Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Cacace Angela Marie"'
Autor:
Anthony Accorsi, Cacace Angela Marie, Erin Valentine, Peter B. Rahl, Aaron N. Chang, Lorin A. Thompson, Lucienne Ronco, Joseph Maglio, Alan J. Robertson, Wallace Owen Brendan, L. Alejandro Rojas, Steven Kazmirski, Diego Cadavid, Rabi Tawil, Ning Shen
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 374:489-498
Facioscapulohumeral muscular dystrophy (FSHD) is caused by the loss of repression at the D4Z4 locus leading to aberrant double homeobox 4 (DUX4) expression in skeletal muscle. Activation of this early embryonic transcription factor results in the exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::391910836251b5c32c0c18a31cee0733
https://doi.org/10.1124/jpet.119.264689
https://doi.org/10.1124/jpet.119.264689
Autor:
Hao Wu, Wallace Owen Brendan, Rudolf Jaenisch, John D. Graef, Chicheng Sun, Deena Qadir, Vivian Villegas, Cacace Angela Marie, Stephen T. Warren, Carrie Ng, Kimberly Jesseman
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88ed3520eef054f566dea7f2034d099d
https://doi.org/10.1111/ejn.14660/v2/response1
https://doi.org/10.1111/ejn.14660/v2/response1
Autor:
Cacace Angela Marie, Peter B. Rahl, Anthony Accorsi, Lucienne Ronco, Aaron N. Chang, Ning Shen, Erin Valentine, Steven Kazmirski, Diego Cadavid, L. Alejandro Rojas, Lorin A. Thompson, Rabi Tawil, Wallace Owen Brendan, Joseph Maglio, Alan J. Robertson
FSHD is caused by the loss of repression at the D4Z4 locus leading to DUX4 expression in skeletal muscle, activation of its early embryonic transcriptional program and muscle fiber death. While progress toward understanding the signals driving DUX4 e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4817be420c5ec18a034e0c9c3e2b9932
https://doi.org/10.1101/700195
https://doi.org/10.1101/700195
Autor:
Kimberly Jesseman, Deena Qadir, Chicheng Sun, Wallace Owen Brendan, Hao Wu, John D. Graef, Carrie Ng, Vivian Villegas, Cacace Angela Marie, Stephen T. Warren, Rudolf Jaenisch
Publikováno v:
The European Journal of Neuroscience
Wiley
Wiley
Fragile X syndrome (FXS) is the most common genetic form of intellectual disability caused by a CGG repeat expansion in the 5′‐UTR of the Fragile X mental retardation gene FMR1, triggering epigenetic silencing and the subsequent absence of the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48a9bafada3dfc8cfd22dc356b810cf8
https://doi.org/10.1101/608331
https://doi.org/10.1101/608331