Year |
Citation |
Score |
2023 |
Arrázola MS, Lira M, Véliz-Valverde F, Quiroz G, Iqbal S, Eaton SL, Lamont DJ, Huerta H, Ureta G, Bernales S, Cárdenas JC, Cerpa W, Wishart TM, Court FA. Necroptosis inhibition counteracts neurodegeneration, memory decline, and key hallmarks of aging, promoting brain rejuvenation. Aging Cell. e13814. PMID 36973898 DOI: 10.1111/acel.13814 |
0.623 |
|
2022 |
Kline RA, Lößlein L, Kurian D, Aguilar Martí J, Eaton SL, Court FA, Gillingwater TH, Wishart TM. An Optimized Comparative Proteomic Approach as a Tool in Neurodegenerative Disease Research. Cells. 11. PMID 36078061 DOI: 10.3390/cells11172653 |
0.678 |
|
2022 |
Ledahawsky LM, Eirini Terzenidou M, Edwards R, Kline RA, Graham LC, Eaton SL, van der Hoorn D, Chaytow H, Huang YT, Groen EJN, Motyl AAL, Lamont DJ, Tokatlidis K, Wishart TM, Gillingwater TH. The mitochondrial protein Sideroflexin 3 (SFXN3) influences neurodegeneration pathways in vivo. The Febs Journal. PMID 35092170 DOI: 10.1111/febs.16377 |
0.637 |
|
2021 |
Graham LC, Kline RA, Lamont DJ, Gillingwater TH, Mabbott NA, Skehel PA, Wishart TM. Temporal Profiling of the Cortical Synaptic Mitochondrial Proteome Identifies Ageing Associated Regulators of Stability. Cells. 10. PMID 34943911 DOI: 10.3390/cells10123403 |
0.565 |
|
2021 |
Roesl C, Evans ER, Dissanayake KN, Boczonadi V, Jones RA, Jordan GR, Ledahawsky L, Allen GCC, Scott M, Thomson A, Wishart TM, Hughes DI, Mead RJ, Shone CC, Slater CR, et al. Confocal Endomicroscopy of Neuromuscular Junctions Stained with Physiologically Inert Protein Fragments of Tetanus Toxin. Biomolecules. 11. PMID 34680132 DOI: 10.3390/biom11101499 |
0.768 |
|
2021 |
Deguise MO, Pileggi C, De Repentigny Y, Beauvais A, Tierney A, Chehade L, Michaud J, Llavero-Hurtado M, Lamont D, Atrih A, Wishart TM, Gillingwater TH, Schneider BL, Harper ME, Parson SH, et al. SMN depleted mice offer a robust and rapid onset model of non-alcoholic fatty liver disease. Cellular and Molecular Gastroenterology and Hepatology. PMID 33545428 DOI: 10.1016/j.jcmgh.2021.01.019 |
0.695 |
|
2021 |
Graham LC, Kline RA, Lamont DJ, Gillingwater TH, Mabbott NA, Skehel PA, Wishart TM. Temporal Profiling of the Cortical Synaptic Mitochondrial Proteome Identifies Ageing Associated Regulators of Stability Cells. 10: 3403. DOI: 10.3390/cells10123403 |
0.566 |
|
2020 |
Lemaitre D, Hurtado ML, De Gregorio C, Oñate M, Martínez G, Catenaccio A, Wishart TM, Court FA. Collateral Sprouting of Peripheral Sensory Neurons Exhibits a Unique Transcriptomic Profile. Molecular Neurobiology. PMID 32696431 DOI: 10.1007/s12035-020-01986-3 |
0.647 |
|
2020 |
Motyl AAL, Faller KME, Groen EJN, Kline RA, Eaton SL, Ledahawsky LM, Chaytow H, Lamont DJ, Wishart TM, Huang YT, Gillingwater TH. Pre-natal manifestation of systemic developmental abnormalities in spinal muscular atrophy. Human Molecular Genetics. PMID 32644120 DOI: 10.1093/hmg/ddaa146 |
0.588 |
|
2020 |
