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The stromal gene encoding the CD274 antigen as a genetic modifier controlling survival of mice with γ-radiation-induced T-cell lymphoblastic lymphomas

Oncogene, 2010-09, Vol.29 (38), p.5265-5273

2010

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Sphingomyelin Degradation is a Key Factor in Dentin and Bone Mineralization: Lessons from the fro/fro Mouse

Journal of dental research, 2008-01, Vol.87 (1), p.9-13

2008

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Rat Gene Mapping Using PCR-Analyzed Microsatellites

Genetics (Austin), 1992-07, Vol.131 (3), p.701-721

1992

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Susceptibility to Experimental Cerebral Malaria Induced by Plasmodium berghei ANKA in Inbred Mouse Strains Recently Derived from Wild Stock

Infection and Immunity, 2002-04, Vol.70 (4), p.2049-2056

2002

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Pax: A murine multigene family of paired box-containing genes

Genomics (San Diego, Calif.), 1991-10, Vol.11 (2), p.424-434

1991

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Sequence interpretation. Functional annotation of mouse genome sequences

Science (American Association for the Advancement of Science), 2001-02, Vol.291 (5507), p.1251

2001

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A Single Base Deletion in the Tfm Androgen Receptor Gene Creates a Short-Lived Messenger RNA that Directs Internal Translation Initiation

Proceedings of the National Academy of Sciences - PNAS, 1991-10, Vol.88 (19), p.8606-8610

1991

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Several classical mouse inbred strains, including DBA/2, NOD/Lt, FVB/N, and SJL/J, carry a putative loss-of-function allele of Gpr84

The Journal of heredity, 2013-07, Vol.104 (4), p.565-571

2013

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A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestine

Genes & development, 1988-12, Vol.2 (12A), p.1647-1654

1988

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Structure and chromosomal assignment of the mouse fra-1 gene, and its exclusion as a candidate gene for oc (osteosclerosis)

Oncogene, 1997-09, Vol.15 (10), p.1171-1178

1997

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A missense mutation in Tbce causes progressive motor neuronopathy in mice

Nature genetics, 2002-11, Vol.32 (3), p.443-447

2002

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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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An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrids

Nature genetics, 1996-04, Vol.12 (4), p.398-403

1996

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cDNA Isolation, Expression, and Chromosomal Localization of the Mouse Survival Motor Neuron Gene (Smn)

Genomics (San Diego, Calif.), 1997-02, Vol.40 (1), p.185-188

1997

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Neurobiological effects of a null mutation depend on genetic context: comparison between two hotfoot alleles of the delta-2 ionotropic glutamate receptor

Neuroscience, 2001-01, Vol.105 (2), p.443-455

2001

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Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1 : structure, function, regulation of expression and chromosomal localization

Biochemical journal, 1994-09, Vol.302 (Pt 3), p.781-790

1994

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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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Innate resistance to flavivirus infections and the functions of 2'-5' oligoadenylate synthetases

Current topics in microbiology and immunology, 2008, Vol.321, p.85

2008

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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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Genetic Analysis of Diabetes and Insulitis in an Interspecific Cross of the Nonobese Diabetic Mouse with Mus spretus

Proceedings of the National Academy of Sciences - PNAS, 1993-03, Vol.90 (5), p.1877-1881

1993

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

Molecular and Cellular Biology, 1995-11, Vol.15 (11), p.5898-5905

1995

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The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice

Nature (London), 1986-06, Vol.321 (6073), p.867-869

1986

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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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Three New Allelic Mouse Mutations that Cause Skeletal Overgrowth Involve the Natriuretic Peptide Receptor C Gene (Npr3)

Proceedings of the National Academy of Sciences - PNAS, 1999-08, Vol.96 (18), p.10278-10283

1999

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The stromal gene encoding the CD274 antigen as a genetic modifier controlling survival of mice with γ-radiation-induced T-cell lymphoblastic lymphomas

Sphingomyelin Degradation is a Key Factor in Dentin and Bone Mineralization: Lessons from the fro/fro Mouse

Rat Gene Mapping Using PCR-Analyzed Microsatellites

Susceptibility to Experimental Cerebral Malaria Induced by Plasmodium berghei ANKA in Inbred Mouse Strains Recently Derived from Wild Stock

Pax: A murine multigene family of paired box-containing genes

Sequence interpretation. Functional annotation of mouse genome sequences

A Single Base Deletion in the Tfm Androgen Receptor Gene Creates a Short-Lived Messenger RNA that Directs Internal Translation Initiation

Several classical mouse inbred strains, including DBA/2, NOD/Lt, FVB/N, and SJL/J, carry a putative loss-of-function allele of Gpr84

Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders

A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestine

Structure and chromosomal assignment of the mouse fra-1 gene, and its exclusion as a candidate gene for oc (osteosclerosis)

A missense mutation in Tbce causes progressive motor neuronopathy in mice

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

An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrids

cDNA Isolation, Expression, and Chromosomal Localization of the Mouse Survival Motor Neuron Gene (Smn)

Neurobiological effects of a null mutation depend on genetic context: comparison between two hotfoot alleles of the delta-2 ionotropic glutamate receptor

Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1 : structure, function, regulation of expression and chromosomal localization

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

Innate resistance to flavivirus infections and the functions of 2'-5' oligoadenylate synthetases

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

Genetic Analysis of Diabetes and Insulitis in an Interspecific Cross of the Nonobese Diabetic Mouse with Mus spretus

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

The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice

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

Three New Allelic Mouse Mutations that Cause Skeletal Overgrowth Involve the Natriuretic Peptide Receptor C Gene (Npr3)

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