| Year |
Citation |
Score |
| 2023 |
Huang YT, Crick HR, Chaytow H, van der Hoorn D, Alhindi A, Jones RA, Hector RD, Cobb SR, Gillingwater TH. Long-term muscle-specific overexpression of DOK7 in mice using AAV9-tMCK-DOK7. Molecular Therapy. Nucleic Acids. 33: 617-628. PMID 37637210 DOI: 10.1016/j.omtn.2023.07.036 |
0.303 |
|
| 2022 |
Zhou H, Hong Y, Scoto M, Thomson A, Pead E, MacGillivray T, Hernandez-Gerez E, Catapano F, Meng J, Zhang Q, Hunter G, Shorrock HK, Ng TK, Hamida A, Sanson M, ... ... Gillingwater TH, et al. Microvasculopathy in SMA is driven by a reversible autonomous endothelial cell defect. The Journal of Clinical Investigation. PMID 36099045 DOI: 10.1172/JCI153430 |
0.64 |
|
| 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 |
0.717 |
|
| 2022 |
Bauer CS, Cohen RN, Sironi F, Livesey MR, Gillingwater TH, Highley JR, Fillingham DJ, Coldicott I, Smith EF, Gibson YB, Webster CP, Grierson AJ, Bendotti C, De Vos KJ. An interaction between synapsin and C9orf72 regulates excitatory synapses and is impaired in ALS/FTD. Acta Neuropathologica. PMID 35876881 DOI: 10.1007/s00401-022-02470-z |
0.307 |
|
| 2022 |
Gillingwater TH, McWilliam C, Horrocks I, McWilliam K, Hamilton M, Fletcher E, Williams N, Smith S, Parson SH. A call to introduce newborn screening for spinal muscular atrophy (SMA) in Scotland. Scottish Medical Journal. 369330221078994. PMID 35147460 DOI: 10.1177/00369330221078994 |
0.592 |
|
| 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 |
0.689 |
|
| 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 |
0.638 |
|
| 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, ... Gillingwater TH, et al. Confocal Endomicroscopy of Neuromuscular Junctions Stained with Physiologically Inert Protein Fragments of Tetanus Toxin. Biomolecules. 11. PMID 34680132 DOI: 10.3390/biom11101499 |
0.788 |
|
| 2021 |
Quondamatteo F, Corzo-Leon DE, Brassett C, Colquhoun I, Davies DC, Dockery P, Grenham S, Guild S, Hunter A, Jones J, Lee TC, Tracey C, Wilkinson T, Munro CA, Gillingwater TH, et al. Neutralisation of SARS-CoV-2 by anatomical embalming solutions. Journal of Anatomy. PMID 34633083 DOI: 10.1111/joa.13549 |
0.565 |
|
| 2021 |
Alhindi A, Boehm I, Forsythe RO, Miller J, Skipworth RJE, Simpson H, Jones RA, Gillingwater TH. Terminal Schwann cells at the human neuromuscular junction. Brain Communications. 3: fcab081. PMID 33977269 DOI: 10.1093/braincomms/fcab081 |
0.304 |
|
| 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 |
0.736 |
|
| 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 |
0.638 |
|
| 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 |
0.668 |
|
| 2020 |
Brassett C, Cosker T, Davies DC, Dockery P, Gillingwater TH, Lee TC, Milz S, Parson SH, Quondamatteo F, Wilkinson T. COVID-19 and anatomy: Stimulus and initial response. Journal of Anatomy. PMID 32628795 DOI: 10.1111/joa.13274 |
0.57 |
|
| 2020 |
Allardyce H, Kuhn D, Hernandez-Gerez E, Hensel N, Huang YT, Faller K, Gillingwater TH, Quondamatteo F, Claus P, Parson SH. Renal pathology in a mouse model of severe Spinal Muscular Atrophy is associated with downregulation of Glial Cell-Line Derived Neurotrophic Factor (GDNF). Human Molecular Genetics. PMID 32588893 DOI: 10.1093/hmg/ddaa126 |
0.668 |
|
| 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 |
0.646 |
|
| 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 |
0.631 |
|
| 2019 |
Deguise MO, Baranello G, Mastella C, Beauvais A, Michaud J, Leone A, De Amicis R, Battezzati A, Dunham C, Selby K, Warman Chardon J, McMillan HJ, Huang YT, Courtney NL, Mole AJ, ... ... Gillingwater TH, et al. Abnormal fatty acid metabolism is a core component of spinal muscular atrophy. Annals of Clinical and Translational Neurology. 6: 1519-1532. PMID 31402618 DOI: 10.1002/Acn3.50855 |
0.658 |
|
| 2019 |
