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Titlebook: Cell Neurobiology Techniques; Alan A. Boulton,Glen B. Baker,Alan N. Bateson Book 1999 Springer Science+Business Media New York 1999

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書(shū)目名稱(chēng)Cell Neurobiology Techniques
編輯Alan A. Boulton,Glen B. Baker,Alan N. Bateson
視頻videohttp://file.papertrans.cn/223/222857/222857.mp4
叢書(shū)名稱(chēng)Neuromethods
圖書(shū)封面Titlebook: Cell Neurobiology Techniques;  Alan A. Boulton,Glen B. Baker,Alan N. Bateson Book 1999 Springer Science+Business Media New York 1999
描述The cutting-edge techniques detailed here include those that are particularly popular in multidisciplinary neuroscience research. There are readily reproducible methods for establishing neural cell cultures, measuring enzymes and their inhibitors, and using quantitative autoradiography to study monoamine uptake sites and receptors in the brain. Additional methods cover the use of flow cytometry to study developmental neurobiology, applications of magnetic resonance spectroscopy (MRS) to human brain metabolism, and the study of drug metabolism. Together with its companion volumes, In Vivo Neuromethods and In Vitro Neurochemical Techniques, all three cutting-edge works will prove exceptionally useful to those basic and clinical neuroscientists who want to expand the range of their current research or develop competence in complementary methods.. .....
出版日期Book 1999
版次1
doihttps://doi.org/10.1385/0896035107
isbn_softcover978-1-4899-4333-0
isbn_ebook978-1-59259-638-6Series ISSN 0893-2336 Series E-ISSN 1940-6045
issn_series 0893-2336
copyrightSpringer Science+Business Media New York 1999
The information of publication is updating

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Structural Imsets: Fundamentals, textbook, with no apparent necessity to understand the fundamentals of how enzymes and their inhibitors work in order to obtain results. More often than not, the researcher alters the original protocol slightly to suit the materials and apparatus available or to address a different question from th
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Description of Probabilistic Models, of the techniques that were supplanted by Fos immunohistochemistry will be followed by a discussion of . and why its expression as a marker of functional activity has gained such popularity in the neurosciences. Techniques for Fos immunohistochemistry, their compatibility with other techniques, and
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https://doi.org/10.1007/b138573 diseases using postmortem brain tissue. Such a success story has yet to be repeated. Nevertheless, neurochemical and other molecular approaches to studying the diseased brain have generated a large amount of information that has increased enormously our understanding of the molecular neuropathology
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https://doi.org/10.1007/b138573idative state of the brain, or (3) to detect regions of membrane abnormality. This list is growing as new MRS technology emerges. The adoption of MRS as a routine diagnostic and patient management tool in clinical medicine has, however, been quite slow when compared to the rapid acceptance of magnet
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Neural Cell Adhesion Molecules,r (Bastiani et al, 1986; Bastiani and Goodman, 1986; du-Lac et al, 1986), zebrafish embryo (Kuwada, 1986,1992), and chick retinal ganglion cells (Silver and Sapiro, 1981) indicate that these connectivities are carried out in a highly stereospecific fashion. There are many theories regarding these se
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c-fos Expression as a Marker of Functional Activity in the Brain, of the techniques that were supplanted by Fos immunohistochemistry will be followed by a discussion of . and why its expression as a marker of functional activity has gained such popularity in the neurosciences. Techniques for Fos immunohistochemistry, their compatibility with other techniques, and
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