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Research 571–600 of 1000+
- Annual Convention in the Time of COVID
- Zebrafish Model of Hereditary Pigmentary Disorders
- Trailing the Path to Preventive Oncology
- Pathological Skin Scarring: From Mechanism to Targeted Local Therapy
- Dercum Disease: Exploratory Therapeutic Approaches in the Absence of Standardized Medical Treatment—A Single Center Case Series
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Computational Drug Repositioning in Cardiorenal Disease: Opportunities, Challenges, and Approaches
- Uncommon Presentation of Pityriasis Rubra Pilaris of the Scalp: Clinical, Trichoscopic, and Histopathologic Features and Review of the Literature
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- E-Poster
- Gastric cancer; actualities and perspectives of early diagnosis and targeted therapy
- Endocrinology
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- Acne Vulgaris
- Trichilemmal cysts of the scrotal wall
- Molecular Mechanisms Regulating Hair Follicle Development
- The JAK/STAT signaling pathway: from bench to clinic
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Advances and Challenges in Plant Sterol Research: Fundamentals, Analysis, Applications and Production
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Fecal Microbiota and Hair Glucocorticoid Concentration Show Associations with Growth during Early Life in a Pig Model
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis