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Glutamine repeats and neurodegeneration

Annual review of neuroscience, 2000-01, Vol.23 (1), p.217-247

2000

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Requirement of Math1 for Secretory Cell Lineage Commitment in the Mouse Intestine

Science (American Association for the Advancement of Science), 2001-12, Vol.294 (5549), p.2155-2158

2001

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Rett syndrome is caused by mutations in X-linked MECP2 , encoding methyl-CpG-binding protein 2

Nature genetics, 1999-10, Vol.23 (2), p.185-188

1999

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TRINUCLEOTIDE REPEATS: Mechanisms and Pathophysiology

Annual review of genomics and human genetics, 2000-01, Vol.1 (1), p.281-328

2000

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Fourteen and counting: unraveling trinucleotide repeat diseases

Human molecular genetics, 2000-04, Vol.9 (6), p.909-916

2000

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Math1: An Essential Gene for the Generation of Inner Ear Hair Cells

Science (American Association for the Advancement of Science), 1999-06, Vol.284 (5421), p.1837-1841

1999

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The clinical and genetic spectrum of spinocerebellar ataxia 14

Neurology, 2005-04, Vol.64 (7), p.1258-1260

2005

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Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1

Nature genetics, 1998-06, Vol.19 (2), p.148-154

1998

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Proprioceptor Pathway Development Is Dependent on MATH1

Neuron (Cambridge, Mass.), 2001-05, Vol.30 (2), p.411-422

2001

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Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype

Neurology, 1998-10, Vol.51 (4), p.1081-1086

1998

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Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots

American journal of human genetics, 1999-12, Vol.65 (6), p.1520-1529

1999

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Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

Nature (London), 1997-10, Vol.389 (6654), p.971-974

1997

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Functional conservation of atonal and Math1 in the CNS and PNS

Development (Cambridge), 2000-03, Vol.127 (5), p.1039-1048

2000

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Identification and characterization of the gene causing type 1 spinocerebellar ataxia

Nature genetics, 1994-08, Vol.7 (4), p.513-520

1994

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The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1

Nature (London), 1997-10, Vol.389 (6654), p.974-978

1997

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Identification and characterization of an ataxin-1-interacting protein : A1Up, a ubiquitin-like nuclear protein

Human molecular genetics, 2000-09, Vol.9 (15), p.2305-2312

2000

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Insights from mouse models into the molecular basis of neurodegeneration

Annual review of physiology, 2000-01, Vol.62 (1), p.779-802

2000

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Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

Nature genetics, 1995-05, Vol.10 (1), p.94-98

1995

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Spinocerebellar ataxia type 10 is rare in populations other than Mexicans

Neurology, 2002-03, Vol.58 (6), p.983-983

2002

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Genetic regulation of cerebellar development

Nature reviews. Neuroscience, 2001-07, Vol.2 (7), p.484-491

2001

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atonal Regulates Neurite Arborization but Does Not Act as a Proneural Gene in the Drosophila Brain

Neuron (Cambridge, Mass.), 2000-03, Vol.25 (3), p.549-561

2000

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Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

Journal of medical genetics, 2005-02, Vol.42 (2), p.e15-e15

2005

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Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice

Human molecular genetics, 2001-07, Vol.10 (14), p.1511-1518

2001

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Repeat instability and motor incoordination in mice with a targeted expanded CAG repeat in the Sca1 locus

Human molecular genetics, 2000-03, Vol.9 (5), p.779-785

2000

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Increased Trinucleotide Repeat Instability with Advanced Maternal Age

Human molecular genetics, 1997-11, Vol.6 (12), p.2135-2139

1997

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Glutamine repeats and neurodegeneration

Requirement of Math1 for Secretory Cell Lineage Commitment in the Mouse Intestine

Rett syndrome is caused by mutations in X-linked MECP2 , encoding methyl-CpG-binding protein 2

TRINUCLEOTIDE REPEATS: Mechanisms and Pathophysiology

Fourteen and counting: unraveling trinucleotide repeat diseases

Math1: An Essential Gene for the Generation of Inner Ear Hair Cells

The clinical and genetic spectrum of spinocerebellar ataxia 14

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1

Proprioceptor Pathway Development Is Dependent on MATH1

Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype

Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots

Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

Functional conservation of atonal and Math1 in the CNS and PNS

Identification and characterization of the gene causing type 1 spinocerebellar ataxia

The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1

Identification and characterization of an ataxin-1-interacting protein : A1Up, a ubiquitin-like nuclear protein

Insights from mouse models into the molecular basis of neurodegeneration

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans

Genetic regulation of cerebellar development

atonal Regulates Neurite Arborization but Does Not Act as a Proneural Gene in the Drosophila Brain

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice

Repeat instability and motor incoordination in mice with a targeted expanded CAG repeat in the Sca1 locus

Increased Trinucleotide Repeat Instability with Advanced Maternal Age

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