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Shultz, Leonard
One or more keywords matched the following items that are connected to
Shultz, Leonard
Item Type
Name
Academic Article
Mapping of the flaky skin (fsn) mutation on distal mouse chromosome 17.
Academic Article
The interleukin-12 beta subunit (p40) maps to mouse chromosome 11.
Academic Article
Effect of the mouse scid mutation on meiotic recombination.
Academic Article
The nonobese diabetic scid mouse: model for spontaneous thymomagenesis associated with immunodeficiency.
Academic Article
Genetic mapping of the IL-12 alpha chain gene (Il12a) on mouse chromosome 3.
Academic Article
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.
Academic Article
Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) mice.
Academic Article
Pleiotropic mutations causing abnormalities in the murine immune system and the skin.
Academic Article
Immunodeficiency and reticulum cell sarcoma in mice segregating for HRS/J and SJL/J genes.
Academic Article
"Viable motheaten," a new allele at the motheaten locus. I. Pathology.
Academic Article
The flaky skin (fsn) mutation in mice: map location and description of the anemia.
Academic Article
The mouse mutation severe combined immune deficiency (scid) is on chromosome 16.
Academic Article
Genetically determined murine models of immunodeficiency.
Academic Article
Motheaten, an immunodeficient mutant of the mouse. I. Genetics and pathology.
Academic Article
Mutations at the murine motheaten locus are within the hematopoietic cell protein-tyrosine phosphatase (Hcph) gene.
Concept
Chromosome Mapping
Search Criteria
Chromosome Mapping