| Year |
Citation |
Score |
| 2024 |
Aubrey LD, Ninkina N, Ulamec SM, Abramycheva NY, Vasili E, Devine OM, Wilkinson M, Mackinnon E, Limorenko G, Walko M, Muwanga S, Amadio L, Peters OM, Illarioshkin SN, Outeiro TF, et al. Substitution of Met-38 to Ile in γ-synuclein found in two patients with amyotrophic lateral sclerosis induces aggregation into amyloid. Proceedings of the National Academy of Sciences of the United States of America. 121: e2309700120. PMID 38170745 DOI: 10.1073/pnas.2309700120 |
0.605 |
|
| 2023 |
Kahriman A, Bouley J, Tuncali I, Dogan EO, Pereira M, Luu T, Bosco DA, Jaber S, Peters OM, Brown RH, Henninger N. Repeated mild traumatic brain injury triggers pathology in asymptomatic C9ORF72 transgenic mice. Brain : a Journal of Neurology. PMID 37527465 DOI: 10.1093/brain/awad264 |
0.644 |
|
| 2023 |
Maddison DC, Malik B, Amadio L, Bis-Brewer DM, Züchner S, Peters OM, Smith GA. COPI-regulated mitochondria-ER contact site formation maintains axonal integrity. Cell Reports. 42: 112883. PMID 37498742 DOI: 10.1016/j.celrep.2023.112883 |
0.745 |
|
| 2021 |
Ninkina N, Millership SJ, Peters OM, Connor-Robson N, Chaprov K, Kopylov AT, Montoya A, Kramer H, Withers DJ, Buchman VL. β-synuclein potentiates synaptic vesicle dopamine uptake and rescues dopaminergic neurons from MPTP-induced death in the absence of other synucleins. The Journal of Biological Chemistry. 101375. PMID 34736896 DOI: 10.1016/j.jbc.2021.101375 |
0.627 |
|
| 2021 |
Peters OM, Smith GA. A nod and a Wnk to axon branching and destruction. Neuron. 109: 2799-2802. PMID 34534451 DOI: 10.1016/j.neuron.2021.08.027 |
0.76 |
|
| 2021 |
Peters OM, Weiss A, Metterville J, Song L, Logan R, Smith GA, Schwarzschild MA, Mueller C, Brown RH, Freeman M. Genetic diversity of axon degenerative mechanisms in models of Parkinson's disease. Neurobiology of Disease. 105368. PMID 33892050 DOI: 10.1016/j.nbd.2021.105368 |
0.738 |
|
| 2020 |
Hsu JM, Kang Y, Corty MM, Mathieson D, Peters OM, Freeman MR. Injury-Induced Inhibition of Bystander Neurons Requires dSarm and Signaling from Glia. Neuron. PMID 33296670 DOI: 10.1016/j.neuron.2020.11.012 |
0.583 |
|
| 2019 |
Malik BR, Maddison DC, Smith GA, Peters OM. Autophagic and endo-lysosomal dysfunction in neurodegenerative disease. Molecular Brain. 12: 100. PMID 31783880 DOI: 10.1186/S13041-019-0504-X |
0.758 |
|
| 2019 |
Kant S, Craige SM, Chen K, Reif MM, Learnard H, Kelly M, Caliz AD, Tran KV, Ramo K, Peters OM, Freeman M, Davis RJ, Keaney JF. Neural JNK3 regulates blood flow recovery after hindlimb ischemia in mice via an Egr1/Creb1 axis. Nature Communications. 10: 4223. PMID 31530804 DOI: 10.1038/S41467-019-11982-4 |
0.479 |
|
| 2018 |
Peters OM, Lewis EA, Osterloh JM, Weiss A, Salameh JS, Metterville J, Brown RH, Freeman MR. Loss of Sarm1 does not suppress motor neuron degeneration in the SOD1G93A mouse model of amyotrophic lateral sclerosis. Human Molecular Genetics. PMID 30010873 DOI: 10.1093/Hmg/Ddy260 |
0.69 |
|
| 2018 |
White MA, Kim E, Duffy A, Adalbert R, Phillips BU, Peters OM, Stephenson J, Yang S, Massenzio F, Lin Z, Andrews S, Segonds-Pichon A, Metterville J, Saksida LM, Mead R, et al. TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTD. Nature Neuroscience. PMID 29556029 DOI: 10.1038/S41593-018-0113-5 |
0.485 |
|
| 2016 |
Fil D, DeLoach A, Yadav S, Alkam D, MacNicol M, Singh A, Compadre CM, Goellner JJ, O'Brien CA, Fahmi T, Basnakian AG, Calingasan NY, Klessner JL, Flint Beal M, Peters OM, et al. Mutant Profilin1 Transgenic Mice Recapitulate Cardinal Features of Motor Neuron Disease. Human Molecular Genetics. PMID 28040732 DOI: 10.1093/Hmg/Ddw429 |
0.558 |
|
| 2016 |
Connor-Robson N, Peters OM, Millership S, Ninkina N, Buchman VL. Combinational losses of synucleins reveal their differential requirements for compensating age-dependent alterations in motor behavior and dopamine metabolism. Neurobiology of Aging. 46: 107-112. PMID 27614017 DOI: 10.1016/j.neurobiolaging.2016.06.020 |
0.623 |
|
| 2015 |