Šoltić D, Shorrock HK, Allardyce H, Wilson EL, Holt I, Synowsky SA, Shirran SL, Parson SH, Gillingwater TH, Fuller HR. Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy. Human Molecular Genetics. PMID 31397869 DOI: 10.1093/hmg/ddz195 |
0.647 |
|
| 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 |
0.637 |
|
| 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 |
0.555 |
|
| 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 |
0.667 |
|
| 2018 |
Fergusson SJ, Aka JJ, Hennessy CM, Wilson AJ, Parson SH, Harrison EM, Finn GM, Gillingwater TH. Examining the impact of audience response systems on student performance in anatomy education: a randomised controlled trial. Scottish Medical Journal. 36933017741409. PMID 29911503 DOI: 10.1177/0036933017741409 |
0.566 |
|
| 2018 |
Jn Groen E, Perenthaler E, Courtney NL, Jordan CY, Shorrock HK, van der Hoorn D, Huang YT, Murray LM, Viero G, Gillingwater TH. Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy. Human Molecular Genetics. PMID 29790918 DOI: 10.1093/hmg/ddy195 |
0.311 |
|
| 2018 |
Maxwell GK, Szunyogova E, Shorrock HK, Gillingwater TH, Parson SH. Developmental and degenerative cardiac defects in the Taiwanese mouse model of severe spinal muscular atrophy. Journal of Anatomy. PMID 29473159 DOI: 10.1111/joa.12793 |
0.642 |
|
| 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 |
0.679 |
|
| 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 |
0.676 |
|
| 2017 |
Bernabò P, Tebaldi T, Groen EJN, Lane FM, Perenthaler E, Mattedi F, Newbery HJ, Zhou H, Zuccotti P, Potrich V, Shorrock HK, Muntoni F, Quattrone A, Gillingwater TH, Viero G. In Vivo Translatome Profiling in Spinal Muscular Atrophy Reveals a Role for SMN Protein in Ribosome Biology. Cell Reports. 21: 953-965. PMID 29069603 DOI: 10.1016/j.celrep.2017.10.010 |
0.329 |
|
| 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 |
0.686 |
|
| 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 |
0.579 |
|
| 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, ... ... Gillingwater TH, 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 |
0.681 |
|
| 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 |
0.616 |
|
| 2017 |
Jones RA, Reich CD, Dissanayake KN, Kristmundsdottir F, Findlater GS, Ribchester RR, Simmen MW, Gillingwater TH. Correction to 'NMJ-morph reveals principal components of synaptic morphology influencing structure-function relationships at the neuromuscular junction'. Open Biology. 7. PMID 28100668 DOI: 10.1098/rsob.160335 |
0.778 |
|
| 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 |
0.635 |
|
| 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 |
0.549 |
|
| 2016 |
Jones RA, Reich CD, Dissanayake KN, Kristmundsdottir F, Findlater GS, Ribchester RR, Simmen MW, Gillingwater TH. NMJ-morph reveals principal components of synaptic morphology influencing structure-function relationships at the neuromuscular junction. Open Biology. 6. PMID 27927794 DOI: 10.1098/Rsob.160240 |
0.787 |
|
| 2016 |
Szunyogova E, Zhou H, Maxwell GK, Powis RA, Muntoni F, Gillingwater TH, Parson SH. Corrigendum: Survival Motor Neuron (SMN) protein is required for normal mouse liver development. Scientific Reports. 6: 35898. PMID 27830828 DOI: 10.1038/srep35898 |
0.659 |
|
| 2016 |
Thomson AK, Somers E, Powis RA, Shorrock HK, Murphy K, Swoboda KJ, Gillingwater TH, Parson SH. Survival of motor neurone protein is required for normal postnatal development of the spleen. Journal of Anatomy. PMID 27726134 DOI: 10.1111/joa.12546 |
0.685 |
|
| 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, ... Gillingwater TH, et al. Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy. Jci Insight. 1: e87908. PMID 27699224 DOI: 10.1172/jci.insight.87908 |
0.786 |
|
| 2016 |
Szunyogova E, Zhou H, Maxwell GK, Powis RA, Francesco M, Gillingwater TH, Parson SH. Survival Motor Neuron (SMN) protein is required for normal mouse liver development. Scientific Reports. 6: 34635. PMID 27698380 DOI: 10.1038/srep34635 |
