A Neurochemical Basis for Phenotypic Differentiation in Alzheimer's Disease? Turing's Morphogens Revisited

Por Whittaker, Heather T., Warren, Jason D.
Publicado no Front Aging Neurosci (2017)

Multiple system atrophy: genetic risks and alpha-synuclein mutations

Por Whittaker, Heather T, Qui, Yichen, Bettencourt, Conceição, Houlden, Henry
Publicado no F1000Res (2017)

Damage to the Optic Chiasm in Myelin Oligodendrocyte Glycoprotein–Experimental Autoimmune Encephalomyelitis Mice

Por Herrera, Sheryl L, Palmer, Vanessa L, Whittaker, Heather, Smith, Blair Cardigan, Kim, Annie, Schellenberg, Angela E, Thiessen, Jonathan D, Buist, Richard, Del Bigio, Marc R, Martin, Melanie
Publicado no Magn Reson Insights (2014)

Trisomy of human chromosome 21 enhances amyloid-β deposition independently of an extra copy of APP

Por Wiseman, Frances K, Pulford, Laura J, Barkus, Chris, Liao, Fan, Portelius, Erik, Webb, Robin, Chávez-Gutiérrez, Lucia, Cleverley, Karen, Noy, Sue, Sheppard, Olivia, Collins, Toby, Powell, Caroline, Sarell, Claire J, Rickman, Matthew, Choong, Xun, Tosh, Justin L, Siganporia, Carlos, Whittaker, Heather T, Stewart, Floy, Szaruga, Maria, Murphy, Michael P, Blennow, Kaj, de Strooper, Bart, Zetterberg, Henrik, Bannerman, David, Holtzman, David M, Tybulewicz, Victor L J, Fisher, Elizabeth M C
Publicado no Brain (2018)