Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Wallace Owen Brendan"'
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
Autor:
Mriganka Sur, Angela Cacace, Dongdong Fu, Aaron N. Chang, Rudolf Jaenisch, Jennifer Shih, Bingbing Yuan, Carrie M. Garrett-Engele, X. Shawn Liu, Kristin R. Andrykovich, Bhav Jain, Hao Wu, Troy W. Whitfield, Marine Krzisch, Rosalie G. J. Rietjens, Stephen T. Warren, Wallace Owen Brendan
Abnormal neuronal development in Fragile X syndrome (FXS) is poorly understood. Data on FXS patients remain scarce and FXS animal models have failed to yield successful therapies. In vitro models do not fully recapitulate the morphology and function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0ee7510fb36960d0bd667cd7f6496be
https://doi.org/10.1101/2021.09.27.461739
https://doi.org/10.1101/2021.09.27.461739
Autor:
S. Silver, C. Moxham, Wallace Owen Brendan, C. Sartain, D. Plioudakis, R. Lieberman, L. Rojas, Erin Valentine, A. Ergun, A. Raman, E. Townsend, Anthony Accorsi, G. Wilson, M. Wertz
Publikováno v:
Neuromuscular Disorders. 31:S147
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
/SummaryPatients with Prader-Willi-Syndrome (PWS) display intellectual impairment, hyperphagia, and various behavioral problems during childhood that converge on a neurologic deficit. The majority of PWS patients have genetic deletions of the paterna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6f759d1c5d04904b629e2f81191ed0a
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
Autor:
Diego Cadavid, Peter B. Rahl, Billy Stuart, Keqiang Xie, Kingsley Appiah, Kim Stickland, Paul Bruno, Lorin A. Thompson, David Peters, Ivan Efremov, Li Qingyi, Wallace Owen Brendan, Lucienne Ronco, Steven Kazmirski, Christopher Moxham, Richard F. W. Barnes, Mark S. Roth
Publikováno v:
Blood. 136:1-1
Red blood cell disorders like Sickle Cell Disease (SCD) and β-thalassemias are caused by mutations within the gene for the hemoglobin β (HBβ) subunit. A fetal ortholog of HBβ, hemoglobin γ (HBγ) can prevent or reduce disease-related pathophysio
Autor:
Leo H. Wang, L. Ronco, A. Rojas, A. Chang, Diego Cadavid, Wallace Owen Brendan, S. Tapscott, Michelle Mellion, Rabi Tawil, Ning Shen
Publikováno v:
Neuromuscular Disorders. 29:S54-S55
Autor:
A. Chang, Richard F. W. Barnes, D. Eyerman, Diego Cadavid, Joseph Maglio, Ning Shen, Angela Cacace, P. Rahl, Wallace Owen Brendan, Erin Valentine, L. Ronco, A. Rojas, Alan S. Robertson, Anthony Accorsi, R. Gould, Steven Kazmirski, Michelle Mellion, L. Thompson
Publikováno v:
Neuromuscular Disorders. 29:S53-S54