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Research 721–750 of 735
- Vitamin D and the Skin: A Review for Dermatologists
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Pathology and pathogenesis of cutaneous lesions in beef cattle associated with buffalo fly infestation
- Immunostaining study of cytokeratins in human hair follicle development
- Segmental Vitiligo
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- The Mechanisms of Fur Development and Color Formation in American Mink Revealed Using Comparative Transcriptomics
- Psychosocial Distress and Quality of Life Among Patients With a Chronic Skin Disorder at a Tertiary Care Hospital in Eastern India: A Hospital-Based Case-Control Study
- Acne Syndromes and Mosaicism
- Hair and Nail Manifestations of Systemic Disease
- Role of MEG3-miRNAs in immune-inflammatory regulation in age-dependent wool follicle remodeling in Tan sheep
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Blue Light Therapy in Dermatological Practice: A Review
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Recently Identified Forms of Epidermolysis Bullosa
- Epidermolysis bullosa in animals: a review
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Alopecia in Epidermolysis Bullosa
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Epidermolysis Bullosa in Calves in the United Kingdom
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Childhood epidermolysis bullosa acquisita during squaric acid dibutyl ester immunotherapy for alopecia areata
- Semidominant Inheritance in Epidermolytic Ichthyosis