C. Maguire

发表

Nkx2.5 homeoprotein regulates expression of gap junction protein connexin 43 and sarcomere organization in postnatal cardiomyocytes.

W. Manning, P. Kang, C. Berul, 2003, Journal of molecular and cellular cardiology.

A mouse model of congenital heart disease: cardiac arrhythmias and atrial septal defect caused by haploinsufficiency of the cardiac transcription factor Csx/Nkx2.5.

J. Seidman, C. Seidman, C. Berul, 2002, Cold Spring Harbor symposia on quantitative biology.

Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein.

W. Manning, C. Berul, H. Wakimoto, 2001, The Journal of clinical investigation.

Maturational Atrioventricular Nodal Physiology in the Mouse

C. Berul, H. Wakimoto, C. Maguire, 2000, Journal of cardiovascular electrophysiology.

Cardiomyopathy in Irx4-Deficient Mice Is Preceded by Abnormal Ventricular Gene Expression

D. Kass, N. Rosenthal, J. Seidman, 2001, Molecular and Cellular Biology.

Function follows form: cardiac conduction system defects in Nkx2-5 mutation.

C. Berul, S. Izumo, R. Gourdie, 2004, The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology.

Deriving Cardiomyocytes from Human Amniocytes

H. Yost, Ryan Sunderland, B. Demarest, 2018, bioRxiv.

Focal Adhesion Kinase Regulates Smooth Muscle Cell Recruitment to the Developing Vasculature

M. Majesky, Joan M. Taylor, C. Mack, 2011, Arteriosclerosis, thrombosis, and vascular biology.

A sonic hedgehog signaling domain in the arterial adventitia supports resident Sca1+ smooth muscle progenitor cells

M. Majesky, V. Bautch, X. Dong, 2008, Proceedings of the National Academy of Sciences.

Chapter 9. Development of coronary vessels.

M. Majesky, X. Dong, San-pin Wu, 2008, Methods in enzymology.

In Vivo Electrophysiologic Studies in Endothelial Nitric Oxide Synthase (eNOS)‐Deficient Mice

C. Berul, H. Wakimoto, T. Michel, 2001, Journal of cardiovascular electrophysiology.

Evaluation of the role of I(KACh) in atrial fibrillation using a mouse knockout model.

D. Clapham, W. Pu, C. Berul, 2001, Journal of the American College of Cardiology.

A Targeted Disruption in Connexin40 Leads to Distinct Atrioventricular Conduction Defects

C. Berul, H. Wakimoto, D. Paul, 2000, Journal of Interventional Cardiac Electrophysiology.

Neurite outgrowth deficits caused by rare PLXNB1 mutation in pediatric bipolar disorder

H. Coon, Jeffrey S. Anderson, M. Yandell, 2022, medRxiv.

Implications of ventricular arrhythmia vulnerability during murine electrophysiology studies.

K. Gauvreau, P. Hammer, C. Berul, 2003, Physiological genomics.

Familial Hypertrophic Cardiomyopathy Mice Display Gender Differences in Electrophysiological Abnormalities

J. Seidman, C. Seidman, C. Berul, 1997, Journal of Interventional Cardiac Electrophysiology.

Relationship of lipoprotein-associated phospholipase A2 and oxidized low density lipoprotein in carotid atherosclerosis[S]

R. Wolfert, K. Vickers, A. Burns, 2009, Journal of Lipid Research.

QT Dispersion in α-Myosin Heavy-Chain Familial Hypertrophic Cardiomyopathy Mice

J. Seidman, C. Seidman, C. Berul, 1999, Pediatric Research.

Nkx 2-5 mutation causes anatomic hypoplasia of the cardiac conduction system

D. Roden, C. Berul, H. Wakimoto, 2022 .

Mitochondrial calcium uniporter stabilization preserves energetic homeostasis during Complex I impairment

S. Franklin, M. Tristani-Firouzi, S. Sommakia, 2022, Nature Communications.

The mitochondrial calcium uniporter compensates for Complex I dysfunction

S. Franklin, M. Tristani-Firouzi, S. Sommakia, 2021 .

Cardiac electrophysiological phenotypes in postnatal expression of Nkx2.5 transgenic mice

