On the public citation graph

Molecular and cellular neurocardiology: development, and cellular and molecular adaptations to heart disease

https://doi.org/10.1113/jp271840
0 signed · 345 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

1 of the 200 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1016/j.bpj.2014.10.054 (notice 2015-11-03).

Dataset join, best-effort; this page does not check the publisher record. Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0); dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1096-9861(19990510)407:3<303::aid-cne1>3.0.co;2-#openalex-snapshot
Regional distribution and extrinsic innervation of intrinsic cardiac neurons in the guinea pig
inferredcites →https://doi.org/10.1002/(sici)1097-4695(200003)42:4<460::aid-neu7>3.0.co;2-#openalex-snapshot
Nerve growth factor collaborates with myocyte‐derived factors to promote development of presynaptic sites in cultured sympathetic neurons
inferredcites →https://doi.org/10.1002/1096-9861(20000717)423:1<26::aid-cne3>3.0.co;2-copenalex-snapshot
Origin of pituitary adenylate cyclase-activating polypeptide (PACAP)-immunoreactive fibers innervating guinea pig parasympathetic cardiac ganglia
inferredcites →https://doi.org/10.1002/1097-0177(2000)9999:9999<::aid-dvdy1031>3.0.co;2-popenalex-snapshot
GDNF family receptors in the embryonic and postnatal rat heart and reduced cholinergic innervation in mice hearts lacking Ret or GFR?2
inferredcites →https://doi.org/10.1002/1097-0185(20000801)259:4<353::aid-ar10>3.0.co;2-ropenalex-snapshot
Morphology, distribution, and variability of the epicardiac neural ganglionated subplexuses in the human heart
inferredcites →https://doi.org/10.1002/1097-0185(20000801)259:4<424::aid-ar60>3.0.co;2-jopenalex-snapshot
Pathology of intrinsic cardiac neurons from ischemic human hearts
inferredcites →https://doi.org/10.1002/ca.20695openalex-snapshot
Autonomic innervation of the developing heart: Origins and function
inferredcites →https://doi.org/10.1002/cne.1336openalex-snapshot
Distribution of cocaine‐ and amphetamine‐regulated transcript peptide in the guinea pig intrinsic cardiac nervous system and colocalization with neuropeptides or transmitter synthetic enzymes
inferredcites →https://doi.org/10.1002/jnr.490260217openalex-snapshot
Endogenous levels of nerve growth factor (NGF) are altered in experimental diabetes mellitus: A possible role for NGF in the pathogenesis of diabetic neuropathy
inferredcites →https://doi.org/10.1006/jmcc.1995.0232openalex-snapshot
Sympathetic Innervation Modulates the Expression of Angiotensin II Receptors in Embryonic Rat Heart Graftedin Oculo
inferredcites →https://doi.org/10.1006/jmcc.1996.0163openalex-snapshot
Rapid Transition of Cardiac Myocytes from Hyperplasia to Hypertrophy During Postnatal Development
inferredcites →https://doi.org/10.1006/jmcc.2000.1214openalex-snapshot
Pre-synaptic NO-cGMP Pathway Modulates Vagal Control of Heart Rate in Isolated Adult Guinea Pig Atria
inferredcites →https://doi.org/10.1006/jmcc.2000.1218openalex-snapshot
Augmented Expression of Cardiotrophin-1 and its Receptor Component, gp130, in both Left and Right Ventricles after Myocardial Infarction in the Rat
inferredcites →https://doi.org/10.1007/s00395-004-0474-7openalex-snapshot
Adrenergic regulation of the rapid component of the cardiac delayed rectifier potassium current, IKr, and the underlying hERG ion channel
inferredcites →https://doi.org/10.1007/s004290000132openalex-snapshot
Ingrowth of sympathetic innervation occurs concomitantly with a decrease of ANP in the growing rat cardiac ventricles
inferredcites →https://doi.org/10.1007/s00441-006-0215-3openalex-snapshot
Localization of cholinergic innervation and neurturin receptors in adult mouse heart and expression of the neurturin gene
inferredcites →https://doi.org/10.1007/s12031-012-9720-xopenalex-snapshot
Nerve Sprouting Contributes to Increased Severity of Ventricular Tachyarrhythmias by Upregulating iGluRs in Rats with Healed Myocardial Necrotic Injury
inferredcites →https://doi.org/10.1016/0002-8703(92)90968-2openalex-snapshot
Prevention of life-threatening arrhythmias by pharmacologic stimulation of the muscarinic receptors with oxotremorine
inferredcites →https://doi.org/10.1016/0002-9149(73)91034-5openalex-snapshot
Cell proliferation during cardiac growth
inferredcites →https://doi.org/10.1016/0006-291x(90)92401-kopenalex-snapshot
C-Type natriuretic peptide (CNP): A new member of natriuretic peptide family identified in porcine brain
inferredcites →https://doi.org/10.1016/0008-6363(95)00039-9openalex-snapshot
Acute and chronic effects of transient myocardial ischemia on sympathetic nerve activity, density, and norepinephrine content
inferredcites →https://doi.org/10.1016/0012-1606(83)90365-2openalex-snapshot
Evidence for neurotransmitter plasticity in vivo: Developmental changes in properties of cholinergic sympathetic neurons
inferredcites →https://doi.org/10.1016/0165-1838(94)90179-1openalex-snapshot
Innervation of the pacemaker in guinea-pig sinoatrial node
inferredcites →https://doi.org/10.1016/0304-3940(90)90681-xopenalex-snapshot
Innervation patterns of the middle cervical - stellate ganglion complex in the rat
inferredcites →https://doi.org/10.1016/0735-1097(89)90391-4openalex-snapshot
Regional sympathetic denervation after myocardial infarction in humans detected noninvasively using I-123-metaiodobenzylguanidine
inferredcites →https://doi.org/10.1016/0735-1097(93)90845-ropenalex-snapshot
Pharmacologic modulation of the autonomic nervous system in the prevention of sudden cardiac death
inferredcites →https://doi.org/10.1016/j.autneu.2008.03.002openalex-snapshot
Regulation of cardiac innervation and function via the p75 neurotrophin receptor
inferredcites →https://doi.org/10.1016/j.autneu.2008.04.010openalex-snapshot
Neurochemical diversity of afferent neurons that transduce sensory signals from dog ventricular myocardium
inferredcites →https://doi.org/10.1016/j.autneu.2010.02.005openalex-snapshot
Norepinephrine-induced nerve growth factor depletion causes cardiac sympathetic denervation in severe heart failure
inferredcites →https://doi.org/10.1016/j.autneu.2011.01.008openalex-snapshot
Remodeling of cardiac cholinergic innervation and control of heart rate in mice with streptozotocin-induced diabetes
inferredcites →https://doi.org/10.1016/j.bbamcr.2003.09.005openalex-snapshot
Calcitonin gene-related peptide partly protects cultured smooth muscle cells from apoptosis induced by an oxidative stress via activation of ERK1/2 MAPK
inferredcites →https://doi.org/10.1016/j.biopsycho.2005.11.013openalex-snapshot
The role of vagal function in the risk for cardiovascular disease and mortality
inferredcites →https://doi.org/10.1016/j.bpj.2008.11.034openalex-snapshot
Characterization of Engineered Channelrhodopsin Variants with Improved Properties and Kinetics
inferredcites →https://doi.org/10.1016/j.bpj.2014.10.054openalex-snapshot
RETRACTED: Oxidative Stress and Ca2+ Release Events in Mouse Cardiomyocytes
inferredcites →https://doi.org/10.1016/j.brainres.2006.09.054openalex-snapshot
Sympathetic hyperinnervation and inflammatory cell NGF synthesis following myocardial infarction in rats
inferredcites →https://doi.org/10.1016/j.cardfail.2006.05.006openalex-snapshot