Boehm I, Alhindi A, Leite AS, Logie C, Gibbs A, Murray O, Farrukh R, Pirie R, Proudfoot C, Clutton R, Wishart TM, Jones RA, Gillingwater TH. Comparative anatomy of the mammalian neuromuscular junction. Journal of Anatomy. PMID 32573802 DOI: 10.1111/joa.13260 |
0.566 |
|
2019 |
Boehm I, Miller J, Wishart TM, Wigmore SJ, Skipworth RJ, Jones RA, Gillingwater TH. Neuromuscular junctions are stable in patients with cancer cachexia. The Journal of Clinical Investigation. PMID 31794435 DOI: 10.1172/JCI128411 |
0.548 |
|
2019 |
Kline RA, Dissanayake KN, Hurtado ML, Martínez NW, Ahl A, Mole AJ, Lamont DJ, Court FA, Ribchester RR, Wishart TM, Murray LM. Altered mitochondrial bioenergetics are responsible for the delay in Wallerian degeneration observed in neonatal mice. Neurobiology of Disease. 104496. PMID 31176719 DOI: 10.1016/J.Nbd.2019.104496 |
0.786 |
|
2019 |
Graham LC, Naldrett MJ, Kohama SG, Smith C, Lamont DJ, McColl BW, Gillingwater TH, Skehel P, Urbanski HF, Wishart TM. Regional Molecular Mapping of Primate Synapses during Normal Healthy Aging. Cell Reports. 27: 1018-1026.e4. PMID 31018120 DOI: 10.1016/J.Celrep.2019.03.096 |
0.561 |
|
2019 |
Boehm I, Miller J, Wishart T, Wigmore S, Jones R, Skipworth R, Gillingwater T. SUN-LB665: Stability of the Neuromuscular Junction in Cancer Cachexia Clinical Nutrition. 38: S306. DOI: 10.1016/S0261-5614(19)32631-7 |
0.452 |
|
2018 |
Shorrock HK, van der Hoorn D, Boyd PJ, Llavero Hurtado M, Lamont DJ, Wirth B, Sleigh JN, Schiavo G, Wishart TM, Groen EJN, Gillingwater TH. UBA1/GARS-dependent pathways drive sensory-motor connectivity defects in spinal muscular atrophy. Brain : a Journal of Neurology. 141: 2878-2894. PMID 30239612 DOI: 10.1093/Brain/Awy237 |
0.581 |
|
2017 |
Jones RA, Harrison C, Eaton SL, Llavero Hurtado M, Graham LC, Alkhammash L, Oladiran OA, Gale A, Lamont DJ, Simpson H, Simmen MW, Soeller C, Wishart TM, Gillingwater TH. Cellular and Molecular Anatomy of the Human Neuromuscular Junction. Cell Reports. 21: 2348-2356. PMID 29186674 DOI: 10.1016/j.celrep.2017.11.008 |
0.613 |
|
2017 |
Catenaccio A, Llavero Hurtado M, Diaz P, Lamont DJ, Wishart TM, Court FA. Molecular analysis of axonal-intrinsic and glial-associated co-regulation of axon degeneration. Cell Death & Disease. 8: e3166. PMID 29120410 DOI: 10.1038/cddis.2017.489 |
0.615 |
|
2017 |
Graham LC, Eaton SL, Brunton PJ, Atrih A, Smith C, Lamont DJ, Gillingwater TH, Pennetta G, Skehel P, Wishart TM. Proteomic profiling of neuronal mitochondria reveals modulators of synaptic architecture. Molecular Neurodegeneration. 12: 77. PMID 29078798 DOI: 10.1186/S13024-017-0221-9 |
0.608 |
|
2017 |
Llavero Hurtado M, Fuller HR, Wong AMS, Eaton SL, Gillingwater TH, Pennetta G, Cooper JD, Wishart TM. Proteomic mapping of differentially vulnerable pre-synaptic populations identifies regulators of neuronal stability in vivo. Scientific Reports. 7: 12412. PMID 28963550 DOI: 10.1038/s41598-017-12603-0 |
0.626 |
|
2017 |
