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  • Book
    Asher Bashiri, Avi Harlev, Ashok Agarwal, editors.
    Contents:
    Part I: Introduction to Recurrent Pregnancy Loss
    Recurrent pregnancy loss: definitions, epidemiology, and prognosis
    Implantation, Physiology of Placentation
    Part II: Causes of Recurrent Pregnancy Loss
    Endocrine abnormalities in RPL
    Genetics of recurrent pregnancy loss
    Inherited and Acquired Thrombophilias and Adverse Pregnancy Outcomes
    Immunological causes of recurrent pregnancy loss
    Anatomical aspects in recurrent pregnancy loss
    Male Factors in Recurrent Pregnancy Loss
    Lifestyle and RPL
    The common characteristics between Infertility and recurrent pregnancy loss
    Part III: Management of Recurrent Pregnancy Loss. Contemporary Prevention and treatment of recurrent pregnancy loss
    Part IV: Psychological and Supporting Aspects of Recurrent Pregnancy Loss
    The healthcare giver's perspective
    The importance of emotional support for women with recurrent RPL
    A Patient's Perspective
    Part V: The Future
    New Frontiers in RPL research and treatment.
    Digital Access Springer 2016
  • Article
    Sato T, Ishikawa K, Ogata K.
    Biochim Biophys Acta. 1977 Feb 16;474(4):549-61.
    Incubation medium II causes release of ribosomal subunits from isolated prelabeled nuclei of regenerating rat liver in vitro (Sato, T., Ishikawa, K. and Ogato, K. (1976) Biochim. Biophys. Acta 000, 000-000). The effects of individual components of this medium on release of subunits were studied and the following results were obtained. 1. Dialyzed cytosol was effective in causing release of total labeled RNA, but its effect on release of labeled ribosomal subunits was rather lower than that of low molecular yeast RNA. Spermidine inhibited the release of total labeled RNA as well as that of labeled ribosomal subunits. 2. Low molecular yeast RNA was the most effective component for inducing release of labeled ribosomal subunits. Homologous ribosomal RNA was as effective as yeast RNA. Cytoplasmic ribosomes, prepared by washing with solution of high salt concentration, and their subunits were also effective. 3. Transfer RNA was not so effective as yeast RNA and ribosomal RNA and even after heat treatment it had little effect. 4. Among the homopolyribonucleotides tested, polyuridylic acid had a strong effect but polyadenylic acid, polycytidylic acid and polyinosinic acid had no effect. 5. The effects of yeast RNA and polyuridylic acid in causing release of labeled ribosomal subunits were dependent upon their concentrations in the reaction mixture. The characteristics of the factors which cause release of labeled ribosomal subunits in vitro are discussed on the basis of the results.
    Digital Access Access Options