Search
for
Sort by
Research 241–270 of 693
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- New developments in the molecular treatment of ichthyosis: review of the literature
- Exploring the Interplay between Arsenic and Cutaneous Physiology, Pathology, and Regeneration
- Cell death by cornification
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Anti-programmed cell death protein 1-induced lichenoid changes of the nail unit: Histopathologic description
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- EGFR inhibitor-induced folliculitis decalvans: a case series and management guidelines
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- A linear and reticulate crusted keratotic papulopustular eruption: a rare presentation of PRIDE (Papulopustules and/or paronychia, Regulatory abnormalities of hair growth, Itching, and Dryness due to Epidermal growth factor receptor inhibitors) complex
- Efficacy and Safety of Fractional CO2 Laser Combined with Halometasone Cream for Treatment of Moderate-to-Severe Chronic Hand Eczema: A Prospective, Single-Center, Parallel-Group, Open-Label Randomized Trial
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Circle Hairs in a Patient with Multiple Myeloma
- Adnexotropic Variants of the Interface Dermatitides: A Review
- Two Mechanisms Regulate Keratin K15 Expression In Keratinocytes: Role of PKC/AP-1 and FOXM1 Mediated Signalling
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- TRPV3 Ion Channel: From Gene to Pharmacology
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Dynamic expression of Runx1 in skin affects hair structure
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Genetic Hair Disorders: A Review
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family