Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Chris M. Morris"'
Autor:
Michael J. Keogh, Wei Wei, Juvid Aryaman, Lauren Walker, Jelle van den Ameele, Jon Coxhead, Ian Wilson, Matthew Bashton, Jon Beck, John West, Richard Chen, Christian Haudenschild, Gabor Bartha, Shujun Luo, Chris M. Morris, Nick S. Jones, Johannes Attems, Patrick F. Chinnery
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-12 (2018)
Similar to cancers, somatic mutations might lead to neurodegenerative diseases. Here, the authors perform ultra-deep sequencing of 102 genes in 173 adult human brains, detect somatic mutations in 54 brains, and develop a mathematical model to estimat
Externí odkaz:
https://doaj.org/article/4340dcba8f0b45e0b3cd339e05e6fd88
Autor:
Amanda J. Myers, Alan M. Pittman, Alice S. Zhao, Kristen Rohrer, Mona Kaleem, Lauren Marlowe, Andrew Lees, Doris Leung, Ian G. McKeith, Robert H. Perry, Chris M. Morris, John Q. Trojanowski, Christopher Clark, Jason Karlawish, Steve Arnold, Mark S. Forman, Vivianna Van Deerlin, Rohan de Silva, John Hardy
Publikováno v:
Neurobiology of Disease, Vol 25, Iss 3, Pp 561-570 (2007)
Previously we have shown that the H1c haplotype on the background of the H1 clade of haplotypes at the MAPT locus is associated with increased risk for progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and Alzheimer’s disease (A
Externí odkaz:
https://doaj.org/article/8d634a24426e480a820cfa3b11293a36
Autor:
David J. Burn, Elaine K. Perry, John T. O’Brien, Neil Archibald, Elizabeta B. Mukaetova-Ladinska, Joaquim Cerejeira, Daniel Collerton, Evelyn Jaros, Robert Perry, Margaret A. Piggott, Chris M. Morris, Andrew Mclaren, Clive G. Ballard, Ian G. Mckeith
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba214833f2d03b6ed3fb21c101613e2
https://doi.org/10.1093/med/9780199798261.003.0062
https://doi.org/10.1093/med/9780199798261.003.0062
Autor:
Parastoo, Momeni, Ekaterina, Rogaeva, Vivianna, Van Deerlin, Wuxing, Yuan, Jordan, Grafman, Michael, Tierney, Edward, Huey, Jason, Bell, Chris M, Morris, Rajesh N, Kalaria, Susan J, van Rensburg, Dana, Niehaus, Felix, Potocnik, Toshitaka, Kawarai, Shabnam, Salehi-Rad, Christine, Sato, Peter, St George-Hyslop, John, Hardy
Publikováno v:
Neuro-degenerative diseases. 3(3)
A nonsense/protein chain-terminating mutation in the CHMP2B gene has recently been reported as a cause of frontotemporal dementia (FTD) in the single large family known to show linkage to chromosome 3. Screening for mutations in this gene in a large
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::72d75d76dc416954f1d76a34d9cc0b25
https://pubmed.ncbi.nlm.nih.gov/16954699
https://pubmed.ncbi.nlm.nih.gov/16954699
Autor:
Scott Smemo, Petra Nowotny, Anthony L. Hinrichs, John S. K. Kauwe, Sara Cherny, Katherine Erickson, Amanda J. Myers, Mona Kaleem, Lauren Marlowe, Alison M. Gibson, Paul Hollingworth, Michael C. O'Donovan, Chris M. Morris, Peter Holmans, Simon Lovestone, John C. Morris, Leon Thal, Yonghong Li, Andrew Grupe, John Hardy
Publikováno v:
Annals of Neurology; Jan2006, Vol. 59 Issue 1, p21-26, 0p
Autor:
Heike Vollbach, Reinhard Heun, Chris M. Morris, Jim A. Edwardson, Ian G. McKeith, Frank Jessen, Anne Schulz, Wolfgang Maier, Heike Kölsch
Publikováno v:
Annals of Neurology; Sep2005, Vol. 58 Issue 3, p436-441, 0p
Autor:
Tim H Ward, Duncan C Gilbert, George Higginbotham, Chris M Morris, Valerie Speirs, Nicola J Curtin
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 8, Iss 1, Pp 3-13 (2022)
Abstract Half of all cancer patients receive radiotherapy, which makes a substantial contribution to their long‐term disease control/cure. There are significant inter‐patient differences in response, both in terms of efficacy and toxicity (freque
Externí odkaz:
https://doaj.org/article/09dae4cbd5104361b79da6053436b26d