Related references
Note: Only part of the references are listed.Thoracic Aortic Aneurysm A Clinical Review
Ethan M. Senser et al.
CARDIOLOGY CLINICS (2021)
Introduction to Updated Guideline on Treatment and Management of Craniosynostosis
Irene M. J. Mathijssen
JOURNAL OF CRANIOFACIAL SURGERY (2021)
Genetic Etiology of Left-Sided Obstructive Heart Lesions: A Story in Development
Lauren E. Parker et al.
JOURNAL OF THE AMERICAN HEART ASSOCIATION (2021)
Essential function and targets of BMP signaling during midbrain neural crest delamination
Michael L. Piacentino et al.
DEVELOPMENTAL BIOLOGY (2021)
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis
Cristina M. Justice et al.
HUMAN GENETICS (2020)
SMAD6 variants in craniosynostosis: genotype and phenotype evaluation
Eduardo Calpena et al.
GENETICS IN MEDICINE (2020)
Recent Advances of Osterix Transcription Factor in Osteoblast Differentiation and Bone Formation
Qian Liu et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2020)
Cranial Neural Crest Cells and Their Role in the Pathogenesis of Craniofacial Anomalies and Coronal Craniosynostosis
Erica M. Siismets et al.
JOURNAL OF DEVELOPMENTAL BIOLOGY (2020)
Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathy
Ilse Luyckx et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2019)
Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies
Yingjuan Liu et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2019)
Efficacy and feasibility of proximal radioulnar derotational osteotomy and internal fixation for the treatment of congenital radioulnar synostosis
Xinjian Pei et al.
JOURNAL OF ORTHOPAEDIC SURGERY AND RESEARCH (2019)
A novel SMAD6 variant in a patient with severely calcified bicuspid aortic valve and thoracic aortic aneurysm
Jong Eun Park et al.
MOLECULAR GENETICS & GENOMIC MEDICINE (2019)
SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis
Yongjia Yang et al.
GENETICS IN MEDICINE (2019)
Biallelic variants in SMAD6 are associated with a complex cardiovascular phenotype
Katja Kloth et al.
HUMAN GENETICS (2019)
Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study
Marian K. Bakker et al.
BMJ OPEN (2019)
Endothelial to Mesenchymal Transition in Cardiovascular Disease JACC State-of-the-Art Review
Jason C. Kovacic et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2019)
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm
Russell A. Gould et al.
NATURE GENETICS (2019)
Management of Congenital Heart Disease: State of the ArtPart IICyanotic Heart Defects
P. Syamasundar Rao
CHILDREN-BASEL (2019)
Genetic Causes of Craniosynostosis: An Update
Jacqueline A. C. Goos et al.
MOLECULAR SYNDROMOLOGY (2019)
Bone Morphogenetic Proteins in Vascular Homeostasis and Disease
Marie-Jose Goumans et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2018)
TGF-β Family Signaling in Epithelial Differentiation and Epithelial-Mesenchymal Transition
Kaoru Kahata et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2018)
Genetics of Nonsyndromic Craniosynostosis
Andrew T. Timberlake et al.
PLASTIC AND RECONSTRUCTIVE SURGERY (2018)
Cooperation of BMP and IHH signaling in interdigital cell fate determination
Arunima Murgai et al.
PLOS ONE (2018)
Developmental SMAD6 loss leads to blood vessel hemorrhage and disrupted endothelial cell junctions
Lyndsay A. Wylie et al.
DEVELOPMENTAL BIOLOGY (2018)
Mortality Following Pediatric Congenital Heart Surgery: An Analysis of the Causes of Death Derived From the National Death Index
Courtney McCracken et al.
JOURNAL OF THE AMERICAN HEART ASSOCIATION (2018)
Cardiovascular Health in Turner Syndrome A Scientific Statement From the American Heart Association
Michael Silberbach et al.
CIRCULATION-GENOMIC AND PRECISION MEDICINE (2018)
Regulation of TGF-β Family Signaling by Inhibitory Smads
Keiji Miyazawa et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2017)
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
Sheng Chih Jin et al.
NATURE GENETICS (2017)
De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis
Andrew T. Timberlake et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor
Elisabeth Gillis et al.
FRONTIERS IN PHYSIOLOGY (2017)
Bone Morphogenetic Protein Signaling Is Required for Aortic Valve Calcification
M. Victoria Gomez-Stallons et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2016)
LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections
Dong-chuan Guo et al.
