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Purkinje cell death: differences between developmental cell death and neurodegenerative death in mutant mice

Cerebellum (London, England), 2006-06, Vol.5 (2), p.163-173

2006

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Pathologic changes in the CNS of Dystonia musculorum mutant mouse: An animal model for human spinocerebellar ataxia

Neuroscience, 1988-11, Vol.27 (2), p.403-424

1988

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Pax8, a murine paired box gene expressed in the developing excretory system and thyroid gland

Development (Cambridge), 1990-10, Vol.110 (2), p.643-651

1990

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Inducing mutations in the mouse genome with the chemical mutagen ethylnitrosourea

Brazilian journal of medical and biological research, 2006-09, Vol.39 (9), p.1217-1226

2006

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Progressive Purkinje cell degeneration in tambaleante mutant mice is a consequence of a missense mutation in HERC1 E3 ubiquitin ligase

PLoS genetics, 2009-12, Vol.5 (12), p.e1000784-e1000784

2009

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A mouse model provides evidence that genetic background modulates anemia and liver injury in erythropoietic protoporphyria

American journal of physiology: Gastrointestinal and liver physiology, 2005, Vol.288, p.G1208-G1216

2005

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Expression of the L14 lectin during mouse embryogenesis suggests multiple roles during pre- and post-implantation development

Development (Cambridge), 1992-05, Vol.115 (1), p.143-155

1992

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The genome

Biochimie, 1991-09, Vol.73 (9), p.1257-1257

Guenet, J.L.

1991

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Comparative Mapping of Lipocalin Genes in Human and Mouse: The Four Genes for Complement C8 γ Chain, Prostaglandin-d-Synthase, Oncogene-24P3, and Progestagen-Associated Endometrial Protein Map to HSA9 and MMU2

Genomics (San Diego, Calif.), 1994-09, Vol.23 (1), p.145-150

1994

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aku, a Mutation of the Mouse Homologous to Human Alkaptonuria, Maps to Chromosome 16

Genomics (San Diego, Calif.), 1994-01, Vol.19 (1), p.9-11

1994

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The Human Gene for Alkaptonuria (AKU) Maps to Chromosome 3q

Genomics (San Diego, Calif.), 1994-01, Vol.19 (1), p.5-8

1994

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Phenotypic reversion at the W/Kit locus mediated by mitotic recombination in mice

Molecular and cellular biology, 1995, Vol.15 (11), p.5898-5905

1995

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The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13

Genomics (San Diego, Calif.), 1995-09, Vol.29 (1), p.131-135

1995

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Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus

Human genetics, 1990-08, Vol.85 (3), p.324-326

1990

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The DDK inbred strain as a model for the study of interactions between parental genomes and egg cytoplasm in mouse preimplantation development

Development (Cambridge), 1990 (Suppl), p.81-87

1990

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Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7

The EMBO journal, 1986-11, Vol.5 (11), p.2899-2905

1986

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The Mouse Mutation Sarcosinemia (sar) Maps to Chromosome 2 in a Region Homologous to Human 9q33–q34

Genomics (San Diego, Calif.), 1996-08, Vol.36 (1), p.182-184

1996

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Homologous chromosomal locations of the four genes for inter- α-inhibitor and pre- α-inhibitor family in human and mouse: Assignment of the ancestral gene for the lipocalin superfamily

Genomics (San Diego, Calif.), 1992-09, Vol.14 (1), p.83-88

1992

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Comparative Assignments of the Genes of the Inter-α-inhibitor Family in Human and Mouse:ITIH4Is Close toITIH1andITIH3,on HSA 3 and MMU 14

Genomics (San Diego, Calif.), 1997-04, Vol.41 (1), p.139-140

1997

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The locus Om, responsible for the DDK syndrome, maps close to Sigje on mouse chromosome 11

Mammalian genome, 1992-01, Vol.2 (2), p.100-105

1992

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Assignment of the Chromogranin A ( Chga) Locus to Homologous Regions on Mouse Chromosome 12 and Rat Chromosome 6

Genomics (San Diego, Calif.), 1993-07, Vol.17 (1), p.252-255

1993

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Genetic analysis of the mouse using interspecific crosses

Trends in Genetics, 1988, Vol.4 (1), p.18-23

1988

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Mapping of the mouse X chromosome using random genomic probes and an interspecific mouse cross

The EMBO journal, 1985-12, Vol.4 (13B), p.3695-3700

1985

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Chromosomal Mapping of the Structural Gene Coding for the Mouse Cell Adhesion Molecule Uvomorulin

Proceedings of the National Academy of Sciences - PNAS, 1988-05, Vol.85 (10), p.3489-3493

1988

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Structural analysis of mouse glycine receptor alpha subunit genes. Identification and chromosomal localization of a novel variant

The Journal of biological chemistry, 1994-01, Vol.269 (4), p.2607-2612

1994

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Purkinje cell death: differences between developmental cell death and neurodegenerative death in mutant mice

Pathologic changes in the CNS of Dystonia musculorum mutant mouse: An animal model for human spinocerebellar ataxia

Pax8, a murine paired box gene expressed in the developing excretory system and thyroid gland

Inducing mutations in the mouse genome with the chemical mutagen ethylnitrosourea

Progressive Purkinje cell degeneration in tambaleante mutant mice is a consequence of a missense mutation in HERC1 E3 ubiquitin ligase

A mouse model provides evidence that genetic background modulates anemia and liver injury in erythropoietic protoporphyria

Expression of the L14 lectin during mouse embryogenesis suggests multiple roles during pre- and post-implantation development

The genome

Comparative Mapping of Lipocalin Genes in Human and Mouse: The Four Genes for Complement C8 γ Chain, Prostaglandin-d-Synthase, Oncogene-24P3, and Progestagen-Associated Endometrial Protein Map to HSA9 and MMU2

aku, a Mutation of the Mouse Homologous to Human Alkaptonuria, Maps to Chromosome 16

The Human Gene for Alkaptonuria (AKU) Maps to Chromosome 3q

Phenotypic reversion at the W/Kit locus mediated by mitotic recombination in mice

The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13

Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus

The DDK inbred strain as a model for the study of interactions between parental genomes and egg cytoplasm in mouse preimplantation development

Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7

The Mouse Mutation Sarcosinemia (sar) Maps to Chromosome 2 in a Region Homologous to Human 9q33–q34

Homologous chromosomal locations of the four genes for inter- α-inhibitor and pre- α-inhibitor family in human and mouse: Assignment of the ancestral gene for the lipocalin superfamily

Comparative Assignments of the Genes of the Inter-α-inhibitor Family in Human and Mouse:ITIH4Is Close toITIH1andITIH3,on HSA 3 and MMU 14

The locus Om, responsible for the DDK syndrome, maps close to Sigje on mouse chromosome 11

Assignment of the Chromogranin A ( Chga) Locus to Homologous Regions on Mouse Chromosome 12 and Rat Chromosome 6

Genetic analysis of the mouse using interspecific crosses

Mapping of the mouse X chromosome using random genomic probes and an interspecific mouse cross

Chromosomal Mapping of the Structural Gene Coding for the Mouse Cell Adhesion Molecule Uvomorulin

Structural analysis of mouse glycine receptor alpha subunit genes. Identification and chromosomal localization of a novel variant

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