0.638 |
|
| 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 |
0.659 |
|
| 2016 |
Hunter G, Powis RA, Jones RA, Groen EJ, Shorrock HK, Lane FM, Zheng Y, Sherman DL, Brophy PJ, Gillingwater TH. Restoration of SMN in Schwann cells reverses myelination defects and improves neuromuscular function in spinal muscular atrophy. Human Molecular Genetics. PMID 27170316 DOI: 10.1093/hmg/ddw141 |
0.334 |
|
| 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 |
0.68 |
|
| 2015 |
Somers E, Lees RD, Hoban K, Sleigh JN, Zhou H, Muntoni F, Talbot K, Gillingwater TH, Parson SH. Vascular defects and spinal cord hypoxia in spinal muscular atrophy. Annals of Neurology. PMID 26506088 DOI: 10.1002/Ana.24549 |
0.657 |
|
| 2015 |
Little D, Valori CF, Mutsaers CA, Bennett EJ, Wyles M, Sharrack B, Shaw PJ, Gillingwater TH, Azzouz M, Ning K. PTEN depletion decreases disease severity and modestly prolongs survival in a mouse model of spinal muscular atrophy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 23: 270-7. PMID 25369768 DOI: 10.1038/mt.2014.209 |
0.333 |
|
| 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 |
0.579 |
|
| 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 |
0.815 |
|
| 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 |
0.68 |
|
| 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 |
0.631 |
|
| 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 |
0.687 |
|
| 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, ... ... Gillingwater TH, 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 |
0.769 |
|
| 2014 |
Sleigh JN, Burgess RW, Gillingwater TH, Cader MZ. Morphological analysis of neuromuscular junction development and degeneration in rodent lumbrical muscles. Journal of Neuroscience Methods. 227: 159-65. PMID 24530702 DOI: 10.1016/J.Jneumeth.2014.02.005 |
0.325 |
|
| 2014 |
Hunter G, Aghamaleky Sarvestany A, Roche SL, Symes RC, Gillingwater TH. SMN-dependent intrinsic defects in Schwann cells in mouse models of spinal muscular atrophy. Human Molecular Genetics. 23: 2235-50. PMID 24301677 DOI: 10.1093/hmg/ddt612 |
0.328 |
|
| 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 |
0.637 |
|
| 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 |
0.606 |
|
| 2013 |
Somers E, Riessland M, Schreml J, Wirth B, Gillingwater TH, Parson SH. Increasing SMN levels using the histone deacetylase inhibitor SAHA ameliorates defects in skeletal muscle microvasculature in a mouse model of severe spinal muscular atrophy. Neuroscience Letters. 544: 100-4. PMID 23583590 DOI: 10.1016/j.neulet.2013.03.052 |
0.681 |
|
| 2013 |
Simpson AH, Gillingwater TH, Anderson H, Cottrell D, Sherman DL, Ribchester RR, Brophy PJ. Effect of limb lengthening on internodal length and conduction velocity of peripheral nerve. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 4536-9. PMID 23467369 DOI: 10.1523/JNEUROSCI.4176-12.2013 |
0.573 |
|
| 2013 |
Hamilton G, Gillingwater TH. Spinal muscular atrophy: Going beyond the motor neuron Trends in Molecular Medicine. 19: 40-50. PMID 23228902 DOI: 10.1016/j.molmed.2012.11.002 |
0.327 |
|
| 2012 |
Thomson SR, Nahon JE, Mutsaers CA, Thomson D, Hamilton G, Parson SH, Gillingwater TH. Morphological Characteristics of Motor Neurons Do Not Determine Their Relative Susceptibility to Degeneration in a Mouse Model of Severe Spinal Muscular Atrophy Plos One. 7. PMID 23285108 DOI: 10.1371/journal.pone.0052605 |
0.68 |
|
| 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 |
0.693 |
|
| 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 |
0.62 |
|
| 2012 |
Findlater GS, Kristmundsdottir F, Parson SH, Gillingwater TH. Development of a supported self-directed learning approach for anatomy education. Anatomical Sciences Education. 5: 114-21. PMID 22223487 DOI: 10.1002/ase.1255 |
0.566 |
|
| 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 |
