Additional sex combs-likefamily genes are required for normal cardiovascular development
出版年份 2014 全文链接
标题
Additional sex combs-likefamily genes are required for normal cardiovascular development
作者
关键词
-
出版物
GENESIS
Volume 52, Issue 7, Pages 671-686
出版商
Wiley
发表日期
2014-05-24
DOI
10.1002/dvg.22793
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Loss of Asxl1 leads to myelodysplastic syndrome-like disease in mice
- (2013) J. Wang et al. BLOOD
- De novoframeshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies
- (2013) Darrell L Dinwiddie et al. BMC Medical Genomics
- Functional and cancer genomics of ASXL family members
- (2013) M Katoh BRITISH JOURNAL OF CANCER
- Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
- (2013) Omar Abdel-Wahab et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Additional Sex Combs-Like 2 Is Required for Polycomb Repressive Complex 2 Binding at Select Targets
- (2013) Hsiao-Lei Lai et al. PLoS One
- De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
- (2013) Matthew N Bainbridge et al. Genome Medicine
- The prevalence of adult congenital heart disease, results from a systematic review and evidence based calculation
- (2012) Teun van der Bom et al. AMERICAN HEART JOURNAL
- Two novel patients with Bohring-Opitz syndrome caused by de novo ASXL1 mutations
- (2012) Pamela Magini et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- ASXL1 Mutations Promote Myeloid Transformation through Loss of PRC2-Mediated Gene Repression
- (2012) Omar Abdel-Wahab et al. CANCER CELL
- Epigenetic regulation of cardiac development and function by polycomb group and trithorax group proteins
- (2012) Q. Tian Wang DEVELOPMENTAL DYNAMICS
- Maintenance of adult cardiac function requires the chromatin factor Asxl2
- (2012) Hsiao-Lei Lai et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Trials with ‘epigenetic’ drugs: An update
- (2012) Angela Nebbioso et al. Molecular Oncology
- Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis
- (2012) Paul Delgado-Olguín et al. NATURE GENETICS
- Loss of the Tumor Suppressor BAP1 Causes Myeloid Transformation
- (2012) A. Dey et al. SCIENCE
- Modifier Genes and the Plasticity of Genetic Networks in Mice
- (2012) Bruce A. Hamilton et al. PLoS Genetics
- Epigenetic mechanisms in cardiac development and disease
- (2011) Marcus Vallaster et al. ACTA BIOCHIMICA ET BIOPHYSICA SINICA
- Epigenetics and Cardiovascular Development
- (2011) Ching-Pin Chang et al. Annual Review of Physiology
- Mutational spectrum analysis of chronic myelomonocytic leukemia includes genes associated with epigenetic regulation: UTX, EZH2, and DNMT3A
- (2011) A. M. Jankowska et al. BLOOD
- Epigenetic factors and cardiac development
- (2011) J. H. van Weerd et al. CARDIOVASCULAR RESEARCH
- Epigenetic Modifications of Stem Cells
- (2011) Yonggang Zhou et al. CIRCULATION RESEARCH
- Polycomb Repressive Complex 2 Regulates Normal Development of the Mouse Heart
- (2011) Aibin He et al. CIRCULATION RESEARCH
- Mesenchymal Nuclear factor I B regulates cell proliferation and epithelial differentiation during lung maturation
- (2011) Yu-Chih Hsu et al. DEVELOPMENTAL BIOLOGY
- Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis
- (2011) Rob Hastings et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- SWI/SNF Complexes Containing Brahma or Brahma-Related Gene 1 Play Distinct Roles in Smooth Muscle Development
- (2011) M. Zhang et al. MOLECULAR AND CELLULAR BIOLOGY
- De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome
- (2011) Alexander Hoischen et al. NATURE GENETICS
- Clinical Effect of Point Mutations in Myelodysplastic Syndromes
- (2011) Rafael Bejar et al. NEW ENGLAND JOURNAL OF MEDICINE
- Fetal Programming of Adult Disease
- (2011) Christopher Lau et al. OBSTETRICS AND GYNECOLOGY
- Critical Congenital Heart Disease-Utility of Routine Screening for Chromosomal and Other Extracardiac Malformations
- (2011) Kimberly Baker et al. Congenital Heart Disease
- Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations
- (2011) Javier T. Granados-Riveron et al. Congenital Heart Disease
- Failure of Postnatal Ductus Arteriosus Closure in Prostaglandin Transporter–Deficient Mice
- (2010) Hee-Yoon Chang et al. CIRCULATION
- Heterogeneity of Genetic Modifiers Ensures Normal Cardiac Development
- (2010) Julia B. Winston et al. CIRCULATION
- Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB
- (2010) Johanna C. Scheuermann et al. NATURE
- Epigenetic modifications as therapeutic targets
- (2010) Theresa K Kelly et al. NATURE BIOTECHNOLOGY
- Epigenetics and cardiovascular disease
- (2010) José M. Ordovás et al. Nature Reviews Cardiology
- Lunatic Fringe-mediated Notch signaling is required for lung alveogenesis
- (2009) Keli Xu et al. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
- Loss-of-function Additional sex combs like 1 mutations disrupt hematopoiesis but do not cause severe myelodysplasia or leukemia
- (2009) C. L. Fisher et al. BLOOD
- Mutations of polycomb-associated geneASXL1in myelodysplastic syndromes and chronic myelomonocytic leukaemia
- (2009) Véronique Gelsi-Boyer et al. BRITISH JOURNAL OF HAEMATOLOGY
- Heart Malformation
- (2009) Joseph T.C. Shieh et al. CIRCULATION
- Recurrence of Congenital Heart Defects in Families
- (2009) Nina Øyen et al. CIRCULATION
- Additional sex combs-like 1 belongs to the enhancer of trithorax and polycomb group and genetically interacts with Cbx2 in mice
- (2009) C.L. Fisher et al. DEVELOPMENTAL BIOLOGY
- Cardiac Fibroblasts Regulate Myocardial Proliferation through β1 Integrin Signaling
- (2009) Masaki Ieda et al. DEVELOPMENTAL CELL
- Platelets contribute to postnatal occlusion of the ductus arteriosus
- (2009) Katrin Echtler et al. NATURE MEDICINE
- Interpreting Neonatal Lethal Phenotypes in Mouse Mutants: Insights Into Gene Function and Human Diseases
- (2009) Benjamin Turgeon et al. PHYSIOLOGICAL REVIEWS
- Functional Conservation of Asxl2, a Murine Homolog for the Drosophila Enhancer of Trithorax and Polycomb Group Gene Asx
- (2009) Heather A. Baskind et al. PLoS One
- Identification of a Cardiac Disease Modifier Gene Using Forward Genetics in the Mouse
- (2009) William T. Pu PLoS Genetics
- Tnni3k Modifies Disease Progression in Murine Models of Cardiomyopathy
- (2009) Ferrin C. Wheeler et al. PLoS Genetics
- ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease
- (2008) Carole A. Warnes et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- An optimized procedure for whole-mount in situ hybridization on mouse embryos and embryoid bodies
- (2008) Denis Piette et al. Nature Protocols
- A chemical method for fast and sensitive detection of DNA synthesis in vivo
- (2008) A. Salic et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Genetic insights into normal and abnormal heart development
- (2007) Mona Nemer CARDIOVASCULAR PATHOLOGY
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