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Computing characterizations of drugs...
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Lines, Glenn T.
Computing characterizations of drugs for ion channels and receptors using Markov models[electronic resource] /
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
杜威分類號:
571.64015118
書名/作者:
Computing characterizations of drugs for ion channels and receptors using Markov models/ by Aslak Tveito, Glenn T. Lines.
作者:
Tveito, Aslak.
其他作者:
Lines, Glenn T.
出版者:
Cham : : Springer International Publishing :, 2016.
面頁冊數:
xvi, 261 p. : : ill. (some col.), digital ;; 24 cm.
Contained By:
Springer eBooks
標題:
Ion channels - Effect of drugs on
標題:
Markov processes.
標題:
Mathematics.
標題:
Computational Science and Engineering.
標題:
Biomedicine general.
標題:
Computer Imaging, Vision, Pattern Recognition and Graphics.
ISBN:
9783319300306
ISBN:
9783319300290
內容註:
Preface -- Background: Contents and Method -- One-dimensional calcium release -- Models of open and state blockers -- Two-dimensional calcium release -- Computing theoretical drugs in the two-dimensional case -- Generalized systems -- Calcium-induced calcium release -- Numerical release for CICR -- A prototypical model of an ion channel -- Inactivated ion channels -- A simple model of the sodium channel -- Mutations affecting the mean open time -- The burst mode -- Whole sale action potentials.
摘要、提要註:
Flow of ions through voltage gated channels can be represented theoretically using stochastic differential equations where the gating mechanism is represented by a Markov model. The flow through a channel can be manipulated using various drugs, and the effect of a given drug can be reflected by changing the Markov model. These lecture notes provide an accessible introduction to the mathematical methods needed to deal with these models. They emphasize the use of numerical methods and provide sufficient details for the reader to implement the models and thereby study the effect of various drugs. Examples in the text include stochastic calcium release from internal storage systems in cells, as well as stochastic models of the transmembrane potential. Well known Markov models are studied and a systematic approach to including the effect of mutations is presented. Lastly, the book shows how to derive the optimal properties of a theoretical model of a drug for a given mutation defined in terms of a Markov model.
電子資源:
http://dx.doi.org/10.1007/978-3-319-30030-6
Computing characterizations of drugs for ion channels and receptors using Markov models[electronic resource] /
Tveito, Aslak.
Computing characterizations of drugs for ion channels and receptors using Markov models
[electronic resource] /by Aslak Tveito, Glenn T. Lines. - Cham :Springer International Publishing :2016. - xvi, 261 p. :ill. (some col.), digital ;24 cm. - Lecture notes in computational science and engineering,1111439-7358 ;. - Lecture notes in computational science and engineering ;82..
Preface -- Background: Contents and Method -- One-dimensional calcium release -- Models of open and state blockers -- Two-dimensional calcium release -- Computing theoretical drugs in the two-dimensional case -- Generalized systems -- Calcium-induced calcium release -- Numerical release for CICR -- A prototypical model of an ion channel -- Inactivated ion channels -- A simple model of the sodium channel -- Mutations affecting the mean open time -- The burst mode -- Whole sale action potentials.
Open access.
Flow of ions through voltage gated channels can be represented theoretically using stochastic differential equations where the gating mechanism is represented by a Markov model. The flow through a channel can be manipulated using various drugs, and the effect of a given drug can be reflected by changing the Markov model. These lecture notes provide an accessible introduction to the mathematical methods needed to deal with these models. They emphasize the use of numerical methods and provide sufficient details for the reader to implement the models and thereby study the effect of various drugs. Examples in the text include stochastic calcium release from internal storage systems in cells, as well as stochastic models of the transmembrane potential. Well known Markov models are studied and a systematic approach to including the effect of mutations is presented. Lastly, the book shows how to derive the optimal properties of a theoretical model of a drug for a given mutation defined in terms of a Markov model.
ISBN: 9783319300306
Standard No.: 10.1007/978-3-319-30030-6doiSubjects--Topical Terms:
641135
Ion channels
--Effect of drugs on
LC Class. No.: QH603.I54
Dewey Class. No.: 571.64015118
Computing characterizations of drugs for ion channels and receptors using Markov models[electronic resource] /
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Preface -- Background: Contents and Method -- One-dimensional calcium release -- Models of open and state blockers -- Two-dimensional calcium release -- Computing theoretical drugs in the two-dimensional case -- Generalized systems -- Calcium-induced calcium release -- Numerical release for CICR -- A prototypical model of an ion channel -- Inactivated ion channels -- A simple model of the sodium channel -- Mutations affecting the mean open time -- The burst mode -- Whole sale action potentials.
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Flow of ions through voltage gated channels can be represented theoretically using stochastic differential equations where the gating mechanism is represented by a Markov model. The flow through a channel can be manipulated using various drugs, and the effect of a given drug can be reflected by changing the Markov model. These lecture notes provide an accessible introduction to the mathematical methods needed to deal with these models. They emphasize the use of numerical methods and provide sufficient details for the reader to implement the models and thereby study the effect of various drugs. Examples in the text include stochastic calcium release from internal storage systems in cells, as well as stochastic models of the transmembrane potential. Well known Markov models are studied and a systematic approach to including the effect of mutations is presented. Lastly, the book shows how to derive the optimal properties of a theoretical model of a drug for a given mutation defined in terms of a Markov model.
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