UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Delayed rectifier K+ currents and cardiac repolarization

Journal of molecular and cellular cardiology, 2010-01, Vol.48 (1), p.37-44

2010

Volltextzugriff (PDF)

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

Circulation (New York, N.Y.), 2004-05, Vol.109 (20), p.2394-2397

2004

Volltextzugriff (PDF)

Impaired KCNQ1–KCNE1 and Phosphatidylinositol-4,5-Bisphosphate Interaction Underlies the Long QT Syndrome

Circulation research, 2005-04, Vol.96 (7), p.730-739

2005

Volltextzugriff (PDF)

Transforming growth factor β receptor inhibition prevents ventricular fibrosis in a mouse model of progressive cardiac conduction disease

Cardiovascular research, 2017-04, Vol.113 (5), p.464-474

2017

Volltextzugriff (PDF)

14-3-3 Is a Regulator of the Cardiac Voltage-Gated Sodium Channel Nav1.5

Circulation research, 2006-06, Vol.98 (12), p.1538-1546

2006

Volltextzugriff (PDF)

Marine n-3 PUFAs modulate IKs gating, channel expression, and location in membrane microdomains

Cardiovascular research, 2015-02, Vol.105 (2), p.223-232

2015

Volltextzugriff (PDF)

Computer modeling of whole-cell voltage-clamp analyses to delineate guidelines for good practice of manual and automated patch-clamp

Scientific reports, 2021-02, Vol.11 (1), p.3282-3282, Article 3282

2021

Volltextzugriff (PDF)

Kv7.1 (KCNQ1) properties and channelopathies

The Journal of physiology, 2008-04, Vol.586 (7), p.1785-1789

2008

Volltextzugriff (PDF)

Phosphatidylinositol-4,5-Bisphosphate (PIP2) Stabilizes the Open Pore Conformation of the Kv11.1 (hERG) Channel

Biophysical journal, 2010-08, Vol.99 (4), p.1110-1118

2010

Volltextzugriff (PDF)

LQT1-associated Mutations Increase KCNQ1 Proteasomal Degradation Independently of Derlin-1

The Journal of biological chemistry, 2009-02, Vol.284 (8), p.5250-5256

2009

Volltextzugriff (PDF)

The N-Terminal Juxtamembranous Domain of KCNQ1 Is Critical for Channel Surface Expression: Implications in the Romano-Ward LQT1 Syndrome

Circulation research, 2006-11, Vol.99 (10), p.1076-1083

2006

Volltextzugriff (PDF)

KCNQ1 Channels Voltage Dependence through a Voltage-dependent Binding of the S4-S5 Linker to the Pore Domain

The Journal of biological chemistry, 2011-01, Vol.286 (1), p.707-716

2011

Volltextzugriff (PDF)

Neural modulation of ion channels in cardiac arrhythmias: Clinical implications and future investigations

Heart rhythm, 2010-06, Vol.7 (6), p.847-849

2010

Volltextzugriff (PDF)

Dysfunction of the Voltage‐Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

Journal of the American Heart Association, 2016-06, Vol.5 (6), p.n/a

2016

Volltextzugriff (PDF)

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Journal of the American College of Cardiology, 2003-02, Vol.41 (4), p.643-652

2003

Volltextzugriff (PDF)

KCNE1–KCNQ1 osmoregulation by interaction of phosphatidylinositol‐4,5‐bisphosphate with Mg2+ and polyamines

The Journal of physiology, 2010-09, Vol.588 (18), p.3471-3483

2010

Volltextzugriff (PDF)

Microarray Analysis Reveals Complex Remodeling of Cardiac Ion Channel Expression With Altered Thyroid Status: Relation to Cellular and Integrated Electrophysiology

Circulation research, 2003-02, Vol.92 (2), p.234-242

2003

Volltextzugriff (PDF)

Toward Personalized Medicine: Using Cardiomyocytes Differentiated From Urine-Derived Pluripotent Stem Cells to Recapitulate Electrophysiological Characteristics of Type 2 Long QT Syndrome

Journal of the American Heart Association, 2015-09, Vol.4 (9), p.e002159-e002159

2015

Volltextzugriff (PDF)

Atrial fibrillation: Is NO an answer for refractoriness?

