Article
Tumour predisposition in mice heterozygous for a targeted mutation in Nf1.
Nature genetics - 1 Jul 1994
Jacks T, Shih T S, Schmitt E M, Bronson R T, Bernards A, Weinberg R A
Abstract excerpt
Human neurofibromatosis type 1 is a dominant disease caused by the inheritance of a mutant allele of the NF1 gene. In order to study NF1 function, we have constructed a mouse strain carrying a germline mutation in the murine homologue. Heterozygous animals do not exhibit the classical symptoms of...
Topics
- Adrenal Gland Neoplasms
- Alleles
- Animals
- Base Sequence
- Disease Models, Animal
- Fetal Death
- Genes, Lethal
- Genes, Neurofibromatosis 1
- Genes, Synthetic
- Genetic Predisposition to Disease
- Heart Defects, Congenital
- Heterozygote
- Humans
- Leukemia, Myeloid
- Mice
- Mice, Knockout
- Mice, Mutant Strains
- Molecular Sequence Data
