12 research outputs found

    Etiology and long-term outcome of extrahepatic portal vein obstruction in children

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    AIM: To study the management and outcome of children with extrahepatic portal vein obstruction (EHPVO) in a whole country population

    Effects of MTX on body weight changes (A), bowel and mucosal weight (B) and mucosal DNA and protein (C).

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    <p>Values are mean ± SEM. CONTR- control, MTX-methotrexate. * P<0.05 MTX-2 and MTX-4 vs CONTR rats, † P<0.05 MTX-4 vs MTX-2 rats.</p

    The effect of MTX on Caco-2 cells proliferation and apoptosis.

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    <p>Two color FACS systems analysis using anti-BrdU and propidium iodide (PI) to determine cell proliferation. FITC Annexin V assay for identifying cells that are undergoing apoptosis. MTX-methotrexate., EA-early apoptosis, LA-late apoptosis, VC-viable cells, DC-dead cells, PI- propidium iodide. Values are mean ± SEM. * P<0.05 MTX-early vs non-treated Caco-2 cells, †P<0.05 MTX-late vs MTX- early.</p

    Changes in intestinal mucosal β-catenin, Akt 1/2/3, GSK3 protein levels following methotrexate induced intestinal damage.

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    <p>Values are mean ± SEM. CONTR- control, MTX-methotrexate. * P<0.05 MTX-2 and MTX-4 vs CONTR rats, † P<0.05 MTX-4 vs MTX-2 rats.</p

    Grade of intestinal mucosal injury and microscopic intestinal appearance after administration of MTX.

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    <p>Values are mean ± SEM. CONTR- control, MTX-methotrexate. * P<0.05 MTX-2 and MTX-4 vs CONTR rats, † P<0.05 MTX-4 vs MTX-2 rats.</p

    Effects of MTX on crypt cell proliferation (A) and apoptosis (B).

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    <p>The number of labeled cells in 10 well-oriented, longitudinal crypts per section from each rat was determined using light microscopy (B). The apoptotic index is expressed as the percentage of apoptotic cells per 10 villi. Values are mean ± SEM. CONTR- control, MTX-methotrexate. * P<0.05 MTX-2 and MTX-4 vs CONTR rats, † P<0.05 MTX-4 vs MTX-2 rats.</p
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