Zobrazeno 1 - 10
of 46
pro vyhledávání: '"J. H. West"'
Autor:
E Beckstead, G Mulokozi, M Jensen, J Smith, M Baldauf, K. A. Dearden, M. Linehan, S. Torres, J. Glenn, J. H. West, P. C. Hall, B. T. Crookston
Publikováno v:
BMC Nutrition, Vol 8, Iss 1, Pp 1-11 (2022)
Abstract Background Optimal infant and young child feeding practices (IYCFP) reduce childhood stunting and are associated with additional health benefits. In Tanzania, IYCFP are far from optimal where 32% of children under the age of 5 years are stun
Externí odkaz:
https://doaj.org/article/1a12f99deb8f4b638b13981a9ec0e218
Autor:
Craig L. Bennett, Somasish Dastidar, Frederick J. Arnold, Spencer U. McKinstry, Cameron Stockford, Brian D. Freibaum, Bryce L. Sopher, Meilin Wu, Glen Seidner, William Joiner, J. Paul Taylor, Ryan J. H. West, Albert R. La Spada
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-18 (2023)
Abstract Identifying genetic modifiers of familial amyotrophic lateral sclerosis (ALS) may reveal targets for therapeutic modulation with potential application to sporadic ALS. GGGGCC (G4C2) repeat expansions in the C9orf72 gene underlie the most com
Externí odkaz:
https://doaj.org/article/6f3ba7e74a9b45459c4b799036492c5d
Autor:
Ryan J. H. West, Joanne L. Sharpe, André Voelzmann, Anna L. Munro, Ines Hahn, Richard A. Baines, Stuart Pickering-Brown
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-19 (2020)
Abstract A large intronic hexanucleotide repeat expansion (GGGGCC) within the C9orf72 (C9orf72-SMCR8 Complex Subunit) locus is the most prevalent genetic cause of both Frontotemporal Dementia (FTD) and Motor Neuron Disease (MND). In patients this exp
Externí odkaz:
https://doaj.org/article/4e9a52c5a5ea4a479ca7cd7829ad0e49
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2021)
An intronic hexanucleotide (GGGGCC) expansion in the C9orf72 gene is the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). In the decade following its discovery, much progress has been made in enhanci
Externí odkaz:
https://doaj.org/article/c2cbff587b784e84af2115e8b3a0ad07
Publikováno v:
Frontiers in Cellular Neuroscience
An intronic hexanucleotide (GGGGCC) expansion in the C9orf72 gene is the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). In the decade following its discovery, much progress has been made in enhanci
Publikováno v:
Parkinson's Disease, Vol 2015 (2015)
We provide an insight into the role Drosophila has played in elucidating neurophysiological perturbations associated with Parkinson’s disease- (PD-) related genes. Synaptic signalling deficits are observed in motor, central, and sensory systems. Gi
Externí odkaz:
https://doaj.org/article/f4088b78b2734b019d65fa3a66440ec1
Autor:
Anna L. Munro, Ines Hahn, Ryan J. H. West, Stuart Pickering-Brown, Richard A. Baines, Joanne L. Sharpe, André Voelzmann
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-19 (2020)
Hahn, I, Sharpe, J, Voelzmann, A, Munro, A, Baines, R, Pickering-Brown, S & West, R 2020, ' Co-expression of C9orf72 related dipeptide-repeats over 1000 repeat units reveals age-and combination-specific phenotypic profiles in Drosophila ', Acta Neuropathologica Communications, vol. 8, no. 158 . https://doi.org/10.1186/s40478-020-01028-y
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-19 (2020)
Hahn, I, Sharpe, J, Voelzmann, A, Munro, A, Baines, R, Pickering-Brown, S & West, R 2020, ' Co-expression of C9orf72 related dipeptide-repeats over 1000 repeat units reveals age-and combination-specific phenotypic profiles in Drosophila ', Acta Neuropathologica Communications, vol. 8, no. 158 . https://doi.org/10.1186/s40478-020-01028-y
A large intronic hexanucleotide repeat expansion (GGGGCC) within the C9orf72 (C9orf72-SMCR8 Complex Subunit) locus is the most prevalent genetic cause of both Frontotemporal Dementia (FTD) and Motor Neuron Disease (MND). In patients this expansion is
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Mutations in CHMP2B, encoding a protein in the endosomal sorting complexes required for transport (ESCRT) machinery, causes frontotemporal dementia linked to chromosome 3 (FTD3). FTD, the second most common form of pre-senile dementia, can also be ca
Autor:
Ryan J. H. West, Khomgrit Morarach, Matthias Landgraf, Matthew C. W. Oswald, Maarten Zwart, Paul S Brooks, Richard A. Baines, Carlo N.G. Giachello, Sean T. Sweeney, Amrita Mukherjee
Publikováno v:
Oswald, M C W, Brooks, P S, Zwart, M F, Mukherjee, A, West, R J H, Giachello, C N G, Morarach, K, Baines, R A, Sweeney, S T & Landgraf, M 2018, ' Reactive oxygen species regulate activity-dependent neuronal plasticity in Drosophila ', eLife, vol. 7, e39393 . https://doi.org/10.7554/eLife.39393
eLife, Vol 7 (2018)
eLife
eLife, Vol 7 (2018)
eLife
Reactive oxygen species (ROS) have been extensively studied as damaging agents associated with ageing and neurodegenerative conditions. Their role in the nervous system under non-pathological conditions has remained poorly understood. Working with th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0acee3003e81ad0d77721c876988d0
https://www.repository.cam.ac.uk/handle/1810/289769
https://www.repository.cam.ac.uk/handle/1810/289769
Autor:
Ryan J. H. West, Chris Ugbode
Publikováno v:
Neurobiology of Disease, Vol 147, Iss, Pp 105144-(2021)
Frontotemporal dementia (FTD) and Amyotrophic Lateral Sclerosis (ALS) are two neurodegenerative diseases with clinical, genetic and pathological overlap. As such, they are commonly regarded as a single spectrum disorder, with pure FTD and pure ALS re