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The mouse mutation “thrombocytopenia and cardiomyopathy” (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia

Blood, 2010-02, Vol.115 (6), p.1267-1276

2010

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Curly bare ( cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene ( mcub) on chromosome 5

Genomics (San Diego, Calif.), 2003, Vol.81 (1), p.6-14

2003

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Downeast Anemia (dea), a New Mouse Model of Severe Nonspherocytic Hemolytic Anemia Caused by Hexokinase (HKI) Deficiency

Blood cells, molecules, & diseases, 2001-09, Vol.27 (5), p.850-860

2001

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In collaboration: the Jackson Laboratory Craniofacial Resource

Critical reviews in eukaryotic gene expression, 2003, Vol.13 (2-4), p.107

2003

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In Collaboration: The Jackson Laboratory Craniofacial Resource

Critical reviews in eukaryotic gene expression, 2003, Vol.13 (2-4), p.2

2003

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Urogenital syndrome (us): a developmental mutation on Chromosome 2 of the mouse

Mammalian genome, 1993-09, Vol.4 (9), p.481-484

1993

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Mapping the Mouse Dactylaplasia Mutation,Dac,and a Gene That Controls Its Expression,mdac

Genomics (San Diego, Calif.), 1995-09, Vol.29 (2), p.457-464

1995

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Anorexia, a recessive mutation causing starvation in preweanling mice

The Journal of heredity, 1984-11, Vol.75 (6), p.468-472

1984

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Osteopetrosis, a New Recessive Skeletal Mutation on Chromosome 12 of the Mouse

The Journal of heredity, 1976-01, Vol.67 (1), p.11-18

1976

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Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9

American journal of medical genetics, 1998-05, Vol.77 (4), p.289-297

1998

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Staggerer, a New Mutation in the Mouse Affecting the Cerebellum

Science (American Association for the Advancement of Science), 1962-08, Vol.137 (3530), p.610-612

1962

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SUSCEPTIBILITY TO SPONTANEOUS PNEUMONITIS IN AN INBRED STRAIN OF BEIGE AND SATIN MICE

Genetics (Austin), 1972-11, Vol.72 (3), p.451-460

1972

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Two New Mutations in Linkage Group XVI of the House Mouse

The Journal of heredity, 1972-05, Vol.63 (3), p.135-140

LANE, PRISCILLA W.

1972

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Patchy fur,a Mouse Coat Mutation Associated with X–Y Nondisjunction, Maps to the Pseudoautosomal Boundary Region

Genomics (San Diego, Calif.), 1998-12, Vol.54 (3), p.556-559

1998

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The influence of genetic background on expression of mutations at the diabetes locus in the mouse. I. C57BL-KsJ and C57BL-6J strains

Biochemical genetics, 1972-08, Vol.7 (1), p.1-13

1972

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Association of megacolon with a new dominant spotting gene (Dom) in the mouse

The Journal of heredity, 1984-11, Vol.75 (6), p.435-439

1984

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Three Recessive Mutations Producing Disproportionate Dwarfing in Mice

The Journal of heredity, 1968-09, Vol.59 (5), p.300-308

1968

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Hydrocephalus with hop gait ( hyh): a new mutation on chromosome 7 in the mouse

Brain research. Developmental brain research, 1990-06, Vol.54 (1), p.131-136

1990

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MAHOGANY, A RECESSIVE COLOR MUTATION IN LINKAGE GROUP V OF THE MOUSE

The Journal of heredity, 1960-09, Vol.51 (5), p.228-230

1960

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Jimpy 4J: A New X-Linked Mouse Mutation Producing Severe CNS Hypomyelination (Part 2 of 2)

Developmental neuroscience, 1995-12, Vol.17 (5-6), p.306-310

1995

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Not Normal Littermates

Science (American Association for the Advancement of Science), 1982-12, Vol.218 (4577), p.1070-1070

Lane, Priscilla W.

1982

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Jimpy 4J: a new X-linked mouse mutation producing severe CNS hypomyelination

Developmental neuroscience, 1995, Vol.17 (5-6), p.300-305

1995

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Parasitoid wasp controls blue gum psyllid

California agriculture (Berkeley, Calif.), 1998-01, Vol.52 (1), p.31-34

1998

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A new gene affecting the morphogenesis of the vestibular part of the inner ear in the mouse

Development (Cambridge), 1966-12, Vol.16 (3), p.543-558

1966

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Linkage Groups III and XVII in the Mouse and the Position of the Light-Ear Locus

The Journal of heredity, 1967-01, Vol.58 (1), p.21-24

LANE, PRISCILLA W.

1967

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The mouse mutation “thrombocytopenia and cardiomyopathy” (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia

Curly bare ( cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene ( mcub) on chromosome 5

Downeast Anemia (dea), a New Mouse Model of Severe Nonspherocytic Hemolytic Anemia Caused by Hexokinase (HKI) Deficiency

In collaboration: the Jackson Laboratory Craniofacial Resource

In Collaboration: The Jackson Laboratory Craniofacial Resource

Urogenital syndrome (us): a developmental mutation on Chromosome 2 of the mouse

Mapping the Mouse Dactylaplasia Mutation,Dac,and a Gene That Controls Its Expression,mdac

Anorexia, a recessive mutation causing starvation in preweanling mice

Osteopetrosis, a New Recessive Skeletal Mutation on Chromosome 12 of the Mouse

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9

Staggerer, a New Mutation in the Mouse Affecting the Cerebellum

SUSCEPTIBILITY TO SPONTANEOUS PNEUMONITIS IN AN INBRED STRAIN OF BEIGE AND SATIN MICE

Two New Mutations in Linkage Group XVI of the House Mouse

Patchy fur,a Mouse Coat Mutation Associated with X–Y Nondisjunction, Maps to the Pseudoautosomal Boundary Region

The influence of genetic background on expression of mutations at the diabetes locus in the mouse. I. C57BL-KsJ and C57BL-6J strains

Association of megacolon with a new dominant spotting gene (Dom) in the mouse

Three Recessive Mutations Producing Disproportionate Dwarfing in Mice

Hydrocephalus with hop gait ( hyh): a new mutation on chromosome 7 in the mouse

MAHOGANY, A RECESSIVE COLOR MUTATION IN LINKAGE GROUP V OF THE MOUSE

Jimpy 4J: A New X-Linked Mouse Mutation Producing Severe CNS Hypomyelination (Part 2 of 2)

Not Normal Littermates

Jimpy 4J: a new X-linked mouse mutation producing severe CNS hypomyelination

Parasitoid wasp controls blue gum psyllid

A new gene affecting the morphogenesis of the vestibular part of the inner ear in the mouse

Linkage Groups III and XVII in the Mouse and the Position of the Light-Ear Locus

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