Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sharlynn Wu"'
Autor:
Stephanie L. Rayner, Alison Hogan, Jennilee M. Davidson, Tyler Chapman, Flora Cheng, Luan Luu, Sharlynn Wu, Selina Zhang, Shu Yang, Ian Blair, Marco Morsch, Roger Chung, Albert Lee
Publikováno v:
Neurobiology of Disease, Vol 192, Iss , Pp 106421- (2024)
Previously, we demonstrated that the SCFcyclin F complex directly mediates the poly-ubiquitylation of TDP-43, raising the question of whether cyclin F can be used to enhance the turnover of TDP-43. A hurdle to the use of cyclin F, however, is that th
Externí odkaz:
https://doaj.org/article/938a323b072b422dbb397509b51afada
Autor:
Denis C. Bauer, Britt A. Berning, Jennifer A. Fifita, Olivier Piguet, Julie D. Atkin, John B.J. Kwok, Adam K. Walker, Sarah E. Freckleton, Alison L. Hogan, Prachi Mehta, Sandrine Chan Moi Fat, Kelly L. Williams, Emily P. McCann, Shu Yang, Dominic B. Rowe, Garth A. Nicholson, Natalie A. Twine, Glenda M. Halliday, Matthew C. Kiernan, Ian P. Blair, Sharlynn Wu, Katharine Y. Zhang, Cyril J. Jagaraj, John R. Hodges, Jasmin Galper, Lyndal Henden, Natalie Grima
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 91:162-171
ObjectiveSince the first report of CHCHD10 gene mutations in amyotrophiclateral sclerosis (ALS)/frontotemporaldementia (FTD) patients, genetic variation in CHCHD10 has been inconsistently linked to disease. A pathological assessment of the CHCHD10 pr
Autor:
Shu Yang, Ian P. Blair, Emily P. McCann, Jasmin Galper, Sharlynn Wu, Sarah E. Freckleton, Fat Scm, Jennifer A. Fifita, Katharine Y. Zhang
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 20:135-159
Background: Ongoing disease gene discoveries continue to drive our understanding of the molecular and cellular mechanisms underlying ALS. Causative genes from 60% of ALS families have been identified using modern genetic techniques, but the causal ge
Autor:
Ram Maharjan, Lyndal Henden, Kelly L. Williams, Alison L. Hogan, Benjamin Heng, Ian P. Blair, Sandrine Chan Moi Fat, Ingrid S. Tarr, Natalie Grima, Shu Yang, Katharine Y. Zhang, Amy K. Cain, Qiongyi Zhao, Sharlynn Wu, Marco Morsch, Amanda L. Wright, Jennifer A. Fifita, Albert Lee, Stephanie L. Rayner, Zong-Hong Zhang, Emily P. McCann
Publikováno v:
Neuropathology and applied neurobiologyREFERENCES. 47(7)
Aim Splicing factor proline and glutamine rich (SFPQ) is an RNA-DNA binding protein that is dysregulated in Alzheimer's disease and frontotemporal dementia. Dysregulation of SFPQ, specifically increased intron retention and nuclear depletion, has bee
Autor:
Lyndal Henden, Qiongyi Zhao, Benjamin Heng, Ram Maharjan, Shu Yang, Sharlynn Wu, Ian P. Blair, Amy K. Cain, Ingrid S. Tarr, Zong-Hong Zhang, Natalie Grima, Katharine Y. Zang, Emily P. McCann, Kelly L. Williams, Sandrine Chan Moi Fat, Alison L. Hogan, Jennifer A. Fifita, Marco Morsch, Amanda L. Wright
BackgroundSplicing factor proline and glutamine rich (SFPQ, also known as polypyrimidine tract-binding protein-associated-splicing factor, PSF) is a RNA-DNA binding protein with roles in key cellular pathways such as DNA transcription and repair, RNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aef207e003688cad0957ec184671e642
https://doi.org/10.1101/2020.09.22.309062
https://doi.org/10.1101/2020.09.22.309062
Autor:
Shu Yang, Sharlynn Wu, Jennifer Fifita, Emily McCann, Sandrine Chan Moi Fat, Jasmin Galper, Sarah Freckleton, Zhang, Kathrine Y., Ian Blair
Publikováno v:
Macquarie University
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::00cac5f16c75a4c089b0f8909c769b63
https://researchers.mq.edu.au/en/publications/87d71738-5421-407b-a797-43b297253164
https://researchers.mq.edu.au/en/publications/87d71738-5421-407b-a797-43b297253164