A mild mutator phenotype arises in a mouse model for malignancies associated with neurofibromatosis type 1

Biochemistry, Genetics and Molecular Biology

• P53 100%
• Mutant 62%
• Mouse 50%
• Mutation 37%
• Nested Gene 37%
• Phenotype 37%
• DNA Repair 37%
• Apoptosis 25%
• Wild Type 25%
• Mouse Model 25%
• Genome Instability 25%
• Transgene 12%
• Human 12%
• Tumor Progression 12%
• Animal 12%
• DNA Damage Response 12%
• Development 12%
• Loss of Heterozygosity 12%
• Indel 12%
• Nucleic Acid Base Substitution 12%
• Big Blue Mouse 12%

Neuroscience

• P53 100%
• Neurofibromatosis Type 1 62%
• Phenotype 37%
• Peripheral Nerve 37%
• DNA Repair 37%
• Gene 37%
• Apoptosis 25%
• Nerve Sheath Tumor 25%
• Brain 25%
• Genomic DNA 12%
• Transgene 12%
• DNA Damage Response 12%
• Spleen 12%
• Neurofibroma 12%
• Indel Mutation 12%