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  • Book
    Vineet Bhandari, editor.
    Contents:
    Hyperoxia in the pathogenesis of Bronchopulmonary Dysplasia
    Invasive mechanical ventilation in the pathogenesis of Bronchopulmonary Dysplasia
    Pre- and post-natal inflammation in the pathogenesis of Bronchopulmonary Dysplasia
    Mycoplasma in Bronchopulmonary Dysplasia
    Chronic obstructive pulmonary disease following Bronchopulmonary Dysplasia
    Genetics of Bronchopulmonary Dysplasia
    Biomarkers of Bronchopulmonary Dysplasia
    Pathology of Bronchopulmonary Dysplasia
    Bronchopulmonary Dysplasia: Definitions and Epidemiology
    Oxygen modulation and Bronchopulmonary Dysplasia: Delivery Room and Beyond
    Non-invasive ventilation for the prevention of Bronchopulmonary Dysplasia
    Nutrition in Bronchopulmonary Dysplasia: In the NICU and Beyond
    Radiology of Bronchopulmonary Dysplasia: from preterm birth to adulthood
    Pulmonary Hypertension in Bronchopulmonary Dysplasia
    Pulmonary Function in Survivors of Bronchopulmonary Dysplasia
    Stem cells for the prevention of Bronchopulmonary Dysplasia
    Less invasive surfactant administration (LISA) for the prevention of Bronchopulmonary Dysplasia
    Anti-Inflammatory Agents for the Prevention of Bronchopulmonary Dysplasia.
    Digital Access Springer 2016
  • Article
    Millard PR, Rabin BS, Whiteside TL, Hubbard JD.
    Am J Clin Pathol. 1977 Mar;67(3):230-5.
    Suspensions of lymphoid cells from tissues have been used for the determination of the quantitative relationship between the T and B cell populations. The distribution of the lymphocytes within a given tissue, however, cannot be demonstrated once such a suspension has been prepared. Various methods of characterizing lymphocytes within tissues were evaluated. The method of tissue preparation can alter the capability of detecting the lymphocyte markers. Fluorescein-labeled anti-immunoglobulin sera reacted equally well with lymphocytes in tissue regardless of the method of tissue preparation. Complement-coated sheep erythrocytes were less effective in detecting lymphocyte markers in tissue sections than in cell suspensions. Quantitative assays of lymphocytes could be done in suspensions only. Unaltered sheep erythrocytes did not bind to T lymphocytes in tissue. T lymphocytes could be identified in tissue sections, however, by the use of anti-human T cell serum.
    Digital Access Access Options