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Titlebook: Cell Surface Receptors: A Short Course on Theory and Methods; A Short Course on Th Lee E. Limbird Book 1996Latest edition Kluwer Academic P

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發(fā)表于 2025-3-21 16:56:49 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Cell Surface Receptors: A Short Course on Theory and Methods
副標題A Short Course on Th
編輯Lee E. Limbird
視頻videohttp://file.papertrans.cn/223/222882/222882.mp4
圖書封面Titlebook: Cell Surface Receptors: A Short Course on Theory and Methods; A Short Course on Th Lee E. Limbird Book 1996Latest edition Kluwer Academic P
描述.Cell Surface Receptors: A Short Course on Theory andMethods, Second. .Edition. is a primer for the study of cellsurface receptors. The simplified discussion of methods and theirunderlying principles removes the usual intimidation caused by thespecialized vocabulary or sophisticated mathematics that characterizemany of the primary papers in this field. In this way, the basicconcepts become emphasized. This volume is a starting point: atextbook as well as a manual to which the investigator can return fora refresher course, when needed.
出版日期Book 1996Latest edition
關(guān)鍵詞cell; cell surface receptors; membrane; pharmacology; research; tissue
版次2
doihttps://doi.org/10.1007/978-1-4613-1255-0
isbn_softcover978-1-4612-8535-9
isbn_ebook978-1-4613-1255-0
copyrightKluwer Academic Publishers 1996
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Anatomy and Physiology of the Ocular Surfacehat elicits an observed response, and (2) outlines methods for determining the affinity constants of agonist, partial agonist, and antagonist agents. It will become clear to the reader that these latter methods exploit early insights regarding efficacy and receptor reserve.
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Languages for Building Ontologies,ractions in a purified preparation. Similarly, determining whether receptor affinity states are a manifestation of receptor interaction with components of an effector system is best accomplished by reconstituting isolated receptor and effector components into lipid vesicles of defined composition.
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The Most Outstanding Ontologies,eptor population accessible for interaction with ligand at the cell surface is continually changing. Figure 6–1 provides a schematic diagram of some of the possible fates of a cell surface receptor following ligand occupancy.
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