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The multiple lives of DEAD-box RNA helicase DP103/DDX20/Gemin3

Biochemical Society transactions, 2018-04, Vol.46 (2), p.329-341

2018

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SCFD1 in amyotrophic lateral sclerosis: reconciling a genetic association with in vivo functional analysis

Neural regeneration research, 2024-06, Vol.19 (6), p.1201-1202

Cauchi, Ruben J

2024

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Cardiolipin Promotes Pore-Forming Activity of Alpha-Synuclein Oligomers in Mitochondrial Membranes

ACS chemical neuroscience, 2019-08, Vol.10 (8), p.3815-3829

2019

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ACE and ACE2: insights from Drosophila and implications for COVID-19

Heliyon, 2021-12, Vol.7 (12), p.e08555-e08555, Article e08555

2021

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Extract from the Marine Seaweed Padina pavonica Protects Mitochondrial Biomembranes from Damage by Amyloidogenic Peptides

Molecules (Basel, Switzerland), 2021-03, Vol.26 (5), p.1444

2021

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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, 2016-10, Vol.94, p.245-258

2016

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Genetic Interactions between the Members of the SMN-Gemins Complex in Drosophila

PloS one, 2015-06, Vol.10 (6), p.e0130974

2015

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Novel interactors of the Drosophila Survival Motor Neuron (SMN) Complex suggest its full conservation

FEBS letters, 2017-11, Vol.591 (21), p.3600-3614

2017

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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, 2023-12, Vol.1869 (8), p.166818-166818, Article 166818

2023

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Disruption of Survival Motor Neuron in Glia Impacts Survival but has no Effect on Neuromuscular Function in Drosophila

Neuroscience, 2022-05, Vol.491, p.32-42

2022

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GEMINs: potential therapeutic targets for spinal muscular atrophy?

Frontiers in neuroscience, 2014-10, Vol.8, p.325-325

2014

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Spinal Muscular Atrophy: From Defective Chaperoning of snRNP Assembly to Neuromuscular Dysfunction

Frontiers in molecular biosciences, 2017-06, Vol.4, p.41-41

2017

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SMN and Gemins: ‘We are family' … or are we?: Insights into the partnership between Gemins and the spinal muscular atrophy disease protein SMN

BioEssays, 2010-12, Vol.32 (12), p.1077-1089

Cauchi, Ruben J

2010

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Loss of amyotrophic lateral sclerosis risk factor SCFD1 causes motor dysfunction in Drosophila

Neurobiology of aging, 2023-06, Vol.126, p.67-76

2023

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Modelling motor neuron disease in fruit flies: Lessons from spinal muscular atrophy

Journal of neuroscience methods, 2018-12, Vol.310, p.3-11

2018

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Tau-induced mitochondrial membrane perturbation is dependent upon cardiolipin

Biochimica et biophysica acta. Biomembranes, 2020-02, Vol.1862 (2), p.183064, Article 183064

2020

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SMN and Gemins: 'We are family' ... or are we?

BioEssays, 2010-12, Vol.32 (12), p.1077-1089

Cauchi, Ruben J.

2010

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Splicing Defects of the Profilin Gene Alter Actin Dynamics in an S. pombe SMN Mutant

iScience, 2020-01, Vol.23 (1), p.100809-100809, Article 100809

2020

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Gem Depletion: Amyotrophic Lateral Sclerosis and Spinal Muscular Atrophy Crossover

CNS neuroscience & therapeutics, 2014-07, Vol.20 (7), p.574-581

Cauchi, Ruben J.

2014

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SMN complex member Gemin3 self-interacts and has a functional relationship with ALS-linked proteins TDP-43, FUS and Sod1

Scientific reports, 2019-12, Vol.9 (1), p.18666-19, Article 18666

2019

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Genetic landscape of ALS in Malta based on a quinquennial analysis

Neurobiology of aging, 2023-03, Vol.123, p.200-207

2023

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Toxic oligomers of the amyloidogenic HypF-N protein form pores in mitochondrial membranes

Scientific reports, 2020-10, Vol.10 (1), p.17733, Article 17733

2020

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Occupation and amyotrophic lateral sclerosis risk: a case-control study in the isolated island population of Malta

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2021-10, Vol.22 (7-8), p.528-534

2021

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Gem formation upon constitutive Gemin3 overexpression in Drosophila

Cell biology international, 2011-12, Vol.35 (12), p.1233-1238

Cauchi, Ruben J.

2011

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Drosophila SMN complex proteins Gemin2, Gemin3, and Gemin5 are components of U bodies

Experimental cell research, 2010-08, Vol.316 (14), p.2354-2364

2010

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The multiple lives of DEAD-box RNA helicase DP103/DDX20/Gemin3

SCFD1 in amyotrophic lateral sclerosis: reconciling a genetic association with in vivo functional analysis

Cardiolipin Promotes Pore-Forming Activity of Alpha-Synuclein Oligomers in Mitochondrial Membranes

ACE and ACE2: insights from Drosophila and implications for COVID-19

Extract from the Marine Seaweed Padina pavonica Protects Mitochondrial Biomembranes from Damage by Amyloidogenic Peptides

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

Genetic Interactions between the Members of the SMN-Gemins Complex in Drosophila

Novel interactors of the Drosophila Survival Motor Neuron (SMN) Complex suggest its full conservation

Functional characterisation of the ACE2 orthologues in Drosophila provides insights into the neuromuscular complications of COVID-19

Disruption of Survival Motor Neuron in Glia Impacts Survival but has no Effect on Neuromuscular Function in Drosophila

GEMINs: potential therapeutic targets for spinal muscular atrophy?

Spinal Muscular Atrophy: From Defective Chaperoning of snRNP Assembly to Neuromuscular Dysfunction

SMN and Gemins: ‘We are family' … or are we?: Insights into the partnership between Gemins and the spinal muscular atrophy disease protein SMN

Loss of amyotrophic lateral sclerosis risk factor SCFD1 causes motor dysfunction in Drosophila

Modelling motor neuron disease in fruit flies: Lessons from spinal muscular atrophy

Tau-induced mitochondrial membrane perturbation is dependent upon cardiolipin

SMN and Gemins: 'We are family' ... or are we?

Splicing Defects of the Profilin Gene Alter Actin Dynamics in an S. pombe SMN Mutant

Gem Depletion: Amyotrophic Lateral Sclerosis and Spinal Muscular Atrophy Crossover

SMN complex member Gemin3 self-interacts and has a functional relationship with ALS-linked proteins TDP-43, FUS and Sod1

Genetic landscape of ALS in Malta based on a quinquennial analysis

Toxic oligomers of the amyloidogenic HypF-N protein form pores in mitochondrial membranes

Occupation and amyotrophic lateral sclerosis risk: a case-control study in the isolated island population of Malta

Gem formation upon constitutive Gemin3 overexpression in Drosophila

Drosophila SMN complex proteins Gemin2, Gemin3, and Gemin5 are components of U bodies

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