porosity in Sp7 R342C knock-in mice. a R342C mutation does not affect femur length of 8-week-old mice. b H&E-stained paraffin-embedded sections from the tibia show no growth plate morphological differences between Sp7 R342C/R342C mice and wild-type littermates. Scale bars are shown in the images. c μCT images from the femoral metaphysis and diaphysis of 8-week-old mice show bone loss and increased cortical porosity in Sp7 R342C/R342C mice compared to wild-type littermates. Scale bars are shown in the images. d Quantification of metaphysis parameters. e Quantification of midshaft diaphysis. BMD: bone mineral density, BV/TV: bone volume fraction, Ct. TMD: cortical bone tissue mineral density, Ct. porosity: cortical porosity. Two-way <t>ANOVA</t> analysis followed by post <t>hoc</t> <t>Tukey–Kramer</t> test was performed (* P < 0.05; ** P < 0.01, *** P < 0.001, **** P < 0.000 1)
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    Bone loss and cortical porosity in Sp7 R342C knock-in mice. a R342C mutation does not affect femur length of 8-week-old mice. b H&E-stained paraffin-embedded sections from the tibia show no growth plate morphological differences between Sp7 R342C/R342C mice and wild-type littermates. Scale bars are shown in the images. c μCT images from the femoral metaphysis and diaphysis of 8-week-old mice show bone loss and increased cortical porosity in Sp7 R342C/R342C mice compared to wild-type littermates. Scale bars are shown in the images. d Quantification of metaphysis parameters. e Quantification of midshaft diaphysis. BMD: bone mineral density, BV/TV: bone volume fraction, Ct. TMD: cortical bone tissue mineral density, Ct. porosity: cortical porosity. Two-way <t>ANOVA</t> analysis followed by post <t>hoc</t> <t>Tukey–Kramer</t> test was performed (* P < 0.05; ** P < 0.01, *** P < 0.001, **** P < 0.000 1)
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    Image Search Results


    Bone loss and cortical porosity in Sp7 R342C knock-in mice. a R342C mutation does not affect femur length of 8-week-old mice. b H&E-stained paraffin-embedded sections from the tibia show no growth plate morphological differences between Sp7 R342C/R342C mice and wild-type littermates. Scale bars are shown in the images. c μCT images from the femoral metaphysis and diaphysis of 8-week-old mice show bone loss and increased cortical porosity in Sp7 R342C/R342C mice compared to wild-type littermates. Scale bars are shown in the images. d Quantification of metaphysis parameters. e Quantification of midshaft diaphysis. BMD: bone mineral density, BV/TV: bone volume fraction, Ct. TMD: cortical bone tissue mineral density, Ct. porosity: cortical porosity. Two-way ANOVA analysis followed by post hoc Tukey–Kramer test was performed (* P < 0.05; ** P < 0.01, *** P < 0.001, **** P < 0.000 1)

    Journal: Bone Research

    Article Title: Osteoclast-independent osteocyte dendrite defects in mice bearing the osteogenesis imperfecta-causing Sp7 R342C mutation

    doi: 10.1038/s41413-025-00440-1

    Figure Lengend Snippet: Bone loss and cortical porosity in Sp7 R342C knock-in mice. a R342C mutation does not affect femur length of 8-week-old mice. b H&E-stained paraffin-embedded sections from the tibia show no growth plate morphological differences between Sp7 R342C/R342C mice and wild-type littermates. Scale bars are shown in the images. c μCT images from the femoral metaphysis and diaphysis of 8-week-old mice show bone loss and increased cortical porosity in Sp7 R342C/R342C mice compared to wild-type littermates. Scale bars are shown in the images. d Quantification of metaphysis parameters. e Quantification of midshaft diaphysis. BMD: bone mineral density, BV/TV: bone volume fraction, Ct. TMD: cortical bone tissue mineral density, Ct. porosity: cortical porosity. Two-way ANOVA analysis followed by post hoc Tukey–Kramer test was performed (* P < 0.05; ** P < 0.01, *** P < 0.001, **** P < 0.000 1)

    Article Snippet: When more than two experimental groups were present, ANOVA analysis followed by post hoc Tukey–Kramer test was performed (GraphPad Prism 9).

    Techniques: Knock-In, Mutagenesis, Staining

    Osteocyte dendrite defects caused by R342C mutation are independent of osteoclast activity. a Schematic illustration of OPG-Fc injection. b Serum CTX-1 level is significantly reduced in OPG-Fc injected wild-type and R342C mutant mice. c TRAP staining of decalcified, paraffin-embedded tibia sections reveals decreased osteoclasts in both wild-type and Sp7 R342C mice following OPG-Fc treatment. Bottom left: low magnification image showing the staining of the whole section. The region with red dashed lines is zoomed in. Right: Quantification of TRAP + multinucleated osteoclasts per bone area (N.Oc/BA) in the cortical bone with Image J. d Silver nitrate staining shows no difference in the canaliculi number per cell between OPG-Fc and vehicle-treated Sp7 R342C mice. Bottom right: low magnification image showing the staining of the whole section. The region with red dashed lines is zoomed in. e Phalloidin staining shows no difference in the dendrite filament density between OPG-Fc and vehicle-treated Sp7 R342C mice. Two-way ANOVA analysis followed by post hoc Tukey–Kramer test was performed (* P < 0.05; ** P < 0.01, *** P < 0.001, **** P < 0.000 1). Scale bars are shown in the images

    Journal: Bone Research

    Article Title: Osteoclast-independent osteocyte dendrite defects in mice bearing the osteogenesis imperfecta-causing Sp7 R342C mutation

    doi: 10.1038/s41413-025-00440-1

    Figure Lengend Snippet: Osteocyte dendrite defects caused by R342C mutation are independent of osteoclast activity. a Schematic illustration of OPG-Fc injection. b Serum CTX-1 level is significantly reduced in OPG-Fc injected wild-type and R342C mutant mice. c TRAP staining of decalcified, paraffin-embedded tibia sections reveals decreased osteoclasts in both wild-type and Sp7 R342C mice following OPG-Fc treatment. Bottom left: low magnification image showing the staining of the whole section. The region with red dashed lines is zoomed in. Right: Quantification of TRAP + multinucleated osteoclasts per bone area (N.Oc/BA) in the cortical bone with Image J. d Silver nitrate staining shows no difference in the canaliculi number per cell between OPG-Fc and vehicle-treated Sp7 R342C mice. Bottom right: low magnification image showing the staining of the whole section. The region with red dashed lines is zoomed in. e Phalloidin staining shows no difference in the dendrite filament density between OPG-Fc and vehicle-treated Sp7 R342C mice. Two-way ANOVA analysis followed by post hoc Tukey–Kramer test was performed (* P < 0.05; ** P < 0.01, *** P < 0.001, **** P < 0.000 1). Scale bars are shown in the images

    Article Snippet: When more than two experimental groups were present, ANOVA analysis followed by post hoc Tukey–Kramer test was performed (GraphPad Prism 9).

    Techniques: Mutagenesis, Activity Assay, Injection, Staining