标题
Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function
作者
关键词
-
出版物
JOURNAL OF CLINICAL INVESTIGATION
Volume 121, Issue 12, Pages 4640-4654
出版商
American Society for Clinical Investigation
发表日期
2011-11-14
DOI
10.1172/jci59472
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。- Genome-wide identification of conserved regulatory function in diverged sequences
- (2011) L. Taher et al. GENOME RESEARCH
- Inherited Cardiomyopathies
- (2011) Hugh Watkins et al. NEW ENGLAND JOURNAL OF MEDICINE
- Co-occupancy by multiple cardiac transcription factors identifies transcriptional enhancers active in heart
- (2011) A. He et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Hippo Pathway Inhibits Wnt Signaling to Restrain Cardiomyocyte Proliferation and Heart Size
- (2011) T. Heallen et al. SCIENCE
- Functional and physiological genomics of estrogen-related receptors (ERRs) in health and disease
- (2010) Geneviève Deblois et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Dilated Cardiomyopathy With Conduction Disease and Arrhythmia
- (2010) Neal K. Lakdawala et al. CIRCULATION
- The BMP pathway acts to directly regulate Tbx20 in the developing heart
- (2010) E. M. Mandel et al. DEVELOPMENT
- Genome-wide discovery of human heart enhancers
- (2010) L. Narlikar et al. GENOME RESEARCH
- Homotypic clusters of transcription factor binding sites are a key component of human promoters and enhancers
- (2010) V. Gotea et al. GENOME RESEARCH
- Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
- (2010) Nona Sotoodehnia et al. NATURE GENETICS
- Genome-wide association study of PR interval
- (2010) Arne Pfeufer et al. NATURE GENETICS
- Variable locus length in the human genome leads to ascertainment bias in functional inference for non-coding elements
- (2009) Leila Taher et al. BIOINFORMATICS
- Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot
- (2009) R. Rauch et al. JOURNAL OF MEDICAL GENETICS
- A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects
- (2009) M. G. Posch et al. JOURNAL OF MEDICAL GENETICS
- Conformational Stability and DNA Binding Specificity of the Cardiac T-Box Transcription Factor Tbx20
- (2009) Ingrid Macindoe et al. JOURNAL OF MOLECULAR BIOLOGY
- ChIP-seq accurately predicts tissue-specific activity of enhancers
- (2009) Axel Visel et al. NATURE
- T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease
- (2008) Caixia Liu et al. European Journal of Medical Genetics
- Cardiac-specific ablation of Cypher leads to a severe form of dilated cardiomyopathy with premature death
- (2008) M. Zheng et al. HUMAN MOLECULAR GENETICS
- Characterization of TBX20 in human hearts and its regulation by TFAP2
- (2008) Stefanie Hammer et al. JOURNAL OF CELLULAR BIOCHEMISTRY
- Redundant Roles of Tead1 and Tead2 in Notochord Development and the Regulation of Cell Proliferation and Survival
- (2008) A. Sawada et al. MOLECULAR AND CELLULAR BIOLOGY
- Genome-wide analysis of transcription factor binding sites based on ChIP-Seq data
- (2008) Anton Valouev et al. NATURE METHODS
- Phenotypic engineering by reprogramming gene transcription using novel artificial transcription factors in Escherichia coli
- (2008) J. Y. Lee et al. NUCLEIC ACIDS RESEARCH
- UniPROBE: an online database of protein binding microarray data on protein-DNA interactions
- (2008) D. E. Newburger et al. NUCLEIC ACIDS RESEARCH
- Transcription factor neuromancer/TBX20 is required for cardiac function in Drosophila with implications for human heart disease
- (2008) L. Qian et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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