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...

SARS-CoV-2 spike protein-mediated cardiomyocyte fusion may contribute to increased arrhythmic risk in COVID-19

PloS one, 2023-03, Vol.18 (3), p.e0282151-e0282151

2023

Volltextzugriff (PDF)

MRAS Variants Cause Cardiomyocyte Hypertrophy in Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes: Additional Evidence for MRAS as a Definitive Noonan Syndrome-Susceptibility Gene

Circulation. Genomic and precision medicine, 2019-11, Vol.12 (11), p.e002648-e002648

2019

Volltextzugriff (PDF)

Patient-specific, re-engineered cardiomyocyte model confirms the circumstance-dependent arrhythmia risk associated with the African-specific common SCN5A polymorphism p.S1103Y: Implications for the increased sudden deaths observed in black individuals during the COVID-19 pandemic

Heart rhythm, 2022-05, Vol.19 (5), p.822-827

2022

Volltextzugriff (PDF)

Molecular characterization of the calcium release channel deficiency syndrome

JCI insight, 2020-08, Vol.5 (15)

2020

Volltextzugriff (PDF)

Acacetin, a Potent Transient Outward Current Blocker, May Be a Novel Therapeutic for KCND3 -Encoded Kv4.3 Gain-of-Function-Associated J-Wave Syndromes

Circulation. Genomic and precision medicine, 2022-10, Vol.15 (5), p.e003238-e003238

2022

Volltextzugriff (PDF)

Suppression-Replacement KCNQ1 Gene Therapy for Type 1 Long QT Syndrome

Circulation (New York, N.Y.), 2021-04, Vol.143 (14), p.1411-1425

2021

Volltextzugriff (PDF)

Single Construct Suppression and Replacement Gene Therapy for the Treatment of All CALM1 -, CALM2 -, and CALM3 -Mediated Arrhythmia Disorders

Circulation. Arrhythmia and electrophysiology, 2024-08, Vol.17 (8), p.e012036

2024

Volltextzugriff (PDF)

Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes

Stem cell reports, 2023-05, Vol.18 (5), p.1075-1089

2023

Volltextzugriff (PDF)

Characterization of N-terminal RYR2 variants outside CPVT1 hotspot regions using patient iPSCs reveal pathogenesis and therapeutic potential

Stem cell reports, 2022-09, Vol.17 (9), p.2023-2036

2022

Volltextzugriff (PDF)

Promise and Potential Peril With Lumacaftor for the Trafficking Defective Type 2 Long-QT Syndrome-Causative Variants, p.G604S, p.N633S, and p.R685P, Using Patient-Specific Re-Engineered Cardiomyocytes

Circulation. Genomic and precision medicine, 2020-10, Vol.13 (5), p.466-475

2020

Volltextzugriff (PDF)

Development of a Patient-Specific p.D85N-Potassium Voltage-Gated Channel Subfamily E Member 1–Induced Pluripotent Stem Cell–Derived Cardiomyocyte Model for Drug-Induced Long QT Syndrome

Circulation. Genomic and precision medicine, 2021-06, Vol.14 (3), p.e003234-e003234

2021

Volltextzugriff (PDF)

Characterization of the CACNA1C-R518C Missense Mutation in the Pathobiology of Long-QT Syndrome Using Human Induced Pluripotent Stem Cell Cardiomyocytes Shows Action Potential Prolongation and L-Type Calcium Channel Perturbation

Circulation. Genomic and precision medicine, 2019-08, Vol.12 (8), p.e002534-e002534

2019

Volltextzugriff (PDF)

Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish Community

JAMA cardiology, 2020-03, Vol.5 (3), p.13

2020

Volltextzugriff (PDF)

Suppression and Replacement Gene Therapy for KCNH2 -Mediated Arrhythmias

Circulation. Genomic and precision medicine, 2022-12, Vol.15 (6), p.e003719-e003719

2022

Volltextzugriff (PDF)

Abstract 11976: Functional Characterization of Calcium Handling Kinetics in Patient-Derived Ipsc-Cm Models of Pkp2-Mediated Arrhythmogenic Right Ventricular Cardiomyopathy

Circulation (New York, N.Y.), 2022-11, Vol.146 (Suppl_1), p.A11976-A11976

2022

Volltextzugriff (PDF)

Abstract 15036: Suppression-Replacement Gene Therapy for CALM1-Mediated Long QT Syndrome