Cardiovascular research, 2006-10, Vol.72 (1), p.7-8

BARO, I

2006

Volltextzugriff (PDF)

Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr -IKs α-subunit interaction

Heart rhythm, 2009-12, Vol.6 (12), p.1792-1801

2009

Volltextzugriff (PDF)

Torsades de pointes complicating atrioventricular block: Evidence for a genetic predisposition

Heart rhythm, 2007-02, Vol.4 (2), p.170-174

2007

Volltextzugriff (PDF)

HIV-Tat induces a decrease in I Kr and I Ks via reduction in phosphatidylinositol-(4,5)-bisphosphate availability

Journal of molecular and cellular cardiology, 2016-10, Vol.99, p.1-13

2016

Volltextzugriff (PDF)

sigma(2)-receptor ligand-mediated inhibition of inwardly rectifying K(+) channels in the heart

The Journal of pharmacology and experimental therapeutics, 2007-07, Vol.322 (1), p.341

2007

Volltextzugriff (PDF)

Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy

Journal of the American College of Cardiology, 2012-07, Vol.60 (2), p.144-156

2012

Volltextzugriff (PDF)

Transfer of Rolf S3-S4 Linker to hERG Eliminates Activation Gating but Spares Inactivation

Biophysical journal, 2009-09, Vol.97 (5), p.1323-1334

2009

Volltextzugriff (PDF)

1 – 25 von 63

Suche als RSS-Feed

Aktive Filter

KollektionMEDLINE

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(62)
Mit Volltextzugriff
(59)

Publikationsform

Artikel
(63)

Sprache

Englisch
(63)

Erscheinungsjahr

n.n

Thema

Science & Technology
(52)
Life Sciences & Biomedicine
(50)
Humans
(49)
Animals
(37)
Cos Cells
(27)
Male
(25)
Cardiac & Cardiovascular Systems
(24)
Cardiovascular System & Cardiology
(24)
Female
(21)
Life Sciences
(20)
Patch-Clamp Techniques
(18)
Biological And Medical Sciences
(15)
Adult
(13)
Cercopithecus Aethiops
(13)
Kcnq1 Potassium Channel - Metabolism
(13)
Long Qt Syndrome - Genetics
(12)
Mutation
(12)
Medical Sciences
(11)
Middle Aged
(11)
Electrocardiography
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Delayed rectifier K+ currents and cardiac repolarization

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

Impaired KCNQ1–KCNE1 and Phosphatidylinositol-4,5-Bisphosphate Interaction Underlies the Long QT Syndrome

Transforming growth factor β receptor inhibition prevents ventricular fibrosis in a mouse model of progressive cardiac conduction disease

14-3-3 Is a Regulator of the Cardiac Voltage-Gated Sodium Channel Nav1.5

Marine n-3 PUFAs modulate IKs gating, channel expression, and location in membrane microdomains

Computer modeling of whole-cell voltage-clamp analyses to delineate guidelines for good practice of manual and automated patch-clamp

Kv7.1 (KCNQ1) properties and channelopathies

Phosphatidylinositol-4,5-Bisphosphate (PIP2) Stabilizes the Open Pore Conformation of the Kv11.1 (hERG) Channel

LQT1-associated Mutations Increase KCNQ1 Proteasomal Degradation Independently of Derlin-1

The N-Terminal Juxtamembranous Domain of KCNQ1 Is Critical for Channel Surface Expression: Implications in the Romano-Ward LQT1 Syndrome

KCNQ1 Channels Voltage Dependence through a Voltage-dependent Binding of the S4-S5 Linker to the Pore Domain

Neural modulation of ion channels in cardiac arrhythmias: Clinical implications and future investigations

Dysfunction of the Voltage‐Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

KCNE1–KCNQ1 osmoregulation by interaction of phosphatidylinositol‐4,5‐bisphosphate with Mg2+ and polyamines

Microarray Analysis Reveals Complex Remodeling of Cardiac Ion Channel Expression With Altered Thyroid Status: Relation to Cellular and Integrated Electrophysiology

Toward Personalized Medicine: Using Cardiomyocytes Differentiated From Urine-Derived Pluripotent Stem Cells to Recapitulate Electrophysiological Characteristics of Type 2 Long QT Syndrome

Atrial fibrillation: Is NO an answer for refractoriness?

Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr -IKs α-subunit interaction

Torsades de pointes complicating atrioventricular block: Evidence for a genetic predisposition

HIV-Tat induces a decrease in I Kr and I Ks via reduction in phosphatidylinositol-(4,5)-bisphosphate availability

sigma(2)-receptor ligand-mediated inhibition of inwardly rectifying K(+) channels in the heart

Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy

Transfer of Rolf S3-S4 Linker to hERG Eliminates Activation Gating but Spares Inactivation

Aktive Filter

Suchergebnisse filtern