about
Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathyMutations in sarcomere protein genes in left ventricular noncompactionMutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathyAlpha1A-adrenergic receptor-directed autoimmunity induces left ventricular damage and diastolic dysfunction in rats.Bcl10 mediates angiotensin II-induced cardiac damage and electrical remodeling.Muscle RING-finger 2 and 3 maintain striated-muscle structure and functionEmbryonic cardiomyocytes can orchestrate various cell protective mechanisms to survive mitochondrial stress.CD74-Downregulation of Placental Macrophage-Trophoblastic Interactions in Preeclampsia.Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease.Inhibition of chymotryptic-like standard proteasome activity exacerbates doxorubicin-induced cytotoxicity in primary cardiomyocytes.Growth arrest specific protein 6 participates in DOCA-induced target-organ damage.Role of the multidomain protein spinophilin in blood pressure and cardiac function regulation.Cardiac troponin C-L29Q, related to hypertrophic cardiomyopathy, hinders the transduction of the protein kinase A dependent phosphorylation signal from cardiac troponin I to C.Dietary n-3 polyunsaturated fatty acids and direct renin inhibition improve electrical remodeling in a model of high human renin hypertension.Impaired myocardial development resulting in neonatal cardiac hypoplasia alters postnatal growth and stress response in the heart.Activation of Peroxisome Proliferator-Activated Receptor-δ as Novel Therapeutic Strategy to Prevent In-Stent Restenosis and Stent Thrombosis.Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease.TAT-apoptosis repressor with caspase recruitment domain protein transduction rescues mice from fulminant liver failure.Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy.The sGC stimulator BAY 41-8543 in a rat model of hypertension-induced heart failure.A Novel Locus for Dilated Cardiomyopathy, Diffuse Myocardial Fibrosis, and Sudden Death on Chromosome 10q25-26
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description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Arnd Heuser
@ast
Arnd Heuser
@en
Arnd Heuser
@es
Arnd Heuser
@nl
type
label
Arnd Heuser
@ast
Arnd Heuser
@en
Arnd Heuser
@es
Arnd Heuser
@nl
prefLabel
Arnd Heuser
@ast
Arnd Heuser
@en
Arnd Heuser
@es
Arnd Heuser
@nl
P106
P21
P31
P496
0000-0002-3334-960X