
Embryonic Stem Cells not only hold a lot of potential for use in regenerative medicine, but also provide an elegant and efficient way to study specific developmental processes and pathways in mammals when whole animal gene knock out experiments fail. We have investigated a pathway through which HDAC1 affects cardiovascular and more specifically cardiomyocyte differentiation in ES cells by controlling expression of SOX17 and BMP2 during early differentiation. This data explains current discrepancies in the role of HDAC1 in cardiovascular differentiation and sheds light into a new pathway through which ES cells determine cardiovascular cell fate.
Time Factors, Science, Bone Morphogenetic Protein 2, Fluorescent Antibody Technique, Gene Expression, Histone Deacetylase 1, Cell Line, Mice, HMGB Proteins, SOXF Transcription Factors, Animals, Myocytes, Cardiac, Embryoid Bodies, Embryonic Stem Cells, Models, Genetic, Reverse Transcriptase Polymerase Chain Reaction, Q, R, Cell Differentiation, Mice, Inbred C57BL, Gene Knockdown Techniques, Medicine, Research Article, Signal Transduction
Time Factors, Science, Bone Morphogenetic Protein 2, Fluorescent Antibody Technique, Gene Expression, Histone Deacetylase 1, Cell Line, Mice, HMGB Proteins, SOXF Transcription Factors, Animals, Myocytes, Cardiac, Embryoid Bodies, Embryonic Stem Cells, Models, Genetic, Reverse Transcriptase Polymerase Chain Reaction, Q, R, Cell Differentiation, Mice, Inbred C57BL, Gene Knockdown Techniques, Medicine, Research Article, Signal Transduction
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| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