McQueen J, Ryan TJ, McKay S, Marwick KF, Baxter PE, Carpanini SM, Wishart TM, Gillingwater TH, Manson JC, Wyllie DJ, Grant SG, McColl B, Komiyama N, Hardingham GE. Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of DAPK1. Elife. 6. PMID 28731405 DOI: 10.7554/Elife.17161 |
0.49 |
|
2017 |
Boyd PJ, Tu WY, Shorrock HK, Groen EJN, Carter RN, Powis RA, Thomson SR, Thomson D, Graham LC, Motyl AAL, Wishart TM, Highley JR, Morton NM, Becker T, Becker CG, et al. Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy. Plos Genetics. 13: e1006744. PMID 28426667 DOI: 10.1371/journal.pgen.1006744 |
0.61 |
|
2017 |
Carpanini SM, Wishart TM, Gillingwater TH, Manson JC, Summers KM. Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and disease. Neurogenetics. PMID 28190221 DOI: 10.1007/s10048-017-0509-5 |
0.535 |
|
2017 |
Amorim IS, Graham LC, Carter RN, Morton NM, Hammachi F, Kunath T, Pennetta G, Carpanini SM, Manson JC, Lamont DJ, Wishart TM, Gillingwater TH. Sideroflexin 3 is a α-synuclein-dependent mitochondrial protein that regulates synaptic morphology. Journal of Cell Science. PMID 28049716 DOI: 10.1242/Jcs.194241 |
0.565 |
|
2017 |
McQueen J, Ryan TJ, McKay S, Marwick K, Baxter P, Carpanini SM, Wishart TM, Gillingwater TH, Manson JC, Wyllie DJA, Grant SGN, McColl BW, Komiyama NH, Hardingham GE. Author response: Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1 Elife. DOI: 10.7554/Elife.17161.024 |
0.445 |
|
2016 |
Powis RA, Karyka E, Boyd P, Côme J, Jones RA, Zheng Y, Szunyogova E, Groen EJ, Hunter G, Thomson D, Wishart TM, Becker CG, Parson SH, Martinat C, Azzouz M, et al. Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy. Jci Insight. 1: e87908. PMID 27699224 DOI: 10.1172/jci.insight.87908 |
0.754 |
|
2016 |
Fuller HR, Gillingwater TH, Wishart TM. Commonality amid diversity: Multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy. Neuromuscular Disorders : Nmd. PMID 27460344 DOI: 10.1016/j.nmd.2016.06.004 |
0.592 |
|
2016 |
Mcgorum B, Scholes S, Milne E, Eaton S, Wishart T, Poxton I, Moss S, Wernery U, Davey T, Harris J, Pirie R. Equine grass sickness, but not botulism, causes autonomic and enteric neurodegeneration and increases SNARE protein expression within neuronal perikarya Journal of Equine Veterinary Science. 39: S40-S41. DOI: 10.1016/J.JEVS.2016.02.089 |
0.517 |
|
2015 |
Amorim IS, Mitchell NL, Palmer DN, Sawiak SJ, Mason R, Wishart TM, Gillingwater TH. Molecular neuropathology of the synapse in sheep with CLN5 Batten disease. Brain and Behavior. 5: e00401. PMID 26664787 DOI: 10.1002/Brb3.401 |
0.612 |
|
2015 |
McGorum BC, Pirie RS, Eaton SL, Keen JA, Cumyn EM, Arnott DM, Chen W, Lamont DJ, Graham LC, Llavero Hurtado M, Pemberton A, Wishart TM. Proteomic Profiling of Cranial (Superior) Cervical Ganglia Reveals Beta-Amyloid & Ubiquitin Proteasome System Perturbations in an Equine Multiple System Neuropathy. Molecular & Cellular Proteomics : McP. PMID 26364976 DOI: 10.1074/mcp.M115.054635 |
0.313 |
|
2014 |
