Titlebook: Quantitative Neuroanatomy in Transmitter Research; Luigi F. Agnati,Kjell Fuxe Book 1985 Palgrave Macmillan, a division of Macmillan Publis

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Quantitative Analysis of Three-Dimensional Structures in Neuroanatomymitters and nuclei are only first steps towards understanding functions — quantitation of all these components at the cellular or at the ultrastructural level is almost inevitable for understanding fully the complex function of their aggregate.

BRIDE

Studies of Local Blood Flow and Glucose Utilization in Brain by Computer Assisted Autoradiographyextensively supplied with several systems of perivascular nerve fibres (Owman et al., 1984). This has led to the additional concept of “neurogenic” control mechanisms for the brain circulation (Owman and Edvins- son, 1977; Heistad and Marcus, 1982; MacKenzie et al., 1984).

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Topographic Distribution of Catecholaminergic Neurons in the Rat Medulla Oblongata Using Quantitativgroups (Dahlstrom and Fuxe, 1964) and dopamine containing neurons. Historically, the question of monoaminergic neurons located in the brain stem has been addressed using fluorescence histochemistry and immunof luorescence techniques (1,2,3,18,19,30).

GENRE

Image Understanding and the Cell World Model applied to the field of cytology (Preston, 1980) with the development of automated cell scanners (chiefly for blood cell analysis). For biomedical research, however, the real promise of computer vision systems—that is, the automated analysis of cells in stained tissue—has yet to be met.

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Tasks in Computer-Assisted Neuroanatomy: Data Acquisition, Imaging and Databaseble in the late 1960’s and early ‘70’s. The benefits of being able to quantitate what could only be photographed and verbally described were obvious to many workers. It was also a hope that machine storage of two and three dimensional information would lead to new methods of imaging of what could on

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Population Characteristics of Nerve Cell Bodies Illustrated by the Postnatal Development of Cerebell change in emphasis to quantitation in TIN studies, for example Fuxe et al (1983), may be hampered by lack of objective data on various aspects of the technique. The “totality” of staining of target cells under any particular experimental circumstance is yet not fully understood. For meaningful ster