Preserved Norepinephrine Reuptake but Reduced Sympathetic Nerve Endings in Hypertrophic Volume-Overloaded Rat Hearts
inferredcites →https://doi.org/10.1016/j.cardiores.2004.01.012openalex-snapshot
Localization of cholinergic innervation in guinea pig heart by immunohistochemistry for high-affinity choline transporters
inferredcites →https://doi.org/10.1016/j.cardiores.2006.12.001openalex-snapshot
Autonomic modulation of electrical restitution, alternans and ventricular fibrillation initiation in the isolated heart
inferredcites →https://doi.org/10.1016/j.cell.2008.02.048openalex-snapshot
A Dynamic Pathway for Calcium-Independent Activation of CaMKII by Methionine Oxidation
inferredcites →https://doi.org/10.1016/j.cell.2011.07.038openalex-snapshot
A Mechanism for Tunable Autoinhibition in the Structure of a Human Ca2+/Calmodulin- Dependent Kinase II Holoenzyme
inferredcites →https://doi.org/10.1016/j.cyto.2006.10.004openalex-snapshot
The lack of cardiotrophin-1 alters expression of interleukin-6 and leukemia inhibitory factor mRNA but does not impair cardiac injury response
inferredcites →https://doi.org/10.1016/j.devcel.2015.06.017openalex-snapshot
Nerves Regulate Cardiomyocyte Proliferation and Heart Regeneration
inferredcites →https://doi.org/10.1016/j.ejphar.2005.12.039openalex-snapshot
The role of calcitonin gene-related peptide (CGRP) in ischemic preconditioning in isolated rat hearts
inferredcites →https://doi.org/10.1016/j.hrthm.2013.11.028openalex-snapshot
Cardiac sympathetic denervation in patients with refractory ventricular arrhythmias or electrical storm: Intermediate and long-term follow-up
inferredcites →https://doi.org/10.1016/j.hrthm.2014.08.001openalex-snapshot
Vagus nerve stimulation initiated late during ischemia, but not reperfusion, exerts cardioprotection via amelioration of cardiac mitochondrial dysfunction
inferredcites →https://doi.org/10.1016/j.hrthm.2015.06.005openalex-snapshot
Control of ventricular excitability by neurons of the dorsal motor nucleus of the vagus nerve
inferredcites →https://doi.org/10.1016/j.jacc.2009.12.066openalex-snapshot
Cardiac Sympathetic Denervation Assessed With 123-Iodine Metaiodobenzylguanidine Imaging Predicts Ventricular Arrhythmias in Implantable Cardioverter-Defibrillator Patients
inferredcites →https://doi.org/10.1016/j.jacc.2013.07.096openalex-snapshot
Regional Myocardial Sympathetic Denervation Predicts the Risk of Sudden Cardiac Arrest in Ischemic Cardiomyopathy
inferredcites →https://doi.org/10.1016/j.jneumeth.2013.09.005openalex-snapshot
In situ three-dimensional reconstruction of mouse heart sympathetic innervation by two-photon excitation fluorescence imaging
inferredcites →https://doi.org/10.1016/j.neulet.2012.08.089openalex-snapshot
Altered atrial neurotransmitter release in transgenic p75−/− and gp130 KO mice
inferredcites →https://doi.org/10.1016/j.neulet.2013.05.028openalex-snapshot
CGRP inhibits norepinephrine induced apoptosis with restoration of Bcl-2/Bax in cultured cardiomyocytes of rat
inferredcites →https://doi.org/10.1016/j.neuron.2006.06.018openalex-snapshot
Selective and Quickly Reversible Inactivation of Mammalian Neurons In Vivo Using the Drosophila Allatostatin Receptor
inferredcites →https://doi.org/10.1016/j.neuroscience.2008.06.063openalex-snapshot
Cholinergic neurons of mouse intrinsic cardiac ganglia contain noradrenergic enzymes, norepinephrine transporters, and the neurotrophin receptors tropomyosin-related kinase A and p75
inferredcites →https://doi.org/10.1016/j.neuroscience.2009.09.001openalex-snapshot
Localization of multiple neurotransmitters in surgically derived specimens of human atrial ganglia
inferredcites →https://doi.org/10.1016/j.neuroscience.2012.06.061openalex-snapshot
Development of cardiac parasympathetic neurons, glial cells, and regional cholinergic innervation of the mouse heart
inferredcites →https://doi.org/10.1016/j.pbiomolbio.2014.07.001openalex-snapshot
Cardiac applications of optogenetics
inferredcites →https://doi.org/10.1016/j.regpep.2013.06.008openalex-snapshot
Alpha-calcitonin gene-related peptide is protective against pressure overload-induced heart failure
inferredcites →https://doi.org/10.1016/j.tips.2010.12.001openalex-snapshot
Cardiac electrical remodeling in health and disease
inferredcites →https://doi.org/10.1016/j.ydbio.2007.12.041openalex-snapshot
Target-dependent inhibition of sympathetic neuron growth via modulation of a BMP signaling pathway
inferredcites →https://doi.org/10.1016/j.yexcr.2007.01.009openalex-snapshot
Re-expression of proteins involved in cytokinesis during cardiac hypertrophy
inferredcites →https://doi.org/10.1016/j.yjmcc.2004.05.009openalex-snapshot
Cardiac ion channel expression and regulation: the role of innervation
inferredcites →https://doi.org/10.1016/j.yjmcc.2006.02.002openalex-snapshot
Down regulation of the L-type Ca2+ channel, GRK2, and phosphorylated phospholamban: protective mechanisms for the denervated failing heart
inferredcites →https://doi.org/10.1016/j.yjmcc.2007.09.005openalex-snapshot
Neuronal nitric oxide synthase gene transfer decreases [Ca2+]i in cardiac sympathetic neurons
inferredcites →https://doi.org/10.1016/j.yjmcc.2007.10.001openalex-snapshot
Neuropeptide Y reduces acetylcholine release and vagal bradycardia via a Y2 receptor-mediated, protein kinase C-dependent pathway
inferredcites →https://doi.org/10.1016/j.yjmcc.2008.12.006openalex-snapshot
Regulation of nerve growth factor in the heart: The role of the calcineurin–NFAT pathway
inferredcites →https://doi.org/10.1016/j.yjmcc.2010.09.025openalex-snapshot
Pravastatin normalises peripheral cardiac sympathetic hyperactivity in the spontaneously hypertensive rat
inferredcites →https://doi.org/10.1016/j.yjmcc.2011.11.016openalex-snapshot
The cardiac sympathetic co-transmitter galanin reduces acetylcholine release and vagal bradycardia: Implications for neural control of cardiac excitability
inferredcites →https://doi.org/10.1016/j.yjmcc.2014.12.011openalex-snapshot
A systematic analysis of neonatal mouse heart regeneration after apical resection
inferredcites →https://doi.org/10.1016/j.yjmcc.2015.06.007openalex-snapshot
CaMKIIδ mediates β-adrenergic effects on RyR2 phosphorylation and SR Ca2+ leak and the pathophysiological response to chronic β-adrenergic stimulation
inferredcites →https://doi.org/10.1016/s0002-8703(77)80172-5openalex-snapshot
Effects of vagal stimulation, atropine, and propranolol on fibrillation threshold of normal and ischemic ventricles
inferredcites →https://doi.org/10.1016/s0002-9149(97)00844-8openalex-snapshot
Adrenergic Nervous System in Heart Failure
inferredcites →https://doi.org/10.1016/s0006-3495(00)76595-7openalex-snapshot
Reverse Mode of the Sarcoplasmic Reticulum Calcium Pump and Load-Dependent Cytosolic Calcium Decline in Voltage-Clamped Cardiac Ventricular Myocytes
inferredcites →https://doi.org/10.1016/s0008-6363(01)00425-4openalex-snapshot
NO-cGMP pathway increases the hyperpolarisation-activated current, If, and heart rate during adrenergic stimulation
inferredcites →https://doi.org/10.1016/s0021-9258(18)88990-6openalex-snapshot
Mechanism of autophosphorylation of the multifunctional Ca2+/calmodulin-dependent protein kinase.
