Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Emily C Troiano"'
Autor:
Guo-Cheng Yuan, Yuxuan Guo, Eric M. Small, Qing Ma, Michael A. Trembley, Alan H. Beggs, Behzad Moghadaszadeh, Emily C Troiano, Blake D. Jardin, Yangpo Cao, Isha Sethi, Neil Mazumdar, William T. Pu
Publikováno v:
Proc Natl Acad Sci U S A
The paucity of knowledge about cardiomyocyte maturation is a major bottleneck in cardiac regenerative medicine. In development, cardiomyocyte maturation is characterized by orchestrated structural, transcriptional, and functional specializations that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a68716eed2520b43d1bba0c2aecf3c6
https://pubmed.ncbi.nlm.nih.gov/33361330
https://pubmed.ncbi.nlm.nih.gov/33361330
Autor:
Jeffrey J. Widrick, Alexandra C. Stanton, Behzad Moghadaszadeh, Amy J. Wagers, Naftali Horwitz, Emily C Troiano, Bryan L Peacker, Mohammadsharif Tabebordbar, Emily M King, Krystynne A Leacock, Pardis C. Sabeti, Simon Ye, Sahar Tavakoli, Kim A. Lagerborg, Kathleen A. Messemer, Alan H. Beggs, Liana Tellez, Allison Krunnfusz
Publikováno v:
Cell. 184(19)
Replacing or editing disease-causing mutations holds great promise for treating many human diseases. Yet, delivering therapeutic genetic modifiers to specific cells in vivo has been challenging, particularly in large, anatomically distributed tissues
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e45d7a4abfeb5420171f7106bf4755
https://pubmed.ncbi.nlm.nih.gov/34732902
https://pubmed.ncbi.nlm.nih.gov/34732902
Autor:
Blake D. Jardin, Emily C Troiano, Behzad Moghadaszadeh, Yuxuan Guo, Isha Sethi, William T. Pu, Michael A. Trembley, Eric M. Small, Guo-Cheng Yuan, Qing Ma, Alan H. Beggs
Cardiomyocyte maturation is essential for robust heart contraction throughout life. The signaling networks governing cardiomyocyte maturation remain poorly defined. Our prior studies established the transcription factor SRF as a key regulator of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::238b043814854f2a3afbd96a000251dd
https://doi.org/10.1101/824185
https://doi.org/10.1101/824185
Autor:
Rebecca Robertson, Jason Karamchandani, Xavier Allard-Chamard, Marc Petitclerc, Benjamin Ellezam, Vandana Gupta, Denis Brunet, Nicolas Chrestian, Emily C Troiano, Bernard Brais, Marie-Josée Dicaire, Chamindra G. Konersman, Alan H. Beggs, David Pellerin, Jodi Warman Chardon, Asli Aykanat, Jean Mathieu
Publikováno v:
Ann Neurol
Objective Recessive null variants of the slow skeletal muscle troponin T1 (TNNT1) gene are a rare cause of nemaline myopathy that is fatal in infancy due to respiratory insufficiency. Muscle biopsy shows rods and fiber type disproportion. We report o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d07b17f72d32bb998dc8bd2e8d814387
https://pubmed.ncbi.nlm.nih.gov/31970803
https://pubmed.ncbi.nlm.nih.gov/31970803
Autor:
Behzad Moghadaszadeh, Emily C Troiano, G. Diane Shelton, Georgina Child, Branden E. Rider, Alan H. Beggs, Claire M. Wade, Ling T. Guo, Bianca Haase, Sophia Tzannes
Publikováno v:
Skeletal Muscle
Background Congenital and inherited myopathies in dogs are faithful models of human muscle diseases and are being recognized with increasing frequency. In fact, canine models of dystrophin deficient muscular dystrophy and X-linked myotubular myopathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aa428b7d3bac4544c3412c0b6332de9
https://doi.org/10.1186/s13395-014-0025-3
https://doi.org/10.1186/s13395-014-0025-3