Conditional Creation and Rescue of Nipbl-Deficiency in Mice Reveals Multiple Determinants of Risk for Congenital Heart Defects

MESP1 Mutations in Patients with Congenital Heart Defects

(2016) Petra Werner et al.   HUMAN MUTATION

De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects

(2016) James R. Priest et al.   PLoS Genetics

Drosophila Nipped-B Mutants Model Cornelia de Lange Syndrome in Growth and Behavior

(2015) Yaning Wu et al.   PLoS Genetics

Morphogenesis and molecular considerations on congenital cardiac septal defects

(2014) Adriana C. Gittenberger-de Groot et al.   ANNALS OF MEDICINE

Neural crest cell-specific inactivation ofNipblorMau2during mouse development results in a late onset of craniofacial defects

(2014) Terence Gordon Smith et al.   GENESIS

Nipbl and Mediator Cooperatively Regulate Gene Expression to Control Limb Development

(2014) Akihiko Muto et al.   PLoS Genetics

Genetics of Congenital Heart Disease

(2013) Akl C. Fahed et al.   CIRCULATION RESEARCH

Conditionals by inversion provide a universal method for the generation of conditional alleles

(2013) Aris N. Economides et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Homeobox transcription factor Pitx2: The rise of an asymmetry gene in cardiogenesis and arrhythmogenesis

(2013) Diego Franco et al.   TRENDS IN CARDIOVASCULAR MEDICINE

Congenital heart disease in Cornelia de Lange syndrome: Phenotype and genotype analysis

(2012) Kathryn C. Chatfield et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Early cardiac development: a view from stem cells to embryos

(2012) P. Van Vliet et al.   CARDIOVASCULAR RESEARCH

Epistatic Rescue of Nkx2.5 Adult Cardiac Conduction Disease Phenotypes by Prospero-Related Homeobox Protein 1 and HDAC3

(2012) Catherine A. Risebro et al.   CIRCULATION RESEARCH

The Ancient and Evolving Roles of Cohesin in Gene Expression and DNA Repair

(2012) Dale Dorsett et al.   CURRENT BIOLOGY

The neural crest in cardiac congenital anomalies

(2012) Anna Keyte et al.   DIFFERENTIATION

Fate Mapping Identifies the Origin of SHF/AHF Progenitors in the Chick Primitive Streak

(2012) Esther Camp et al.   PLoS One

Mind bomb 1 is required for pancreatic  -cell formation

(2012) S. Horn et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Dual Lineage-Specific Expression of Sox17 During Mouse Embryogenesis

(2012) Eunyoung Choi et al.   STEM CELLS

Reduced Glutathione Enhances Fertility of Frozen/Thawed C57BL/6 Mouse Sperm after Exposure to Methyl-Beta-Cyclodextrin1

(2011) Toru Takeo et al.   BIOLOGY OF REPRODUCTION

Cohesin: genomic insights into controlling gene transcription and development

(2011) Dale Dorsett   CURRENT OPINION IN GENETICS & DEVELOPMENT

The Contribution of Chromosomal Abnormalities to Congenital Heart Defects: A Population-Based Study

(2011) Robert J. Hartman et al.   PEDIATRIC CARDIOLOGY

Multifactorial Origins of Heart and Gut Defects in nipbl-Deficient Zebrafish, a Model of Cornelia de Lange Syndrome

(2011) Akihiko Muto et al.   PLOS BIOLOGY

Updated national birth prevalence estimates for selected birth defects in the United States, 2004-2006

(2010) Samantha E. Parker et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Mesp1

(2010) Antoine Bondue et al.   CIRCULATION RESEARCH

Positive regulation of c-Myc by cohesin is direct, and evolutionarily conserved

(2010) Jenny M. Rhodes et al.   DEVELOPMENTAL BIOLOGY

Dissecting spatio-temporal protein networks driving human heart development and related disorders

(2010) Kasper Lage et al.   Molecular Systems Biology

Analysis of congenital heart defects in 87 consecutive patients with Brachmann-de Lange syndrome

(2009) Angelo Selicorni et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Globally optimal stitching of tiled 3D microscopic image acquisitions

(2009) S. Preibisch et al.   BIOINFORMATICS

Cohesin, gene expression and development: Lessons from Drosophila

(2009) Dale Dorsett   CHROMOSOME RESEARCH

Cornelia de Lange syndrome, cohesin, and beyond

(2009) J Liu et al.   CLINICAL GENETICS

Sox17-2A-iCre: A knock-in mouse line expressing Cre recombinase in endoderm and vascular endothelial cells

(2009) Silvia Engert et al.   GENESIS

Reptilian heart development and the molecular basis of cardiac chamber evolution

(2009) Kazuko Koshiba-Takeuchi et al.   NATURE

Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells

(2009) Jinglan Liu et al.   PLOS BIOLOGY

Multiple Organ System Defects and Transcriptional Dysregulation in the Nipbl+/− Mouse, a Model of Cornelia de Lange Syndrome

(2009) Shimako Kawauchi et al.   PLoS Genetics

Mesp1 Acts as a Master Regulator of Multipotent Cardiovascular Progenitor Specification

(2008) Antoine Bondue et al.   Cell Stem Cell

Does Size Matter?

(2008) Frederick E. Dewey et al.   CIRCULATION

Prevalence of Congenital Heart Defects in Metropolitan Atlanta, 1998-2005

(2008) Mark D. Reller et al.   JOURNAL OF PEDIATRICS

The developmental genetics of congenital heart disease

(2008) Benoit G. Bruneau   NATURE

Enhanced gene trapping in mouse embryonic stem cells

(2008) Frank Schnütgen et al.   NUCLEIC ACIDS RESEARCH