Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jennilee M. Davidson"'
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:
Stephanie L. Rayner, Shu Yang, Natalie E. Farrawell, Cyril J. Jagaraj, Flora Cheng, Jennilee M. Davidson, Luan Luu, Alberto G. Redondo, Alberto Rábano, Daniel Borrego-Hernández, Julie D. Atkin, Marco Morsch, Ian P. Blair, Justin J. Yerbury, Roger Chung, Albert Lee
Publikováno v:
Neurobiology of Disease, Vol 167, Iss , Pp 105673- (2022)
Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterised by the loss of upper and lower motor neurons in the brain and spinal cord. ALS and frontotemporal dementia (FTD) are overlapping diseases with shared p
Externí odkaz:
https://doaj.org/article/8b0375252ae3453588b0ea1234e98d29
Publikováno v:
Neurobiology of Disease, Vol 166, Iss , Pp 105653- (2022)
Investigations into the pathogenetic mechanisms underlying amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) have provided significant insight into the disease. At the cellular level, ALS and FTD are classified as proteinopathies,
Externí odkaz:
https://doaj.org/article/2308bff4aca04d7ab283a63ee4159659
Autor:
Flora Cheng, Alana De Luca, Alison L. Hogan, Stephanie L. Rayner, Jennilee M. Davidson, Maxinne Watchon, Claire H. Stevens, Sonia Sanz Muñoz, Lezanne Ooi, Justin J. Yerbury, Emily K. Don, Jennifer A. Fifita, Maria D. Villalva, Hannah Suddull, Tyler R. Chapman, Thomas J. Hedl, Adam K. Walker, Shu Yang, Marco Morsch, Bingyang Shi, Ian P. Blair, Angela S. Laird, Roger S. Chung, Albert Lee
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
The past decade has seen a rapid acceleration in the discovery of new genetic causes of ALS, with more than 20 putative ALS-causing genes now cited. These genes encode proteins that cover a diverse range of molecular functions, including free radical
Externí odkaz:
https://doaj.org/article/6d9d5478214e4a43b5c90d1b2ff9a16b
Autor:
Thomas J. Hedl, Rebecca San Gil, Flora Cheng, Stephanie L. Rayner, Jennilee M. Davidson, Alana De Luca, Maria D. Villalva, Heath Ecroyd, Adam K. Walker, Albert Lee
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are increasing in prevalence but lack targeted therapeutics. Although the pathological mechanisms behind these diseases remain unclear, both ALS
Externí odkaz:
https://doaj.org/article/9fb158da4d31476494289e43bada051d
Autor:
Jennilee M. Davidson, Sharlynn S. L. Wu, Stephanie L. Rayner, Flora Cheng, Kimberley Duncan, Carlo Russo, Michelle Newbery, Kunjie Ding, Natalie M. Scherer, Rachelle Balez, Alberto García-Redondo, Alberto Rábano, Livia Rosa-Fernandes, Lezanne Ooi, Kelly L. Williams, Marco Morsch, Ian P. Blair, Antonio Di Ieva, Shu Yang, Roger S. Chung, Albert Lee
Publikováno v:
Molecular Neurobiology.
Amyotrophic lateral sclerosis (ALS)- and frontotemporal dementia (FTD)-linked mutations in CCNF have been shown to cause dysregulation to protein homeostasis. CCNF encodes for cyclin F, which is part of the cyclin F-E3 ligase complex SCFcyclinF known
Autor:
Stephanie L, Rayner, Shu, Yang, Natalie E, Farrawell, Cyril J, Jagaraj, Flora, Cheng, Jennilee M, Davidson, Luan, Luu, Alberto G, Redondo, Alberto, Rábano, Daniel, Borrego-Hernández, Julie D, Atkin, Marco, Morsch, Ian P, Blair, Justin J, Yerbury, Roger, Chung, Albert, Lee
Publikováno v:
Neurobiology of disease. 167
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterised by the loss of upper and lower motor neurons in the brain and spinal cord. ALS and frontotemporal dementia (FTD) are overlapping diseases with shared pathological
Autor:
Stephanie L. Rayner, Alison Hogan, Jennilee M. Davidson, Flora Cheng, Luan Luu, Marco Morsch, Ian Blair, Roger Chung, Albert Lee
Publikováno v:
The Neuroscientist. :107385842211201
Amyotrophic lateral sclerosis (ALS) is the most common form of motor neuron disease and is characterized by the degeneration of upper and lower motor neurons of the brain and spinal cord. ALS is also linked clinically, genetically, and pathologically
Autor:
Andrew J. Lee, Justin J. Yerbury, C. Cluning, Sarah L. Rea, P.A. Akkari, Jennilee M. Davidson, R. Mejzini, A. D. Foster, Flora Cheng, N. Polain, Loren L. Flynn, Natalie E. Farrawell, Robert Layfield
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) that exist on a spectrum of neurodegenerative disease. A hallmark of pathology is cytoplasmic TDP-43 aggregates within neurons, observed in 97% of ALS cases and ~ 50% of
Autor:
Maria D. Villalva, Claire H. Stevens, Alison L. Hogan, Maxinne Watchon, Hannah J. Suddull, Angela S. Laird, Alana De Luca, Ian P. Blair, Flora Cheng, Emily K. Don, Jennilee M. Davidson, Bingyang Shi, Thomas J. Hedl, Shu Yang, Marco Morsch, Albert Lee, Justin J. Yerbury, Sonia Sanz Muñoz, Roger S. Chung, Jennifer A. Fifita, Stephanie L. Rayner, Adam K. Walker, Tyler R. Chapman, Lezanne Ooi
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Frontiers in Molecular Neuroscience
Frontiers in Molecular Neuroscience
The past decade has seen a rapid acceleration in the discovery of new genetic causes of ALS, with more than 20 putative ALS-causing genes now cited. These genes encode proteins that cover a diverse range of molecular functions, including free radical