0.656 |
|
| 2011 |
Koch S, Molchanova SM, Wright AK, Edwards A, Cooper JD, Taira T, Gillingwater TH, Tyynelä J. Morphologic and functional correlates of synaptic pathology in the cathepsin D knockout mouse model of congenital neuronal ceroid lipofuscinosis. Journal of Neuropathology and Experimental Neurology. 70: 1089-96. PMID 22082660 DOI: 10.1097/NEN.0b013e318238fc28 |
0.343 |
|
| 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 |
0.779 |
|
| 2011 |
Sleigh JN, Gillingwater TH, Talbot K. The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy. Disease Models & Mechanisms. 4: 457-67. PMID 21708901 DOI: 10.1242/Dmm.007245 |
0.319 |
|
| 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 |
0.791 |
|
| 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 |
0.757 |
|
| 2011 |
Murray LM, Comley LH, Gillingwater TH, Parson SH. The response of neuromuscular junctions to injury is developmentally regulated. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 1306-13. PMID 21228222 DOI: 10.1096/fj.10-171934 |
0.704 |
|
| 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 |
0.667 |
|
| 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 |
0.783 |
|
| 2010 |
Murray LM, Gillingwater TH, Parson SH. Using mouse cranial muscles to investigate neuromuscular pathology in vivo Neuromuscular Disorders. 20: 740-743. PMID 20637618 DOI: 10.1016/J.Nmd.2010.06.013 |
0.648 |
|
| 2010 |
de Waard MC, van der Pluijm I, Zuiderveen Borgesius N, Comley LH, Haasdijk ED, Rijksen Y, Ridwan Y, Zondag G, Hoeijmakers JH, Elgersma Y, Gillingwater TH, Jaarsma D. Age-related motor neuron degeneration in DNA repair-deficient Ercc1 mice. Acta Neuropathologica. 120: 461-75. PMID 20602234 DOI: 10.1007/s00401-010-0715-9 |
0.336 |
|
| 2010 |
Murray LM, Lee S, Bäumer D, Parson SH, Talbot K, Gillingwater TH. Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy. Human Molecular Genetics. 19: 420-33. PMID 19884170 DOI: 10.1093/Hmg/Ddp506 |
0.701 |
|
| 2009 |
Bäumer D, Lee S, Nicholson G, Davies JL, Parkinson NJ, Murray LM, Gillingwater TH, Ansorge O, Davies KE, Talbot K. Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy. Plos Genetics. 5: e1000773. PMID 20019802 DOI: 10.1371/Journal.Pgen.1000773 |
0.35 |
|
| 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 |
0.677 |
|
| 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 |
0.693 |
|
| 2009 |
Mackenzie FE, Romero R, Williams D, Gillingwater T, Hilton H, Dick J, Riddoch-Contreras J, Wong F, Ireson L, Powles-Glover N, Riley G, Underhill P, Hough T, Arkell R, Greensmith L, et al. Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse Human Molecular Genetics. 18: 3553-3566. PMID 19578180 DOI: 10.1093/Hmg/Ddp304 |
0.638 |
|
| 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 |
0.609 |
|
| 2009 |
Baxter B, Parsons MJ, Gillingwater T, Parson S. Hypoxia induces rapid and selective injury to alpha-motor nerve terminals Journal of Anatomy. 214: 792-793. DOI: 10.1111/J.1469-7580.2009.01069.X |
0.615 |
|
| 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 |
0.715 |
|
| 2008 |
Court FA, Gillingwater TH, Melrose S, Sherman DL, Greenshields KN, Morton AJ, Harris JB, Willison HJ, Ribchester RR. Identity, developmental restriction and reactivity of extralaminar cells capping mammalian neuromuscular junctions. Journal of Cell Science. 121: 3901-11. PMID 19001504 DOI: 10.1242/Jcs.031047 |
0.786 |
|
| 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 |
0.678 |
|
| 2008 |
Baxter B, Gillingwater TH, Parson SH. Rapid loss of motor nerve terminals following hypoxia-reperfusion injury occurs via mechanisms distinct from classic Wallerian degeneration. Journal of Anatomy. 212: 827-35. PMID 18510509 DOI: 10.1111/j.1469-7580.2008.00909.x |
0.683 |
|
| 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 |
0.766 |
|
| 2008 |
