טוען...
Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function
Human mutations in or variants of TBX20 are associated with congenital heart disease, cardiomyopathy, and arrhythmias. To investigate whether cardiac disease in patients with these conditions results from an embryonic or ongoing requirement for Tbx20 in myocardium, we ablated Tbx20 specifically in a...
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| Main Authors: | , , , , , , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Clinical Investigation
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3223071/ https://ncbi.nlm.nih.gov/pubmed/22080862 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI59472 |
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