Eaton SL, Hurtado ML, Oldknow KJ, Graham LC, Marchant TW, Gillingwater TH, Farquharson C, Wishart TM. A guide to modern quantitative fluorescent western blotting with troubleshooting strategies. Journal of Visualized Experiments : Jove. e52099. PMID 25490604 DOI: 10.3791/52099 |
0.489 |
|
2014 |
Roche SL, Sherman DL, Dissanayake K, Soucy G, Desmazieres A, Lamont DJ, Peles E, Julien JP, Wishart TM, Ribchester RR, Brophy PJ, Gillingwater TH. Loss of glial neurofascin155 delays developmental synapse elimination at the neuromuscular junction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 12904-18. PMID 25232125 DOI: 10.1523/Jneurosci.1725-14.2014 |
0.798 |
|
2014 |
Aghamaleky Sarvestany A, Hunter G, Tavendale A, Lamont DJ, Llavero Hurtado M, Graham LC, Wishart TM, Gillingwater TH. Label-free quantitative proteomic profiling identifies disruption of ubiquitin homeostasis as a key driver of Schwann cell defects in spinal muscular atrophy. Journal of Proteome Research. 13: 4546-57. PMID 25151848 DOI: 10.1021/pr500492j |
0.618 |
|
2014 |
Powis RA, Mutsaers CA, Wishart TM, Hunter G, Wirth B, Gillingwater TH. Increased levels of UCHL1 are a compensatory response to disrupted ubiquitin homeostasis in spinal muscular atrophy and do not represent a viable therapeutic target. Neuropathology and Applied Neurobiology. 40: 873-87. PMID 25041530 DOI: 10.1111/nan.12168 |
0.543 |
|
2014 |
Carpanini SM, McKie L, Thomson D, Wright AK, Gordon SL, Roche SL, Handley MT, Morrison H, Brownstein D, Wishart TM, Cousin MA, Gillingwater TH, Aligianis IA, Jackson IJ. A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton. Disease Models & Mechanisms. 7: 711-22. PMID 24764192 DOI: 10.1242/Dmm.015222 |
0.621 |
|
2014 |
Wishart TM, Mutsaers CA, Riessland M, Reimer MM, Hunter G, Hannam ML, Eaton SL, Fuller HR, Roche SL, Somers E, Morse R, Young PJ, Lamont DJ, Hammerschmidt M, Joshi A, et al. Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy. The Journal of Clinical Investigation. 124: 1821-34. PMID 24590288 DOI: 10.1172/Jci71318 |
0.734 |
|
2013 |
Mutsaers CA, Lamont DJ, Hunter G, Wishart TM, Gillingwater TH. Label-free proteomics identifies Calreticulin and GRP75/Mortalin as peripherally accessible protein biomarkers for spinal muscular atrophy. Genome Medicine. 5: 95. PMID 24134804 DOI: 10.1186/gm498 |
0.554 |
|
2013 |
Eaton SL, Roche SL, Llavero Hurtado M, Oldknow KJ, Farquharson C, Gillingwater TH, Wishart TM. Total protein analysis as a reliable loading control for quantitative fluorescent Western blotting. Plos One. 8: e72457. PMID 24023619 DOI: 10.1371/journal.pone.0072457 |
0.523 |
|
2012 |
Wishart TM, Rooney TM, Lamont DJ, Wright AK, Morton AJ, Jackson M, Freeman MR, Gillingwater TH. Combining comparative proteomics and molecular genetics uncovers regulators of synaptic and axonal stability and degeneration in vivo. Plos Genetics. 8: e1002936. PMID 22952455 DOI: 10.1371/Journal.Pgen.1002936 |
0.647 |
|
2012 |
Avery MA, Rooney TM, Pandya JD, Wishart TM, Gillingwater TH, Geddes JW, Sullivan PG, Freeman MR. WldS prevents axon degeneration through increased mitochondrial flux and enhanced mitochondrial Ca2+ buffering. Current Biology : Cb. 22: 596-600. PMID 22425157 DOI: 10.1016/J.Cub.2012.02.043 |