Partanen S, Haapanen A, Kielar C, Pontikis C, Alexander N, Inkinen T, Saftig P, Gillingwater TH, Cooper JD, Tyynelä J. Synaptic changes in the thalamocortical system of cathepsin D-deficient mice: a model of human congenital neuronal ceroid-lipofuscinosis. Journal of Neuropathology and Experimental Neurology. 67: 16-29. PMID 18091563 DOI: 10.1097/nen.0b013e31815f3899 |
0.33 |
|
| 2008 |
Murray LM, Comley LH, Thomson D, Parkinson N, Talbot K, Gillingwater TH. Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy. Human Molecular Genetics. 17: 949-62. PMID 18065780 DOI: 10.1093/Hmg/Ddm367 |
0.392 |
|
| 2008 |
Findlater GS, Gillingwater TH, Kristmundsdottir F, Parson SH. Eldred Wright Walls, MD, FRCS, FRCSE, FRSE Journal of Anatomy. 213: 230-231. DOI: 10.1111/j.1469-7580.2008.00923.x |
0.548 |
|
| 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 |
0.762 |
|
| 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 |
0.693 |
|
| 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 |
0.78 |
|
| 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 |
0.802 |
|
| 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 |
0.781 |
|
| 2005 |
Newbery HJ, Gillingwater TH, Dharmasaroja P, Peters J, Wharton SB, Thomson D, Ribchester RR, Abbott CM. Progressive loss of motor neuron function in wasted mice: Effects of a spontaneous null mutation in the gene for the eEF1A2 translation factor Journal of Neuropathology and Experimental Neurology. 64: 295-303. PMID 15835265 DOI: 10.1093/Jnen/64.4.295 |
0.67 |
|
| 2005 |
Adalbert R, Gillingwater TH, Haley JE, Bridge K, Beirowski B, Berek L, Wagner D, Grumme D, Thomson D, Celik A, Addicks K, Ribchester RR, Coleman MP. A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapses. The European Journal of Neuroscience. 21: 271-7. PMID 15654865 DOI: 10.1111/J.1460-9568.2004.03833.X |
0.706 |
|
| 2005 |
Mi W, Beirowski B, Gillingwater TH, Adalbert R, Wagner D, Grumme D, Osaka H, Conforti L, Arnhold S, Addicks K, Wada K, Ribchester RR, Coleman MP. The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy mice Brain. 128: 405-416. PMID 15644421 DOI: 10.1093/brain/awh368 |
0.606 |
|
| 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 |
0.807 |
|
| 2004 |
Gillingwater TH, Thomson D, Ribchester RR. Myo-GDNF increases non-functional polyinnervation of reinnervated mouse muscle Neuroreport. 15: 21-25. PMID 15106825 DOI: 10.1097/00001756-200401190-00006 |
0.653 |
|
| 2004 |
Parson SH, Ribchester RR, Davie N, Gandhi NP, Malik RQ, Gillingwater TH, Thomson D. Axotomy-Dependent and -Independent Synapse Elimination in Organ Cultures of WldS Mutant Mouse Skeletal Muscle Journal of Neuroscience Research. 76: 64-75. PMID 15048930 DOI: 10.1002/Jnr.20016 |
0.79 |
|
| 2004 |
Gillingwater TH, Haley JE, Ribchester RR, Horsburgh K. Neuroprotection after transient global cerebral ischemia in Wld(s) mutant mice. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 24: 62-6. PMID 14688617 DOI: 10.1097/01.Wcb.0000095798.98378.34 |
0.705 |
|
| 2003 |
Gillingwater TH, Ribchester RR. The relationship of neuromuscular synapse elimination to synaptic degeneration and pathology: Insights from Wlds and other mutant mice Journal of Neurocytology. 32: 863-881. PMID 15034273 DOI: 10.1023/B:Neur.0000020629.51673.F5 |
0.704 |
|
| 2003 |
Gillingwater TH, Ingham CA, Coleman MP, Ribchester RR. Ultrastructural correlates of synapse withdrawal at axotomized neuromuscular junctions in mutant and transgenic mice expressing the Wld gene. Journal of Anatomy. 203: 265-76. PMID 14529044 DOI: 10.1046/j.1469-7580.2003.00214.x |
0.673 |
|
| 2002 |
Gillingwater TH, Thomson D, Mack TGA, Soffin EM, Mattison RJ, Coleman MP, Ribchester RR. Age-dependent synapse withdrawal at axotomised neuromuscular junctions in Wlds mutant and Ube4b/Nmnat transgenic mice Journal of Physiology. 543: 739-755. PMID 12231635 DOI: 10.1113/Jphysiol.2002.022343 |
0.779 |
|
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