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  • Book
    edited by Grant J. Jensen.
    Contents:
    Chapter 1. Fundamentals of three-dimensional reconstruction from projections / Pawel A. Penczek
    Chapter 2. Image restoration in cryo-electron microscopy / Pawel A. Penczek
    Chapter 3. Resolution measures in molecular electron microscopy / Pawel A. Penczek
    Chapter 4. 3D reconstruction from 2D crystal image and diffraction data / Andreas D. Schenk ... [et al.]
    Chapter 5. Fourier-Bessel reconstruction of helical assemblies / Ruben Diaz, William J. Rice, David L. Stokes
    Chapter 6. Reconstruction of helical filaments and tubes / Edward H. Egelman
    Chapter 7. Three-dimensional asymmetric reconstruction of tailed bacteriophage / Jinghua Tang, Robert S. Sinkovits, Timothy S. Baker
    Chapter 8. Single particle analysis at high resolution / Yao Cong, Steven J. Ludtke
    Chapter 9. The Orthogonal tilt reconstruction method / Andres Leschziner
    Chapter 10. An Introduction to maximum-likelihood methods in cryo-EM / Fred J. Sigworth ... [et al.]
    Chapter 11. Classification of structural heterogeneity by maximum-likelihood methods / Sjors H.W. Scheres
    Chapter 12. Methods for three-dimensional reconstruction of heterogeneous assemblies / Elena V. Orlova, Helen R. Saibil
    Chapter 13. Alignment of cryo-electron tomography datasets / Fernando Amat ... [et al.]
    Chapter 14. Correcting for the Ewald sphere in high-resolution single-particle reconstructions / Peter A. Leong ... [et al.]
    Chapter 15. Software tools for molecular microscopy: an open-text wikibook / Neil R. Voss ... [et al.].
    Digital Access ScienceDirect 2010
    Access via Methods in enzymology ; 2010; 482
    Location
    Version
    Call Number
    Items
    Methods in enzymology ; 2010; 482
    2010
    QP601 .M49 v.482 2010
  • Article
    Nakamura T, Kuroda T, Noguchi K, Funaki J.
    Bull Tokyo Med Dent Univ. 1979 Dec;26(4):273-8.
    The purpose of this experiment was to examine the growth of condylar, epiphyseal, and spheno-occipital synchrondrosal cartilages cultured on medium BGJ. Materials from 12 neonatal rabbits were cultured for 7 days on this medium with the addition of 0, 10, or 20% fetal calf serum. Epiphyseal cartilages cultured with the addition of 20% fetal calf serum showed slightly better maintenance of in situ state, though little morphological changes were observed during 7 days. Spheno-occipital synchondrosal cartilages cultured with the addition of 10% or 20% fetal calf serum were histologically relatively similar to in situ state than those cultured without fetal calf serum, but no growth in length and width of these cartilages was observed. On the other hand, cultured condylar cartilages showed the least maintenance of histological and histochemical features. It was assumed that medium BGJ was not a recommendable medium for the organ culture of condylar cartilage.
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