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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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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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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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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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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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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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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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CAG Repeat Expansion in Autosomal Dominant Familial Spastic Paraparesis: Novel Expansion in a Subset of Patients

Human molecular genetics, 1998-10, Vol.7 (11), p.1779-1786

1998

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Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246

American journal of human genetics, 1996-03, Vol.58 (3), p.523-534

1996

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Familial Mediterranean fever (FMF) in Moroccan Jews : demonstration of a founder effect by extended haplotype analysis

American journal of human genetics, 1993-09, Vol.53 (3), p.644-651

1993

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Refined mapping of the gene causing familial mediterranean fever, by linkage and homozygosity studies

American journal of human genetics, 1993-08, Vol.53 (2), p.451-461

1993

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Fragile X syndrome : diagnosis using highly polymorphic microsatellite markers

American journal of human genetics, 1991-06, Vol.48 (6), p.1051-1057

1991

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Human prostate specific antigen (PSA) gene: structure and linkage to the kallikrein-like gene, hGK-1

Nucleic acids research, 1989-03, Vol.17 (5), p.2137-2137

1989

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Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21-hydroxylase deficiency

Medical journal of Australia, 1992-01, Vol.156 (2), p.132-135

1992

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Fragile X syndrome: The most common cause of familial intellectual handicap

Medical journal of Australia, 1993-04, Vol.158 (7), p.482-485

1993

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Sequence of the mouse glandular kallikrein gene, mGK-5

Nucleic acids research, 1987-12, Vol.15 (23), p.10052-10052

1987

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Sequence of mGK-11, a mouse glandular kallikrein gene

Nucleic acids research, 1988-11, Vol.16 (22), p.10918-10918

1988

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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

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

Common chromosomal fragile site FRA16D mutation in cancer cells

Chromosomal fragile site FRA16D and DNA instability in cancer

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

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

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

CAG Repeat Expansion in Autosomal Dominant Familial Spastic Paraparesis: Novel Expansion in a Subset of Patients

Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246

Familial Mediterranean fever (FMF) in Moroccan Jews : demonstration of a founder effect by extended haplotype analysis

Refined mapping of the gene causing familial mediterranean fever, by linkage and homozygosity studies

Fragile X syndrome : diagnosis using highly polymorphic microsatellite markers

Human prostate specific antigen (PSA) gene: structure and linkage to the kallikrein-like gene, hGK-1

Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21-hydroxylase deficiency

Fragile X syndrome: The most common cause of familial intellectual handicap

Sequence of the mouse glandular kallikrein gene, mGK-5

Sequence of mGK-11, a mouse glandular kallikrein gene

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