Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kendall E Martin"'
Autor:
Kendall E Martin, Padmapriyadarshini Ravisankar, Manu Beerens, Calum A MacRae, Joshua S Waxman
Publikováno v:
eLife, Vol 12 (2023)
Maintenance of cardiomyocyte identity is vital for normal heart development and function. However, our understanding of cardiomyocyte plasticity remains incomplete. Here, we show that sustained expression of the zebrafish transcription factor Nr2f1a
Externí odkaz:
https://doaj.org/article/f836804f17944076be9c284e9dd8ddfc
Autor:
Tracy E Dohn, Padmapriyadarshini Ravisankar, Fouley T Tirera, Kendall E Martin, Jacob T Gafranek, Tiffany B Duong, Terri L VanDyke, Melissa Touvron, Lindsey A Barske, J Gage Crump, Joshua S Waxman
Publikováno v:
PLoS Genetics, Vol 15, Iss 2, p e1007962 (2019)
Multiple syndromes share congenital heart and craniofacial muscle defects, indicating there is an intimate relationship between the adjacent cardiac and pharyngeal muscle (PM) progenitor fields. However, mechanisms that direct antagonistic lineage de
Externí odkaz:
https://doaj.org/article/240d1ba88b8b4c0cb4b6ef2a5e18629f
Autor:
Kendall E. Martin, Padmapriyadarshini Ravisankar, Manu E. M. Beerens, Calum A. MacRae, Joshua S. Waxman
Maintenance of cardiomyocyte identity is vital for normal heart development and function. However, our understanding of cardiomyocyte plasticity remains incomplete. Here, we show that sustained expression of the zebrafish transcription factor (TF) Nr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99b6eddb8062bfef345bea268ec6d9d1
https://doi.org/10.1101/2022.02.24.481762
https://doi.org/10.1101/2022.02.24.481762
Autor:
Joshua S. Waxman, Kendall E Martin
Publikováno v:
Journal of Cardiovascular Development and Disease
Journal of Cardiovascular Development and Disease, Vol 8, Iss 15, p 15 (2021)
Journal of Cardiovascular Development and Disease, Vol 8, Iss 15, p 15 (2021)
Proper development and function of the vertebrate heart is vital for embryonic and postnatal life. Many congenital heart defects in humans are associated with disruption of genes that direct the formation or maintenance of atrial and pacemaker cardio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::427cc9288987540e34bd042447d5879f
https://pubmed.ncbi.nlm.nih.gov/33572147
https://pubmed.ncbi.nlm.nih.gov/33572147
Autor:
Melissa Touvron, Tracy E. Dohn, Joshua S. Waxman, J. Gage Crump, Padmapriyadarshini Ravisankar, Fouley T. Tirera, Terri L. VanDyke, Lindsey Barske, Tiffany B. Duong, Kendall E. Martin, Jacob T. Gafranek
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 15, Iss 2, p e1007962 (2019)
PLoS Genetics, Vol 15, Iss 2, p e1007962 (2019)
Multiple syndromes share congenital heart and craniofacial muscle defects, indicating there is an intimate relationship between the adjacent cardiac and pharyngeal muscle (PM) progenitor fields. However, mechanisms that direct antagonistic lineage de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::377e3ca00a98dc02583c5249192d450e
https://doi.org/10.1371/journal.pgen.1007962
https://doi.org/10.1371/journal.pgen.1007962
Autor:
Kendall E. Martin, Joshua S. Waxman
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 8, Iss 2, p 15 (2021)
Proper development and function of the vertebrate heart is vital for embryonic and postnatal life. Many congenital heart defects in humans are associated with disruption of genes that direct the formation or maintenance of atrial and pacemaker cardio
Externí odkaz:
https://doaj.org/article/1990d7dbf6d14849b0121bf1e37e13e9