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bm-cyclin test  (Boehringer Mannheim)

 
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    Boehringer Mannheim bm-cyclin test
    Bm Cyclin Test, supplied by Boehringer Mannheim, 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/result/bm-cyclin test/product/Boehringer Mannheim
    Average 90 stars, based on 1 article reviews
    bm-cyclin test - by Bioz Stars, 2026-02
    90/100 stars

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    <t>After</t> <t>SCI,</t> Aged Mice Exhibit More Severe Defects than Young Mice (A) Time courses of changes in the <t>BMS</t> scores of the young and aged mice after SCI (n = 5 mice/group). ∗∗ p < 0.01. (B) Rotarod treadmill test performed 6 weeks after SCI (n = 5 mice/group). ∗∗ p < 0.01. (C) Mortality rates of the young and aged mice after SCI (n = 4 independent experiments, young SCI: 2/24, 1/9, 2/15, 1/12; aged SCI: 8/22, 2/10, 5/14, 4/11). ∗∗ p < 0.01. (D) Representative images of H&E-stained and GFAP-immunostained sagittal sections of the spinal cord 9 days after SCI (upper panels: ∗ indicates the lesion epicenter). The damaged areas are enclosed by dashed lines. Scale bars, 500 μm. Representative images of NF200-immunostained sections of the injured spinal cord and quantification of the NF200-positive cells in the aged and young mice (lower panels; n = 4 mice/group). Scale bar, 100 μm. ∗∗ p < 0.01. (E) Principal component analysis (PCA) of the mRNA microarray data from the spinal cord samples collected from the young and aged mice with and without SCI. (F) Heatmap depicting the mRNA microarray profile of the spinal cord samples collected from the aged mice with SCI relative to that of the young mice with SCI (left panel). Up- and downregulated genes are shown in shades of magenta and green, respectively. Ontology analysis of the genes that were differentially expressed between the young and aged mice with SCI (right panel). Yellow marks indicate p = 0.5. Values are means with SEMs.
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    Accuracy of non‐invasive tests for H pylori infection at different levels of prevalence

    Journal: The Cochrane Database of Systematic Reviews

    Article Title: Non‐invasive diagnostic tests for Helicobacter pylori infection

    doi: 10.1002/14651858.CD012080.pub2

    Figure Lengend Snippet: Accuracy of non‐invasive tests for H pylori infection at different levels of prevalence

    Article Snippet: Comparison of a new rapid blood assay for detection of antibodies to Helicobacter pylori (bm‐test Helicobacter pylori rapid assay, boehringer mannheim) with an enzyme‐linked immunosorbent assay (enzygnost, behringwerke marburg) .

    Techniques: Infection

    Summary ROC plot of non‐invasive tests for H pylori infection. The SROC curves for the four tests are parallel. The curve for each test is drawn within the range of estimates of specificity from the studies included for the test.

    Journal: The Cochrane Database of Systematic Reviews

    Article Title: Non‐invasive diagnostic tests for Helicobacter pylori infection

    doi: 10.1002/14651858.CD012080.pub2

    Figure Lengend Snippet: Summary ROC plot of non‐invasive tests for H pylori infection. The SROC curves for the four tests are parallel. The curve for each test is drawn within the range of estimates of specificity from the studies included for the test.

    Article Snippet: Comparison of a new rapid blood assay for detection of antibodies to Helicobacter pylori (bm‐test Helicobacter pylori rapid assay, boehringer mannheim) with an enzyme‐linked immunosorbent assay (enzygnost, behringwerke marburg) .

    Techniques: Infection

    Indirect comparison of the accuracy of non‐invasive tests for H pylori infection

    Journal: The Cochrane Database of Systematic Reviews

    Article Title: Non‐invasive diagnostic tests for Helicobacter pylori infection

    doi: 10.1002/14651858.CD012080.pub2

    Figure Lengend Snippet: Indirect comparison of the accuracy of non‐invasive tests for H pylori infection

    Article Snippet: Comparison of a new rapid blood assay for detection of antibodies to Helicobacter pylori (bm‐test Helicobacter pylori rapid assay, boehringer mannheim) with an enzyme‐linked immunosorbent assay (enzygnost, behringwerke marburg) .

