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  • Book
    Kim Vaiphei.
    Summary: The book covers all aspects of endoscopic biopsies of the stomach inclusive of gastritis and gastropathies. It highlights the best way of handling of endoscopic biopsies in the endoscopic room by the gastroenterologist. It elucidates various steps involved in processing of the biopsy, tissue embedding and paraffin sectioning, approach to interpretation, various precautions that require to be taken while interpreting the biopsies, and the essential background knowledge of the interpreter. The book highlights the importance of the little things for a proper reading like matching of the tissue fragments received and the number of tissue present on a slide after the paraffin section. Chapters cover various forms of gastritis, and the easiest approach for daily routine by avoiding the cumbersome classifications and staging formulated for gastritis. It also discusses the utilization of the right nomenclature for acute and chronic gastritis and various other subtypes of gastritis. Chapters include various rarer and infrequently come across conditions of both acute and chronic gastritis, special form of gastritis and infective conditions. It also includes unusual forms of non-neoplastic gastric pathologies such as, a condition, where the gastric mucosa is affected not only by direct exposure to various irritants but may also be affected by many systemic diseases. It also highlights the frequently observed changes in chronic renal and liver failures. The book is targeted to all the practicing pathologists as well as graduate and post graduate students who are keen to learn about non-neoplastic gastric pathology at various levels.

    Contents:
    Introduction to endoscopic biopsies
    Handling of biopsies
    Interpretation of endoscopic biopsies
    Special approach to commonly observed organisms in stomach
    Endoscopic biopsy in acute gastritis infective and non-infective
    Endoscopic biopsy in chronic gastritis infective and non-infective
    Endoscopic biopsy in diffuse antral gastritis
    Endoscopic biopsy in lymphocytic gastritis and collagenous gastritis
    Endoscopic biopsy in autoimmune gastritis
    Endoscopic biopsy in focally enhanced gastritis
    Endoscopic biopsy in reactive gastropathy
    Endoscopic biopsy in granulomatous gastritis ; infective and non-infective
    Endoscopic biopsy in gastric polyps
    Endoscopic biopsy in gastritis cystica profunda
    Endoscopic biopsy in hyperplastic gastropathies
    Endoscopic biopsy in peptic ulcer disease
    Endoscopic biopsy of gastric mucosa in kidney disease
    Endoscopic biopsy in gastric microvasculature
    Endoscopic biopsy in portal hypertensive gastropathies
    Endoscopic biopsy in paediatric gastritis, gastropathies and peptic ulcer disease
    Endoscopic biopsy in gastrointestinal duplications
    Endoscopic biopsy - gastritis versus gastropathy.
    Digital Access Springer 2022
  • Journal
    Digital Access Full text via HathiTrust, Vol. 1, no. 1 (May 25, 1878)-v. 149, no. 15 (Oct. 10, 1952) whole no. 1-3878.
  • Article
    Kanbayashi Y, Nakamura T, Hosoda K, Nogimori K, Yajima M, Ui M.
    J Biochem. 1978 Aug;84(2):453-60.
    Based on the finding reported in the preceding paper (Kanbayashi, et al.: J. Biochem) that subunits of islets-activating protein (IAP), a new protein purified from the culture media of Bordetella pertussis, were inactive as such, but regained the original biological activities when recombined, the conditions required for recovery of the biological activities were studied. Essentially the same biological activities as the native IAP were recovered when the smallest subunit, F-3, was incubated with one of the other subunits, F-1 and F-2, at a pH of around 7, at temperatures below 30 degrees C and for longer than 12 h. During the incubation, association products were formed which were isolated by gel filtration as homogenous proteins that consisted of two subunits probably in a molar ratio of 1 : 1. The native IAP (consisting of two IAP subunits including F-3) were equipotent in enhancing insulin secretory responses, in inhibiting epinephrine-induced hyperglycemia, in inducing leukocytosis and in increasing histamine sensitivity in experimental animals.
    Digital Access Access Options