Search
for
Sort by
Research 61–90 of 596
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- Role of the Wnt signaling pathway in keratoacanthoma
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Acne
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Molecular Genetics of Human Hair Diseases
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- JAK1 gain-of-function variant causes alopecia areata, atopic dermatitis, and autoimmune thyroid disease
- p63: a crucial player in epithelial stemness regulation
- The molecular basis of human keratin disorders
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- FGF Family: From Drug Development to Clinical Application
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Developing Patient-Derived 3D-Bioprinting models of pancreatic cancer
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Hair & Cutaneous Development
- Modeling animal genomics in mice: An authentic approach for the functional interrogation of evolutionarily and agriculturally critical variants
- Revolutionary Approaches to Hair Regrowth: Follicle Neogenesis, Wnt/ß-Catenin Signaling, and Emerging Therapies