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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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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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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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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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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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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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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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Fragile sites still breaking

Trends in Genetics, 1998-12, Vol.14 (12), p.501-506

1998

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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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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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Mouse glandular kallikrein genes: identification and characterization of the genes encoding the epidermal growth factor binding proteins

Biochemistry (Easton), 1987-10, Vol.26 (21), p.6750-6756

1987

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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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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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Incidence and origin of null alleles in the (AC)n microsatellite markers

American journal of human genetics, 1993-05, Vol.52 (5), p.922-927

1993

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Dynamic mutations: A new class of mutations causing human disease

Cell, 1992-09, Vol.70 (5), p.709-712

1992

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Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

Human genetics, 1999-09, Vol.105 (3), p.261-265

1999

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Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal disease

Journal of medical genetics, 1997-03, Vol.34 (3), p.213-216

1997

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Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2

American journal of human genetics, 1997-10, Vol.61 (4), p.873-881

1997

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

Huntingtin-deficient zebrafish exhibit defects in iron utilization and development

Fragile and unstable chromosomes in cancer: causes and consequences

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

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

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

Common chromosomal fragile site FRA16D mutation in cancer cells

Fragile sites still breaking

Chromosomal fragile site FRA16D and DNA instability in cancer

Know thy fly

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

Mouse glandular kallikrein genes: identification and characterization of the genes encoding the epidermal growth factor binding proteins

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

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

Incidence and origin of null alleles in the (AC)n microsatellite markers

Dynamic mutations: A new class of mutations causing human disease

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal disease

Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2

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