Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Richard Wroe"'
Autor:
Michelle K Lupton, Petroula Proitsi, Makrina Danillidou, Magda Tsolaki, Gillian Hamilton, Richard Wroe, Megan Pritchard, Kathryn Lord, Belinda M Martin, Iwona Kloszewska, Hilkka Soininen, Patrizia Mecocci, Bruno Vellas, Denise Harold, Paul Hollingworth, Simon Lovestone, John F Powell
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e17298 (2011)
Nicastrin is an obligatory component of the γ-secretase; the enzyme complex that leads to the production of Aβ fragments critically central to the pathogenesis of Alzheimer's disease (AD). Analyses of the effects of common variation in this gene on
Externí odkaz:
https://doaj.org/article/23a00884875846cc8154fa1c9d1e808c
Autor:
Bilal Malik, Stuart Kellie, C. Hugh Reynolds, Cathy Fernandes, Richard Killick, Ritchie Williamson, Brian H. Anderton, Richard Wroe, Alessia Usardi
Publikováno v:
Neurochemistry International. 61:321-333
Amyloid-β peptide (Aβ) is the principal component of plaques in the brains of patients with Alzheimer's disease (AD), and the most toxic form of Aβ may be as soluble oligomers. We report here the results of a microarray study of gene expression pr
Autor:
Chantelle Fernandes, John Stephenson, Karelle Leroy, Alessia Usardi, Anbarasu Lourdusamy, Richard Williamson, Patrick M. Nolan, Elena M. Ribe, Wendy Noble, Angela Hodges, Christopher A. Reynolds, Richard Wroe, Chantal Bazenet, Claudie Hooper, Mirsada Causevic, Stuart Kellie, Alvina W.M. To, J-P. Brion, Raya Al-Shawi, Simon Lovestone, Katie Lunnon, Gerome Breen, Richard Dobson, Martha Robinson, J. Paul Simons, Simon J. Furney, Richard Killick, Kuang Lin, Bilal Malik
Publikováno v:
Molecular psychiatry, 19 (1
Molecular Psychiatry
Killick, R, Ribe, E M, Al-Shawi, R, Malik, B, Hooper, C, Fernandes, C, Dobson, R, Nolan, P M, Lourdusamy, A, Furney, S, Lin, K, Breen, G, Wroe, R, To, A W M, Leroy, K, Causevic, M, Usardi, A, Robinson, M, Noble, W, Williamson, R, Lunnon, K, Kellie, S, Reynolds, C H, Bazenet, C, Hodges, A, Brion, J-P, Stephenson, J, Paul Simons, J & Lovestone, S 2014, ' Clusterin regulates β-amyloid toxicity via Dickkopf-1-driven induction of the wnt-PCP-JNK pathway ', Molecular Psychiatry, vol. 19, no. 1, pp. 88-98 . https://doi.org/10.1038/mp.2012.163
Molecular Psychiatry
Killick, R, Ribe, E M, Al-Shawi, R, Malik, B, Hooper, C, Fernandes, C, Dobson, R, Nolan, P M, Lourdusamy, A, Furney, S, Lin, K, Breen, G, Wroe, R, To, A W M, Leroy, K, Causevic, M, Usardi, A, Robinson, M, Noble, W, Williamson, R, Lunnon, K, Kellie, S, Reynolds, C H, Bazenet, C, Hodges, A, Brion, J-P, Stephenson, J, Paul Simons, J & Lovestone, S 2014, ' Clusterin regulates β-amyloid toxicity via Dickkopf-1-driven induction of the wnt-PCP-JNK pathway ', Molecular Psychiatry, vol. 19, no. 1, pp. 88-98 . https://doi.org/10.1038/mp.2012.163
Although the mechanism of Aβ action in the pathogenesis of Alzheimer's disease (AD) has remained elusive, it is known to increase the expression of the antagonist of canonical wnt signalling, Dickkopf-1 (Dkk1), whereas the silencing of Dkk1 blocks A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08d852d2e28fab1f69dcf47924b534aa
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/132854
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/132854
Autor:
Kathryn Lord, Simon Lovestone, Michelle K. Lupton, Bruno Vellas, Patrizia Mecocci, Richard Wroe, Gillian Hamilton, John Powell, Makrina Danillidou, Denise Harold, Magda Tsolaki, Hilkka Soininen, Megan Pritchard, Paul Hollingworth, Iwona Kłoszewska, Petroula Proitsi, Belinda M. Martin
Publikováno v:
Lupton, M K, Proitsi, P, Danillidou, M, Tsolaki, M, Hamilton, G, Wroe, R, Pritchard, M, Lord, K, Martin, B M, Kloszewska, I, Soininen, H, Mecocci, P, Vellas, B, Harold, D, Hollingworth, P, Lovestone, S & Powell, J F 2011, ' Deep Sequencing of the Nicastrin Gene in Pooled DNA, the Identification of Genetic Variants That Affect Risk of Alzheimer's Disease ', PLoS ONE, vol. 6, no. 2, e17298, pp.-. https://doi.org/10.1371/journal.pone.0017298
King's College London
PLoS ONE, Vol 6, Iss 2, p e17298 (2011)
PLoS ONE
PLoS ONE; Vol 6
King's College London
PLoS ONE, Vol 6, Iss 2, p e17298 (2011)
PLoS ONE
PLoS ONE; Vol 6
Nicastrin is an obligatory component of the c-secretase; the enzyme complex that leads to the production of Ab fragments critically central to the pathogenesis of Alzheimer's disease (AD). Analyses of the effects of common variation in this gene on r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e4b9e277b1b36bdfc49316bacb8085c
https://orca.cardiff.ac.uk/id/eprint/80475/1/journal.pone.0017298.pdf
https://orca.cardiff.ac.uk/id/eprint/80475/1/journal.pone.0017298.pdf
Autor:
Mandy Y.M. Ng, Richard Wroe, Amy W. Butler, Paola Forabosco, Ammar Al-Chalabi, Marian L. Hamshere, John Powell, Cathryn M. Lewis
Publikováno v:
Neurobiology of aging. 30(7)
Familial late-onset Alzheimer's disease (LOAD) shows high heritability. However, with the exception of ApoE, no well-replicated susceptibility genes have been identified to date. Several genome-wide linkage studies have nominated potential susceptibi
A central question in molecular evolution concerns the nature of phenotypic transitions, in particular, if neutral mutations hamper or somehow facilitate adaptability of proteins to new requirements. Proteins have been found to fluctuate between diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b45cad47c8b9683287363a9453947e3
https://europepmc.org/articles/PMC2645552/
https://europepmc.org/articles/PMC2645552/
Understanding the evolution of biopolymers is a key element in rationalizing their structures and functions. Simple exact models (SEMs) are well-positioned to address general principles of evolution as they permit the exhaustive enumeration of both s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc1882001ebb340d7cea7d46ab49f50b
https://europepmc.org/articles/PMC1304991/
https://europepmc.org/articles/PMC1304991/
Publikováno v:
Amyotrophic Lateral Sclerosis. 9:249-250
More than 100 point mutations spanning the 153 amino acid SOD1 sequence have been identified in individuals with ALS. In 1999 the Amyotrophic Lateral Sclerosis Database (ALSOD) was generated to store these mutations along with ALS patient information