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Research 151–180 of 1000+
- Skin, Genetic Defects, and Aging
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- New clinico‐genetic classification of trichothiodystrophy
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Current Genetics in Hair Diseases
- Trichothiodystrophy
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands
- Diagnosis of common, benign neonatal dermatoses
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Hair and scalp disorders in ethnic populations
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- “Structural imprinting” of the cutaneous immune effector function
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hair follicles modulate skin barrier function
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.