Circulation (New York, N.Y.), 2022-11, Vol.146 (Suppl_1), p.A15036-A15036

2022

Volltextzugriff (PDF)

B-AB13-04 A PATIENT-SPECIFIC RE-ENGINEERED CARDIOMYOCYTE MODEL CONFIRMS THE CIRCUMSTANCE-DEPENDENT ARRHYTHMIA RISK ASSOCIATED WITH THE AFRICAN-SPECIFIC COMMON SCN5A POLYMORPHISM (P.SER1103TYR): IMPLICATIONS FOR THE INCREASED SUDDEN DEATHS OBSERVED IN BLACKS DURING THE COVID-19 PANDEMIC

Heart rhythm, 2021-08, Vol.18 (8), p.S26-S26

2021

Volltextzugriff (PDF)

Abstract 14260: Suppression and Replacement Gene Therapy for Type 2 Long QT Syndrome

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1), p.A14260-A14260

2021

Volltextzugriff (PDF)

Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias

Circulation. Genomic and precision medicine, 2022-10

2022

Volltextzugriff (PDF)

Abstract 12327: Precision Medicine for the Trafficking Defective Mutation, p. N633S, in the Type 2 Long QT Syndrome-associated, KCNH2-encoded Kv11.1 Channel Using Patient-specific Re-engineered Cardiomyocytes

Circulation (New York, N.Y.), 2019-11, Vol.140 (Suppl_1 Suppl 1), p.A12327-A12327

2019

Volltextzugriff (PDF)

Abstract 12295: Characterization of a Novel Homozygous Multi-exon Ryr2 Duplication Associated With Exertion-related Sudden Unexplained Death in the Young in the Amish Community Using Patient-specific Hipsc-cardiomyocytes

Circulation (New York, N.Y.), 2019-11, Vol.140 (Suppl_1 Suppl 1), p.A12295-A12295

2019

Volltextzugriff (PDF)

Abstract 12260: Whole Exome Molecular Autopsy With Copy Number Variant Analysis of Multiple Autopsy Negative Sudden Unexplained Deaths Among Amish Siblings Yields the Discovery of a Novel Homozygous Multi-exon Duplication in the Ryr2-Encoded Ryanodine Receptor

Circulation (New York, N.Y.), 2019-11, Vol.140 (Suppl_1 Suppl 1), p.A12260-A12260

2019

Volltextzugriff (PDF)

Skin-interfaced biosensors for advanced wireless physiological monitoring in neonatal and pediatric intensive-care units

Nature medicine, 2020-03, Vol.26 (3), p.418-429

2020

Volltextzugriff (PDF)

Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome

The New England journal of medicine, 2018-11, Vol.379 (22), p.2097-2107

2018

Volltextzugriff (PDF)

1 – 25 von 10.365

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(9.180)
Mit Volltextzugriff
(8.791)

Publikationsform

6 weitere anzeigen...

Weniger anzeigen...

Sprache

5 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(7.424)
Life Sciences & Biomedicine
(5.509)
Humans
(4.289)
Male
(2.374)
Female
(2.356)
Biological And Medical Sciences
(1.466)
Middle Aged
(1.388)
Animals
(1.302)
Adult
(1.276)
Physical Sciences
(1.133)
Aged
(1.128)
Medical Sciences
(1.121)
Technology
(950)
Science & Technology - Other Topics
(726)
Oncology
(623)
Mice
(615)
Neurosciences & Neurology
(560)
Surgery
(551)
Risk Factors
(534)
Adolescent
(528)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(5.302)
Electronic Journals Library
(4.840)
Ingenta
(3.941)
Journals@Ovid Full Text
(3.554)
Publisher website
(2.864)
Elsevier ScienceDirect Journals Complete
(1.866)
IngentaConnect Journals
(1.422)
Wiley Online Library
(1.117)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(1.024)
Wiley Online Library Full Collection 2018
(760)
Springer Nature - Connect here FIRST to enable access
(662)
springer (창간호~2014)
(655)
Ebook Central Perpetual and DDA
(547)
eBooks on EBSCOhost
(540)
JSTOR
(514)
Oxford Journals
(513)
Nexis Uni
(416)
Oxford Journals 2020 Medicine
(372)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(338)
Psychology & Behavioral Sciences Collection (EBSCO)
(263)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

