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Voltage-gated CA2+ channels = pharma...
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Striessnig, Jorg.
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Voltage-gated CA2+ channels = pharmacology, modulation and their role in human disease /
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Voltage-gated CA2+ channels/ edited by Jorg Striessnig.
其他題名:
pharmacology, modulation and their role in human disease /
其他作者:
Striessnig, Jorg.
出版者:
Cham :Springer International Publishing : : 2023.,
面頁冊數:
xii, 316 p. :ill., digital ;24 cm.
內容註:
Preface -- Part 1 Modulation -- Cav1.1Calcium Channel Signaling Complexes in Excitation-Contraction Coupling: Insights from Channelopathies -- Mechanisms of Vascular CaV1.2 Channel Regulation During Diabetic Hyperglycemia -- Sympathetic Nervous System Regulation of Cardiac Calcium Channels -- Modulation of CaV1.2 Channel Function by Interacting Proteins and Post-Translational Modifications: Implications in Cardiovascular Diseases and COVID-19 -- Part 2 Pharmacological Approaches -- Pathophysiological Roles of Auxiliary Calcium Channel α2δ Subunits -- Design and Applications of Genetically-Encoded Voltage-Dependent Calcium Channel Inhibitors -- Part 3 Disease insight from channelopathies: consequences for pharmacology and therapeutic strategies -- CACNA1C-Related Channelopathies -- CACNA1D-Related Channelopathies: From Hypertension to Autism -- CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options -- CaV3.2 (CACNA1H) in Primary Aldosteronism,- CaV3.3 Channelopathies -- Pathophysiological Roles of Auxiliary Calcium Channel α2δ Subunits.
Contained By:
Springer Nature eBook
標題:
Calcium channels. -
電子資源:
https://doi.org/10.1007/978-3-031-38437-0
ISBN:
9783031384370
Voltage-gated CA2+ channels = pharmacology, modulation and their role in human disease /
Voltage-gated CA2+ channels
pharmacology, modulation and their role in human disease /[electronic resource] :edited by Jorg Striessnig. - Cham :Springer International Publishing :2023. - xii, 316 p. :ill., digital ;24 cm. - Handbook of experimental pharmacology,v. 2791865-0325 ;. - Handbook of experimental pharmacology ;v. 279..
Preface -- Part 1 Modulation -- Cav1.1Calcium Channel Signaling Complexes in Excitation-Contraction Coupling: Insights from Channelopathies -- Mechanisms of Vascular CaV1.2 Channel Regulation During Diabetic Hyperglycemia -- Sympathetic Nervous System Regulation of Cardiac Calcium Channels -- Modulation of CaV1.2 Channel Function by Interacting Proteins and Post-Translational Modifications: Implications in Cardiovascular Diseases and COVID-19 -- Part 2 Pharmacological Approaches -- Pathophysiological Roles of Auxiliary Calcium Channel α2δ Subunits -- Design and Applications of Genetically-Encoded Voltage-Dependent Calcium Channel Inhibitors -- Part 3 Disease insight from channelopathies: consequences for pharmacology and therapeutic strategies -- CACNA1C-Related Channelopathies -- CACNA1D-Related Channelopathies: From Hypertension to Autism -- CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options -- CaV3.2 (CACNA1H) in Primary Aldosteronism,- CaV3.3 Channelopathies -- Pathophysiological Roles of Auxiliary Calcium Channel α2δ Subunits.
The aim of this volume is to summarize novel findings on the function, pathophysiology, and regulation of voltage-gated Ca2+ channels and on novel concepts of their pharmacological modulation. Impressive insights into the role of channel function and regulation have come from Ca2+ channelopathies affecting the pore-forming as well as accessory subunits and channel-interacting proteins. Moreover, the long-sought molecular basis for key regulatory pathways have been discovered as well as exciting concepts of their subtype-selective pharmacological modulation.
ISBN: 9783031384370
Standard No.: 10.1007/978-3-031-38437-0doiSubjects--Topical Terms:
845987
Calcium channels.
LC Class. No.: QP535.C2
Dewey Class. No.: 572.696
Voltage-gated CA2+ channels = pharmacology, modulation and their role in human disease /
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The aim of this volume is to summarize novel findings on the function, pathophysiology, and regulation of voltage-gated Ca2+ channels and on novel concepts of their pharmacological modulation. Impressive insights into the role of channel function and regulation have come from Ca2+ channelopathies affecting the pore-forming as well as accessory subunits and channel-interacting proteins. Moreover, the long-sought molecular basis for key regulatory pathways have been discovered as well as exciting concepts of their subtype-selective pharmacological modulation.
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