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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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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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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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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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Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiency

Journal of endocrinology, 1994-04, Vol.141 (1), p.33

1994

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The mouse mutation severe combined immune deficiency (scid) is on chromosome 16

Immunogenetics (New York), 1989, Vol.29 (1), p.54-57

1989

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Genomic, Transcriptional and Mutational Analysis of the Mouse microphthalmia Locus

Genetics (Austin), 2000-05, Vol.155 (1), p.291-300

2000

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A new allelic series for the underwhite gene on mouse chromosome 15

The Journal of heredity, 1998-11, Vol.89 (6), p.546-551

1998

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Cerebellar Disorganization Characteristic of Reeler in Scrambler Mutant Mice Despite Presence of Reelin

The Journal of neuroscience, 1997-11, Vol.17 (22), p.8767-8777

1997

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Genetic and Physical Maps of the Stargazer Locus on Mouse Chromosome 15

Genomics (San Diego, Calif.), 1997-07, Vol.43 (1), p.62-68

1997

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Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage

Genes & development, 1994-06, Vol.8 (12), p.1463-1472

1994

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The Neurological Mouse Mutations Jittery and Hesitant Are Allelic and Map to the Region of Mouse Chromosome 10 Homologous to 19p13.3

Genomics (San Diego, Calif.), 1996-08, Vol.35 (3), p.533-538

1996

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Mesenchymal Dysplasia: A Recessive Mutation on Chromosome 13 of the Mouse

The Journal of heredity, 1996-03, Vol.87 (2), p.87-95

1996

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Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype

The Journal of neuroscience, 1997-12, Vol.17 (23), p.9204-9211

1997

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Cocoa: a new mouse model for platelet storage pool deficiency

British journal of haematology, 1988-07, Vol.69 (3), p.371-378

1988

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The fld mutation maps near to but distinct from the Apob locus on mouse chromosome 12

Mammalian genome, 1996-07, Vol.7 (7), p.555-557

1996

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Osteochondrodystrophy (ocd): A New Autosomal Recessive Mutation in the Mouse

The Journal of heredity, 1991-03, Vol.82 (2), p.140-144

1991

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'Wasted' , a new mutant of the mouse with abnormalities characteristic of ataxia telangiectasia

Nature (London), 1982-06, Vol.297 (5865), p.402-404

1982

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A Road Map Toward a Globally Harmonized Approach for Occupational Health Surveillance and Epidemiology in Nanomaterial Workers

Journal of occupational and environmental medicine, 2012-10, Vol.54 (10), p.1214-1223

2012

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Transmissible Spongiform Encephalopathy in the Gray Tremor Mutant Mouse

Proceedings of the National Academy of Sciences - PNAS, 1985-01, Vol.82 (1), p.253-257

1985

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The stumbler mutation maps to proximal mouse chromosome 2

Mammalian genome, 1994-11, Vol.5 (11), p.659-662

1994

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Dense Incisors (din): A New Mouse Mutation on Chromosome 16 Affecting Tooth Eruption and Body Size

The Journal of heredity, 1996-03, Vol.87 (2), p.162-167

1996

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Dilute suppressor, a new suppressor gene in the house mouse

The Journal of heredity, 1983-07, Vol.74 (4), p.305-306

Sweet, H O

1983

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Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton

The American journal of pathology, 1976-03, Vol.82 (3), p.493-512

1976

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

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

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

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

Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiency

The mouse mutation severe combined immune deficiency (scid) is on chromosome 16

Genomic, Transcriptional and Mutational Analysis of the Mouse microphthalmia Locus

A new allelic series for the underwhite gene on mouse chromosome 15

Cerebellar Disorganization Characteristic of Reeler in Scrambler Mutant Mice Despite Presence of Reelin

Genetic and Physical Maps of the Stargazer Locus on Mouse Chromosome 15

Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage

The Neurological Mouse Mutations Jittery and Hesitant Are Allelic and Map to the Region of Mouse Chromosome 10 Homologous to 19p13.3

Mesenchymal Dysplasia: A Recessive Mutation on Chromosome 13 of the Mouse

Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype

Cocoa: a new mouse model for platelet storage pool deficiency

The fld mutation maps near to but distinct from the Apob locus on mouse chromosome 12

Osteochondrodystrophy (ocd): A New Autosomal Recessive Mutation in the Mouse

'Wasted' , a new mutant of the mouse with abnormalities characteristic of ataxia telangiectasia

A Road Map Toward a Globally Harmonized Approach for Occupational Health Surveillance and Epidemiology in Nanomaterial Workers

Transmissible Spongiform Encephalopathy in the Gray Tremor Mutant Mouse

The stumbler mutation maps to proximal mouse chromosome 2

Dense Incisors (din): A New Mouse Mutation on Chromosome 16 Affecting Tooth Eruption and Body Size

Dilute suppressor, a new suppressor gene in the house mouse

Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton

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