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  • Book
    Antigoni Delantoni, Kaan Orhan, editors.
    Summary: This atlas is a detailed and complete guide on imaging of the dentomaxillofacial region, a region of high interest to a wide range of specialists. A large number of injuries and patient's treatment involve the facial skeleton. Enriched by radiographic images and illustrations, this book explores the anatomy of this region presenting its imaging characteristics through the most commonly available techniques (MDCT, CBCT, MRI and US). In addition, two special chapters on angiography and micro-CT expand the limits of dentomaxillofacial imaging. This comprehensive book will be an invaluable tool for radiologists, dentists, surgeons and ENT specialists in their training and daily practice.

    Contents:
    Chapter 1) Introduction to Dentomaxillofacial Imaging
    Chapter 2) Basic Principles of Intraoral Radiography
    Chapter 3) Intraoral Radiographic Anatomy
    Chapter 4Basic Principles of Panoramic Radiography
    Chapter 5) Panoramic Radiographic Anatomy
    Chapter 6) Cephalometric Radiography
    Chapter 7) Basic Principles of Computer Tomography (MDCT/CBCT). The Use of MDCT and CBCT in Dentomaxillofacial Imaging
    Chapter 8) CBCT Anatomical Imaging
    Chapter 9) MDCT Soft Tissue Anatomy
    Chapter 10) Dentomaxillofacial Ultrasonography: Basic Principles and Radiographic Anatomy
    Chapter 11) Basics of Magnetic Resonance Imaging (MRI)
    Chapter 12) MRI Anatomy
    Chapter 13) Principles of Maxillofacial Angiography
    Chapter 14) Imaging of the Most Common Dental Pathologies
    Chapter 15) Micro CT.
    Digital Access Springer 2022
  • Article
    Mock M, Schwartz M.
    J Bacteriol. 1978 Nov;136(2):700-7.
    As previously reported by others, more than 90% of the colicin E3 synthesized soon after induction of colicinogenic bacteria was found to be cell bound, about half of it being in a salt-extractable state at the cell surface. Evidence is presented that the colicin molecules remain preferentially bound to the cell which produced them, rather than being secreted and randomly distributed in the cell population. Secretion of colicin E3 may in fact never occur, all or most of the colicin found free in the medium perhaps being released during lysis of the producing cells long after induction. Among 19 mutant plasmids selected on the basis of their inability to produce an active colicin, only 3 were found to code for a protein which although it lacked any bactericidal activity, had the same molecular weight as wild-type colicin E3 and displayed a reaction of immunological identity with it. These three inactive colicins fail to be exported to the cell surface and seem to be blocked at some intermediate stage in the export process.
    Digital Access Access Options