Year |
Citation |
Score |
2016 |
Decker JM, Krüger L, Sydow A, Dennissen F, Siskovà Z, Mandelkow E, Mandelkow EM. The Tau/A152T mutation, a risk factor for frontotemporal-spectrum disorders, leads to NR2B receptor-mediated excitotoxicity. Embo Reports. PMID 26931569 DOI: 10.15252/Embr.201541439 |
0.403 |
|
2012 |
Caleo M, Restani L, Vannini E, Siskova Z, Al-Malki H, Morgan R, O'Connor V, Perry VH. The role of activity in synaptic degeneration in a protein misfolding disease, prion disease. Plos One. 7: e41182. PMID 22815961 DOI: 10.1371/Journal.Pone.0041182 |
0.489 |
|
2010 |
Sisková Z, Mahad DJ, Pudney C, Campbell G, Cadogan M, Asuni A, O'Connor V, Perry VH. Morphological and functional abnormalities in mitochondria associated with synaptic degeneration in prion disease. The American Journal of Pathology. 177: 1411-21. PMID 20651247 DOI: 10.2353/Ajpath.2010.091037 |
0.321 |
|
2010 |
Sisková Z, Sanyal NK, Orban A, O'Connor V, Perry VH. Reactive hypertrophy of synaptic varicosities within the hippocampus of prion-infected mice. Biochemical Society Transactions. 38: 471-5. PMID 20298205 DOI: 10.1042/Bst0380471 |
0.465 |
|
2010 |
Asuni AA, Hilton K, Siskova Z, Lunnon K, Reynolds R, Perry VH, O'Connor V. Alpha-synuclein deficiency in the C57BL/6JOlaHsd strain does not modify disease progression in the ME7-model of prion disease. Neuroscience. 165: 662-74. PMID 19879926 DOI: 10.1016/J.Neuroscience.2009.10.047 |
0.326 |
|
2009 |
Sisková Z, Page A, O'Connor V, Perry VH. Degenerating synaptic boutons in prion disease: microglia activation without synaptic stripping. The American Journal of Pathology. 175: 1610-21. PMID 19779137 DOI: 10.2353/Ajpath.2009.090372 |
0.487 |
|
2009 |
Gray BC, Siskova Z, Perry VH, O'Connor V. Selective presynaptic degeneration in the synaptopathy associated with ME7-induced hippocampal pathology. Neurobiology of Disease. 35: 63-74. PMID 19362593 DOI: 10.1016/J.Nbd.2009.04.001 |
0.517 |
|
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