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Molecular characterization of Pax6(2Neu) through Pax6(10Neu): an extension of the Pax6 allelic series and the identification of two possible hypomorph alleles in the mouse Mus musculus

Genetics (Austin), 2001-12, Vol.159 (4), p.1689-1700

2001

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Saturation mutagenesis for dominant eye morphological defects in the mouse Mus musculus

Mammalian genome, 2000-07, Vol.11 (7), p.520-525

2000

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The mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion

Mammalian genome, 2008-05, Vol.19 (5), p.378-378

2008

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Reevaluation of the induction of specific-locus mutations in spermatogonia of the mouse by acrylamide

Mutation research, 1992-11, Vol.283 (3), p.185-191

1992

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The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

Proceedings of the National Academy of Sciences - PNAS, 1996-11, Vol.93 (24), p.13870-13875

1996

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mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion

Mammalian genome, 1997-06, Vol.8 (6), p.403-406

1997

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Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16

Investigative ophthalmology & visual science, 1997-11, Vol.38 (12), p.2502-2507

1997

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Genetic Mosaicism in the House Mouse

Annual review of genetics, 1994-01, Vol.28 (1), p.27-47

1994

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A 76-bp Deletion in the Mip Gene Causes Autosomal Dominant Cataract in Hfi Mice

Genomics (San Diego, Calif.), 2001-06, Vol.74 (3), p.313-319

2001

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Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8

Investigative ophthalmology & visual science, 1998-09, Vol.39 (10), p.1863-1869

1998

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Mutagenicity testing of vincristine sulfate in germ cells of male mice

Mutation research, 1988-11, Vol.209 (3), p.107-113

1988

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Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion

Mammalian genome, 1996-11, Vol.7 (11), p.843-846

1996

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Detection of a point mutation (A to G) in exon 5 of the murine Mgf gene defines a novel allele at the Steel locus with a weak phenotype

Mutation research, 1997-09, Vol.382 (1-2), p.75-78

1997

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Induction of specific-locus and dominant lethal mutations in male mice by ifosfamide (Holoxan)

Genetical Research, 1998-12, Vol.72 (3), p.177-183

1998

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Induction of specific-locus and dominant lethal mutations in male mice by 1-methyl-1-nitrosourea (MNU)

Mutation research, 1991-09, Vol.250 (1-2), p.447-456

1991

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Induction of specific-locus and dominant lethal mutations in male mice by n-propyl and isopropyl methanesulfonate

Mutation research, 1995-04, Vol.328 (1), p.73-82

1995

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Mutagenic activity of 2-amino- N6-hydroxyadenine in the mouse spot test

Mutation Research/Environmental Mutagenesis and Related Subjects, 1991-08, Vol.253 (1), p.109-114

Neuhäuser-Klaus, A.

1991

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The mutagenic effect of caprolactam in the spot test with (T x HT) F1 mouse embryos

Mutation Research/Genetic Toxicology, 1989-11, Vol.224 (3), p.369-371

1989

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Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice

Investigative ophthalmology & visual science, 2004-02, Vol.45 (2), p.601-609

2004

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Induction of specific-locus and dominant lethal mutations in male mice by busulfan

Mutation research, 1991-08, Vol.249 (2), p.285-292

1991

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Three Murine Cataract Mutants (Cat2) Are Defective in Different γ-Crystallin Genes

Genomics (San Diego, Calif.), 1998-09, Vol.52 (2), p.152-158

1998

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Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4

Mammalian genome, 1997-03, Vol.8 (3), p.178-181

1997

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Loss of heterozygosity at the dilute-short ear (Myo5a-Bmp5) region of the mouse: mitotic recombination or double non-disjunction?

Genetical Research, 1998-12, Vol.72 (3), p.199-204

1998

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Dominant cataract mutations and specific-locus mutations in mice induced by radiation or ethylnitrosourea

Mutation research, 1982-02, Vol.92 (1-2), p.181-192

1982

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Induction of gene mutations in mice: the multiple endpoint approach

Mutation research, 1985-06, Vol.150 (1-2), p.393-401

1985

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Molecular characterization of Pax6(2Neu) through Pax6(10Neu): an extension of the Pax6 allelic series and the identification of two possible hypomorph alleles in the mouse Mus musculus

Saturation mutagenesis for dominant eye morphological defects in the mouse Mus musculus

The mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion

Reevaluation of the induction of specific-locus mutations in spermatogonia of the mouse by acrylamide

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion

Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16

Genetic Mosaicism in the House Mouse

A 76-bp Deletion in the Mip Gene Causes Autosomal Dominant Cataract in Hfi Mice

Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8

Mutagenicity testing of vincristine sulfate in germ cells of male mice

Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion

Detection of a point mutation (A to G) in exon 5 of the murine Mgf gene defines a novel allele at the Steel locus with a weak phenotype

Induction of specific-locus and dominant lethal mutations in male mice by ifosfamide (Holoxan)

Induction of specific-locus and dominant lethal mutations in male mice by 1-methyl-1-nitrosourea (MNU)

Induction of specific-locus and dominant lethal mutations in male mice by n-propyl and isopropyl methanesulfonate

Mutagenic activity of 2-amino- N6-hydroxyadenine in the mouse spot test

The mutagenic effect of caprolactam in the spot test with (T x HT) F1 mouse embryos

Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice

Induction of specific-locus and dominant lethal mutations in male mice by busulfan

Three Murine Cataract Mutants (Cat2) Are Defective in Different γ-Crystallin Genes

Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4

Loss of heterozygosity at the dilute-short ear (Myo5a-Bmp5) region of the mouse: mitotic recombination or double non-disjunction?

Dominant cataract mutations and specific-locus mutations in mice induced by radiation or ethylnitrosourea

Induction of gene mutations in mice: the multiple endpoint approach

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