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  • Book
    Ashutosh Kumar Shukla, editor.
    Summary: Nanotechnology is expected to bring revolutionary changes in a variety of fields. This volume describes nanoparticles and their biomedical applications, and covers metal nanoparticles, metal oxide nanoparticles, rare earth based nanoparticles and graphene oxide nanoparticles. It elaborates on a number of biomedical applications, including therapeutic applications. It addresses the topic of green synthesis, in view of increasing health and environmental concerns.

    Contents:
    Chapter 1. Rare Earth Based Nanoparticles: Biomedical Applications, Pharmacological and Toxicological Significance
    Chapter 2. Nanomedicine for Hepatic Fibrosis
    Chapter 3. Biomedical Applications of Zinc oxide nanoparticles synthesized using Eco-friendly method
    Chapter 4. Potential Applications of Greener synthesized Silver and Gold Nanoparticles in Medicine
    Chapter 5. Nanofinished Medical Textiles and Their Potential Impact to Health and Environment
    Chapter 6. Therapeutic Applications of Graphene Oxides in Angiogenesis and Cancers
    Chapter 7. Use of nanoparticles to manage Candida biofilms
    Chapter 8. Biomedical applications of lignin-based nanoparticles
    Chapter 9. Green nanoparticles for biomedical and bioengineering applications
    Chapter 10. Nanoparticles: A boon to target mitochondrial diseases.
    Digital Access Springer 2020
  • Journal
    Print 1930/31-
  • Article
    Uyeki EM, Nishimura T, Bisel TU.
    Eur J Immunol. 1978 Feb;8(2):138-41.
    Differences in suiciding by various tritiated nucleosides were observed between two functional assays for in vitro lymphocytic precursor cell development, the hemolysin plaque-forming cell (PFC) assay and the B lymphocytic colony-forming cell (CFC-L) assay, using BDF1 mouse spleen cells. PFC growth was markedly reduced by an early (days 0-1) pulse of tritiated deoxyadenosine ([3H]dAdo), but relatively unaffected by a pulse of tritiated thymidine ([3H]dThd) during the same interval. In contrast, CFC-L formation significantly dropped after an early (day 0) [3H]dThd pulse, as well as after pulses of [3H]dAdo and the corresponding tritiated ribosides, uridine and adenosine. This implied a cycling state in an early lymphocytic precursor cell, as opposed to the PFC insensitivity to an early [3H]dThd pulse. The response pattern of colonies and clusters to [3H]dThd supported our notion of a delayed suiciding of CFC contributing to the increase in cluster numbers.
    Digital Access Access Options