Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jillian, Gallagher"'
Autor:
Hector Ribeiro Benatti, Rachel D. Prestigiacomo, Toloo Taghian, Rachael Miller, Robert King, Matthew J. Gounis, Ugur Celik, Stephanie Bertrand, Susan Tuominen, Lindsey Bierfeldt, Elizabeth Parsley, Jillian Gallagher, Erin F. Hall, Abigail W. McElroy, Miguel Sena-Esteves, Anastasia Khvorova, Neil Aronin, Heather L. Gray-Edwards
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 31, Iss , Pp 101122- (2023)
Oligonucleotide therapeutics offer great promise in the treatment of previously untreatable neurodegenerative disorders; however, there are some challenges to overcome in pre-clinical studies. (1) They carry a well-established dose-related acute neur
Externí odkaz:
https://doaj.org/article/47746a402a8d49c9b29336720b82daae
Autor:
Toloo Taghian, Jillian Gallagher, Erin Batcho, Caitlin Pullan, Tim Kuchel, Thomas Denney, Raj Perumal, Shamika Moore, Robb Muirhead, Paul Herde, Daniel Johns, Chris Christou, Amanda Taylor, Thomas Passler, Sanjana Pulaparthi, Erin Hall, Sundeep Chandra, Charles A. O’Neill, Heather Gray-Edwards
Publikováno v:
Journal of Huntington's disease. 11(4)
Background: Huntington’s disease (HD) is a fatal neurodegenerative autosomal dominant disorder with prevalence of 1 : 20000 that has no effective treatment to date. Translatability of candidate therapeutics could be enhanced by additional testing i
Autor:
Jillian Gallagher, Judith Gallant, Ping Xu, Rachael Gately, Stephanie Bertrand, Abigail McElroy, Erin Hall, Hector Benatti, Rachel Prestigiacomo, Kevin Luk, Leigh E. Fremuth, Diantha van de Vlekkert, Huimin Hu, Camilo Toro, Alessandra d'Azzo, Cynthia J. Tifft, Scot Wolfe, Jaime Rivera, Miguel Sena-Esteves, Heather Gray-Edwards
Publikováno v:
Molecular Genetics and Metabolism. 138:107109
Autor:
Jey W. Koehler, Ashley N. Randle, Jillian Gallagher, Amanda L. Gross, Elise B. Diffie, Brett D. Story, Sundeep Chandra, Sara Carl, Kayly Nielsen, Paul Cuddon, Miguel Sena-Esteves, Edwin H. Kolodny, Deborah Fernau, Amanda R. Taylor, Douglas R. Martin, Carly Corado, Xuntian Jiang, Heather L. Gray-Edwards, Annie S. Maguire, Toloo Taghian, Siauna Johnson
Publikováno v:
Mol Genet Metab
Tay-Sachs disease (TSD) is a fatal neurodegenerative disease caused by a deficiency of the enzyme β-N-acetylhexosaminidase A (HexA). TSD naturally occurs in Jacob sheep is the only experimental model of TSD. TSD in sheep recapitulates neurologic fea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69a0c7cda10ecdd0ead870203e1fd7ba
https://europepmc.org/articles/PMC8811770/
https://europepmc.org/articles/PMC8811770/
Autor:
Jillian Gallagher, Judith Gallant, Ping Xu, Rachael Gately, Stephanie Bertrand, Kevin Luk, Camilo Toro, Alessandra d'Azzo, Scot Wolfe, Jaime Rivera, Miguel Sena-Esteves, Heather Gray-Edwards
Publikováno v:
Molecular Genetics and Metabolism. 135:S45
Autor:
Jillian Gallagher
Publikováno v:
International Journal of Case Studies in Clinical Research. 1:155-155
Autor:
Barbara, Liebert, Michael, Parle, Celia, Roberts, Sally, Redman, Sue, Carrick, Jillian, Gallagher, Judy, Simpson, Kitty, Ng, M Asaduzzaman, Khan, Kate, White, Glenn, Salkeld, Meg, Lewis, Ian, Olver, Grantly, Gill, Mary, Marchant, Alan, Coates, Robert, North, Gina, Akers, Andrea, Cannon, Christine, Gray, Jeanette, Liebelt, Alan, Rodger, Michael, Henderson, David, Stoney, Pat, Hickey, Stephen, Archer, Cecily, Metcalf, James, Trotter
Publikováno v:
European journal of cancer care. 12(1)
The objective of this study was to examine the feasibility, implementation, acceptability and impact of an evidence-based specialist breast care nurse (SBN) model of care in Australia. Primary data were collected from four diverse Australian breast c