inferredcites →https://doi.org/10.1016/s0021-9258(19)84416-2openalex-snapshot
Reversible generation of a Ca2+-independent form of Ca2+(calmodulin)-dependent protein kinase II by an autophosphorylation mechanism.
inferredcites →https://doi.org/10.1016/s0022-2828(02)00290-0openalex-snapshot
Expression of heart K+ channels in adrenalectomized and catecholamine-depleted reserpine-treated rats
inferredcites →https://doi.org/10.1016/s0092-8674(00)80847-8openalex-snapshot
PKA Phosphorylation Dissociates FKBP12.6 from the Calcium Release Channel (Ryanodine Receptor)
inferredcites →https://doi.org/10.1016/s1044-7431(03)00102-7openalex-snapshot
BDNF and CNTF regulate cholinergic properties of sympathetic neurons through independent mechanisms
inferredcites →https://doi.org/10.1016/s1566-0702(00)00215-0openalex-snapshot
Functional and chemical anatomy of the afferent vagal system
inferredcites →https://doi.org/10.1016/s1566-0702(00)00244-7openalex-snapshot
Local opiate receptors in the sinoatrial node moderate vagal bradycardia
inferredcites →https://doi.org/10.1038/415198aopenalex-snapshot
Cardiac excitation–contraction coupling
inferredcites →https://doi.org/10.1038/nature11444openalex-snapshot
CaMKII determines mitochondrial stress responses in heart
inferredcites →https://doi.org/10.1038/nature12537openalex-snapshot
Diabetic hyperglycaemia activates CaMKII and arrhythmias by O-linked glycosylation
inferredcites →https://doi.org/10.1038/nbt.3268openalex-snapshot
Optogenetics for in vivo cardiac pacing and resynchronization therapies
inferredcites →https://doi.org/10.1038/ncomms4329openalex-snapshot
3D multifunctional integumentary membranes for spatiotemporal cardiac measurements and stimulation across the entire epicardium
inferredcites →https://doi.org/10.1038/ncomms7235openalex-snapshot
Targeting protein tyrosine phosphatase σ after myocardial infarction restores cardiac sympathetic innervation and prevents arrhythmias
inferredcites →https://doi.org/10.1038/ng1790openalex-snapshot
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
inferredcites →https://doi.org/10.1038/nm.2506openalex-snapshot
Oxidation of CaMKII determines the cardiotoxic effects of aldosterone
inferredcites →https://doi.org/10.1038/nm1215openalex-snapshot
Calmodulin kinase II inhibition protects against structural heart disease
inferredcites →https://doi.org/10.1038/nm1570openalex-snapshot
Sema3a maintains normal heart rhythm through sympathetic innervation patterning
inferredcites →https://doi.org/10.1038/nmat2879openalex-snapshot
Waterproof AlInGaP optoelectronics on stretchable substrates with applications in biomedicine and robotics
inferredcites →https://doi.org/10.1038/nn1525openalex-snapshot
Millisecond-timescale, genetically targeted optical control of neural activity
inferredcites →https://doi.org/10.1038/nrcardio.2014.19openalex-snapshot
Cardiac sympathetic denervation to prevent life-threatening arrhythmias
inferredcites →https://doi.org/10.1038/nrendo.2012.21openalex-snapshot
Cardiovascular autonomic neuropathies as complications of diabetes mellitus
inferredcites →https://doi.org/10.1046/j.1540-8167.2002.00735.xopenalex-snapshot
Identification and Characterization of Atrioventricular Parasympathetic Innervation in Humans
inferredcites →https://doi.org/10.1056/nejmoa1100171openalex-snapshot
Effect of Nesiritide in Patients with Acute Decompensated Heart Failure
inferredcites →https://doi.org/10.1073/pnas.0806422106openalex-snapshot
Calmodulin kinase II is required for fight or flight sinoatrial node physiology
inferredcites →https://doi.org/10.1073/pnas.0813013106openalex-snapshot
The δ isoform of CaM kinase II is required for pathological cardiac hypertrophy and remodeling after pressure overload
inferredcites →https://doi.org/10.1073/pnas.1509380112openalex-snapshot
Optogenetic determination of the myocardial requirements for extrasystoles by cell type-specific targeting of ChannelRhodopsin-2
inferredcites →https://doi.org/10.1073/pnas.95.18.10890openalex-snapshot
Characterization of a calmodulin kinase II inhibitor protein in brain
inferredcites →https://doi.org/10.1074/jbc.m115.650234openalex-snapshot
S-Nitrosylation Induces Both Autonomous Activation and Inhibition of Calcium/Calmodulin-dependent Protein Kinase II δ
inferredcites →https://doi.org/10.1083/jcb.75.3.694openalex-snapshot
Role of nerve growth factor in the development of rat sympathetic neurons in vitro. I. Survival, growth, and differentiation of catecholamine production.
