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Research 511–540 of 845
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Nilotinib-Induced Keratosis Pilaris
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Topical tacalcitol ointment can be a good therapeutic choice in erythromelanosis follicularis faciei et colli
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Vitamin D and the Skin: A Review for Dermatologists
- AN UPDATE OF HAIR SHAFT DISORDERS
- Hair and Scalp Disorders in a Tuscan Pediatric Dermatological Outpatient Clinic: A Clinical and Epidemiological Evaluation
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Topical corticosteroid in foam vehicle offers comparable coverage compared with traditional vehicles
- Regulation of Epidermal Ferritin Expression Influences Systemic Iron Homeostasis
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Off-label uses of retinoids in dermatology
- Madarosis from mitochondriopathy
- Retinoids in Dermatology
- ELL Facilitates RNA Polymerase II–Mediated Transcription of Human Epidermal Proliferation Genes
- “Structural imprinting” of the cutaneous immune effector function
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Connexin mutations in human disease
- An audit of dermatoses at Baqai Institute of Skin Diseases, Karachi
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- “Peeling paint” dermatosis in a leukemia patient
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Trichilemmal cyst of the neck: case report and review of the literature