Results 131 to 140 of about 46,008 (253)

Inhibitory effect of oestradiol on the cardiac KV7.1/KCNE1 channel is species dependent

open access: yesExperimental Physiology, Volume 111, Issue 1, Page 54-68, 1 January 2026.
Abstract Oestradiol (17β‐E2) is reported to prolong the cardiac action potential duration and QT interval, in part by affecting cardiac ion channels. Previous studies found inhibiting 17β‐E2 effects on the repolarizating cardiac KV7.1/KCNE1 channel, or its native current, in heterologous expression systems or tissue from animal species.
Veronika A. Linhart   +2 more
wiley   +1 more source

Insufficient or Excessive Niacin Intake Induced Glucose and Lipid Metabolic Disorders and Impaired Liver Health in Nile Tilapia

open access: yesAquaculture Nutrition, Volume 2026, Issue 1, 2026.
Niacin (vitamin B3) is involved in the metabolic regulation of energy metabolism in animals. However, both deficiency and excess supplementation of niacin can induce profound physiological disturbances in fish. The present study investigated the effect of niacin on energy metabolism and liver health in Nile tilapia (Oreochromis niloticus).
Ruixin Li   +11 more
wiley   +1 more source

Facilitation of I Kr current by some hERG channel blockers suppresses early afterdepolarizations. [PDF]

open access: yes, 2019
Drug-induced block of the cardiac rapid delayed rectifying potassium current (I Kr), carried by the human ether-a-go-go-related gene (hERG) channel, is the most common cause of acquired long QT syndrome.
Chen, I-Shan   +6 more
core   +1 more source

Arrhythmogenic Mechanisms of Novel Biomarkers in Cardiac Electrophysiology

open access: yesCardiology Research and Practice, Volume 2026, Issue 1, 2026.
Arrhythmia is an important cause of cardiovascular disease deaths and a serious threat to human health, but the current means of identification are limited. Biomarkers, with the advantages of easy access and rapid detection, have shown significant value in arrhythmia risk prediction, precision diagnosis, and prognosis assessment.
Jin Liu   +4 more
wiley   +1 more source

Molecular and clinical determinants of drug-induced long QT syndrome: an iatrogenic channelopathy. [PDF]

open access: yes, 2004
More than 70 drugs present on the Swiss market can cause drug-induced long QT syndrome (LQTS), which is associated with torsades de pointes (TdP) arrhythmias, potentially leading to sudden cardiac death. Basic and clinical investigations performed during
Abriel, H.   +7 more
core  

Personalizing therapies over the course of hormone receptor‐positive/HER2‐negative metastatic breast cancer

open access: yesCA: A Cancer Journal for Clinicians, Volume 76, Issue 1, January/February 2026.
ABSTRACT The hormone receptor (HR)‐positive/human epidermal growth factor receptor 2 (HER2)‐negative breast cancer subtype accounts for most early and metastatic breast cancer (MBC) cases. HR‐positive/HER2‐negative MBC is characterized by a relatively prolonged, although variable, disease course and substantial intertumoral and intratumoral ...
Akshara Singareeka Raghavendra   +5 more
wiley   +1 more source

Upgrade from ICD to CRT-D: clinical andhaemodynamic impact of biventricular pacing in apatient with acquired long QT syndrome [PDF]

open access: gold, 2015
Damian Kawecki   +6 more
openalex   +1 more source

Electrocardiographic manifestation of cardiac repolarization dispersion [PDF]

open access: yes, 2019
Alterations of repolarization heterogeneity in the heart have been established as anAlterations of repolarization heterogeneity in the heart have been established as ...
Sedova Ksenia
core  

Ventricular Fibrillation Caused by a Low-Rate Pacemaker

open access: yesForbes Tıp Dergisi
After undergoing surgery for a perimembranous ventricular septal defect and discrete membrane resection, a 7-year-old patient developed complete atrioventricular block and received an epicardial pacemaker.
Hüseyin YILDIZ   +2 more
doaj   +1 more source

Early LQT2 Nonsense Mutation Generates N-Terminally Truncated hERG Channels with Altered Gating Properties by the Reinitiation of Translation

open access: yes, 2012
Mutations in the human ether-a-go-go-related gene (hERG) result in long QT syndrome type 2 (LQT2). The hERG gene encodes a K+ channel that contributes to the repolarization of the cardiac action potential.
Gong, Qiuming   +3 more
core   +1 more source

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