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Research 211–240 of 227
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Trichothiodystrophy
- Skin, Genetic Defects, and Aging
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Sarcoidosis: Are there differences in your skin of color patients?
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Ichthyosiform Rash and Fever in a Child
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Description of skin lesions
- Bad Hair Days: A Clinical and Trichoscopic Evaluation of Scalp Lesions
- Skin changes in pediatric transplant patients
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- “Degeneration” in Dermatopathology
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution