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- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- An in vivo method for the detection of somatic mutations at the cellular level in mice
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Identification of Somatic <i>KRAS</i> Mutation in a Korean Baby with Nevus Sebaceus Syndrome
- Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Androgen Receptor Mutations and Polymorphisms in African American Prostate Cancer
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
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