inferredcites →https://doi.org/10.1089/104303401750476230openalex-snapshot
A High-Efficiency Synthetic Promoter That Drives Transgene Expression Selectively in Noradrenergic Neurons
inferredcites →https://doi.org/10.1093/cvr/24.2.102openalex-snapshot
Plasma neuropeptide Y on admission to a coronary care unit: raised levels in patients with left heart failure
inferredcites →https://doi.org/10.1093/cvr/cvp029openalex-snapshot
Structural and functional cardiac cholinergic deficits in adult neurturin knockout mice
inferredcites →https://doi.org/10.1093/cvr/cvr105openalex-snapshot
Vagus nerve stimulation protects against ventricular fibrillation independent of muscarinic receptor activation
inferredcites →https://doi.org/10.1093/cvr/cvr244openalex-snapshot
Substance P induces adverse myocardial remodelling via a mechanism involving cardiac mast cells
inferredcites →https://doi.org/10.1093/cvr/cvs212openalex-snapshot
Cardioprotection evoked by remote ischaemic preconditioning is critically dependent on the activity of vagal pre-ganglionic neurones
inferredcites →https://doi.org/10.1093/cvr/cvt081openalex-snapshot
Nerves projecting from the intrinsic cardiac ganglia of the pulmonary veins modulate sinoatrial node pacemaker function
inferredcites →https://doi.org/10.1093/cvr/cvt201openalex-snapshot
NO-dependent CaMKII activation during β-adrenergic stimulation of cardiac muscle
inferredcites →https://doi.org/10.1093/cvr/cvu258openalex-snapshot
Optogenetic release of norepinephrine from cardiac sympathetic neurons alters mechanical and electrical function
inferredcites →https://doi.org/10.1093/emboj/21.8.1889openalex-snapshot
14‐3‐3 amplifies and prolongs adrenergic stimulation of HERG K+ channel activity
inferredcites →https://doi.org/10.1093/oso/9780195141290.001.0001openalex-snapshot
Basic and Clinical Neurocardiology
inferredcites →https://doi.org/10.1093/oxfordjournals.eurheartj.a060088openalex-snapshot
Plasma calcitonin gene-related peptide decreases in chronic congestive heart failure
inferredcites →https://doi.org/10.1093/oxfordjournals.eurheartj.a060526openalex-snapshot
Prognostic value of plasma neuropeptide-Y in coronary care unit patients with and without acute myocardial infarction
inferredcites →https://doi.org/10.1111/j.1469-7793.1998.779bd.xopenalex-snapshot
Overexpression of nerve growth factor in the heart alters ion channel activity and β‐adrenergic signalling in an adult transgenic mouse
inferredcites →https://doi.org/10.1111/j.1469-7793.2001.00507.xopenalex-snapshot
Nitric oxide‐cGMP pathway facilitates acetylcholine release and bradycardia during vagal nerve stimulation in the guinea‐pig in vitro
inferredcites →https://doi.org/10.1111/j.1469-7793.2001.00547.xopenalex-snapshot
Vagus nerve stimulation decreases left ventricular contractility in vivo in the human and pig heart
inferredcites →https://doi.org/10.1111/j.1540-8167.1999.tb00278.xopenalex-snapshot
Characterization of Sinoatrial Parasympathetic Innervation in Humans
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07208.xopenalex-snapshot
Cholinoceptive and cholinergic properties of cardiomyocytes involving an amplification mechanism for vagal efferent effects in sparsely innervated ventricular myocardium
inferredcites →https://doi.org/10.1111/j.1749-6632.2001.tb03667.xopenalex-snapshot
Cardiac Vagal Chemosensory Afferents
inferredcites →https://doi.org/10.1111/j.1749-6632.2001.tb03668.xopenalex-snapshot
Cardiac Sympathetic Afferent Activation Provoked by Myocardial Ischemia and Reperfusion
inferredcites →https://doi.org/10.1113/eph8602146openalex-snapshot
Effects of Direct Sympathetic and Vagus Nerve Stimulation on the Physiology of the Whole Heart – A Novel Model of Isolated Langendorff Perfused Rabbit Heart with Intact Dual Autonomic Innervation
inferredcites →https://doi.org/10.1113/expphysiol.2003.002654openalex-snapshot
Interaction between direct sympathetic and vagus nerve stimulation on heart rate in the isolated rabbit heart
inferredcites →https://doi.org/10.1113/expphysiol.2006.033605openalex-snapshot
Vasoactive intestinal polypeptide receptor antagonism enhances the vagally induced increase in cardiac interval of the rat atriumin vitro
inferredcites →https://doi.org/10.1113/expphysiol.2007.041178openalex-snapshot
Potential clinical relevance of the ‘little brain’ on the mammalian heart
inferredcites →https://doi.org/10.1113/expphysiol.2009.048710openalex-snapshot
Control of cardiac contractility in the rat working heart–brainstem preparation
inferredcites →https://doi.org/10.1113/expphysiol.2009.049965openalex-snapshot
Infarction‐induced cytokines cause local depletion of tyrosine hydroxylase in cardiac sympathetic nerves
inferredcites →https://doi.org/10.1113/expphysiol.2014.080184openalex-snapshot
Autonomic control of the heart: going beyond the classical neurotransmitters
inferredcites →https://doi.org/10.1113/jp270917openalex-snapshot
Innervating sympathetic neurons regulate heart size and the timing of cardiomyocyte cell cycle withdrawal
inferredcites →https://doi.org/10.1113/jp271588openalex-snapshot
Protection against ventricular fibrillation via cholinergic receptor stimulation and the generation of nitric oxide
inferredcites →https://doi.org/10.1113/jphysiol.1976.sp011414openalex-snapshot
The location of cardiac vagal preganglionic motoneurones in the medulla of the cat.
inferredcites →https://doi.org/10.1113/jphysiol.2004.063347openalex-snapshot
Heterogeneous expression of repolarizing, voltage‐gated K+ currents in adult mouse ventricles
inferredcites →https://doi.org/10.1113/jphysiol.2009.169417openalex-snapshot
Direct evidence of nitric oxide release from neuronal nitric oxide synthase activation in the left ventricle as a result of cervical vagus nerve stimulation
inferredcites →https://doi.org/10.1113/jphysiol.2013.257758openalex-snapshot
Myths and realities of the cardiac vagus
inferredcites →https://doi.org/10.1113/jphysiol.2014.278051openalex-snapshot
Maximal acceleration of Ca2+ release refractoriness by β‐adrenergic stimulation requires dual activation of kinases PKA and CaMKII in mouse ventricular myocytes
inferredcites →https://doi.org/10.1113/jphysiol.2014.279638openalex-snapshot
Decreased inward rectifying K+current and increased ryanodine receptor sensitivity synergistically contribute to sustained focal arrhythmia in the intact rabbit heart
inferredcites →https://doi.org/10.1126/science.1066843openalex-snapshot
Requirement of a Macromolecular Signaling Complex for β Adrenergic Receptor Modulation of the KCNQ1-KCNE1 Potassium Channel
inferredcites →https://doi.org/10.1126/science.1161748openalex-snapshot
Membrane Fusion: Grappling with SNARE and SM Proteins
inferredcites →https://doi.org/10.1126/science.1200708openalex-snapshot
Transient Regenerative Potential of the Neonatal Mouse Heart
inferredcites →https://doi.org/10.1126/science.2512641openalex-snapshot
The Cholinergic Neuronal Differentiation Factor from Heart Cells Is Identical to Leukemia Inhibitory Factor
inferredcites →https://doi.org/10.1126/science.256.5060.1199openalex-snapshot
Calmodulin Trapping by Calcium-Calmodulin-Dependent Protein Kinase
