22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Herrera P, Cauchi RJ. Functional characterisation of the ACE2 orthologues in Drosophila provides insights into the neuromuscular complications of COVID-19. Biochimica Et Biophysica Acta. Molecular Basis of Disease. 1869: 166818. PMID 37495086 DOI: 10.1016/j.bbadis.2023.166818  0.424
2023 Borg R, Herrera P, Purkiss A, Cacciottolo R, Cauchi RJ. Reduced levels of ALS gene induce motor defects in . Frontiers in Neuroscience. 17: 1164251. PMID 37360176 DOI: 10.3389/fnins.2023.1164251  0.537
2023 Borg R, Purkiss A, Cacciottolo R, Herrera P, Cauchi RJ. Loss of amyotrophic lateral sclerosis risk factor SCFD1 causes motor dysfunction in Drosophila. Neurobiology of Aging. 126: 67-76. PMID 36944290 DOI: 10.1016/j.neurobiolaging.2023.02.005  0.433
2022 Farrugia M, Vassallo N, Cauchi RJ. Disruption of Survival Motor Neuron in Glia Impacts Survival but has no Effect on Neuromuscular Function in Drosophila. Neuroscience. 491: 32-42. PMID 35314252 DOI: 10.1016/j.neuroscience.2022.03.013  0.578
2020 Antoine M, Patrick KL, Soret J, Duc P, Rage F, Cacciottolo R, Nissen KE, Cauchi RJ, Krogan NJ, Guthrie C, Gachet Y, Bordonné R. Splicing Defects of the Profilin Gene Alter Actin Dynamics in an S. pombe SMN Mutant. Iscience. 23: 100809. PMID 31927482 DOI: 10.1016/J.Isci.2019.100809  0.407
2019 Cacciottolo R, Ciantar J, Lanfranco M, Borg RM, Vassallo N, Bordonné R, Cauchi RJ. SMN complex member Gemin3 self-interacts and has a functional relationship with ALS-linked proteins TDP-43, FUS and Sod1. Scientific Reports. 9: 18666. PMID 31822699 DOI: 10.1038/S41598-019-53508-4  0.534
2018 Aquilina B, Cauchi RJ. Genetic screen identifies a requirement for SMN in mRNA localisation within the Drosophila oocyte. Bmc Research Notes. 11: 378. PMID 29895323 DOI: 10.1186/S13104-018-3496-1  0.325
2018 Aquilina B, Cauchi RJ. Modelling motor neuron disease in fruit flies: Lessons from spinal muscular atrophy. Journal of Neuroscience Methods. PMID 29649521 DOI: 10.1016/J.Jneumeth.2018.04.003  0.441
2018 Curmi F, Cauchi RJ. The multiple lives of DEAD-box RNA helicase DP103/DDX20/Gemin3. Biochemical Society Transactions. PMID 29523774 DOI: 10.1042/Bst20180016  0.38
2017 Lanfranco M, Cacciottolo R, Borg RM, Vassallo N, Juge F, Bordonné R, Cauchi RJ. Novel interactors of the Drosophila Survival Motor Neuron (SMN) Complex suggest its full conservation. Febs Letters. PMID 28949413 DOI: 10.1002/1873-3468.12853  0.487
2017 Lanfranco M, Vassallo N, Cauchi RJ. Spinal Muscular Atrophy: From Defective Chaperoning of snRNP Assembly to Neuromuscular Dysfunction. Frontiers in Molecular Biosciences. 4: 41. PMID 28642865 DOI: 10.3389/Fmolb.2017.00041  0.486
2016 Borg RM, Salerno BF, Vassallo N, Bordonne R, Cauchi RJ. Disruption of snRNP biogenesis factors Tgs1 and pICln induces phenotypes that mirror aspects of SMN-Gemins complex perturbation in Drosophila, providing new insights into spinal muscular atrophy. Neurobiology of Disease. PMID 27388936 DOI: 10.1016/J.Nbd.2016.06.015  0.595
2015 Borg RM, Bordonne R, Vassallo N, Cauchi RJ. Genetic Interactions between the Members of the SMN-Gemins Complex in Drosophila. Plos One. 10: e0130974. PMID 26098872 DOI: 10.1371/Journal.Pone.0130974  0.573
2014 Borg R, Cauchi RJ. GEMINs: potential therapeutic targets for spinal muscular atrophy? Frontiers in Neuroscience. 8: 325. PMID 25360080 DOI: 10.3389/Fnins.2014.00325  0.514
2014 Cauchi RJ. Gem depletion: amyotrophic lateral sclerosis and spinal muscular atrophy crossover. Cns Neuroscience & Therapeutics. 20: 574-81. PMID 24645792 DOI: 10.1111/Cns.12242  0.503
2013 Borg R, Cauchi RJ. The Gemin associates of survival motor neuron are required for motor function in Drosophila. Plos One. 8: e83878. PMID 24391840 DOI: 10.1371/Journal.Pone.0083878  0.594
2013 Cauchi RJ. Drosophila melanogaster models of motor neuron disease Drosophila Melanogaster Models of Motor Neuron Disease. 1-223.  0.397
2012 Cauchi RJ. Conserved requirement for DEAD-box RNA helicase Gemin3 in Drosophila oogenesis. Bmc Research Notes. 5: 120. PMID 22361416 DOI: 10.1186/1756-0500-5-120  0.452
2011 Cauchi RJ. Gem formation upon constitutive Gemin3 overexpression in Drosophila. Cell Biology International. 35: 1233-8. PMID 21627586 DOI: 10.1042/Cbi20110147  0.347
2010 Cauchi RJ. SMN and Gemins: 'we are family' … or are we?: insights into the partnership between Gemins and the spinal muscular atrophy disease protein SMN. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 32: 1077-89. PMID 20954180 DOI: 10.1002/Bies.201000088  0.57
2010 Cauchi RJ, Sanchez-Pulido L, Liu JL. Drosophila SMN complex proteins Gemin2, Gemin3, and Gemin5 are components of U bodies. Experimental Cell Research. 316: 2354-64. PMID 20452345 DOI: 10.1016/J.Yexcr.2010.05.001  0.302
2008 Lee S, Sayin A, Cauchi RJ, Grice S, Burdett H, Baban D, van den Heuvel M. Genome-wide expression analysis of a spinal muscular atrophy model: towards discovery of new drug targets. Plos One. 3: e1404. PMID 18167563 DOI: 10.1371/journal.pone.0001404  0.409
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