Peters OM, Cabrera GT, Tran H, Gendron TF, McKeon JE, Metterville J, Weiss A, Wightman N, Salameh J, Kim J, Sun H, Boylan KB, Dickson D, Kennedy Z, Lin Z, et al. Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice. Neuron. 88: 902-909. PMID 26637797 DOI: 10.1016/J.Neuron.2015.11.018 |
0.462 |
|
| 2015 |
Peters OM, Ghasemi M, Brown RH. Emerging mechanisms of molecular pathology in ALS. The Journal of Clinical Investigation. 125: 2548. PMID 26030230 DOI: 10.1172/JCI82693 |
0.347 |
|
| 2015 |
Peters OM, Ghasemi M, Brown RH. Emerging mechanisms of molecular pathology in ALS. The Journal of Clinical Investigation. 125: 1767-79. PMID 25932674 DOI: 10.1172/Jci71601 |
0.436 |
|
| 2014 |
Peters OM, Shelkovnikova T, Highley JR, Cooper-Knock J, Hortobágyi T, Troakes C, Ninkina N, Buchman VL. Gamma-synuclein pathology in amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology. 2: 29-37. PMID 25642432 DOI: 10.1002/acn3.143 |
0.689 |
|
| 2013 |
Shelkovnikova TA, Peters OM, Deykin AV, Connor-Robson N, Robinson H, Ustyugov AA, Bachurin SO, Ermolkevich TG, Goldman IL, Sadchikova ER, Kovrazhkina EA, Skvortsova VI, Ling SC, Da Cruz S, Parone PA, et al. Fused in sarcoma (FUS) protein lacking nuclear localization signal (NLS) and major RNA binding motifs triggers proteinopathy and severe motor phenotype in transgenic mice. The Journal of Biological Chemistry. 288: 25266-74. PMID 23867462 DOI: 10.1074/Jbc.M113.492017 |
0.694 |
|
| 2013 |
Peters OM, Shelkovnikova T, Tarasova T, Springe S, Kukharsky MS, Smith GA, Brooks S, Kozin SA, Kotelevtsev Y, Bachurin SO, Ninkina N, Buchman VL. Chronic administration of Dimebon does not ameliorate amyloid-β pathology in 5xFAD transgenic mice. Journal of Alzheimer's Disease : Jad. 36: 589-96. PMID 23645096 DOI: 10.3233/Jad-130071 |
0.716 |
|
| 2013 |
Peters OM, Connor-Robson N, Sokolov VB, Aksinenko AY, Kukharsky MS, Bachurin SO, Ninkina N, Buchman VL. Chronic administration of dimebon ameliorates pathology in TauP301S transgenic mice. Journal of Alzheimer's Disease : Jad. 33: 1041-9. PMID 23099813 DOI: 10.3233/JAD-2012-121732 |
0.593 |
|
| 2012 |
Ninkina N, Peters OM, Connor-Robson N, Lytkina O, Sharfeddin E, Buchman VL. Contrasting effects of α-synuclein and γ-synuclein on the phenotype of cysteine string protein α (CSPα) null mutant mice suggest distinct function of these proteins in neuronal synapses. The Journal of Biological Chemistry. 287: 44471-7. PMID 23129765 DOI: 10.1074/jbc.M112.422402 |
0.628 |
|
| 2012 |
Peters OM, Millership S, Shelkovnikova TA, Soto I, Keeling L, Hann A, Marsh-Armstrong N, Buchman VL, Ninkina N. Selective pattern of motor system damage in gamma-synuclein transgenic mice mirrors the respective pathology in amyotrophic lateral sclerosis. Neurobiology of Disease. 48: 124-31. PMID 22750530 DOI: 10.1016/j.nbd.2012.06.016 |
0.69 |
|
| 2011 |
Bachurin SO, Shelkovnikova TA, Ustyugov AA, Peters O, Khritankova I, Afanasieva MA, Tarasova TV, Alentov II, Buchman VL, Ninkina NN. Dimebon slows progression of proteinopathy in γ-synuclein transgenic mice. Neurotoxicity Research. 22: 33-42. PMID 22179976 DOI: 10.1007/s12640-011-9299-y |
0.673 |
|
| 2011 |
Anwar S, Peters O, Millership S, Ninkina N, Doig N, Connor-Robson N, Threlfell S, Kooner G, Deacon RM, Bannerman DM, Bolam JP, Chandra SS, Cragg SJ, Wade-Martins R, Buchman VL. Functional alterations to the nigrostriatal system in mice lacking all three members of the synuclein family. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 7264-74. PMID 21593311 DOI: 10.1523/Jneurosci.6194-10.2011 |
0.644 |
|
| 2011 |
Shelkovnikova TA, Ustyugov AA, Millership S, Peters O, Anichtchik O, Spillantini MG, Buchman VL, Bachurin SO, Ninkina NN. Dimebon does not ameliorate pathological changes caused by expression of truncated (1-120) human alpha-synuclein in dopaminergic neurons of transgenic mice. Neuro-Degenerative Diseases. 8: 430-7. PMID 21576917 DOI: 10.1159/000324989 |
0.66 |
|
| 2009 |
Ninkina N, Peters O, Millership S, Salem H, van der Putten H, Buchman VL. Gamma-synucleinopathy: neurodegeneration associated with overexpression of the mouse protein. Human Molecular Genetics. 18: 1779-94. PMID 19246516 DOI: 10.1093/hmg/ddp090 |
0.661 |
|
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