inferredcites →https://doi.org/10.1126/science.7701323openalex-snapshot
Rapid Adaptation of Cardiac Ryanodine Receptors: Modulation by Mg 2+ and Phosphorylation
inferredcites →https://doi.org/10.1136/bmj.330.7492.625openalex-snapshot
How well does B-type natriuretic peptide predict death and cardiac events in patients with heart failure: systematic review
inferredcites →https://doi.org/10.1136/heartjnl-2012-303443openalex-snapshot
Relationship of plasma neuropeptide Y with angiographic, electrocardiographic and coronary physiology indices of reperfusion during ST elevation myocardial infarction
inferredcites →https://doi.org/10.1139/y08-075openalex-snapshot
Chemical sympathetic denervation, suppression of myocardial transient outward potassium current, and ventricular fibrillation in the rat
inferredcites →https://doi.org/10.1146/annurev.neuro.28.061604.135659openalex-snapshot
GROWTH AND SURVIVAL SIGNALS CONTROLLING SYMPATHETIC NERVOUS SYSTEM DEVELOPMENT
inferredcites →https://doi.org/10.1146/annurev.pharmtox.052808.102215openalex-snapshot
Autonomic Neurotransmission: 60 Years Since Sir Henry Dale
inferredcites →https://doi.org/10.1146/annurev.physiol.70.113006.100455openalex-snapshot
Calcium Cycling and Signaling in Cardiac Myocytes
inferredcites →https://doi.org/10.1152/ajpheart.00255.2013openalex-snapshot
Cardiac sympathetic dysfunction in the prehypertensive spontaneously hypertensive rat
inferredcites →https://doi.org/10.1152/ajpheart.00319.2001openalex-snapshot
Loss of cardiac sympathetic neurotransmitters in heart failure and NE infusion is associated with reduced NGF
inferredcites →https://doi.org/10.1152/ajpheart.00353.2006openalex-snapshot
Calmodulin kinase II inhibition protects against myocardial cell apoptosis in vivo
inferredcites →https://doi.org/10.1152/ajpheart.00424.2007openalex-snapshot
Angiotensin II attenuates myocardial interstitial acetylcholine release in response to vagal stimulation
inferredcites →https://doi.org/10.1152/ajpheart.00434.2013openalex-snapshot
Focal myocardial infarction induces global remodeling of cardiac sympathetic innervation: neural remodeling in a spatial context
inferredcites →https://doi.org/10.1152/ajpheart.00445.2015openalex-snapshot
Neurotransmission to parasympathetic cardiac vagal neurons in the brain stem is altered with left ventricular hypertrophy-induced heart failure
inferredcites →https://doi.org/10.1152/ajpheart.00492.2008openalex-snapshot
Cardiac cholinergic NO-cGMP signaling following acute myocardial infarction and nNOS gene transfer
inferredcites →https://doi.org/10.1152/ajpheart.00557.2015openalex-snapshot
Central-peripheral neural network interactions evoked by vagus nerve stimulation: functional consequences on control of cardiac function
inferredcites →https://doi.org/10.1152/ajpheart.00724.2007openalex-snapshot
Deficiency of M2muscarinic acetylcholine receptors increases susceptibility of ventricular function to chronic adrenergic stress
inferredcites →https://doi.org/10.1152/ajpheart.00730.2002openalex-snapshot
Cardiac enkephalins interrupt vagal bradycardia via δ2-opioid receptors in sinoatrial node
inferredcites →https://doi.org/10.1152/ajpheart.00754.2012openalex-snapshot
Functional differences between junctional and extrajunctional adrenergic receptor activation in mammalian ventricle
inferredcites →https://doi.org/10.1152/ajpheart.00768.2003openalex-snapshot
Infarction alters both the distribution and noradrenergic properties of cardiac sympathetic neurons
inferredcites →https://doi.org/10.1152/ajpheart.01106.2011openalex-snapshot
Sympathetic stimulation increases dispersion of repolarization in humans with myocardial infarction
inferredcites →https://doi.org/10.1152/ajpheart.01128.2009openalex-snapshot
Heterogeneous ventricular sympathetic innervation, altered β-adrenergic receptor expression, and rhythm instability in mice lacking the p75 neurotrophin receptor
inferredcites →https://doi.org/10.1152/ajpheart.1977.232.6.h590openalex-snapshot
Ventral root mapping of cardiac nerves in the canine using evoked potentials
inferredcites →https://doi.org/10.1152/ajpheart.1985.249.4.h876openalex-snapshot
Innervation of bat heart: cholinergic and adrenergic nerves innervate all chambers
inferredcites →https://doi.org/10.1152/ajpheart.1987.253.6.h1618openalex-snapshot
Angiotensin II binding sites in the conduction system of rat hearts
inferredcites →https://doi.org/10.1152/ajpheart.1994.266.6.h2167openalex-snapshot
The effect of vagal stimulation on left ventricular systolic and diastolic performance
inferredcites →https://doi.org/10.1152/ajpheart.1999.276.2.h608openalex-snapshot
β-Adrenergic modulation of L-type Ca2+-channel currents in early-stage embryonic mouse heart
inferredcites →https://doi.org/10.1152/ajpheart.2000.279.4.h1989openalex-snapshot
Cardiac synthesis, processing, and coronary release of enkephalin-related peptides
inferredcites →https://doi.org/10.1152/ajpheart.2001.281.6.h2318openalex-snapshot
Natriuretic peptides like NO facilitate cardiac vagal neurotransmission and bradycardia via a cGMP pathway
inferredcites →https://doi.org/10.1152/ajplegacy.1974.227.1.9openalex-snapshot
Responses of the canine heart to stimulation of the first five ventral thoracic roots
inferredcites →https://doi.org/10.1152/ajpregu.00118.2013openalex-snapshot
Peripheral cardiac sympathetic hyperactivity in cardiovascular disease: role of neuropeptides
inferredcites →https://doi.org/10.1152/jappl.2001.90.1.287openalex-snapshot
Ventricular activation during sympathetic imbalance and its computational reconstruction
inferredcites →https://doi.org/10.1152/jn.00870.2011openalex-snapshot
Selective optogenetic stimulation of cholinergic axons in neocortex
inferredcites →https://doi.org/10.1152/jn.01078.2005openalex-snapshot
Nerve Growth Factor Decreases Potassium Currents and Alters Repetitive Firing in Rat Sympathetic Neurons
inferredcites →https://doi.org/10.1152/physiol.00037.2013openalex-snapshot
Neural Mechanisms of Cardioprotection
inferredcites →https://doi.org/10.1152/physrev.00037.2003openalex-snapshot
Vascular Actions of Calcitonin Gene-Related Peptide and Adrenomedullin
inferredcites →https://doi.org/10.1152/physrev.1991.71.3.617openalex-snapshot
Reflexes from the heart.
inferredcites →https://doi.org/10.1161/01.cir.0000105721.71640.daopenalex-snapshot
Vagal Nerve Stimulation Markedly Improves Long-Term Survival After Chronic Heart Failure in Rats
inferredcites →https://doi.org/10.1161/01.cir.101.14.1634openalex-snapshot
Catecholamines, Cardiac β-Adrenergic Receptors, and Heart Failure
inferredcites →https://doi.org/10.1161/01.cir.101.16.1960openalex-snapshot
Relationship Between Regional Cardiac Hyperinnervation and Ventricular Arrhythmia
inferredcites →https://doi.org/10.1161/01.cir.49.1.86openalex-snapshot
Role of the Vagus Nerves in the Cardiovascular Changes Induced by Coronary Occlusion
inferredcites →https://doi.org/10.1161/01.cir.67.4.787openalex-snapshot
Transmural myocardial infarction in the dog produces sympathectomy in noninfarcted myocardium.
inferredcites →https://doi.org/10.1161/01.cir.88.3.1004openalex-snapshot
Natriuretic peptide system in human heart failure.
