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The Enemy within: Innate Surveillance-Mediated Cell Death, the Common Mechanism of Neurodegenerative Disease

Frontiers in neuroscience, 2016-05, Vol.10, p.193-193

2016

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Tumor suppressor WWOX moderates the mitochondrial respiratory complex

Genes chromosomes & cancer, 2015-12, Vol.54 (12), p.745-761

2015

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Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat disease

Human molecular genetics, 2012-02, Vol.21 (3), p.536-547

2012

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Common chromosomal fragile sites and cancer: Focus on FRA16D

Cancer letters, 2006-01, Vol.232 (1), p.37-47

2006

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Tumor Suppressor WWOX Contributes to the Elimination of Tumorigenic Cells in Drosophila melanogaster

PloS one, 2015-08, Vol.10 (8), p.e0136356-e0136356

2015

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Drosophila melanogaster models of MPS IIIC (Hgsnat‐deficiency) highlight the role of glia in disease presentation

Journal of inherited metabolic disease, 2024-03, Vol.47 (2), p.340-354

2024

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The pathogenic agent in Drosophila models of ‘polyglutamine’ diseases

Human molecular genetics, 2005-04, Vol.14 (8), p.1041-1048

2005

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Common chromosomal fragile site FRA16D tumor suppressor WWOX gene expression and metabolic reprograming in cells

Genes chromosomes & cancer, 2013-09, Vol.52 (9), p.823-831

2013

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Non-self mutation: double-stranded RNA elicits antiviral pathogenic response in a Drosophila model of expanded CAG repeat neurodegenerative diseases

Human molecular genetics, 2019-09, Vol.28 (18), p.3000-3012

2019

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Neuronal-specific impairment of heparan sulfate degradation in Drosophila reveals pathogenic mechanisms for Mucopolysaccharidosis type IIIA

Experimental neurology, 2018-05, Vol.303, p.38-47

2018

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Molecular Biology of the WWOX Gene That Spans Chromosomal Fragile Site FRA16D

Cells (Basel, Switzerland), 2021-06, Vol.10 (7), p.1637

2021

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Drosophila orthologue of WWOX, the chromosomal fragile site FRA16D tumour suppressor gene, functions in aerobic metabolism and regulates reactive oxygen species

Human molecular genetics, 2011-02, Vol.20 (3), p.497-509

2011

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Distinct roles for Toll and autophagy pathways in double-stranded RNA toxicity in a Drosophila model of expanded repeat neurodegenerative diseases

Human molecular genetics, 2013-07, Vol.22 (14), p.2811-2819

2013

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Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases

Human molecular genetics, 2011-10, Vol.20 (19), p.3757-3768

2011

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Ubiquitous expression of CUG or CAG trinucleotide repeat RNA causes common morphological defects in a Drosophila model of RNA-mediated pathology

PloS one, 2012-06, Vol.7 (6), p.e38516

2012

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Perturbation of the Akt/Gsk3-β signalling pathway is common to Drosophila expressing expanded untranslated CAG, CUG and AUUCU repeat RNAs

Human molecular genetics, 2011-07, Vol.20 (14), p.2783-2794

2011

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RNA pathogenesis via Toll-like receptor-activated inflammation in expanded repeat neurodegenerative diseases

Frontiers in molecular neuroscience, 2013-09, Vol.6, p.25-25

2013

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Know thy fly

Trends in genetics, 2007-05, Vol.23 (5), p.238-242

2007

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FRA16D common chromosomal fragile site oxido-reductase (FOR/WWOX) protects against the effects of ionizing radiation in Drosophila

Oncogene, 2005-09, Vol.24 (43), p.6590-6596

2005

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Tumor Suppressor WWOX Contributes to the Elimination of Tumorigenic Cells in Drosophila melanogaster: e0136356

PloS one, 2015-08, Vol.10 (8)

2015

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A Drosophila G1-specific cyclin E homolog exhibits different modes of expression during embryogenesis

Development (Cambridge), 1993-11, Vol.119 (3), p.673-690

1993

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Ectopic cyclin E expression induces premature entry into S phase and disrupts pattern formation in the Drosophila eye imaginal disc

Development (Cambridge), 1995-10, Vol.121 (10), p.3371-3379

1995

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Regulation of the Elongation Phase of Protein Synthesis Enhances Translation Accuracy and Modulates Lifespan

Current biology, 2019-03, Vol.29 (5), p.737-749.e5

2019

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The Enemy within: Innate Surveillance-Mediated Cell Death, the Common Mechanism of Neurodegenerative Disease

Tumor suppressor WWOX moderates the mitochondrial respiratory complex

Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat disease

Common chromosomal fragile sites and cancer: Focus on FRA16D

Tumor Suppressor WWOX Contributes to the Elimination of Tumorigenic Cells in Drosophila melanogaster

Drosophila melanogaster models of MPS IIIC (Hgsnat‐deficiency) highlight the role of glia in disease presentation

The pathogenic agent in Drosophila models of ‘polyglutamine’ diseases

Common chromosomal fragile site FRA16D tumor suppressor WWOX gene expression and metabolic reprograming in cells

Non-self mutation: double-stranded RNA elicits antiviral pathogenic response in a Drosophila model of expanded CAG repeat neurodegenerative diseases

Neuronal-specific impairment of heparan sulfate degradation in Drosophila reveals pathogenic mechanisms for Mucopolysaccharidosis type IIIA

Molecular Biology of the WWOX Gene That Spans Chromosomal Fragile Site FRA16D

Drosophila orthologue of WWOX, the chromosomal fragile site FRA16D tumour suppressor gene, functions in aerobic metabolism and regulates reactive oxygen species

Distinct roles for Toll and autophagy pathways in double-stranded RNA toxicity in a Drosophila model of expanded repeat neurodegenerative diseases

Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases

Ubiquitous expression of CUG or CAG trinucleotide repeat RNA causes common morphological defects in a Drosophila model of RNA-mediated pathology

Perturbation of the Akt/Gsk3-β signalling pathway is common to Drosophila expressing expanded untranslated CAG, CUG and AUUCU repeat RNAs

RNA pathogenesis via Toll-like receptor-activated inflammation in expanded repeat neurodegenerative diseases

Know thy fly

FRA16D common chromosomal fragile site oxido-reductase (FOR/WWOX) protects against the effects of ionizing radiation in Drosophila

Tumor Suppressor WWOX Contributes to the Elimination of Tumorigenic Cells in Drosophila melanogaster: e0136356

A Drosophila G1-specific cyclin E homolog exhibits different modes of expression during embryogenesis

Ectopic cyclin E expression induces premature entry into S phase and disrupts pattern formation in the Drosophila eye imaginal disc

Regulation of the Elongation Phase of Protein Synthesis Enhances Translation Accuracy and Modulates Lifespan

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