| scholarly article | Q13442814 |
| P50 | author | Lia Crotti | Q56944927 |
| P2093 | author name string | Alfred L George | |
| Walter J Chazin | |||
| Christopher N Johnson | |||
| Zahurul A Bhuiyan | |||
| Florence Fellmann | |||
| Nicole Sekarski | |||
| Gregory Webster | |||
| Daniel C Pipilas | |||
| Jurg Schlaepfer | |||
| Lisa M Wren | |||
| Daniel M Chazin | |||
| Kateryna V Ogorodnik | |||
| P2860 | cites work | Calmodulin mutations associated with long QT syndrome prevent inactivation of cardiac L-type Ca(2+) currents and promote proarrhythmic behavior in ventricular myocytes | Q42551776 |
| Brugada Syndrome | Q56140211 | ||
| A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence | Q86057040 | ||
| Calmodulinopathy: a genetic trilogy | Q86146914 | ||
| An integrated map of genetic variation from 1,092 human genomes | Q22122153 | ||
| Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death | Q24300356 | ||
| Long-QT syndrome: from genetics to management | Q26823298 | ||
| Molecular and genetic basis of sudden cardiac death | Q26825973 | ||
| Novel calmodulin mutations associated with congenital arrhythmia susceptibility | Q33164413 | ||
| Impact of genetics on the clinical management of channelopathies | Q34036797 | ||
| Calcium binding to calmodulin mutants monitored by domain-specific intrinsic phenylalanine and tyrosine fluorescence. | Q34179216 | ||
| CALM3 mutation associated with long QT syndrome | Q34451319 | ||
| CaBP1 regulates voltage-dependent inactivation and activation of Ca(V)1.2 (L-type) calcium channels. | Q34799937 | ||
| Competitive and non-competitive regulation of calcium-dependent inactivation in CaV1.2 L-type Ca2+ channels by calmodulin and Ca2+-binding protein 1 | Q36812386 | ||
| Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants | Q36913464 | ||
| Calmodulin mutations associated with recurrent cardiac arrest in infants | Q37327429 | ||
| Inherited calcium channelopathies in the pathophysiology of arrhythmias | Q38021673 | ||
| Induced pluripotent stem cell-derived cardiomyocytes: a versatile tool for arrhythmia research | Q38097412 | ||
| Induced pluripotent stem cell-derived cardiomyocytes: boutique science or valuable arrhythmia model? | Q38097414 | ||
| Arrhythmogenic calmodulin mutations disrupt intracellular cardiomyocyte Ca2+ regulation by distinct mechanisms | Q42065538 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | long QT syndrome | Q653924 |
| congenital disorder | Q727096 | ||
| P304 | page(s) | 2012-2019 | |
| P577 | publication date | 2016-06-30 | |
| P1433 | published in | Heart Rhythm | Q2058605 |
| P1476 | title | Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes | |
| P478 | volume | 13 |
| Q92949059 | An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome |
| Q89861027 | Calmodulin Mutations Associated with Heart Arrhythmia: A Status Report |
| Q60046053 | Calmodulinopathy: A Novel, Life-Threatening Clinical Entity Affecting the Young |
| Q60959820 | Calmodulinopathy: Functional Effects of CALM Mutations and Their Relationship With Clinical Phenotypes |
| Q99421604 | Complex Arrhythmia Syndrome in a Knock-In Mouse Model Carrier of the N98S Calm1 Mutation |
| Q33168530 | Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT. |
| Q59335621 | Human Calmodulin Mutations |
| Q90519863 | Impact of arrhythmogenic calmodulin variants on small conductance Ca2+ -activated K+ (SK3) channels |
| Q58801873 | Long QT Syndrome and Sinus Bradycardia-A Mini Review |
| Q52590940 | Small-conductance Ca2+-activated K+ channels: insights into their roles in cardiovascular disease. |
| Q46179717 | The Arrhythmogenic Calmodulin Mutation D129G Dysregulates Cell Growth, Calmodulin-dependent Kinase II Activity, and Cardiac Function in Zebrafish |
| Q60937346 | The multifunctional role of phospho-calmodulin in pathophysiological processes |
| Q38636096 | Treatment of calmodulinopathy with verapamil |
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