Literature DB >> 2709405

Three-dimensional visualization methods for confocal microscopy.

H T van der Voort1, G J Brakenhoff, M W Baarslag.   

Abstract

Three-dimensional images of microscopic objects can be obtained by confocal scanning laser microscopy (CSLM). The imaging process in a CSLM consists of sampling a specific volume in the object and storing the result in a three-dimensional memory array of a digital computer. Methods are needed to visualize these images. In this paper three methods are discussed, each suitable in a specific area of application. For purposes where realistic rendering of solid or semi-transparent objects is required, an algorithm based on simulation of a fluorescence process is most suitable. When speed is essential, as for interactive purposes, a simple procedure to generate anaglyphs can be used. Both methods have in common that they require no previous interpretation or analysis of the image. When the study of an object imaged by CSLM involves analysis in terms of a geometrical model, sophisticated graphics techniques can be used to display the results of the analysis.

Mesh:

Year:  1989        PMID: 2709405     DOI: 10.1111/j.1365-2818.1989.tb00553.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  11 in total

1.  Chromosome no. 1 of Crepis capillaris shows defined 3D-shapes in mitotic prophase.

Authors:  A B Houtsmuller; J L Oud; M B Montijn; M Worring; A W Smeulders; N Nanninga
Journal:  Chromosome Res       Date:  2000       Impact factor: 5.239

2.  Three-dimensional organization of the ribosomal genes and Ag-NOR proteins during interphase and mitosis in PtK1 cells studied by confocal microscopy.

Authors:  I Robert-Fortel; H R Junéra; G Géraud; D Hernandez-Verdun
Journal:  Chromosoma       Date:  1993-02       Impact factor: 4.316

3.  Visualization of silver-enhanced reaction products from protein-and immuno-colloidal gold probes by laser scanning confocal microscopy in reflection mode.

Authors:  J Uriel; H K Lorenzo; A Macho; A W de Feijter; Z Mishal
Journal:  Histochem Cell Biol       Date:  1995-05       Impact factor: 4.304

Review 4.  Spatial analysis of intranuclear human repetitive DNA regions by in situ hybridization and digital fluorescence microscopy.

Authors:  H van Dekken; R Hulspas
Journal:  Histochem J       Date:  1993-03

5.  A dual fluorescence technique for visualization of Staphylococcus epidermidis biofilm using scanning confocal laser microscopy.

Authors:  B A Sanford; A W de Feijter; M H Wade; V L Thomas
Journal:  J Ind Microbiol       Date:  1996-01

6.  Carbohydrate binding activities of Bradyrhizobium japonicum: unipolar localization of the lectin BJ38 on the bacterial cell surface.

Authors:  J T Loh; S C Ho; A W de Feijter; J L Wang; M Schindler
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-01       Impact factor: 11.205

7.  Primary culture of rat hepatocytes entrapped in cylindrical collagen gels: an in vitro system with application to the bioartificial liver. Rat hepatocytes cultured in cylindrical collagen gels.

Authors:  S L Nyberg; R A Shatford; W D Payne; W S Hu; F B Cerra
Journal:  Cytotechnology       Date:  1992       Impact factor: 2.058

8.  Effects of growth conditions on mitochondrial morphology in Saccharomyces cerevisiae.

Authors:  W Visser; E A van Spronsen; N Nanninga; J T Pronk; J Gijs Kuenen; J P van Dijken
Journal:  Antonie Van Leeuwenhoek       Date:  1995       Impact factor: 2.271

9.  High level expression of transfected beta- and gamma-actin genes differentially impacts on myoblast cytoarchitecture.

Authors:  G Schevzov; C Lloyd; P Gunning
Journal:  J Cell Biol       Date:  1992-05       Impact factor: 10.539

10.  Adult rat cardiomyocytes cultured in creatine-deficient medium display large mitochondria with paracrystalline inclusions, enriched for creatine kinase.

Authors:  M Eppenberger-Eberhardt; I Riesinger; M Messerli; P Schwarb; M Müller; H M Eppenberger; T Wallimann
Journal:  J Cell Biol       Date:  1991-04       Impact factor: 10.539

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