Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas

Medicine and Dentistry

• Thyroid Tumor 50%
• Heterozygosity 50%
• Pathogenesis 40%
• Thyroid Adenoma 40%
• Gene 40%
• Patient 40%
• Neoplasm 20%
• Somatics 20%
• Cowden Syndrome 20%
• Inpatient 20%
• Disease Predisposition 10%
• Phosphate 10%
• Tumor Suppressor Gene 10%
• Penetrance 10%
• Somatic Mutation 10%
• Thyroid Carcinoma 10%
• Benign Tumor 10%
• Germline Mutation 10%
• Inositol Phosphate 10%
• Dual Specificity Phosphatase 10%
• Thyroid Follicular Carcinoma 10%
• Marker 10%
• Tissues 10%
• Syndrome 10%
• Aptitude 10%

Biochemistry, Genetics and Molecular Biology

• Loss of Heterozygosity 50%
• Mutation 30%
• Nested Gene 30%
• Phosphatase 20%
• Germline 20%
• Allele 10%
• Candidate Gene 10%
• Penetrance 10%
• Somatic Mutation 10%
• Germline Mutation 10%
• Inositol Phosphate 10%
• Dual-Specificity Phosphatase 10%
• Aptitude 10%
• Phosphate 10%

Neuroscience

• Thyroid 100%
• Gene 30%
• Somatic 20%
• Phosphatase 20%
• DNA 10%
• Inositol Phosphate 10%
• Dual Specificity Phosphatase 10%