inferredcites →https://doi.org/10.1161/01.cir.93.1.168openalex-snapshot
Regional Differences in Current Density and Rate-Dependent Properties of the Transient Outward Current in Subepicardial and Subendocardial Myocytes of Human Left Ventricle
inferredcites →https://doi.org/10.1161/01.cir.97.13.1282openalex-snapshot
Ischemic Preconditioning in the Intact Rat Heart Is Mediated by δ1- But Not μ- or κ-Opioid Receptors
inferredcites →https://doi.org/10.1161/01.cir.98.17.1783openalex-snapshot
Reciprocal In Vivo Regulation of Myocardial G Protein–Coupled Receptor Kinase Expression by β-Adrenergic Receptor Stimulation and Blockade
inferredcites →https://doi.org/10.1161/01.hyp.0000255792.97033.f7openalex-snapshot
Gene Transfer of Neuronal Nitric Oxide Synthase into Intracardiac Ganglia Reverses Vagal Impairment in Hypertensive Rats
inferredcites →https://doi.org/10.1161/01.res.0000072999.51484.92openalex-snapshot
Sympathetic Nerve Sprouting, Electrical Remodeling, and Increased Vulnerability to Ventricular Fibrillation in Hypercholesterolemic Rabbits
inferredcites →https://doi.org/10.1161/01.res.0000133678.22968.e3openalex-snapshot
Mechanisms of Cardiac Nerve Sprouting After Myocardial Infarction in Dogs
inferredcites →https://doi.org/10.1161/01.res.0000269828.62250.abopenalex-snapshot
Cardiac Sympathetic Rejuvenation
inferredcites →https://doi.org/10.1161/01.res.17.3.222openalex-snapshot
Depression of Ventricular Contractility by Stimulation of the Vagus Nerves
inferredcites →https://doi.org/10.1161/01.res.21.5.691openalex-snapshot
Localized Myocardial Responses to Stimulation of Cardiac Sympathetic Nerves
inferredcites →https://doi.org/10.1161/01.res.57.1.55openalex-snapshot
Mechanisms of supersensitivity to sympathomimetic amines in the chronically denervated heart of the conscious dog.
inferredcites →https://doi.org/10.1161/01.res.62.6.1075openalex-snapshot
Expression of cellular oncogenes in the myocardium during the developmental stage and pressure-overloaded hypertrophy of the rat heart.
inferredcites →https://doi.org/10.1161/01.res.68.5.1471openalex-snapshot
Vagal stimulation and prevention of sudden death in conscious dogs with a healed myocardial infarction.
inferredcites →https://doi.org/10.1161/01.res.69.6.1427openalex-snapshot
Heterogeneity within the ventricular wall. Electrophysiology and pharmacology of epicardial, endocardial, and M cells.
inferredcites →https://doi.org/10.1161/01.res.77.4.841openalex-snapshot
Endogenous and Exogenous Nitric Oxide Inhibits Norepinephrine Release From Rat Heart Sympathetic Nerves
inferredcites →https://doi.org/10.1161/01.res.86.7.816openalex-snapshot
Nerve Sprouting and Sudden Cardiac Death
inferredcites →https://doi.org/10.1161/01.res.86.7.e80openalex-snapshot
Reduced Myocardial Nerve Growth Factor Expression in Human and Experimental Heart Failure
showing the first 200 of 243

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3950133openalex-extracted
inferred← citeshttps://doi.org/10.1001/jamacardio.2019.4717openalex-snapshot
Coronary Sinus Neuropeptide Y Levels and Adverse Outcomes in Patients With Stable Chronic Heart Failure
inferred← citeshttps://doi.org/10.1001/jamacardio.2019.4766openalex-snapshot
Correlating Cardiac Origin Neurohormonal Stress Levels With Heart Failure Outcomes
inferred← citeshttps://doi.org/10.1002/adbi.202000190openalex-snapshot
Drawing Inspiration from Developmental Biology for Cardiac Tissue Engineers
inferred← citeshttps://doi.org/10.1002/ar.25686openalex-snapshot
Noradrenergic and cholinergic innervation of the normal human heart and changes associated with cardiomyopathy
inferred← citeshttps://doi.org/10.1002/ehf2.13138openalex-snapshot
Pleiotropic Activity of Nerve Growth Factor in Regulating Cardiac Functions and Counteracting Pathogenesis
inferred← citeshttps://doi.org/10.1002/jnr.23924openalex-snapshot
Studying the pathophysiologic connection between cardiovascular and nervous systems using stem cells
inferred← citeshttps://doi.org/10.1007/978-3-030-28008-6_2openalex-snapshot
Brain-Heart Afferent-Efferent Traffic
inferred← citeshttps://doi.org/10.1007/978-3-031-08309-9_11openalex-snapshot
Neural Regulation of Cardiac Rhythm
inferred← citeshttps://doi.org/10.1007/978-3-319-90305-7_2-1openalex-snapshot
Brain-Heart Afferent-Efferent Traffic
inferred← citeshttps://doi.org/10.1007/s00018-017-2452-xopenalex-snapshot
The role of neuropeptides in adverse myocardial remodeling and heart failure
inferred← citeshttps://doi.org/10.1007/s00441-020-03279-6openalex-snapshot
The diversity of neuronal phenotypes in rodent and human autonomic ganglia
inferred← citeshttps://doi.org/10.1016/b978-0-12-805353-9.00129-7openalex-snapshot
Neuromodulation Therapies for Cardiac Disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-85492-4.00042-9openalex-snapshot
Sympathetic control of the heart
inferred← citeshttps://doi.org/10.1016/j.autneu.2016.08.016openalex-snapshot
Cardiac sympatho-vagal balance and ventricular arrhythmia
inferred← citeshttps://doi.org/10.1016/j.autneu.2021.102897openalex-snapshot
Aberrant autonomic pattern during the post-exercise recovery phase in long QT syndrome patients
inferred← citeshttps://doi.org/10.1016/j.autneu.2023.103134openalex-snapshot
Sympathetic remodeling and altered angiotensin-converting enzyme 2 localization occur in patients with cardiac disease but are not exacerbated by severe COVID-19
inferred← citeshttps://doi.org/10.1016/j.bbadis.2022.166511openalex-snapshot
Cognitive decline in heart failure: Biomolecular mechanisms and benefits of exercise
inferred← citeshttps://doi.org/10.1016/j.ccep.2017.08.002openalex-snapshot
Cardiac Innervation and the Autonomic Nervous System in Sudden Cardiac Death
inferred← citeshttps://doi.org/10.1016/j.hlc.2019.11.002openalex-snapshot
The Brain-Heart Connection in Sympathetically Triggered Inherited Arrhythmia Syndromes
inferred← citeshttps://doi.org/10.1016/j.ijcard.2019.01.010openalex-snapshot
The effects of interleukin 17A on left stellate ganglion remodeling are mediated by neuroimmune communication in normal structural hearts
inferred← citeshttps://doi.org/10.1016/j.ijcard.2021.11.033openalex-snapshot
Cellular pathophysiology of Friedreich's ataxia cardiomyopathy
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102713openalex-snapshot
A single cell transcriptomics map of paracrine networks in the intrinsic cardiac nervous system
inferred← citeshttps://doi.org/10.1016/j.isci.2023.107709openalex-snapshot
Parasympathetic and sympathetic axons are bundled in the cardiac ventricles and undergo physiological reinnervation during heart regeneration