C. Berul, H. Wakimoto, S. Izumo, 2003, Genesis.

Developmentally Modulated Cardiac Conduction Failure in Transgenic Mice with Fetal or Postnatal Overexpression of DNA Nonbinding Mutant Nkx2.5

C. Berul, H. Wakimoto, S. Izumo, 2002, Journal of cardiovascular electrophysiology.

Absence of Msx2 Does Not Affect Cardiac Conduction or Rescue Conduction Defects Associated with Nkx2‐5 Mutation

C. Berul, H. Wakimoto, S. Izumo, 2005, Journal of cardiovascular electrophysiology.

Loss of MicroRNAs in Neural Crest Leads to Cardiovascular Syndromes Resembling Human Congenital Heart Defects

Jian-Fu Chen, Da-Zhi Wang, Ruhang Tang, 2010, Arteriosclerosis, thrombosis, and vascular biology.

14-3-3ε Plays a Role in Cardiac Ventricular Compaction by Regulating the Cardiomyocyte Cell Cycle

Y. Saijoh, A. Baldini, A. Wynshaw-Boris, 2012, Molecular and Cellular Biology.

Heart block, ventricular tachycardia, and sudden death in ACE2 transgenic mice with downregulated connexins.

C. Berul, H. Wakimoto, M. Donoghue, 2003, Journal of molecular and cellular cardiology.

Genome-Wide Analysis Reveals the Unique Stem Cell Identity of Human Amniocytes

Jonathon T. Hill, H. Yost, B. Demarest, 2013, PloS one.

Progressive Atrioventricular Conduction Block in a Mouse Myotonic Dystrophy Model

C. Berul, S. Reddy, C. Maguire, 2000, Journal of Interventional Cardiac Electrophysiology.

DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model.

D. Housman, C. Berul, M. Aronovitz, 1999, The Journal of clinical investigation.

The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele

Brett J. Kennedy, C. Ball, J. Carlquist, 2021, Nature Communications.

Induction of atrial tachycardia and fibrillation in the mouse heart.

J. Triedman, P. Hammer, C. Berul, 2001, Cardiovascular research.

Transgenic Mice Overexpressing Mutant PRKAG2 Define the Cause of Wolff-Parkinson-White Syndrome in Glycogen Storage Cardiomyopathy

Ferhaan Ahmad, J. Schmitt, J. Seidman, 2003, Circulation.

Electrophysiological characterization of murine myocardial ischemia and infarction

Richard T. Lee, A. Ducharme, C. Berul, 2001, Basic Research in Cardiology.

Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome.

J. Seidman, C. Seidman, C. Berul, 2003, Journal of the American College of Cardiology.

Comparison of Two Murine Models of Familial Hypertrophic Cardiomyopathy

F J Schoen, James O. Mudd, D. Kass, 2001, Circulation research.

Characterization of Cardiac Conduction System Abnormalities in Mice with Targeted Disruption of Six5 Gene

C. Berul, H. Wakimoto, S. Reddy, 2002, Journal of Interventional Cardiac Electrophysiology.

Phenotypic screening for heart rate variability in the mouse.

J K Triedman, J. Triedman, P. Hammer, 2000, American journal of physiology. Heart and circulatory physiology.

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.

D. Roden, C. Berul, H. Wakimoto, 2004, The Journal of clinical investigation.

Ventricular Arrhythmia Vulnerability in Cardiomyopathic Mice With Homozygous Mutant Myosin-Binding Protein C Gene

J. Seidman, C. Seidman, C. Berul, 2001, Circulation.

Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem Cells

D. Dykxhoorn, X. Liu, C. Maguire, 2021, Genes.

Impaired parasympathetic heart rate control in mice with a reduction of functional G protein βγ-subunits

E. Neer, P. Hammer, C. Berul, 2002 .

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.

D. Roden, C. Berul, H. Wakimoto, 2004, The Journal of clinical investigation.

Impaired parasympathetic heart rate control in mice with a reduction of functional G protein betagamma-subunits.

E. Neer, P. Hammer, C. Berul, 2002, American journal of physiology. Heart and circulatory physiology.