    Techniques: Comparison, Diagnostic Assay

    Direct comparison of the accuracy of non‐invasive tests for H pylori infection

    Journal: The Cochrane Database of Systematic Reviews

    Article Title: Non‐invasive diagnostic tests for Helicobacter pylori infection

    doi: 10.1002/14651858.CD012080.pub2

    Figure Lengend Snippet: Direct comparison of the accuracy of non‐invasive tests for H pylori infection

    Article Snippet: Comparison of a new rapid blood assay for detection of antibodies to Helicobacter pylori (bm‐test Helicobacter pylori rapid assay, boehringer mannheim) with an enzyme‐linked immunosorbent assay (enzygnost, behringwerke marburg) .

    Techniques: Comparison

    Performance of non‐invasive tests for diagnosis of H pylori infection

    Journal: The Cochrane Database of Systematic Reviews

    Article Title: Non‐invasive diagnostic tests for Helicobacter pylori infection

    doi: 10.1002/14651858.CD012080.pub2

    Figure Lengend Snippet: Performance of non‐invasive tests for diagnosis of H pylori infection

    Article Snippet: Comparison of a new rapid blood assay for detection of antibodies to Helicobacter pylori (bm‐test Helicobacter pylori rapid assay, boehringer mannheim) with an enzyme‐linked immunosorbent assay (enzygnost, behringwerke marburg) .

    Techniques: Biomarker Discovery, Infection, Staining, Selection, Diagnostic Assay, Comparison

    Journal: The Cochrane Database of Systematic Reviews

    Article Title: Non‐invasive diagnostic tests for Helicobacter pylori infection

    doi: 10.1002/14651858.CD012080.pub2

    Figure Lengend Snippet:

    Article Snippet: Comparison of a new rapid blood assay for detection of antibodies to Helicobacter pylori (bm‐test Helicobacter pylori rapid assay, boehringer mannheim) with an enzyme‐linked immunosorbent assay (enzygnost, behringwerke marburg) .

    Techniques: Selection, Sampling, Infection, Immunohistochemical staining, Staining

    After SCI, Aged Mice Exhibit More Severe Defects than Young Mice (A) Time courses of changes in the BMS scores of the young and aged mice after SCI (n = 5 mice/group). ∗∗ p < 0.01. (B) Rotarod treadmill test performed 6 weeks after SCI (n = 5 mice/group). ∗∗ p < 0.01. (C) Mortality rates of the young and aged mice after SCI (n = 4 independent experiments, young SCI: 2/24, 1/9, 2/15, 1/12; aged SCI: 8/22, 2/10, 5/14, 4/11). ∗∗ p < 0.01. (D) Representative images of H&E-stained and GFAP-immunostained sagittal sections of the spinal cord 9 days after SCI (upper panels: ∗ indicates the lesion epicenter). The damaged areas are enclosed by dashed lines. Scale bars, 500 μm. Representative images of NF200-immunostained sections of the injured spinal cord and quantification of the NF200-positive cells in the aged and young mice (lower panels; n = 4 mice/group). Scale bar, 100 μm. ∗∗ p < 0.01. (E) Principal component analysis (PCA) of the mRNA microarray data from the spinal cord samples collected from the young and aged mice with and without SCI. (F) Heatmap depicting the mRNA microarray profile of the spinal cord samples collected from the aged mice with SCI relative to that of the young mice with SCI (left panel). Up- and downregulated genes are shown in shades of magenta and green, respectively. Ontology analysis of the genes that were differentially expressed between the young and aged mice with SCI (right panel). Yellow marks indicate p = 0.5. Values are means with SEMs.

    Journal: Stem Cell Reports

    Article Title: Enhanced Functional Recovery from Spinal Cord Injury in Aged Mice after Stem Cell Transplantation through HGF Induction

