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Research 241–270 of 1000+
- EVALUATION OF EFFICACY AND SAFETY OF PLATELET RICH PLASMA (PRP) IN THE TREATMENT OF ANDROGENIC ALOPECIA AND BACTERIAL ULCERATIVE LESION
- Action of isotretinoin in acne rosacea and gram-negative folliculitis
- Vitamin D and the skin: Focus on a complex relationship: A review
- Hidradenitis Suppurativa
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Molecular Genetics of Alopecias
- Primary cicatricial alopecias
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Enzymology of the hair follicle.
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- AN UPDATE OF HAIR SHAFT DISORDERS
- Topical corticosteroid in foam vehicle offers comparable coverage compared with traditional vehicles
- Keratins and skin disease
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- A Comprehensive Review of Acne Treatments: Unpacking the Chemical Structures and Effective Bioactive Compounds
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Cell death in the skin
- Trichoscopy in genetic hair shaft abnormalities
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Hypotrichosis in a child with olmsted syndrome
- TONGUE, RED
- Cell death by cornification
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit