Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Megan J. Dowie"'
Publikováno v:
PLoS Biology, Vol 10, Iss 6, p e1001340 (2012)
Externí odkaz:
https://doaj.org/article/1f43c0e074964d6e866bd1a6f624e087
Publikováno v:
The Neuroscientist. 23:7-15
Engaging young people with science is essential to ensuring a scientifically literate society. Furthermore, it is important to enable access to a variety of sciences during adolescence, when individuals are making decisions about their future educati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fcdc8eb923ced4ea6e3b6282c3cdae4
https://doi.org/10.1177/1073858415600150
https://doi.org/10.1177/1073858415600150
The endogenous cannabinoid system is integral to normal physiology and has been implicated in the pathology of a number of neurological conditions. Components of the endocannabinoid system display an abundant and widespread distribution throughout th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6473a83b3e08eb032d254aac796af829
https://doi.org/10.1016/b978-0-12-809666-6.00005-8
https://doi.org/10.1016/b978-0-12-809666-6.00005-8
Autor:
John C. Ashton, Balapal S. Basavarajappa, Natalia Battista, Megan J. Dowie, Andrea Giuffrida, Michelle Glass, Bernard Le Foll, F. Markus Leweke, Mauro Maccarrone, Alex Martinez, Cathrin Rohleder, Jose M. Trigo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24c19d9db4987826bcb7ea37c0f22bab
https://doi.org/10.1016/b978-0-12-809666-6.01002-9
https://doi.org/10.1016/b978-0-12-809666-6.01002-9
Publikováno v:
Journal of Chemical Neuroanatomy. :62-71
Huntington's disease (HD) is an inherited neurological disease with motor, cognitive and psychiatric symptoms. Characterised by neuronal degeneration, HD pathology is initially apparent in the striatum and cortex. Considerable research has recently s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fe8ff06f0d6c18d582bcdb3fc5c3c31
https://doi.org/10.1016/j.jchemneu.2014.06.004
https://doi.org/10.1016/j.jchemneu.2014.06.004
Autor:
Louise F.B. Nicholson, Richard L.M. Faull, Megan J. Dowie, Michelle Glass, Anthony J. Hannan, Monique L. Howard
Publikováno v:
Neuroscience. 170:324-336
Early loss of CB1 receptors is a hallmark of human Huntington's disease. Data from rodent studies suggest that preservation and activation of CB1 receptors may be protective against disease progression. R6/1 transgenic mice are considered to be a mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aadb5f3cafbe76975ccc1718dc3932b5
https://doi.org/10.1016/j.neuroscience.2010.06.056
https://doi.org/10.1016/j.neuroscience.2010.06.056
Autor:
Megan J. Dowie, Louise F.B. Nicholson
Publikováno v:
The Neuroscientist. 17:9-17
The 3rd hosting of the Auckland region New Zealand Brain Bee Challenge was held in 2009. Designed as a neuroscience quiz for high school students, the competition provides a valuable case study for science outreach. By engaging with teenagers, the fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a193c4e3a6b584672a867db04d2dd78a
https://doi.org/10.1177/1073858410367520
https://doi.org/10.1177/1073858410367520
Autor:
Monique L. Howard, Richard L.M. Faull, Michelle Glass, Megan J. Dowie, Louise F.B. Nicholson, Anthony J. Hannan, Heather B. Bradshaw
Publikováno v:
Neuroscience. 163:456-465
Huntington's disease (HD) is an inherited neurodegenerative disease characterised by cell dysfunction and death in the basal ganglia and cortex. Currently there are no effective pharmacological treatments available. Loss of cannabinoid CB1 receptor l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc19c9a65908dbc3a0ff9db33ffe5f46
https://doi.org/10.1016/j.neuroscience.2009.06.014
https://doi.org/10.1016/j.neuroscience.2009.06.014
Publikováno v:
Pharmacologytherapeutics. 128(2)
Huntington's disease is a late-onset autosomal dominant inherited neurodegenerative disease characterised by increased symptom severity over time and ultimately premature death. An expanded CAG repeat sequence in the huntingtin gene leads to a polygl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ef525529ccd9122574f7c214dc18c42
https://pubmed.ncbi.nlm.nih.gov/20708032
https://pubmed.ncbi.nlm.nih.gov/20708032
Autor:
John C. Ashton, J. Wilkerson, Philip W. Brownjohn, E. Milligan, Michelle Glass, Megan J. Dowie
Publikováno v:
European Journal of Pain. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c2acd7360a1b3221296e1b06a951d34
https://doi.org/10.1016/s1090-3801(09)60169-5
https://doi.org/10.1016/s1090-3801(09)60169-5