0.557 |
|
2012 |
Thomson SR, Wishart TM, Patani R, Chandran S, Gillingwater TH. Using induced pluripotent stem cells (iPSC) to model human neuromuscular connectivity: promise or reality? Journal of Anatomy. 220: 122-30. PMID 22133357 DOI: 10.1111/j.1469-7580.2011.01459.x |
0.577 |
|
2011 |
Mutsaers CA, Wishart TM, Lamont DJ, Riessland M, Schreml J, Comley LH, Murray LM, Parson SH, Lochmüller H, Wirth B, Talbot K, Gillingwater TH. Reversible molecular pathology of skeletal muscle in spinal muscular atrophy. Human Molecular Genetics. 20: 4334-44. PMID 21840928 DOI: 10.1093/Hmg/Ddr360 |
0.743 |
|
2011 |
Comley LH, Fuller HR, Wishart TM, Mutsaers CA, Thomson D, Wright AK, Ribchester RR, Morris GE, Parson SH, Horsburgh K, Gillingwater TH. ApoE isoform-specific regulation of regeneration in the peripheral nervous system. Human Molecular Genetics. 20: 2406-21. PMID 21478199 DOI: 10.1093/Hmg/Ddr147 |
0.783 |
|
2011 |
Comley LH, Wishart TM, Baxter B, Murray LM, Nimmo A, Thomson D, Parson SH, Gillingwater TH. Induction of cell stress in neurons from transgenic mice expressing yellow fluorescent protein: implications for neurodegeneration research. Plos One. 6: e17639. PMID 21408118 DOI: 10.1371/journal.pone.0017639 |
0.725 |
|
2010 |
Wright AK, Wishart TM, Ingham CA, Gillingwater TH. Synaptic protection in the brain of WldS mice occurs independently of age but is sensitive to gene-dose. Plos One. 5: e15108. PMID 21124744 DOI: 10.1371/journal.pone.0015108 |
0.601 |
|
2010 |
Wishart TM, Huang JP, Murray LM, Lamont DJ, Mutsaers CA, Ross J, Geldsetzer P, Ansorge O, Talbot K, Parson SH, Gillingwater TH. SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy. Human Molecular Genetics. 19: 4216-28. PMID 20705736 DOI: 10.1093/Hmg/Ddq340 |
0.751 |
|
2009 |
Wishart TM, Brownstein DG, Thomson D, Tabakova AM, Boothe KM, Tsao JW, Gillingwater TH. Expression of the neuroprotective slow Wallerian degeneration (WldS) gene in non-neuronal tissues. Bmc Neuroscience. 10: 148. PMID 20015399 DOI: 10.1186/1471-2202-10-148 |
0.622 |
|
2009 |
Kielar C, Wishart TM, Palmer A, Dihanich S, Wong AM, Macauley SL, Chan CH, Sands MS, Pearce DA, Cooper JD, Gillingwater TH. Molecular correlates of axonal and synaptic pathology in mouse models of Batten disease. Human Molecular Genetics. 18: 4066-80. PMID 19640925 DOI: 10.1093/hmg/ddp355 |
0.646 |
|
2009 |
Benedict JW, Getty AL, Wishart TM, Gillingwater TH, Pearce DA. Protein product of CLN6 gene responsible for variant late-onset infantile neuronal ceroid lipofuscinosis interacts with CRMP-2. Journal of Neuroscience Research. 87: 2157-66. PMID 19235893 DOI: 10.1002/Jnr.22032 |
0.529 |
|
2008 |
Murray LM, Thomson D, Conklin A, Wishart TM, Gillingwater TH. Loss of translation elongation factor (eEF1A2) expression in vivo differentiates between Wallerian degeneration and dying-back neuronal pathology. Journal of Anatomy. 213: 633-45. PMID 19094180 DOI: 10.1111/j.1469-7580.2008.01007.x |