The New England Journal Of Medicine
(161)
Nature
(151)
Nature Communications
(129)
Blood
(128)
Proceedings Of The National Academy Of Sciences - Pnas
(119)
Journal Of The American College Of Cardiology
(113)
Journal Of Clinical Oncology
(111)
Journal Of Medicinal Chemistry
(104)
Plos One
(96)
Circulation
(86)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

SARS-CoV-2 spike protein-mediated cardiomyocyte fusion may contribute to increased arrhythmic risk in COVID-19

MRAS Variants Cause Cardiomyocyte Hypertrophy in Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes: Additional Evidence for MRAS as a Definitive Noonan Syndrome-Susceptibility Gene

Patient-specific, re-engineered cardiomyocyte model confirms the circumstance-dependent arrhythmia risk associated with the African-specific common SCN5A polymorphism p.S1103Y: Implications for the increased sudden deaths observed in black individuals during the COVID-19 pandemic

Molecular characterization of the calcium release channel deficiency syndrome

Acacetin, a Potent Transient Outward Current Blocker, May Be a Novel Therapeutic for KCND3 -Encoded Kv4.3 Gain-of-Function-Associated J-Wave Syndromes

Suppression-Replacement KCNQ1 Gene Therapy for Type 1 Long QT Syndrome

Single Construct Suppression and Replacement Gene Therapy for the Treatment of All CALM1 -, CALM2 -, and CALM3 -Mediated Arrhythmia Disorders

KCNQ1 suppression-replacement gene therapy in transgenic rabbits with type 1 long QT syndrome

Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes

Characterization of N-terminal RYR2 variants outside CPVT1 hotspot regions using patient iPSCs reveal pathogenesis and therapeutic potential

Promise and Potential Peril With Lumacaftor for the Trafficking Defective Type 2 Long-QT Syndrome-Causative Variants, p.G604S, p.N633S, and p.R685P, Using Patient-Specific Re-Engineered Cardiomyocytes

Development of a Patient-Specific p.D85N-Potassium Voltage-Gated Channel Subfamily E Member 1–Induced Pluripotent Stem Cell–Derived Cardiomyocyte Model for Drug-Induced Long QT Syndrome

Characterization of the CACNA1C-R518C Missense Mutation in the Pathobiology of Long-QT Syndrome Using Human Induced Pluripotent Stem Cell Cardiomyocytes Shows Action Potential Prolongation and L-Type Calcium Channel Perturbation

Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish Community

Suppression and Replacement Gene Therapy for KCNH2 -Mediated Arrhythmias

Abstract 11976: Functional Characterization of Calcium Handling Kinetics in Patient-Derived Ipsc-Cm Models of Pkp2-Mediated Arrhythmogenic Right Ventricular Cardiomyopathy

Abstract 15036: Suppression-Replacement Gene Therapy for CALM1-Mediated Long QT Syndrome

B-AB13-04 A PATIENT-SPECIFIC RE-ENGINEERED CARDIOMYOCYTE MODEL CONFIRMS THE CIRCUMSTANCE-DEPENDENT ARRHYTHMIA RISK ASSOCIATED WITH THE AFRICAN-SPECIFIC COMMON SCN5A POLYMORPHISM (P.SER1103TYR): IMPLICATIONS FOR THE INCREASED SUDDEN DEATHS OBSERVED IN BLACKS DURING THE COVID-19 PANDEMIC

Abstract 14260: Suppression and Replacement Gene Therapy for Type 2 Long QT Syndrome

Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias

Abstract 12327: Precision Medicine for the Trafficking Defective Mutation, p. N633S, in the Type 2 Long QT Syndrome-associated, KCNH2-encoded Kv11.1 Channel Using Patient-specific Re-engineered Cardiomyocytes

Abstract 12295: Characterization of a Novel Homozygous Multi-exon Ryr2 Duplication Associated With Exertion-related Sudden Unexplained Death in the Young in the Amish Community Using Patient-specific Hipsc-cardiomyocytes

Abstract 12260: Whole Exome Molecular Autopsy With Copy Number Variant Analysis of Multiple Autopsy Negative Sudden Unexplained Deaths Among Amish Siblings Yields the Discovery of a Novel Homozygous Multi-exon Duplication in the Ryr2-Encoded Ryanodine Receptor

Skin-interfaced biosensors for advanced wireless physiological monitoring in neonatal and pediatric intensive-care units

Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome

Suchergebnisse filtern