Diseases associated with altered ryanodine receptor activity

Sub-cellular Biochemistry
W J DurhamSusan L Hamilton

Abstract

Mutations in two intracellular Ca2+ release channels or ryanodine receptors (RyR1 and RyR2) are associated with a number of human skeletal and cardiac diseases. This chapter discusses these diseases in terms of known mechanisms, controversies, and unanswered questions. We also compare the cardiac and skeletal muscle diseases to explore common mechanisms.

Citations

Oct 18, 2008·The Journal of Biological Chemistry·Susan L Hamilton, Irina I Serysheva
Jun 16, 2010·The Journal of General Physiology·Alexandra ZahradníkováIvan Zahradník
Jul 18, 2017·Frontiers in Physiology·Andrea FaltinovaAlexandra Zahradnikova
Nov 6, 2014·Acta Crystallographica. Section D, Biological Crystallography·Lubomír BorkoJozef Sevčík
Oct 17, 2008·Developmental Dynamics : an Official Publication of the American Association of Anatomists·Thulasimala ReddyMoira K O'Bryan
May 24, 2012·Developmental Medicine and Child Neurology·Ros Quinlivan, Heinz Jungbluth
Nov 4, 2009·The Journal of Clinical Investigation·Ahlke HeydemannElizabeth M McNally
May 27, 2015·The Journal of General Physiology·Eduardo RíosSheila Riazi
May 27, 2015·The Journal of General Physiology·Pavol PetrovičAlexandra Zahradníková
Aug 11, 2017·Molecular BioSystems·Phonindra Nath DasSamrat Chatterjee
Jan 6, 2021·Pflügers Archiv : European journal of physiology·Satadru K LahiriXander H T Wehrens
Mar 2, 2010·Cell Calcium·Eva SammelsGeert Bultynck
Dec 2, 2010·Biochimica Et Biophysica Acta·David H Maclennan, Elena Zvaritch

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