0.662 |
|
2008 |
Wishart TM, Pemberton HN, James SR, McCabe CJ, Gillingwater TH. Modified cell cycle status in a mouse model of altered neuronal vulnerability (slow Wallerian degeneration; Wlds) Genome Biology. 9. PMID 18570652 DOI: 10.1186/gb-2008-9-6-r101 |
0.619 |
|
2008 |
Wilbrey AL, Haley JE, Wishart TM, Conforti L, Morreale G, Beirowski B, Babetto E, Adalbert R, Gillingwater TH, Smith T, Wyllie DJ, Ribchester RR, Coleman MP. VCP binding influences intracellular distribution of the slow Wallerian degeneration protein, Wld(S). Molecular and Cellular Neurosciences. 38: 325-40. PMID 18468455 DOI: 10.1016/J.Mcn.2008.03.004 |
0.744 |
|
2007 |
Wishart TM, Macdonald SH, Chen PE, Shipston MJ, Coleman MP, Gillingwater TH, Ribchester RR. Design of a novel quantitative PCR (QPCR)-based protocol for genotyping mice carrying the neuroprotective Wallerian degeneration slow (Wlds) gene. Molecular Neurodegeneration. 2: 21. PMID 17971231 DOI: 10.1186/1750-1326-2-21 |
0.731 |
|
2007 |
Wishart TM, Paterson JM, Short DM, Meredith S, Robertson KA, Sutherland C, Cousin MA, Dutia MB, Gillingwater TH. Differential proteomics analysis of synaptic proteins identifies potential cellular targets and protein mediators of synaptic neuroprotection conferred by the slow Wallerian degeneration (Wlds) gene. Molecular & Cellular Proteomics : McP. 6: 1318-30. PMID 17470424 DOI: 10.1074/Mcp.M600457-Mcp200 |
0.647 |
|
2006 |
Wishart TM, Parson SH, Gillingwater TH. Synaptic vulnerability in neurodegenerative disease. Journal of Neuropathology and Experimental Neurology. 65: 733-9. PMID 16896307 DOI: 10.1097/01.jnen.0000228202.35163.c4 |
0.746 |
|
2006 |
Gillingwater TH, Ingham CA, Parry KE, Wright AK, Haley JE, Wishart TM, Arbuthnott GW, Ribchester RR. Delayed synaptic degeneration in the CNS of Wlds mice after cortical lesion. Brain : a Journal of Neurology. 129: 1546-56. PMID 16738060 DOI: 10.1093/brain/awl101 |
0.77 |
|
2006 |
Gillingwater TH, Wishart TM, Chen PE, Haley JE, Robertson K, MacDonald SH, Middleton S, Wawrowski K, Shipston MJ, Melmed S, Wyllie DJ, Skehel PA, Coleman MP, Ribchester RR. The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells. Human Molecular Genetics. 15: 625-35. PMID 16403805 DOI: 10.1093/Hmg/Ddi478 |
0.753 |
|
2006 |
Laser H, Conforti L, Morreale G, Mack TG, Heyer M, Haley JE, Wishart TM, Beirowski B, Walker SA, Haase G, Celik A, Adalbert R, Wagner D, Grumme D, Ribchester RR, et al. The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus. Molecular Biology of the Cell. 17: 1075-84. PMID 16371511 DOI: 10.1091/mbc.E05-04-0375 |
0.671 |
|
2004 |
Ribchester RR, Thomson D, Wood NI, Hinks T, Gillingwater TH, Wishart TM, Court FA, Morton AJ. Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation European Journal of Neuroscience. 20: 3092-3114. PMID 15579164 DOI: 10.1111/J.1460-9568.2004.03783.X |
0.783 |
|
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