    doi: 10.1016/j.stemcr.2017.01.013

    Figure Lengend Snippet: After SCI, Aged Mice Exhibit More Severe Defects than Young Mice (A) Time courses of changes in the BMS scores of the young and aged mice after SCI (n = 5 mice/group). ∗∗ p < 0.01. (B) Rotarod treadmill test performed 6 weeks after SCI (n = 5 mice/group). ∗∗ p < 0.01. (C) Mortality rates of the young and aged mice after SCI (n = 4 independent experiments, young SCI: 2/24, 1/9, 2/15, 1/12; aged SCI: 8/22, 2/10, 5/14, 4/11). ∗∗ p < 0.01. (D) Representative images of H&E-stained and GFAP-immunostained sagittal sections of the spinal cord 9 days after SCI (upper panels: ∗ indicates the lesion epicenter). The damaged areas are enclosed by dashed lines. Scale bars, 500 μm. Representative images of NF200-immunostained sections of the injured spinal cord and quantification of the NF200-positive cells in the aged and young mice (lower panels; n = 4 mice/group). Scale bar, 100 μm. ∗∗ p < 0.01. (E) Principal component analysis (PCA) of the mRNA microarray data from the spinal cord samples collected from the young and aged mice with and without SCI. (F) Heatmap depicting the mRNA microarray profile of the spinal cord samples collected from the aged mice with SCI relative to that of the young mice with SCI (left panel). Up- and downregulated genes are shown in shades of magenta and green, respectively. Ontology analysis of the genes that were differentially expressed between the young and aged mice with SCI (right panel). Yellow marks indicate p = 0.5. Values are means with SEMs.

    Article Snippet: The motor function of the hind limbs after SCI was evaluated using the locomotor rating test of the BMS ( ) and the rotarod treadmill test ( ) (Muromachi Kikai).

    Techniques: Staining, Microarray

    NSC TP Is as Effective in Aged Mice as It Is in Young Mice after SCI (A and B) Representative bioluminescence images and photon-count quantifications for young and aged mice after TP on days 0 (A), 7, 21, and 35 (B) (n = 10 mice/group). ∗∗ p < 0.01. (C) Representative GFP-immunostained images of sagittally sectioned spinal cords collected 5 weeks after TP. Scale bars, 500 μm (left), 50 μm (right). (D) Axial sections of the spinal cord after TP were stained for GFP, and the GFP-positive area was quantified (n = 5 mice/group). ∗ p < 0.05, ∗∗ p < 0.01. (E) Representative images stained for GFP and bromodeoxyuridine (BrdU). The experimental plan is illustrated in (F), upper panel. Arrowheads indicate GFP + BrdU + cells. Scale bar, 50 μm. (F) Quantification of BrdU + GFP + NSCs from the experiments shown in (E) (n = 4 mice/group). ∗ p < 0.05. (G) Time courses of the BMS scores of vehicle control mice (vehicle) and mice with NSC TP (n = 10 mice/group). ∗ p < 0.05, ∗∗ p < 0.01, †† p < 0.01. (H) Rotarod treadmill test performed 6 weeks after SCI (n = 10 mice/group). ∗∗ p < 0.01, †† p < 0.01. Values are means with SEM.

    Journal: Stem Cell Reports

    Article Title: Enhanced Functional Recovery from Spinal Cord Injury in Aged Mice after Stem Cell Transplantation through HGF Induction

    doi: 10.1016/j.stemcr.2017.01.013

    Figure Lengend Snippet: NSC TP Is as Effective in Aged Mice as It Is in Young Mice after SCI (A and B) Representative bioluminescence images and photon-count quantifications for young and aged mice after TP on days 0 (A), 7, 21, and 35 (B) (n = 10 mice/group). ∗∗ p < 0.01. (C) Representative GFP-immunostained images of sagittally sectioned spinal cords collected 5 weeks after TP. Scale bars, 500 μm (left), 50 μm (right). (D) Axial sections of the spinal cord after TP were stained for GFP, and the GFP-positive area was quantified (n = 5 mice/group). ∗ p < 0.05, ∗∗ p < 0.01. (E) Representative images stained for GFP and bromodeoxyuridine (BrdU). The experimental plan is illustrated in (F), upper panel. Arrowheads indicate GFP + BrdU + cells. Scale bar, 50 μm. (F) Quantification of BrdU + GFP + NSCs from the experiments shown in (E) (n = 4 mice/group). ∗ p < 0.05. (G) Time courses of the BMS scores of vehicle control mice (vehicle) and mice with NSC TP (n = 10 mice/group). ∗ p < 0.05, ∗∗ p < 0.01, †† p < 0.01. (H) Rotarod treadmill test performed 6 weeks after SCI (n = 10 mice/group). ∗∗ p < 0.01, †† p < 0.01. Values are means with SEM.

    Article Snippet: The motor function of the hind limbs after SCI was evaluated using the locomotor rating test of the BMS ( ) and the rotarod treadmill test ( ) (Muromachi Kikai).

    Techniques: Staining, Control