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Katja Elisabeth Odening (1978-)

Ärztin

Name	Katja Elisabeth Odening
Zeit	1978- (Lebensdaten)
Ort	Mainz (Geburtsort) Deutschland
Akademischer Grad bzw. Titel	Dr. (an der Medizinischen Fakultät der Universität Heidelberg) (2004)
Beruf	Ärztin (charakteristischer Beruf)
Weitere Angaben	Habil.-Schr. an der Medizinischen Fakultät der Universität Freiburg (Breisgau), 2012
Datensatztyp	Person
GND-Nummer	129240664
Datensatz-ID	129240664
Beteiligt an alle anzeigen Beneficial normalization of cardiac repolarization by carnitine in transgenic SQT1 rabbit models KCNQ1 suppression-replacement gene therapy in transgenic rabbits with type 1 long QT syndrome Mechano‐electrical interactions and heterogeneities in wild‐type and drug‐induced long QT syndrome rabbits Whole-heart computational modelling provides further mechanistic insights into ST-elevation in Brugada syndrome Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2 vhl-1 beeinflusst osmotische und oxidative Stressantwort in C. elegans A computational model of rabbit geometry and ECG: Optimizing ventricular activation sequence and APD distribution Catheter ablation of short-coupled variant of torsade de pointes Effects of short term adiponectin receptor agonism on cardiac function and energetics in diabetic db/db mice Genotype-specific ECG-based risk stratification approaches in patients with long-QT syndrome Oxytocin exerts harmful cardiac repolarization prolonging effects in drug-induced LQTS Transgenic rabbit models for cardiac disease research Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing Rolle von TRAF1 und NF-kappaB als potentielle therapeutische Zielstrukturen in der Chronischen Lymphatischen Leukämie Sex-differences in short QT syndrome: a systematic literature review and pooled analysis Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome Transgenic LQT2, LQT5, and LQT2‐5 rabbit models with decreased repolarisation reserve for prediction of drug‐induced ventricular arrhythmias Transgenic rabbit models in proarrhythmia research Dysregulation of the mitochondrial proteome occurs in mice lacking adiponectin receptor 1 Dysregulation of the mitochondrial proteome occurs in mice lacking adiponectin receptor 1 Fascicular parasystole and recurrent syncope – a case report Genotype-specific beneficial QT-shortening effects of docosahexaenoic acid in transgenic LQT1, LQT2, LQT5 and LQT2-5 rabbit models In vivo und ex vivo Charakterisierung des arrhythmogenen Phänotyps transgener SQT1 Kaninchen = In vivo and ex vivo characterization of the arrhythmic phenotype of transgenic SQT1 rabbits Der Einfluss von Zellzyklusregulatoren auf die Entwicklung, Gesundheit und Lebensdauer von C. elegans Genotyp- und geschlechtsspezifische Unterschiede der zellulären Elektrophysiologie und Kalziumhomöostase in transgenen LQT1 und Wildtyp Kaninchen Normalization of QT interval duration in a long QT syndrome patient during pregnancy and the postpartum period due to sex hormone effects on cardiac repolarization Hormonelle und medikamentöse Beeinflussung der Arrhythmogenese in transgenen Tiermodellen des Long-QT-Syndroms Komplementresistenz P-gp exprimierender Multidrug-resistenter Ovarialkarzinomzelllinien

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Katalog der Deutschen Nationalbibliothek

Katja Elisabeth Odening (1978-)

Beneficial normalization of cardiac repolarization by carnitine in transgenic SQT1 rabbit models

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

Mechano‐electrical interactions and heterogeneities in wild‐type and drug‐induced long QT syndrome rabbits

Whole-heart computational modelling provides further mechanistic insights into ST-elevation in Brugada syndrome

Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2

vhl-1 beeinflusst osmotische und oxidative Stressantwort in C. elegans

A computational model of rabbit geometry and ECG: Optimizing ventricular activation sequence and APD distribution

Catheter ablation of short-coupled variant of torsade de pointes

Effects of short term adiponectin receptor agonism on cardiac function and energetics in diabetic db/db mice

Genotype-specific ECG-based risk stratification approaches in patients with long-QT syndrome

Oxytocin exerts harmful cardiac repolarization prolonging effects in drug-induced LQTS

Transgenic rabbit models for cardiac disease research

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing

Rolle von TRAF1 und NF-kappaB als potentielle therapeutische Zielstrukturen in der Chronischen Lymphatischen Leukämie

Sex-differences in short QT syndrome: a systematic literature review and pooled analysis

Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome

Transgenic LQT2, LQT5, and LQT2‐5 rabbit models with decreased repolarisation reserve for prediction of drug‐induced ventricular arrhythmias

Transgenic rabbit models in proarrhythmia research

Dysregulation of the mitochondrial proteome occurs in mice lacking adiponectin receptor 1

Dysregulation of the mitochondrial proteome occurs in mice lacking adiponectin receptor 1

Fascicular parasystole and recurrent syncope – a case report

Genotype-specific beneficial QT-shortening effects of docosahexaenoic acid in transgenic LQT1, LQT2, LQT5 and LQT2-5 rabbit models

In vivo und ex vivo Charakterisierung des arrhythmogenen Phänotyps transgener SQT1 Kaninchen = In vivo and ex vivo characterization of the arrhythmic phenotype of transgenic SQT1 rabbits

Der Einfluss von Zellzyklusregulatoren auf die Entwicklung, Gesundheit und Lebensdauer von C. elegans

Genotyp- und geschlechtsspezifische Unterschiede der zellulären Elektrophysiologie und Kalziumhomöostase in transgenen LQT1 und Wildtyp Kaninchen

Normalization of QT interval duration in a long QT syndrome patient during pregnancy and the postpartum period due to sex hormone effects on cardiac repolarization

Hormonelle und medikamentöse Beeinflussung der Arrhythmogenese in transgenen Tiermodellen des Long-QT-Syndroms

Komplementresistenz P-gp exprimierender Multidrug-resistenter Ovarialkarzinomzelllinien