inferred← citeshttps://doi.org/10.1016/j.jacbts.2021.11.003openalex-snapshot
Research Opportunities in Autonomic Neural Mechanisms of Cardiopulmonary Regulation
inferred← citeshttps://doi.org/10.1016/j.jacep.2022.01.018openalex-snapshot
Proarrhythmic Effects of Sympathetic Activation Are Mitigated by Vagal Nerve Stimulation in Infarcted Hearts
inferred← citeshttps://doi.org/10.1016/j.jacep.2025.08.016openalex-snapshot
Adrenergic Hypersensitivity Drives Ventricular Arrhythmias Following Loss of Plexin-Mediated Cardiac Innervation
inferred← citeshttps://doi.org/10.1016/j.jjcc.2025.08.013openalex-snapshot
Cardiopulmonary neuro-immune reflex: From afferent stress signaling to peripheral myeloid memory
inferred← citeshttps://doi.org/10.1016/j.mehy.2020.109563openalex-snapshot
Neurogenic inflammation in fulminant myocarditis: May be a trigger
inferred← citeshttps://doi.org/10.1016/j.phymed.2018.01.019openalex-snapshot
Identifying potential quality markers of Xin-Su-Ning capsules acting on arrhythmia by integrating UHPLC-LTQ-Orbitrap, ADME prediction and network target analysis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.01.010openalex-snapshot
Pre-synaptic sympathetic calcium channels, cyclic nucleotide-coupled phosphodiesterases and cardiac excitability
inferred← citeshttps://doi.org/10.1016/j.semcdb.2023.01.001openalex-snapshot
The vagus nerve in cardiovascular physiology and pathophysiology: From evolutionary insights to clinical medicine
inferred← citeshttps://doi.org/10.1016/j.tins.2023.11.007openalex-snapshot
Identifying vagal sensory neurons driving the Bezold-Jarisch reflex
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.1c00636openalex-snapshot
Engineering Models of the Heart Left Ventricle
inferred← citeshttps://doi.org/10.1038/d41586-022-00508-6openalex-snapshot
Crosstalk between nerves, immune cells and plaques drives atherosclerosis
inferred← citeshttps://doi.org/10.1038/s41536-020-0096-1openalex-snapshot
Innervation: the missing link for biofabricated tissues and organs
inferred← citeshttps://doi.org/10.1038/s41569-019-0221-2openalex-snapshot
The autonomic nervous system and cardiac arrhythmias: current concepts and emerging therapies
inferred← citeshttps://doi.org/10.1038/s41586-023-06311-1openalex-snapshot
Spatially resolved multiomics of human cardiac niches
inferred← citeshttps://doi.org/10.1038/s44161-025-00746-7openalex-snapshot
Development and modeling of cardiac autonomic innervation
inferred← citeshttps://doi.org/10.1038/srep38898openalex-snapshot
Sympathetic neurons are a powerful driver of myocyte function in cardiovascular disease
inferred← citeshttps://doi.org/10.1039/d6lc00320fopenalex-snapshot
Modeling sympathetic neuro–cardiac interactions in a hiPSC-based microphysiological system
inferred← citeshttps://doi.org/10.1093/cvr/cvw225openalex-snapshot
Natriuretic peptides and peripheral autonomic neurotransmission: back to the A, B, and C’s.
inferred← citeshttps://doi.org/10.1093/cvr/cvz053openalex-snapshot
Cardiac innervation in acute myocardial ischaemia/reperfusion injury and cardioprotection
inferred← citeshttps://doi.org/10.1097/hco.0000000000001267openalex-snapshot
Assessment of cardiac autonomic function: from bench to bedside
inferred← citeshttps://doi.org/10.1098/rsos.200265openalex-snapshot
Combining tissue engineering and optical imaging approaches to explore interactions along the neuro-cardiac axis
inferred← citeshttps://doi.org/10.1098/rstb.2022.0173openalex-snapshot
Human induced pluripotent stem cell-derived cardiac myocytes and sympathetic neurons in disease modelling
inferred← citeshttps://doi.org/10.1101/2021.07.19.452502openalex-snapshot
Cardiac adenylyl cyclase type 8 overexpression increases locomotor activity in mice by modulating EEG-gamma oscillations
inferred← citeshttps://doi.org/10.1111/febs.70195openalex-snapshot
In vivo modeling of lethal congenital contracture syndrome 1 suggests pathomechanisms in cellular stress responses
inferred← citeshttps://doi.org/10.1111/jcmm.17344openalex-snapshot
17β‐Oestradiol facilitates M2 macrophage skewing and ameliorates arrhythmias in ovariectomized female infarcted rats
inferred← citeshttps://doi.org/10.1111/jocs.15652openalex-snapshot
Bilateral thoracoscopic sympathectomy for cardiac denervation in pediatric population: Does Kuntz nerve cauterization have an impact on success?
inferred← citeshttps://doi.org/10.1113/jp271869openalex-snapshot
Translational neurocardiology: preclinical models and cardioneural integrative aspects
inferred← citeshttps://doi.org/10.1113/jp272580openalex-snapshot
Cardiac autonomic control in health and disease
inferred← citeshttps://doi.org/10.1113/jp273120openalex-snapshot
Cardiac sympathetic innervation, from a different point of (re)view
inferred← citeshttps://doi.org/10.1113/jp274678openalex-snapshot
Defining the neural fulcrum for chronic vagus nerve stimulation: implications for integrated cardiac control
inferred← citeshttps://doi.org/10.1113/jp275693openalex-snapshot
Dynamics of neuroeffector coupling at cardiac sympathetic synapses
inferred← citeshttps://doi.org/10.1113/jp278839openalex-snapshot
Altered adrenergic response in myocytes bordering a chronic myocardial infarction underlies in vivo triggered activity and repolarization instability
inferred← citeshttps://doi.org/10.1113/jp281118openalex-snapshot
What gets on the nerves of cardiac patients? Pathophysiological changes in cardiac innervation
inferred← citeshttps://doi.org/10.1113/jp282828openalex-snapshot
Nerve growth factor transfer from cardiomyocytes to innervating sympathetic neurons activates TrkA receptors at the neuro‐cardiac junction
inferred← citeshttps://doi.org/10.1113/jp284059openalex-snapshot
Cholinergic collaterals arising from noradrenergic sympathetic neurons in mice
inferred← citeshttps://doi.org/10.1113/jp284739openalex-snapshot
Molecular and cellular neurocardiology in heart disease
inferred← citeshttps://doi.org/10.1113/jp286845openalex-snapshot
Cardiac sympathetic neurons are additional cells affected in genetically determined arrhythmogenic cardiomyopathy
inferred← citeshttps://doi.org/10.1126/science.adj0217openalex-snapshot
Heart failure causes sleepless nights
inferred← citeshttps://doi.org/10.1136/bjsports-2018-099578openalex-snapshot
Sudden cardiac arrest in sports: a video analysis
inferred← citeshttps://doi.org/10.1152/ajpheart.00546.2020openalex-snapshot
Functional coculture of sympathetic neurons and cardiomyocytes derived from human-induced pluripotent stem cells
inferred← citeshttps://doi.org/10.1152/ajpheart.00674.2020openalex-snapshot
Rapid measurement of cardiac neuropeptide dynamics by capacitive immunoprobe in the porcine heart
