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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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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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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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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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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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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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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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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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Common chromosomal fragile site FRA16D mutation in cancer cells

Human molecular genetics, 2005-05, Vol.14 (10), p.1341-1349

2005

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Simple Tandem DNA Repeats and Human Genetic Disease

Proceedings of the National Academy of Sciences - PNAS, 1995-04, Vol.92 (9), p.3636-3641

1995

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Simple repeat DNA is not replicated simply

Nature genetics, 1994-02, Vol.6 (2), p.114-116

1994

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Chromosomal fragile site FRA16D and DNA instability in cancer

Cancer research (Chicago, Ill.), 2000-03, Vol.60 (6), p.1683-1689

2000

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Structure of mouse kallikrein gene family suggests a role in specific processing of biologically active peptides

Nature (London), 1983-05, Vol.303 (5915), p.300-307

1983

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Dynamic mutations on the move in Banff

Nature genetics, 2004-07, Vol.36 (7), p.667-670

2004

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Heritable unstable DNA sequences

Nature genetics, 1992-04, Vol.1 (1), p.7-9

1992

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Physical linkage of the fragile site FRA11B and a Jacobsen Syndrome chromosome deletion breakpoint in 11q23. 3

Human molecular genetics, 1994-12, Vol.3 (12), p.2123-2130

1994

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Characterization of DNA sequences through which cadmium and glucocorticoid hormones induce human metallothionein-IIA gene

Nature (London), 1984-04, Vol.308 (5959), p.513-519

1984

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Human metallothionein genes-primary structure of the metallothionein-II gene and a related processed gene

Nature (London), 1982-10, Vol.299 (5886), p.797-802

1982

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Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence

The New England journal of medicine, 1991-12, Vol.325 (24), p.1720-1722

1991

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DNA Repeats -- A Treasury of Human Variation

The New England journal of medicine, 1994-07, Vol.331 (3), p.191-193

1994

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

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

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

Huntingtin-deficient zebrafish exhibit defects in iron utilization and development

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

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

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

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

Common chromosomal fragile site FRA16D mutation in cancer cells

Simple Tandem DNA Repeats and Human Genetic Disease

Simple repeat DNA is not replicated simply

Chromosomal fragile site FRA16D and DNA instability in cancer

Structure of mouse kallikrein gene family suggests a role in specific processing of biologically active peptides

Dynamic mutations on the move in Banff

Heritable unstable DNA sequences

Physical linkage of the fragile site FRA11B and a Jacobsen Syndrome chromosome deletion breakpoint in 11q23. 3

Characterization of DNA sequences through which cadmium and glucocorticoid hormones induce human metallothionein-IIA gene

Human metallothionein genes-primary structure of the metallothionein-II gene and a related processed gene

Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence

DNA Repeats -- A Treasury of Human Variation

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