Search Results - "KOENEN, Michael"
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The Symptom Complex of Familial Sinus Node Dysfunction and Myocardial Noncompaction Is Associated With Mutations in the HCN4 Channel
Published in Journal of the American College of Cardiology (26-08-2014)“…Abstract Background Inherited arrhythmias were originally considered isolated electrical defects. There is growing evidence that ion channel dysfunction also…”
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Augmentation of myocardial If dysregulates calcium homeostasis and causes adverse cardiac remodeling
Published in Nature communications (23-07-2019)“…HCN channels underlie the depolarizing funny current (I f ) that contributes importantly to cardiac pacemaking. I f is upregulated in failing and infarcted…”
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Improved Generation of Human Induced Pluripotent Stem Cell-Derived Cardiac Pacemaker Cells Using Novel Differentiation Protocols
Published in International journal of molecular sciences (01-07-2022)“…Current protocols for the differentiation of human-induced pluripotent stem cells (hiPSC) into cardiomyocytes only generate a small amount of cardiac pacemaker…”
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4
Tiotropium Respimat Inhaler and the Risk of Death in COPD
Published in The New England journal of medicine (17-10-2013)“…This large trial involving patients with chronic obstructive pulmonary disease examined the relative safety of tiotropium inhalation delivered by two different…”
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Subtype-specific differentiation of cardiac pacemaker cell clusters from human induced pluripotent stem cells
Published in Stem cell research & therapy (16-10-2017)“…Human induced pluripotent stem cells (hiPSC) harbor the potential to differentiate into diverse cardiac cell types. Previous experimental efforts were…”
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Quantitative Efficacy and Fate of Mesenchymal Stromal Cells Targeted to Cardiac Sites by Radiofrequency Catheter Ablation
Published in Cell transplantation (01-01-2020)“…Engraftment and functional integration of stem cells or stem cell-derived cells within cardiac tissue is an important prerequisite for cell replacement therapy…”
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A Distinct Cardiomyopathy
Published in Journal of the American College of Cardiology (01-03-2017)Get full text
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8
Genetic suppression of atrial fibrillation using a dominant-negative ether-a-go-go–related gene mutant
Published in Heart rhythm (01-02-2012)“…Background Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia. Gene therapy–dependent modulation of atrial electrophysiology may provide…”
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Novel mouse model reveals distinct activity-dependent and -independent contributions to synapse development
Published in PloS one (31-01-2011)“…The balanced action of both pre- and postsynaptic organizers regulates the formation of neuromuscular junctions (NMJ). The precise mechanisms that control the…”
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10
Acetylcholine receptor channel subtype directs the innervation pattern of skeletal muscle
Published in EMBO reports (01-06-2005)“…Acetylcholine receptors (AChRs) mediate synaptic transmission at the neuromuscular junction, and structural and functional analysis has assigned distinct…”
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Decrease in the oral bioavailability of dabigatran etexilate after co‐medication with rifampicin
Published in British journal of clinical pharmacology (01-09-2012)“…WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • Dabigatran etexilate is an oral prodrug that is rapidly converted to dabigatran, a direct and reversible thrombin…”
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12
Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1
Published in Journal of molecular and cellular cardiology (01-01-2010)“…Abstract Hereditary long QT syndrome (LQTS) is a cardiovascular disorder characterized by prolongation of the QT interval on the surface ECG and a high risk…”
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13
Skipping of Exon 1 in the KCNQ1 Gene Causes Jervell and Lange-Nielsen Syndrome
Published in The Journal of biological chemistry (17-11-2006)“…The Jervell and Lange-Nielsen syndrome (JLNS) is a rare autosomal recessive form of the long QT syndrome linked with a profound hearing loss caused by…”
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14
Regulation of fast inactivation of cloned mammalian Ik(A) channels by cysteine oxidation
Published in Nature (London) (22-08-1991)“…Modulation of neuronal excitability by regulation of K+ channels potentially plays a part in short-term memory but has not yet been studied at the molecular…”
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15
Pharmacokinetic and Safety Evaluation of BILR 355, a Second-Generation Nonnucleoside Reverse Transcriptase Inhibitor, in Healthy Volunteers
Published in Antimicrobial Agents and Chemotherapy (01-12-2008)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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BS-452757-4 ANTI-ARRHYTHMIC EFFECTS OF ANDROGEN DEPRIVATION THERAPIES IN A SCN5A LOSS-OF-FUNCTION MOUSE MODEL
Published in Heart rhythm (01-05-2023)Get full text
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17
Location of a Threonine Residue in the $\alpha $-subunit M2 Transmembrane Segment that Determines the Ion Flow through the Acetylcholine Receptor Channel
Published in Proceedings of the Royal Society. B, Biological sciences (22-01-1991)“…By the combination of cDNA manipulation and functional analysis of normal and mutant acetylcholine receptor (AChR) channels of Torpedo expressed in Xenopus…”
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A Distinct Cardiomyopathy: HCN4Syndrome Comprising Myocardial Noncompaction, Bradycardia, Mitral Valve Defects, and Aortic Dilation
Published in Journal of the American College of Cardiology (07-03-2017)“…Given the challenging analysis of mechanistic pathways leading to LVNC associated with previously identified mutations, this specific entity is expected to…”
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GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndrome
Published in Pflügers Archiv (01-02-2024)“…Loss-of-function variants of SCN5A , encoding the sodium channel alpha subunit Nav1.5 are associated with high phenotypic variability and multiple cardiac…”
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Response to the letter by Dr Chin and co‐workers
Published in British journal of clinical pharmacology (01-02-2013)Get full text
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