inferred← citeshttps://doi.org/10.1152/physrev.00007.2020openalex-snapshot
Sympathetic and sensory-motor nerves in peripheral small arteries
inferred← citeshttps://doi.org/10.1155/2021/2492286openalex-snapshot
The Preventive Effect of Cardiac Sympathetic Denervation Induced by 6‐OHDA on Myocardial Ischemia–Reperfusion Injury: The Changes of lncRNA/circRNAs‐miRNA‐mRNA Network of the Upper Thoracic Spinal Cord in Rats
inferred← citeshttps://doi.org/10.1159/000533405openalex-snapshot
Circulating Neuropeptide Y May Be a Biomarker for Diagnosing Atrial Fibrillation
inferred← citeshttps://doi.org/10.1161/circresaha.116.308446openalex-snapshot
Heart–Brain Axis
inferred← citeshttps://doi.org/10.1161/circresaha.121.319148openalex-snapshot
The Heart’s Little Brain
inferred← citeshttps://doi.org/10.1161/strokeaha.119.027732openalex-snapshot
Brain-Heart Interactions During Ischemic Processes
inferred← citeshttps://doi.org/10.1172/jci.insight.153913openalex-snapshot
High-resolution structure-function mapping of intact hearts reveals altered sympathetic control of infarct border zones
inferred← citeshttps://doi.org/10.1186/s12576-021-00794-1openalex-snapshot
Successful induction of deep hypothermia by isoflurane anesthesia and cooling in a non-hibernator, the rat
inferred← citeshttps://doi.org/10.1186/s12872-025-05442-9openalex-snapshot
Reprogramming heart failure: physiological orchestration and mechanistic decoding of exercise benefits
inferred← citeshttps://doi.org/10.1186/s12967-026-08085-2openalex-snapshot
Biological tissue engineering for Fontan failure using decellularized extracellular matrix: a systematic review
inferred← citeshttps://doi.org/10.1371/journal.pone.0180194openalex-snapshot
Recurrent myocardial infarction: Mechanisms of free-floating adaptation and autonomic derangement in networked cardiac neural control
inferred← citeshttps://doi.org/10.15829/1560-4071-2021-4035openalex-snapshot
Dynamics of heart failure markers and cardiac reverse remodeling in patients receiving cardiac contractility modulation therapy
inferred← citeshttps://doi.org/10.21203/rs.3.rs-543638/v1openalex-snapshot
Altered Sympathetic Control of Myocardial Infarct Border Zones: High-Resolution Mapping with Automated Structure Detection
inferred← citeshttps://doi.org/10.22541/au.158861363.33722117openalex-snapshot
An Integral Approach for Understanding the Bioactive Small Molecules in Cardiovascular Diseases
inferred← citeshttps://doi.org/10.23925/2176-901x.2011v14iespecial9p89-104openalex-snapshot
Fisioterapia no Cuidado ao Sistema Familiar: Uma Abordagem à Pessoa Idosa Fragilizada
inferred← citeshttps://doi.org/10.26538/tjnpr/v8i7.18openalex-snapshot
Antioxidant Activity and Cardioprotective Potential of a Nanoemulsion Mix of Rosmarinus officinalis and Centella asiatica in Gestational Diabetes Mellitus Zebrafish Larvae Model
inferred← citeshttps://doi.org/10.26538/tjnpr/v9i5.65openalex-snapshot
ERRATUM: Antioxidant Activity and Cardioprotective Potential of Nanoemulsion Mix of Rosmarinus officinalis and Centella asiatica in Gestational Diabetes Mellitus Zebrafish Larvae Model
inferred← citeshttps://doi.org/10.3389/fcvm.2022.842656openalex-snapshot
Untangling Peripheral Sympathetic Neurocircuits
inferred← citeshttps://doi.org/10.3389/fcvm.2026.1814067openalex-snapshot
Chemogenetic activation of cholinergic intrinsic cardiac ganglia improves border zone oxygenation and reduces arrhythmias during acute local ischemia
inferred← citeshttps://doi.org/10.3389/fncel.2024.1386355openalex-snapshot
Exploring the prospects, advancements, and challenges of in vitro modeling of the heart-brain axis
inferred← citeshttps://doi.org/10.3389/fnsyn.2022.949150openalex-snapshot
Healthy cardiac myocytes can decrease sympathetic hyperexcitability in the early stages of hypertension
inferred← citeshttps://doi.org/10.3389/fped.2021.680923openalex-snapshot
The Changes of T-Wave Amplitude and QT Interval Between the Supine and Orthostatic Electrocardiogram in Children With Dilated Cardiomyopathy
inferred← citeshttps://doi.org/10.3389/fphys.2019.00350openalex-snapshot
β-Adrenergic Receptor Stimulation and Alternans in the Border Zone of a Healed Infarct: An ex vivo Study and Computational Investigation of Arrhythmogenesis
inferred← citeshttps://doi.org/10.3389/fphys.2020.617459openalex-snapshot
Autonomic Modulation for Cardiovascular Disease
inferred← citeshttps://doi.org/10.3389/fphys.2023.1213959openalex-snapshot
Building blocks of microphysiological system to model physiology and pathophysiology of human heart
inferred← citeshttps://doi.org/10.3390/biology13020105openalex-snapshot
The Intrinsic Cardiac Nervous System: From Pathophysiology to Therapeutic Implications
inferred← citeshttps://doi.org/10.3390/cells10102629openalex-snapshot
Ventricular Arrhythmias in Ischemic Cardiomyopathy—New Avenues for Mechanism-Guided Treatment
inferred← citeshttps://doi.org/10.3390/cells14181434openalex-snapshot
Defined Composition of Culture Media Promotes Rodent Neonatal Cardiomyocyte Maturation and Enables Functional Neuro-Cardiac Co-Culture
inferred← citeshttps://doi.org/10.3390/ijms23063148openalex-snapshot
Human Neurons Form Axon-Mediated Functional Connections with Human Cardiomyocytes in Compartmentalized Microfluidic Chip
inferred← citeshttps://doi.org/10.3390/ijms25136959openalex-snapshot
The Brain–Heart Network of Syncope
inferred← citeshttps://doi.org/10.3390/jcdd8110149openalex-snapshot
From Mice to Mainframes: Experimental Models for Investigation of the Intracardiac Nervous System
inferred← citeshttps://doi.org/10.3791/60482openalex-snapshot
Capturing the Cardiac Injury Response of Targeted Cell Populations via Cleared Heart Three-Dimensional Imaging
inferred← citeshttps://doi.org/10.4022/jafib.2398openalex-snapshot
Vagal Stimulation and Arrhythmias
inferred← citeshttps://doi.org/10.4330/wjc.v12.i8.373openalex-snapshot
Sympathetic nervous system activation and heart failure: Current state of evidence and the pathophysiology in the light of novel biomarkers
inferred← citeshttps://doi.org/10.4330/wjc.v9.i6.508openalex-snapshot
Influence of cardiac nerve status on cardiovascular regulation and cardioprotection
inferred← citeshttps://doi.org/10.64898/2026.06.18.733286openalex-snapshot
Generative Modeling of Mouse Embryogenesis for Fate and Disease Prediction
inferred← citeshttps://doi.org/10.70675/bd0fceeaz96eez4a2fza380zdaaeaa5f3df8openalex-snapshot
Identification d'un réseau neuronal responsable de l'amplification ocytocinergique de l'arythmie sinusale respiratoire : implication dans les comportements de relaxation
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.