Heather Tian Whittaker

Affiliations: 
McGill University (Montreal Neurological Institute) 
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"Heather Whittaker"
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Wu Y, Whittaker HT, Noy S, et al. (2021) The effects of Cstb duplication on APP/amyloid-β pathology and cathepsin B activity in a mouse model. Plos One. 16: e0242236
Tosh JL, Rhymes ER, Mumford P, et al. (2021) Publisher Correction: Genetic dissection of down syndrome‑associated alterations in APP/amyloid‑β biology using mouse models. Scientific Reports. 11: 14966
Tosh JL, Rhymes ER, Mumford P, et al. (2021) Genetic dissection of down syndrome-associated alterations in APP/amyloid-β biology using mouse models. Scientific Reports. 11: 5736
Wiseman FK, Pulford LJ, Barkus C, et al. (2019) Trisomy of human chromosome 21 enhances amyloid-beta 3 deposition independently of an extra copy of APP (vol 141, pg 2457, 2018) Brain. 142
Wiseman FK, Pulford LJ, Barkus C, et al. (2018) Trisomy of human chromosome 21 enhances amyloid-β deposition independently of an extra copy of APP. Brain : a Journal of Neurology
Whittaker HT, Zhu S, Di Curzio DL, et al. (2018) T, diffusion tensor, and quantitative magnetization transfer imaging of the hippocampus in an Alzheimer's disease mouse model. Magnetic Resonance Imaging
Wiseman FK, Pulford LJ, Barkus C, et al. (2017) TRISOMY 21 CAUSES A DEFICIT IN LYSOSOMAL CATHEPSINS AND ALTERS APP/Aβ PROCESSING, INDEPENDENTLY OF AN EXTRA COPY OF APP Alzheimers & Dementia. 13
Herrera SL, Palmer VL, Whittaker H, et al. (2014) Damage to the optic chiasm in myelin oligodendrocyte glycoprotein-experimental autoimmune encephalomyelitis mice. Magnetic Resonance Insights. 7: 23-31
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