Heterogeneous Nuclear Ribonucleoproteins: Implications in Neurological Diseases

von Low, Yi-Hua, Asi, Yasmine, Foti, Sandrine C., Lashley, Tammaryn
Veröffentlicht in Mol Neurobiol (2020)

Identification and Quantification of Oligodendrocyte Precursor Cells in Multiple System Atrophy, Progressive Supranuclear Palsy and Parkinson's Disease

von Ahmed, Zeshan, Asi, Yasmine T., Lees, Andrew J., Revesz, Tamas, Holton, Janice L.
Veröffentlicht in Brain Pathol (2012)

Alpha-synuclein mRNA expression in oligodendrocytes in MSA

von Asi, Yasmine T, Simpson, Julie E, Heath, Paul R, Wharton, Stephen B, Lees, Andrew J, Revesz, Tamas, Houlden, Henry, Holton, Janice L
Veröffentlicht in Glia (2014)

Alzheimer’s disease phospholipase C-gamma-2 (PLCG2) protective variant is a functional hypermorph

von Magno, Lorenza, Lessard, Christian B., Martins, Marta, Lang, Verena, Cruz, Pedro, Asi, Yasmine, Katan, Matilda, Bilsland, Jamie, Lashley, Tammaryn, Chakrabarty, Paramita, Golde, Todd E., Whiting, Paul J.
Veröffentlicht in Alzheimers Res Ther (2019)

α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy?

von Kiely, Aoife P., Asi, Yasmine T., Kara, Eleanna, Limousin, Patricia, Ling, Helen, Lewis, Patrick, Proukakis, Christos, Quinn, Niall, Lees, Andrew J., Hardy, John, Revesz, Tamas, Houlden, Henry, Holton, Janice L.
Veröffentlicht 2013

Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemp...

von Davidson, Yvonne S., Robinson, Andrew C., Flood, Louis, Rollinson, Sara, Benson, Bridget C., Asi, Yasmine T., Richardson, Anna, Jones, Matthew, Snowden, Julie S., Pickering-Brown, Stuart, Lashley, Tammaryn, Mann, David M. A.
Veröffentlicht in Acta Neuropathol Commun (2017)

Identification of multiple system atrophy mimicking Parkinson’s disease or progressive supranuclear palsy

von Miki, Yasuo, Tsushima, Eiki, Foti, Sandrine C, Strand, Kate M, Asi, Yasmine T, Yamamoto, Adam Kenji, Bettencourt, Conceição, Oliveira, Marcos C B, De Pablo-Fernández, Eduardo, Jaunmuktane, Zane, Lees, Andrew J, Wakabayashi, Koichi, Warner, Thomas T, Quinn, Niall, Holton, Janice L, Ling, Helen
Veröffentlicht in Brain (2021)

Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation

von Kiely, Aoife P., Ling, Helen, Asi, Yasmine T., Kara, Eleanna, Proukakis, Christos, Schapira, Anthony H., Morris, Huw R., Roberts, Helen C., Lubbe, Steven, Limousin, Patricia, Lewis, Patrick A., Lees, Andrew J., Quinn, Niall, Hardy, John, Love, Seth, Revesz, Tamas, Houlden, Henry, Holton, Janice L.
Veröffentlicht in Mol Neurodegener (2015)