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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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An activator of voltage-gated K + channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1

Proceedings of the National Academy of Sciences - PNAS, 2023-08, Vol.120 (31), p.e2207978120-e2207978120

2023

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Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Nature genetics, 2022-03, Vol.54 (3), p.361-361

2022

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Conserved requirement for DEAD-box RNA helicase Gemin3 in Drosophila oogenesis

BMC research notes, 2012-02, Vol.5 (1), p.120-120, Article 120

Cauchi, Ruben J

2012

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Correction: Genome-Wide Expression Analysis of a Spinal Muscular Atrophy Model: Towards Discovery of New Drug Targets

PloS one, 2008-04, Vol.3 (4)

2008

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Correction: Genome-Wide Expression Analysis of a Spinal Muscular Atrophy Model: Towards Discovery of New Drug Targets

PloS one, 2008-01, Vol.3 (4)

2008

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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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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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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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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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Extracts from two ubiquitous Mediterranean plants ameliorate cellular and animal models of neurodegenerative proteinopathies

Neuroscience letters, 2017-01, Vol.638, p.12-20

2017

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The Fly as a Model for Neurodegenerative Diseases: Is It Worth the Jump?

Neuro-degenerative diseases, 2006-01, Vol.3 (6), p.338-356

2006

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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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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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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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The Gemin associates of survival motor neuron are required for motor function in Drosophila

PloS one, 2013-12, Vol.8 (12), p.e83878-e83878

2013

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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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Genetic analysis of ALS cases in the isolated island population of Malta

European journal of human genetics : EJHG, 2021-04, Vol.29 (4), p.604-614

2021

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Genetic animal models of Tourette syndrome: The long and winding road from lab to clinic

Translational neuroscience, 2012-06, Vol.3 (2), p.153-159

2012

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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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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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Genetic screen identifies a requirement for SMN in mRNA localisation within the Drosophila oocyte

BMC research notes, 2018-06, Vol.11 (1), p.378-378, Article 378

2018

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Genome-wide expression analysis of a spinal muscular atrophy model: towards discovery of new drug targets

PloS one, 2008-01, Vol.3 (1), p.e1404-e1404

2008

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Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis

Neuron (Cambridge, Mass.), 2022-03, Vol.110 (6), p.992-1008.e11

2022

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

An activator of voltage-gated K + channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Conserved requirement for DEAD-box RNA helicase Gemin3 in Drosophila oogenesis

Correction: Genome-Wide Expression Analysis of a Spinal Muscular Atrophy Model: Towards Discovery of New Drug Targets

Correction: Genome-Wide Expression Analysis of a Spinal Muscular Atrophy Model: Towards Discovery of New Drug Targets

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

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

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

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

Extracts from two ubiquitous Mediterranean plants ameliorate cellular and animal models of neurodegenerative proteinopathies

The Fly as a Model for Neurodegenerative Diseases: Is It Worth the Jump?

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

Gem Depletion: Amyotrophic Lateral Sclerosis and Spinal Muscular Atrophy Crossover

Gem formation upon constitutive Gemin3 overexpression in Drosophila

The Gemin associates of survival motor neuron are required for motor function in Drosophila

GEMINs: potential therapeutic targets for spinal muscular atrophy?

Genetic analysis of ALS cases in the isolated island population of Malta

Genetic animal models of Tourette syndrome: The long and winding road from lab to clinic

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

Genetic landscape of ALS in Malta based on a quinquennial analysis

Genetic screen identifies a requirement for SMN in mRNA localisation within the Drosophila oocyte

Genome-wide expression analysis of a spinal muscular atrophy model: towards discovery of new drug targets

Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis

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

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