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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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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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Single-cell sequencing shows mosaic aneuploidy in most human embryos

The Journal of clinical investigation, 2024-03, Vol.134 (6)

2024

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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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Neurodegenerative diseases have genetic hallmarks of autoinflammatory disease

Human molecular genetics, 2018-08, Vol.27 (R2), p.R108-R118

2018

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Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome

Human molecular genetics, 2006-12, Vol.15 (23), p.3446-3458

2006

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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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WWOX, the chromosomal fragile site FRA16D spanning gene: Its role in metabolism and contribution to cancer

Experimental biology and medicine (Maywood, N.J.), 2015-03, Vol.240 (3), p.338-344

2015

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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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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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Huntingtin-deficient zebrafish exhibit defects in iron utilization and development

Human molecular genetics, 2007-08, Vol.16 (16), p.1905-1920

2007

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Fragile and unstable chromosomes in cancer: causes and consequences

Trends in Genetics, 2001-06, Vol.17 (6), p.339-345

Richards, Robert I.

2001

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Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

Cell, 1997-02, Vol.88 (3), p.367-374

1997

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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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Selective neuronal requirement for huntingtin in the developing zebrafish

Human molecular genetics, 2009-12, Vol.18 (24), p.4830-4842

2009

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Common chromosomal fragile site FRA16D sequence : identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Human molecular genetics, 2000-07, Vol.9 (11), p.1651-1663

2000

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Dynamic mutations : a decade of unstable expanded repeats in human genetic disease

Human molecular genetics, 2001-10, Vol.10 (20), p.2187-2194

RICHARDS, Robert I

2001

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The molecular basis of fragile sites in human chromosomes

Current opinion in genetics & development, 1995-06, Vol.5 (3), p.323-327

1995

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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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A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene : implications for mutation analysis in pseudoxanthoma elasticum

Journal of molecular medicine (Berlin, Germany), 2001-09, Vol.79 (9), p.536-546

2001

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Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6

Human mutation, 2005-09, Vol.26 (3), p.235-248

2005

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

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

Tumor suppressor WWOX moderates the mitochondrial respiratory complex

Single-cell sequencing shows mosaic aneuploidy in most human embryos

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

Common chromosomal fragile sites and cancer: Focus on FRA16D

Neurodegenerative diseases have genetic hallmarks of autoinflammatory disease

Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome

The pathogenic agent in Drosophila models of ‘polyglutamine’ diseases

WWOX, the chromosomal fragile site FRA16D spanning gene: Its role in metabolism and contribution to cancer

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

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

Huntingtin-deficient zebrafish exhibit defects in iron utilization and development

Fragile and unstable chromosomes in cancer: causes and consequences

Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

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

Selective neuronal requirement for huntingtin in the developing zebrafish

Common chromosomal fragile site FRA16D sequence : identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Dynamic mutations : a decade of unstable expanded repeats in human genetic disease

The molecular basis of fragile sites in human chromosomes

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

A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene : implications for mutation analysis in pseudoxanthoma elasticum

Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6

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