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Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene

Vision research (Oxford), 2007-03, Vol.47 (5), p.624-633

2007

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Retinal degeneration mutants in the mouse

Vision research (Oxford), 2002-02, Vol.42 (4), p.517-525

2002

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Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

Nature genetics, 1997-05, Vol.16 (1), p.19-27

1997

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Mouse models of ocular diseases

Visual neuroscience, 2005-09, Vol.22 (5), p.587-593

2005

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A mouse model for Down syndrome exhibits learning and behaviour deficits

Nature genetics, 1995-10, Vol.11 (2), p.177-184

1995

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Motor dysfunction in a mouse model for Down syndrome

Physiology & behavior, 1999-12, Vol.68 (1), p.211-220

1999

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Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice

Nature genetics, 1999-04, Vol.21 (4), p.405-409

1999

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Retinal Degeneration 6 (rd6): A New Mouse Model for Human Retinitis Punctata Albescens

Investigative ophthalmology & visual science, 2000-09, Vol.41 (10), p.3149-3157

2000

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Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome

Cytogenetic and genome research, 2001-01, Vol.93 (3-4), p.270-276

2001

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Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions

Gene, 2003-10, Vol.318, p.137-147

2003

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Discovery genetics: Serendipity in basic research

ILAR journal, 2005, Vol.46 (4), p.338-345

Davisson, M.T

2005

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Mutations in the Human Orthologue of the Mouse underwhite Gene ( uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

American journal of human genetics, 2001-11, Vol.69 (5), p.981-988

2001

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A New Spontaneous Mouse Mutation of Hoxd13 with a Polyalanine Expansion and Phenotype Similar to Human Synpolydactyly

Human molecular genetics, 1998-06, Vol.7 (6), p.1033-1038

1998

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Recombination Suppression by Heterozygous Robertsonian Chromosomes in the Mouse

Genetics (Austin), 1993-03, Vol.133 (3), p.649-667

1993

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Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta

Proceedings of the National Academy of Sciences - PNAS, 1993-03, Vol.90 (5), p.1701-1705

1993

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Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (at) and white-bellied agouti (AW) reveals alternative forms of agouti transcripts

Genes & development, 1994-02, Vol.8 (4), p.481-490

1994

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Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis

The American journal of pathology, 1997-07, Vol.151 (1), p.293-310

1997

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Murine mucopolysaccharidosis type VII: characterization of a mouse with β-glucuronidase deficiency

The Journal of clinical investigation, 1989-04, Vol.83 (4), p.1258-1266

1989

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Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration

Mammalian genome, 1996-11, Vol.7 (11), p.798-802

1996

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Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome

Behavioural brain research, 2002-08, Vol.134 (1), p.185-200

2002

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The Mouse Genome Database (MGD). A comprehensive public resource of genetic, phenotypic and genomic data

Nucleic acids research, 1997-01, Vol.25 (1), p.85-91

1997

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Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)

Annals of neurology, 1993-04, Vol.33 (4), p.381-385

1993

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Lop12, a Mutation in Mouse Crygd Causing Lens Opacity Similar to Human Coppock Cataract

Genomics (San Diego, Calif.), 2000-02, Vol.63 (3), p.314-320

2000

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Mouse chromosome classification by radial basis function network with fast orthogonal search

Neural networks, 1998-06, Vol.11 (4), p.769-777

1998

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The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities

The Journal of biological chemistry, 1989-05, Vol.264 (14), p.7994-8003

1989

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Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene

Retinal degeneration mutants in the mouse

Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

Mouse models of ocular diseases

A mouse model for Down syndrome exhibits learning and behaviour deficits

Motor dysfunction in a mouse model for Down syndrome

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice

Retinal Degeneration 6 (rd6): A New Mouse Model for Human Retinitis Punctata Albescens

Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome

Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions

Discovery genetics: Serendipity in basic research

Mutations in the Human Orthologue of the Mouse underwhite Gene ( uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

A New Spontaneous Mouse Mutation of Hoxd13 with a Polyalanine Expansion and Phenotype Similar to Human Synpolydactyly

Recombination Suppression by Heterozygous Robertsonian Chromosomes in the Mouse

Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta

Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (at) and white-bellied agouti (AW) reveals alternative forms of agouti transcripts

Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis

Murine mucopolysaccharidosis type VII: characterization of a mouse with β-glucuronidase deficiency

Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration

Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome

The Mouse Genome Database (MGD). A comprehensive public resource of genetic, phenotypic and genomic data

Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)

Lop12, a Mutation in Mouse Crygd Causing Lens Opacity Similar to Human Coppock Cataract

Mouse chromosome classification by radial basis function network with fast orthogonal search

The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities

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