UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.617

Sortiert nach

Home smoking bans and secondhand smoke exposure in Mexico and the US

Preventive medicine, 2009-03, Vol.48 (3), p.207-212

2009

Volltextzugriff (PDF)

Alterations in Calcium Handling Are a Common Feature in an Arrhythmogenic Cardiomyopathy Cell Model Triggered by Desmosome Genes Loss

International journal of molecular sciences, 2023-01, Vol.24 (3), p.2109

2023

Volltextzugriff (PDF)

Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient

Journal of molecular and cellular cardiology, 2018-01, Vol.114, p.10-19

2018

Volltextzugriff (PDF)

Loss of sodium current caused by a Brugada syndrome–associated variant is determined by patient-specific genetic background

Heart rhythm, 2024-03, Vol.21 (3), p.331-339

2024

Volltextzugriff (PDF)

Crossing Borders: The Impact of the California Tobacco Control Program on Both Sides of the US-Mexico Border

American journal of public health (1971), 2008-02, Vol.98 (2), p.258-267

2008

Volltextzugriff (PDF)

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

Heart rhythm, 2015-07, Vol.12 (7), p.1636-1643

2015

Volltextzugriff (PDF)

Experimental Models of Brugada syndrome

International journal of molecular sciences, 2019-04, Vol.20 (9), p.2123

2019

Volltextzugriff (PDF)

Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient

Stem cell research, 2023-12, Vol.73, p.103239-103239, Article 103239

2023

Volltextzugriff (PDF)

A Missense Mutation in the Sodium Channel [beta]2 Subunit Reveals SCN2B as a New Candidate Gene for Brugada Syndrome

Human mutation, 2013-07, Vol.34 (7), p.961-966

2013

Volltextzugriff (PDF)

Epigenetic Changes Governing Scn5a Expression in Denervated Skeletal Muscle

International journal of molecular sciences, 2021-03, Vol.22 (5), p.2755

2021

Volltextzugriff (PDF)

A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome

PloS one, 2013-01, Vol.8 (1), p.e53220-e53220

2013

Volltextzugriff (PDF)

Generation of an induced pluripotent stem cell line from a healthy Caucasian male

Stem cell research, 2022-04, Vol.60, p.102717-102717, Article 102717

2022

Volltextzugriff (PDF)

Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males

Circulation (New York, N.Y.), 2002-10, Vol.106 (15), p.2004-2011

2002

Volltextzugriff (PDF)

Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A

Stem cell research, 2022-08, Vol.63, p.102847-102847, Article 102847

2022

Volltextzugriff (PDF)

Competencia clínica de médicos de seguridad social guatemaltecos para manejar hepatitis virales en atención primaria

Revista de salud pública (Bogotá, Colombia), 2017-02, Vol.19 (1), p.94-98

2017

Volltextzugriff (PDF)

Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A

Nutrients, 2019-07, Vol.11 (7), p.1656

2019

Volltextzugriff (PDF)

Protein arginine methyl transferases-3 and -5 increase cell surface expression of cardiac sodium channel

FEBS letters, 2013-10, Vol.587 (19), p.3159-3165

2013

Volltextzugriff (PDF)

Vasoregulation by the β1 subunit of the calcium-activated potassium channel

Nature (London), 2000-10, Vol.407 (6806), p.870-876

2000

Volltextzugriff (PDF)

A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death

Circulation. Cardiovascular genetics, 2010-04, Vol.3 (2), p.199

2010

Volltextzugriff (PDF)

Kir2.3 knock-down decreases IK1 current in neonatal rat cardiomyocytes

FEBS letters, 2008-06, Vol.582 (15), p.2338-2342

2008

Volltextzugriff (PDF)

Correlates of Home Smoking Bans among Mexican-Americans

American journal of health promotion, 2007-03, Vol.21 (4), p.229-236

2007

Volltextzugriff (PDF)

Large-conductance calcium-activated potassium current modulates excitability in isolated canine intracardiac neurons

American Journal of Physiology: Cell Physiology, 2013-02, Vol.304 (3), p.C280-C286

2013

Volltextzugriff (PDF)

SAFETY THRESHOLD FOR CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA IN CHILDHOOD UNDER BETABLOCKER TREATMENT

Journal of the American College of Cardiology, 2014-04, Vol.63 (12), p.A425-A425

2014

Volltextzugriff (PDF)

Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation

Forensic science international : genetics, 2019-11, Vol.43, p.102159-102159, Article 102159

2019

Volltextzugriff (PDF)

A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome

Heart rhythm, 2014-07, Vol.11 (7), p.1202-1209

2014

Volltextzugriff (PDF)

1 – 25 von 1.617

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.473)
Mit Volltextzugriff
(1.474)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

4 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)
... seit 90 Tagen
(8)

Menü

Weitere Dienste

Einstellungen

Home smoking bans and secondhand smoke exposure in Mexico and the US

Alterations in Calcium Handling Are a Common Feature in an Arrhythmogenic Cardiomyopathy Cell Model Triggered by Desmosome Genes Loss

Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient

Loss of sodium current caused by a Brugada syndrome–associated variant is determined by patient-specific genetic background

Crossing Borders: The Impact of the California Tobacco Control Program on Both Sides of the US-Mexico Border

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

Experimental Models of Brugada syndrome

Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient

A Missense Mutation in the Sodium Channel [beta]2 Subunit Reveals SCN2B as a New Candidate Gene for Brugada Syndrome

Epigenetic Changes Governing Scn5a Expression in Denervated Skeletal Muscle

A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome

Generation of an induced pluripotent stem cell line from a healthy Caucasian male

Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males

Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A

Competencia clínica de médicos de seguridad social guatemaltecos para manejar hepatitis virales en atención primaria

Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A

Protein arginine methyl transferases-3 and -5 increase cell surface expression of cardiac sodium channel

Vasoregulation by the β1 subunit of the calcium-activated potassium channel

A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death

Kir2.3 knock-down decreases IK1 current in neonatal rat cardiomyocytes

Correlates of Home Smoking Bans among Mexican-Americans

Large-conductance calcium-activated potassium current modulates excitability in isolated canine intracardiac neurons

SAFETY THRESHOLD FOR CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA IN CHILDHOOD UNDER BETABLOCKER TREATMENT

Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation

A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome

Suchergebnisse filtern