CIRCULATION RESEARCH (2016)
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles
Andrew T. Timberlake et al.
ELIFE (2016)
A Genetic-Pathophysiological Framework for Craniosynostosis
Stephen R. F. Twigg et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
The Importance of Timing in Optimizing Cranial Vault Remodeling in Syndromic Craniosynostosis
Alan F. Utria et al.
PLASTIC AND RECONSTRUCTIVE SURGERY (2015)
Birth prevalence of congenital heart defects in Norway 1994-2009-A nationwide study
Elisabeth Leirgul et al.
AMERICAN HEART JOURNAL (2014)
GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve
Lin-Mei Shi et al.
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE (2014)
Aortic Dilatation in Patients with Bicuspid Aortic Valve
Subodh Verma et al.
NEW ENGLAND JOURNAL OF MEDICINE (2014)
Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve
Elizabeth M. Bonachea et al.
PEDIATRIC RESEARCH (2014)
Signaling mechanisms of the epithelial-mesenchymal transition
David M. Gonzalez et al.
SCIENCE SIGNALING (2014)
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
Richard N. Wang et al.
GENES & DISEASES (2014)
Co-ordinating Notch, BMP, and TGF-β signaling during heart valve development
Victoria C. Garside et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2013)
Augmentation of smad-dependent BMP signaling in neural crest cells causes craniosynostosis in mice
Yoshihiro Komatsu et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2013)
Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation
Huay L. Tan et al.
HUMAN MUTATION (2012)
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
Cristina M. Justice et al.
NATURE GENETICS (2012)
Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm
Alexander J. Doyle et al.
NATURE GENETICS (2012)
Congenital heart disease: current knowledge about causes and inheritance
Gillian M. Blue et al.
MEDICAL JOURNAL OF AUSTRALIA (2012)
BMP Signaling in Congenital Heart Disease: New Developments and Future Directions
Jun Wang et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2011)
Cooperative activity of noggin and gremlin 1 in axial skeleton development
David A. Stafford et al.
DEVELOPMENT (2011)
Smad6 Is Essential to Limit BMP Signaling During Cartilage Development
Kristine D. Estrada et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2011)
Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease
Dong-Chuan Guo et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Epithelial-Mesenchymal Transitions in Development and Disease
Jean Paul Thiery et al.
CELL (2009)
The basics of epithelial-mesenchymal transition
Raghu Kalluri et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
Hypoplastic Left Heart Syndrome Links to Chromosomes 10q and 6q and Is Genetically Related to Bicuspid Aortic Valve
Robert B. Hinton et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2009)
A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003
Sheree L. Boulet et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Selective inhibitory effects of Smad6 on bone morphogenetic protein type I receptors
Kouichiro Goto et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
BMP signaling is required for RUNX2-dependent induction of the osteoblast phenotype
M Phimphilai et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2006)
A case of hypoplastic left heart syndrome and bicuspid aortic valve in monochorionic twins
TS Mu et al.
PEDIATRIC CARDIOLOGY (2005)
Mutations in NOTCH1 cause aortic valve disease
V Garg et al.
NATURE (2005)
Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability
KL McBride et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Activin receptor-like kinase 2 and Smad6 regulate epithelial-mesenchymal transformation during cardiac valve formation
JS Desgrosellier et al.
DEVELOPMENTAL BIOLOGY (2005)
The bicuspid aortic valve
AC Braverman et al.
CURRENT PROBLEMS IN CARDIOLOGY (2005)
Epistatic interactions between modifier genes confer strain-specific redundancy for Tgfb1 in developmental angiogenesis
Y Tanga et al.
GENOMICS (2005)
Smad-dependent and Smad-independent pathways in TGF-β family signalling
R Derynck et al.
NATURE (2003)
Control of endocardial cushion and cardiac valve maturation by BMP signaling pathways
EC Délot
MOLECULAR GENETICS AND METABOLISM (2003)
Genetic modifiers interact with maternal determinants in vascular development of Tgfb1-/- mice
Y Tang et al.
HUMAN MOLECULAR GENETICS (2003)
The role of Smads in BMP signaling
R Nishimura et al.
FRONTIERS IN BIOSCIENCE (2003)
A role for Smad6 in development and homeostasis of the cardiovascular system
KM Galvin et al.
NATURE GENETICS (2000)