Progressive Atrioventricular Conduction Defects and Heart Failure in Mice Expressing a Mutant CSX/Nkx2.5 Homeoprotein

Journal of Clinical Investigation - United States
doi 10.1172/jci12694
Full Text
Abstract

Available in full text

Categories
Medicine
Date
Authors
Publisher

American Society for Clinical Investigation

Related search

Atrioventricular Conduction in Secundum Atrial Septal Defects

Circulation
Cardiovascular MedicinePhysiologyCardiology
1973English

Atrial Septal Defect-Atrioventricular Conduction Defects Syndrome

2020English

Cardiac and Extracardiac Expression of CSX/Nkx2.5 Homeodomain Protein

Circulation Research
Cardiovascular MedicinePhysiologyCardiology
1998English

Patterns of Atrioventricular Conduction in the Human Heart

Circulation Research
Cardiovascular MedicinePhysiologyCardiology
1970English

Erratum: Neurofibrillary Tangles, Amyotrophy and Progressive Motor Disturbance in Mice Expressing Mutant (P301L) Tau Protein

Nature Genetics
Genetics
2000English

Atrioventricular Conduction Defects in Patients Presenting With Syncope and Normal PR Interval.

Heart
Cardiovascular MedicineCardiology
1972English

Phenomenon of the Gap in Atrioventricular Conduction in the Human Heart

Circulation Research
Cardiovascular MedicinePhysiologyCardiology
1970English

Cis-Acting Elements Regulate Expression of the Cardiac Specific Homeobox Gene, CSX/Nkx2.5

Pediatric Research
Child HealthPediatricsPerinatology
1999English

Concealed and Supernormal Atrioventricular Conduction

Circulation
Cardiovascular MedicinePhysiologyCardiology
1971English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy