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Research 91–120 of 582
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Chromatographic Method for Simultaneous Quantification of Gemcitabine and Olaparib Recovered from Isolated Pancreatic Tissue
- Epigenetic regulation in adult stem cells and cancers
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Genetic Defects of Female Sexual Differentiation
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Biology and Genetics of Hair
- Diagnostic approach to low‐renin hypertension
- Dermatopathology and molecular genetics
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Inherited Disorders of the Hair
- Aging and Immortality: Quasi-Programmed Senescence and Its Pharmacologic Inhibition
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Birt–Hogg–Dubé syndrome
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer